Detalhe da pesquisa
1.
A deep catalogue of protein-coding variation in 983,578 individuals.
Nature
; 2024 May 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-38768635
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.
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
4.
Author Correction: Common and rare variant associations with clonal haematopoiesis phenotypes.
Nature
; 615(7950): E3, 2023 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-36807635
5.
Genome-wide Study Identifies Association between HLA-B∗55:01 and Self-Reported Penicillin Allergy.
Am J Hum Genet
; 107(4): 612-621, 2020 10 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32888428
6.
GWAS Identifies Risk Locus for Erectile Dysfunction and Implicates Hypothalamic Neurobiology and Diabetes in Etiology.
Am J Hum Genet
; 104(1): 157-163, 2019 01 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-30583798
7.
Causal relationships between obesity and the leading causes of death in women and men.
PLoS Genet
; 15(10): e1008405, 2019 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-31647808
8.
Converging evidence from exome sequencing and common variants implicates target genes for osteoporosis.
Nat Genet
; 55(8): 1277-1287, 2023 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-37558884
9.
A deep catalog of protein-coding variation in 985,830 individuals.
bioRxiv
; 2023 Nov 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-37214792
10.
Genetically predicted vitamin K levels and risk of osteoarthritis: Mendelian randomization study.
Semin Arthritis Rheum
; 55: 152030, 2022 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-35667331
11.
Multiancestry exome sequencing reveals INHBE mutations associated with favorable fat distribution and protection from diabetes.
Nat Commun
; 13(1): 4844, 2022 08 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-35999217
12.
Colocalization analysis of polycystic ovary syndrome to identify potential disease-mediating genes and proteins.
Eur J Hum Genet
; 29(9): 1446-1454, 2021 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-33664499
13.
Response to comment on "Evaluating the cardiovascular safety of sclerostin inhibition using evidence from meta-analysis of clinical trials and human genetics".
Sci Transl Med
; 13(622): eabf4530, 2021 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-34851696
14.
Evaluating the cardiovascular safety of sclerostin inhibition using evidence from meta-analysis of clinical trials and human genetics.
Sci Transl Med
; 12(549)2020 06 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-32581134
15.
Genetic IL-6R variants and therapeutic inhibition of IL-6 receptor signalling in COVID-19 - Authors' reply.
Lancet Rheumatol
; 3(2): e97-e98, 2021 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-33521676
16.
Genetic variants mimicking therapeutic inhibition of IL-6 receptor signaling and risk of COVID-19.
Lancet Rheumatol
; 2(11): e658-e659, 2020 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-33015641
17.
Commentary: Using human genetics to guide the repurposing of medicines.
Int J Epidemiol
; 49(4): 1140-1146, 2020 08 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32097451
18.
Commentary: Mendelian randomization and women's health.
Int J Epidemiol
; 48(3): 830-833, 2019 06 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31292646