Faculty > Tracey L. Petryshen.    
       

Tracey L. Petryshen, Ph.D.

Selected Publications

Petryshen TL, Kaplan BJ, Liu MF, Field LL. Absence of significant linkage between phonological coding dyslexia and chromosome 6p23-21.3, as determined by use of quantitative-trait methods: confirmation of qualitative analyses. Am J Hum Genet 2000;66:708-14.
 
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Petryshen TL, Kaplan BJ, Liu MF, Schmill de French N, Tobias R, Hughes ML, Field LL. Evidence for a susceptibility locus (DYX4) on chromosome 6q influencing phonological coding dyslexia. Am J Med Genet 2001;105:507-17.

Petryshen TL, Kaplan BJ, Hughes ML, Tzenova J, Field LL. Supportive evidence for the DYX3 dyslexia susceptibility gene in Canadian families. J Med Genet 2002;39:125-6.

Hsiung GY, Kaplan BJ, Petryshen TL, Lu S, Field LL. A dyslexia susceptibility locus (DYX7) linked to dopamine D4 receptor (DRD4) region on chromosome 11p15.5. Am J Med Genet 2004;125B:112-9.

Tzenova J, Kaplan BJ, PetryshenTL, Field LL. Confirmation of a dyslexia susceptibility locus on chromosome 1p34-p36 in a set of 100 Canadian families. Am J Med Genet 2004;127B:117-24.

Sklar P, Pato CN, Kirby A, Petryshen TL, Medeiros H, Carvalho C, Macedo A, Dourado A, Coelho I, Valente J, Soares MJ, Ferreira CP, Lei M, Verner A, Hudson TJ, Morley CP, Kennedy JL, Azevedo MH, Lander E, Daly MJ, Pato MT. Genome-wide scan in Portuguese island families Identifies 5q31-5q35 as a susceptibility locus for schizophrenia and psychosis. Mol Psychiatry 2004;9:213-8.

Pato CN, Pato MT, Kirby A, Petryshen TL, Medeiros H, Carvalho C, Macedo A, Dourado A, Coelho I, Valente J, Soares MJ, Ferreira CP, Lei M, Verner A, Hudson TJ, Morley CP, Kennedy JL, Azevedo MH, Daly MJ, Sklar P. Genome-wide scan in Portuguese island families supports chromosome 6q16.3-21 as a susceptibility locus for bipolar disorder. Neuropsychiatric Genetics 2004;127B:30-4.

Freedman MI, Reich DE, Penney K, McDonald G, Patterson N, Gabriel S, Topol EJ, Smoller JW, Pato CN, Pato MT, Petryshen TL, Kolonel L, Sklar P, Lander ES, Henderson B, Hirschhorn JN, Altshuler D. The impact of population stratification on genetic association studies. Nat Genetics 2004;36(4):388-393.

Middleton FA, Pato MT, Gentile KL, Morley CP, Zhao X, Eisner A, Brown A, Petryshen TL, Kirby A, Medeiros H, Carvalho C, Macedo A, Dourado A, Coelho I, Valente J, Soares MJ, Ferreira CP, Lei M, Azevedo MH, Kennedy JL, Daly MJ, Sklar P, Pato CN. Genome-wide linkage analysis of bipolar disorder using high density single nucleotide polymorphism (SNP) genotyping array: a comparison with microsatellite markers and finding of significant linkage to chromosome 6q22. Am J Hum Gen 2004;74(5):886-897.

Petryshen TL, Kirby A, Hammer RP Jr. Purcell S, O’Leary S, Singer JB, Hill AE, Nadeau JH, Daly MJ, Sklar P. Two QTLs for prepulse inhibition of startle identified on mouse chromosome 16 using chromosome substitution strains. Genetics 2005a;171:1895-904.

Petryshen TL, Middleton FA, Kirby A, Aldinger KA, Purcell S, Tahl AR, Morley CP, McGann L, Gentile KL, Rockwell GN, Medeiros HM, Carvalho C, Macedo A, Dourado A, Valente J, Ferreira CP, Patterson NJ, Azevedo MH, Daly MJ, Pato CN, Pato MT, Sklar P. Support for involvement of neuregulin 1 in schizophrenia pathophysiology. Mol Psychiatry 2005b;10:366-374.

Petryshen TL, Middleton FA, Tahl AR, Rockwell GN, Purcell S, Aldinger KA, Kirby A, Morley CP, McGann L, Gentile KL, Waggoner SG, Medeiros HM, Carvalho C, Macedo A, Albus M, Maier W, Trixler M, Eichhammer P, Schwab SG, Wildenauer DB, Azevedo MH, Pato MT, Pato CN, Daly MJ, Sklar P. Genetic investigation of chromosome 5q GABAA receptor subunit genes in schizophrenia. Mol Psychiatry 2005c; 10:1074-88,1057.

Scolnick EM, Petryshen T, Sklar P. Schizophrenia: Do the genetics and neurobiology of neuregulin provide a pathogenesis model? Harv Rev Psychiatry 2006; 14:64-77.