21 results for author:"Feingold E." in Literature citations
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| GWAS of dental caries patterns in the permanent dentition. Shaffer J.R., Feingold E., Wang X., Lee M., Tcuenco K., Weeks D.E., Weyant R.J., Crout R., McNeil D.W., Marazita M.L. J. Dent. Res. 92:38-44(2013) · Mapped (2) |
| An excess of deleterious variants in VEGF-A pathway genes in Down-syndrome-associated atrioventricular septal defects. Ackerman C., Locke A.E., Feingold E., Reshey B., Espana K., Thusberg J., Mooney S., Bean L.J., Dooley K.J., Cua C.L. et al. Am. J. Hum. Genet. 91:646-659(2012) · Mapped (6) |
| Connexin 47 mutations increase risk for secondary lymphedema following breast cancer treatment. Finegold D.N., Baty C.J., Knickelbein K.Z., Perschke S., Noon S.E., Campbell D., Karlsson J.M., Huang D., Kimak M.A., Lawrence E.C. et al. Clin. Cancer Res. 18:2382-2390(2012) · Mapped (1) |
| Genome-wide association analysis of age-at-onset in Alzheimer's disease. Kamboh M.I., Barmada M.M., Demirci F.Y., Minster R.L., Carrasquillo M.M., Pankratz V.S., Younkin S.G., Saykin A.J., Sweet R.A., Feingold E. et al. Mol. Psychiatry 17:1340-1346(2012) · Mapped (8) |
| Genotype-phenotype correlations of pheochromocytoma in two large von Hippel-Lindau (VHL) type 2A kindreds with different missense mutations. Nielsen S.M., Rubinstein W.S., Thull D.L., Armstrong M.J., Feingold E., Stang M.T., Gnarra J.R., Carty S.E. Am. J. Med. Genet. A 155A:168-173(2011) · Mapped (3) |
| Identification of functional elements and regulatory circuits by Drosophila modENCODE. modENCODE Consortium Science 330:1787-1797(2010) · Mapped (47) |
| Association between NEDD4L gene and sodium lithium countertransport. Zheng X., Morrison A.C., Feingold E., Turner S.T., Ferrell R.E. Am. J. Hypertens. 24:145-148(2011) · Mapped (6) |
| Variation in folate pathway genes contributes to risk of congenital heart defects among individuals with Down syndrome. Locke A.E., Dooley K.J., Tinker S.W., Cheong S.Y., Feingold E., Allen E.G., Freeman S.B., Torfs C.P., Cua C.L., Epstein M.P. et al. Genet. Epidemiol. 34:613-623(2010) · Mapped (13) |
| GJC2 missense mutations cause human lymphedema. Ferrell R.E., Baty C.J., Kimak M.A., Karlsson J.M., Lawrence E.C., Franke-Snyder M., Meriney S.D., Feingold E., Finegold D.N. Am. J. Hum. Genet. 86:943-948(2010) · UniProtKB (1) |
| Pooling-based genome-wide association study implicates gamma-glutamyltransferase 1 (GGT1) gene in pancreatic carcinogenesis. Diergaarde B., Brand R., Lamb J., Cheong S.Y., Stello K., Barmada M.M., Feingold E., Whitcomb D.C. Pancreatology 10:194-200(2010) · Mapped (9) |
| Host genetics, steatosis and insulin resistance among African Americans and Caucasian Americans with hepatitis C virus genotype-1 infection. Iuliano A.D., Feingold E., Wahed A.S., Kleiner D.E., Belle S.H., Conjeevaram H.S., Zmuda J., Liang T.J., Yee L.J., Afdhal N. et al. Intervirology 52:49-56(2009) · Mapped (24) |
| Genome-wide microarray expression analysis of CD4+ T Cells from nonobese diabetic congenic mice identifies Cd55 (Daf1) and Acadl as candidate genes for type 1 diabetes. Irie J., Reck B., Wu Y., Wicker L.S., Howlett S., Rainbow D., Feingold E., Ridgway W.M. J. Immunol. 180:1071-1079(2008) · Mapped (2) |
| Gender-specific association of ATP-binding cassette transporter 1 (ABCA1) polymorphisms with the risk of late-onset Alzheimer's disease. Sundar P.D., Feingold E., Minster R.L., DeKosky S.T., Kamboh M.I. Neurobiol. Aging 28:856-862(2007) · Mapped (17) |
| Genetic association of ubiquilin with Alzheimer's disease and related quantitative measures. Kamboh M.I., Minster R.L., Feingold E., DeKosky S.T. Mol. Psychiatry 11:273-279(2006) · Mapped (4) |
| The C161-->T polymorphism in peroxisome proliferator-activated receptor gamma, but not P12A, is associated with insulin resistance in Hispanic and non-Hispanic white women: evidence for another functional variant in peroxisome proliferator-activated receptor gamma. Moffett S.P., Feingold E., Barmada M.M., Damcott C.M., Marshall J.A., Hamman R.F., Ferrell R.E. Metab. Clin. Exp. 54:1552-1556(2005) · Mapped (9) |
| Genetic variation in uncoupling protein 3 is associated with dietary intake and body composition in females. Damcott C.M., Feingold E., Moffett S.P., Barmada M.M., Marshall J.A., Hamman R.F., Ferrell R.E. Metab. Clin. Exp. 53:458-464(2004) · Mapped (6) |
| Genetic variation in fatty acid-binding protein-4 and peroxisome proliferator-activated receptor gamma interactively influence insulin sensitivity and body composition in males. Damcott C.M., Moffett S.P., Feingold E., Barmada M.M., Marshall J.A., Hamman R.F., Ferrell R.E. Metab. Clin. Exp. 53:303-309(2004) · Mapped (11) |
| Evaluation of human leukocyte N-formylpeptide receptor (FPR1) SNPs in aggressive periodontitis patients. Zhang Y., Syed R., Uygar C., Pallos D., Gorry M.C., Firatli E., Cortelli J.R., VanDyke T.E., Hart P.S., Feingold E. et al. Genes Immun. 4:22-29(2003) · Mapped (2) |
| Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. Strausberg R.L., Feingold E.A., Grouse L.H., Derge J.G., Klausner R.D., Collins F.S., Wagner L., Shenmen C.M., Schuler G.D., Altschul S.F. et al. Proc. Natl. Acad. Sci. U.S.A. 99:16899-16903(2002) · UniProtKB (495) · Mapped (4,838) |
| A variant of the glucocorticoid receptor gene is not associated with adrenal androgen excess in women with polycystic ovary syndrome. Kahsar-Miller M., Azziz R., Feingold E., Witchel S.F. Fertil. Steril. 74:1237-1240(2000) · Mapped (12) |
| An olfactory receptor gene is located in the extended human beta-globin gene cluster and is expressed in erythroid cells. Feingold E.A., Penny L.A., Nienhuis A.W., Forget B.G. |