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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.
Artículo
en Inglés
| MEDLINE | ID: mdl-29216383
2.
Race/ethnicity difference in the pharmacogenetics of bilirubin-related atazanavir discontinuation.
Pharmacogenet Genomics
; 28(1): 1-6, 2018 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-29117017
3.
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.
Artículo
en Inglés
| MEDLINE | ID: mdl-24899048
4.
Pharmacogenetics of efavirenz discontinuation for reported central nervous system symptoms appears to differ by race.
Pharmacogenet Genomics
; 26(10): 473-80, 2016 10.
Artículo
en Inglés
| MEDLINE | ID: mdl-27509478
5.
Rare variants in RTEL1 are associated with familial interstitial pneumonia.
Am J Respir Crit Care Med
; 191(6): 646-55, 2015 Mar 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-25607374
6.
Common variants at 9p21 and 8q22 are associated with increased susceptibility to optic nerve degeneration in glaucoma.
PLoS Genet
; 8(4): e1002654, 2012.
Artículo
en Inglés
| MEDLINE | ID: mdl-22570617
7.
Association of CAV1/CAV2 genomic variants with primary open-angle glaucoma overall and by gender and pattern of visual field loss.
Ophthalmology
; 121(2): 508-16, 2014 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-24572674
8.
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.
Artículo
en Inglés
| MEDLINE | ID: mdl-21379321
9.
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.
Artículo
en Inglés
| MEDLINE | ID: mdl-21873608
10.
Estrogen pathway polymorphisms in relation to primary open angle glaucoma: an analysis accounting for gender from the United States.
Mol Vis
; 19: 1471-81, 2013.
Artículo
en Inglés
| MEDLINE | ID: mdl-23869166
11.
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.
Artículo
en Inglés
| MEDLINE | ID: mdl-22125226
12.
Deletion of CFHR3 and CFHR1 genes in age-related macular degeneration.
Hum Mol Genet
; 17(7): 971-7, 2008 Apr 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-18084039
13.
C3 R102G polymorphism increases risk of age-related macular degeneration.
Hum Mol Genet
; 17(12): 1821-4, 2008 Jun 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-18325906
14.
Haplotypes spanning the complement factor H gene are protective against age-related macular degeneration.
Invest Ophthalmol Vis Sci
; 48(9): 4277-83, 2007 Sep.
Artículo
en Inglés
| MEDLINE | ID: mdl-17724217
15.
Single nucleotide polymorphisms related to cystic fibrosis in chronic rhinositus-a pilot study.
Int Forum Allergy Rhinol
; 7(5): 467-473, 2017 05.
Artículo
en Inglés
| MEDLINE | ID: mdl-28236359
16.
Functional candidate genes in age-related macular degeneration: significant association with VEGF, VLDLR, and LRP6.
Invest Ophthalmol Vis Sci
; 47(1): 329-35, 2006 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-16384981
17.
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.
Artículo
en Inglés
| MEDLINE | ID: mdl-15647115
18.
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.
Artículo
en Inglés
| MEDLINE | ID: mdl-26180834
19.
Genome-Wide Association Study of Serum Creatinine Levels during Vancomycin Therapy.
PLoS One
; 10(6): e0127791, 2015.
Artículo
en Inglés
| MEDLINE | ID: mdl-26030142
20.
Examination of NRCAM, LRRN3, KIAA0716, and LAMB1 as autism candidate genes.
BMC Med Genet
; 5: 12, 2004 May 05.
Artículo
en Inglés
| MEDLINE | ID: mdl-15128462