Detalhe da pesquisa
1.
Machine learning-based marker for coronary artery disease: derivation and validation in two longitudinal cohorts.
Lancet
; 401(10372): 215-225, 2023 Jan 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-36563696
2.
Cholesterol Contributes to Risk, Severity, and Machine Learning-Driven Diagnosis of Lyme Disease.
Clin Infect Dis
; 77(6): 839-847, 2023 09 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-37227948
3.
Genome-wide polygenic risk score for retinopathy of type 2 diabetes.
Hum Mol Genet
; 30(10): 952-960, 2021 05 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-33704450
4.
Genome-first recall of healthy individuals by polygenic risk score reveals differences in coronary artery calcium.
Am Heart J
; 250: 29-33, 2022 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-35526571
5.
Population-Based Penetrance of Deleterious Clinical Variants.
JAMA
; 327(4): 350-359, 2022 01 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-35076666
6.
Genetic pleiotropy of ERCC6 loss-of-function and deleterious missense variants links retinal dystrophy, arrhythmia, and immunodeficiency in diverse ancestries.
Hum Mutat
; 42(8): 969-977, 2021 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-34005834
7.
Non-invasive ventilation versus mechanical ventilation in hypoxemic patients with COVID-19.
Infection
; 49(5): 989-997, 2021 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-34089483
8.
Derivation and validation of genome-wide polygenic score for urinary tract stone diagnosis.
Kidney Int
; 98(5): 1323-1330, 2020 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-32540406
9.
Machine learning-based markers for CAD - Authors' reply.
Lancet
; 402(10397): 184, 2023 07 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-37453750
10.
Penetrance of Deleterious Clinical Variants-Reply.
JAMA
; 327(19): 1927, 2022 05 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-35579644
11.
Genome-first evaluation with exome sequence and clinical data uncovers underdiagnosed genetic disorders in a large healthcare system.
Cell Rep Med
; 5(5): 101518, 2024 May 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-38642551
12.
Muesli Intake May Protect Against Coronary Artery Disease: Mendelian Randomization on 13 Dietary Traits.
JACC Adv
; 3(4)2024 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-38737007
13.
Development of a human genetics-guided priority score for 19,365 genes and 399 drug indications.
Nat Genet
; 56(1): 51-59, 2024 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-38172303
14.
A machine learning model identifies patients in need of autoimmune disease testing using electronic health records.
Nat Commun
; 14(1): 2385, 2023 04 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-37169741
15.
Phenome-wide Mendelian randomization study of plasma triglyceride levels and 2600 disease traits.
Elife
; 122023 03 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-36988189
16.
Deep learning on electronic medical records identifies distinct subphenotypes of diabetic kidney disease driven by genetic variations in the Rho pathway.
medRxiv
; 2023 Sep 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-37732187
17.
Genetic and phenotypic profiling of supranormal ejection fraction reveals decreased survival and underdiagnosed heart failure.
Eur J Heart Fail
; 24(11): 2118-2127, 2022 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-35278270
18.
Coronary Risk Estimation Based on Clinical Data in Electronic Health Records.
J Am Coll Cardiol
; 79(12): 1155-1166, 2022 03 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-35331410
19.
A tissue-level phenome-wide network map of colocalized genes and phenotypes in the UK Biobank.
Commun Biol
; 5(1): 849, 2022 08 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-35987940
20.
Derivation and Validation of Genome-Wide Polygenic Score for Ischemic Heart Failure.
J Am Heart Assoc
; 10(22): e021916, 2021 11 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-34713709