Coon, Hilary , PhD

Research Interests

  • Suicide
  • Autism Spectrum Disorders
  • Statistical Genetics
  • Genetic Epidemiology
  • Child Psychiatry
  • Obesity
  • Pulmonary fibrosis
  • Nicotine Dependence

Languages

  • English

Academic Information

  • Departments: Biomedical Informatics - Adjunct Professor, Internal Medicine - Adjunct Professor, Psychiatry - Professor
  • Divisions: Adult Psychiatry, Epidemiology

Academic Office Information

  • Biomedical Polymers Research Bldg
    Psychiatry Genetics Laboratory
    20 S 2030 E, Room: 408
    Salt Lake City, UT 84112

Research Statement

Hilary Coon's primary research interests within the Department of Psychiatry include finding genes that lead to susceptibility to autism and, genetic risk factors for suicide, and the genetics of nicotine and alcohol addiction. Work to achieve these goals is accomplished through collaborations with national, and international collaborators, and locally through analyses of extended families ascertained through the Utah Population Data Base (UPDB). Gene findings may lead to better understanding of underlying mechanisms. Intermediate traits and co-morbid conditions associated with disease have also been a focus of Dr. Coon's research. Traits that are correlated with disease are often observed at increased rates also in clinically unaffected family members. These traits may indicate the presence of relatively common gene changes that, together with other genetic and environmental factors, contribute to increased risk of carrying a diagnosis. In addition, appearance of particular traits or co-morbid conditions in affected pedigree members and their clinically unaffected relatives may indicate particular genetic subtypes of disease present in the family. The study of these phenotypes within families may reveal susceptibility mutations that would otherwise not be detected. Pedigrees also offer a chance to study protective mechanisms in unaffected relatives, and environmental exposures that may be particularly important for genetically susceptible individuals. Interests outside the Psychiatry Department include the development and application of statistical methods to genetic and phenotypic data, cardiovascular genetics, genetics of obesity, and genetics of lung disorders. Dr. Coon is also interested in research ethics, and is a long time member of the University of Utah Institutional Review Board.

Education History

Type School Degree
Doctoral Training University of Colorado
Psychology/Behavioral Genetics
Ph.D.
Fellowship University of Colorado, Institute for Behavioral Genetics, Colorado Adoption Project
Biostatistics
Fellow
Graduate Training University of Colorado
Psychology/Behavioral Genetics
M.A.
Undergraduate University of Colorado
Mathematics
B.A.
Undergraduate University of Colorado
Music
B.A.

Selected Publications

Journal Article

  1. Keeshin BR, Gray D, Zhang C, Presson AP, Coon H (2017 Aug 22). Youth Suicide Deaths: Investigation of Clinical Predictors in a Statewide Sample.LID - 10.1111/sltb.12386 [doi]. (Epub ahead of print) Suicide Life Threat Behav.
  2. Weiner DJ, Wigdor EM, Ripke S, Walters RK, Kosmicki JA, Grove J, Samocha KE, Goldstein JI, Okbay A, Bybjerg-Grauholm J, Werge T, Hougaard DM, Taylor J, iPSYCH-Broad Autism Group, Psychiatric Genomics Consortium Autism Group, Skuse D, Devlin B, Anney R, Sanders SJ, Bishop S, Mortensen PB, Brglum AD, Smith GD, Daly MJ, Robinson EB (). Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders. Nat Genet, May 15(10:1038).
  3. Autism Spectrum Disorders Working Group of The Psychiatric Genomics Consortium (). Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia. Mol Autism, 8(21).
  4. Woodbury-Smith M, Bilder DA, Morgan J, Jerominski L, Darlington T, Dyer T, Paterson AD, Coon H (2017). Combined genome-wide linkage and targeted association analysis of head circumference in autism spectrum disorder families. J Neurodev Disord, 9, 5.
  5. Figueroa KP, Coon H, Santos N, Velazquez L, Mederos LA, Pulst SM (2017 Jun). Genetic analysis of age at onset variation in spinocerebellar ataxia type 2. Neurol Genet, 3(3), e155.
  6. Christensen ED, Berger J, Alashari MM, Coon H, Robison C, Ho HT, Adams DR, Gahl WA, Smith KR, Opitz JM, Johnson DR (2017 Jan). Sudden infant death "syndrome"-Insights and future directions from a Utah population database analysis. Am J Med Genet A, 173(1), 177-182.
  7. Hasstedt SJ, Coon H, Xin Y, Adams TD, Hunt SC (2016 Feb). APOH interacts with FTO to predispose to healthy thinness. Hum Genet, 135(2), 201-7.
  8. Hollingshaus MS, Coon H, Crowell SE, Gray DD, Hanson HA, Pimentel R, Smith KR (2016). Differential Vulnerability to Early-Life Parental Death: The Moderating Effects of Family Suicide History on Risks for Major Depression and Substance Abuse in Later Life. Biodemography Soc Biol, 62(1), 105-25.
  9. McGlade E, Bakian A, Coon H, Yurgelun-Todd D, Callor WB, Byrd J, Gray D (2016 Aug). Male suspected suicide decedents in Utah: A comparison of Veterans and nonveterans. Compr Psychiatry, 69, 1-10.
  10. Hu H, Coon H, Li M, Yandell M, Huff CD (2016 Aug 25). VARPRISM: incorporating variant prioritization in tests of de novo mutation association. Genome Medicine, 8(1), 91.
  11. Cannon DS, Medina TR, Mermelstein RJ, Hedeker D, Bakian AV, Coon H, Cook EH, Hamil C, Weiss RB (2016 Feb). CYP2A6 Longitudinal Effects in Young Smokers. Nicotine Tob Res, 18(2), 196-203.
  12. Jones KB, Cottle K, Bakian A, Farley M, Bilder D, Coon H, McMahon WM (2016 Jul). A description of medical conditions in adults with autism spectrum disorder: A follow-up of the 1980s Utah/UCLA Autism Epidemiologic Study. Autism, 20(5), 551-61.
  13. Schwantes-An TH, Zhang J, Chen LS, Hartz SM, Culverhouse RC, Chen X, Coon H, Frank J, Kamens HM, Konte B, Kovanen L, Latvala A, Legrand LN, Maher BS, Melroy WE, Nelson EC, Reid MW, Robinson JD, Shen PH, Yang BZ, Andrews JA, Aveyard P, Beltcheva O, Brown SA, Cannon DS, Cichon S, Corley RP, Dahmen N, Degenhardt L, Foroud T, Gaebel W, Giegling I, Glatt SJ, Grucza RA, Hardin J, Hartmann AM, Heath AC, Herms S, Hodgkinson CA, Hoffmann P, Hops H, Huizinga D, Ising M, Johnson EO, Johnstone E, Kaneva RP, Kendler KS, Kiefer F, Kranzler HR, Krauter KS, Levran O, Lucae S, Lynskey MT, Maier W, Mann K, Martin NG, Mattheisen M, Montgomery GW, Muller-Myhsok B, Murphy MF, Neale MC, Nikolov MA, Nishita D, Nothen MM, Nurnberger J, Partonen T, Pergadia ML, Reynolds M, Ridinger M, Rose RJ, Rouvinen-Lagerstrom N, Scherbaum N, Schmal C, Soyka M, Stallings MC, Steffens M, Treutlein J, Tsuang M, Wall TL, Wodarz N, Yuferov V, Zill P, Bergen AW, Chen J, Cinciripini PM, Edenberg HJ, Ehringer MA, Ferrell RE, Gelernter J, Goldman D, Hewitt JK, Hopfer CJ, Iacono WG, Kaprio J, Kreek MJ, Kremensky IM, Madden PA, McGue M, Munafo MR, Philibert RA, Rietschel M, Roy A, Rujescu D, Saarikoski ST, Swan GE, Todorov AA, Vanyukov MM, Weiss RB, Bierut LJ, Saccone NL (2016 Mar). Association of the OPRM1 Variant rs1799971 (A118G) with Non-Specific Liability to Substance Dependence in a Collaborative de novo Meta-Analysis of European-Ancestry Cohorts. Behav Genet, 46(2), 151-69.
  14. Bakian AV, Huber RS, Coon H, Gray D, Wilson P, McMahon WM, Renshaw PF (2015 Mar 01). Bakian et al. respond to "Assessing air pollution and suicide risk". Am J Epidemiol, 181(5), 309-10.
  15. Bakian AV, Huber RS, Coon H, Gray D, Wilson P, McMahon WM, Renshaw PF (2015 Mar 01). Acute air pollution exposure and risk of suicide completion. Am J Epidemiol, 181(5), 295-303.
  16. Addis L, Ahn JW, Dobson R, Dixit A, Ogilvie CM, Pinto D, Vaags AK, Coon H, Chaste P, Wilson S, Parr JR, Andrieux J, Lenne B, Tumer Z, Leuzzi V, Aubell K, Koillinen H, Curran S, Marshall CR, Scherer SW, Strug LJ, Collier DA, Pal DK (2015 Sep). Microdeletions of ELP4 Are Associated with Language Impairment, Autism Spectrum Disorder, and Mental Retardation. Hum Mutat, 36(9), 842-50.
  17. Chapman NH, Nato AQ Jr, Bernier R, Ankenman K, Sohi H, Munson J, Patowary A, Archer M, Blue EM, Webb SJ, Coon H, Raskind WH, Brkanac Z, Wijsman EM (2015 Oct). Whole exome sequencing in extended families with autism spectrum disorder implicates four candidate genes. Hum Genet, 134(10), 1055-68.
  18. Bakian AV, Bilder DA, Coon H, McMahon WM (2015 Apr). Spatial relative risk patterns of autism spectrum disorders in Utah. J Autism Dev Disord, 45(4), 988-1000.
  19. Bowton E, Saunders C, Reddy IA, Campbell NG, Hamilton PJ, Henry LK, Coon H, Sakrikar D, Veenstra-VanderWeele JM, Blakely RD, Sutcliffe J, Matthies HJ, Erreger K, Galli A (2014 Oct 14). SLC6A3 coding variant Ala559Val found in two autism probands alters dopamine transporter function and trafficking. Transl Psychiatry, 4, e464.
  20. Darlington TM, Pimentel R, Smith K, Bakian AV, Jerominski L, Cardon J, Camp NJ, Callor WB, Grey T, Singleton M, Yandell M, Renshaw PF, Yurgelun-Todd DA, Gray D, Coon H (2014 Oct 21). Identifying rare variants for genetic risk through a combined pedigree and phenotype approach: application to suicide and asthma. Transl Psychiatry, 4, e471.
  21. De Rubeis S, He X, Goldberg AP, Poultney CS, Samocha K, Cicek AE, Kou Y, Liu L, Fromer M, Walker S, Singh T, Klei L, Kosmicki J, Shih-Chen F, Aleksic B, Biscaldi M, Bolton PF, Brownfeld JM, Cai J, Campbell NG, Carracedo A, Chahrour MH, Chiocchetti AG, Coon H, Crawford EL, Curran SR, Dawson G, Duketis E, Fernandez BA, Gallagher L, Geller E, Guter SJ, Hill RS, Ionita-Laza J, Jimenz Gonzalez P, Kilpinen H, Klauck SM, Kolevzon A, Lee I, Lei I, Lei J, Lehtimaki T, Lin CF, Maayan A, Marshall CR, McInnes AL, Neale B, Owen MJ, Ozaki N, Parellada M, Parr JR, Purcell S, Puura K, Rajagopalan D, Rehnstrom K, Reichenberg A, Sabo A, Sachse M, Sanders SJ, Schafer C, Schulte-Ruther M, Skuse D, Stevens C, Szatmari P, Tammimies K, Valladares O, Voran A, Li-San W, Weiss LA, Willsey AJ, Yu TW, Yuen RK, Cook EH, Freitag CM, Gill M, Hultman CM, Lehner T, Palotie A, Schellenberg GD, Sklar P, State MW, Sutcliffe JS, Walsh CA, Scherer SW, Zwick ME, Barett JC, Cutler DJ, Roeder K, Devlin B, Daly MJ, Buxbaum JD (2014 Nov 13). Synaptic, transcriptional and chromatin genes disrupted in autism. Nature, 515(7526), 209-15.
  22. Buxbaum JD, Bolshakova N, Brownfeld JM, Anney RJ, Bender P, Bernier R, Cook EH, Coon H, Cuccaro M, Freitag CM, Hallmayer J, Geschwind D, Klauck SM, Nurnberger JI, Oliveira G, Pinto D, Poustka F, Scherer SW, Shih A, Sutcliffe JS, Szatmari P, Vicente AM, Vieland V, Gallagher L (2014). The Autism Simplex Collection: an international, expertly phenotyped autism sample for genetic and phenotypic analyses. Mol Autism, 5, 34.
  23. Coon H, Piasecki TM, Cook EH, Dunn D, Mermelstein RJ, Weiss RB, Cannon DS (2014 Apr). Association of the CHRNA4 neuronal nicotinic receptor subunit gene with frequency of binge drinking in young adults. Alcohol Clin Exp Res, 38(4), 930-7.
  24. Huber RS, Coon H, Kim N, Renshaw PF, Kondo DG (2014 Mar). Altitude is a risk factor for completed suicide in bipolar disorder. Med Hypotheses, 82(3), 377-81.
  25. Scholand MB, Wolff R, Crossno PF, Sundar K, Winegar M, Whipple S, Carey P, Sunchild N, Coon H (2014). Severity of cough in idiopathic pulmonary fibrosis is associated with MUC5 B genotype. Cough, 10, 3.
  26. Pinto D, Delaby E, Merico D, Barbosa M, Merikangas A, Klei L, Thiruvahindrapuram B, Xu X, Ziman R, Wang Z, Vorstman JA, Thompson A, Regan R, Pilorge M, Pellecchia G, Pagnamenta AT, Oliveira B, Marshall CR, Magalhaes TR, Lowe JK, Howe JL, Griswold AJ, Gilbert J, Duketis E, Dombroski BA, De Jonge MV, Cuccaro M, Crawford EL, Correia CT, Conroy J, Conceicao IC, Chiocchetti AG, Casey JP, Cai G, Cabrol C, Bolshakova N, Bacchelli E, Anney R, Gallinger S, Cotterchio M, Casey G, Zwaigenbaum L, Wittemeyer K, Wing K, Wallace S, van Engeland H, Tryfon A, Thomson S, Soorya L, Roge B, Roberts W, Poustka F, Mouga S, Minshew N, McInnes LA, McGrew SG, Lord C, Leboyer M, Le Couteur AS, Kolevzon A, Jimenez Gonzalez P, Jacob S, Holt R, Guter S, Green J, Green A, Gillberg C, Fernandez BA, Duque F, Delorme R, Dawson G, Chaste P, Cafe C, Brennan S, Bourgeron T, Bolton PF, Bolte S, Bernier R, Baird G, Bailey AJ, Anagnostou E, Almeida J, Wijsman EM, Vieland VJ, Vicente AM, Schellenberg GD, Pericak-Vance M, Paterson AD, Parr JR, Oliveira G, Nurnberger JI, Monaco AP, Maestrini E, Klauck SM, Hakonarson H, Haines JL, Geschwind DH, Freitag CM, Folstein SE, Ennis S, Coon H, Battaglia A, Szatmari P, Sutcliffe JS, Hallmayer J, Gill M, Cook EH, Buxbaum JD, Devlin B, Gallagher L, Betancur C, Scherer SW (2014 May 01). Convergence of genes and cellular pathways dysregulated in autism spectrum disorders. Am J Hum Genet, 94(5), 677-94.
  27. Hu H, Roach JC, Coon H, Guthery SL, Voelkerding KV, Margraf RL, Durtschi JD, Tavtigian SV, Shankaracharya, Wu W, Scheet P, Wang S, Xing J, Glusman G, Hubley R, Li H, Garg V, Moore B, Hood L, Galas DJ, Srivastava D, Reese MG, Jorde LB, Yandell M, Huff CD (2014 Jul). A unified test of linkage analysis and rare-variant association for analysis of pedigree sequence data. Nat Biotechnol, 32(7), 663-9.
  28. Buck TR, Viskochil J, Farley M, Coon H, McMahon WM, Morgan J, Bilder DA (2014 Dec). Psychiatric comorbidity and medication use in adults with autism spectrum disorder. J Autism Dev Disord, 44(12), 3063-71.
  29. Gray D, Coon H, McGlade E, Callor WB, Byrd J, Viskochil J, Bakian A, Yurgelun-Todd D, Grey T, McMahon WM (2014 Jun). Comparative analysis of suicide, accidental, and undetermined cause of death classification. Suicide Life Threat Behav, 44(3), 304-16.
  30. Cannon DS, Mermelstein RJ, Hedeker D, Coon H, Cook EH, McMahon WM, Hamil C, Dunn D, Weiss RB (2014 Feb). Effect of neuronal nicotinic acetylcholine receptor genes (CHRN) on longitudinal cigarettes per day in adolescents and young adults. Nicotine Tob Res, 16(2), 137-44.
  31. Coon H, Darlington T, Pimentel R, Smith KR, Huff CD, Hu H, Jerominski L, Hansen J, Klein M, Callor WB, Byrd J, Bakian A, Crowell SE, McMahon WM, Rajamanickam V, Camp NJ, McGlade E, Yurgelun-Todd D, Grey T, Gray D (2013 Nov 19). Genetic risk factors in two Utah pedigrees at high risk for suicide. Transl Psychiatry, 3, e325.
  32. Bilder DA, Bakian AV, Viskochil J, Clark EA, Botts EL, Smith KR, Pimentel R, McMahon WM, Coon H (2013 Nov). Maternal prenatal weight gain and autism spectrum disorders. Pediatrics, 132(5), e1276-83.
  33. Stephens SH, Hartz SM, Hoft NR, Saccone NL, Corley RC, Hewitt JK, Hopfer CJ, Breslau N, Coon H, Chen X, Ducci F, Dueker N, Franceschini N, Frank J, Han Y, Hansel NN, Jiang C, Korhonen T, Lind PA, Liu J, Lyytikainen LP, Michel M, Shaffer JR, Short SE, Sun J, Teumer A, Thompson JR, Vogelzangs N, Vink JM, Wenzlaff A, Wheeler W, Yang BZ, Aggen SH, Balmforth AJ, Baumeister SE, Beaty TH, Benjamin DJ, Bergen AW, Broms U, Cesarini D, Chatterjee N, Chen J, Cheng YC, Cichon S, Couper D, Cucca F, Dick D, Foroud T, Furberg H, Giegling I, Gillespie NA, Gu F, Hall AS, Hallfors J, Han S, Hartmann AM, Heikkila K, Hickie IB, Hottenga JJ, Jousilahti P, Kaakinen M, Kahonen M, Koellinger PD, Kittner S, Konte B, Landi MT, Laatikainen T, Leppert M, Levy SM, Mathias RA, McNeil DW, Medland SE, Montgomery GW, Murray T, Nauck M, North KE, Pare PD, Pergadia M, Ruczinski I, Salomaa V, Viikari J, Willemsen G, Barnes KC, Boerwinkle E, Boomsma DI, Caporaso N, Edenberg HJ, Francks C, Gelernter J, Grabe HJ, Hops H, Jarvelin MR, Johannesson M, Kendler KS, Lehtimaki T, Magnusson PK, Marazita ML, Marchini J, Mitchell BD, Nothen MM, Penninx BW, Raitakari O, Rietschel M, Rujescu D, Samani NJ, Schwartz AG, Shete S, Spitz M, Swan GE, Volzke H, Veijola J, Wei Q, Amos C, Cannon DS, Grucza R, Hatsukami D, Heath A, Johnson EO, Kaprio J, Madden P, Martin NG, Stevens VL, Weiss RB, Kraft P, Bierut LJ, Ehringer MA (2013 Dec). Distinct loci in the CHRNA5/CHRNA3/CHRNB4 gene cluster are associated with onset of regular smoking. Genet Epidemiol, 37(8), 846-59.
  34. Miller JS, Bilder D, Farley M, Coon H, Pinborough-Zimmerman J, Jenson W, Rice CE, Fombonne E, Pingree CB, Ritvo E, Ritvo RA, McMahon WM (2013 Jan). Autism spectrum disorder reclassified: a second look at the 1980s Utah/UCLA Autism Epidemiologic Study. J Autism Dev Disord, 43(1), 200-10.
  35. Bilder D, Botts EL, Smith KR, Pimentel R, Farley M, Viskochil J, McMahon WM, Block H, Ritvo E, Ritvo RA, Coon H (2013 May). Excess mortality and causes of death in autism spectrum disorders: a follow up of the 1980s Utah/UCLA autism epidemiologic study. J Autism Dev Disord, 43(5), 1196-204.
  36. Burton BK, Leviton L, Vespa H, Coon H, Longo N, Lundy BD, Johnson M, Angelino A, Hamosh A, Bilder D (2013 Jan). A diversified approach for PKU treatment: routine screening yields high incidence of psychiatric distress in phenylketonuria clinics. Mol Genet Metab, 108(1), 8-12.
  37. Bilder DA, Burton BK, Coon H, Leviton L, Ashworth J, Lundy BD, Vespa H, Bakian AV, Longo N (2013 Mar). Psychiatric symptoms in adults with phenylketonuria. Mol Genet Metab, 108(3), 155-60.
  38. Liu L, Sabo A, Neale BM, Nagaswamy U, Stevens C, Lim E, Bodea CA, Muzny D, Reid JG, Banks E, Coon H, Depristo M, Dinh H, Fennel T, Flannick J, Gabriel S, Garimella K, Gross S, Hawes A, Lewis L, Makarov V, Maguire J, Newsham I, Poplin R, Ripke S, Shakir K, Samocha KE, Wu Y, Boerwinkle E, Buxbaum JD, Cook EH Jr, Devlin B, Schellenberg GD, Sutcliffe JS, Daly MJ, Gibbs RA, Roeder K (2013 Apr). Analysis of rare, exonic variation amongst subjects with autism spectrum disorders and population controls. PLoS Genet, 9(4), e1003443.
  39. Scholand MB, Coon H, Wolff R, Cannon-Albright L (2013 Oct). Use of a genealogical database demonstrates heritability of pulmonary fibrosis. Lung, 191(5), 475-81.
  40. Lee SH, Ripke S, Neale BM, Faraone SV, Purcell SM, Perlis RH, Mowry BJ, Thapar A, Goddard ME, Witte JS, Absher D, Agartz I, Akil H, Amin F, Andreassen OA, Anjorin A, Anney R, Anttila V, Arking DE, Asherson P, Azevedo MH, Backlund L, Badner JA, Bailey AJ, Banaschewski T, Barchas JD, Barnes MR, Barrett TB, Bass N, Battaglia A, Bauer M, Bayes M, Bellivier F, Bergen SE, Berrettini W, Betancur C, Bettecken T, Biederman J, Binder EB, Black DW, Blackwood DH, Bloss CS, Boehnke M, Boomsma DI, Breen G, Breuer R, Bruggeman R, Cormican P, Buccola NG, Buitelaar JK, Bunney WE, Buxbaum JD, Byerley WF, Byrne EM, Caesar S, Cahn W, Cantor RM, Casas M, Chakravarti A, Chambert K, Choudhury K, Cichon S, Cloninger CR, Collier DA, Cook EH, Coon H, Cormand B, Corvin A, Coryell WH, Craig DW, Craig IW, Crosbie J, Cuccaro ML, Curtis D, Czamara D, Datta S, Dawson G, Day R, De Geus EJ, Degenhardt F, Djurovic S, Donohoe GJ, Doyle AE, Duan J, Dudbridge F, Duketis E, Ebstein RP, Edenberg HJ, Elia J, Ennis S, Etain B, Fanous A, Farmer AE, Ferrier IN, Flickinger M, Fombonne E, Foroud T, Frank J, Franke B, Fraser C, Freedman R, Freimer NB, Freitag CM, Friedl M, Frisen L, Gallagher L, Gejman PV, Georgieva L, Gershon ES, Geschwind DH, Giegling I, Gill M, Gordon SD, Gordon-Smith K, Green EK, Greenwood TA, Grice DE, Gross M, Grozeva D, Guan W, Gurling H, De Haan L, Haines JL, Hakonarson H, Hallmayer J, Hamilton SP, Hamshere ML, Hansen TF, Hartmann AM, Hautzinger M, Heath AC, Henders AK, Herms S, Hickie IB, Hipolito M, Hoefels S, Holmans PA, Holsboer F, Hoogendijk WJ, Hottenga JJ, Hultman CM, Hus V, Ingason A, Ising M, Jamain S, Jones EG, Jones I, Jones L, Tzeng JY, Kahler AK, Kahn RS, Kandaswamy R, Keller MC, Kennedy JL, Kenny E, Kent L, Kim Y, Kirov GK, Klauck SM, Klei L, Knowles JA, Kohli MA, Koller DL, Konte B, Korszun A, Krabbendam L, Krasucki R, Kuntsi J, Kwan P, Landen M, Langstrom N, Lathrop M, Lawrence J, Lawson WB, Leboyer M, Ledbetter DH, Lee PH, Lencz T, Lesch KP, Levinson DF, Lewis CM, Li J, Lichtenstein P, Lieberman JA, Lin DY, Linszen DH, Liu C, Lohoff FW, Loo SK, Lord C, Lowe JK, Lucae S, MacIntyre DJ, Madden PA, Maestrini E, Magnusson PK, Mahon PB, Maier W, Malhotra AK, Mane SM, Martin CL, Martin NG, Mattheisen M, Matthews K, Mattingsdal M, McCarroll SA, McGhee KA, McGough JJ, McGrath PJ, McGuffin P, McInnis MG, McIntosh A, McKinney R, McLean AW, McMahon FJ, McMahon WM, McQuillin A, Medeiros H, Medland SE, Meier S, Melle I, Meng F, Meyer J, Middeldorp CM, Middleton L, Milanova V, Miranda A, Monaco AP, Montgomery GW, Moran JL, Moreno-De-Luca D, Morken G, Morris DW, Morrow EM, Moskvina V, Muglia P, Muhleisen TW, Muir WJ, Muller-Myhsok B, Murtha M, Myers RM, Myin-Germeys I, Neale MC, Nelson SF, Nievergelt CM, Nikolov I, Nimgaonkar V, Nolen WA, Nothen MM, Nurnberger JI, Nwulia EA, Nyholt DR, ODushlaine C, Oades RD, Olincy A, Oliveira G, Olsen L, Ophoff RA, Osby U, Owen MJ, Palotie A, Parr JR, Paterson AD, Pato CN, Pato MT, Penninx BW, Pergadia ML, Pericak-Vance MA, Pickard BS, Pimm J, Piven J, Posthuma D, Potash JB, Poustka F, Propping P, Puri V, Quested DJ, Quinn EM, Ramos-Quiroga JA, Rasmussen HB, Raychaudhuri S, Rehnstrom K, Reif A, Ribases M, Rice JP, Rietschel M, Roeder K, Roeyers H, Rossin L, Rothenberger A, Rouleau G, Ruderfer D, Rujescu D, Sanders AR, Sanders SJ, Santangelo SL, Sergeant JA, Schachar R, Schalling M, Schatzberg AF, Scheftner WA, Schellenberg GD, Scherer SW, Schork NJ, Schulze TG, Schumacher J, Schwarz M, Scolnick E, Scott LJ, Shi J, Shilling PD, Shyn SI, Silverman JM, Slager SL, Smalley SL, Smit JH, Smith EN, Sonuga-Barke EJ, St Clair D, State M, Steffens M, Steinhausen HC, Strauss JS, Strohmaier J, Stroup TS, Sutcliffe JS, Szatmari P, Szelinger S, Thirumalai S, Thompson RC, Todorov AA, Tozzi F, Treutlein J, Uhr M, van den Oord EJ, Van Grootheest G, Van Os J, Vicente AM, Vieland VJ, Vincent JB, Visscher PM, Walsh CA, Wassink TH, Watson SJ, Weissman MM, Werge T, Wienker TF, Wijsman EM, Willemsen G, Williams N, Willsey AJ, Witt SH (2013 Sep). Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs. Nat Genet, 45(9), 984-94.
  41. Casey JP, Magalhaes T, Conroy JM, Regan R, Shah N, Anney R, Shields DC, Abrahams BS, Almeida J, Bacchelli E, Bailey AJ, Baird G, Battaglia A, Berney T, Bolshakova N, Bolton PF, Bourgeron T, Brennan S, Cali P, Correia C, Corsello C, Coutanche M, Dawson G, de Jonge M, Delorme R, Duketis E, Duque F, Estes A, Farrar P, Fernandez BA, Folstein SE, Foley S, Fombonne E, Freitag CM, Gilbert J, Gillberg C, Glessner JT, Green J, Guter SJ, Hakonarson H, Holt R, Hughes G, Hus V, Igliozzi R, Kim C, Klauck SM, Kolevzon A, Lamb JA, Leboyer M, Le Couteur A, Leventhal BL, Lord C, Lund SC, Maestrini E, Mantoulan C, Marshall CR, McConachie H, McDougle CJ, McGrath J, McMahon WM, Merikangas A, Miller J, Minopoli F, Mirza GK, Munson J, Nelson SF, Nygren G, Oliveira G, Pagnamenta AT, Papanikolaou K, Parr JR, Parrini B, Pickles A, Pinto D, Piven J, Posey DJ, Poustka A, Poustka F, Ragoussis J, Roge B, Rutter ML, Sequeira AF, Soorya L, Sousa I, Sykes N, Stoppioni V, Tancredi R, Tauber M, Thompson AP, Thomson S, Tsiantis J, Van Engeland H, Vincent JB, Volkmar F, Vorstman JA, Wallace S, Wang K, Wassink TH, White K, Wing K, Wittemeyer K, Yaspan BL, Zwaigenbaum L, Betancur C, Buxbaum JD, Cantor RM, Cook EH, Coon H, Cuccaro ML, Geschwind DH, Haines JL, Hallmayer J, Monaco AP, Nurnberger JI Jr, Pericak-Vance MA, Schellenberg GD, Scherer SW, Sutcliffe JS, Szatmari P, Vieland VJ, Wijsman EM, Green A, Gill M, Gallagher L, Vicente A, Ennis S (2012 Apr). A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder. Hum Genet, 131(4), 565-79.
  42. Marchani EE, Chapman NH, Cheung CY, Ankenman K, Stanaway IB, Coon HH, Nickerson D, Bernier R, Brkanac Z, Wijsman EM (2012). Identification of rare variants from exome sequence in a large pedigree with autism. Hum Hered, 74(3-4), 153-64.
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  94. Arnett DK, Miller MB, Coon H, Ellison RC, North KE, Province M, Leppert M, Eckfeldt JH (2004 Nov). Genome-wide linkage analysis replicates susceptibility locus for fasting plasma triglycerides: NHLBI Family Heart Study. Hum Genet, 115(6), 468-74.
  95. Hasstedt SJ, Camp NJ, Hopkins PN, Coon H, McKinney JT, Cawthon RM, Hunt SC (2004 Dec). Model-fitting and linkage analysis of sodium-lithium countertransport. Eur J Hum Genet, 12(12), 1055-61.
  96. Segurado R, Detera-Wadleigh SD, Levinson DF, Lewis CM, Gill M, Nurnberger JI Jr, Craddock N, DePaulo JR, Baron M, Gershon ES, Ekholm J, Cichon S, Turecki G, Claes S, Kelsoe JR, Schofield PR, Badenhop RF, Morissette J, Coon H, Blackwood D, McInnes LA, Foroud T, et al (2003). Genome scan meta-analysis of schizophrenia and bipolar disorder, part III: Bipolar disorder. Am J Hum Genet, 73, 49-62.
  97. Lewis CM, Levinson DF, Wise LH, DeLisi LE, Straub RE, Hovatta I, Williams NM, Schwab SG, Pulver AE, Faraone SV, Brzustowicz LM, Kaufmann CA, Garver DL, Gurling HM, Lindholm E, Coon H, Moises HW, et al (2003). Genome scan meta-analysis of schizophrenia and bipolar disorder, part II: Schizophrenia. Am J Hum Genet, 73, 34-48.
  98. Kim UK, Jorgenson E, Coon H, Leppert M, Risch N, Drayna D (2003 Feb 21). Positional cloning of the human quantitative trait locus underlying taste sensitivity to phenylthiocarbamide. Science, 299(5610), 1221-5.
  99. Drayna D, Coon H, Kim UK, Elsner T, Cromer K, Otterud B, Baird L, Peiffer AP, Leppert M (2003 May). Genetic analysis of a complex trait in the Utah Genetic Reference Project: a major locus for PTC taste ability on chromosome 7q and a secondary locus on chromosome 16p. Hum Genet, 112(5-6), 567-72.
  100. Camp NJ, Hopkins PN, Hasstedt SJ, Coon H, Malhotra A, Cawthon RM, Hunt SC (2003 Sep). Genome-wide multipoint parametric linkage analysis of pulse pressure in large, extended utah pedigrees. Hypertension, 42(3), 322-8.
  101. Bigler ED, Tate DF, Neeley ES, Wolfson LJ, Miller MJ, Rice SA, Cleavinger H, Anderson C, Coon H, Ozonoff S, Johnson M, Dinh E, Lu J, Mc Mahon W, Lainhart JE (2003 Nov-Dec). Temporal lobe, autism, and macrocephaly. AJNR Am J Neuroradiol, 24(10), 2066-76.
  102. Drayna D, Kim UK, Coon H, Jorgenson E, Risch N, Leppert M (2003). A model system for identifying genes underlying complex traits. Cold Spring Harb Symp Quant Biol, 68, 365-71.
  103. Kronenberg F, Coon H, Ellison RC, Borecki I, Arnett DK, Province MA, Eckfeldt JH, Hopkins PN, Hunt SC (2002). Segregation analysis of HDL cholesterol in the NHLBI Family Heart Study and in Utah pedigrees. Eur J Hum Genet, 10, 367-374.
  104. Kronenberg F, Coon H, Gutin A, Abkevich V, Samuels ME, Ballinger DG, Hopkins PN, Hunt SC (2002 Sep). A genome scan for loci influencing anti-atherogenic serum bilirubin levels. Eur J Hum Genet, 10(9), 539-46.
  105. Coon H, Eckfeldt JH, Leppert MF, Myers RH, Arnett DK, Heiss G, Province MA, Hunt SC (2002 Sep). A genome-wide screen reveals evidence for a locus on chromosome 11 influencing variation in LDL cholesterol in the NHLBI Family Heart Study. Hum Genet, 111(3), 263-9.
  106. Hunt SC, Hasstedt SJ, Coon H, Camp NJ, Cawthon RM, Wu LL, Hopkins PN (2002 Oct). Linkage of creatinine clearance to chromosome 10 in Utah pedigrees replicates a locus for end-stage renal disease in humans and renal failure in the fawn-hooded rat. Kidney Int, 62(4), 1143-8.
  107. Hobbs MR, Udhayakumar V, Levesque MC, Booth J, Roberts JM, Tkachuk AN, Pole A, Coon H, Kariuki S, Nahlen BL, Mwaikambo ED, Lal AL, Granger DL, Anstey NM, Weinberg JB (2002 Nov 09). A new NOS2 promoter polymorphism associated with increased nitric oxide production and protection from severe malaria in Tanzanian and Kenyan children. Lancet, 360(9344), 1468-75.
  108. Lainhart JE, Ozonoff S, Coon H, Krasny L, Dinh E, Nice J, McMahon W (2002 Dec 01). Autism, regression, and the broader autism phenotype. Am J Med Genet, 113(3), 231-7.
  109. McDowell JE, Brenner CA, Myles-Worsley M, Coon H, Byerley W, Clementz BA (2001 Jan). Ocular motor delayed-response task performance among patients with schizophrenia and their biological relatives. Psychophysiology, 38(1), 153-6.
  110. Camp NJ, Neuhausen SL, Tiobech J, Polloi A, Coon H, Myles-Worsley M (2001 Dec). Genomewide multipoint linkage analysis of seven extended Palauan pedigrees with schizophrenia, by a Markov-chain Monte Carlo method. Am J Hum Genet, 69(6), 1278-89.
  111. Peacock JM, Arnett DK, Atwood LD, Myers RH, Coon H, Rich SS, Province MA, Heiss G (2001 Nov). Genome scan for quantitative trait loci linked to high-density lipoprotein cholesterol: The NHLBI Family Heart Study. Arterioscler Thromb Vasc Biol, 21(11), 1823-8.
  112. Coon H, Leppert MF, Eckfeldt JH, Oberman A, Myers RH, Peacock JM, Province MA, Hopkins PN, Heiss G (2001 Dec). Genome-wide linkage analysis of lipids in the Hypertension Genetic Epidemiology Network (HyperGEN) Blood Pressure Study. Arterioscler Thromb Vasc Biol, 21(12), 1969-76.
  113. Lehman DM, Sponsel WE, Stratton RF, Mensah J, Macdonald JC, Johnson-Pais TL, Coon H, Reveles XT, Cody JD, Leach RJ (2001 Jun 15). Genetic mapping of a novel X-linked recessive colobomatous microphthalmia. Am J Med Genet, 101(2), 114-9.
  114. Bennett PJ, McMahon WM, Watabe J, Achilles J, Bacon M, Coon H, Grey T, Keller T, Tate D, Tcaciuc I, Workman J, Gray D (2000 Mar). Tryptophan hydroxylase polymorphisms in suicide victims. Psychiatr Genet, 10(1), 13-7.
  115. Bennett PJ, Hoff M, Rosenthal J, Zhao M, Coon H, Myles-Worsley M, Byerley WF (2000 Jun). Mutation screening of a neutral amino acid transporter, ASCT1, and its potential role in schizophrenia. Psychiatr Genet, 10(2), 79-82.
  116. Coon H, Myers RH, Borecki IB, Arnett DK, Hunt SC, Province MA, Djousse L, Leppert MF (2000 Oct). Replication of linkage of familial combined hyperlipidemia to chromosome 1q with additional heterogeneous effect of apolipoprotein A-I/C-III/A-IV locus. The NHLBI Family Heart Study. Arterioscler Thromb Vasc Biol, 20(10), 2275-80.
  117. McDowell JE, Myles-Worsley M, Coon H, Byerley W, Clementz B (2000). Antisaccade performance as an endophenotype for schizophrenia: A transcultural replication. Neuropsychobiology.
  118. Djousse L, Myers RH, Coon H, Arnett DK, Province MA, Ellison RC (2000 Aug). Smoking influences the association between apolipoprotein E and lipids: the National Heart, Lung, and Blood Institute Family Heart Study. Lipids, 35(8), 827-31.
  119. Hobbs MR, Pole AR, Pidwirny GN, Rosen IB, Zarbo RJ, Coon H, Heath H 3rd, Leppert M, Jackson CE (1999 Feb). Hyperparathyroidism-jaw tumor syndrome: the HRPT2 locus is within a 0.7-cM region on chromosome 1q. Am J Hum Genet, 64(2), 518-25.
  120. Myles-Worsley M, Coon H, Tiobech J, Collier J, Dale P, Wender P, Reimherr F, Polloi A, Byerley W (1999 Feb 05). Genetic epidemiological study of schizophrenia in Palau, Micronesia: prevalence and familiality. Am J Med Genet, 88(1), 4-10.
  121. McDowell JE, Myles-Worsley M, Coon H, Byerley W, Clementz BA (1999 Jan). Measuring liability for schizophrenia using optimized antisaccade stimulus parameters. Psychophysiology, 36(1), 138-41.
  122. Myles-Worsley M, Coon H, McDowell J, Brenner C, Hoff M, Lind B, Bennett P, Freedman R, Clementz B, Byerley W (1999 Oct 15). Linkage of a composite inhibitory phenotype to a chromosome 22q locus in eight Utah families. Am J Med Genet, 88(5), 544-50.
  123. Coon H, Leppert MF, Kronenberg F, Province MA, Myers RH, Arnett DK, Eckfeldt JH, Heiss G, Williams RR, Hunt SC (1999 Sep). Evidence for a major gene accounting for mild elevation in LDL cholesterol: the NHLBI Family Heart Study. Ann Hum Genet, 63(Pt 5), 401-12.
  124. Cody JD, Reveles XT, Hale DE, Lehman D, Coon H, Leach RJ (1999 Nov). Haplosufficiency of the melancortin-4 receptor gene in individuals with deletions of 18q. Hum Genet, 105(5), 424-7.
  125. Bennett P, Coon H, Lenox RH, Hoff M, Rosenthal J, Byerley W (1999 Mar). Tests for linkage to MDI with a new trinucleotide repeat polymorphism in the 80K-H gene on chromosome 19. Psychiatr Genet, 9(1), 39-42.
  126. Myles-Worsley M, Coon H, Byerley W (1998 May 25). The sensitivity of the Spontaneous Selective Attention Test (SSAT): a study of schizophrenic inpatients and outpatients versus normal controls. Schizophr Res, 31(2-3), 131-9.
  127. Coon H, Myles-Worsley M, Tiobech J, Hoff M, Rosenthal J, Bennett P, Reimherr F, Wender P, Dale P, Polloi A, Byerley W (1998 Nov). Evidence for a chromosome 2p13-14 schizophrenia susceptibility locus in families from Palau, Micronesia. Mol Psychiatry, 3(6), 521-7.
  128. Jensen J, Coon H, Hoff M, Rosenthal J, Reimherr F, Wender P, Myles-Worsley M, Freedman R, Byerley W (1998 Winter). Search for a schizophrenia susceptibility gene on chromosome 13. Psychiatr Genet, 8(4), 239-43.
  129. Lind B, Hoff M, Rosenthal J, Byerley W, Coon H (1998). Analysis of chromosome 6 markers in 8 Utah schizophrenia pedigrees. Psychiatr Genet, 8, 171-173.
  130. Lind B, Hoff M, Rosenthal J, Byerley W, Coon H (1998 Autumn). Analysis of chromosome 6 markers in eight Utah schizophrenia pedigrees. Psychiatr Genet, 8(3), 171-3.
  131. Freedman R, Coon H, Myles-Worsley M, Orr-Urtreger A, Olincy A, Davis A, Polymeropoulos M, Holik J, Hopkins J, Hoff M, Rosenthal J, Waldo MC, Reimherr F, Wender P, Yaw J, Young DA, Breese CR, Adams C, Patterson D, Adler LE, Kruglyak L, Leonard S, Byerley W (1997 Jan 21). Linkage of a neurophysiological deficit in schizophrenia to a chromosome 15 locus. Proc Natl Acad Sci U S A, 94(2), 587-92.
  132. Lainhart JE, Piven J, Wzorek M, Landa R, Santangelo SL, Coon H, Folstein SE (1997 Feb). Macrocephaly in children and adults with autism. J Am Acad Child Adolesc Psychiatry, 36(2), 282-90.
  133. Myles-Worsley M, Coon H (1997 Aug 08). Genetic and developmental factors in spontaneous selective attention: a study of normal twins. Psychiatry Res, 71(3), 163-74.
  134. Yaw J, Myles-Worsley M, Hoff M, Holik J, Freedman R, Byerley W, Coon H (1996 Spring). Anticipation in multiplex schizophrenia pedigrees. Psychiatr Genet, 6(1), 7-11.
  135. Myles-Worsley M, Coon H, Byerley W, Waldo M, Young D, Freedman R (1996 Feb 15). Developmental and genetic influences on the P50 sensory gating phenotype. Biol Psychiatry, 39(4), 289-95.
  136. Coon H, Hoff M, Holik J, Hadley D, Fang N, Reimherr F, Wender P, Byerley W (1996 Apr 15). Analysis of chromosome 18 DNA markers in multiplex pedigrees with manic depression. Biol Psychiatry, 39(8), 689-96.
  137. McMahon WM, van de Wetering BJ, Filloux F, Betit K, Coon H, Leppert M (1996 May). Bilineal transmission and phenotypic variation of Tourette's disorder in a large pedigree. J Am Acad Child Adolesc Psychiatry, 35(5), 672-80.
  138. Coon H, Schizophrenia Collaborative Linkage Group for Chromosome 3, 6, and 8, et al (1996). Support for schizophrenia linkage findings on chromosomes 6 and 8: a multicenter study. Am J Med Genet B Neuropsychiatr Genet, 67, 580-594.
  139. Gill M, Vallada H, Collier D, Sham P, Holmans P, Murray R, McGuffin P, Nanko S, Owen M, Antonarakis S, Housman D, Kazazian H, Nestadt G, Pulver AE, Straub RE, MacLean CJ, Walsh D, Kendler KS, DeLisi L, Polymeropoulos M, Coon H, Byerley W, Lofthouse R, Gershon E, Read CM, et al (1996 Feb 16). A combined analysis of D22S278 marker alleles in affected sib-pairs: support for a susceptibility locus for schizophrenia at chromosome 22q12. Schizophrenia Collaborative Linkage Group (Chromosome 22). Am J Med Genet, 67(1), 40-5.
  140. Fang N, Coon H, Hoff M, Holik J, Hadley D, Reimherr F, Wender P, Myles-Worsley M, Waldo M, Freedman R, et al (1995 Spring). Search for a schizophrenia susceptibility gene on chromosome 18. Psychiatr Genet, 5(1), 31-5.
  141. Byerley W, Hoff M, Holik J, Myles-Worsley M, Waldo M, Freedman R, Coon H (1995 Jan-Feb). Linkage analysis between schizophrenia and index simple-sequence repeat loci for chromosome 21. Hum Hered, 45(1), 49-52.
  142. Shah M, Coon H, Holik J, Hoff M, Helmer V, Panos P, Byerley W (1995 Apr 24). Mutation scan of the D1 dopamine receptor gene in 22 cases of bipolar I disorder. Am J Med Genet, 60(2), 150-3.
  143. Hadley D, Hoff M, Holik J, Reimherr F, Wender P, Coon H, Byerley W (1995 May-Jun). Manic-depression and the norepinephrine transporter gene. Hum Hered, 45(3), 165-8.
  144. Byerley W, Bailey M, Hicks AA, Riley BP, Darlison MG, Holik J, Hoff M, Umar F, ReimherrF, Wender P, Myles-Worsley M, Waldo M, Freedman R, Johnson KJ, Coon H (1995). Schizophrenia and GABAA receptor subunit genes. Psychiatr Genet, 5, 23-9.
  145. Daviss WB, Coon H, Whitehead P, Ryan K, Burkley M, McMahon W (1995 Dec). Predicting diabetic control from competence, adherence, adjustment, and psychopathology. J Am Acad Child Adolesc Psychiatry, 34(12), 1629-36.
  146. Byerley W, Holik J, Hoff M, Coon H (1995 Jun 19). Search for a gene predisposing to manic-depression on chromosome 21. Am J Med Genet, 60(3), 231-3.
  147. Pariseau C, Gregor P, Myles-Worsley M, Holik J, Hoff M, Waldo M, Freedman R, Coon H, Byerley W (1994 Fall). Schizophrenia and glutamate receptor genes. Psychiatr Genet, 4(3), 161-5.
  148. Coon H, Hicks AA, Bailey ME, Hoff M, Holik J, Harvey RJ, Johnson KJ, Darlison MG, Reimherr F, Wender P, et al (1994 Fall). Analysis of GABAA receptor subunit genes in multiplex pedigrees with manic depression. Psychiatr Genet, 4(3), 185-91.
  149. Coon H, Jensen S, Holik J, Hoff M, Myles-Worsley M, Reimherr F, Wender P, Waldo M, Freedman R, Leppert M, et al (1994 Mar 15). Genomic scan for genes predisposing to schizophrenia. Am J Med Genet, 54(1), 59-71.
  150. Coon H, Holik J, Hoff M, Reimherr F, Wender P, Myles-Worsley M, Waldo M, Freedman R, Byerley W (1994 Mar 15). Analysis of chromosome 22 markers in nine schizophrenia pedigrees. Am J Med Genet, 54(1), 72-9.
  151. Coon H, Sobell J, Heston L, Sommer S, Hoff M, Holik J, Umar F, Robertson M, Reimherr F, Wender P, et al (1994 Mar 15). Search for mutations in the beta 1 GABAA receptor subunit gene in patients with schizophrenia. Am J Med Genet, 54(1), 12-20.
  152. Kasapi M, Holik J, Shah M, Hoff M, Coon H, Byerley W (1994 Aug). SSCP at the HTR1DA locus. Hum Mol Genet, 3(8), 1444.
  153. Byerley W, Hoff M, Holik J, Coon H (1994 Fall). A linkage study with D5 dopamine and alpha 2C-adrenergic receptor genes in six multiplex bipolar pedigrees. Psychiatr Genet, 4(3), 121-4.
  154. Ravindranathan A, Coon H, DeLisi L, Holik J, Hoff M, Brown A, Shields G, Crow T, Byerley W (1994 Summer). Linkage analysis between schizophrenia and a microsatellite polymorphism for the D5 dopamine receptor gene. Psychiatr Genet, 4(2), 77-80.
  155. Gregor P, Hoff M, Holik J, Hadley D, Fang N, Coon H, Byerley W (1994 Dec). Dinucleotide repeat polymorphism in the human taurine transporter gene (TAUT). Hum Mol Genet, 3(12), 2263.
  156. Polymeropoulos MH, Coon H, Byerley W, Gershon ES, Goldin L, Crow TJ, Rubenstein J, Hoff M, Holik J, Smith AM, et al (1994 Jun 15). Search for a schizophrenia susceptibility locus on human chromosome 22. Am J Med Genet, 54(2), 93-9.
  157. Jensen S, Plaetke R, Holik J, Hoff M, Myles-Worsley M, Leppert M, Coon H, Vest K, Freedman R, Waldo M, et al (1993 Jan-Feb). Linkage analysis of schizophrenia: the D1 dopamine receptor gene and several flanking DNA markers. Hum Hered, 43(1), 58-62.
  158. Coon H, Byerley W, Holik J, Hoff M, Myles-Worsley M, Lannfelt L, Sokoloff P, Schwartz JC, Waldo M, Freedman R, et al (1993 Feb). Linkage analysis of schizophrenia with five dopamine receptor genes in nine pedigrees. Am J Hum Genet, 52(2), 327-34.
  159. Coon H, Hoff M, Holik J, Delisi LE, Crowe T, Freedman R, Shields G, Boccio AM, Lerman M, Gershon ES, et al (1993 May 01). C to T nucleotide substitution in codon 713 of amyloid precursor protein gene not found in 86 unrelated schizophrenics from multiplex families. Am J Med Genet, 48(1), 36-9.
  160. Coon H, Jensen S, Hoff M, Holik J, Plaetke R, Reimherr F, Wender P, Leppert M, Byerley W (1993 Jun). A genome-wide search for genes predisposing to manic-depression, assuming autosomal dominant inheritance. Am J Hum Genet, 52(6), 1234-49.
  161. Coon H, Plaetke R, Holik J, Hoff M, Myles-Worsley M, Waldo M, Freedman R, Byerley W (1993 Sep 01). Use of a neurophysiological trait in linkage analysis of schizophrenia. Biol Psychiatry, 34(5), 277-89.
  162. Byerley W, Coon H, Hoff M, Holik J, Waldo M, Freedman R, Caron MG, Giros B (1993 Sep-Oct). Human dopamine transporter gene not linked to schizophrenia in multigenerational pedigrees. Hum Hered, 43(5), 319-22.
  163. Coon H, Carey G, Fulker DW, DeFries JC (1993). Influences of school environment on the achievement scores of adopted and nonadopted first grade children. Intelligence, 17, 79-104.
  164. Coon H, Carey G, Fulker DW (1992). Community influences on cognitive ability. Intelligence, 16, 169-188.
  165. Coon H, Carey G, Corley R, Fulker DW (1992 May). Identifying children in the Colorado Adoption Project at risk for conduct disorder. J Am Acad Child Adolesc Psychiatry, 31(3), 503-11.
  166. Plomin R, Coon H, Carey G, DeFries JC, Fulker DW (1991 Dec). Parent-offspring and sibling adoption analyses of parental ratings of temperament in infancy and childhood. J Pers, 59(4), 705-32.
  167. Coon H, Carey G, Fulker DW (1990 May). A simple method of model fitting for adoption data. Behav Genet, 20(3), 385-404.
  168. Coon H, Carey G (1989 Mar). Genetic and environmental determinants of musical ability in twins. Behav Genet, 19(2), 183-93.

Review

  1. Coon H (2006 Feb 15). Current perspectives on the genetic analysis of autism. [Review]. Am J Med Genet C Semin Med Genet, 142C(1), 24-32.
  2. Ramig LO, Gray S, Baker K, Corbin-Lewis K, Buder E, Luschei E, Coon H, Smith M (2001 Sep-Oct). The aging voice: a review, treatment data and familial and genetic perspectives. [Review]. Folia Phoniatr Logop, 53(5), 252-65.
  3. Leonard S, Adams C, Breese CR, Adler LE, Bickford P, Byerley W, Coon H, Griffith JM, Miller C, Myles-Worsley M, Nagamoto HT, Rollins Y, Stevens KE, Waldo M, Freedman R (1996). Nicotinic receptor function in schizophrenia. [Review]. Schizophr Bull, 22(3), 431-45.
  4. Freedman R, Adler LE, Bickford P, Byerley W, Coon H, Cullum CM, Griffith JM, Harris JG, Leonard S, Miller C, et al (1994 Nov-Dec). Schizophrenia and nicotinic receptors. [Review]. Harv Rev Psychiatry, 2(4), 179-92.

Book Chapter

  1. Coon, H (1999). New techniques in the genetic analysis of complex illness. In JR Botkin, WM McMahon, LP Francis (Eds.), Genetics and Criminality. Washington, D.C.: American Psychological Association.
  2. Coon H (1997). Genetic analysis of complex diseases. In Labuda MC, Grigorenko EL (Eds.), On the Way to Individuality. Commack: Nova.
  3. Freedman R, Leonard S, Adler L, Bickford P, Byerley W, Coon H, Miller C, Luntz-Leybman V, Myles-Worsley M, Nagamoto H, Rose G, Stevens K, Waldo M (1997). Nicotinic receptors and the pathophysiology of schizophrenia. In Clarke P, Quick M (Eds.), The Effects of Nicotine on Biological Systems. Basel: Birkhauser-Verlag.
  4. Byerley W, Coon H (1995). Strategies to identify genes for schizophrenia. In Oldham JM, Riba MB (Eds.), Review of Psychiatry (pp. 361-381). Washington, D.C.: American Psychiatric Press.

Letter

  1. Wang S, Detera-Wadleigh SD, Coon H, Sun CE, Goldin LR, Duffy DL, Byerley WF, Gershon ES, Diehl SR (1996 Sep). Evidence of linkage disequilibrium between schizophrenia and the SCa1 CAG repeat on chromosome 6p23 [Letter to the editor]. Am J Hum Genet, 59(3), 731-6.

Abstract

  1. Coon H, Matsunami N, Stevens J, Miller J, Pingree C, Krasny L, Lainhart J, Leppert MF, McMahon, WM (In Press). Evidence for linkage on chromosome 3q25-27 in a large autism extended pedigree [Abstract]. Hum Hered, 60(4), 220-6.
  2. Weis KA, Arnett DK, Tsai MY, Coon H, Heiss G, Atwood LD, Hong Y (2002). Genome scans for apolipoproteins A-1 and B in the NHLBI Family Heart Study (FHS) [Abstract]. Am J Hum Genet, 69, A2025.
  3. Lin JP, Sholinsky P, Coon H, Hunt SC, Myres RH, Arnett DK, Hong Y (2001). Linkage between cholesterol 7 alpha hydroxylase (CYP7) gene and low-density lipoprotein cholesterol (LDL-C) in increased CHD risk Caucasian families-the NHLBI Family Heart Study [Abstract]. Am J Hum Genet, 69, A2055.
  4. Peacock JM, Arnett KD, Atwood LD, Myers RH, Province MA, Coon H, Rich SS, Heiss G (2000). Full genome scan of HDL-cholesterol in the NHLBI Family Heart Study (FHS) [Abstract]. Am J Hum Genet, 67, A1684.
  5. Neklason DW, Otterud BE, Coon H, Hunt SC, Metherall JE (2000). Multidrug resistance (MDR) genetic locus influences circulating triglyceride levels in a population with coronary heart disease [Abstract]. Am J Hum Genet, 67, A1913.
  6. Leppert MF, Coon H, Borecki I, Arnett DK, Hunt SC, Province MA, Djousse L, Myers RH (1999). Analysis of familial combined hyperlipidemia with chromosome 1q21-23 markers and the APOAI/CIII/AIV gene cluster in the NHLBI Family Heart Study [Abstract]. Am J Hum Genet, 65, A2594.
  7. Lewis CE, Arnett DK, Borecki I, Coon H, Ellison RC, Hunt S, Oberman A, Rich S, Province MA (1999). Genome-wide linkage analysis of human fatness: The HyperGEN Blood Pressure Study [Abstract]. Am J Hum Genet, 65, A1150.
  8. Fisher KA, Arnett DK, Atwood L, Hunt S, Coon H, Province M, Rao DC, Myers R, Oberman A, Lewis CE (1999). A genome-wide linkage analysis in hypertensive African American and White siblings for loci that influence variation in pulse pressure: The HyperGEN network of the Family Blood Pressure Program [Abstract]. Am J Hum Genet, 65, A1113.
  9. Feitosa M, Borecki I, Hunt S, Coon H, Ellison C, Arnett D, Heiss G, Eckfeldt J, Province M (1999). Evidence for a second major gene for APO-A1 beyond the AI/CIII/AIV gene cluster: the NHLBI Family Heart Study (FHS) [Abstract]. Am J Hum Genet, 65, A84.
  10. Lehman DM, Stratton RF, Mensah JM, Sponsel WE, Coon H, Leach RJ (1998). Apparent X-linked colobomatous microphthalmia [Abstract]. Am J Hum Genet, 63, A111.
  11. Coon H, Leppert MF, Province MA, Myers RH, Arnett DK, Heiss G, Williams RR, Hunt SC (1998). Evidence for a major gene unlinked to the LDL receptor accounting for mild elevation in LDL cholesterol: The NHLBI Family Heart Study [Abstract]. American Journal of Human Genetics, 63, A285.
  12. Myles-Worsley M, McDowell J, Clementz B, Hasstedt S, Byerley W, Coon H (1997). Cosegregation of a neurophysiological inhibitory dysfunction and schizophrenia in large multiplex families in Palau, Micronesia [Abstract]. Neuropsychiatric Genetics, 74, 599.
  13. McDowell JE, Coon H, Myles-Worsley M, Clementz BA, Byerley W (1997). Linkage analysis of antisaccade performance among schizophrenia pedigrees [Abstract]. Neuropsychiatric Genetics, 74, 599.
  14. Coon H, Myles-Worsley m, James S, Tiobech J, Polloi A, Byerley W (1997). Anticipation for schizophrenia in the isolated population of Palau, Micronesia [Abstract]. Neuropsychiat Genet, 74, 607.
  15. Coon H, Myles-Worsley M, Hasstedt SJ, Freedman R, Tiobech J, Polloi A, McDowell JE, Clementz BA, Byerley W (1997). Using correlated physiological abnormalities to create a sensitive phenotype for detecting schizophrenia susceptibility genes [Abstract]. Neuropsychiatric Genetics, 74, 596.
  16. Clementz BA, McDowell JE, Brenner C, Coon H, Byerley W, Myles-Worsley M (1997). Measures of eye movement performance for identifying unaffected gene carriers in schizophrenia pedigrees [Abstract]. Neuropsychiatric Genetics, 74, 595.
  17. Byerley W, Polloi A, Dale P, Hoff M, Rosenthal J, Tiobech J, Reimherr F, Wender P, Myles-Worsley M, Coon H (1997). Genome-wide linkage analysis of a large schizophrenia pedigree ascertained from Palau, Micronesia [Abstract]. Neuropsychiatric Genetics, 74, 559.
  18. Leppert M, Peiffer A, Snyder B, van de Wetering BJM, Filoux F, Coon H, McMahon WM (1996). Two loci of interest in a family with Tourette syndrome [Abstract]. Am J Hum Genet, 59[Suppl], 225.
  19. Leonard S, Byerley W, Myles-Worsley M, Orr-Urtreger A, Olincy A, Polymeropoulos M, Holik J, Hopkins J, Hoff M, Rosenthal J, Waldo MC, Reimherr F, Wender P, Yaw J, Young DA, Breese CR, Adams C, Patterson D, Adler LE, Krugyak L, Freedman R, Coon H (1996). Linkage of a chromosome 15 locus to a neurophysiological deficit in schizophrenia [Abstract]. Am J Hum Genet, 59[Suppl], 225.
  20. Byerley W, Polloi A, Myles-Worsley M, Hoff M, Rosenthal J, Yaw J, Reimherr F, Wender P, Dale P, Coon H (1996). Strategies for mapping a schizophrenia gene in the isolated population of Palau, Micronesia [Abstract]. Am J Hum Genet, 59[Suppl], 214.
  21. Coon H, Myles-Worsley M, Hoff M, Rosenthal J, Yaw J, Dale P, Reimherr F, Wender P, Polloi A, Byerley W (1996). Segregation and genetic anticipation of schizophrenia in the isolated population of Palau, Micronesia [Abstract]. Am J Hum Genet, 59[Suppl], 215.
  22. Myles-Worsley M, Coon H, Polloi A, Tiobech J, Hoff M, Rosenthal J, Yaw J, Byerley W (1996). A genetic study of schizophrenia in Palau, Micronesia [Abstract]. Psychiatr Genet, 6, 171.
  23. Wang S, Detera-Wadleigh S, Coon H, Sun C, Goldin LR, Byerley W, Gershon ES, Diehl SR (1995). Further evidence for a susceptibility locus for schizophrenia on chromosome 6p23 [Abstract]. Am J Hum Genet, 57[Suppl], 177.
  24. McMahon WM, Peiffer A, Coon H, Filloux F, van de Wetering BJM, Lepper M (1995). Validation of a quantitative measure for genetic studies of Tourette's syndrome [Abstract]. Psychiatr Genet, 5, S107.
  25. Moises HW, Kristbjarnarson H, Yang L, Wiese C, Arolt V, Schwinger E, Macciardi F, Blackwood, D, Coon H, Byerley W, Aschauer H, Sjogren B, Kennedy JL, Kidd KK, Wetterberg L, Gottesman II, Helgason T (1995). A two-stage genome-wide search for schizophrenia susceptibility genes [Abstract]. Psychiatr Genet, 5, S33.
  26. Coon H, Myles-Worsley M, Waldo M, Holik J, Hoff M, Yaw J, Dale P, Polloi A, Freedman R, Byerley W (1995). Segregation, linkage, and linkage disequilibrium analysis of Micronesian schizophrenia families [Abstract]. Psychiatr Genet, 5, S49.
  27. Myles-Worsley M, Coon H, Waldo M, Polloi A, Freedman R, Byerley W (1994). Genetic study of schizophrenia in large multiplex clans in Palau, Micronesia [Abstract]. Schizophr Bull.
  28. Myles-Worsley M, Yaw J, Coon H, Byerley W, Freedman R (1994). P50 sensory gating in children of multiplex schizophrenia families [Abstract]. Schizophr Bull.
  29. Nelson A, Yaw J, Holik J, Hoff M, Myles-Worsley M, Waldo M, Freedman R, Byerley W, Coon H (1994). Anticipation in multiplex schizophrenia families [Abstract]. Schizophr Bull.
  30. Diehl SR, Wang S, Detera-Wadleigh S, Coon H, Sun C, Goldin LR, Walczak C, Pickar D, DeLisis LE, Byerley W, Gershon ES (1994). Evidence suggesting possible SCA1 gene involvement in schizophrenia [Abstract]. Am J Hum Genet, 55[Suppl], 867.
  31. Polymeropoulos MH, Coon H, Byerley W, Gershon ES, Crow T, Delisi L, Merril CR (1993). Search for a schizophrenia locus on chromosome 22 [Abstract]. Psychiatr Genet, 3, 126.
  32. Waldo MC, Myles-Worsley M, Coon H, Byerley W, Polloi A, Freedman R (1993). Familial schizophrenia in a Micronesian population [Abstract]. Psychiatr Genet, 3, 117.
  33. Byerley W, Holik J, Hoff M, Myles-Worsley M, Waldo M, Freedman R, Leppert M, Coon H (1993). Strategies to identify genes for complex diseases [Abstract]. Psychiatr Genet, 3, 125.
  34. Coon H, Holik J, Hoff M, Myles-Worsley M, Waldo M, Freedman R, Byerley W (1993). Neurophysiological variables in linkage analysis of schizophrenia [Abstract]. Schizophr Res, 9, 116.
  35. Elliott AJ, Carey G, Coon H, Cardon L, Fulker DW (1991). Adolescent substance abuse: A family study [Abstract]. Behavior Genetics, 21, 567.
  36. Corley R, Coon H (1991). Resemblance for TV viewing and other interests at age 7 in adoptive and nonadoptive siblings [Abstract]. Behav Genet, 21, 567.
  37. Coon H, Corley R, Carey G (1991). Identifying boys at risk for conduct disorder in the Colorado Adoption Project [Abstract]. Behavior Genetics, 21, 567.
  38. Coon H, Carey G (1991). A multifactorial model of cultural transmission [Abstract]. Behav Genet, 21, 566.
  39. Coon H, Lewark T, Carey G (1990). Influences of the neighborhood environment on the cognitive development of adopted and nonadopted children in the Colorado Adoption Project [Abstract]. Behav Genet, 20, 712.
  40. Coon H (1989). Environmental transmission in adoptive families: Alternative models [Abstract]. Behav Genet, 19, 750.
  41. Coon H, Carey G (1988). Systematic rating bias of childhood temperament: Effect on behavior genetic data [Abstract]. Behavior Genetics, 18, 711.
  42. Coon H, Carey G (1987). Twins and musical ability: An analysis of if-then relationships [Abstract]. Behav Genet, 17, 620.

Other

  1. Levinson DF, Coon H (1998 Summer). Chromosome 22 workshop. Psychiatr Genet (8(2), pp. 115-20). England.