Detalles de la búsqueda
1.
A Phenome-Wide Association Study of genes associated with COVID-19 severity reveals shared genetics with complex diseases in the Million Veteran Program.
PLoS Genet
; 18(4): e1010113, 2022 04.
Artículo
en Inglés
| MEDLINE | ID: mdl-35482673
2.
Correction: A missense variant in Mitochondrial Amidoxime Reducing Component 1 gene and protection against liver disease.
PLoS Genet
; 17(4): e1009503, 2021 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-33822779
3.
Genetically proxied glucose-lowering drug target perturbation and risk of cancer: a Mendelian randomisation analysis.
Diabetologia
; 66(8): 1481-1500, 2023 08.
Artículo
en Inglés
| MEDLINE | ID: mdl-37171501
4.
A missense variant in Mitochondrial Amidoxime Reducing Component 1 gene and protection against liver disease.
PLoS Genet
; 16(4): e1008629, 2020 04.
Artículo
en Inglés
| MEDLINE | ID: mdl-32282858
5.
Mendelian randomization study of diabetes and dementia in the Million Veteran Program.
Alzheimers Dement
; 19(10): 4367-4376, 2023 10.
Artículo
en Inglés
| MEDLINE | ID: mdl-37417779
6.
Separating the direct effects of traits on atherosclerotic cardiovascular disease from those mediated by type 2 diabetes.
Diabetologia
; 65(5): 790-799, 2022 05.
Artículo
en Inglés
| MEDLINE | ID: mdl-35129650
7.
Genetic determinants of increased body mass index mediate the effect of smoking on increased risk for type 2 diabetes but not coronary artery disease.
Hum Mol Genet
; 29(19): 3327-3337, 2020 11 25.
Artículo
en Inglés
| MEDLINE | ID: mdl-32833022
8.
Harmonizing Genetic Ancestry and Self-identified Race/Ethnicity in Genome-wide Association Studies.
Am J Hum Genet
; 105(4): 763-772, 2019 10 03.
Artículo
en Inglés
| MEDLINE | ID: mdl-31564439
9.
Dietary Vitamin E Intake Is Associated With a Reduced Risk of Developing Digestive Diseases and Nonalcoholic Fatty Liver Disease.
Am J Gastroenterol
; 117(6): 927-930, 2022 06 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-35288522
10.
Leveraging human genetic data to investigate the cardiometabolic effects of glucose-dependent insulinotropic polypeptide signalling.
Diabetologia
; 64(12): 2773-2778, 2021 12.
Artículo
en Inglés
| MEDLINE | ID: mdl-34505161
11.
Metabolic Traits and Stroke Risk in Individuals of African Ancestry: Mendelian Randomization Analysis.
Stroke
; 52(8): 2680-2684, 2021 08.
Artículo
en Inglés
| MEDLINE | ID: mdl-34078102
12.
Genome-first approach to rare EYA4 variants and cardio-auditory phenotypes in adults.
Hum Genet
; 140(6): 957-967, 2021 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-33745059
13.
Genetics of height and risk of atrial fibrillation: A Mendelian randomization study.
PLoS Med
; 17(10): e1003288, 2020 10.
Artículo
en Inglés
| MEDLINE | ID: mdl-33031386
14.
Genomic architecture and treatment outcome in pediatric acute myeloid leukemia: a Children's Oncology Group report.
Blood
; 129(23): 3051-3058, 2017 06 08.
Artículo
en Inglés
| MEDLINE | ID: mdl-28411282
15.
Polymorphisms in cytochrome P450 are associated with extensive efavirenz pharmacokinetics and CNS toxicities in an HIV cohort in Botswana.
Pharmacogenomics J
; 18(5): 678-688, 2018 09.
Artículo
en Inglés
| MEDLINE | ID: mdl-29855606
16.
TPMT and MTHFR genotype is not associated with altered risk of thioguanine-related sinusoidal obstruction syndrome in pediatric acute lymphoblastic leukemia: a report from the Children's Oncology Group.
Pediatr Blood Cancer
; 61(11): 2086-8, 2014 Nov.
Artículo
en Inglés
| MEDLINE | ID: mdl-24737678
17.
Patient and hospital factors associated with induction mortality in acute lymphoblastic leukemia.
Pediatr Blood Cancer
; 61(5): 846-52, 2014 May.
Artículo
en Inglés
| MEDLINE | ID: mdl-24249480
18.
Validity of a questionnaire measuring the world health organization concept of health system responsiveness with respect to perinatal services in the Dutch obstetric care system.
BMC Health Serv Res
; 14: 622, 2014 Dec 03.
Artículo
en Inglés
| MEDLINE | ID: mdl-25465053
19.
Session Introduction: Drug-repurposing and discovery in the era of "big" real-world data: how the incorporation of observational data, genetics, and other -omic technologies can move us forward.
Pac Symp Biocomput
; 29: 226-231, 2024.
Artículo
en Inglés
| MEDLINE | ID: mdl-38160282
20.
A genome-first approach to variants in MLXIPL and their association with hepatic steatosis and plasma lipids.
Hepatol Commun
; 8(5)2024 May 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-38668731