Kristina Lisa Allen-Brady

Kristina Lisa Allen-Brady, PhD, MSPH, MPT

Languages spoken: English

Academic Information

Departments Adjunct - Family & Preventive Medicine , Primary - Internal Medicine

Divisions: Public Health , Epidemiology

Kristina Allen-Brady, PhD, MSPH, MPH, is a Research Assistant Professor at the University of Utah School of Medicine, Division of Genetic Epidemiology. As a genetic epidemiologist, her research interests include pelvic floor disorders, food allergies, autism, cancer, and development of new methods to analyze genetic data.

Allen-Brady has always been interested in research and seeking to understand the underlying causes of chronic diseases. This curiosity has led her to publish her findings in a number of different journals. She reviews frequently for different journals as well as various grant funding agencies.

Allen-Brady received her PhD, MSPH, and MPT degrees all from the University of Utah. She is currently a member of the American Society of Human Genetics, the International Society of Genetic Epidemiology, a licensed physical therapist in the state of Utah, and serves on the University of Utah Institutional Review Board (IRB).

Education History

Undergraduate University of Utah
 BA
Other Training Cambridge University
Other Training Brigham Young University Jerusalem Center
Graduate Training University of Utah
 MPT
Other Training Intermountain Healthcare
Graduate Training University of Utah
 MSPH
Doctoral Training University of Utah
 PhD
Postdoctoral Fellowship University of Utah
 Postdoctoral Fellow
Postdoctoral Fellowship University of Utah, Department of Biomedical Informatics
 Postdoctoral Fellow

Selected Publications

Journal Article

  1. Peterson K, Firszt R, Fang J, Wong J, Smith KR, Allen-Brady K (2016). Risk of autoimmunity in EoE and families - A population-based cohort study. Am J Gastroenterol, 111, 926-32.
  2. Easton DF, Deffenbaugh AM, Pruss D, Frye C, Wenstrup RJ, Allen-Brady K, Tavtigian SV, Monteiro AN, Iversen ES, Couch FJ, Goldgar DE (2007). A systematic genetic assessment of 1,433 sequence variants of unknown clinical significance in the BRCA1 and BRCA2 breast cancer-predisposition genes. Am J Hum Genet, 81(5), 873-83.
  3. Allen-Brady K, Norton PA, Farnham JM, Teerlink C, Cannon-Albright LA (2009). Significant linkage evidence for a predisposition gene for pelvic floor disorders on chromosome 9q21. Am J Hum Genet, 84(5), 678-82.
  4. Wu JM, Ward RM, Allen-Brady KL, Edwards TL, Norton PA, Hartmann KE, Hauser ER, Velez Edwards DR (2013). Phenotyping clinical disorders: lessons learned from pelvic organ prolapse. Am J Obstet Gynecol, 208(5), 360-5.
  5. Morgan TK, Allen-Brady KL, Monson MA, Leclair CM, Sharp HT, Cannon-Albright LA (2016). Familiality analysis of provoked vestibulodynia treated by vestibulectomy supports genetic predisposition. Am J Obstet Gynecol, 214(5), 609.e1-7.
  6. Allen-Brady K, Cannon-Albright LA, Farnham JM, Norton P (2015). Evidence for pelvic organ prolapse predisposition genes on chromosomes 10 and 17. American journal of obstetrics and gynecology, 212(6), 771.e1-7.
  7. Allen-Brady K, Norton PA, Hill AJ, Rowe K, Cannon-Albright L (2020). Risk of pelvic organ prolapse treatment based on extended family history. American journal of obstetrics and gynecology, 223(1), 105.e1-105.e8.
  8. Thomas A, Camp NJ, Farnham JM, Allen-Brady K, Cannon-Albright L (2008). Shared genomic segment analysis. Mapping disease predisposition genes in extended pedigrees using SNP genotype assays. Annals of human genetics, 72(Pt 2), 279-87.
  9. Kim SH, Lee S, Piccolo SR, Allen-Brady K, Park EJ, Chun JN, Kim TW, Cho NH, Kim IG, So I, Jeon J (2012). Menthol induces cell-cycle arrest in PC-3 cells by down-regulating G2/M genes, including polo-like kinase 1. Biochemical and biophysical research communications, 422(3), 436-41.
  10. Allen BG, Allen-Brady K, Weeks D (2006). Reduction of XNkx2-10 expression leads to anterior defects and malformation of the embryonic heart. Mechanisms of development, 123(10), 719-29.
  11. Allen-Brady K, Cannon-Albright LA, Neuhausen SL, Camp N (2006). A role for XRCC4 in age at diagnosis and breast cancer risk. Cancer epidemiology, biomarkers & prevention, 15(7), 1306-10.
  12. Gaudet MM, Milne RL, Cox A, Camp NJ, Goode EL, Humphreys MK, Dunning AM, Morrison J, Giles GG, Severi G, Baglietto L, English DR, Couch FJ, Olson JE, Wang X, Chang-Claude J, Flesch-Janys D, Abbas S, Salazar R, Mannermaa A, Kataja V, Kosma VM, Lindblom A, Margolin S, Heikkinen T, Kämpjärvi K, Aaltonen K, Nevanlinna H, Bogdanova N, Coinac I, Schürmann P, Dörk T, Bartram CR, Schmutzler RK, Tchatchou S, Burwinkel B, Brauch H, Torres D, Hamann U, Justenhoven C, Ribas G, Arias JI, Benitez J, Bojesen SE, Nordestgaard BG, Flyger HL, Peto J, Fletcher O, Johnson N, Dos Santos Silva I, Fasching PA, Beckmann MW, Strick R, Ekici AB, Broeks A, Schmidt MK, van Leeuwen FE, Van't Veer LJ, Southey MC, Hopper JL, Apicella C, Haiman CA, Henderson BE, Le Marchand L, Kolonel LN, Kristensen V, Grenaker Alnaes G, Hunter DJ, Kraft P, Cox DG, Hankinson SE, Seynaeve C, Vreeswijk MP, Tollenaar RA, Devilee P, Chanock S, Lissowska J, Brinton L, Peplonska B, Czene K, Hall P, Li Y, Liu J, Balasubramanian S, Rafii S, Reed MW, Pooley KA, Conroy D, Baynes C, Kang D, Yoo KY, Noh DY, Ahn SH, Shen CY, Wang HC, Yu JC, Wu PE, Anton-Culver H, Ziogoas A, Egan K, Newcomb P, Titus-Ernstoff L, Trentham Dietz A, Sigurdson AJ, Alexander BH, Bhatti P, Allen-Brady K, Cannon-Albright LA, Wong J, Australian Ovarian Cancer Study Group., Chenevix-Trench G, Spurdle AB, Beesley J, Pharoah PD, Easton DF, Garcia-Closas M, Breast Cancer Association Consortium (2009). Five polymorphisms and breast cancer risk: results from the Breast Cancer Association Consortium. Cancer epidemiology, biomarkers & prevention, 18(5), 1610-6.
  13. Allen-Brady K, Camp N (2011). Genetic distance and markers used in linkage mapping. Methods in molecular biology (Clifton, N.J.), 713, 43-53.
  14. Shephard ND, Abo R, Rigas SH, Frank B, Lin WY, Brock IW, Shippen A, Balasubramanian SP, Reed MW, Bartram CR, Meindl A, Schmutzler RK, Engel C, Burwinkel B, Cannon-Albright LA, Allen-Brady K, Camp NJ, Cox (2009). A breast cancer risk haplotype in the caspase-8 gene. Cancer research, 69(7), 2724-8.
  15. Dodson MW*, Allen-Brady K*, Brown LM, Elliott CG, Cannon-Albright L (2019). Chronic Thromboembolic Pulmonary Hypertension Cases Cluster in Families. Chest, 155(2), 384-390.
  16. Dupuis J, Albers K, Allen-Brady K, Cho K, Elston RC, Kappen HJ, Tang H, Thomas A, Thomson G, Tsung E, Yang Q, Zhang W, Zhao K, Zheng G, Ziegler J (2007). Effect of linkage disequilibrium between markers in linkage and association analyses. Genetic epidemiology, 31 Suppl 1, S139-48.
  17. Teerlink C, Farnham J, Allen-Brady K, Camp NJ, Thomas A, Leachman S, Cannon-Albright (2012). A unique genome-wide association analysis in extended Utah high-risk pedigrees identifies a novel melanoma risk variant on chromosome arm 10q. Human genetics, 131(1), 77-85.
  18. Allen-Brady K, Camp NJ, Ward JH, Cannon-Albright L (2005). Lobular breast cancer: excess familiality observed in the Utah Population Database. International journal of cancer, 117(4), 655-61.
  19. Allen-Brady K, Firszt R, Fang JC, Wong J, Smith KR, Peterson K (2017). Population-based familial aggregation of eosinophilic esophagitis suggests a genetic contribution. The Journal of allergy and clinical immunology, 140(4), 1138-1143.
  20. Lin WY, Camp NJ, Cannon-Albright LA, Allen-Brady K, Balasubramanian S, Reed MW, Hopper JL, Apicella C, Giles GG, Southey MC, Milne RL, Arias-Pérez JI, Menéndez-Rodríguez P, Benítez J, Grundmann M, Dubrowinskaja N, Park-Simon TW, Dörk T, Garcia-Closas M, Figueroa J, Sherman M, Lissowska J, Easton DF, Dunning AM, Rajaraman P, Sigurdson AJ, Doody MM, Linet MS, Pharoah PD, Schmidt MK, Cox (2011). A role for XRCC2 gene polymorphisms in breast cancer risk and survival. Journal of medical genetics, 48(7), 477-84.
  21. Robson J, Korgenski K, Parsons K, McClain A, Barbagelata C, Allen-Brady K, Patel R, O'Gorman M, Peterson K, Guthery (2019). Sensitivity and Specificity of Administrative Medical Coding for Pediatric Eosinophilic Esophagitis. Journal of pediatric gastroenterology and nutrition, 69(2), e49-e53.
  22. Allen-Brady K, Rowe K, Cessna M, Lenherr S, Norton (2018). Significant Linkage Evidence for Interstitial Cystitis/Painful Bladder Syndrome on Chromosome 3. The Journal of urology, 199(1), 172-177.
  23. Richter HE, Whitehead N, Arya L, Ridgeway B, Allen-Brady K, Norton P, Sung V, Shepherd JP, Komesu Y, Gaddis N, Fraser MO, Tan-Kim J, Meikle S, Page GP, Pelvic Floor Disorders Network (2015). Genetic contributions to urgency urinary incontinence in women. The Journal of urology, 193(6), 2020-7.
  24. Beddhu S, Allen-Brady K, Cheung AK, Horne BD, Bair T, Muhlestein JB, Anderson J (2002). Impact of renal failure on the risk of myocardial infarction and death. Kidney international, 62(5), 1776-83.
  25. Krikov S, Price RC, Matney SA, Allen-Brady K, Facelli J (2011). Enabling GeneHunter as a grid service: a case study for implementing analytical services in biomedical grids. Methods of information in medicine, 50(4), 364-71.
  26. Allen-Brady K, Cannon-Albright L, Farnham JM, Teerlink C, Vierhout ME, van Kempen LCL, Kluivers KB, Norton P (2011). Identification of six loci associated with pelvic organ prolapse using genome-wide association analysis. Obstetrics and gynecology, 118(6), 1345-1353.
  27. Hemmert R, Schliep KC, Willis S, Peterson CM, Louis GB, Allen-Brady K, Simonsen SE, Stanford JB, Byun J, Smith K (2019). Modifiable life style factors and risk for incident endometriosis. Paediatric and perinatal epidemiology, 33(1), 19-25.
  28. Camp NJ, Farnham JM, Allen-Brady K, Cannon-Albright L (2007). Statistical recombinant mapping in extended high-risk Utah pedigrees narrows the 8q24 prostate cancer locus to 2.0 Mb. The Prostate, 67(13), 1456-64.
  29. Allen-Brady K, Miller J, Matsunami N, Stevens J, Block H, Farley M, Krasny L, Pingree C, Lainhart J, Leppert M, McMahon WM, Coon (2009). A high-density SNP genome-wide linkage scan in a large autism extended pedigree. Molecular psychiatry, 14(6), 590-600.
  30. Allen-Brady K, Robison R, Cannon D, Varvil T, Villalobos M, Pingree C, Leppert MF, Miller J, McMahon WM, Coon (2010). Genome-wide linkage in Utah autism pedigrees. Molecular psychiatry, 15(10), 1006-15.
  31. Allen KL, Miskulin D, Yan G, Dwyer JT, Frydrych A, Leung J, Poole D, and the Hemodialysis (HEMO) Study Grou (2002). Association of nutritional and behavioral markers on the physical and mental health status in prevalent hemodialysis patients from the HEMO Study. Journal of renal nutrition, 12(3), 160-9.
  32. Allen-Brady K, Wong J, Camp N (2006). PedGenie: an analysis approach for genetic association testing in extended pedigrees and genealogies of arbitrary size. BMC bioinformatics, 7, 209.
  33. Curtin K, Wong J, Allen-Brady K, Camp N (2007). PedGenie: meta genetic association testing in mixed family and case-control designs. BMC bioinformatics, 8, 448.
  34. Allen-Brady K, Farnham JM, Weiler J, Camp N (2003). A cautionary note on the appropriateness of using a linkage resource for an association study. BMC genetics, 4 Suppl 1, S89.
  35. Allen-Brady K, Camp N (2005). Characterization of the linkage disequilibrium structure and identification of tagging-SNPs in five DNA repair genes. BMC cancer, 5, 99.
  36. Peterson K, Clayton F, Qeadan F, Gorman D, Robson J, Allen-Brady K, Fang J (2020). Esophageal Eosinophilia Is Common Among Relatives of Eosinophilic Esophagitis Patients. Clinical gastroenterology and hepatology, 20(5), e957-e963.
  37. Krikov S, Price RC, Allen-Brady K, Cannon-Albright L, Facelli J (2008). Enabling GeneHunter as a grid service: a case study for implementing analytical services for biomedical grids. AMIA ... Annual Symposium proceedings. AMIA Symposium, 1014.
  38. Brune CW, Korvatska E, Allen-Brady K, Cook EH Jr, Dawson G, Devlin B, Estes A, Hennelly M, Hyman SL, McMahon WM, Munson J, Rodier PM, Schellenberg GD, Stodgell CJ, Coon (2008). Heterogeneous association between engrailed-2 and autism in the CPEA network. American journal of medical genetics. Part B, Neuropsychiatric genetics, 147B(2), 187-93.
  39. Byun J, Peterson CM, Backonja U, Taylor RN, Stanford JB, Allen-Brady KL, Smith KR, Louis GMB, Schliep K (2020). Adiposity and Endometriosis Severity and Typology. Journal of minimally invasive gynecology, 27(7), 1516-1523.
  40. Allen-Brady (2007). Genetic polymorphisms and metastatic breast cancer survival. Future oncology (London, England), 3(2), 155-8.
  41. Curtin K, Wong J, Allen-Brady K, Camp N (2007). Meta-genetic association of rheumatoid arthritis and PTPN22 using PedGenie 2.1. BMC proceedings, 1 Suppl 1, S12.
  42. Allen-Brady K, Horne BD, Malhotra A, Teerlink C, Camp NJ, Thomas (2007). Analysis of high-density single-nucleotide polymorphism data: three novel methods that control for linkage disequilibrium between markers in a linkage analysis. BMC proceedings, 1 Suppl 1, S160.
  43. Piccolo SR, Abo RP, Allen-Brady K, Camp NJ, Knight S, Anderson JL, Horne B (2009). Evaluation of genetic risk scores for lipid levels using genome-wide markers in the Framingham Heart Study. BMC proceedings, 3 Suppl 7, S46.
  44. Allen-Brady K, Farnham J, Cannon-Albright L (2011). Strategies for selection of subjects for sequencing after detection of a linkage peak. BMC proceedings, 5(Suppl 9), S77.
  45. Allen-Brady K, Farnham J, Cannon-Albright (2011). Strategies for selection of subjects for sequencing after detection of a linkage peak. BMC proceedings, 5 Suppl 9, S77.
  46. Allen-Brady K, Farnham JM, Camp NJ, Karlins E, Ostrander EA, Cannon-Albright L (2009). No evidence of BRCA2 mutations in chromosome 13q-linked Utah high-risk prostate cancer pedigrees. BMC research notes, 2, 94.
  47. Allen-Brady K, Cannon D, Robison R, McMahon WM, Coon (2010). A unified theory of autism revisited: linkage evidence points to chromosome X using a high-risk subset of AGRE families. Autism research, 3(2), 47-52.
  48. Allen-Brady K, Cai G, Cannon D, Robison R, McMahon WM, Coon H, Buxbaum J (2011). No evidence for IL1RAPL1 involvement in selected high-risk autism pedigrees from the AGRE data set. Autism research, 4(4), 293-6.
  49. Allen KL,Gappmaier (2001). Exercise Habits and Attitudes of Patients Undergoing Hemodialysis. Cardiopulmonary physical therapy journal, 12(1), 11-16.
  50. Cannon DS, Miller JS, Robison RJ, Villalobos ME, Wahmhoff NK, Allen-Brady K, McMahon WM, Coon (2010). Genome-wide linkage analyses of two repetitive behavior phenotypes in Utah pedigrees with autism spectrum disorders. Molecular autism, 1(1), 3.
  51. Coon H, Villalobos ME, Robison RJ, Camp NJ, Cannon DS, Allen-Brady K, Miller JS, McMahon W (2010). Genome-wide linkage using the Social Responsiveness Scale in Utah autism pedigrees. Molecular autism, 1(1), 8.
  52. Allen-Brady K, Norton PA, Cannon-Albright (2015). Risk of associated conditions in relatives of subjects with interstitial cystitis. Female pelvic medicine & reconstructive surgery, 21(2), 93-8.
  53. Lee S, Piccolo SR, Allen-Brady (2014). Robust meta-analysis shows that glioma transcriptional subtyping complements traditional approaches. Cellular oncology (Dordrecht, Netherlands), 37(5), 317-29.
  54. Norton PA, Allen-Brady K, Cannon-Albright L (2013). The familiality of pelvic organ prolapse in the Utah Population Database. International urogynecology journal, 24(3), 413-8.
  55. Norton PA, Allen-Brady K, Wu J, Egger M, Cannon-Albright (2015). Clinical characteristics of women with familial pelvic floor disorders. International urogynecology journal, 26(3), 401-6.
  56. Allen-Brady K, Chua JWF, Cuffolo R, Koch M, Sorrentino F, Cartwright (2021). Systematic review and meta-analysis of genetic association studies of pelvic organ prolapse. International urogynecology journal,
  57. Wirostko BM, Curtin K, Ritch R, Thomas S, Allen-Brady K, Smith KR, Hageman GS, Allingham R (2016). Risk for Exfoliation Syndrome in Women With Pelvic Organ Prolapse : A Utah Project on Exfoliation Syndrome (UPEXS) Study. JAMA ophthalmology, 134(11), 1255-1262.
  58. Allen-Brady K, Miller J, Matsunami N, Stevens J, Block H, Farley M, Krasny L, Pingree C, Lainhart J, Leppert M, McMahon WM, Coon (2008). The Value of Large Pedigrees for Chromosome Mapping in the Era of Dense Marker Sets. International journal of medical and biological frontiers, 14(1/2), 9-24.
  59. Brockmeyer DL, Cheshier SH, Stevens J, Facelli JC, Rowe K, Heiss JD, Musolf A, Viskochil DH, Allen-Brady KL, Cannon-Albright L (2022). A likely HOXC4 predisposition variant for Chiari malformations. Journal of neurosurgery, 139(1), 1-9.
  60. Allen-Brady KL, Christensen MB, Sandberg AD, Pastuszak A (2022). Significant familial clustering of Peyronie's disease in close and distant relatives. Andrology, 10(7), 1361-1367.
  61. Cannon-Albright LA, Teerlink CC, Stevens J, Facelli JC, Carr SR, Allen-Brady K, Puri S, Bailey-Wilson JE, Musolf AM, Genetic Epidemiology of Lung Cancer Consortium, Akerley (2023). A rare FGF5 candidate variant (rs112475347) for predisposition to nonsquamous, nonsmall-cell lung cancer. International journal of cancer, 153(2), 364-372.
  62. Cohan JN, Horns JJ, Hanson HA, Allen-Brady K, Kieffer MC, Huang LC, Brooke B (2023). The Association Between Family History and Diverticulitis Recurrence: A Population-Based Study. Diseases of the colon and rectum, 66(2), 269-277.
  63. Allen-Brady K, Colletier KJ, Woller S, Eliason K, Uchida AM, Ro G, Newman M, Peterson K (2023). Eosinophilic Gastritis and Enteritis Are Increased in Families With Eosinophilic Esophagitis. The American journal of gastroenterology, 118(2), 263-268.
  64. Verrilli L, Johnstone E, Welt C, Allen-Brady (2023). Primary ovarian insufficiency has strong familiality: results of a multigenerational genealogical study. Fertility and sterility, 119(1), 128-134.
  65. Schliep KC, Farland LV, Pollack AZ, Buck Louis G, Stanford JB, Allen-Brady K, Varner MW, Kah K, Peterson C (2022). Endometriosis diagnosis, staging and typology and adverse pregnancy outcome history. Paediatric and perinatal epidemiology, 36(6), 771-781.
  66. Verrilli L, Johnstone E, Allen-Brady K, Welt (2021). Shared genetics between nonobstructive azoospermia and primary ovarian insufficiency. F&S reviews, 2(3), 204-213.
  67. Cohan JN, Horns JJ, Ramsay JM, Huang LC, Allen-Brady (2023). Diverticulitis Familiality: A Statewide Case-Control Study. Journal of the American College of Surgeons, 237(5), 689-696.
  68. Cannon-Albright LA, Stevens J, Facelli JC, Teerlink CC, Allen-Brady K, Agarwal (2023). High-Risk Pedigree Study Identifies LRBA (rs62346982) as a Likely Predisposition Variant for Prostate Cancer. Cancers, 15(7),
  69. Kluivers KB, Lince SL, Ruiz-Zapata AM, Post WM, Cartwright R, Kerkhof MH, Widomska J, De Witte W, Pecanka J, Kiemeney LA, Vermeulen SH, Goeman JJ, Allen-Brady K, Oosterwijk E, Poelmans (2023). Molecular Landscape of Pelvic Organ Prolapse Provides Insights into Disease Etiology. International journal of molecular sciences, 24(7),
  70. Reddy CA*, Allen-Brady K*, Uchida AM, Peterson KA, Hoffman AM, Souza RF, Spechler S (2023). Achalasia is Strongly Associated with Eosinophilic Esophagitis and Other Allergic Disorders. Clinical gastroenterology and hepatology, 22(1), 34-41.e2.
  71. Allen-Brady K, Fyer AJ, Weissman (2023). The multi-generational familial aggregation of interstitial cystitis, other chronic nociplastic pain disorders, depression, and panic disorder. Psychological medicine, 53(16), 7847-7856.
  72. Cannon-Albright LA, Stevens J, Teerlink CC, Facelli JC, Allen-Brady K, Welm A (2023). A Rare Variant in MDH2 (rs111879470) Is Associated with Predisposition to Recurrent Breast Cancer in an Extended High-Risk Pedigree. Cancers, 15(24),
  73. Verrilli LE, Allen-Brady K, Johnstone EB, Alvord MA, Welt C (2023). Family size for women with primary ovarian insufficiency and their relatives. Human reproduction (Oxford, England), 38(10), 1991-1997.
  74. da Silva RSP, Bortolini MAT, Teixeira JB, Batista NC, Fitz FF, Allen-Brady K, Castro R (2023). Association between the rs1036819 polymorphism of the ZFAT gene and pelvic organ prolapse: a case-control study. International urogynecology journal, 34(10), 2611-2617.
  75. Schliep KC, Ghabayen L, Shaaban M, Hughes FR, Pollack AZ, Stanford JB, Brady KA, Kiser A, Peterson C (2023). Examining the co-occurrence of endometriosis and polycystic ovarian syndrome. AJOG global reports, 3(3), 100259.
  76. Peterson K, Firszt R, Fang J, Wong J, Smith KR, Brady K (2016). Risk of Autoimmunity in EoE and Families: A Population-Based Cohort Study. The American journal of gastroenterology, 111(7), 926-32.
  77. Barnard ME, Farland LV, Yan B, Wang J, Trabert B, Doherty JA, Meeks HD, Madsen M, Guinto E, Collin LJ, Maurer KA, Page JM, Kiser AC, Varner MW, Allen-Brady K, Pollack AZ, Peterson KR, Peterson CM, Schliep K (2024). Endometriosis Typology and Ovarian Cancer Risk. JAMA, 332(6), 482-489.
  78. Allen-Brady K, Moore B, Verrilli LE, Alvord MA, Kern M, Camp N, Kelley K, Letourneau J, Cannon-Albright L, Yandell M, Johnstone EB, Welt C (2024). Breast Cancer is Increased in Women with Primary Ovarian Insufficiency. The Journal of clinical endocrinology and metabolism, 110(5), e1678-e1686.
  79. Pyne AL, Uchida AM, Hazel MW, Stubben CJ, Chang JW, Bailey DD, Gonsalves N, Allen-Brady K, Peterson KA, Pletneva M (2024). Effect of benralizumab on histopathology and inflammatory signatures in a clinical cohort of eosinophilic esophagitis. Diseases of the esophagus,
  80. Tashjian RZ, Jurynec MJ, Christy K, Stevens J, Teerlink CC, Cannon-Albright L, Allen-Brady (2024). Identification of rare genetic variants for rotator cuff tearing and repair in high-risk pedigrees. JSES international, 8(4), 815-821.
  81. Teixeira JB, Bortolini MAT, Silva RSP, Batista NC, Costa E Silva CL, Allen-Brady K, Castro R (2024). The rs2018736 fibulin-5 polymorphism as a determinant for pelvic organ prolapse: a case-control study. Climacteric, 27(3), 321-325.
  82. Leonard ME, Horns JJ, Allen-Brady K, Ozanne EM, Wallace AS, Brooke BS, Supiano MA, Cohan J (2024). Recurrence of severe diverticulitis is associated with age and birth decade. Journal of gastrointestinal surgery, 28(4), 507-512.
  83. Allen KL, Miskulin D, Yan G, Dwyer JT, Frydrych A, Leung J, Poole D, Hemodialysis (HEMO) Study Grou (2002). Association of nutritional markers with physical and mental health status in prevalent hemodialysis patients from the HEMO study. Journal of renal nutrition, 12(3), 160-9.
  84. Allen-Brady K, Clayton F, Hazel MW, Stevens J, Pyne AL, Pletneva MA, Cessna M, Stubben C, Robson J, Fang J, Peterson K (2025). Overlap of Genomic and Transcriptomic Genes Identified in Familial Eosinophilic Esophagitis. Gastroenterology, 168(6), 1101-1113.e18.
  85. Allen-Brady K, Verrilli LE, Austin BA, Letourneau JM, Johnstone EB, Welt C (2025). Turner syndrome: fertility, familial clustering, and cancer risk. Human reproduction (Oxford, England), 40(2), 391-396.
  86. Allen-Brady K, Johnstone EB, Welt C (2024). Response to Letter to the Editor: Breast Cancer is Increased in Women with Primary Ovarian Insufficiency. The Journal of clinical endocrinology and metabolism, 110(5), e1725-e1726.
  87. Wang V, Walsh J, Zell J, Verrilli LE, Letourneau J, Johnstone EB, Allen-Brady K, Welt C (2024). Autoimmune Disease is Increased in Women with Primary Ovarian Insufficiency. The Journal of clinical endocrinology and metabolism, 110(8), e2614-e2620.
  88. Pyne AL, Uchida AM, Hazel MW, Pletneva MA, Allen-Brady K, Peterson K (2024). Differing Epithelial and Immunologic Activation Patterns Following Food Reintroduction Reveal Different Transcriptional Profiles in Active Eosinophilic Esophagitis. Gastroenterology, 168(3), 598-600.e3.
  89. Armon C, Cannon-Albright LA, Allen-Brady K, Wolfson (2024). Chasing shadows: Investigating X chromosome mediation in late-onset Alzheimer's disease. Advanced neurology, 3(2),
  90. Dodson MW, Allen-Brady K, Stevens J, Cirulis MM, Alotaibi M, Fernandes TM, Kim NH, Kerr KM, Papamatheakis DG, Poch DS, Desmarais J, Best DH, Hatton ND, Ryan JJ, Elliott CG, Cannon-Albright L (2025). Rare variants in STAB2 in patients with chronic thromboembolic pulmonary hypertension. ERJ open research, 11(4),
  91. Allen-Brady K, Kodama S, Verrilli LE, Ramsay JM, Johnstone EB, Horns JJ, Emery BR, Cannon-Albright L, Aston KI, Hotaling JM, Welt C (2025). Azoospermia/Oligozoospermia and Prostate Cancer Are Increased in Families of Women With Primary Ovarian Insufficiency. Journal of the Endocrine Society, 9(4), bvaf030.

Review

  1. Davies M, Jurynec MJ, Gomez-Alvarado F, Hu D, Feeley SE, Allen-Brady K, Tashjian RZ, Feeley B (2023). Current cellular and molecular biology techniques for the orthopedic surgeon-scientist. Journal of shoulder and elbow surgery, 32(1), e11-e22.
  2. Deprest JA, Cartwright R, Dietz HP, Brito LGO, Koch M, Allen-Brady K, Manonai J, Weintraub AY, Chua JWF, Cuffolo R, Sorrentino F, Cattani L, Decoene J, Page AS, Weeg N, Varella Pereira GM, Mori da Cunha de Carvalho MGMC, Mackova K, Hympanova LH, Moalli P, Shynlova O, Alperin M, Bortolini MA (2022). International Urogynecological Consultation (IUC): pathophysiology of pelvic organ prolapse (POP). International urogynecology journal, 33(7), 1699-1710.
  3. Allen-Brady K, Bortolini MAT, Damaser M (2022). Mouse Knockout Models for Pelvic Organ Prolapse: a Systematic Review. International urogynecology journal, 33(7), 1765-1788.
  4. Yu J, Varella Pereira GM, Allen-Brady K, Cuffolo R, Siddharth A, Koch M, Chua JWF, Sorrentino F, Dytko O, Ng KY, Violette P, Khullar V, Wang ZT, Cartwright (2023). Genetic polymorphisms associated with urinary tract infection in children and adults: a systematic review and meta-analysis. American journal of obstetrics and gynecology,

Editorial

  1. Guo Q, Allen-Brady K, Olszewska (2024). Editorial: Women in applied genetic epidemiology. Frontiers in genetics, 15, 1508169.

Letter

  1. May Maestas M, Perry KD, Smith K, Firszt R, Allen-Brady K, Robson J, Joy E, Peterson K (2019). Food impactions in Eosinophilic esophagitis and acute exposures to fine particulate pollution. [Letter to the editor]. Allergy, 74(12), 2529-2530.
  2. Spechler SJ, Reddy CA, Allen-Brady K, Uchida AM, Peterson KA, Hoffman AM, Souza R (2023). Reply. Clinical gastroenterology and hepatology,
  3. Allen-Brady (2025). Commentary on "Whole Exome Sequencing Reveals Candidate Variants in Ion Channel Genes for Pelvic Muscle Dysfunction in Young Females with a Family History". International urogynecology journal, 36(4), 935.