Detalhe da pesquisa
1.
Mucus sialylation determines intestinal host-commensal homeostasis.
Cell
; 185(7): 1172-1188.e28, 2022 03 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-35303419
2.
Genotyping, sequencing and analysis of 140,000 adults from Mexico City.
Nature
; 622(7984): 784-793, 2023 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-37821707
3.
Common and rare variant associations with clonal haematopoiesis phenotypes.
Nature
; 612(7939): 301-309, 2022 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-36450978
4.
Whole-genome sequencing reveals host factors underlying critical COVID-19.
Nature
; 607(7917): 97-103, 2022 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-35255492
5.
Exome sequencing and analysis of 454,787 UK Biobank participants.
Nature
; 599(7886): 628-634, 2021 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-34662886
6.
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
7.
Author Correction: Genotyping, sequencing and analysis of 140,000 adults from Mexico City.
Nature
; 626(8001): E18, 2024 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-38332034
8.
A Genetic Risk Variant for Multiple Sclerosis Severity is Associated with Brain Atrophy.
Ann Neurol
; 94(6): 1080-1085, 2023 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-37753809
9.
Author Correction: Common and rare variant associations with clonal haematopoiesis phenotypes.
Nature
; 615(7950): E3, 2023 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-36807635
10.
Genome-wide association analysis of serum alanine and aspartate aminotransferase, and the modifying effects of BMI in 388k European individuals.
Genet Epidemiol
; 45(6): 664-681, 2021 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-34184762
11.
Efficacy and Safety of Sarilumab in Hospitalized Patients With Coronavirus Disease 2019: A Randomized Clinical Trial.
Clin Infect Dis
; 75(1): e380-e388, 2022 08 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-35219277
12.
UGT1A1 genetic variants are associated with increases in bilirubin levels in rheumatoid arthritis patients treated with sarilumab.
Pharmacogenomics J
; 22(3): 160-165, 2022 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-35149777
13.
Clinical Implications of the Amyloidogenic V122I Transthyretin Variant in the General Population.
J Card Fail
; 28(3): 403-414, 2022 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-34634447
14.
Heterozygosity for a Pathogenic Variant in SLC12A3 That Causes Autosomal Recessive Gitelman Syndrome Is Associated with Lower Serum Potassium.
J Am Soc Nephrol
; 32(3): 756-765, 2021 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-33542107
15.
Patients With High Genome-Wide Polygenic Risk Scores for Coronary Artery Disease May Receive Greater Clinical Benefit From Alirocumab Treatment in the ODYSSEY OUTCOMES Trial.
Circulation
; 141(8): 624-636, 2020 02 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-31707832
16.
Homozygosity for a mutation affecting the catalytic domain of tyrosyl-tRNA synthetase (YARS) causes multisystem disease.
Hum Mol Genet
; 28(4): 525-538, 2019 02 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-30304524
17.
An international genome-wide meta-analysis of primary biliary cholangitis: Novel risk loci and candidate drugs.
J Hepatol
; 75(3): 572-581, 2021 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-34033851
18.
Profiling and Leveraging Relatedness in a Precision Medicine Cohort of 92,455 Exomes.
Am J Hum Genet
; 102(5): 874-889, 2018 05 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-29727688
19.
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
20.
A Protein-Truncating HSD17B13 Variant and Protection from Chronic Liver Disease.
N Engl J Med
; 378(12): 1096-1106, 2018 03 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-29562163