Detalhe da pesquisa
1.
Ancestry- and sex-specific effects underlying inguinal hernia susceptibility identified in a multiethnic genome-wide association study meta-analysis.
Hum Mol Genet
; 31(13): 2279-2293, 2022 07 07.
Artigo
Inglês
| MEDLINE | ID: mdl-35022708
2.
Multitrait genetic association analysis identifies 50 new risk loci for gastro-oesophageal reflux, seven new loci for Barrett's oesophagus and provides insights into clinical heterogeneity in reflux diagnosis.
Gut
; 71(6): 1053-1061, 2022 06.
Artigo
Inglês
| MEDLINE | ID: mdl-34187846
3.
Insights into the genetic basis of retinal detachment.
Hum Mol Genet
; 29(4): 689-702, 2020 03 13.
Artigo
Inglês
| MEDLINE | ID: mdl-31816047
4.
Analysis of putative cis-regulatory elements regulating blood pressure variation.
Hum Mol Genet
; 29(11): 1922-1932, 2020 07 21.
Artigo
Inglês
| MEDLINE | ID: mdl-32436959
5.
Gene- and tissue-level interactions in normal gastrointestinal development and Hirschsprung disease.
Proc Natl Acad Sci U S A
; 116(52): 26697-26708, 2019 Dec 26.
Artigo
Inglês
| MEDLINE | ID: mdl-31818953
6.
Rare variants in fox-1 homolog A (RBFOX1) are associated with lower blood pressure.
PLoS Genet
; 13(3): e1006678, 2017 03.
Artigo
Inglês
| MEDLINE | ID: mdl-28346479
7.
Trans-ethnic meta-analysis of genome-wide association studies for Hirschsprung disease.
Hum Mol Genet
; 25(23): 5265-5275, 2016 12 01.
Artigo
Inglês
| MEDLINE | ID: mdl-27702942
8.
The role of rare variants in systolic blood pressure: analysis of ExomeChip data in HyperGEN African Americans.
Hum Hered
; 79(1): 20-7, 2015.
Artigo
Inglês
| MEDLINE | ID: mdl-25765051
9.
Genome-wide meta-analysis of insomnia prioritizes genes associated with metabolic and psychiatric pathways.
Nat Genet
; 54(8): 1125-1132, 2022 08.
Artigo
Inglês
| MEDLINE | ID: mdl-35835914
10.
Biophysical and structural considerations for protein sequence evolution.
BMC Evol Biol
; 11: 361, 2011 Dec 16.
Artigo
Inglês
| MEDLINE | ID: mdl-22171550
11.
Nuclear genome-wide associations with mitochondrial heteroplasmy.
Sci Adv
; 7(12)2021 03.
Artigo
Inglês
| MEDLINE | ID: mdl-33731350
12.
Multiple, independent, common variants at RET, SEMA3 and NRG1 gut enhancers specify Hirschsprung disease risk in European ancestry subjects.
J Pediatr Surg
; 56(12): 2286-2294, 2021 Dec.
Artigo
Inglês
| MEDLINE | ID: mdl-34006365
13.
Genetic analyses identify widespread sex-differential participation bias.
Nat Genet
; 53(5): 663-671, 2021 05.
Artigo
Inglês
| MEDLINE | ID: mdl-33888908
14.
Combined linkage and association analysis identifies rare and low frequency variants for blood pressure at 1q31.
Eur J Hum Genet
; 27(2): 269-277, 2019 02.
Artigo
Inglês
| MEDLINE | ID: mdl-30262922
15.
Contributions of rare coding variants in hypotension syndrome genes to population blood pressure variation.
Medicine (Baltimore)
; 97(33): e11865, 2018 Aug.
Artigo
Inglês
| MEDLINE | ID: mdl-30113482
16.
Genome-wide association study of Hirschsprung disease detects a novel low-frequency variant at the RET locus.
Eur J Hum Genet
; 26(4): 561-569, 2018 04.
Artigo
Inglês
| MEDLINE | ID: mdl-29379196
17.
MicroRNAs in the miR-17 and miR-15 families are downregulated in chronic kidney disease with hypertension.
PLoS One
; 12(8): e0176734, 2017.
Artigo
Inglês
| MEDLINE | ID: mdl-28771472
18.
Genome-wide association analyses using electronic health records identify new loci influencing blood pressure variation.
Nat Genet
; 49(1): 54-64, 2017 01.
Artigo
Inglês
| MEDLINE | ID: mdl-27841878
19.
Rare coding variants associated with blood pressure variation in 15â914 individuals of African ancestry.
J Hypertens
; 35(7): 1381-1389, 2017 07.
Artigo
Inglês
| MEDLINE | ID: mdl-28234671
20.
Rare coding TTN variants are associated with electrocardiographic QT interval in the general population.
Sci Rep
; 6: 28356, 2016 06 20.
Artigo
Inglês
| MEDLINE | ID: mdl-27321809