Detalhe da pesquisa
1.
Genetic Susceptibility to Postdiarrheal Hemolytic-Uremic Syndrome After Shiga Toxin-Producing Escherichia coli Infection: A Centers for Disease Control and Prevention FoodNet Study.
J Infect Dis
; 217(6): 1000-1010, 2018 03 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-29216383
2.
Rare and common variants in extracellular matrix gene Fibrillin 2 (FBN2) are associated with macular degeneration.
Hum Mol Genet
; 23(21): 5827-37, 2014 Nov 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-24899048
3.
Rare variants in RTEL1 are associated with familial interstitial pneumonia.
Am J Respir Crit Care Med
; 191(6): 646-55, 2015 Mar 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-25607374
4.
Common variants at 9p21 and 8q22 are associated with increased susceptibility to optic nerve degeneration in glaucoma.
PLoS Genet
; 8(4): e1002654, 2012.
Artigo
em Inglês
| MEDLINE | ID: mdl-22570617
5.
Mapping of the disease locus and identification of ADAMTS10 as a candidate gene in a canine model of primary open angle glaucoma.
PLoS Genet
; 7(2): e1001306, 2011 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-21379321
6.
Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma in Caucasians from the USA.
Hum Mol Genet
; 20(23): 4707-13, 2011 Dec 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-21873608
7.
Pitfalls of merging GWAS data: lessons learned in the eMERGE network and quality control procedures to maintain high data quality.
Genet Epidemiol
; 35(8): 887-98, 2011 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-22125226
8.
Deletion of CFHR3 and CFHR1 genes in age-related macular degeneration.
Hum Mol Genet
; 17(7): 971-7, 2008 Apr 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-18084039
9.
C3 R102G polymorphism increases risk of age-related macular degeneration.
Hum Mol Genet
; 17(12): 1821-4, 2008 Jun 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-18325906
10.
Haplotypes spanning the complement factor H gene are protective against age-related macular degeneration.
Invest Ophthalmol Vis Sci
; 48(9): 4277-83, 2007 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-17724217
11.
Genome-wide and Ordered-Subset linkage analyses provide support for autism loci on 17q and 19p with evidence of phenotypic and interlocus genetic correlates.
BMC Med Genet
; 6: 1, 2005 Jan 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-15647115
12.
Screening for UGT1A1 Genotype in Study A5257 Would Have Markedly Reduced Premature Discontinuation of Atazanavir for Hyperbilirubinemia.
Open Forum Infect Dis
; 2(3): ofv085, 2015 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-26180834
13.
Genome-Wide Association Study of Serum Creatinine Levels during Vancomycin Therapy.
PLoS One
; 10(6): e0127791, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-26030142
14.
Examination of NRCAM, LRRN3, KIAA0716, and LAMB1 as autism candidate genes.
BMC Med Genet
; 5: 12, 2004 May 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-15128462
15.
Mechanistic phenotypes: an aggregative phenotyping strategy to identify disease mechanisms using GWAS data.
PLoS One
; 8(12): e81503, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-24349080
16.
The NEIGHBOR consortium primary open-angle glaucoma genome-wide association study: rationale, study design, and clinical variables.
J Glaucoma
; 22(7): 517-25, 2013 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-22828004
17.
CDKN2B-AS1 genotype-glaucoma feature correlations in primary open-angle glaucoma patients from the United States.
Am J Ophthalmol
; 155(2): 342-353.e5, 2013 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-23111177
18.
Identification of a rare coding variant in complement 3 associated with age-related macular degeneration.
Nat Genet
; 45(11): 1375-9, 2013 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-24036949
19.
Dissection of chromosome 16p12 linkage peak suggests a possible role for CACNG3 variants in age-related macular degeneration susceptibility.
Invest Ophthalmol Vis Sci
; 52(3): 1748-54, 2011 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-21169531
20.
Using genetic variation and environmental risk factor data to identify individuals at high risk for age-related macular degeneration.
PLoS One
; 6(3): e17784, 2011 Mar 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-21455292