Detalhe da pesquisa
1.
The phenotype-genotype reference map: Improving biobank data science through replication.
Am J Hum Genet
; 110(9): 1522-1533, 2023 09 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-37607538
2.
Next-generation phenotyping: introducing phecodeX for enhanced discovery research in medical phenomics.
Bioinformatics
; 39(11)2023 11 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37930895
3.
Predictive Utility of Polygenic Risk Scores for Coronary Heart Disease in Three Major Racial and Ethnic Groups.
Am J Hum Genet
; 106(5): 707-716, 2020 05 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-32386537
4.
Antibacterial and Cytocompatible pH-Responsive Peptide Hydrogel.
Molecules
; 28(11)2023 May 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-37298865
5.
Genetic loci and prioritization of genes for kidney function decline derived from a meta-analysis of 62 longitudinal genome-wide association studies.
Kidney Int
; 102(3): 624-639, 2022 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-35716955
6.
Extracellular Vimentin as a Target Against SARS-CoV-2 Host Cell Invasion.
Small
; 18(6): e2105640, 2022 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-34866333
7.
Under-specification as the source of ambiguity and vagueness in narrative phenotype algorithm definitions.
BMC Med Inform Decis Mak
; 22(1): 23, 2022 01 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-35090449
8.
Meta-analysis uncovers genome-wide significant variants for rapid kidney function decline.
Kidney Int
; 99(4): 926-939, 2021 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-33137338
9.
The eMERGE genotype set of 83,717 subjects imputed to ~40 million variants genome wide and association with the herpes zoster medical record phenotype.
Genet Epidemiol
; 43(1): 63-81, 2019 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-30298529
10.
The vimentin cytoskeleton: when polymer physics meets cell biology.
Phys Biol
; 18(1): 011001, 2020 12 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32992303
11.
Genetics of rheumatoid arthritis contributes to biology and drug discovery.
Nature
; 506(7488): 376-81, 2014 Feb 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-24390342
12.
Association of Genetic Risk of Obesity with Postoperative Complications Using Mendelian Randomization.
World J Surg
; 44(1): 84-94, 2020 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31605180
13.
Unfolding of hidden white blood cell count phenotypes for gene discovery using latent class mixed modeling.
Genes Immun
; 20(7): 555-565, 2019 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-30459343
14.
GWAS and enrichment analyses of non-alcoholic fatty liver disease identify new trait-associated genes and pathways across eMERGE Network.
BMC Med
; 17(1): 135, 2019 07 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-31311600
15.
Evaluating statistical approaches to leverage large clinical datasets for uncovering therapeutic and adverse medication effects.
Bioinformatics
; 34(17): 2988-2996, 2018 09 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29912272
16.
CYP2D6 genotype and adverse events to risperidone in children and adolescents.
Pediatr Res
; 85(5): 602-606, 2019 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-30661084
17.
Facilitating phenotype transfer using a common data model.
J Biomed Inform
; 96: 103253, 2019 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-31325501
18.
SOS2 and ACP1 Loci Identified through Large-Scale Exome Chip Analysis Regulate Kidney Development and Function.
J Am Soc Nephrol
; 28(3): 981-994, 2017 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-27920155
19.
R PheWAS: data analysis and plotting tools for phenome-wide association studies in the R environment.
Bioinformatics
; 30(16): 2375-6, 2014 Aug 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-24733291
20.
PheWAS analysis on large-scale biobank data with PheTK.
medRxiv
; 2024 Feb 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-38410487