Detalhe da pesquisa
1.
Genetic variants regulating immune cell levels in health and disease.
Cell
; 155(1): 242-56, 2013 Sep 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-24074872
2.
Common and rare variant associations with clonal haematopoiesis phenotypes.
Nature
; 612(7939): 301-309, 2022 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-36450978
3.
Exome sequencing and analysis of 454,787 UK Biobank participants.
Nature
; 599(7886): 628-634, 2021 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-34662886
4.
Germline Mutations in CIDEB and Protection against Liver Disease.
N Engl J Med
; 387(4): 332-344, 2022 07 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-35939579
5.
Pan-ancestry exome-wide association analyses of COVID-19 outcomes in 586,157 individuals.
Am J Hum Genet
; 108(7): 1350-1355, 2021 07 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34115965
6.
Author Correction: Common and rare variant associations with clonal haematopoiesis phenotypes.
Nature
; 615(7950): E3, 2023 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-36807635
7.
Correlations between H2 Permeation and Physical/Mechanical Properties in Ethylene Propylene Diene Monomer Polymers Blended with Carbon Black and Silica Fillers.
Int J Mol Sci
; 24(3)2023 Feb 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-36769186
8.
Genome-wide Study of Atrial Fibrillation Identifies Seven Risk Loci and Highlights Biological Pathways and Regulatory Elements Involved in Cardiac Development.
Am J Hum Genet
; 102(1): 103-115, 2018 01 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-29290336
9.
Whole-Genome Sequencing Identifies Novel Functional Loci Associated with Lung Function in Puerto Rican Youth.
Am J Respir Crit Care Med
; 202(7): 962-972, 2020 10 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32459537
10.
Common α-globin variants modify hematologic and other clinical phenotypes in sickle cell trait and disease.
PLoS Genet
; 14(3): e1007293, 2018 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-29590102
11.
Genome-Wide Association Study of Diabetic Kidney Disease Highlights Biology Involved in Glomerular Basement Membrane Collagen.
J Am Soc Nephrol
; 30(10): 2000-2016, 2019 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-31537649
12.
Comparing variant calling algorithms for target-exon sequencing in a large sample.
BMC Bioinformatics
; 16: 75, 2015 Mar 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-25884587
13.
Systems genetic analysis of osteoblast-lineage cells.
PLoS Genet
; 8(12): e1003150, 2012.
Artigo
em Inglês
| MEDLINE | ID: mdl-23300464
14.
A likelihood-based framework for variant calling and de novo mutation detection in families.
PLoS Genet
; 8(10): e1002944, 2012.
Artigo
em Inglês
| MEDLINE | ID: mdl-23055937
15.
Comparative analysis of proteome and transcriptome variation in mouse.
PLoS Genet
; 7(6): e1001393, 2011 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-21695224
16.
Fine mapping of five loci associated with low-density lipoprotein cholesterol detects variants that double the explained heritability.
PLoS Genet
; 7(7): e1002198, 2011 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-21829380
17.
Rare coding variants in CHRNB2 reduce the likelihood of smoking.
Nat Genet
; 55(7): 1138-1148, 2023 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-37308787
18.
Genome-wide analysis provides genetic evidence that ACE2 influences COVID-19 risk and yields risk scores associated with severe disease.
Nat Genet
; 54(4): 382-392, 2022 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-35241825
19.
Sequencing of 640,000 exomes identifies GPR75 variants associated with protection from obesity.
Science
; 373(6550)2021 07 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-34210852
20.
Genetic signature to provide robust risk assessment of psoriatic arthritis development in psoriasis patients.
Nat Commun
; 9(1): 4178, 2018 10 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-30301895