1 - 25 of 146 results for author:"Haines J.L." in Literature citations
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| Variants in the ATP-binding cassette transporter (ABCA7), apolipoprotein E ϵ4,and the risk of late-onset Alzheimer disease in African Americans. Alzheimer Disease Genetics Consortium JAMA 309:1483-1492(2013) · Mapped (5) |
| Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus. NEIGHBOR Consortium Nat. Genet. 45:155-163(2013) · Mapped (2) |
| Common genetic variants in the CLDN2 and PRSS1-PRSS2 loci alter risk for alcohol-related and sporadic pancreatitis. Alzheimer's Disease Genetics Consortium Nat. Genet. 44:1349-1354(2012) · Mapped (25) |
| The p53 codon 72 PRO/PRO genotype may be associated with initial central visual field defects in caucasians with primary open angle glaucoma. Wiggs J.L., Hewitt A.W., Fan B.J., Wang D.Y., Figueiredo Sena D.R., O'Brien C., Realini A., Craig J.E., Dimasi D.P., Mackey D.A. et al. PLoS ONE 7:e45613-e45613(2012) · Mapped (33) |
| Identification and confirmation of an exonic splicing enhancer variation in exon 5 of the Alzheimer disease associated PICALM gene. Schnetz-Boutaud N.C., Hoffman J., Coe J.E., Murdock D.G., Pericak-Vance M.A., Haines J.L. Ann. Hum. Genet. 76:448-453(2012) · Mapped (6) |
| Comprehensive search for Alzheimer disease susceptibility loci in the APOE region. Alzheimer's Disease Genetics Consortium Arch. Neurol. 69:1270-1279(2012) · Mapped (5) |
| The ARMS2 A69S variant and bilateral advanced age-related macular degeneration. Schwartz S.G., Agarwal A., Kovach J.L., Gallins P.J., Cade W., Postel E.A., Wang G., Ayala-Haedo J., Spencer K.M., Haines J.L. et al. Retina (Philadelphia, Pa.) 32:1486-1491(2012) · Mapped (1) |
| Meta-analysis of Parkinson's disease: identification of a novel locus, RIT2. PD GWAS Consortium Ann. Neurol. 71:370-384(2012) · Mapped (1) |
| 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) |
| Population differences in genetic risk for age-related macular degeneration and implications for genetic testing. Spencer K.L., Glenn K., Brown-Gentry K., Haines J.L., Crawford D.C. Arch. Ophthalmol. 130:116-117(2012) · Mapped (1) |
| A novel ARMS2 splice variant is identified in human retina. Wang G., Scott W.K., Whitehead P., Court B.L., Kovach J.L., Schwartz S.G., Agarwal A., Dubovy S., Haines J.L., Pericak-Vance M.A. Exp. Eye Res. 94:187-191(2012) · Mapped (1) |
| Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma in Caucasians from the USA. GENEVA Consortium Hum. Mol. Genet. 20:4707-4713(2011) · Mapped (9) |
| Mutations in UBQLN2 cause dominant X-linked juvenile and adult-onset ALS and ALS/dementia. Deng H.X., Chen W., Hong S.T., Boycott K.M., Gorrie G.H., Siddique N., Yang Y., Fecto F., Shi Y., Zhai H. et al. |
| Lack of association between autism and four heavy metal regulatory genes. Owens S.E., Summar M.L., Ryckman K.K., Haines J.L., Reiss S., Summar S.R., Aschner M. Neurotoxicology 32:769-775(2011) · Mapped (12) |
| Interrogating the complex role of chromosome 16p13.13 in multiple sclerosis susceptibility: independent genetic signals in the CIITA-CLEC16A-SOCS1 gene complex. International Multiple Sclerosis Genetics Consortium Hum. Mol. Genet. 20:3517-3524(2011) · Mapped (8) |
| 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 (14) |
| Whole-exome sequencing links a variant in DHDDS to retinitis pigmentosa. Zuchner S., Dallman J., Wen R., Beecham G., Naj A., Farooq A., Kohli M.A., Whitehead P.L., Hulme W., Konidari I. et al. Am. J. Hum. Genet. 88:201-206(2011) · UniProtKB (1) · Mapped (2) |
| Meta-analysis of the association between variants in SORL1 and Alzheimer disease. Genetic and Environmental Risk in Alzheimer Disease 1 Consortium Arch. Neurol. 68:99-106(2011) · Mapped (5) |
| LOXL1 promoter haplotypes are associated with exfoliation syndrome in a U.S. Caucasian population. Fan B.J., Pasquale L.R., Rhee D., Li T., Haines J.L., Wiggs J.L. Invest. Ophthalmol. Vis. Sci. 52:2372-2378(2011) · Mapped (2) |
| Dissection of chromosome 16p12 linkage peak suggests a possible role for CACNG3 variants in age-related macular degeneration susceptibility. Spencer K.L., Olson L.M., Schnetz-Boutaud N., Gallins P., Wang G., Scott W.K., Agarwal A., Jakobsdottir J., Conley Y., Weeks D.E. et al. Invest. Ophthalmol. Vis. Sci. 52:1748-1754(2011) · Mapped (4) |
| Distribution of COL8A2 and COL8A1 gene variants in Caucasian primary open angle glaucoma patients with thin central corneal thickness. Desronvil T., Logan-Wyatt D., Abdrabou W., Triana M., Jones R., Taheri S., Del Bono E., Pasquale L.R., Olivier M., Haines J.L. et al. Mol. Vis. 16:2185-2191(2010) · Mapped (7) |
| Genotype at polymorphism rs11200638 and HTRA1 expression level. Wang G., Scott W.K., Haines J.L., Pericak-Vance M.A. Arch. Ophthalmol. 128:1491-1493(2010) · Mapped (4) |
| Identification of genomic predictors of atrioventricular conduction: using electronic medical records as a tool for genome science. Denny J.C., Ritchie M.D., Crawford D.C., Schildcrout J.S., Ramirez A.H., Pulley J.M., Basford M.A., Masys D.R., Haines J.L., Roden D.M. Circulation 122:2016-2021(2010) · Mapped (1) |
| 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. 6:878-880(2010) · Mapped (3) |
| The CALHM1 P86L polymorphism is a genetic modifier of age at onset in Alzheimer's disease: a meta-analysis study. Lambert J.C., Sleegers K., Gonzalez-Perez A., Ingelsson M., Beecham G.W., Hiltunen M., Combarros O., Bullido M.J., Brouwers N., Bettens K. et al. J. Alzheimers Dis. 22:247-255(2010) · UniProtKB (1) · Mapped (5) |