1 - 25 of 54 results for author:"Gilbert J.R." in Literature citations
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| MCP1 SNPs and pulmonary tuberculosis in cohorts from West Africa, the USA and Argentina: lack of association or epistasis with IL12B polymorphisms. Velez Edwards D.R., Tacconelli A., Wejse C., Hill P.C., Morris G.A., Edwards T.L., Gilbert J.R., Myers J.L., Park Y.S., Stryjewski M.E. et al. PLoS ONE 7:e32275-e32275(2012) · Mapped (6) |
| Vitamin D receptor and Alzheimer's disease: a genetic and functional study. Wang L., Hara K., Van Baaren J.M., Price J.C., Beecham G.W., Gallins P.J., Whitehead P.L., Wang G., Lu C., Slifer M.A. et al. Neurobiol. Aging 33:1844.e1-9(2012) · Mapped (6) |
| Hippocampal leptin signaling reduces food intake and modulates food-related memory processing. Kanoski S.E., Hayes M.R., Greenwald H.S., Fortin S.M., Gianessi C.A., Gilbert J.R., Grill H.J. Neuropsychopharmacology 36:1859-1870(2011) · Mapped (1) |
| Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease. Naj A.C., Jun G., Beecham G.W., Wang L.S., Vardarajan B.N., Buros J., Gallins P.J., Buxbaum J.D., Jarvik G.P., Crane P.K. et al. Nat. Genet. 43:436-441(2011) · Mapped (15) |
| A de novo 1.5 Mb microdeletion on chromosome 14q23.2-23.3 in a patient with autism and spherocytosis. Griswold A.J., Ma D., Sacharow S.J., Robinson J.L., Jaworski J.M., Wright H.H., Abramson R.K., Lybaek H., Oyen N., Cuccaro M.L. et al. Autism Res 4:221-227(2011) · Mapped (10) |
| Interleukin 12B (IL12B) genetic variation and pulmonary tuberculosis: a study of cohorts from The Gambia, Guinea-Bissau, United States and Argentina. Morris G.A., Edwards D.R., Hill P.C., Wejse C., Bisseye C., Olesen R., Edwards T.L., Gilbert J.R., Myers J.L., Stryjewski M.E. et al. PLoS ONE 6:e16656-e16656(2011) · Mapped (3) |
| Dementia revealed: novel chromosome 6 locus for late-onset Alzheimer disease provides genetic evidence for folate-pathway abnormalities. Naj A.C., Beecham G.W., Martin E.R., Gallins P.J., Powell E.H., Konidari I., Whitehead P.L., Cai G., Haroutunian V., Scott W.K. et al. PLoS Genet. 6:0-0(2010) · Mapped (12) |
| APOE is not associated with Alzheimer disease: a cautionary tale of genotype imputation. Beecham G.W., Martin E.R., Gilbert J.R., Haines J.L., Pericak-Vance M.A. Ann. Hum. Genet. 74:189-194(2010) · Mapped (5) |
| PCDH11X variation is not associated with late-onset Alzheimer disease susceptibility. Beecham G.W., Naj A.C., Gilbert J.R., Haines J.L., Buxbaum J.D., Pericak-Vance M.A. Psychiatr. Genet. 20:321-324(2010) · Mapped (9) |
| Quantification of the sulfated cholecystokinin CCK-8 in hamster plasma using immunoprecipitation liquid chromatography-mass spectrometry/mass spectrometry. Young S.A., Julka S., Bartley G., Gilbert J.R., Wendelburg B.M., Hung S.C., Anderson W.H., Yokoyama W.H. Anal. Chem. 81:9120-9128(2009) · UniProtKB (1) |
| Variants in toll-like receptors 2 and 9 influence susceptibility to pulmonary tuberculosis in Caucasians, African-Americans, and West Africans. Velez D.R., Wejse C., Stryjewski M.E., Abbate E., Hulme W.F., Myers J.L., Estevan R., Patillo S.G., Olesen R., Tacconelli A. et al. Hum. Genet. 127:65-73(2010) · Mapped (18) |
| Association of SLC11A1 with tuberculosis and interactions with NOS2A and TLR2 in African-Americans and Caucasians. Velez D.R., Hulme W.F., Myers J.L., Stryjewski M.E., Abbate E., Estevan R., Patillo S.G., Gilbert J.R., Hamilton C.D., Scott W.K. Int. J. Tuberc. Lung Dis. 13:1068-1076(2009) · Mapped (48) |
| Examination of tetrahydrobiopterin pathway genes in autism. Schnetz-Boutaud N.C., Anderson B.M., Brown K.D., Wright H.H., Abramson R.K., Cuccaro M.L., Gilbert J.R., Pericak-Vance M.A., Haines J.L. Genes Brain Behav. 8:753-757(2009) · Mapped (49) |
| Association and gene-gene interaction of SLC6A4 and ITGB3 in autism. Ma D.Q., Rabionet R., Konidari I., Jaworski J., Cukier H.N., Wright H.H., Abramson R.K., Gilbert J.R., Cuccaro M.L., Pericak-Vance M.A. et al. Am. J. Med. Genet. B Neuropsychiatr. Genet. 153B:477-483(2010) · Mapped (8) |
| NOS2A, TLR4, and IFNGR1 interactions influence pulmonary tuberculosis susceptibility in African-Americans. Velez D.R., Hulme W.F., Myers J.L., Weinberg J.B., Levesque M.C., Stryjewski M.E., Abbate E., Estevan R., Patillo S.G., Gilbert J.R. et al. Hum. Genet. 126:643-653(2009) · Mapped (19) |
| Common genetic variants on 5p14.1 associate with autism spectrum disorders. Wang K., Zhang H., Ma D., Bucan M., Glessner J.T., Abrahams B.S., Salyakina D., Imielinski M., Bradfield J.P., Sleiman P.M. et al. Nature 459:528-533(2009) · Mapped (4) |
| Resolving the relationship between ApolipoproteinE and depression. Slifer M.A., Martin E.R., Gilbert J.R., Haines J.L., Pericak-Vance M.A. Neurosci. Lett. 455:116-119(2009) · Mapped (5) |
| Examination of association to autism of common genetic variationin genes related to dopamine. Anderson B.M., Schnetz-Boutaud N., Bartlett J., Wright H.H., Abramson R.K., Cuccaro M.L., Gilbert J.R., Pericak-Vance M.A., Haines J.L. Autism Res 1:364-369(2008) · Mapped (50) |
| Genomic convergence to identify candidate genes for Alzheimer disease on chromosome 10. Liang X., Slifer M., Martin E.R., Schnetz-Boutaud N., Bartlett J., Anderson B., Zuchner S., Gwirtsman H., Gilbert J.R., Pericak-Vance M.A. et al. Hum. Mutat. 30:463-471(2009) · Mapped (23) |
| Examination of association of genes in the serotonin system to autism. Anderson B.M., Schnetz-Boutaud N.C., Bartlett J., Wotawa A.M., Wright H.H., Abramson R.K., Cuccaro M.L., Gilbert J.R., Pericak-Vance M.A., Haines J.L. Neurogenetics 10:209-216(2009) · Mapped (42) |
| Genome-wide association study implicates a chromosome 12 risk locus for late-onset Alzheimer disease. Beecham G.W., Martin E.R., Li Y.J., Slifer M.A., Gilbert J.R., Haines J.L., Pericak-Vance M.A. Am. J. Hum. Genet. 84:35-43(2009) · Mapped (38) |
| An association analysis of Alzheimer disease candidate genes detects an ancestral risk haplotype clade in ACE and putative multilocus association between ACE, A2M, and LRRTM3. Edwards T.L., Pericak-Vance M., Gilbert J.R., Haines J.L., Martin E.R., Ritchie M.D. Am. J. Med. Genet. B Neuropsychiatr. Genet. 150B:721-735(2009) · Mapped (47) |
| A SAGE study of apolipoprotein E3/3, E3/4 and E4/4 allele-specific gene expression in hippocampus in Alzheimer disease. Xu P.T., Li Y.J., Qin X.J., Kroner C., Green-Odlum A., Xu H., Wang T.Y., Schmechel D.E., Hulette C.M., Ervin J. et al. Mol. Cell. Neurosci. 36:313-331(2007) · Mapped (5) |
| Investigation of potential gene-gene interactions between APOE and RELN contributing to autism risk. Ashley-Koch A.E., Jaworski J., Ma d.e. Q., Mei H., Ritchie M.D., Skaar D.A., Robert Delong G., Worley G., Abramson R.K., Wright H.H. et al. Psychiatr. Genet. 17:221-226(2007) · Mapped (10) |
| Transforming growth factor-beta1 regulates fibronectin isoform expression and splicing factor SRp40 expression during ATDC5 chondrogenic maturation. Han F., Gilbert J.R., Harrison G., Adams C.S., Freeman T., Tao Z., Zaka R., Liang H., Williams C., Tuan R.S. et al. Exp. Cell Res. 313:1518-1532(2007) · Mapped (3) |