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Goubran M, Mills BD, Georgiadic M, Karimpoor M, Mouchawar N, Sami S, Dennis EL, Akers C, Mitchell L, Boldt B, Douglas D, DiGiacomo PS, Rosenberg J, Grant G, Wintermark M, Camarillo DB, Zeineh M (). Microstructural Alterations in Tract Development in College Football and Volleyball Players: A Longitudinal Diffusion MRI Study. (Epub ahead of print) Neurology.
Wade BSC, Tate DF, Kennedy E, Bigler ED, York GE, Taylor BA, Troyanskaya M, Hovenden ES, Goodrich-Hunsaker N, Newsome MR, Dennis EL, Abildskov T, Pugh MJ, Walker WC, Kenney K, Betts A, Shih R, Welsh RC, Wilde EA (). Microstructural Organization of Distributed White Matter Associated with Fine Motor Control in US Service Members with Mild Traumatic Brain Injury. (Epub ahead of print) J Neurotrauma.
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Hammers DB, Kostadinova R, Unverzagt F, Apostolova L (2022). Assessing and validating reliable change across ADNI protocols. J Clin Exp Neuropsychol.
Ikanga, J, Taiwo, Z, Lengu, K, Epenge, E, Esambo, H, Gikelekele, G, Esilakoy, Kavugho, I, Mampunza, S, Hammers, DB, Stringer, A, Spencer, RJ (2022). Developing Learning Slope Scores for the African Neuropsychology Battery in a Sample of Healthy Congolese. J Int Neuropsychol Soc.
Liu S, Wright M, Wong K, Mizenko C, Kammeyer R, Schreiner T, Kadish R, Smith T, Galli J, Klein J, Greenlee JE, Rose JW, Paz Soldan MM, Bennett J, Bonkowsky J, Peterson L, Piquet A, Clardy SL (2022). MOGAD in the Mountain West: Epidemiology and Outcomes in Pediatric and Adult Patients at Two Large Academic Referral Centers [Abstract]. 98(18 Supplement), P16.003.
Wong K, Bacharach R, Fjeldstad A, Klein J, Paz Soldan MM, Rose JW (2022). Longitudinal Assessment of Optical Coherence Tomography in Patients with Relapsing-Remitting Multiple Sclerosis on Interferon beta-1a [Abstract]. 98(18 Supplement), P15.009.
Lord J, Rose JW, Paz Soldan MM (2022). Autologous HSCT Outside of Clinical Trials in Patients with Multiple Sclerosis [Abstract]. 98(18 Supplement), P6.009.
Rodenbeck S, Abbatemarco J, Poon J, Liu S, Paz Soldan MM, Greenlee JE, Rose JW, Peterson L, Johnson L, Clardy SL (2022). Matched or Unique Cerebrospinal Fluid Oligoclonal Bands: Clinical Characteristics and Diagnostic Utility [Abstract]. 98(18 Supplement), S3.009.
Hoshina Y, Galli J, Wong K, Kovacsovics T, Steinbach M, Lancaster E, Paz Soldan MM, Clardy SL (2022). Anti-GABAA receptor encephalitis in patients with multiple myeloma after autologous stem cell transplant: A report of 3 cases [Abstract]. 98(18 Supplement), P1.001.
Hammers, DB, Duff, K, Apostolova, LG (2022). Examining the role of repeated test exposure over 12 months across ADNI protocols. Alzheimers Dement (Amst).
Hammers DB, Spencer RJ, Apostolova LG (2022). Validation of and demographically-corrected normative data for the Learning Ratio derived from the RAVLT in robustly intact older adults. Arch Clin Neuropsychol.
Suhrie K, Hammers D, Porter S, Dixon A, King J, Anderson J, Duff K, Hoffman J (2021). Predicting Biomarkers in Intact Older Adults and those with Amnestic Mild Cognitive Impairment, and mild Alzheimer’s Disease Using the Repeatable Battery for the Assessment of Neuropsychological Status. J Clin Exp Neuropsychol.
Shepard SJ, Chesney SA, Larsen SE, Fuller S, Liebel SW (2021). Program evaluation of an integrated approach to group CPT in VA residential treatment. J Aggress Maltreat Trauma.
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Cortez MM, Millsap L, Rea NA, Sciarretta C, Brennan KC (2021). Photophobia and allodynia in persistent post-traumatic headache are associated with higher disease burden. Cephalalgia, 41(10), 1089-1099.
Hammers DB, Duff K, Spencer R (2021). Demographically-corrected normative data for the HVLT-R, BVMT-R, and Aggregated Learning Ratio values in a sample of older adults. J Clin Exp Neuropsychol.
Baldassari LE, Paz Soldan MM (2021). Natural History of Multiple Sclerosis. In Piquet AL, Alvarez E (Eds.), Neuroimmunology: Multiple Sclerosis, Autoimmune Neurology and Related Diseases (1st, pp. 535 pages). Switzerland: Springer International Publishing.
Mis EK, Sega AG, Signer RH, Cartwright T, Ji W, Martinez-Agosto JA, Nelson SF, Palmer CGS, Lee H, Mitzelfelt T, Konstantino M, Undiagnosed Diseases Network Moretti P, Jeffries L, Khokha MK, Marco E, Martin MG, Lakhani SA (2021). Expansion of NEUROD2 phenotypes to include developmental delay without seizures, . Am J Med Genet A, 185(4), 1076-1080.
Studwell CM, Kelley EG, Undiagnosed Diseases Network - Moretti P, Sinsheimer JS, Palmer CGS, LeBlanc K (2021). Family genetic result communication in rare and undiagnosed disease communities: Understanding the practice. J Genet Couns, 30(2), 439-447.
Ferdinandusse S, McWalter K, Te Brinke H, IJlst L, Mooijer PM, Ruiter JPN, van Lint AEM, Pras-Raves M, Wever E, Millan F, Guillen Sacoto MJ, Begtrup A, Tarnopolsky M, Brady L, Ladda RL, Sell SL, Nowak CB, Douglas J, Tian C, Ulm E, Perlman S, Drack AV, Chong K, Martin N, Brault J, Brokamp E, Toro C, Gahl WA, Macnamara EF, Wolfe L, Undiagnosed Diseases Network Moretti P, Waisfisz Q, Zwijnenburg PJG, Ziegler A, Barth M, Smith R, Ellingwood S, Gaebler-Spira D, Bakhtiari S, Kruer MC, van Kampen AHC, Wanders RJA, Waterham HR, Cassiman D, Vaz FM (2021). An autosomal dominant neurological disorder caused by de novo variants in FAR1 resulting in uncontrolled synthesis of ether lipids. . Genet Med, 23(4), 740-750.
Hammers D, Suhrie K, Dixon A, Gradwohl B, Duff K, Spencer R (2021). Validation of HVLT-R, BVMT-R, and RBANS learning slope scores along the Alzheimer’s continuum. Arch Clin Neuropsychol.
Hammers DB, Miranda M, Abildskov TJ, Tate DF, Wilde EA, Spencer RJ (2021). Consideration of Different Scoring Approaches for a Verbal Incidental Learning Measure from the WAIS-IV Using Hippocampal Volumes. Appl Neuropsychol Adult.
Frost NA, Haggart A, Sohal VS (2021). Dynamic patterns of correlated activity in the prefrontal cortex encode information about social behavior. PLoS Biol, May 3;19(5), e3001235.
Patrick D Parker, Pratyush Suryavanshi, Marcello Melone, Punam A Sawant-Pokam, Katelyn M Reinhart, Dan Kaufmann, Jeremy J Theriot, Arianna Pugliese, Fiorenzo Conti, C William Shuttleworth, Daniela Pietrobon, KC Brennan (2021). Non-canonical glutamate signaling in a genetic model of migraine with aura. Neuron, 109(4), 611-628.
Porter SM, Dixon A, Suhrie K, Hammers DB, Duff K (2021). Longitudinal changes on the Independent Living Scale in Amnestic Mild Cognitive Impairment. Appl Neuropsychol Adult.
Rossetti LZ, Bekheirnia MR, Lewis AM, Mefford HC, Golden-Grant K, Tarczy-Hornoch K, Briere LC, Sweetser DA, Walker MA, Kravets E, Stevenson DA, Bruenner G, Sebastian J, Knapo J, Rosenfeld JA, Marcogliese PC, Undiagnosed Diseases Network Moretti P, Wangler MF (2020). Missense variants in CTNNB1 can be associated with vitreoretinopathy-Seven new cases of CTNNB1-associated neurodevelopmental disorder including a previously unreported retinal phenotype. 2020 Dec 22;:e1542. [Epub ahead of print] PMID: 33350591. Mol Genet Genomic Med.
Parkhouse RME, Sciutto E, Hernndez M, Cortez MM, Carpio A, Fleury A (2020). Extraparenchymal human neurocysticercosis induces autoantibodies against brain tubulin and MOG35-55 in cerebral spinal fluid. J Neuroimmunol, 349, 577389.
Meissner LE, Macnamara EF, DSouza P, Yang J, Vezina G, Undiagnosed Diseases Network Moretti P, Ferreira CR, Zein WM, Tifft CJ, Adams (2020). DR. DYRK1A pathogenic variants in two patients with syndromic intellectual disability and a review of the literature. 2020 Dec;8(12):e1544. PMID: 33159716. Mol Genet Genomic Med.
Bryant L, Li D, Cox SG, Marchione D, Joiner EF, Wilson K, Janssen K, Lee P, March ME, Nair D, Sherr E, Fregeau B, Wierenga KJ, Wadley A, Mancini GMS, Powell-Hamilton N, van de Kamp J, Grebe T, Dean J, Ross A, Crawford HP, Powis Z, Cho MT, Willing MC, Manwaring L, Schot R, Nava C, Afenjar A, Lessel D, Wagner M, Klopstock T, Winkelmann J, Catarino CB, Retterer K, Schuette JL, Innis JW, Pizzino A, Lttgen S, Denecke J, Strom TM, Monaghan KG, Yuan ZF, Dubbs H, Bend R, Lee JA, Lyons MJ, Hoefele J, Gnthner R, Reutter H, Keren B, Radtke K, Sherbini O, Mrokse C, Helbig KL, Odent S, Cogne B, Mercier S, Bezieau S, Besnard T, Kury S, Redon R, Reinson K, Wojcik MH, unap K, Ilves P, Innes AM, Kernohan KD, Costain G, Meyn MS, Chitayat D, Zackai E, Lehman A, Kitson H, Martin MG, Martinez-Agosto JA, Undiagnosed Diseases Network Moretti P, Nelson SF, Palmer CGS, Papp JC, Parker NH, Sinsheimer JS, Vilain E, Wan J, Yoon AJ, Zheng A, Brimble E, Ferrero GB, Radio FC, Carli D, Barresi S, Brusco A, Tartaglia M, Thomas JM, Umana L, Weiss MM, Gotway G, Stuurman KE, Thompson ML, McWalter K, Stumpel CTRM, Stevens SJC, Stegmann APA, Tveten K, Vllo A, Prescott T, Fagerberg C, Laulund LW, Larsen MJ, Byler M, Lebel RR, Hurst AC, Dean J, Schrier Vergano SA, Norman J, Mercimek-Andrews S, Neira J, Van Allen MI, Longo N, Sellars E, Louie RJ, Cathey SS, Brokamp E, Heron D, Snyder M, Vanderver A, Simon C, de la Cruz X, Padilla N, Crump JG, Chung W, Garcia B, Hakonarson HH, Bhoj (2020). HistoneH3.3 beyond cancer: Germline mutations in Histone 3 Family 3A and 3B cause a previously unidentified neurodegenerative disorder in 46 patients 2020 Dec;6(49). PMID: 33268356 . Sci Adv.
Cif L, Demailly D, Lin JP, Barwick KE, Sa M, Abela L, Malhotra S, Chong WK, Steel D, Sanchis-Juan A, Ngoh A, Trump N, Meyer E, Vasques X, Rankin J, Allain MW, Applegate CD, Attaripour Isfahani S, Baleine J, Balint B, Bassetti JA, Baple EL, Bhatia KP, Blanchet C, Burglen L, Cambonie G, Seng EC, Bastaraud SC, Cyprien F, Coubes C, dHardemare V, Doja A, Dorison N, Doummar D, Dy-Hollins ME, Farrelly E, Fitzpatrick DR, Fearon C, Fieg EL, Fogel BL, Forman EB, Fox RG, Gahl WA, Galosi S, Gonzalez V, Graves TD, Gregory A, Hallett M, Hasegawa H, Hayflick SJ, Hamosh A, Hully M, Jansen S, Jeong SY, Krier JB, Krystal S, Kumar KR, Laurencin C, Lee H, Lesca G, Franois LL, Lynch T, Mahant N, Martinez-Agosto JA, Milesi C, Mills KA, Mondain M, Morales-Briceno H, Ostergaard JR, Pal S, Pallais JC, Pavillard F, Perrigault PF, Petersen AK, Polo G, Poulen G, Rinne T, Roujeau T, Rogers C, Roubertie A, Sahagian M, Schaefer E, Selim L, Selway R, Sharma N, Signer R, Soldatos AG, Stevenson DA, Stewart F, Tchan M, Undiagnosed Diseases Network Moretti P, Verma IC, de Vries BBA, Wilson JL, Wong DA, Zaitoun R, Zhen D, Znaczko A, Dale RC, de Gusmo CM, Friedman J, Fung VSC, King MD, Mohammad SS, Rohena L, Waugh JL, Toro C, Raymond FL, Topf M, Coubes P, Gorman KM, Kurian MA (2020). KMT2B-related disorders: expansion of the phenotypic spectrum and long-term efficacy of deep brain stimulation. 2020 Dec 5;143(11):3242-3261. PMID: 33150406. Brain.
Barish S, Barakat TS, Michel BC, Mashtalir N, Phillips JB, Valencia AM, Ugur B, Wegner J, Scott TM, Bostwick B, Undiagnosed Diseases Network Moretti P, Murdock DR, Dai H, Perenthaler E, Nikoncuk A, van Slegtenhorst M, Brooks AS, Keren B, Nava C, Mignot C, Douglas J, Rodan L, Nowak C, Ellard S, Stals K, Lynch SA, Faoucher M, Lesca G, Edery P, Engleman KL, Zhou D, Thiffault I, Herriges J, Gass J, Louie RJ, Stolerman E, Washington C, Vetrini F, Otsubo A, Pratt VM, Conboy E, Treat K, Shannon N, Camacho J, Wakeling E, Yuan B, Chen CA, Rosenfeld JA, Westerfield M, Wangler M, Yamamoto S, Kadoch C, Scott DA, Bellen HJ (2020). BICRA, a SWI/SNF Complex Member, Is Associated with BAF-Disorder Related Phenotypes in Humans and Model Organisms 2020 Dec 3;107(6):1096-1112. PMID: 33232675. Am J Med Genet.
Granadillo JL, Wegner DJ, Paul AJ, Willing M, Sisco K, Tedder ML, Sadikovic B, Wambach JA, Baldridge D, Cole FS, Undiagnosed Diseases Network Moretti P (2020). Discovery of a novel CHD7 CHARGE syndrome variant by integrated omics analyses. 2020 Nov 13;. [Epub ahead of print] PMID: 33184947. Am J Med Genet.
Diaz F, Khosa S, Niyazov D, Lee H, Person R, Morrow MM, Signer R, Dorrani N, Zheng A, Herzog M, Freundlich R, Undiagnosed Diseases Network Moretti P, Birath JB, Cervantes-Manzo Y, Martinez-Agosto JA, Palmer C, Nelson SF, Fogel BL, Mishra SK (2020). Novel NUDT2 variant causes intellectual disability and polyneuropathy. 2020 Nov;7(11):2320-2325. PMID: 33058507. Ann Clin Transl Neurol.
Ng BG, Eklund EA, Shiryaev SA, Dong YY, Abbott MA, Asteggiano C, Bamshad MJ, Barr E, Bernstein JA, Chelakkadan S, Christodoulou J, Chung WK, Ciliberto MA, Cousin J, Gardiner F, Ghosh S, Graf WD, Grunewald S, Hammond K, Hauser NS, Hoganson GE, Houck KM, Kohler JN, Morava E, Larson AA, Liu P, Madathil S, McCormack C, Meeks NJL, Miller R, Monaghan KG, Nickerson DA, Palculict TB, Papazoglu GM, Pletcher BA, Scheffer IE, Schenone AB, Schnur RE, Si Y, Rowe LJ, Serrano Russi AH, Russo RS, Thabet F, Tuite A, Villanueva MM, Wang RY, Webster RI, Wilson D, Zalan A, Undiagnosed Diseases Network Moretti P, University of Washington Center for Mendelian Genomics UW-CMG Wolfe LA, Rosenfeld JA, Rhodes L, Freeze HH (2020). Predominant and novel de novo variants in 29 individuals with ALG13 deficiency: Clinical description, biomarker status, biochemical analysis, and treatment suggestions. 2020 Nov;43(6):1333-1348. PMID: 32681751. J Inherit Metab Dis.
Castillo-Pinto C, Lamotte G, et al (2020). Healthcare Worker With Large Vessel Acute Ischemic Stroke Likely Related to Mild SARS-CoV-2 Infection. Neurohospitalist.
Anadani M, Lapergue B, Blanc R, Kyheng M, Labreuche J, Machaa MB, Duhamel A, Marnat G, Saleme S, Costalat V, Bracard S, Anxionnat R, Spiotta AM, DeHavenon A, Richard S, Desal H, Mazighi M, Consoli A, Piotin M, Gory B (2020). Admission Blood Pressure and Outcome of Endovascular Therapy: Secondary Analysis of ASTER Trial. J Stroke Cerebrovasc Dis.
Hammers DB, Gradwohl B, Kucera A, Abildskov T, Wilde E, Spencer R (2020). Preliminary validation of a measure for learning slope for the HVLT-R and BVMT-R in older adults. Cogn Behav Neurol.
Punam A Sawant-Pokam, Tyler J Vail, Cameron S Metcalf, Jamie L Maguire, Thomas O McKean, Nick O McKean, KC Brennan (2020). Preventing neuronal edema increases network excitability after traumatic brain injury. J Clin Invest, 130(11), 6005–6020.
Cope H, Spillmann R, Rosenfeld JA, Brokamp E, Signer R, Schoch K, Kelley EG, Sullivan JA, Macnamara E, Lincoln S, Golden-Grant K, Undiagnosed Diseases Network Moretti P, Orengo JP, Clark G, Burrage LC, Posey JE, Punetha J, Robertson A, Cogan J, Phillips JA 3rd, Martinez-Agosto J, Shashi V (2020). Missed diagnoses: Clinically relevant lessons learned through medical mysteries solved by the Undiagnosed Diseases Network. 2020 Oct;8(10):e1397. PMID: 32730690. Mol Genet Genomics.
Hammers DB, Stolwyk R, Harder L, Cullum MC (2020). A Survey of International Clinical Teleneuropsychology Service Provision Prior to and in the Context of COVID-19. https://doi.org/10.1080/13854046.2020.1810323. Clin Neuropsychol.
Guillen Sacoto MJ, Tchasovnikarova IA, Torti E, Forster C, Andrew EH, Anselm I, Baranano KW, Briere LC, Cohen JS, Craigen WJ, Cytrynbaum C, Ekhilevitch N, Elrick MJ, Fatemi A, Fraser JL, Gallagher RC, Guerin A, Haynes D, High FA, Inglese CN, Kiss C, Koenig MK, Krier J, Lindstrom K, Marble M, Meddaugh H, Moran ES, Morel CF, Mu W, Muller EA 2nd, Nance J, Natowicz MR, Numis AL, Ostrem B, Pappas J, Stafstrom CE, Streff H, Sweetser DA, Szybowska M, Undiagnosed Diseases Network Moretti P, Walker MA, Wang W, Weiss K, Weksberg R, Wheeler PG, Yoon G, Kingston RE, Juusola J De Novo (2020). De Novo Variants in the ATPase Module of MORC2 Cause a Neurodevelopmental Disorder with Growth Retardation and Variable Craniofacial Dysmorphism. 2020 Aug 6;107(2):352-363. PMID: 32693025. Am J Hum Genet.
Schneeberger PE, Kortm F, Korenke GC, Alawi M, Santer R, Woidy M, Buhas D, Fox S, Juusola J, Alfadhel M, Webb BD, Coci EG, Abou Jamra R, Siekmeyer M, Biskup S, Heller C, Maier EM, Javaher-Haghighi P, Bedeschi MF, Ajmone PF, Iascone M, Peeters H, Ballon K, Jaeken J, Rodrguez Alonso A, Palomares-Bralo M, Santos-Simarro F, Meuwissen MEC, Beysen D, Kooy RF, Houlden H, Murphy D, Doosti M, Karimiani EG, Mojarrad M, Maroofian R, Noskova L, Kmoch S, Honzik T, Cope H, Sanchez-Valle A, Undiagnosed Diseases Network Moretti P, Gelb BD, Kurth I, Hempel M, Kutsche K Biallelic (2020). MADD variants cause a phenotypic spectrum ranging from developmental delay to a multisystem disorder2020 Aug 1;143(8):2437-2453. PMID: 32761064. Brain.
Hammers DB, Suhrie KR, Porter SM, Dixon AM, and Duff K (2020). Validation of one-year reliable change in the RBANS for community-dwelling older adults with Mild Cognitive Impairment. doi: 10.1080/13854046.2020.1807058. Clin Neuropsychol.
Castilla-Vallmanya L, Selmer KK, Dimartino C, Rabionet R, Blanco-Snchez B, Yang S, Reijnders MRF, van Essen AJ, Oufadem M, Vigeland MD, Stadheim B, Houge G, Cox H, Kingston H, Clayton-Smith J, Innis JW, Iascone M, Cereda A, Gabbiadini S, Chung WK, Sanders V, Charrow J, Bryant E, Millichap J, Vitobello A, Thauvin C, Mau-Them FT, Faivre L, Lesca G, Labalme A, Rougeot C, Chatron N, Sanlaville D, Christensen KM, Kirby A, Lewandowski R, Gannaway R, Aly M, Lehman A, Clarke L, Graul-Neumann L, Zweier C, Lessel D, Lozic B, Aukrust I, Peretz R, Stratton R, Smol T, Dieux-Coslier A, Meira J, Wohler E, Sobreira N, Beaver EM, Heeley J, Briere LC, High FA, Sweetser DA, Walker MA, Keegan CE, Jayakar P, Shinawi M, Kerstjens-Frederikse WS, Earl DL, Siu VM, Reesor E, Yao T, Hegele RA, Vaske OM, Rego S, Undiagnosed Diseases Network Moretti P, Care4Rare Canada Consortium Shapiro KA, Wong B, Gambello MJ, McDonald M, Karlowicz D, Colombo R, Serretti A, Pais L, ODonnell-Luria A, Wray A, Sadedin S, Chong B, Tan TY, Christodoulou J, White SM, Slavotinek A, Barbouth D, Morel Swols D, Parisot M, Bole-Feysot C, Nitschk P, Pingault V, Munnich A, Cho MT, Cormier-Daire V, Balcells S, Lyonnet S, Grinberg D, Amiel J, Urreizti R, Gordon CT (2020). Phenotypic spectrum and transcriptomic profile associated with germline variants in TRAF7. 2020 Jul;22(7):1215-1226. PMID: 32376980. Genet Med.
Schoch K, Tan QK, Stong N, Deak KL, McConkie-Rosell A, McDonald MT, Undiagnosed Diseases Network Moretti P, Goldstein DB, Jiang YH, Shashi V (2020). Alternative transcripts in variant interpretation: the potential for missed diagnoses and misdiagnoses. Jul;22(7):1269-1275. PMID: 32366967. Genet Med.
Duff K, Porter S, Dixon A, Suhrie K, Hammers DB (2020). The Independent Living Scale in Amnestic Mild Cognitive Impairment: Relationships to demographic variables and cognitive performance. J Clin Exp Neuropsychol.
Spencer R, Gradwohl B, Williams T, Kordovski V, Hammers D (2020). Developing Learning Slope Scores for the Repeatable Battery for the Assessment of Neuropsychological Status. Appl Neuropsychol Adult.
Woods JD, Khanlou N, Lee H, Signer R, Shieh P, Chen J, Herzog M, Palmer C, Martinez-Agosto J, Undiagnosed Diseases Network Moretti P Nelson SF (2020). Myopathy associated with homozygous PYROXD1 pathogenic variants detected by genome sequencing. Neuropathology. 2020 Jun;40(3):302-307. PMID: 32037607. Neuropathology.
Bornali Kundu, Tyler S Davis, Brian Philip, Elliot H Smith, Amir Arain, Angela Peters, Blake Newman, Christopher R Butson, John D Rolston (2020). A systematic exploration of parameters affecting evoked intracranial potentials in patients with epilepsy. Brain Stimul, 13(5), 1232-1244.
Burdick KJ, Cogan JD, Rives LC, Robertson AK, Koziura ME, Brokamp E, Duncan L, Hannig V, Pfotenhauer J, Vanzo R, Paul MS, Bican A, Morgan T, Duis J, Newman JH, Hamid R, Phillips JA 3rd, Undiagnosed Diseases Network Moretti P (2020). Limitations of exome sequencing in detecting rare and undiagnosed diseases. 2020 Jun;182(6):1400-1406. PMID: 32190976. Am J Med Genet A.
Dutta D, Briere LC, Kanca O, Marcogliese PC, Walker MA, High FA, Vanderver A, Krier J, Carmichael N, Callahan C, Taft RJ, Simons C, Helman G, Undiagnosed Diseases Network Moretti P, Wangler MF, Yamamoto S, Sweetser DA, Bellen HJ (2020). De novo mutations in TOMM70, a receptor of the mitochondrial import translocase, cause neurological impairment. 2020 Jun 3;29(9):1568-1579. PMID: 32356556. Hum Mol Genet.
Bziat V, Tavernier SJ, Chen YH, Ma CS, Materna M, Laurence A, Staal J, Aschenbrenner D, Roels L, Worley L, Claes K, Gartner L, Kohn LA, De Bruyne M, Schmitz-Abe K, Charbonnier LM, Keles S, Nammour J, Vladikine N, Luxman Maglorius Renkilaraj MR, Seeleuthner Y, Migaud M, Rosain J, Jeljeli M, Boisson B, Van Braeckel E, Rosenfeld JA, Dai H, Burrage LC, Murdock DR, Lambrecht BN, Avettand-Fenoel V, Vogel TP, Undiagnosed Diseases Network Moretti P Esther CR, Haskologlu S, Dogu F, Ciznar P, Boutboul D, Ouache-Chardin M, Amourette J, Lebras MN, Gauvain C, Tcherakian C, Ikinciogullari A, Beyaert R, Abel L, Milner JD, Grimbacher B, Couderc LJ, Butte MJ, Freeman AF, Catherinot, Fieschi C, Chatila TA, Tangye SG, Uhlig HH, Haerynck F, Casanova JL, Puel A (2020). Correction: Dominant-negative mutations in human IL6ST underlie hyper-IgE syndrome. 2020 Jun 1;217(7). PMID: 32516385. Jpn J Exp Med.
Shieh C, Jones N, Vanle B, Au M, Huang AY, Silva APG, Lee H, Douine ED, Otero MG, Choi A, Grand K, Taff IP, Delgado MR, Hajianpour MJ, Seeley A, Rohena L, Vernon H, Gripp KW, Vergano SA, Mahida S, Naidu S, Sousa AB, Wain KE, Challman TD, Beek G, Basel D, Ranells J, Smith R, Yusupov R, Freckmann ML, Ohden L, Davis-Keppen L, Chitayat D, Dowling JJ, Finkel R, Dauber A, Spillmann R, Pena LDM, Undiagnosed Diseases Network Moretti P, Metcalfe K, Splitt M, Lachlan K, McKee SA, Hurst J, Fitzpatrick DR, Morton JEV, Cox H, Venkateswaran S, Young JI, Marsh ED, Nelson SF, Martinez JA, Graham JM Jr, Kini U, Mackay JP, Pierson TM (2020). GATAD2B-associated neurodevelopmental disorder (GAND): clinical and molecular insights into a NuRD-related disorder. 2020 May;22(5):878-888. PMID: 31949314. Genet Med.
Chung HL, Wangler MF, Marcogliese PC, Jo J, Ravenscroft TA, Zuo Z, Duraine L, Sadeghzadeh S, Li-Kroeger D, Schmidt RE, Pestronk A, Rosenfeld JA, Burrage L, Herndon MJ, Chen S, Members of Undiagnosed Diseases Network Moretti P Shillington A, Vawter-Lee M, Hopkin R, Rodriguez-Smith J, Henrickson M, Lee B, Moser AB, Jones RO, Watkins P, Yoo T, Mar S, Choi M, Bucelli RC, Yamamoto S, Lee HK, Prada CE, Chae JH, Vogel TP, Bellen HJ (2020). Loss- or Gain-of-Function Mutations in ACOX1 Cause Axonal Loss via Different Mechanisms. 2020 May 20;106(4):589-606.e6. PMID: 32169171. Neuron.
Chung HL, Mao X, Wang H, Park YJ, Marcogliese PC, Rosenfeld JA, Burrage LC, Liu P, Murdock DR, Yamamoto S, Wangler MF, Undiagnosed Diseases Network Moretti P Chao HT, Long H, Feng L, Bacino CA, Bellen HJ, Xiao B (2020). De Novo Variants in CDK19 Are Associated with a Syndrome Involving Intellectual Disability and Epileptic Encephalopathy. 2020 May 7;106(5):717-725. PMID: 32330417. Am J Hum Genet.
Davids M, Menezes M, Guo Y, McLean SD, Hakonarson H, Collins F, Worgan L, Billington CJ Jr, Maric I, Littlejohn RO, Onyekweli T, Members Of The Udn Moretti P, Adams DR, Tifft CJ, Gahl WA, Wolfe LA, Christodoulou J, Malicdan (2020). MCV. Homozygous splice-variants in human ARV1 cause GPI-anchor synthesis deficiency. 2020 May;130(1):49-57. PMID: 32165008.
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Waslo CS, Paz Soldan MM, Freedman MS, Repovic P, Solomon AJ, Rinker JR, Wallin MT, Haselkorn JK, Spain RI (2020). Challenges and Opportunities in Progressive Multiple Sclerosis Trials: Lessons from Lipoic Acid [Abstract]. 22(s2), 10-11.
Steiner S, Durman G, Paz Soldan MM, Woltz S, Wong K, Rose J (2020). Neurogenic Pain in Multiple Sclerosis: A Single Center Comprehensive Pain Assessment [Abstract]. 94(15 Suppl.), 4592.
Esquibel L, De Almeida B, Millsap L, Galli J, Gundlapalli A, Paz Soldan MM, Klein J, Cortez M, Rose J, Greenlee J, Hill H, Wong K, Clardy SL (2020). Evaluation of the Prevalence of Headache and Pain of Unknown Cause in Patients with Common Variable Immunodeficiency (CVID) [Abstract]. 94(15 Suppl.), 794.
Kadish R, Wong K, Galli J, Greenlee J, Klein J, Paz Soldan MM, Clardy S, Rose J (2020). Characterization of Retinal Nerve Fiber Layer Thickness in a Cohort with Anti-Glutamic Acid Decarboxylase and Anti-Glycine Receptor Autoimmunity [Abstract]. 94(15 Suppl.), 2227.
Wong K, Bacharach R, Klein J, Paz Soldan MM, Rose J (2020). Longitudinal Assessment of Optical Coherence Tomography in Patients with Relapsing-Remitting Multiple Sclerosis on Three Disease Modifying Therapies. Neurology [Abstract]. 94(15 Suppl.), 4691.
Kassa RM, Sechi E, Flanagan EP, Kaufmann TJ, Kantarci OH, Weinshenker BG, Mandrekar J, Schmalstieg WF, Paz Soldan MM, Keegan BM (2020). Onset of Progressive Motor Impairment in Patients with Critical CNS Demyelinating Lesions [Abstract]. 94(15 Suppl.), 4405.
Hammers DB, Kucera A, Spencer RJ, Abildskov TJ, Archibald ZG, Hoffman JM, Wilde EA (2020). Examining the Relationship between a Verbal Incidental Learning Measure from the WAIS-IV and Neuroimaging Biomarkers in Older Adults. Dev Neuropsychol.
De Almeida BI, Esquibel L, Millsap L, Klein J, Galli J, Cortez MM, Paz Soldan MM, Gundlapalli A, Greenlee J, Rose J, Hill H, Wong K, Clardy S (2020). Cognitive and Depressive Symptoms in Adults with Common Variable Immunodeficiency (CVID) [Abstract]. 94(15 Suppl.), 4502.
Macnamara EF, DSouza P, Undiagnosed Diseases Network Moretti P, Tifft CJ (2020). . The undiagnosed diseases program: Approach to diagnosis. 2020 Apr 13;4(3-4):179-188. PMID: 32477883. Transl Sci Rare Dis.
Mao D, Reuter CM, Ruzhnikov MRZ, Beck AE, Farrow EG, Emrick LT, Rosenfeld JA, Mackenzie KM, Robak L, Wheeler MT, Burrage LC, Jain M, Liu P, Calame D, Kry S, Sillesen M, Schmitz-Abe K, Tonduti D, Spaccini L, Iascone M, Genetti CA, Koenig MK, Graf M, Tran A, Alejandro M, Undiagnosed Diseases Network Moretti P, Lee BH, Thiffault I, Agrawal PB, Bernstein JA, Bellen HJ, Chao HT (2020). De novo EIF2AK1 and EIF2AK2 Variants Are Associated with Developmental Delay, Leukoencephalopathy, and Neurologic Decompensation. 2020 Apr 2;106(4):570-583. PMID: 32197074. Am J Hum Genet.
Hammers DB, Suhrie K, Porter S, Dixon A, Duff K (2020). Generalizability of reliable change equations for the RBANS over one year in community-dwelling older adults. https://doi.org/10.1080/13803395.2020.1740654. J Clin Exp Neuropsychol.
Mirzaa GM, Chong JX, Piton A, Popp B, Foss K, Guo H, Harripaul R, Xia K, Scheck J, Aldinger KA, Sajan SA, Tang S, Bonneau D, Beck A, White J, Mahida S, Harris J, Smith-Hicks C, Hoyer J, Zweier C, Reis A, Thiel CT, Jamra RA, Zeid N, Yang A, Farach LS, Walsh L, Payne K, Rohena L, Velinov M, Ziegler A, Schaefer E, Gatinois V, Genevive D, Simon MEH, Kohler J, Rotenberg J, Wheeler P, Larson A, Ernst ME, Akman CI, Westman R, Blanchet P, Schillaci LA, Vincent-Delorme C, Gripp KW, Mattioli F, Guyader GL, Gerard B, Mathieu-Dramard M, Morin G, Sasanfar R, Ayub M, Vasli N, Yang S, Person R, Monaghan KG, Nickerson DA, van Binsbergen E, Enns GM, Dries AM, Rowe LJ, Tsai ACH, Svihovec S, Friedman J, Agha Z, Qamar R, Rodan LH, Martinez-Agosto J, Ockeloen CW, Vincent M, Sunderland WJ, Bernstein JA, Undiagnosed Diseases Network Moretti P, Eichler EE, Vincent JB, University of Washington Center for Mendelian Genomics UW-CMG, Bamshad MJ (2020). De novo and inherited variants in ZNF292 underlie a neurodevelopmental disorder with features of autism spectrum disorder. 2020 Mar;22(3):538-546. PMID: 31723249. Genet Med.
Lee H, Huang AY, Wang LK, Yoon AJ, Renteria G, Eskin A, Signer RH, Dorrani N, Nieves-Rodriguez S, Wan J, Douine ED, Woods JD, DellAngelica EC, Fogel BL, Martin MG, Butte MJ, Parker NH, Wang RT, Shieh PB, Wong DA, Gallant N, Singh KE, Tavyev Asher YJ, Sinsheimer JS, Krakow D, Loo SK, Allard P, Papp JC, Undiagnosed Diseases Network Moretti P, Palmer CGS, Martinez-Agosto JA, Nelson SF (2020). Diagnostic utility of transcriptome sequencing for rare Mendelian diseases. 2020 Mar;22(3):490-499. PMID: 31607746. Genet Med.
Thompson PM, Ching CK, Dennis EL, Salminen LE, Turner JA, van Erp TGM, Jahanshad N (2020). Big Data Initiatives in Psychiatry: Global Neuroimaging Studies. In Kubicki M, Shenton ME (Eds.), Neuroimaging in Schizophrenia (pp. 411-26). Springer-Verlag.
Hammers DB, Suhrie KR, Dixon A, Porter S, Duff K (2020). Reliable change in cognition over 1 week in community-dwelling older adults: a validation and extension study. Arch Clin Neuropsychol.
Aday AW, Krier JB, Pallais JC, Fieg EL, MacRae CA, Loscalzo J, Members of the UDN Moretti P (2020). The Undiagnosed Diseases Network as a Tool for Graduate Medical Education. 2020 Feb;133(2):e18-e22. PMID: 31301294. Ala J Med Sci.
Patrick D Parker, Pratyush Suryavanshi, Marcello Melone, Katelyn M Reinhart, Punam M Sawant-Pokam, Dan Kaufmann, Jeremy J Theriot, Arianna Pugliese, Fiorenzo Conti, C William Shuttleworth, Daniela Pietrobon, KC Brennan (2020). Non-canonical glutamate signaling in a genetic model of migraine with aura. bioRxiv.
Johnson BV, Kumar R, Oishi S, Alexander S, Kasherman M, Vega MS, Ivancevic A, Gardner A, Domingo D, Corbett M, Parnell E, Yoon S, Oh T, Lines M, Lefroy H, Kini U, Van Allen M, Grnborg S, Mercier S, Kry S, Bzieau S, Pasquier L, Raynaud M, Afenjar A, Billette de Villemeur T, Keren B, Dsir J, Van Maldergem L, Marangoni M, Dikow N, Koolen DA, VanHasselt PM, Weiss M, Zwijnenburg P, Sa J, Reis CF, Lpez-Otn C, Santiago-Fernndez O, Fernndez-Jan A, Rauch A, Steindl K, Joset P, Goldstein A, Madan-Khetarpal S, Infante E, Zackai E, Mcdougall C, Narayanan V, Ramsey K, Mercimek-Andrews S, Pena L, Shashi V, Undiagnosed Diseases Network Moretti P, Schoch K, Sullivan JA, Pinto E Vairo F, Pichurin PN, Ewing SA, Barnett SS, Klee EW, Perry MS, Koenig MK, Keegan CE, Schuette JL, Asher S, Perilla-Young Y, Smith LD, Rosenfeld JA, Bhoj E, Kaplan P, Li D, Oegema R, van Binsbergen E, van der Zwaag B, Smeland MF, Cutcutache I, Page M, Armstrong M, Lin AE, Steeves MA, Hollander ND, Hoffer MJV, Reijnders MRF, Demirdas S, Koboldt DC, Bartholomew D, Mosher TM, Hickey SE, Shieh C, Sanchez-Lara PA, Graham JM Jr, Tezcan K, Schaefer GB, Danylchuk NR, Asamoah A, Jackson KE, Yachelevich N, Au M, Prez-Jurado LA, Kleefstra T, Penzes P, Wood SA, Burne T, Pierson TM, Piper M, Gcz J, Jolly LA (2020). Partial Loss of USP9X Function Leads to a Male Neurodevelopmental and Behavioral Disorder Converging on Transforming Growth Factor β Signaling. 2020 Jan 15;87(2):100-112. PMID: 31443933. Biol Psychiatry.
Pratyush Suryavanshi, Punam Sawant Pokam, KC Brennan (2020). Altered synaptic adaptation and gain in sensory circuits of the casein kinase 1 delta (CK1dT44A) mouse model of migraine.
Naoir Zaher, Kevin Haas, Hasan Sonmezturk, Amir Arain, Bassel Abou-Khalil (2019). Rhythmic ictal nonclonic hand (RINCH) motions in general EMU patients with focal epilepsy. Epilepsy Behav, Feb. 2020, 103 pt. A.
Bhatia A, Mobley BC, Cogan J, Koziura ME, Brokamp E, Phillips J, Newman J, Moore SA, Hamid R, Members of the Undiagnosed Diseases Network Moretti P (2019). Magnetic Resonance Imaging characteristics in case of TOR1AIP1 muscular dystrophy. 2019 Nov - Dec;58:108-113. PMID: 31299614. Clin Imaging.
Hammers D, Foster N, Hoffman J, Green T, Duff K (2019). Neuropsychological, psychiatric, and functional correlates of clinical trial enrollment. J Prev Alzheimers Dis, 6(4), 242-247.
Shoeibi A, Litvan I, Juncos JL, Bordelon Y, Riley D, Standaert D, Reich SG, Shprecher D, Hall D, Marras C, Kluger B, Olfati N, Jankovic J (2019). Are the International Parkinson disease and Movement Disorder Society progressive supranuclear palsy (IPMDS-PSP) diagnostic criteria accurate enough to differentiate common PSP phenotypes? Parkinsonism Relat Disord, 69, 34-39.
De Almeida BI, Wong K, Millsap L, Cortez M, Greenlee JE, Gundlapalli A, Hill H, Paz Soldan MM, Rose J, Galli J, Clardy SL (2019). Neurological Manifestations in Common Variable Immunodeficiency [Abstract]. 86(Suppl. 24), S36 (S108).
Geng LN, Kohler JN, Levonian P, Members of the Undiagnosed Diseases Network Moretti P, Bernstein JA, Ford JM, Ahuja N, Witteles R, Hom J, Wheeler M (2019). Genomics in medicine: a novel elective rotation for internal medicine residents. 2019 Oct;95(1128):569-572. PMID: 31439813. Postgrad Med.
Accogli A, Calabretta S, St-Onge J, Boudrahem-Addour N, Dionne-Laporte A, Joset P, Azzarello-Burri S, Rauch A, Krier J, Fieg E, Pallais JC, Undiagnosed Diseases Network Moretti P, McConkie-Rosell A, McDonald M, Freedman SF, Rivire JB, Lafond-Lapalme J, Simpson BN, Hopkin RJ, Trimouille A, Van-Gils J, Begtrup A, McWalter K, Delphine H, Keren B, Genevieve D, Argilli E, Sherr EH, Severino M, Rouleau GA, Yam PT, Charron F, Srour M (2019). De Novo Pathogenic Variants in N-cadherin Cause a Syndromic Neurodevelopmental Disorder with Corpus Collosum, Axon, Cardiac, Ocular, and Genital Defects. 2019 Oct 3;105(4):854-868. PMID: 31585109. Am J Hum Genet.
Kassa RM, Sechi E, Flanagan EP, Weinshenker BG, Kantarci OH, Kaufmann TJ, Schmalstieg WF, Paz Soldan MM, Keegan BM (2019). Age of onset of progressive motor impairment in patients with critical demyelinating lesions [Abstract]. 25(Suppl. 2), 673 (P1243).
Weisenbach SL, Kim J, Hammers D, Konopacki K, Koppelmans V (2019). Linking Late Life Depression and Alzheimer’s Disease: Mechanisms and Resilience. Curr Behav Neurosci Rep, 6, 103-112.
Deisseroth CA, Birgmeier J, Bodle EE, Kohler JN, Matalon DR, Nazarenko Y, Genetti CA, Brownstein CA, Schmitz-Abe K, Schoch K, Cope H, Signer R, Undiagnosed Diseases Network Moretti P, Martinez-Agosto JA, Shashi V, Beggs AH, Wheeler MT, Bernstein JA, Bejerano G (2019). ClinPhen extracts and prioritizes patient phenotypes directly from medical records to expedite genetic disease diagnosis. 2019 Jul;21(7):1585-1593. PMID: 30514889. Genet Med.
Emrick LT, Rosenfeld JA, Lalani SR, Jain M, Desai NK, Larson A, Kripps K, Vanderver A, Taft RJ, Bluske K, Perry D, Nagakura H, Immken LL, Burrage LC, Bacino CA, Belmont JW, Undiagnosed Diseases Network Moretti P, Lee B (2019). Microdeletions excluding YWHAE and PAFAH1B1 cause a unique leukoencephalopathy: further delineation of the 17p13.3 microdeletion spectrum. 2019 Jul;21(7):1652-1656. PMID: 30568308. Genet Med.
Guo L, Tang H, Wang Q, Dennis EL, Zhu D, Huang H, Ajilore O, Leow AD, Zhan L (2019). Identifying Configurational Abnormalities in Alzheimer’s Disease Progression Using Multi-View Structure Connectome. 2019 IEEE 16th International Symposium on Biomedical Imaging (ISBI 2019), Venice, Italy, 169-72.
Nir TM, Thomopoulos SI, Villalon-Reina J, Zavaliangos-Petropulu A, Dennis EL, Reid RI, Bernstein M, Borowski BJ, Jack Jr CR, Weiner M, Jahanshad N, Thompson PM (2019). Multi-shell Diffusion MRI Measures of Brain Aging: a Preliminary Comparison from ADNI3. 2019 IEEE 16th International Symposium on Biomedical Imaging (ISBI 2019), Venice, Italy, 173-7.
Dennis EL, Singh A, Corbin CK, Jahanshad N, Ho TC, King LS, Borchers LR, Humphreys KL, Thompson PM, Gotlib IH (2019). Associations Between Maternal Depression and Infant Fronto-Limbic Connectivity. 2019 IEEE 16th International Symposium on Biomedical Imaging (ISBI 2019), Venice, Italy, 126-30.
Fernandez HH, Stamler D, Davis MD, Factor SA, Hauser RA, Jimenez-Shahed J, Ondo WG, Jarskog LF, Woods SW, Bega D, LeDoux MS, Shprecher DR, Anderson KE (2019). Long-term safety and efficacy of deutetrabenazine for the treatment of tardive dyskinesia. J Neurol Neurosurg Psychiatry, 90(12), 1317-1323.
Hom J, Marwaha S, Postolova A, Kittle J, Vasquez R, Davidson J, Kohler J, Dries A, Fernandez-Betancourt L, Majcherska M, Dearlove J, Raghavan S, Vogel H, Bernstein JA, Fisher P, Ashley E, Sampson J, Wheeler M, Undiagnosed Diseases Network Moretti P (2019). A Patient with Sjogren's Syndrome and Subsequent Diagnosis of Inclusion Body Myositis and Light-Chain Amyloidosis. 2019 Jun;34(6):1058-1062. PMID: 30887439. J Gen Intern Med.
Silverman EK, Allard P, Loscalzo J, Mulvihill JJ, Korrick SA, Undiagnosed Diseases Network Moretti P (2019). Reported environmental exposures are inversely associated with obtaining a genetic diagnosis in the Undiagnosed Diseases Network. 2019 Jun;179(6):958-965. PMID: 30903737. Am J Med Genet.
Kumar A, Zastrow DB, Kravets EJ, Beleford D, Ruzhnikov MRZ, Grove ME, Dries AM, Kohler JN, Waggott DM, Yang Y, Huang Y, Undiagnosed Diseases Network Moretti P, Mackenzie KM, Eng CM, Fisher PG, Ashley EA, Teng JM, Stevenson DA, Shieh JT, Wheeler MT, Bernstein JA (2019). Extracutaneous manifestations in phacomatosis cesioflammea and cesiomarmorata: Case series and literature review. 2019 Jun;179(6):966-977. PMID: 30920161. Am J Med Genet.
Klonoski J, Palmer C, Clardy S, Paz Soldan MM, Lancaster E, Peterson L (2019). Histopathologic presentation of two cases of GABAa-R autoimmune encephalitis [Abstract]. 78(6), 575 (P218).
Newman JH, Shaver A, Sheehan JH, Mallal S, Stone JH, Pillai S, Bastarache L, Riebau D, Allard-Chamard H, Stone WM, Perugino C, Pilkinton M, Smith SA, McDonnell WJ, Capra JA, Meiler J, Cogan J, Xing K, Mahajan VS, Mattoo H, Hamid R, Phillips JA 3rd, Undiagnosed Diseases Network Moretti P (2019). IgG4-related disease: Association with a rare gene variant expressed in cytotoxic T cells. 2019 Jun;7(6):e686. PMID: 30993913. Mol Genet Med.
Nicoli ER, Weston MR, Hackbarth M, Becerril A, Larson A, Zein WM, Baker PR 2nd, Burke JD, Dorward H, Davids M, Huang Y, Adams DR, Zerfas PM, Chen D, Markello TC, Toro C, Wood T, Elliott G, Vu M, Undiagnosed Diseases Network Moretti P, Zheng W, Garrett LJ, Tifft CJ, Gahl WA, Day-Salvatore DL, Mindell JA, Malicdan MCV (2019). Lysosomal Storage and Albinism Due to Effects of a De Novo CLCN7 Variant on Lysosomal Acidification. 2019 Jun 6;104(6):1127-1138. PMID: 31155284. Am J Hum Genet.
Galli J, Piquet A, Kresser J, Klein J, Warner J, Digre K, Peterson L, Tebo A, Haven T, Paz Soldan MM, Rose J, Greenlee J, Clardy S (2019). GAD65 and Glycine Receptor-Associated Neurologic Autoimmunity and Stiff-Person Syndrome within the University of Utah Health Care System [Abstract]. 92(15 Suppl.), P2.2-036.
Lord J, Bacharach R, Galli J, Kresser J, Klein J, DeWitt LD, Paz Soldan MM, Rose J, Greenlee J, Clardy S (2019). Neurosarcoidosis: Longitudinal Experience in a Single-Center, Academic Health Care System [Abstract]. 92(15 Suppl.), P1.2-046.
Shashi V, Geist J, Lee Y, Yoo Y, Shin U, Schoch K, Sullivan J, Stong N, Smith E, Jasien J, Kranz P, Undiagnosed Diseases Network Moretti P, Lee Y, Shin YB, Wright NT, Choi M, Kontrogianni-Konstantopoulos A (2019). Heterozygous variants in MYBPC1 are associated with an expanded neuromuscular phenotype beyond arthrogryposis. Hum Mutat, 40(8), 1115-1126.
Duff, K, Dalley, B, Suhrie, K, Hammers, D (2019). Predicting Premorbid Scores on the Repeatable Battery for the Assessment of Neuropsychological Status and their Validation in an Elderly Sample. Arch Clin Neuropsychol, 34(3), 395-402.
Onofrei LV, Smith AG (2019). Chapter 33: Advocacy for patients with neuropathic pain. In Grisold W, Struhal W, Grisold T (Eds.), Advocacy in Neurology. Oxford: Oxford University Press.
Grove ME, White S, Fisk DG, Rego S, Dagan-Rosenfeld O, Kohler JN, Reuter CM, Bonner D, Undiagnosed Diseases Network Moretti P, Wheeler MT, Bernstein JA, Ormond KE, Hanson-Kahn AK (2019). Developing a genomics rotation: Practical training around variant interpretation for genetic counseling students. 2019 Apr;28(2):466-476. PMID: 30706981. J Genet Couns.
Zastrow DB, Kohler JN, Bonner D, Reuter CM, Fernandez L, Grove ME, Fisk DG, Undiagnosed Diseases Network Moretti P, Yang Y, Eng CM, Ward PA, Bick D, Worthey EA, Fisher PG, Ashley EA, Bernstein JA, Wheeler MT (2019). A toolkit for genetics providers in follow-up of patients with non-diagnostic exome sequencing. 2019 Apr;28(2):213-228. PMID: 30964584. J Genet Couns.
Cassini TA, Duncan L, Rives LC, Newman JH, Phillips JA, Koziura ME, Brault J, Hamid R, Cogan J, Undiagnosed Diseases Network Moretti P (2019). Whole genome sequencing reveals novel IGHMBP2 variant leading to unique cryptic splice-site and Charcot-Marie-Tooth phenotype with early onset symptoms. Mol Genet Med, 7(6), e00676.
Mohanty AK, Vuzman D, Francioli L, Cassa C, Brigham Genomic Medicine Undiagnosed Diseases Network Moretti P Brigham and Womens Hospital FaceBase Project Toth-Petroczy A, Sunyaev S novoCaller a Bayesian network approach for de novo variant calling from pedigree and population sequence data Bioinformatics 2019 Apr 13571174-1180 PMID 30169785 (2019). novoCaller: aBayesian network approach for de novo variant calling from pedigree and population sequence data. Bioinformatics. 2019 Apr 1;35(7):1174-1180. PMID: 30169785. Bioinformatics.
Burrage LC, Reynolds JJ, Baratang NV, Phillips JB, Wegner J, McFarquhar A, Higgs MR, Christiansen AE, Lanza DG, Seavitt JR, Jain M, Li X, Parry DA, Raman V, Chitayat D, Chinn IK, Bertuch AA, Karaviti L, Schlesinger AE, Earl D, Bamshad M, Savarirayan R, Doddapaneni H, Muzny D, Jhangiani SN, Eng CM, Gibbs RA, Bi W, Emrick L, Rosenfeld JA, Postlethwait J, Westerfield M, Dickinson ME, Beaudet AL, Ranza E, Huber C, Cormier-Daire V, Shen W, Mao R, Heaney JD, Orange JS, University of Washington Center for Mendelian Genomics Undiagnosed Diseases Network Moretti P Bertola D, Yamamoto GL, Baratela WAR, Butler MG, Ali A, Adeli M, Cohn DH, Krakow D, Jackson AP, Lees M, Offiah AC, Carlston CM, Carey JC, Stewart GS, Bacino CA, Campeau PM, Lee B (2019). Bi-allelic Variants in TONSL Cause SPONASTRIME Dysplasia and a Spectrum of Skeletal Dysplasia Phenotypes. Am J Hum Genet. 2019 Mar 7;104(3):422-438. PMID: 30773277. Am J Hum Genet.
Kelly M, Park M, Mihalek I, Rochtus A, Gramm M, Prez-Palma E, Axeen ET, Hung CY, Olson H, Swanson L, Anselm I, Briere LC, High FA, Sweetser DA, Undiagnosed Diseases Network Moretti P Kayani S, Snyder M, Calvert S, Scheffer IE, Yang E, Waugh JL, Lal D, Bodamer O, Poduri A (2019). Spectrum of neurodevelopmental disease associated with the GNAO1 guanosine triphosphate-binding region. 2019 Mar;60(3):406-418. PMID: 30682224.
Shashi V, Schoch K, Spillmann R, Cope H, Tan QK, Walley N, Pena L, McConkie-Rosell A, Jiang YH, Stong N, Need AC, Goldstein DB, Undiagnosed Diseases Network Moretti P (2019). A comprehensive iterative approach is highly effective in diagnosing individuals who are exome negative. 2019 Jan;21(1):161-172. PMID: 29907797. Genet Med.
Machol K, Rousseau J, Ehresmann S, Garcia T, Nguyen TTM, Spillmann RC, Sullivan JA, Shashi V, Jiang YH, Stong N, Fiala E, Willing M, Pfundt R, Kleefstra T, Cho MT, McLaughlin H, Rosello Piera M, Orellana C, Martnez F, Caro-Llopis A, Monfort S, Roscioli T, Nixon CY, Buckley MF, Turner A, Jones WD, van Hasselt PM, Hofstede FC, van Gassen KLI, Brooks AS, van Slegtenhorst MA, Lachlan K, Sebastian J, Madan-Khetarpal S, Sonal D, Sakkubai N, Thevenon J, Faivre L, Maurel A, Petrovski S, Krantz ID, Tarpinian JM, Rosenfeld JA, Lee BH, Undiagnosed Diseases Network Moretti P Campeau PM (2019). Expanding the Spectrum of BAF-Related Disorders: De Novo Variants in SMARCC2 Cause a Syndrome with Intellectual Disability and Developmental Delay. 2019 Jan 3;104(1):164-178. PMID: 30580808. Am J Hum Genet.
Ryan Martin, Sarah Peacock, Megan Corry, Kerri L LaRovere and Safdar Ansari (2019). Emergency Neurological Life Support: Spinal Cord Compression. What To Do in the Critical First Hours of a Neurological Emergency Version 4.0.
Liebel SW, Sweet LH (2019). Effects of cardiovascular disease and related risk factors on neurocognition. In Stern RA, Alosco MA (Eds.), The Oxford Handbook of Adult Cognitive Disorders (pp. 84-116). New York, NY: Oxford University Press.
Dennis EL, Caeyenberghs K, Babikian T, Olsen A, Giza CC, Asarnow RF, Levin H, Kochunov P, Jahanshad N, Thompson PM, Tate D, Wilde E (2018). ENIGMA Pediatric msTBI: Preliminary Results from Meta-Analysis of Diffusion MRI. Proc. SPIE 10975, 14th International Symposium on Medical Information Processing and Analysis, 10975, 109750P-1-8.
Handoko M, Emrick LT, Rosenfeld JA, Wang X, Tran AA, Turner A, Belmont JW, Undiagnosed Diseases Network Moretti P, Lee BH, Bacino CA, Chao HT (2018). Recurrent mosaic MTOR c.5930C > T (p.Thr1977Ile) variant causing megalencephaly, asymmetric polymicrogyria, and cutaneous pigmentary mosaicism: Case report and review of the literature. Am J Med Genet A, 179(3), 475-479.
Reilmann R, McGarry A, Grachev ID, Savola JM, Borowsky B, Eyal E, Gross NLangbehn D, Schubert R, Wickenberg AT, Papapetropoulos S, Hayden M, Squitieri F, Kieburtz K, Landwehrmeyer GB, European Huntingtons Disease Network, HuntingtonStudy Group investigators (2018 Dec 14 [Epub ahead of print]). Safety and efficacy of pridopidine in patients with Huntington's disease (PRIDE-HD): a phase 2, randomised, placebo-controlled, multicentre, dose-ranging study. Lancet Neurol.
Ng BG, Rosenfeld JA, Emrick L, Jain M, Burrage LC, Lee B, Undiagnosed Diseases Network members Moretti P, Craigen WJ, Bearden DR, Graham BH, Freeze HH (2018). Pathogenic Variants in Fucokinase Cause a Congenital Disorder of Glycosylation. 2018 Dec 6;103(6):1030-1037. PMID: 30503518. Am J Hum Genet.
Shashi V, Magiera MM, Klein D, Zaki M, Schoch K, Rudnik-Schneborn S, Norman A, Lopes Abath Neto O, Dusl M, Yuan X, Bartesaghi L, De Marco P, Alfares AA, Marom R, Arold ST, Guzmn-Vega FJ, Pena LD, Smith EC, Steinlin M, Babiker MO, Mohassel P, Foley AR, Donkervoort S, Kaur R, Ghosh PS, Stanley V, Musaev D, Nava C, Mignot C, Keren B, Scala M, Tassano E, Picco P, Doneda P, Fiorillo C, Issa MY, Alassiri A, Alahmad A, Gerard A, Liu P, Yang Y, Ertl-Wagner B, Kranz PG, Wentzensen IM, Stucka R, Stong N, Allen AS, Goldstein DB, Undiagnosed Diseases Network members Moretti P, Schoser B, Rsler KM, Alfadhel M, Capra V, Chrast R, Strom TM, Kamsteeg EJ, Bnnemann CG, Gleeson JG, Martini R, Janke C, Senderek J (2018). Loss of tubulin deglutamylase CCP1 causes infantile-onset neurodegeneration. 2018 Dec 3;37(23). PMID: 30420557. EMBO J.
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Johnston JJ, van der Smagt JJ, Rosenfeld JA, Pagnamenta AT, Alswaid A, Baker EH, Blair E, Borck G, Brinkmann J, Craigen W, Dung VC, Emrick L, Everman DB, van Gassen KL, Gulsuner S, Harr MH, Jain M, Kuechler A, Leppig KA, McDonald-McGinn DM, Can NTB, Peleg A, Roeder ER, Rogers RC, Sagi-Dain L, Sapp JC, Schffer AA, Schanze D, Stewart H, Taylor JC, Verbeek NE, Walkiewicz MA, Zackai EH, Zweier C, Members of the Undiagnosed Diseases Network Moretti P Zenker M, Lee B, Biesecker LG (2018). Autosomal recessive Noonan syndrome associated with biallelic LZTR1 variants. 2018 Oct;20(10):1175-1185. PMID: 29469822. Genet Med.
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Hedera P, Moretti P, Howard J, Zhao (2018). Novel Type of Complicated Autosomal Dominant Hereditary Spastic Paraplegia Associated with Congenital Distal Arthrogryposis Type I. Brain Sci, 8(7), e136.
Liu N, Schoch K, Luo X, Pena LDM, Bhavana VH, Kukolich MK, Stringer S, Powis Z, Radtke K, Mroske C, Deak KL, McDonald MT, McConkie-Rosell A, Markert ML, Kranz PG, Stong N, Need AC, Bick D, Amaral MD, Worthey EA, Levy S, Undiagnosed Diseases Network UDN Moretti P Wangler MF, Bellen HJ, Shashi V, Yamamoto S (2018). Functional variants in TBX2 are associated with a syndromic cardiovascular and skeletal developmental disorder. 2018 Jul 15;27(14):2454-2465. PMID: 29726930. Hum Mol Genet.
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Gerard Bischof, Peter Bartenstein, Henryk Barthel, Bart Van Berckel, Vincent Dore, Thilo Van Eimeren, Norman Foster, Jochen Hammes, Adriaan Lammertsma, Satoshi Minoshima, Christopher Rowe, Osama Sabri, John Seibyl, Koen Van Laere, Rik Vandenberghe, Victor Villemagne, Igor Yakushev, amp Alexander Drzezga (05/30/2018). Comparing Amyloid PET Tracers and Interpretation Strategies: First Results from the CAPTAINs Study [Abstract]. J Nucl Med, 2018(59), 485.
Reuter CM, Brimble E, DeFilippo C, Dries AM, Undiagnosed Diseases Network Moretti P, Enns GM, Ashley EA, Bernstein JA, Fisher PG, Wheeler MT (2018). A New Approach to Rare Diseases of Children: The Undiagnosed Diseases Network. 2018 May;196:291-297.e2. PMID: 29331327. J Clin Pediatr Dent.
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Cassini TA, Robertson AK, Bican AG, Cogan JD, Hannig VL, Newman JH, Hamid R, Phillips JA 3rd, Undiagnosed Diseases Network Moretti P (2018). Phenotypic heterogeneity of ZMPSTE24 deficiency. 2018 May;176(5):1175-1179. PMID: 29341437. Am J Med Genet A.
Williams JP, Street M, Badger JK, Peterson LK, Greenlee JE, Carlson NG, Rose JW, Paz Soldan MM, Clardy SL (2018). Characterization and Alternative Diagnoses in Patients with False-positive Aquaporin-4 Autoantibody Detection by Enzyme-Linked Immunosorbent Assay (ELISA) [Abstract]. Neurology, 90(15 Suppl.), P6.420.
Williams JP, Galli JR, Groshans KA, Horvat DE, Austin S, Pittock SJ, Rose JW, Carlson NG, Greenlee JE, Paz Soldan MM, Tagg NT, Clardy SL (2018). Neuromyelitis Optica Spectrum Disorder (NMOSD) in Active Duty Service Members [Abstract]. Neurology, 90(15 Suppl.), P6.424.
Wong K, Marini E, Nguyen TP, Clardy SL, Cortez MM, DeWitt LD, Greenlee JE, Klein JM, Paz Soldan MM, Steffens JD, Rose JW (2018). Dimethyl Fumarate in Relapsing Remitting Multiple Sclerosis: 24 Months Observations of the Effects of Dose Reduction on Lymphopenia [Abstract]. Neurology, 90(15 Suppl.), P6.347.
Keegan BM, Kaufmann TJ, Weinshenker BG, Kantarci OH, Schmalstieg WF, Paz Soldan MM, Flanagan EP (2018). Progressive Motor Impairment from a Critically Located Lesion in Highly Restricted CNS Demyelinating Disease [Abstract]. Neurology, 90(15 Suppl.), P5.034.
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Bennett A, Wilder M, Majersik J, Ansari A, de Havenon A (2016). Increased Systolic Blood Pressure Variability is Associated with Symptomatic Intracerebral Hemorrhage After Endovascular Treatment for Stroke. Poster [Abstract]. InternationalStroke Conference.
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de Havenon A, Tirschwell DL, Chung L, Wang H, Smith G, Majersik J (2016). Prediction of Neurologic Outcome after Ischemic Stroke with Volumetric Measurements on CT and MRI. Poster [Abstract]. International Stroke Conference.
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de Havenon A, Parker D, Kim S, Park M, McNally S (2016). Intracranial High-Resolution Vessel Wall MRI for the Detection of Arterial Inflammation, Unraveling Vascular Inflammation: From Inflammation to Imaging [Abstract]. NHLBI Symposium.
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Bennett A, Wilder M, Majersik J, Ansari S, de Havenon A (2016). Increased Systolic Blood Pressure Variability is Associated with Symptomatic Intracerebral Hemorrhage after Endovascular Treatment for Stroke. Moderated poster session [Abstract]. International Stroke Conference.
Sultan-Qurraie A, de Havenon A, Lynch J, Fred-Fitzsimmons B (2016). Early Platelet Transfusion in Pateints with Subarachnoid Hemorrhage Does Not Improve Outcome. Poster [Abstract]. World Stroke Conference.
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de Havenon A, ODonnell S, Wang H, Smith G, Majersik J (2016). A Comparison of Three Different CTA Collateral Scoring Systems’ Ability to Predict MR Lesion Volume and Outcome After Ischemic Stroke. E-Poster [Abstract]. American Academy ofNeurology Annual Meeting.
Dennis EL, Prasad G, Kernan C, Babikian T, Mink R, Babbitt C, Johnson J, Giza CC, Asarnow RF, Thompson PM (2015). Adaptive Algorithms to Map How Brain Trauma Affects Anatomical Connectivity in Children. Proc. SPIE 9681, 11th International Symposium on Medical Information Processing and Analysis, 96810B, 96810-7.
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Carlson NG, Schmidt L, Redd J, Bellamkonda S, Wood B, Weber LM, Paz Soldn MM, Rose JW (2015). Vulnerability of oligodendrocyte precursor cells to death is modulated by key prostaglandins [Abstract]. Multiple Sclerosis Journal, 21(Suppl. 11), 467-468.
Novotna M, Paz Soldn MM, Abou Zeid N, Kale N, Tutuncu M, Kantarci OH (2015). Defining the overlapping period of relapsing-remitting and progressive phases of multiple sclerosis for continuing disease modifying treatments [Abstract]. Multiple Sclerosis Journal, 21(Suppl. 11), 91-92.
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Arnold DL, Kappos L, Wiendl H, Selmaj K, Havrdova E, Boyko A, Kaufman M, Rose JW, Greenberg S, Amaravadi L, Riestger K, Elkins J (2015). Benefits on brain MRI lesion activity with Daclizumab HYP compared with intramuscular interferon beta- 1a are maintained through 144 weeks’ treatment: results from the DECIDE study [Abstract]. Finale Programme: ECTRIMS 31st Congress. Barcelona, Spain.
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Kappos L, Wiendle H, Selmaj K, Arnold DL, Havrdova E, Boyko A, Kaufman M, Rose JW, Greenberg S, Sweetser M, Riester K, ONeill G, Elkins J (2015). Daclizumab HYP versus Interferon Beta-1a in Relapsing Multiple Sclerosis. N Engl J Med, 373(15), 1418-28.
Chitnis T, Graves J, Weinstock-Guttman B, Belman A, Misra M, Olsen CS, Aaen G, Benson L, Candee M, Gorman M, Greenberg B, Lotze T, Ness J, Rodriquez M, Rose JW, Rubin J, Schreiner T, Mendelt-Tillema J, Casper TC, Waubant E (2015). Effect of obesity and puberty on risk and age at onset of pediatric MS [Abstract]. Finale Programme: ECTRIMS 31st Congress. Barcelona, Spain.
Katz Sand I, Fabian M, Cook L, Telford R, Chehade M, Masilamani M, Kraus T, Farrell C, Phelps S, Riffle ME, Rose JW, Moran T, Lublin F (2015). An open-label add-on trial of cetirizine for neuromyelitis optica: baseline data and preliminary results [Abstract]. Finale Programme: ECTRIMS 31st Congress. Barcelona, Spain.
Wiendl H, Havrdova E, RoseJW, Giovannoni G, Tsao LC, Zhao J, Pan Q, Elkins J, Greenberg SJ (2015). Daclizumab high-yield process (DAC HYP) vs. intramuscular interferon beta-1a in subgroups predictive of active disease: results from the DECIDE study [Abstract]. Finale Programme: ECTRIMS 31st Congress. Barcelona, Spain.
Nourbakhsh B, Graves J, Lulu S, Waldman A, Belman A, Greenberg B, Weinstock-Guttman B, Aaen G, Tillema J-M, Hart J, Lee M, Ness J, Rubin J, Krupp L, Gorman M, Benson L, Rodriguez M, Chitnis T, Simmons T, Casper C, Rose JW, Barcellos L, Waubant E (2015). Association of dietary salt intake and relapse rate in pediatric multiple sclerosis [Abstract]. Finale Programme: ECTRIMS 31st Congress. Barcelona, Spain.
Loughran-Fjeldstad AS, Carlson NG, Cook LJ, Rose JW (2015). Longitudinal reduction of total macular volume in relapsing and remitting multiple sclerosis: indicative of ongoing neurodegeneration [Abstract]. Finale Programme: ECTRIMS 31st Congress. Barcelona, Spain.
Clawson SA, Hill KE, Wood B, Clardy SL, Carlson NG, Greenlee JE (09/28/2015). Intracellular update of immunoglubulin G antibodies is common among CNS neurons and requires the Fc portion of the IgG molecule. Presented at the 140th Annual Meeting of the American Neurological Assocation [Abstract]. Ann Neurol, 78((Supplment 19)), S76.
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McNally JS, Aldred B, Burton T, McLauglin M, Kim S, Miller D, Majersik J, Parker D, Treiman G (2015). Vitamin D and Vulnerable Carotid Plaque. Accepted for oral presentation at the American Society of Neuroradiology, Chicago, USA, 2015. [Abstract]. AJNR.
de Havenon A, Stoddard G, Wang H, Chung L, Majersik JJ (May 2015). Increased blood pressure variable is associated with worse outcome in acute ischemic stroke patients with penumbra. Accepted for oral presentation at the European Stroke Conference, Vienna, Austria, May 2015. [Abstract]. Cerebrovascular Diseases.
Southerland A, Majersik JJ, Worrall BB (04/29/2015). Chapter 15: Cervical Artery Dissection. In Gilbert R. Upchurch Jr., Peter K. Henke (Eds.), Clinical Scenarios in Vascular Surgery, Second Edition. LWW.
Paz Soldn MM, Schmidt LA, Wood BL, Rose JW, Carlson NG (2015). Prostaglandin F2α Receptor Mediates Oligodendrocyte Precursor Injury/Death: Potential Role in Multiple Sclerosis [Abstract]. Neurology, 84(14 Suppl.), P5.210.
Dansithong W, Paul S, Figueroa KP, Rinehart MD, Wiest S, Pfleiger LT, Scoles DR, Pulst SM (2015). Ataxin-2 regulates RGS8 translation in a new BAC-SCA2 transgenic mouse model. PLoS Genet, 11(4), e1005182.
Greenlee JE, Clawson SA, Hill KE, Wood B, Tsunda I, Carlson NG (04/17/2015). Anti-Yo Antibody Interaction with its intracellular target antigen leads to targeted Purkinje Cell death rat cerebellar slice cultures: a possible mechanism for paraneoplastic cerebellar degeneration in humans with gynecological or breast cancers. PLoS One, 10(4), e0123446.
Kinard KI, Smith AG, Singleton JR, Lessard MK, Katz BJ, Warner JE, Crum AV, Mifflin MD, Brennan KC, Digre KB (2015). Chronic migraine is aaociated with reduced corneal nerve fiber density and symptoms of dry eye. Headache, 55(4), 543-9.
Wang V, Clardy T, Rose JW, Burns J, Carlson N, Greenlee J, Clardy S (2015). Neuromyelitis Optica in Veterans [Abstract]. Neurology, 84(14 Supplement), P1.104.
Wiendl H, Havrdova E, Rose JW, Riester K, Tsao C, Greenberg S (2015). Daclizumab HYP Versus Interferon β-1a Across Patient Demographic and Disease Activity Subgroups in the DECIDE Phase 3 Study [Abstract]. Neurology, 84(14 Supplement), P4.007.
Tremlett H, Fadrosh D, Lynch S, Hart J, Gravas J, Lulu S, Aaen G, Belman A, Benson L, Casper C, Chitnis T, Gorman M, Krupp L, Lotze T, Ness J, Roalstac S, Rodriquez M, Rose JW, Tillema JM, Weinstock-Guttman B, Waubant E (2015). Gut Microbiome in Early Pediatric Multiple Sclerosis: A Case-control Study [Abstract]. Neurology, 84(14 Supplement), P4.027.
Rose JW, Wiendl H, Arnold D, Kappos L, Havrdova E, Selmaj K, Boyko A, Kaufman M, Greenberg S, Sweetser M, Riester K, Elkins J (2015). Daclizumab HYP Reduced Brain MRI Lesion Activity Compared with Interferon Beta-1a: Results from the DECIDE Study [Abstract]. Neurology, 84(14 Supplement), P7.252.
Paz Soldan M, Schmidt L, Wood B, Rose JW, Carlson N (2015). Prostaglandin F2a Receptor Mediates Oligodendrocyte Precursor Injury/Death: Potential Rose in Multiple Sclerosis. Washington D.C [Abstract]. Neurology, 84(14 Supplement), P5.210.
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Seminatore B, Graves J, Waldman A, Lotze T, Schreiner T, Belman A, Greenberg B, Weinstock-Guttman B, Aaen G, Tillema JM, Hart J, Ness J, Rubin J, Krupp L, Gorman M, Benson L, Rodriguez M, Chitnis T, Mar S, Barcellos L, Rose JW, Roalstad S, Simmons T, Casper C, Waubant E (2015). Fat, Fiber, and Pediatric MS [Abstract]. Neurology, 84(14 Supplement), S38.002.
Selmaj K, Kappos L, Arnold D, Havrdova E, Boyko A, Kaufman M, Wiendl H, Rose JW, Greenberg S, Riester K, Sweetser M, Elkins J (2015). Safety and Tolerability Results from the DECIDE Study: A Phase 3 Active-comparator Study of Daclizumab HYP in Relapsing-remitting Multiple Sclerosis. [Abstract]. Neurology, 84(14 Supplement), P7.230.
McDonald J, Graves J, Waldman A, Lotze T, Schreiner T, Belman A, Greenberg B, Weinstock-Guttman B, Aaen G, Tilleman JM, Hart J, Ness J, Rubin J, Krupp L, Gorman M, Benson L, Rodriguez M, Chitnis T, Mar S, Barcellos L, Rose JW, Roalstad S, Simmons T, Casper TC, Waubant E (2015). A Case-control Study of Dietary Salt Intake and Risk of Pediatric Multiple Sclerosis (MS). Washington D.C. [Abstract]. Neurology, 84(14 Supplement), S38.003.
Kappos L, Selmaj K, Arnold D, Havrdova E, Boyko A, Kaufman M, Wiendl H, Rose JW, Greenberg S, Sweetser M, Riester K, Elkins J (2015). Daclizumab HYP Versus Interferon Beta-1a in Relapsing-remitting Multiple Sclerosis: Primary Results of the DECIDE Study [Abstract]. Neurology, 84(14 Suppliment), S4.003.
Riaz A, Matsuo F (2015). Lamotrigine. In Shorvon S, Perucca E, Engel J (Eds.), The Treatment of Epilepsy (4th Ed., pp. 498-515). Oxford: Wiley Blackwell.
Majersik JJ, Schmidt RH (03/03/2015). Continued risk of SAH after negative screen in first degree relatives - and persistent questions. Invited editorial on Rasing I, et al. Longterm risk of subarachnoid hemorrhage after a negative aneurysm screen. Neurology, 84(9), 868-9.
Nelson R, Lesko A, Majersik J, Okon N, Bhatt A, Baraban E (2/12/2015). Budget Impact Analysis of Telestroke in the Pacific Northwest, Abstract, # 3732. Accepted for poster presentation at the International Stroke Conference February 11 - 13, 2015, Nashville, TN, USA [Abstract]. Stroke.
Krug A, Ramirez L, Nhoung H, Perese J, Gasparian G, Kazaryan S, Kelly C, Breen J, Majersik JJ, Sanossian N (02/12/2015). A Survey of Certified Stroke Center Medical Directors in the United States. Poster Board Number: P283. Accepted as a poster to the International Stroke Conference, February 11-13, 2015, Nashville, TN, USA [Abstract]. Stroke.
Okon N, Nelson R, Majersik J, Lesko A, Bhatt A, Baraban E (2/11/2015). Telestroke Network Cost-Effectiveness in the Pacific Northwest: Geography and Facility Size Support a Cost-Sharing Model Between Hub and Spoke, Abstract #3176. Accepted as a moderated poster presentation to the International Stroke Conference, February 11 - 13, 2015, Nashville, TN, USA. [Abstract]. Stroke.
Baraban E, Nelson R, Lesko A, Majersik J, Bhatt A, Okon (2/11/2015). The Cost-Effectiveness of Telestroke Varies by Implementation Cost and Stroke Severity: Real World Data From a Pacific Northwest Network, Abstract # 3665. ccepted for poster presentation at the International Stroke Conference, February 11 - 13, 2015, Nashville, TN, USA [Abstract]. Stroke.
Lamotte G, Skender E, Rafferty MR, David F, Sadowsky S, Corcos DM (2015). Effects of progressive resistance exercise training on the motor and non-motor features of Parkinson’s disease: a review. 4, 11-27.
Alshaikh J, Kusner LL, Kaminski HJ (2015). Clinical Trials of Myasthenia Gravis. In Mineo TC (Ed.), Novel Challenges in Myasthenia Gravis (1st Edition). New York, NY: Nova Science Publishers.
Gibson SB, Kasarskis EJ, Hu N, Pulst SM, Mendiondo SM, Matthews DE, Mitsumoto H, Tandan R, Simmons Z, Kryscio RJ, Bromberg MB (2015). Relationship of Creatine Kinase to body composition, disease state, and longevity in ALS. Amyotroph Lateral Scler Frontotemporal Degener, 27, 1-5.
Martini SR, Williams SR, Moretti P, Woo D, Worrall BB (2015). A molecular/genetic approach to Cerebral Small Vessel Disease: Beyond aging and hypertension. Brain Circ, 1(1), 79-87.
Hammers D, Duff K, amp Chelune G (2015). Assessing change of cognitive trajectories over time in later life. In N.A. Pachana and Laidlaw (Eds.), Oxford Handbook of Clinical Geropsychology. Oxford: Oxford University Press.
de Havenon A, Tirschwell DL, Sultan-Qurraie A, Jalal A (2015). Arterial Spin Labeling MRI Identifies Ischemic Stroke Patients with Good Outcome at Hospital Discharge. Poster [Abstract]. International Stroke Conference.
Cortez MM, Singleton JR, Smith AG (2014). Glucose intolerance, metabolic syndrome, and neuropathy. In D.W. Zochodne and R.A. Malik (Eds.), Handbook of Clinical Neurology: Diabetes and the Nervous System (3rd, 126, pp. 109-22). Toronto: Elsevier Publishing.
De Havenon A, Ansari SA (11/4/2014). Combating performance enhancing drug abuse: Detection and punishment are not enough. Perform Enhanc Health, 3(1), 51-53.
Greenlee JE, Clawson SA, Hill KA, Wood B, Clardy SL, Carlson NG (11/1/2014). Anti-Yo antibody, associated with paraneoplastic cerebellar degeneration, specifically produces Purkinje cell death by binding to the 62 kDa intracellular Yo antigen. Presented at Annual Meeting of the International Society for Neuroimmunology, Mainz, Germany [Abstract]. J Neuroimmunology, 275, 36-37.
French KF, Martinez JK, DeHavenon AH et al (2014). Reproducibility of ABC/2 method to determine infarct volume and mismatch percentage with CT perfusion. J Neuroimaging, 24(3), 232-7.
Charvet LE, ODonnell EH, Belman AL, Chitnis T, Ness JM, et al (2014). Longitudinal evaluation of cognitive functioning in pediatric multiple sclerosis: report from the "US Pediatric Multiple Sclerosis Network". Mult Scler, 20(11), 1502-10.
Casper TC, Rose JW, Roalstad S, Waubant E, Aaen G, Belman A, Chitnis T, Gorman M, Krupp L, Lotze TE, Ness J, Patterson M, Rodriguez M, Weinstock-Guttman B, Browning B, Graves J, Tillema JM, Benson L, Harris Y (2014). The US Network of Pediatric Multiple Sclerosis Centers: Development, Progress, and Next Steps. J Child Neurol, 09/30/2014, 1-7.
Shprecher D, Rubenstein L, Gannon K, Frank S, Kurlan R (2014). Temporal Course of the Tourette Syndrome Clinical Triad. Tremor Other Hyperkinet Mov (N Y).
Paz Soldan MM, Flanagan EP, Kantarci OH (2014). Highly active multiple sclerosis and Epstein-Barr virus reactivation [Abstract]. Mult Scler, 20(Suppl. 1), 229-230.
Bennett AE, Hoesch RE, DeWitt LD, Afra P, Ansari SA (09/04/2014). Therapeutic hypothermia for status epilepticus: A report, historical perspective, and review. [Review]. Clin Neurol Neurosurg, 126(2014), 103-109.
Shprecher D, Schrock L, Himle M (2014). Neurobehavioral aspects, pathophysiology, and management of Tourette's syndrome. Curr Opin Neurol, 27(4), 484-92.
Cortez MM, Wilder M, McFadden M, Majersik JM (2014). Quality of Life after Intra-arterial Therapy for Acute Ischemic Stroke. J Stroke Cerebrovasc Dis, 23(7), 1890-6.
Warstadt NM, Jahanshad N, Dennis EL, Kohannim O, McMahon KL, de Zubicaray GI, Montgomery GW, Henders AE, Martin NG, Whitfield JB, Wright MJ, Thompson PM (2014). Identifying Candidate Gene Effects by Restricting Search Space in a Multivariate Genetic Analysis of White Matter Microstructure. 2014 IEEE 11th International Symposium on Biomedical Imaging (ISBI), Beijing, 353-6.
Paz Soldan MM, Gamez JD, Raman M, Macura SI, Johnson AJ, Pirko I (2014). MRI measured brain and spinal cord atrophy differ between mouse strains in a murine model of MS [Abstract]. ISMRM 2014; Abstract No. 3382.
Anderson K, Wold JJ (I). Headaches in Older Adults. In CS Landefeld, BA Williams, A Chang et. al. (Eds.), Current Geriatric Diagnosis and Treatment (2nd, pp. 447-450). Lange Medical Books / McGraw Hill.
Novotna M, Tutuncu M, Paz Soldan MM, Crusan DJ, Atkinson EJ, Kantarci OH (2014). Early relapse-recovery impacts progressive disease course in multiple sclerosis [Abstract]. Neurology, 82(10 Suppl.), S34.006.
Gibson SB, Figueroa KP, Huynh LP, Bromberg MB, Pulst SM (April 29, 2014). Regional Variation of Causative ALS Genes [Abstract]. 66th AAN Annual Meeting.
Adam de Havenon, Kris French and Safdar Ansari (04/25/2014). Extensive Cortical Diffusion Restriction in a 50-Year-Old Female with Hyperammonemic Encephalopathy and Status Epilepticus. Case Rep Neurol Med, 2014.
de Havenon A, French K, Ansari S (2014). Extensive cortical diffusion restriction in a 50-year-old female with hyperammonemic encephalopathy and status epilepticus. Case Rep Neurol Med.
Shprecher D, Gannon K, Agarwal N, Shi X, Anderson J (2014). Elucidating the mechanism of tic improvement in Tourette syndrome: a pilot study. Tremor Other Hyperkinet Mov (N Y).
de Havenon A, Ansari S (2014). Combating performance enhancing drug abuse: detection and punishment are not enough. Perform Enhanc Health, 3(1), 51-53.
Sheridan JP, Robinson RR, Rose JW (2014). Daclizumab, an IL-2 modulating antibody for treatment of multiple sclerosis. Expert Rev Clin Pharmacol, 7(1), 9-19.
de Havenon A, Sultan-Qurraie A, Moore A, Tirschwell D (2014). A Comparison of Transcranial Doppler to Echocardiography for the Detection of Right-to-left Shunt in Ischemic Stroke Patients. Poster [Abstract]. European Stroke Conference.
de Havenon A, Tirschwell DL, Anzai Y et al (2014). Medial occipital lobe hyperperfusion – a poor prognostic sign for patients with hypoxic-anoxic injury. Poster [Abstract]. Radiological Society of North America Annual Meeting.
Mossa-Basha M, Ferndale M, Hwang W, Hatsukami T, de Havenon A et al (2014). The Value of High-Resolution T2-Weighted Vessel Wall MR Imaging for the Differentiation of Intracranial Vasculopathies. Oral abstract [Abstract]. Radiological Society of North America Annual Meeting.
Lopez-Valdes HE, Clarkson AN, Ao Y, Charles AC, Carmichael ST, Sofroniew MV, Brennan K (2014). Memantine enhances recovery from stroke. Stroke, 45(7), 2093-100.
de Havenon A, Joos Z, Longenecker L et al (2014). A Hypertensive Reversible Encephalomyelitis Syndrome (HyRES). Poster [Abstract]. International Stroke Conference.
Sultan-Qurraie A, de Havenon A, Tirschwell DL et al (2014). Performance Metrics for The Interventional Treatment Of Acute Ischemic Stroke: Results from A Comprehensive Stroke Center. Moderated poster [Abstract]. American Academy of Neurology Annual Meeting.
Sultan-Qurraie S, de Havenon A, Becker K et al (2014). Improved Ischemic Stroke Outcomes After Intra-arterial Interventions Associated with Higher HDL Cholesterol. Poster [Abstract]. International Stroke Conference.
Longenecker L, de Havenon A, Joos Z et al (2014). Two Case Reports of Posterior Reversible Encephalopathy Syndrome (PRES) Involving the Spinal Cord. Oral presentation [Abstract]. American Society of Spine Radiology Annual Symposium.
Dennis EL, Zhan L, Jahanshad N, Mueller BA, Jin Y, Lenglet C, Yacoub E, Sapiro G, Ugurbil K, Harel N, Toga AW, Lim KO, Thompson PM (2013). Rich Club Analysis of Structural Brain Connectivity at 7 Tesla versus 3 Tesla. In Schultz T, Nedjati-Gilani G, Venkataraman A, O'Donnell L, Panagiotaki E (Eds.), Computational Diffusion MRI and Brain Connectivity. Mathematics and Visualization, Switzerland: Springer, Cham, 209-18.
Daianu M, Dennis EL, Nir TM, Toga AW, Jack CR, Jr, Weiner MW, Thompson PM and the Alzheimers Disease Neuroimaging Initiative (2013). Disrupted Brain Connectivity in Alzheimer’s Disease: Effects of Network Thresholding. In Schultz T, Nedjati-Gilani G, Venkataraman A, O'Donnell L, Panagiotaki E (Eds.), Computational Diffusion MRI and Brain Connectivity. Mathematics and Visualization, Switzerland: Springer, Cham, 199-208.
Seo HS, Kim SE, Rose JW, Hadley JR, Parker DL, Jeong EK (2013). Diffusion tensor imaging of extraocular muscle using two-dimensional single-shot interleaved multiple inner volume imaging diffusion-weighted EPI at 3 tesla. J Magn Reson Imaging, 38(5), 1162-1168.
Paz Soldan MM, Martina N, Crusan DJ, Atkinson EJ, Kantarci OH (2013). Pre- and post-progression relapses impact disability in progressive multiple sclerosis [Abstract]. Mult Scler, 19(Suppl. 1), 65.
Duff K, Shprecher D, Litvan I, Gerstenecker A, Mast B on behalf of the ENGENE investigators (2013). Correcting for demographic variables on the modified Telephone Interview for Cognitive Status. Am J Geriatr Psychiatry.
Tara M Newcomb, Michael B Himle, Tara M Newcomb, Abby L Smart, Anna G Sharp, Donata Viazzo-Trussell, Perla C Thulin and Kathryn J Swoboda (September 3, 2013). Impact of Sapropterin Dihydrochloride on Mood and Motor Function in Autosomal Dominant Dopa-Responsive Dystonia (AD-DRD): A Pilot Study [Abstract]. Journal of Inherited Metabolic Disease, 36(2), 91.
Chang J, Brennan K, He D, Huang H, Miura R, Wilson P, Wylie J (Summer 2013). A Mathematical Model of the Metabolic and Perfusion Effects on Cortical Spreading Depression. PLoS One.
Ansari SA (2013). Infectious Disease. In Zakaria (Ed.), Neurocritical Care Board Review (1st edition (July 16, 2013), p. 476). Demos Medical.
Duff K, Foster NL, Dennett K, Hammers DB, Zollinger LV, Christian PE, Butterfield RI, Beardmore BE, Wang AY, Morton KA, amp Hoffman JM (2013). Amyloid deposition and cognition in older adults: The effects of premorbid intellect. Arch Clin Neuropsychol, 28(7), 665-71.
Clarkson AN, Lopez-Valdes HE, Overmann JJ, Charles AC, Brennan KC, Thomas Carmichael S (2013). Multimodal examination of structural and functional remapping in the mouse photothrombotic stroke model. J Cereb Blood Flow Metab, 33(5), 716-723.
Carlson NG, Rose JW (2013). Vitamin D as a clinical biomarker in multiple sclerosis. Expert Opin Med Diagn, 7(3), 231-42.
Brennan KC, Bates EA, Shapiro RE, Zyuzin J, Hallows WC, Huang Y, Lee HY, Jones CR, Fu YH, Charles AC, Ptacek LJ (2013). Casein kinase 1 delta mutations in familial migraine and advanced sleep phase. Sci Transl Med, 1(5), 1-11.
Paz Soldan MM, Tutuncu M, Tang J, Abou Zeid N, Kale N, Crusan DJ, Atkinson EJ, Siva A, Pittock SJ, Pirko I, Keegan BM, Lucchinetti CF, Noseworthy JH, Rodriguez M, Weinshenker BG, Kantarci OH (2013). Predicting tempo of post-progression disability accumulation in multiple sclerosis [Abstract]. Neurology, 80(7 Suppl.), P02.147.
de Havenon A (2013). Appearances on Salt Lake City NBC and ABC affiliates to discuss neurologic illness associated with drug use.
Gibson SB, Majersik J, Smith AG, Bromberg MB (2013). Three Cases of Acute Myositis in Adults Following Influenza-like Illness during the H1N1 Pandaemic. J Neurosci Rural Pract, 4, 51.
de Havenon A (2013-present). Monthly contributions to the American Heart Association’s “Blogging Stroke” website [Web]. Available: http://strokeblog.strokeahajournal.org.
Gibson SB, Bromberg MB (2012). Amyotrophic lateral sclerosis: drug therapy from the bench to the bedside. (PMID: 23117941). Semin Neurol, 32(3), 173-8.
Theriot JJ, Toga AW, Prakash N, Ju, YS, Brennan KC (In Press). Cortical sensory plasticity in a model of migraine with aura. J Neurosci, 32(44), 15252-61.
Daianu M, Jahanshad N, Nir T, Dennis E, Toga AW, Jack Jr CR, Weiner MW, Thompson PM, and the Alzheimers Disease Neuroimaging Initiative (2012). Analyzing the Structural k-core of Brain Connectivity Networks in Normal Aging and Alzheimer's Disease. Workshop on Novel Imaging Biomarkers for Alzheimer’s Disease and Related Disorders. MICCAI NIBAD, 12, 52-62.
Shprecher D, Noyes Katia, Biglan Kevin, Wang Dongwen, Dorsey Ray E, Kurlan Roger, Adams Michael Jacob (2012). Willingness of Parkinson Disease Patients to Participate in Research Using Internet Based Technology. Telemed J E Health.
Merrill RP, Hadley JR, Minalga E, Kholmovski EG, Vijayakumar S, Kim SE, Quigley EP, Parker DL, Rose JW (2012). A 28-channel coil array for improved imaging of the optic nerve. Sci Transl Med, 41B(3), 73-84.
Rose JW (August 2012). Anti-CD25 immunotherapy: regulating the regulators. Sci Transl Med, 4(145), 145fs25.
Majersik JJ, Jex RF, Skalabrin EJ, Taillac PP (May 2012). Development and Initial Results of an Inclusive State-Wide Approach to Stroke Care [Abstract]. Quality Care and Outcomes Research in Cardiovascular Disease and Stroke 2012 Scientific Sessions, Atlanta, GA.
Langer HF, Choi EY, Zhou H, Schleicher R, Chung KJ, Tang Z, Gobel K, Bdeir K, Chatzigeorgiou A, Wong C, Bhatia S, Kruhlak MJ, Rose JW, Burns JB, Hill KE, Qu H, Zhang Y, Lehrmann E, Becker KG, Wang Y, Simon DI, Nieswandt B, Lambris JD, Li X, Meuth SC, Kubes P, Chavakis T (Apr 2012). Platelets contribute to the pathogenesis of experimental autoimmune encephalomyelitis [Abstract]. Circ Res, 110(9), 1202-10.
Langer HF, Choi EY, Zhou H, Schleicher R, Chung KJ, Tang Z, Gobel K, Bdeir K, Chatzigeorgiou A, Wong C, Bhatia S Kruhlak MJ, Rose JW, Burns JB, Hill KE, Qu H, Zhang Y, Lehrmann E, Becker KG, Wang Y, Simon DI, Nieswandt B, Lambris JD, Li X, Meuth SG, Kubes P, Chavakis T (2012). Platelets contribute to the pathogenesis of experimental autoimmune encephalomyelitis. Circ Res, 110(9), 1202-10.
Foster NL (2012). Neuroimaging. In Weiner MF, Lipton AM (Eds.), Clinical Manual of Alzheimer Disease and Other Dementias (pp. 89-126). Washington DC: American Psychiatric Publishing, Inc.
Chelune GJ, Duff K (2012). The Assessment of change: Serial assessments in dementia evaluation. In Ravdin LD, Katzen H (Eds.), Handbook on the Neuropsychology of Aging and Dementia (pp. 43-57). New York: Springer.
Brennan K, Digre K, Baggaley S (2012). Headache- A Patient's Guide.
Gibson SB, Figueroa KP, Huynh LP, Bromberg MB, Pulst SM (2012). Evidence for a Genetic Contribution to ALS Mortality in a Population-based Resource. [Abstract]. 64th AAN Annual Meeting.
Chang JC, Brennan KC, Chou T (2011). Tracking monotonically advancing boundaries in image sequences using graph cuts and recursive kernel shape priors. IEEE Trans Med Imaging, PMC2215697.
Hayden KM, Reed BR, Manly JJ, Tommet D, Pietrzak RH, Chelune GJ, Yang FM, Revell AJ, Bennett DA, Jones RN (2011). Cognitive decline in the elderly: an analysis of population heterogeneity. Age Ageing, 40(6), 684-689.
Martins TB, Rose JW, Jaskowski TD, Wilson AR, Husebye D, Seraj HS, Hill HR (2011). Analysis of proinflammatory and anti-inflammatory cytokine serum concentrations in patients with multiple sclerosis by using a multiplexed immunoassay. Am J Clin Pathol, 136(5), 696-704.
Paz Soldan MM, Gamez JD, Johnson AJ, Lohrey AK, Chen Y, Pirko I (2011). Correlation of brain atrophy, disability and spinal cord atrophy in a murine model of MS [Abstract]. Annals of Neurology, 70(Suppl. 15), S70 (T1715).
Waldman AT, Gorman MP, Rensel MR, Austin Te, Hertz DP, et al (2011). Management of pediatric central nervous system demyelinating disorders: consensus of United States neurologists. J Child Neurol, 26(6), 675-82.
Minalga E, Rose JW, Choi SE, Jeong EK, Kholmovski E, et al (2011). A 20-channel coil for improved magnetic resonance imaging of the optic nerve. Concepts Magn Reson Part B Magn Reson Eng, 25(39B(1)), 26-36.
Southerland AM, Malik S, Majersik JJ, Worrall BB (2/1/2011). Age Distribution by Sex and Clinical Characteristic in Cervical Artery Dissection. Presented in poster form at the American Academy of Neurology annual meeting, Honolulu, HI, USA [Abstract].
Brennan KC (2011). Turn down the lights! An irritable occipital cortex in migraine without aura. Neurology, 76(3), 206-7.
Foster NL (2011). Molecular Imaging in Neuropsychiatry. In Coffey CE, Cummings JL (Eds.), The American Psychiatric Publishing Textbook of Geriatric Neuropsychiatry (3rd Ed, pp. 177-209). Washington: American Psychiatric Publishing, Inc.
Livesay S, Suarez J, Bershad E, Smirnakis S, Newmark M, Ansari SA, Mazabob J, Brown G (September 2010). Neurocritical Care Morbidity and Mortality (M&M): A Multidisciplinary Systems-based Approach for Improving Patient Care [Abstract]. Journ of Neurocritical Care, 2010(13), 63.
Livesay S, Suarez J, Bershad E, Smirnakis S, Newmark M, Ansari S, Mazabob J, Brown G, Mokracek M (2010). The neurocritical care telestroke network: Extending high quality care to the underserved community for a reasonable cost. [Abstract]. Neurocritical Care Society 8th Annual Meeting, 2010(13), 64.
Livesay S, Suarez J, Bershad E, Smirnakis S, Newmark M, Ansari S, Mazabob J, Brown G (2010). Neurocritical care morbidity and mortality (M&M): A multidisciplinary systems-based approach for improving patient care. [Abstract]. Neurocritical Care Society 8th Annual Meeting, 13(S3-231), 63.
Majersik JJ, Cannon-Albright LA (2010). Evidence for a Heritable Contribution to Death from Ischemic Stroke. American Academy of Neurology, Toronto, Canada. [Abstract].
Ford C, Goodman AD, Johnson K, Kachuck N, Lindsey JW, Lisak R, Luzzio C, Myers L, Panitch H, Preiningerova J, Pruitt A, Rose J, Rus H, Wolinski J (2010). Continuous long-term immunomodulatory therapy in relapsing multiple sclerosis: results from the 15-year analysis of the US prospective open-label study of glatiramer acetate. Mult Scler, Mar(3), 342-50.
Nelson RE, Saltzman G, Skalabrin EJ, Majersik JJ (2010). Cost-Effectiveness of Telestroke for Ischemic Stroke: A Literature-Based Decision-Analytic Model. International Stroke Conference, San Antonio, TX, USA [Abstract].
Scoles DR, Xu X, Wang H, Tran H, Taylor-Harding B, Li A, Karlan BY (2010). Liver X receptor agonist inhibits proliferation of ovarian carcinoma cells stimulated by oxidized low density lipoprotein. Gynecol Oncol, 116(1), 109-116.
Charles A, Brennan KC (2010). The neurobiology of migraine. In Handb Clin Neurol (97, pp. 99-108).
Carlson N, Rojas M, Redd J, Tang P, Wood B, Hill K, Rose JW (2009). Cyclooxygenase-2 expression in oligodendrocytes increases sensitiity to excitotoxic death [Abstract]. European Committee for Treatment and Research in Multiple Sclerosis (ECTRIMS), Dusseldorf, Germany.
Matsuo F, Riaz A (2009). Lamotrigine. In Shorvon S, Perucca E, Engel J (Eds.), The Treatment of Epilepsy (3rd, pp. 536-58). Blackwell Publishing.
Rose JW, Quigley E, Anderson J, Kim S, Jeong EK, Minalga E, Merrill R, Parker D, Hadley R (2009). Imaging of the optic nerve with improved radiofrequency toils for 3T MRI. [Abstract]. First International Conference on Inflammation and Retinal Disease: Complement Biology and Pathology, Knossos, Crete.
Tumani H, Brettschneider J, Jakowski T, Abdul S, Husebye D, Seraj H, Hill H, Fire E, Spector L, Dotan N, Rose JW (2009). Anti-GAGA4 IgM assay may distinguish primary progressive multiple sclerosis from relapsing remitting multiple sclerosis patients. [Abstract]. ACTRIMS, Atlanta, Geogia.
Benbadis SR, LaFrance WC, Papandonatos GD, Korabathina K, Lin K, Kramer HC, NES Treatment Workshop, Matsuo F EEG-Video Reviewer (2009). Interrater reliability of EEG_Video monitoring. Neurology, 73, 843-6.
Merrill R, Hadley R, Minalga E, Parker D, Vijayakumar S, Choi SEK, Bell L, Rose JW (2009). An improved 28 channel array for optic nerve imaging [Abstract]. International Society for Magnetic Resonance Imaging.
Kim T, Kim SE, Patel A, Zollinger L, Rose JW, Jeong EK (2009). Diffusion tensor imaging of human spinal cords in cervical myelopathy [Abstract]. International Society for Magnetic Resonance Imaging, Honolulu, Hawaii.
Mehta LR, Rose JW (2009). Recurrent granuloma annulare during treatment with daclizumab. Mult Scler, 15(4), 527-8.
Cantu CB, Majersik JJ, Sanchez BS, Morgenstern LB (2009). Physician Perception of Acute Stroke Care in a Mexican Community, American Academy of Neurology, Seattle, WA, USA. [Abstract].
Hills WL, Warner JEA, Katz BJ, Celune GJ, Foster NL, Steffens J, Thulin PC, Chin S, Digre KB (2008). Neuro-opthalmic Findings that May Reliably Differentiate PSP and Parkinson's Disease. (Platform Presentation) [Abstract].
Ansari SA, Harati Y (2009). Anesthesiologist with muscle cramps (Tubular Aggregate Myopathy). [Abstract]. J Clin Neuromuscular Dis, 10(3), 147-162.
Wolinski JS, Sochat T, Weiss S, Ladkani D PROMiSe Trial Study Group J Rose site PI (2009). Glatiramer acetate treatment in PPMS: why males appear to respond favorably. J Neurol Sci, 15, 286-928.
Kim T, Zollinger L, Shu X, Rose JW, Jeong E (2009). Diffusion tensor imaging of ex vivo cervical spinal cord specimens: the immediate and long term effects of fixation on diffusivity. Anat Rec, 292, 234-41.
Lopez-Valdes HE, Clarkson AN, Carmichael ST, Charles AC, Brennan KC (2009). Chronic treatment with memantine enhances recovery of somatosensory maps in a mouse stroke model. Annual Meeting of the Society for Neuroscience, Chicago, IL [Abstract].
Brennan KC, Toga AW (2009). Intraoperative optical imaging. In Frostig R (Ed.), Methods for in vivo Optical Imaging of the Central Nervous System. CRC Press.
Foster NL (2009). Neuroimaging. In Weiner MF, Lipton AM (Eds.), The American Psychiatric Publishing Textbook of Alzheimer Disease and Other Dementias (pp. 105-136). Washington: American Psychiatric Publishing, Inc.
Burt RK, Loh Y, Cohen B, Stefoski D, Balabanov R, Katsamakis G, Oyama Y, Russell EJ, Stern J, Muraro P, Rose JW, Testori A, Bucha J, Jovanovic B, Milanetti F, Storek J, Volterelli JC, Burns WH (2009). Autologous non-myeloablative heamtopoetic stem cell transplantation for relapsing and remitting multiple sclerosis. Lancet Neurol, 8, 244-53.
Brennan KC, Chang J, Shook L, Biag J, Nguyen E, Toga AW, Charles AC (2009). Biphasic DC shift, hemoglobin desaturation, and neurovascular uncoupling in cortical spreading depression. 134th Annual Meeting of the American Neurological Association, Baltimore MD. Selected for Platform Presentation. [Abstract].
Rose J (2009). Multiple Sclerosis: Evidence of Maternal Effects and an Increasing Incidence in Women. Neurology, 73(8), 578-9.
Rose JW, Jaskowski T, Husebye D, Seraj H, Hill H, Carlson N (2008). Anti-thyroid antibodies identify a subgroup of multiple sclerosis patients. [Abstract]. ECTRIMS, Montreal, Canada.
Carlson N, Rojas M, Black J-D, Redd J, Hill K, Rose JW (2008). Neuroprotection by EP1 prostanoid receptor antagonists is modulated by microglia [Abstract]. Society for Neuroscience, Washington, DC.
Lopez-Valdes HE, Biag J, Chang J, Toga AW, Charles AC, Brennan KC (2008). Long term optical intrinsic signal imaging of forepaw and hindpaw cortex in mouse. Annual Meeting of the Society for Neuroscience, Washington, DC [Abstract].
Tsunoda I, Rose JW, Carlson N (2008). Treatment on an animal model for MS with resveratrol, a red wine component [Abstract]. International Society for Neuroimmunology, Dallas, Texas.
Carlson N, Rojas M, Redd J, Wood B, Hill K, Rose JW (2008). The role of COX-2 in experimental oligodendrocytes death and demyelination [Abstract]. International society for Neuroimmunology, Dallas, Texas.
Carlson N, Rojas M, Redd J, Wood B, Hill K, Rose JW (2008). A COX-2 inhibitor limits demyelination in a murine model of MS and protects oligodendrocytes from excitotoxic death in culture. [Abstract]. ECTRIMS, Montreal, Canada.
Mehta L, Rose JW (2008). Recurrent granuloma annulare occurring during treatment with daclizumab [Abstract]. ECTRIMS, Montreal, Canada.
Elmore RG, Ioffe Y, Scoles DR, Karlan BY, Li AJ (2008). Impact of statin therapy on survival in epithelial ovarian cancer. Gynecol Oncol, 111(1), 102-105.
Jaskowski T, Husebye D, Yarden J, Spector L, Fire E, Dotan N, Hill H, Rose JW (2008). Performance of an anti-GAGA4 IgM assay in distinguishing MS patients from control groups in a US cohort: a cross sectional retrospective study [Abstract]. ECTRIMS, Montreal, Canada.
Hadley R, Merrill R, Minalga E, Parker D, Rose JW (2008). Improved radio frequency coils for 3T magnetic resonance imaging of the optic nerve [Abstract]. ECTRIMS, Monteral, Canada.
Tsunoda I, Carlson N, Rose JW (2008). Treatment with a red wine component, resveratrol, in a virus induced model for MS [Abstract]. ECTRIMS, Montreal, Canada.
Burt R, Cohen B, Stefoski D, Balabanov R, Katsamakis G, Rose JW, Testori A, Muraro P, Storek J and Voltarelli J (2008). Autologous non myeloablative hematopoetic stem cell transplantation for relapsing multiple sclerosis [Abstract]. ECTRIMS, Montreal, Canada.
Matsuo F (2008). A case of familial epilepsy with nocturnal recurrences. In Schmidt D, Schacter SC (Eds.), Puzzling Cases of Epilepsy (2nd, pp. 267-9). Elsevier.
Ansari SA, Harati Y (2008). A Case of Nemaline Myopathy masquerading as Fascioscapulohumeral dystrophy. [Abstract]. J Clin Neuromuscular Dis, 9(3), 364-377.
CharlesAC, Brennan KC (2008). Glial cell calcium signaling. In Squire L (Ed.), Encyclopedia of Neuroscience. Elsevier Press.
Shprecher D, Smith SS, Steffens JD, Flanigan K (2008). Clinical and Diagnostic Features of Delayed Hypoxic leukoencephalopathy. J Neuropsychiatry Clin Neurosci.
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Chang J, Shook L, Charles AC, Brennan KC (2008). Significant hemoglobin desaturation during cortical spreading depression. 133rd Annual Meeting of the American Neurological Association, Salt Lake City UT [Abstract].
Brennan KC, Charles AC (2008). Mechanisms of cortical spreading depression as targets for migraine therapy. In OlesenJ, Ramadan N (Eds.), Frontiers in Headache Research: Innovative Drug Development for Headache Disorders. Oxford University Press.
Brennan KC, Romero Reyes M, Lopez-Valdes HE, Arnold AP, Charles AC (2007). Reduced threshold for cortical spreading depression in female mice. 13th Annual Congress of the International Headache Society, Stockholm, Sweden [Abstract].
KC Brennan, Hector E Lpez-Valds, Marcela Romero Reyes, Arthur P Arnold, Andrew C Charles (2007). Reduced threshold for cortical spreading depression in female mice. American Headache Society Annual Scientific Meeting, Chicago IL. Selected for Platform Presentation. [Abstract].
Turchik J, Karpenko V, Hammers D, McNamara J (2007). Practical and ethical assessment issues in rural, impoverished, and managed care settings. Prof Psychol Res Pr, 38(2), 158-168.
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Beltran-Parrazal L, Lpez-Valds HE, Brennan KC, Daz-Muoz M, de Vellis J, Charles AC (2006). Mitochondrial transport in processes of cortical neurons is independent of intracellular calcium. Am J Physiol Cell Physiol, 291(6), C1193-7.
Brennan KC, Shapiro RE, Xu Y, Ptacek LJ, Fu YH, Charles AC (2006). Alterations in spreading depression in a transgenic mouse carrying a novel potential migraine gene. (Selected for Platform Presentation, awarded Best Poster Prize), Migraine Trust International Symposium, London, UK [Abstract].
KC Brennan, Robert Shapiro, Louis Ptcek, and Andrew Charles (2006). Reduced threshold for cortical spreading depression and increased vasodilatation in mice expressing CK1dT44A. American Headache Society Annual Scientific Meeting, Los Angeles CA. Selected for Platform Presentation. [Abstract].
KC Brennan, Ying Xu, Louis Ptcek, and Andrew Charles (2006). Reduced threshold for cortical spreading depression in mice expressing CK1dT44A. Channels, Receptors, and Synapses Meeting. Cold Spring Harbor NY. Selected for Platform Presentation. [Abstract].
Steffens, JD (2006). Parkinson's Disease Medications. National APDA Newsletter (Winter, 2006). New York: National chapter of the American Parkinson's Disease Association.
Matsumoto J, Saver JL, Brennan KC, Ringman JM (2005). Mitochondrial encephalomyopathy with lactic acidosis and stroke (MELAS). [Review]. Rev Neurol Dis, 2(1), 30-4.
Steffens, JD (2005). The Purpose Behind the Pills. Parkinson's News (Fall, 2005). APDA I&R Center, Utah.
KC Brennan, Jeremy Theriot, Kevin Cury, Arthur W Toga, Andrew C Charles (2005). Changes in arterial caliber can precede cortical spreading depression. 12th Annual Congress of the International Headache Society, Kyoto, Japan. Selected for Platform Presentation. [Abstract].
Oh M-K, Scoles DR, Pulst SM (2005). DNA microarray analysis of immediate response to EGF treatment in rat schwannoma cells. Biotechnol Bioprocess Eng, 10(5), 444-450.
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