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Cathy Barr

TitleSenior Scientist
InstitutionThe Hospital for Sick Children
DepartmentNeurosciences & Mental Health
Address555 University Avenue
Toronto ON M5G 1X8
Phone416-813-1500
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    Collapse Bibliographic 
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    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Faculty can login to make corrections and additions.
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    1. Anttila V, Bulik-Sullivan B, Finucane HK, Walters RK, Bras J, Duncan L, Escott-Price V, Falcone GJ, Gormley P, Malik R, Patsopoulos NA, Ripke S, Wei Z, Yu D, Lee PH, Turley P, Grenier-Boley B, Chouraki V, Kamatani Y, Berr C, Letenneur L, Hannequin D, Amouyel P, Boland A, Deleuze JF, Duron E, Vardarajan BN, Reitz C, Goate AM, Huentelman MJ, Kamboh MI, Larson EB, Rogaeva E, St George-Hyslop P, Hakonarson H, Kukull WA, Farrer LA, Barnes LL, Beach TG, Demirci FY, Head E, Hulette CM, Jicha GA, Kauwe JSK, Kaye JA, Leverenz JB, Levey AI, Lieberman AP, Pankratz VS, Poon WW, Quinn JF, Saykin AJ, Schneider LS, Smith AG, Sonnen JA, Stern RA, Van Deerlin VM, Van Eldik LJ, Harold D, Russo G, Rubinsztein DC, Bayer A, Tsolaki M, Proitsi P, Fox NC, Hampel H, Owen MJ, Mead S, Passmore P, Morgan K, Nöthen MM, Rossor M, Lupton MK, Hoffmann P, Kornhuber J, Lawlor B, McQuillin A, Al-Chalabi A, Bis JC, Ruiz A, Boada M, Seshadri S, Beiser A, Rice K, van der Lee SJ, De Jager PL, Geschwind DH, Riemenschneider M, Riedel-Heller S, Rotter JI, Ransmayr G, Hyman BT, Cruchaga C, Alegret M, Winsvold B, Palta P, Farh KH, Cuenca-Leon E, Furlotte N, Kurth T, Ligthart L, Terwindt GM, Freilinger T, Ran C, Gordon SD, Borck G, Adams HHH, Lehtimäki T, Wedenoja J, Buring JE, Schürks M, Hrafnsdottir M, Hottenga JJ, Penninx B, Artto V, Kaunisto M, Vepsäläinen S, Martin NG, Montgomery GW, Kurki MI, Hämäläinen E, Huang H, Huang J, Sandor C, Webber C, Muller-Myhsok B, Schreiber S, Salomaa V, Loehrer E, Göbel H, Macaya A, Pozo-Rosich P, Hansen T, Werge T, Kaprio J, Metspalu A, Kubisch C, Ferrari MD, Belin AC, van den Maagdenberg AMJM, Zwart JA, Boomsma D, Eriksson N, Olesen J, Chasman DI, Nyholt DR, Avbersek A, Baum L, Berkovic S, Bradfield J, Buono R, Catarino CB, Cossette P, De Jonghe P, Depondt C, Dlugos D, Ferraro TN, French J, Hjalgrim H, Jamnadas-Khoda J, Kälviäinen R, Kunz WS, Lerche H, Leu C, Lindhout D, Lo W, Lowenstein D, McCormack M, Møller RS, Molloy A, Ng PW, Oliver K, Privitera M, Radtke R, Ruppert AK, Sander T, Schachter S, Schankin C, Scheffer I, Schoch S, Sisodiya SM, Smith P, Sperling M, Striano P, Surges R, Thomas GN, Visscher F, Whelan CD, Zara F, Heinzen EL, Marson A, Becker F, Stroink H, Zimprich F, Gasser T, Gibbs R, Heutink P, Martinez M, Morris HR, Sharma M, Ryten M, Mok KY, Pulit S, Bevan S, Holliday E, Attia J, Battey T, Boncoraglio G, Thijs V, Chen WM, Mitchell B, Rothwell P, Sharma P, Sudlow C, Vicente A, Markus H, Kourkoulis C, Pera J, Raffeld M, Silliman S, Boraska Perica V, Thornton LM, Huckins LM, William Rayner N, Lewis CM, Gratacos M, Rybakowski F, Keski-Rahkonen A, Raevuori A, Hudson JI, Reichborn-Kjennerud T, Monteleone P, Karwautz A, Mannik K, Baker JH, O'Toole JK, Trace SE, Davis OSP, Helder SG, Ehrlich S, Herpertz-Dahlmann B, Danner UN, van Elburg AA, Clementi M, Forzan M, Docampo E, Lissowska J, Hauser J, Tortorella A, Maj M, Gonidakis F, Tziouvas K, Papezova H, Yilmaz Z, Wagner G, Cohen-Woods S, Herms S, Julià A, Rabionet R, Dick DM, Ripatti S, Andreassen OA, Espeseth T, Lundervold AJ, Steen VM, Pinto D, Scherer SW, Aschauer H, Schosser A, Alfredsson L, Padyukov L, Halmi KA, Mitchell J, Strober M, Bergen AW, Kaye W, Szatkiewicz JP, Cormand B, Ramos-Quiroga JA, Sánchez-Mora C, Ribasés M, Casas M, Hervas A, Arranz MJ, Haavik J, Zayats T, Johansson S, Williams N, Dempfle A, Rothenberger A, Kuntsi J, Oades RD, Banaschewski T, Franke B, Buitelaar JK, Arias Vasquez A, Doyle AE, Reif A, Lesch KP, Freitag C, Rivero O, Palmason H, Romanos M, Langley K, Rietschel M, Witt SH, Dalsgaard S, Børglum AD, Waldman I, Wilmot B, Molly N, Bau CHD, Crosbie J, Schachar R, Loo SK, McGough JJ, Grevet EH, Medland SE, Robinson E, Weiss LA, Bacchelli E, Bailey A, Bal V, Battaglia A, Betancur C, Bolton P, Cantor R, Celestino-Soper P, Dawson G, De Rubeis S, Duque F, Green A, Klauck SM, Leboyer M, Levitt P, Maestrini E, Mane S, De-Luca DM, Parr J, Regan R, Reichenberg A, Sandin S, Vorstman J, Wassink T, Wijsman E, Cook E, Santangelo S, Delorme R, et al. Analysis of shared heritability in common disorders of the brain. Science. 2018 06 22; 360(6395). PMID: 29930110.
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    2. Reble E, Dineen A, Barr CL. The contribution of alternative splicing to genetic risk for psychiatric disorders. Genes Brain Behav. 2018 03; 17(3):e12430. PMID: 29052934.
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    3. Huang AY, Yu D, Davis LK, Sul JH, Tsetsos F, Ramensky V, Zelaya I, Ramos EM, Osiecki L, Chen JA, McGrath LM, Illmann C, Sandor P, Barr CL, Grados M, Singer HS, Nöthen MM, Hebebrand J, King RA, Dion Y, Rouleau G, Budman CL, Depienne C, Worbe Y, Hartmann A, Müller-Vahl KR, Stuhrmann M, Aschauer H, Stamenkovic M, Schloegelhofer M, Konstantinidis A, Lyon GJ, McMahon WM, Barta C, Tarnok Z, Nagy P, Batterson JR, Rizzo R, Cath DC, Wolanczyk T, Berlin C, Malaty IA, Okun MS, Woods DW, Rees E, Pato CN, Pato MT, Knowles JA, Posthuma D, Pauls DL, Cox NJ, Neale BM, Freimer NB, Paschou P, Mathews CA, Scharf JM, Coppola G. Rare Copy Number Variants in NRXN1 and CNTN6 Increase Risk for Tourette Syndrome. Neuron. 2017 Jun 21; 94(6):1101-1111.e7. PMID: 28641109.
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    4. Schmitt AD, Hu M, Jung I, Xu Z, Qiu Y, Tan CL, Li Y, Lin S, Lin Y, Barr CL, Ren B. A Compendium of Chromatin Contact Maps Reveals Spatially Active Regions in the Human Genome. Cell Rep. 2016 11 15; 17(8):2042-2059. PMID: 27851967.
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    5. Alexander J, Potamianou H, Xing J, Deng L, Karagiannidis I, Tsetsos F, Drineas P, Tarnok Z, Rizzo R, Wolanczyk T, Farkas L, Nagy P, Szymanska U, Androutsos C, Tsironi V, Koumoula A, Barta C, Sandor P, Barr CL, Tischfield J, Paschou P, Heiman GA, Georgitsi M. Targeted Re-Sequencing Approach of Candidate Genes Implicates Rare Potentially Functional Variants in Tourette Syndrome Etiology. Front Neurosci. 2016; 10:428. PMID: 27708560.
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    6. Wilson DG, Leventigiannis G, Barr C, Morgan JM. ECG predictors of T wave oversensing in subcutaneous implantable cardioverter defibrillators. Int J Cardiol. 2016 Oct 01; 220:27-31. PMID: 27372039.
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    7. Barr CL, Misener VL. Decoding the non-coding genome: elucidating genetic risk outside the coding genome. Genes Brain Behav. 2016 Jan; 15(1):187-204. PMID: 26515765; PMCID: PMC4833497.
    8. Rimay T, Benak I, Kiss E, Baji I, Feher A, Juhasz A, Strauss J, Kennedy J, Barr C, Kovacs M, Vetro A, Kapornai K. BDNF Val66Met polymorphism and stressful life events in melancholic childhood-onset depression. Psychiatr Genet. 2015 Dec; 25(6):249-55. PMID: 26462036.
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    9. Zhang K, Feng Y, Wigg KG, Sandor P, Barr CL. Association study of the SLITRK5 gene and Tourette syndrome. Psychiatr Genet. 2015 Feb; 25(1):31-4. PMID: 25426764.
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    10. Yu D, Mathews CA, Scharf JM, Neale BM, Davis LK, Gamazon ER, Derks EM, Evans P, Edlund CK, Crane J, Fagerness JA, Osiecki L, Gallagher P, Gerber G, Haddad S, Illmann C, McGrath LM, Mayerfeld C, Arepalli S, Barlassina C, Barr CL, Bellodi L, Benarroch F, Berrió GB, Bienvenu OJ, Black DW, Bloch MH, Brentani H, Bruun RD, Budman CL, Camarena B, Campbell DD, Cappi C, Silgado JC, Cavallini MC, Chavira DA, Chouinard S, Cook EH, Cookson MR, Coric V, Cullen B, Cusi D, Delorme R, Denys D, Dion Y, Eapen V, Egberts K, Falkai P, Fernandez T, Fournier E, Garrido H, Geller D, Gilbert DL, Girard SL, Grabe HJ, Grados MA, Greenberg BD, Gross-Tsur V, Grünblatt E, Hardy J, Heiman GA, Hemmings SM, Herrera LD, Hezel DM, Hoekstra PJ, Jankovic J, Kennedy JL, King RA, Konkashbaev AI, Kremeyer B, Kurlan R, Lanzagorta N, Leboyer M, Leckman JF, Lennertz L, Liu C, Lochner C, Lowe TL, Lupoli S, Macciardi F, Maier W, Manunta P, Marconi M, McCracken JT, Mesa Restrepo SC, Moessner R, Moorjani P, Morgan J, Muller H, Murphy DL, Naarden AL, Nurmi E, Ochoa WC, Ophoff RA, Pakstis AJ, Pato MT, Pato CN, Piacentini J, Pittenger C, Pollak Y, Rauch SL, Renner T, Reus VI, Richter MA, Riddle MA, Robertson MM, Romero R, Rosário MC, Rosenberg D, Ruhrmann S, Sabatti C, Salvi E, Sampaio AS, Samuels J, Sandor P, Service SK, Sheppard B, Singer HS, Smit JH, Stein DJ, Strengman E, Tischfield JA, Turiel M, Valencia Duarte AV, Vallada H, Veenstra-VanderWeele J, Walitza S, Wang Y, Weale M, Weiss R, Wendland JR, Westenberg HG, Shugart YY, Hounie AG, Miguel EC, Nicolini H, Wagner M, Ruiz-Linares A, Cath DC, McMahon W, Posthuma D, Oostra BA, Nestadt G, Rouleau GA, Purcell S, Jenike MA, Heutink P, Hanna GL, Conti DV, Arnold PD, Freimer NB, Stewart SE, Knowles JA, Cox NJ, Pauls DL. Cross-disorder genome-wide analyses suggest a complex genetic relationship between Tourette's syndrome and OCD. Am J Psychiatry. 2015 Jan; 172(1):82-93. PMID: 25158072; PMCID: PMC4282594.
    11. Paschou P, Yu D, Gerber G, Evans P, Tsetsos F, Davis LK, Karagiannidis I, Chaponis J, Gamazon E, Mueller-Vahl K, Stuhrmann M, Schloegelhofer M, Stamenkovic M, Hebebrand J, Noethen M, Nagy P, Barta C, Tarnok Z, Rizzo R, Depienne C, Worbe Y, Hartmann A, Cath DC, Budman CL, Sandor P, Barr C, Wolanczyk T, Singer H, Chou IC, Grados M, Posthuma D, Rouleau GA, Aschauer H, Freimer NB, Pauls DL, Cox NJ, Mathews CA, Scharf JM. Genetic association signal near NTN4 in Tourette syndrome. Ann Neurol. 2014 Aug; 76(2):310-5. PMID: 25042818; PMCID: PMC4140987.
    12. McGrath LM, Yu D, Marshall C, Davis LK, Thiruvahindrapuram B, Li B, Cappi C, Gerber G, Wolf A, Schroeder FA, Osiecki L, O'Dushlaine C, Kirby A, Illmann C, Haddad S, Gallagher P, Fagerness JA, Barr CL, Bellodi L, Benarroch F, Bienvenu OJ, Black DW, Bloch MH, Bruun RD, Budman CL, Camarena B, Cath DC, Cavallini MC, Chouinard S, Coric V, Cullen B, Delorme R, Denys D, Derks EM, Dion Y, Rosário MC, Eapen V, Evans P, Falkai P, Fernandez TV, Garrido H, Geller D, Grabe HJ, Grados MA, Greenberg BD, Gross-Tsur V, Grünblatt E, Heiman GA, Hemmings SM, Herrera LD, Hounie AG, Jankovic J, Kennedy JL, King RA, Kurlan R, Lanzagorta N, Leboyer M, Leckman JF, Lennertz L, Lochner C, Lowe TL, Lyon GJ, Macciardi F, Maier W, McCracken JT, McMahon W, Murphy DL, Naarden AL, Neale BM, Nurmi E, Pakstis AJ, Pato MT, Pato CN, Piacentini J, Pittenger C, Pollak Y, Reus VI, Richter MA, Riddle M, Robertson MM, Rosenberg D, Rouleau GA, Ruhrmann S, Sampaio AS, Samuels J, Sandor P, Sheppard B, Singer HS, Smit JH, Stein DJ, Tischfield JA, Vallada H, Veenstra-VanderWeele J, Walitza S, Wang Y, Wendland JR, Shugart YY, Miguel EC, Nicolini H, Oostra BA, Moessner R, Wagner M, Ruiz-Linares A, Heutink P, Nestadt G, Freimer N, Petryshen T, Posthuma D, Jenike MA, Cox NJ, Hanna GL, Brentani H, Scherer SW, Arnold PD, Stewart SE, Mathews CA, Knowles JA, Cook EH, Pauls DL, Wang K, Scharf JM. Copy number variation in obsessive-compulsive disorder and tourette syndrome: a cross-disorder study. J Am Acad Child Adolesc Psychiatry. 2014 Aug; 53(8):910-9. PMID: 25062598; PMCID: PMC4218748.
    13. Gomez L, Wigg K, Zhang K, Lopez L, Sandor P, Malone M, Barr CL. Association of the KCNJ5 gene with Tourette Syndrome and Attention-Deficit/Hyperactivity Disorder. Genes Brain Behav. 2014 Jul; 13(6):535-42. PMID: 24840790; PMCID: PMC4833495.
    14. Tran C, Wigg KG, Zhang K, Cate-Carter TD, Kerr E, Field LL, Kaplan BJ, Lovett MW, Barr CL. Association of the ROBO1 gene with reading disabilities in a family-based analysis. Genes Brain Behav. 2014 Apr; 13(4):430-8. PMID: 24612512; PMCID: PMC4930671.
    15. Davis LK, Yu D, Keenan CL, Gamazon ER, Konkashbaev AI, Derks EM, Neale BM, Yang J, Lee SH, Evans P, Barr CL, Bellodi L, Benarroch F, Berrio GB, Bienvenu OJ, Bloch MH, Blom RM, Bruun RD, Budman CL, Camarena B, Campbell D, Cappi C, Cardona Silgado JC, Cath DC, Cavallini MC, Chavira DA, Chouinard S, Conti DV, Cook EH, Coric V, Cullen BA, Deforce D, Delorme R, Dion Y, Edlund CK, Egberts K, Falkai P, Fernandez TV, Gallagher PJ, Garrido H, Geller D, Girard SL, Grabe HJ, Grados MA, Greenberg BD, Gross-Tsur V, Haddad S, Heiman GA, Hemmings SM, Hounie AG, Illmann C, Jankovic J, Jenike MA, Kennedy JL, King RA, Kremeyer B, Kurlan R, Lanzagorta N, Leboyer M, Leckman JF, Lennertz L, Liu C, Lochner C, Lowe TL, Macciardi F, McCracken JT, McGrath LM, Mesa Restrepo SC, Moessner R, Morgan J, Muller H, Murphy DL, Naarden AL, Ochoa WC, Ophoff RA, Osiecki L, Pakstis AJ, Pato MT, Pato CN, Piacentini J, Pittenger C, Pollak Y, Rauch SL, Renner TJ, Reus VI, Richter MA, Riddle MA, Robertson MM, Romero R, Rosàrio MC, Rosenberg D, Rouleau GA, Ruhrmann S, Ruiz-Linares A, Sampaio AS, Samuels J, Sandor P, Sheppard B, Singer HS, Smit JH, Stein DJ, Strengman E, Tischfield JA, Valencia Duarte AV, Vallada H, Van Nieuwerburgh F, Veenstra-Vanderweele J, Walitza S, Wang Y, Wendland JR, Westenberg HG, Shugart YY, Miguel EC, McMahon W, Wagner M, Nicolini H, Posthuma D, Hanna GL, Heutink P, Denys D, Arnold PD, Oostra BA, Nestadt G, Freimer NB, Pauls DL, Wray NR, Stewart SE, Mathews CA, Knowles JA, Cox NJ, Scharf JM. Partitioning the heritability of Tourette syndrome and obsessive compulsive disorder reveals differences in genetic architecture. PLoS Genet. 2013 Oct; 9(10):e1003864. PMID: 24204291; PMCID: PMC3812053.
    16. Karagiannidis I, Dehning S, Sandor P, Tarnok Z, Rizzo R, Wolanczyk T, Madruga-Garrido M, Hebebrand J, Nöthen MM, Lehmkuhl G, Farkas L, Nagy P, Szymanska U, Anastasiou Z, Stathias V, Androutsos C, Tsironi V, Koumoula A, Barta C, Zill P, Mir P, Müller N, Barr C, Paschou P. Support of the histaminergic hypothesis in Tourette syndrome: association of the histamine decarboxylase gene in a large sample of families. J Med Genet. 2013 Nov; 50(11):760-4. PMID: 23825391.
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    17. Tran C, Gagnon F, Wigg KG, Feng Y, Gomez L, Cate-Carter TD, Kerr EN, Field LL, Kaplan BJ, Lovett MW, Barr CL. A family-based association analysis and meta-analysis of the reading disabilities candidate gene DYX1C1. Am J Med Genet B Neuropsychiatr Genet. 2013 Mar; 162B(2):146-56. PMID: 23341075.
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    18. Scharf JM, Yu D, Mathews CA, Neale BM, Stewart SE, Fagerness JA, Evans P, Gamazon E, Edlund CK, Service SK, Tikhomirov A, Osiecki L, Illmann C, Pluzhnikov A, Konkashbaev A, Davis LK, Han B, Crane J, Moorjani P, Crenshaw AT, Parkin MA, Reus VI, Lowe TL, Rangel-Lugo M, Chouinard S, Dion Y, Girard S, Cath DC, Smit JH, King RA, Fernandez TV, Leckman JF, Kidd KK, Kidd JR, Pakstis AJ, State MW, Herrera LD, Romero R, Fournier E, Sandor P, Barr CL, Phan N, Gross-Tsur V, Benarroch F, Pollak Y, Budman CL, Bruun RD, Erenberg G, Naarden AL, Lee PC, Weiss N, Kremeyer B, Berrío GB, Campbell DD, Cardona Silgado JC, Ochoa WC, Mesa Restrepo SC, Muller H, Valencia Duarte AV, Lyon GJ, Leppert M, Morgan J, Weiss R, Grados MA, Anderson K, Davarya S, Singer H, Walkup J, Jankovic J, Tischfield JA, Heiman GA, Gilbert DL, Hoekstra PJ, Robertson MM, Kurlan R, Liu C, Gibbs JR, Singleton A, Hardy J, Strengman E, Ophoff RA, Wagner M, Moessner R, Mirel DB, Posthuma D, Sabatti C, Eskin E, Conti DV, Knowles JA, Ruiz-Linares A, Rouleau GA, Purcell S, Heutink P, Oostra BA, McMahon WM, Freimer NB, Cox NJ, Pauls DL. Genome-wide association study of Tourette's syndrome. Mol Psychiatry. 2013 Jun; 18(6):721-8. PMID: 22889924; PMCID: PMC3605224.
    19. Bisceglia R, Jenkins JM, Wigg KG, O'Connor TG, Moran G, Barr CL. Arginine vasopressin 1a receptor gene and maternal behavior: evidence of association and moderation. Genes Brain Behav. 2012 Apr; 11(3):262-8. PMID: 22288734.
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    20. Xie W, Barr CL, Kim A, Yue F, Lee AY, Eubanks J, Dempster EL, Ren B. Base-resolution analyses of sequence and parent-of-origin dependent DNA methylation in the mouse genome. Cell. 2012 Feb 17; 148(4):816-31. PMID: 22341451; PMCID: PMC3343639.
    21. Karagiannidis I, Rizzo R, Tarnok Z, Wolanczyk T, Hebebrand J, Nöthen MM, Lehmkuhl G, Farkas L, Nagy P, Barta C, Szymanska U, Panteloglou G, Miranda DM, Feng Y, Sandor P, Barr C, Paschou P. Replication of association between a SLITRK1 haplotype and Tourette Syndrome in a large sample of families. Mol Psychiatry. 2012 Jul; 17(7):665-8. PMID: 22083730.
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    22. Tobe SW, Baker B, Hunter K, Kiss A, Perkins N, Gomez L, Feng Y, Wigg K, Barr CL. The impact of endothelin-1 genetic analysis and job strain on ambulatory blood pressure. J Psychosom Res. 2011 Aug; 71(2):97-101. PMID: 21767690.
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    23. Elbert A, Lovett MW, Cate-Carter T, Pitch A, Kerr EN, Barr CL. Genetic variation in the KIAA0319 5' region as a possible contributor to dyslexia. Behav Genet. 2011 Jan; 41(1):77-89. PMID: 21207242.
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    24. Feng Y, Kapornai K, Kiss E, Tamás Z, Mayer L, Baji I, Daróczi G, Benák I, Kothencné VO, Dombovári E, Kaczvinszk E, Besnyo M, Gádoros J, Székely J, Kovacs M, Vetró A, Kennedy JL, Barr CL. Association of the GABRD gene and childhood-onset mood disorders. Genes Brain Behav. 2010 Aug; 9(6):668-72. PMID: 20561060; PMCID: PMC2935687.
    25. Strauss JS, Freeman NL, Shaikh SA, Vetró A, Kiss E, Kapornai K, Daróczi G, Rimay T, Kothencné VO, Dombovári E, Kaczvinszk E, Tamás Z, Baji I, Besny M, Gádoros J, DeLuca V, George CJ, Dempster E, Barr CL, Kovacs M, Kennedy JL. No association between oxytocin or prolactin gene variants and childhood-onset mood disorders. Psychoneuroendocrinology. 2010 Oct; 35(9):1422-8. PMID: 20547007; PMCID: PMC2941560.
    26. Couto JM, Livne-Bar I, Huang K, Xu Z, Cate-Carter T, Feng Y, Wigg K, Humphries T, Tannock R, Kerr EN, Lovett MW, Bremner R, Barr CL. Association of reading disabilities with regions marked by acetylated H3 histones in KIAA0319. Am J Med Genet B Neuropsychiatr Genet. 2010 Mar 05; 153B(2):447-462. PMID: 19588467.
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    27. Dempster EL, Kiss E, Kapornai K, Daróczi G, Mayer L, Baji I, Tamas Z, Gadoros J, Kennedy JL, Vetró A, Kovacs M, Barr CL. No evidence of an association between two genes, EDN1 and ACE, and childhood-onset mood disorders. Am J Med Genet B Neuropsychiatr Genet. 2010 Jan 05; 153B(1):341-6. PMID: 19475602.
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    28. Dempster EL, Burcescu I, Wigg K, Kiss E, Baji I, Gadoros J, Tamás Z, Kapornai K, Daróczy G, Kennedy JL, Vetró A, Kovacs M, Barr CL. Further genetic evidence implicates the vasopressin system in childhood-onset mood disorders. Eur J Neurosci. 2009 Oct; 30(8):1615-9. PMID: 19821843.
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    29. Gomez L, Wigg K, Feng Y, Kiss E, Kapornai K, Tamás Z, Mayer L, Baji I, Daróczi G, Benák I, Kothencné VO, Dombovári E, Kaczvinszk E, Besnyo M, Gádoros J, King N, Székely J, Kovacs M, Vetró A, Kennedy JL, Barr CL. G72/G30 (DAOA) and juvenile-onset mood disorders. Am J Med Genet B Neuropsychiatr Genet. 2009 Oct 05; 150B(7):1007-12. PMID: 19089835.
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    30. Mill J, Wigg K, Burcescu I, Vetró A, Kiss E, Kapornai K, Tamás Z, Baji I, Gádoros J, Kennedy JL, Kovacs M, Barr CL. Mutation screen and association analysis of the glucocorticoid receptor gene (NR3C1) in childhood-onset mood disorders (COMD). Am J Med Genet B Neuropsychiatr Genet. 2009 Sep 05; 150B(6):866-73. PMID: 19089807.
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    31. Misener VL, Gomez L, Wigg KG, King N, Kiss E, Daróczi G, Kapornai K, Tamás Z, Mayer L, Gádoros J, Baji I, Kennedy JL, Kovacs M, Vetró A, Barr CL. Tagging SNP association study of the IL-1beta gene (IL1B) and childhood-onset mood disorders. Am J Med Genet B Neuropsychiatr Genet. 2009 Jul 05; 150B(5):653-9. PMID: 19016479.
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    32. Wigg K, Feng Y, Gomez L, Kiss E, Kapornai K, Tamás Z, Mayer L, Baji I, Daróczi G, Benák I, Osváth VK, Dombovári E, Kaczvinszk E, Besnyõ M, Gádoros J, King N, Székely J, Kovacs M, Vetró A, Kennedy JL, Barr CL. Genome scan in sibling pairs with juvenile-onset mood disorders: Evidence for linkage to 13q and Xq. Am J Med Genet B Neuropsychiatr Genet. 2009 Jul 05; 150B(5):638-46. PMID: 19035515.
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    33. Miranda DM, Wigg K, Kabia EM, Feng Y, Sandor P, Barr CL. Association of SLITRK1 to Gilles de la Tourette Syndrome. Am J Med Genet B Neuropsychiatr Genet. 2009 Jun 05; 150B(4):483-6. PMID: 18698576.
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    34. Dorval KM, Burcescu I, Adams J, Wigg KG, King N, Kiss E, Kapornai K, Gádoros J, Tamás Z, Daróczi G, Baji I, Mayer L, Kennedy JL, Vetró A, Kovacs M, Barr CL. Association study of N-methyl-D-aspartate glutamate receptor subunit genes and childhood-onset mood disorders. Psychiatr Genet. 2009 Jun; 19(3):156-7. PMID: 19352217.
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    35. Couto JM, Gomez L, Wigg K, Ickowicz A, Pathare T, Malone M, Kennedy JL, Schachar R, Barr CL. Association of attention-deficit/hyperactivity disorder with a candidate region for reading disabilities on chromosome 6p. Biol Psychiatry. 2009 Aug 15; 66(4):368-75. PMID: 19362708.
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    36. Laurin N, Wigg KG, Feng Y, Sandor P, Barr CL. Chromosome 5 and Gilles de la Tourette syndrome: Linkage in a large pedigree and association study of six candidates in the region. Am J Med Genet B Neuropsychiatr Genet. 2009 Jan 05; 150B(1):95-103. PMID: 18454440.
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    37. Ouellet-Morin I, Wigg KG, Feng Y, Dionne G, Robaey P, Brendgen M, Vitaro F, Simard L, Schachar R, Tremblay RE, Pérusse D, Boivin M, Barr CL. Association of the dopamine transporter gene and ADHD symptoms in a Canadian population-based sample of same-age twins. Am J Med Genet B Neuropsychiatr Genet. 2008 Dec 05; 147B(8):1442-9. PMID: 18165969.
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    38. Wigg KG, Feng Y, Crosbie J, Tannock R, Kennedy JL, Ickowicz A, Malone M, Schachar R, Barr CL. Association of ADHD and the Protogenin gene in the chromosome 15q21.3 reading disabilities linkage region. Genes Brain Behav. 2008 Nov; 7(8):877-86. PMID: 19076634; PMCID: PMC4833493.
    39. Gizer IR, Waldman ID, Abramowitz A, Barr CL, Feng Y, Wigg KG, Misener VL, Rowe DC. Relations between multi-informant assessments of ADHD symptoms, DAT1, and DRD4. J Abnorm Psychol. 2008 Nov; 117(4):869-80. PMID: 19025233.
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    40. Mill J, Kiss E, Baji I, Kapornai K, Daróczy G, Vetró A, Kennedy J, Kovacs M, Barr C. Association study of the estrogen receptor alpha gene (ESR1) and childhood-onset mood disorders. Am J Med Genet B Neuropsychiatr Genet. 2008 Oct 05; 147B(7):1323-6. PMID: 18449864.
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    41. Misener VL, Gomez L, Wigg KG, Luca P, King N, Kiss E, Daróczi G, Kapornai K, Tamas Z, Mayer L, Gádoros J, Baji I, Kennedy JL, Kovacs M, Vetró A, Barr CL. Cytokine Genes TNF, IL1A, IL1B, IL6, IL1RN and IL10, and childhood-onset mood disorders. Neuropsychobiology. 2008; 58(2):71-80. PMID: 18832862.
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    42. Lepoire D, Richmond P, Cheng JJ, Kamboj S, Arnish J, Chen SY, Barr C, McKenney C. Web-based training course for evaluating radiological dose assessment in NRC's license termination process. Health Phys. 2008 Aug; 95 Suppl 2:S137-42. PMID: 18617797.
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    43. Laurin N, Lee J, Ickowicz A, Pathare T, Malone M, Tannock R, Kennedy JL, Schachar RJ, Barr CL. Association study for genes at chromosome 5p13-q11 in attention deficit hyperactivity disorder. Am J Med Genet B Neuropsychiatr Genet. 2008 Jul 05; 147B(5):600-5. PMID: 18081024.
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    44. Bulgin NL, Strauss JS, King NA, Shaikh SA, George CJ, Fox NA, Barr CL, Kovacs M, Kennedy JL. Association study of theta EEG asymmetry and brain-derived neurotrophic factor gene variants in childhood-onset mood disorder. Neuromolecular Med. 2008; 10(4):343-55. PMID: 18543122.
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    45. Laurin N, Ickowicz A, Pathare T, Malone M, Tannock R, Schachar R, Kennedy JL, Barr CL. No evidence for genetic association between DARPP-32 (PP1R1B) polymorphisms and attention deficit hyperactivity disorder. Am J Med Genet B Neuropsychiatr Genet. 2008 Apr 05; 147(3):339-42. PMID: 17948899.
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    46. Shaikh SA, Strauss J, King N, Bulgin NL, Vetró A, Kiss E, George CJ, Kovacs M, Barr CL, Kennedy JL. Association study of serotonin system genes in childhood-onset mood disorder. Psychiatr Genet. 2008 Apr; 18(2):47-52. PMID: 18349694.
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    47. Feng Y, Vetró A, Kiss E, Kapornai K, Daróczi G, Mayer L, Tamás Z, Baji I, Gádoros J, King N, Kennedy JL, Wigg K, Kovacs M, Barr CL. Association of the neurotrophic tyrosine kinase receptor 3 (NTRK3) gene and childhood-onset mood disorders. Am J Psychiatry. 2008 May; 165(5):610-6. PMID: 18347002.
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    48. Miranda DM, Wigg K, Feng Y, Sandor P, Barr CL. Association study between Gilles de la Tourette Syndrome and two genes in the Robo-Slit pathway located in the chromosome 11q24 linked/associated region. Am J Med Genet B Neuropsychiatr Genet. 2008 Jan 05; 147B(1):68-72. PMID: 17671968.
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    49. Couto JM, Gomez L, Wigg K, Cate-Carter T, Archibald J, Anderson B, Tannock R, Kerr EN, Lovett MW, Humphries T, Barr CL. The KIAA0319-like (KIAA0319L) gene on chromosome 1p34 as a candidate for reading disabilities. J Neurogenet. 2008; 22(4):295-313. PMID: 19085271.
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    50. Lee J, Laurin N, Crosbie J, Ickowicz A, Pathare T, Malone M, Tannock R, Kennedy JL, Schachar R, Barr CL. Association study of the brain-derived neurotropic factor (BDNF) gene in attention deficit hyperactivity disorder. Am J Med Genet B Neuropsychiatr Genet. 2007 Dec 05; 144B(8):976-81. PMID: 17918236.
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    51. Dempster EL, Kiss E, Kapornai K, Daróczy G, Mayer L, Baji I, Tamas Z, Gadoros J, Kennedy JL, Vetró A, Kovacs M, Barr CL. No evidence of association between a functional polymorphism in the MTHFR gene and childhood-onset mood disorders. Mol Psychiatry. 2007 Dec; 12(12):1063-4. PMID: 18043712.
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    52. Feng Y, Wigg K, King N, Vetró A, Kiss E, Kapornai K, Mayer L, Gádoros J, Kennedy JL, Kovacs M, Barr CL. GPR50 is not associated with childhood-onset mood disorders in a large sample of Hungarian families. Psychiatr Genet. 2007 Dec; 17(6):347-50. PMID: 18075476.
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    53. Lee SI, Schachar RJ, Chen SX, Ornstein TJ, Charach A, Barr C, Ickowicz A. Predictive validity of DSM-IV and ICD-10 criteria for ADHD and hyperkinetic disorder. J Child Psychol Psychiatry. 2008 Jan; 49(1):70-8. PMID: 17979965.
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    54. Dempster EL, Burcescu I, Wigg K, Kiss E, Baji I, Gadoros J, Tamás Z, Kennedy JL, Vetró A, Kovacs M, Barr CL. Evidence of an association between the vasopressin V1b receptor gene (AVPR1B) and childhood-onset mood disorders. Arch Gen Psychiatry. 2007 Oct; 64(10):1189-95. PMID: 17909131.
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    55. Crosbie J, Pérusse D, Barr CL, Schachar RJ. Validating psychiatric endophenotypes: inhibitory control and attention deficit hyperactivity disorder. Neurosci Biobehav Rev. 2008; 32(1):40-55. PMID: 17976721.
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    56. Lee J, Laurin N, Crosbie J, Ickowicz A, Pathare T, Malone M, Kennedy JL, Tannock R, Schachar R, Barr CL. Association study of the nicotinic acetylcholine receptor alpha4 subunit gene, CHRNA4, in attention-deficit hyperactivity disorder. Genes Brain Behav. 2008 Feb; 7(1):53-60. PMID: 17504247; PMCID: PMC4833496.
    57. Makkar R, Gomez L, Wigg KG, Ickowicz A, Pathare T, Tannock R, Malone M, Kennedy JL, Schachar R, Barr CL. The gene for synapsin III and attention-deficit hyperactivity disorder. Psychiatr Genet. 2007 Apr; 17(2):109-12. PMID: 17413450.
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    58. Schachar R, Logan GD, Robaey P, Chen S, Ickowicz A, Barr C. Restraint and cancellation: multiple inhibition deficits in attention deficit hyperactivity disorder. J Abnorm Child Psychol. 2007 Apr; 35(2):229-38. PMID: 17351752.
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    59. Laurin N, Feng Y, Ickowicz A, Pathare T, Malone M, Tannock R, Schachar R, Kennedy JL, Barr CL. No preferential transmission of paternal alleles at risk genes in attention-deficit hyperactivity disorder. Mol Psychiatry. 2007 Mar; 12(3):226-9. PMID: 17325714.
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    60. Luca P, Laurin N, Misener VL, Wigg KG, Anderson B, Cate-Carter T, Tannock R, Humphries T, Lovett MW, Barr CL. Association of the dopamine receptor D1 gene, DRD1, with inattention symptoms in families selected for reading problems. Mol Psychiatry. 2007 Aug; 12(8):776-85. PMID: 17310237.
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    61. Laurin N, Ickowicz A, Pathare T, Malone M, Tannock R, Schachar R, Kennedy JL, Barr CL. Investigation of the G protein subunit Galphaolf gene (GNAL) in attention deficit/hyperactivity disorder. J Psychiatr Res. 2008 Jan; 42(2):117-24. PMID: 17166517; PMCID: PMC4930670.
    62. Dorval KM, Wigg KG, Crosbie J, Tannock R, Kennedy JL, Ickowicz A, Pathare T, Malone M, Schachar R, Barr CL. Association of the glutamate receptor subunit gene GRIN2B with attention-deficit/hyperactivity disorder. Genes Brain Behav. 2007 Jul; 6(5):444-52. PMID: 17010153; PMCID: PMC4833492.
    63. Ozbay F, Wigg KG, Turanli ET, Asherson P, Yazgan Y, Sandor P, Barr CL. Analysis of the dopamine beta hydroxylase gene in Gilles de la Tourette syndrome. Am J Med Genet B Neuropsychiatr Genet. 2006 Sep 05; 141B(6):673-7. PMID: 16838359.
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    64. Wigg KG, Takhar A, Ickowicz A, Tannock R, Kennedy JL, Pathare T, Malone M, Schachar R, Barr CL. Gene for the serotonin transporter and ADHD: no association with two functional polymorphisms. Am J Med Genet B Neuropsychiatr Genet. 2006 Sep 05; 141B(6):566-70. PMID: 16856124.
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    65. Burcescu I, Wigg K, Gomez L, King N, Vetró A, Kiss E, Kapornai K, Gádoros J, Kennedy JL, Kovacs M, Barr CL. Association study of the adrenergic receptors and childhood-onset mood disorders in Hungarian families. Am J Med Genet B Neuropsychiatr Genet. 2006 Apr 05; 141B(3):227-33. PMID: 16526032.
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    66. Laurin N, Misener VL, Crosbie J, Ickowicz A, Pathare T, Roberts W, Malone M, Tannock R, Schachar R, Kennedy JL, Barr CL. Association of the calcyon gene (DRD1IP) with attention deficit/hyperactivity disorder. Mol Psychiatry. 2005 Dec; 10(12):1117-25. PMID: 16172615.
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    67. Feng Y, Wigg KG, Makkar R, Ickowicz A, Pathare T, Tannock R, Roberts W, Malone M, Kennedy JL, Schachar R, Barr CL. Sequence variation in the 3'-untranslated region of the dopamine transporter gene and attention-deficit hyperactivity disorder (ADHD). Am J Med Genet B Neuropsychiatr Genet. 2005 Nov 05; 139B(1):1-6. PMID: 16082693.
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    68. Feng Y, Crosbie J, Wigg K, Pathare T, Ickowicz A, Schachar R, Tannock R, Roberts W, Malone M, Swanson J, Kennedy JL, Barr CL. The SNAP25 gene as a susceptibility gene contributing to attention-deficit hyperactivity disorder. Mol Psychiatry. 2005 Nov; 10(11):998-1005, 973. PMID: 16088329.
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    69. Strauss J, Barr CL, George CJ, Devlin B, Vetró A, Kiss E, Baji I, King N, Shaikh S, Lanktree M, Kovacs M, Kennedy JL. Brain-derived neurotrophic factor variants are associated with childhood-onset mood disorder: confirmation in a Hungarian sample. Mol Psychiatry. 2005 Sep; 10(9):861-7. PMID: 15940299.
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    70. Burcescu I, Wigg K, King N, Vetró A, Kiss E, Katay L, Kennedy JL, Kovacs M, Barr CL. Association study of CREB1 and childhood-onset mood disorders. Am J Med Genet B Neuropsychiatr Genet. 2005 Aug 05; 137B(1):45-50. PMID: 15999345.
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    71. Schachar RJ, Crosbie J, Barr CL, Ornstein TJ, Kennedy J, Malone M, Roberts W, Ickowicz A, Tannock R, Chen S, Pathare T. Inhibition of motor responses in siblings concordant and discordant for attention deficit hyperactivity disorder. Am J Psychiatry. 2005 Jun; 162(6):1076-82. PMID: 15930055.
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    72. Zai G, King N, Wong GW, Barr CL, Kennedy JL. Possible association between the gamma-aminobutyric acid type B receptor 1 (GABBR1) gene and schizophrenia. Eur Neuropsychopharmacol. 2005 May; 15(3):347-52. PMID: 15820424.
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    73. Zai G, Arnold P, Burroughs E, Barr CL, Richter MA, Kennedy JL. Evidence for the gamma-amino-butyric acid type B receptor 1 (GABBR1) gene as a susceptibility factor in obsessive-compulsive disorder. Am J Med Genet B Neuropsychiatr Genet. 2005 Apr 05; 134B(1):25-9. PMID: 15685626.
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    74. Zai G, King N, Wigg K, Couto J, Wong GW, Honer WG, Barr CL, Kennedy JL. Genetic study of the myelin oligodendrocyte glycoprotein (MOG) gene in schizophrenia. Genes Brain Behav. 2005 Feb; 4(1):2-9. PMID: 15660663.
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    75. Adams JH, Wigg KG, King N, Burcescu I, Vetró A, Kiss E, Baji I, George CJ, Kennedy JL, Kovacs M, Barr CL. Association study of neurotrophic tyrosine kinase receptor type 2 (NTRK2) and childhood-onset mood disorders. Am J Med Genet B Neuropsychiatr Genet. 2005 Jan 05; 132B(1):90-5. PMID: 15389758.
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    76. Wigg KG, Couto JM, Feng Y, Anderson B, Cate-Carter TD, Macciardi F, Tannock R, Lovett MW, Humphries TW, Barr CL. Support for EKN1 as the susceptibility locus for dyslexia on 15q21. Mol Psychiatry. 2004 Dec; 9(12):1111-21. PMID: 15249932.
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    77. Strauss J, Barr CL, George CJ, King N, Shaikh S, Devlin B, Kovacs M, Kennedy JL. Association study of brain-derived neurotrophic factor in adults with a history of childhood onset mood disorder. Am J Med Genet B Neuropsychiatr Genet. 2004 Nov 15; 131B(1):16-9. PMID: 15384083.
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    78. Zai G, Bezchlibnyk YB, Richter MA, Arnold P, Burroughs E, Barr CL, Kennedy JL. Myelin oligodendrocyte glycoprotein (MOG) gene is associated with obsessive-compulsive disorder. Am J Med Genet B Neuropsychiatr Genet. 2004 Aug 15; 129B(1):64-8. PMID: 15274043.
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    79. Paschou P, Feng Y, Pakstis AJ, Speed WC, DeMille MM, Kidd JR, Jaghori B, Kurlan R, Pauls DL, Sandor P, Barr CL, Kidd KK. Indications of linkage and association of Gilles de la Tourette syndrome in two independent family samples: 17q25 is a putative susceptibility region. Am J Hum Genet. 2004 Oct; 75(4):545-60. PMID: 15303240; PMCID: PMC1182043.
    80. Misener VL, Luca P, Azeke O, Crosbie J, Waldman I, Tannock R, Roberts W, Malone M, Schachar R, Ickowicz A, Kennedy JL, Barr CL. Linkage of the dopamine receptor D1 gene to attention-deficit/hyperactivity disorder. Mol Psychiatry. 2004 May; 9(5):500-9. PMID: 14569274.
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    81. Adams J, Crosbie J, Wigg K, Ickowicz A, Pathare T, Roberts W, Malone M, Schachar R, Tannock R, Kennedy JL, Barr CL. Glutamate receptor, ionotropic, N-methyl D-aspartate 2A (GRIN2A) gene as a positional candidate for attention-deficit/hyperactivity disorder in the 16p13 region. Mol Psychiatry. 2004 May; 9(5):494-9. PMID: 14699423.
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    82. Ambrósio AM, Kennedy JL, Macciardi F, Barr C, Soares MJ, Oliveira CR, Pato CN. No evidence of association or linkage disequilibrium between polymorphisms in the 5' upstream and coding regions of the dopamine D4 receptor gene and schizophrenia in a Portuguese population. Am J Med Genet B Neuropsychiatr Genet. 2004 Feb 15; 125B(1):20-4. PMID: 14755438.
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    83. Lowe N, Kirley A, Hawi Z, Sham P, Wickham H, Kratochvil CJ, Smith SD, Lee SY, Levy F, Kent L, Middle F, Rohde LA, Roman T, Tahir E, Yazgan Y, Asherson P, Mill J, Thapar A, Payton A, Todd RD, Stephens T, Ebstein RP, Manor I, Barr CL, Wigg KG, Sinke RJ, Buitelaar JK, Smalley SL, Nelson SF, Biederman J, Faraone SV, Gill M. Joint analysis of the DRD5 marker concludes association with attention-deficit/hyperactivity disorder confined to the predominantly inattentive and combined subtypes. Am J Hum Genet. 2004 Feb; 74(2):348-56. PMID: 14732906; PMCID: PMC1181932.
    84. Strauss J, Barr CL, George CJ, Ryan CM, King N, Shaikh S, Kovacs M, Kennedy JL. BDNF and COMT polymorphisms: relation to memory phenotypes in young adults with childhood-onset mood disorder. Neuromolecular Med. 2004; 5(3):181-92. PMID: 15626819.
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    85. Misener VL, Schachar R, Ickowicz A, Malone M, Roberts W, Tannock R, Kennedy JL, Pathare T, Barr CL. Replication test for association of the IL-1 receptor antagonist gene, IL1RN, with attention-deficit/hyperactivity disorder. Neuropsychobiology. 2004; 50(3):231-4. PMID: 15365221.
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    86. Barr CL, Levin AV, Kovacs R, Muller W, Barsoum-Homsy M, Zachary D, Clark RA, Tsilfidis C. Linkage study between congenital cataracts and five crystallin loci. Am J Med Genet A. 2003 Aug 15; 121A(1):15-9. PMID: 12900895.
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    87. Xu C, Ozbay F, Wigg K, Shulman R, Tahir E, Yazgan Y, Sandor P, Barr CL. Evaluation of the genes for the adrenergic receptors alpha 2A and alpha 1C and Gilles de la Tourette Syndrome. Am J Med Genet B Neuropsychiatr Genet. 2003 May 15; 119B(1):54-9. PMID: 12707939.
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    88. Wong AH, Macciardi F, Klempan T, Kawczynski W, Barr CL, Lakatoo S, Wong M, Buckle C, Trakalo J, Boffa E, Oak J, Azevedo MH, Dourado A, Coelho I, Macedo A, Vicente A, Valente J, Ferreira CP, Pato MT, Pato CN, Kennedy JL, Van Tol HH. Identification of candidate genes for psychosis in rat models, and possible association between schizophrenia and the 14-3-3eta gene. Mol Psychiatry. 2003 Feb; 8(2):156-66. PMID: 12610648.
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    89. Quist JF, Barr CL, Schachar R, Roberts W, Malone M, Tannock R, Basile VS, Beitchman J, Kennedy JL. The serotonin 5-HT1B receptor gene and attention deficit hyperactivity disorder. Mol Psychiatry. 2003 Jan; 8(1):98-102. PMID: 12556913.
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    90. Wigg K, Zai G, Schachar R, Tannock R, Roberts W, Malone M, Kennedy JL, Barr CL. Attention deficit hyperactivity disorder and the gene for dopamine Beta-hydroxylase. Am J Psychiatry. 2002 Jun; 159(6):1046-8. PMID: 12042196.
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    91. Barr CL, Kroft J, Feng Y, Wigg K, Roberts W, Malone M, Ickowicz A, Schachar R, Tannock R, Kennedy JL. The norepinephrine transporter gene and attention-deficit hyperactivity disorder. Am J Med Genet. 2002 Apr 08; 114(3):255-9. PMID: 11920844.
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    92. Barr CL, Best L, Weksberg R. Linkage study in families with posterior helical ear pits and Wiedemann-Beckwith syndrome. Am J Med Genet. 2001 Nov 22; 104(2):120-6. PMID: 11746041.
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    93. Barr CL, Wigg K, Zai G, Roberts W, Malone M, Schachar R, Tannock R, Kennedy JL. Attention-deficit hyperactivity disorder and the adrenergic receptors alpha 1C and alpha 2C. Mol Psychiatry. 2001 May; 6(3):334-7. PMID: 11326305; PMCID: PMC4833494.
    94. Gutkind D, Ventura J, Barr C, Shaner A, Green M, Mintz J. Factors affecting reliability and confidence of DSM-III-R psychosis-related diagnosis. Psychiatry Res. 2001 Apr 15; 101(3):269-75. PMID: 11311930.
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    95. Barr CL, Shulman R, Wigg K, Schachar R, Tannock R, Roberts W, Malone M, Kennedy JL. Linkage study of polymorphisms in the gene for myelin oligodendrocyte glycoprotein located on chromosome 6p and attention deficit hyperactivity disorder. Am J Med Genet. 2001 Apr 08; 105(3):250-4. PMID: 11353444.
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    96. Xu C, Schachar R, Tannock R, Roberts W, Malone M, Kennedy JL, Barr CL. Linkage study of the alpha2A adrenergic receptor in attention-deficit hyperactivity disorder families. Am J Med Genet. 2001 Mar 08; 105(2):159-62. PMID: 11304829.
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    97. Barr CL, Xu C, Kroft J, Feng Y, Wigg K, Zai G, Tannock R, Schachar R, Malone M, Roberts W, Nöthen MM, Grünhage F, Vandenbergh DJ, Uhl G, Sunohara G, King N, Kennedy JL. Haplotype study of three polymorphisms at the dopamine transporter locus confirm linkage to attention-deficit/hyperactivity disorder. Biol Psychiatry. 2001 Feb 15; 49(4):333-9. PMID: 11239904.
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    98. Barr CL, Feng Y, Wigg KG, Schachar R, Tannock R, Roberts W, Malone M, Kennedy JL. 5'-untranslated region of the dopamine D4 receptor gene and attention-deficit hyperactivity disorder. Am J Med Genet. 2001 Jan 08; 105(1):84-90. PMID: 11425008.
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    99. Barr CL. Genetics of childhood disorders: XXII. ADHD, Part 6: The dopamine D4 receptor gene. J Am Acad Child Adolesc Psychiatry. 2001 Jan; 40(1):118-21. PMID: 11195554.
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    100. Sunohara GA, Roberts W, Malone M, Schachar RJ, Tannock R, Basile VS, Wigal T, Wigal SB, Schuck S, Moriarty J, Swanson JM, Kennedy JL, Barr CL. Linkage of the dopamine D4 receptor gene and attention-deficit/hyperactivity disorder. J Am Acad Child Adolesc Psychiatry. 2000 Dec; 39(12):1537-42. PMID: 11128331.
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    101. Quist JF, Barr CL, Schachar R, Roberts W, Malone M, Tannock R, Basile VS, Beitchman J, Kennedy JL. Evidence for the serotonin HTR2A receptor gene as a susceptibility factor in attention deficit hyperactivity disorder (ADHD). Mol Psychiatry. 2000 Sep; 5(5):537-41. PMID: 11032388.
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    102. Barr CL, Wigg KG, Feng Y, Zai G, Malone M, Roberts W, Schachar R, Tannock R, Kennedy JL. Attention-deficit hyperactivity disorder and the gene for the dopamine D5 receptor. Mol Psychiatry. 2000 Sep; 5(5):548-51. PMID: 11032390.
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    103. Barr CL, Feng Y, Wigg K, Bloom S, Roberts W, Malone M, Schachar R, Tannock R, Kennedy JL. Identification of DNA variants in the SNAP-25 gene and linkage study of these polymorphisms and attention-deficit hyperactivity disorder. Mol Psychiatry. 2000 Jul; 5(4):405-9. PMID: 10889551.
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    104. Barr CL, Wigg KG, Bloom S, Schachar R, Tannock R, Roberts W, Malone M, Kennedy JL. Further evidence from haplotype analysis for linkage of the dopamine D4 receptor gene and attention-deficit hyperactivity disorder. Am J Med Genet. 2000 Jun 12; 96(3):262-7. PMID: 10898896.
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    105. Barr CL, Wigg KG, Wu J, Zai C, Bloom S, Tannock R, Roberts W, Malone M, Schachar R, Kennedy JL. Linkage study of two polymorphisms at the dopamine D3 receptor gene and attention-deficit hyperactivity disorder. Am J Med Genet. 2000 Feb 07; 96(1):114-7. PMID: 10686563.
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    106. Zai C, Wigg KG, Barr CL. Genetics and sleep disorders. Semin Clin Neuropsychiatry. 2000 Jan; 5(1):33-43. PMID: 10704536.
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    107. Swanson JM, Flodman P, Kennedy J, Spence MA, Moyzis R, Schuck S, Murias M, Moriarity J, Barr C, Smith M, Posner M. Dopamine genes and ADHD. Neurosci Biobehav Rev. 2000 Jan; 24(1):21-5. PMID: 10654656.
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    108. Barr CL, Wigg K, Malone M, Schachar R, Tannock R, Roberts W, Kennedy JL. Linkage study of catechol-O-methyltransferase and attention-deficit hyperactivity disorder. Am J Med Genet. 1999 Dec 15; 88(6):710-3. PMID: 10581494.
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    109. Barr CL, Wigg KG, Sandor P. Catechol-O-methyltransferase and Gilles de la Tourette syndrome. Mol Psychiatry. 1999 Sep; 4(5):492-5. PMID: 10523824.
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    110. Barr CL, Wigg KG, Pakstis AJ, Kurlan R, Pauls D, Kidd KK, Tsui LC, Sandor P. Genome scan for linkage to Gilles de la Tourette syndrome. Am J Med Genet. 1999 Aug 20; 88(4):437-45. PMID: 10402514.
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    111. Vincent JB, Kovacs M, Krol R, Barr CL, Kennedy JL. Intergenerational CAG repeat expansion at ERDA1 in a family with childhood-onset depression, schizoaffective disorder, and recurrent major depression. Am J Med Genet. 1999 Feb 05; 88(1):79-82. PMID: 10050972.
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    112. Minassian BA, Sainz J, Serratosa JM, Gee M, Sakamoto LM, Bohlega S, Geoffroy G, Barr C, Scherer SW, Tomiyasu U, Carpenter S, Wigg K, Sanghvi AV, Delgado-Escueta AV. Genetic locus heterogeneity in Lafora's progressive myoclonus epilepsy. Ann Neurol. 1999 Feb; 45(2):262-5. PMID: 9989632.
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    113. Barr C. Why two findings which were eventually refuted have been seminal for the field of psychiatric genetics. J Psychosom Res. 1998 Jun; 44(6):625-6. PMID: 9678738.
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    114. Barr CL, Sandor P. Current status of genetic studies of Gilles de la Tourette syndrome. Can J Psychiatry. 1998 May; 43(4):351-7. PMID: 9598271.
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    115. Levy F, Barr C, Sunohara G. Directions of aetiologic research on attention deficit hyperactivity disorder. Aust N Z J Psychiatry. 1998 Feb; 32(1):97-103. PMID: 9565190.
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    116. Barr CL, Wigg KG, Zovko E, Sandor P, Tsui LC. Linkage study of the dopamine D5 receptor gene and Gilles de la Tourette syndrome. Am J Med Genet. 1997 Feb 21; 74(1):58-61. PMID: 9034008.
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    117. Barr CL, Wigg KG, Zovko E, Sandor P, Tsui LC. No evidence for a major gene effect of the dopamine D4 receptor gene in the susceptibility to Gilles de la Tourette syndrome in five Canadian families. Am J Med Genet. 1996 May 31; 67(3):301-5. PMID: 8725747.
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    118. Petronis A, O'Hara K, Barr CL, Kennedy JL, Van Tol HH. (G)n-mononucleotide polymorphism in the human D4 dopamine receptor (DRD4) gene. Hum Genet. 1994 Jun; 93(6):719. PMID: 8005603.
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    119. Barr CL, Kennedy JL, Pakstis AJ, Wetterberg L, Sjögren B, Bierut L, Wadelius C, Wahlström J, Martinsson T, Giuffra L, et al. Progress in a genome scan for linkage in schizophrenia in a large Swedish kindred. Am J Med Genet. 1994 Mar 15; 54(1):51-8. PMID: 7909991.
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    120. Barr CL, Kennedy JL, Pakstis AJ, Castiglione CM, Kidd JR, Wetterberg L, Kidd KK. Linkage study of a susceptibility locus for schizophrenia in the pseudoautosomal region. Schizophr Bull. 1994; 20(2):277-86. PMID: 8085132.
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    121. Barr CL, Kennedy JL, Lichter JB, Van Tol HH, Wetterberg L, Livak KJ, Kidd KK. Alleles at the dopamine D4 receptor locus do not contribute to the genetic susceptibility to schizophrenia in a large Swedish kindred. Am J Med Genet. 1993 Dec 15; 48(4):218-22. PMID: 8135305.
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    122. Barr CL, Kidd KK. Population frequencies of the A1 allele at the dopamine D2 receptor locus. Biol Psychiatry. 1993 Aug 15; 34(4):204-9. PMID: 8399816.
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    123. Lichter JB, Barr CL, Kennedy JL, Van Tol HH, Kidd KK, Livak KJ. A hypervariable segment in the human dopamine receptor D4 (DRD4) gene. Hum Mol Genet. 1993 Jun; 2(6):767-73. PMID: 8353495.
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