1 - 25 of
40
results
for author:"Purcell S."
in Literature Citations
| Support of association between BRD1 and both schizophrenia and bipolar affective disorder. Nyegaard M., Severinsen J.E., Als T.D., Hedemand A., Straarup S., Nordentoft M., McQuillin A., Bass N., Lawrence J., Thirumalai S. et al. Am. J. Med. Genet. B Neuropsychiatr. Genet. 0:0-0(2009) · Mapped (12) |
| Common polygenic variation contributes to risk of schizophrenia and bipolar disorder. International Schizophrenia Consortium Nature 460:748-752(2009) · Mapped (3,235) |
| Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis. Landers J.E., Melki J., Meininger V., Glass J.D., van den Berg L.H., van Es M.A., Sapp P.C., van Vught P.W., McKenna-Yasek D.M., Blauw H.M. et al. Proc. Natl. Acad. Sci. U.S.A. 106:9004-9009(2009) · Mapped (5) |
| A large-scale international meta-analysis of paraoxonase gene polymorphisms in sporadic ALS. Wills A.M., Cronin S., Slowik A., Kasperaviciute D., Van Es M.A., Morahan J.M., Valdmanis P.N., Meininger V., Melki J., Shaw C.E. et al. Neurology 73:16-24(2009) · Mapped (3) |
| Linkage disequilibrium mapping of the chromosome 6q21-22.31 bipolar I disorder susceptibility locus. Fan J., Ionita-Laza I., McQueen M.B., Devlin B., Purcell S., Faraone S.V., Allen M.H., Bowden C.L., Calabrese J.R., Fossey M.D. et al. Am. J. Med. Genet. B Neuropsychiatr. Genet. 0:0-0(2009) · Mapped (4) |
| Use of a genetic isolate to identify rare disease variants: C7 on 5p associated with MS. Kallio S.P., Jakkula E., Purcell S., Suvela M., Koivisto K., Tienari P.J., Elovaara I., Pirttila T., Reunanen M., Bronnikov D. et al. Hum. Mol. Genet. 18:1670-1683(2009) · Mapped (10) |
| Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants. Myocardial Infarction Genetics Consortium Nat. Genet. 41:334-341(2009) · Mapped (41) |
| Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder. Wellcome Trust Case Control Consortium Nat. Genet. 40:1056-1058(2008) · Mapped (25) |
| 50bp deletion in the promoter for superoxide dismutase 1 (SOD1) reduces SOD1 expression in vitro and may correlate with increased age of onset of sporadic amyotrophic lateral sclerosis. Broom W.J., Greenway M., Sadri-Vakili G., Russ C., Auwarter K.E., Glajch K.E., Dupre N., Swingler R.J., Purcell S., Hayward C. et al. Amyotroph Lateral Scler 9:229-237(2008) · Mapped (1) |
| Whole-genome association study of bipolar disorder. Sklar P., Smoller J.W., Fan J., Ferreira M.A., Perlis R.H., Chambert K., Nimgaonkar V.L., McQueen M.B., Faraone S.V., Kirby A. et al. Mol. Psychiatry 13:558-569(2008) · Mapped (34) |
| Influence of RGS2 on anxiety-related temperament, personality, and brain function. Smoller J.W., Paulus M.P., Fagerness J.A., Purcell S., Yamaki L.H., Hirshfeld-Becker D., Biederman J., Rosenbaum J.F., Gelernter J., Stein M.B. Arch. Gen. Psychiatry 65:298-308(2008) · Mapped (2) |
| Pharmacogenetic analysis of genes implicated in rodent models of antidepressant response: association of TREK1 and treatment resistance in the STAR(*)D study. Perlis R.H., Moorjani P., Fagerness J., Purcell S., Trivedi M.H., Fava M., Rush A.J., Smoller J.W. Neuropsychopharmacology 33:2810-2819(2008) · Mapped (10) |
| Family-based association study of lithium-related and other candidate genes in bipolar disorder. Perlis R.H., Purcell S., Fagerness J., Kirby A., Petryshen T.L., Fan J., Sklar P. Arch. Gen. Psychiatry 65:53-61(2008) · Mapped (71) |
| Two independent alleles at 6q23 associated with risk of rheumatoid arthritis. Plenge R.M., Cotsapas C., Davies L., Price A.L., de Bakker P.I., Maller J., Pe'er I., Burtt N.P., Blumenstiel B., DeFelice M. et al. Nat. Genet. 39:1477-1482(2007) · Mapped (5) |
| Further evidence of association between two NET single-nucleotide polymorphisms with ADHD. Kim J.W., Biederman J., McGrath C.L., Doyle A.E., Mick E., Fagerness J., Purcell S., Smoller J.W., Sklar P., Faraone S.V. Mol. Psychiatry 13:624-630(2008) · Mapped (7) |
| Dysbindin (DTNBP1) and the biogenesis of lysosome-related organelles complex 1 (BLOC-1): main and epistatic gene effects are potential contributors to schizophrenia susceptibility. Morris D.W., Murphy K., Kenny N., Purcell S.M., McGhee K.A., Schwaiger S., Nangle J.M., Donohoe G., Clarke S., Scully P. et al. Biol. Psychiatry 63:24-31(2008) · Mapped (5) |
| Association between treatment-emergent suicidal ideation with citalopram and polymorphisms near cyclic adenosine monophosphate response element binding protein in the STAR*D study. Perlis R.H., Purcell S., Fava M., Fagerness J., Rush A.J., Trivedi M.H., Smoller J.W. Arch. Gen. Psychiatry 64:689-697(2007) · Mapped (10) |
| Contribution of methylenetetrahydrofolate reductase (MTHFR) polymorphisms to negative symptoms in schizophrenia. Roffman J.L., Weiss A.P., Purcell S., Caffalette C.A., Freudenreich O., Henderson D.C., Bottiglieri T., Wong D.H., Halsted C.H., Goff D.C. Biol. Psychiatry 63:42-48(2008) · Mapped (9) |
| Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels. Saxena R., Voight B.F., Lyssenko V., Burtt N.P., de Bakker P.I., Chen H., Roix J.J., Kathiresan S., Hirschhorn J.N., Daly M.J. et al. Science 316:1331-1336(2007) · Mapped (21) |
| Investigation of variation in SNAP-25 and ADHD and relationship to co-morbid major depressive disorder. Kim J.W., Biederman J., Arbeitman L., Fagerness J., Doyle A.E., Petty C., Perlis R.H., Purcell S., Smoller J.W., Faraone S.V. et al. Am. J. Med. Genet. B Neuropsychiatr. Genet. 144B:781-790(2007) · Mapped (1) |
| Investigation of parent-of-origin effects in ADHD candidate genes. Kim J.W., Waldman I.D., Faraone S.V., Biederman J., Doyle A.E., Purcell S., Arbeitman L., Fagerness J., Sklar P., Smoller J.W. Am. J. Med. Genet. B Neuropsychiatr. Genet. 144B:776-780(2007) · Mapped (12) |
| Effects of the methylenetetrahydrofolate reductase (MTHFR) C677T polymorphism on executive function in schizophrenia. Roffman J.L., Weiss A.P., Deckersbach T., Freudenreich O., Henderson D.C., Purcell S., Wong D.H., Halsted C.H., Goff D.C. Schizophr. Res. 92:181-188(2007) · Mapped (9) |
| Evaluation of common variants in the six known maturity-onset diabetes of the young (MODY) genes for association with type 2 diabetes. Winckler W., Weedon M.N., Graham R.R., McCarroll S.A., Purcell S., Almgren P., Tuomi T., Gaudet D., Bostrom K.B., Walker M. et al. Diabetes 56:685-693(2007) · Mapped (21) |
| Clinical and genetic dissection of anger expression and CREB1 polymorphisms in major depressive disorder. Perlis R.H., Purcell S., Fagerness J., Cusin C., Yamaki L., Fava M., Smoller J.W. Biol. Psychiatry 62:536-540(2007) · Mapped (10) |
| Identification of EFHC2 as a quantitative trait locus for fear recognition in Turner syndrome. Weiss L.A., Purcell S., Waggoner S., Lawrence K., Spektor D., Daly M.J., Sklar P., Skuse D. Hum. Mol. Genet. 16:107-113(2007) · Mapped (6) |
