1 - 25 of
75
results
for author:"Daly M.J."
in Literature Citations
| A genome-wide linkage and association scan reveals novel loci for autism. Gene Discovery Project of Johns Hopkins & the Autism Consortium Nature 461:802-808(2009) · Mapped (2) |
| Common body mass index-associated variants confer risk of extreme obesity. GIANT Consortium Hum. Mol. Genet. 18:3502-3507(2009) · Mapped (4) |
| Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci. International MS Genetics Consortium Nat. Genet. 41:776-782(2009) · Mapped (15) |
| HLA-B*5701 genotype is a major determinant of drug-induced liver injury due to flucloxacillin. International SAE Consortium Nat. Genet. 41:816-819(2009) · Mapped (1,384) |
| Genome-wide association study of electrocardiographic conduction measures in an isolated founder population: Kosrae. Smith J.G., Lowe J.K., Kovvali S., Maller J.B., Salit J., Daly M.J., Stoffel M., Altshuler D.M., Friedman J.M., Breslow J.L. et al. Heart Rhythm 6:634-641(2009) · Mapped (11) |
| A novel hybrid yeast-human network analysis reveals an essential role for FNBP1L in antibacterial autophagy. Huett A., Ng A., Cao Z., Kuballa P., Komatsu M., Daly M.J., Podolsky D.K., Xavier R.J. J. Immunol. 182:4917-4930(2009) · Mapped (5) |
| The role of the CD58 locus in multiple sclerosis. De Jager P.L., Baecher-Allan C., Maier L.M., Arthur A.T., Ottoboni L., Barcellos L., McCauley J.L., Sawcer S., Goris A., Saarela J. et al. Proc. Natl. Acad. Sci. U.S.A. 106:5264-5269(2009) · Mapped (17) |
| 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) |
| Genetic variants in the region harbouring IL2/IL21 associated with ulcerative colitis. Festen E.A., Goyette P., Scott R., Annese V., Zhernakova A., Lian J., Lefebvre C., Brant S.R., Cho J.H., Silverberg M.S. et al. Gut 58:799-804(2009) · Mapped (13) |
| 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) |
| Deletion polymorphism upstream of IRGM associated with altered IRGM expression and Crohn's disease. McCarroll S.A., Huett A., Kuballa P., Chilewski S.D., Landry A., Goyette P., Zody M.C., Hall J.L., Brant S.R., Cho J.H. et al. Nat. Genet. 40:1107-1112(2008) · Mapped (2) |
| Genetic variants near TNFAIP3 on 6q23 are associated with systemic lupus erythematosus. Graham R.R., Cotsapas C., Davies L., Hackett R., Lessard C.J., Leon J.M., Burtt N.P., Guiducci C., Parkin M., Gates C. et al. Nat. Genet. 40:1059-1061(2008) · Mapped (5) |
| Ulcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study. Silverberg M.S., Cho J.H., Rioux J.D., McGovern D.P., Wu J., Annese V., Achkar J.P., Goyette P., Scott R., Xu W. et al. Nat. Genet. 41:216-220(2009) · Mapped (255) |
| Gene-centric association mapping of chromosome 3p implicates MST1 in IBD pathogenesis. Goyette P., Lefebvre C., Ng A., Brant S.R., Cho J.H., Duerr R.H., Silverberg M.S., Taylor K.D., Latiano A., Aumais G. et al. Mucosal Immunol 1:131-138(2008) · Mapped (8) |
| Impaired autophagy of an intracellular pathogen induced by a Crohn's disease associated ATG16L1 variant. Kuballa P., Huett A., Rioux J.D., Daly M.J., Xavier R.J. PLoS ONE 3:e3391-e3391(2008) · Mapped (9) |
| Common SNPs in HMGCR in micronesians and whites associated with LDL-cholesterol levels affect alternative splicing of exon13. Burkhardt R., Kenny E.E., Lowe J.K., Birkeland A., Josowitz R., Noel M., Salit J., Maller J.B., Pe'er I., Daly M.J. et al. Arterioscler. Thromb. Vasc. Biol. 28:2078-2084(2008) · Mapped (5) |
| Common variants at CD40 and other loci confer risk of rheumatoid arthritis. Raychaudhuri S., Remmers E.F., Lee A.T., Hackett R., Guiducci C., Burtt N.P., Gianniny L., Korman B.D., Padyukov L., Kurreeman F.A. et al. Nat. Genet. 40:1216-1223(2008) · Mapped (4) |
| Multigenic control of tuberculosis resistance: analysis of a QTL on mouse chromosome 7 and its synergism with sst1. Sissons J., Yan B.S., Pichugin A.V., Kirby A., Daly M.J., Kramnik I. Genes Immun. 10:37-46(2009) · Mapped (4) |
| 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) |
| Variation near complement factor I is associated with risk of advanced AMD. Fagerness J.A., Maller J.B., Neale B.M., Reynolds R.C., Daly M.J., Seddon J.M. Eur. J. Hum. Genet. 17:100-104(2009) · Mapped (6) |
| A high-density association screen of 155 ion transport genes for involvement with common migraine. Nyholt D.R., LaForge K.S., Kallela M., Alakurtti K., Anttila V., Farkkila M., Hamalainen E., Kaprio J., Kaunisto M.A., Heath A.C. et al. Hum. Mol. Genet. 17:3318-3331(2008) · Mapped (70) |
| Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease. NIDDK IBD Genetics Consortium Nat. Genet. 40:955-962(2008) · Mapped (15) |
| 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) |
| Disruption of neurexin 1 associated with autism spectrum disorder. Kim H.G., Kishikawa S., Higgins A.W., Seong I.S., Donovan D.J., Shen Y., Lally E., Weiss L.A., Najm J., Kutsche K. et al. Am. J. Hum. Genet. 82:199-207(2008) · UniProtKB (1) · Mapped (8) |
| 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) |
