1 - 25 of 76 results for author:"Schork N.J." in Literature citations
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| Noncoding transcription within the Igh distal V(H) region at PAIR elements affects the 3D structure of the Igh locus in pro-B cells. Verma-Gaur J., Torkamani A., Schaffer L., Head S.R., Schork N.J., Feeney A.J. Proc. Natl. Acad. Sci. U.S.A. 109:17004-17009(2012) · Mapped (4) |
| Neuropeptide Y (NPY): genetic variation in the human promoter alters glucocorticoid signaling, yielding increased NPY secretion and stress responses. Zhang K., Rao F., Miramontes-Gonzalez J.P., Hightower C.M., Vaught B., Chen Y., Greenwood T.A., Schork A.J., Wang L., Mahata M. et al. J. Am. Coll. Cardiol. 60:1678-1689(2012) · Mapped (2) |
| Genome-wide significant association between a 'negative mood delusions' dimension in bipolar disorder and genetic variation on chromosome 3q26.1. Bipolar Disorder Genome Study (BiGS) Consortium Transl Psychiatry 2:e165-e165(2012) · Mapped (3) |
| Association of common genetic variants in GPCPD1 with scaling of visual cortical surface area in humans. Bakken T.E., Roddey J.C., Djurovic S., Akshoomoff N., Amaral D.G., Bloss C.S., Casey B.J., Chang L., Ernst T.M., Gruen J.R. et al. Proc. Natl. Acad. Sci. U.S.A. 109:3985-3990(2012) · Mapped (2) |
| Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4. Psychiatric GWAS Consortium Bipolar Disorder Working Group Nat. Genet. 43:977-983(2011) · Mapped (16) |
| Disruption of vascular homeostasis in patients with Kawasaki disease: involvement of vascular endothelial growth factor and angiopoietins. International Kawasaki Disease Genetics Consortium Arthritis Rheum. 64:306-315(2012) · Mapped (6) |
| Genetic association of recovery from eating disorders: the role of GABA receptor SNPs. Bloss C.S., Berrettini W., Bergen A.W., Magistretti P., Duvvuri V., Strober M., Brandt H., Crawford S., Crow S., Fichter M.M. et al. Neuropsychopharmacology 36:2222-2232(2011) · Mapped (3) |
| Methylenetetrahydrofolate reductase (MTHFR) polymorphism A1298C (Glu429Ala) predicts decline in renal function over time in the African-American Study of Kidney Disease and Hypertension (AASK) Trial and Veterans Affairs Hypertension Cohort (VAHC). Fung M.M., Salem R.M., Lipkowitz M.S., Bhatnagar V., Pandey B., Schork N.J., O'Connor D.T. Nephrol. Dial. Transplant. 27:197-205(2012) · Mapped (2) |
| CCCTC-binding factor (CTCF) and cohesin influence the genomic architecture of the Igh locus and antisense transcription in pro-B cells. Degner S.C., Verma-Gaur J., Wong T.P., Bossen C., Iverson G.M., Torkamani A., Vettermann C., Lin Y.C., Ju Z., Schulz D. et al. Proc. Natl. Acad. Sci. U.S.A. 108:9566-9571(2011) · Mapped (9) |
| Global developmental gene expression and pathway analysis of normal brain development and mouse models of human neuronal migration defects. Pramparo T., Libiger O., Jain S., Li H., Youn Y.H., Hirotsune S., Schork N.J., Wynshaw-Boris A. PLoS Genet. 7:e1001331-e1001331(2011) · Mapped (52) |
| Genome-wide association study identifies genetic variation in neurocan as a susceptibility factor for bipolar disorder. Bipolar Disorder Genome Study (BiGS) Consortium Am. J. Hum. Genet. 88:372-381(2011) · Mapped (4) |
| A genome-wide association study on common SNPs and rare CNVs in anorexia nervosa. Wang K., Zhang H., Bloss C.S., Duvvuri V., Kaye W., Schork N.J., Berrettini W., Hakonarson H., Brandt H., Crawford S. et al. Mol. Psychiatry 16:949-959(2011) · Mapped (24) |
| A covering method for detecting genetic associations between rare variants and common phenotypes. Bhatia G., Bansal V., Harismendy O., Schork N.J., Topol E.J., Frazer K., Bafna V. PLoS Comput. Biol. 6:e1000954-e1000954(2010) · Mapped (6) |
| Longitudinal genome-wide association of cardiovascular disease risk factors in the Bogalusa heart study. Smith E.N., Chen W., Kahonen M., Kettunen J., Lehtimaki T., Peltonen L., Raitakari O.T., Salem R.M., Schork N.J., Shaw M. et al. PLoS Genet. 6:e936-45(2010) · Mapped (11) |
| Progression of chronic kidney disease: Adrenergic genetic influence on glomerular filtration rate decline in hypertensive nephrosclerosis. Chen Y., Lipkowitz M.S., Salem R.M., Fung M.M., Bhatnagar V., Mahata M., Nievergelt C.M., Rao F., Mahata S.K., Schork N.J. et al. Am. J. Nephrol. 32:23-30(2010) · Mapped (5) |
| Association study of 182 candidate genes in anorexia nervosa. Pinheiro A.P., Bulik C.M., Thornton L.M., Sullivan P.F., Root T.L., Bloss C.S., Berrettini W.H., Schork N.J., Kaye W.H., Bergen A.W. et al. Am. J. Med. Genet. B Neuropsychiatr. Genet. 153B:1070-1080(2010) · Mapped (747) |
| Genetic regulation of catecholamine synthesis, storage and secretion in the spontaneously hypertensive rat. Jirout M.L., Friese R.S., Mahapatra N.R., Mahata M., Taupenot L., Mahata S.K., Kren V., Zidek V., Fischer J., Maatz H. et al. Hum. Mol. Genet. 19:2567-2580(2010) · Mapped (2) |
| Sex-dependent association of common variants of microcephaly genes with brain structure. Rimol L.M., Agartz I., Djurovic S., Brown A.A., Roddey J.C., Kahler A.K., Mattingsdal M., Athanasiu L., Joyner A.H., Schork N.J. et al. Proc. Natl. Acad. Sci. U.S.A. 107:384-388(2010) · Mapped (59) |
| CACNA1C gene polymorphisms, cardiovascular disease outcomes, and treatment response. Beitelshees A.L., Navare H., Wang D., Gong Y., Wessel J., Moss J.I., Langaee T.Y., Cooper-DeHoff R.M., Sadee W., Pepine C.J. et al. Circ Cardiovasc Genet 2:362-370(2009) · Mapped (12) |
| Autonomic function in hypertension; role of genetic variation at the catecholamine storage vesicle protein chromogranin B. Zhang K., Rao F., Rana B.K., Gayen J.R., Calegari F., King A., Rosa P., Huttner W.B., Stridsberg M., Mahata M. et al. Circ Cardiovasc Genet 2:46-56(2009) · Mapped (3) |
| Human dopamine beta-hydroxylase (DBH) regulatory polymorphism that influences enzymatic activity, autonomic function, and blood pressure. Chen Y., Wen G., Rao F., Zhang K., Wang L., Rodriguez-Flores J.L., Sanchez A.P., Mahata M., Taupenot L., Sun P. et al. J. Hypertens. 28:76-86(2010) · Mapped (1) |
| Adrenergic beta-1 receptor genetic variation predicts longitudinal rate of GFR decline in hypertensive nephrosclerosis. Fung M.M., Chen Y., Lipkowitz M.S., Salem R.M., Bhatnagar V., Mahata M., Nievergelt C.M., Rao F., Mahata S.K., Schork N.J. et al. Nephrol. Dial. Transplant. 24:3677-3686(2009) · Mapped (5) |
| A common MECP2 haplotype associates with reduced cortical surface area in humans in two independent populations. Joyner A.H., J C.R., Bloss C.S., Bakken T.E., Rimol L.M., Melle I., Agartz I., Djurovic S., Topol E.J., Schork N.J. et al. Proc. Natl. Acad. Sci. U.S.A. 106:15483-15488(2009) · Mapped (15) |
| Natural variation within the neuronal nicotinic acetylcholine receptor cluster on human chromosome 15q24: influence on heritable autonomic traits in twin pairs. Rana B.K., Wessel J., Mahboubi V., Rao F., Haeller J., Gayen J.R., Eskin E., Valle A.M., Das M., Mahata S.K. et al. J. Pharmacol. Exp. Ther. 331:419-428(2009) · Mapped (10) |
| Genome-wide association study of bipolar disorder in European American and African American individuals. Smith E.N., Bloss C.S., Badner J.A., Barrett T., Belmonte P.L., Berrettini W., Byerley W., Coryell W., Craig D., Edenberg H.J. et al. Mol. Psychiatry 14:755-763(2009) · Mapped (14) |