Detalhe da pesquisa
1.
Genomic Disorders in CKD across the Lifespan.
J Am Soc Nephrol
; 34(4): 607-618, 2023 04 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36302597
2.
Variant Classification Concordance using the ACMG-AMP Variant Interpretation Guidelines across Nine Genomic Implementation Research Studies.
Am J Hum Genet
; 107(5): 932-941, 2020 11 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-33108757
3.
Genome-wide Modeling of Polygenic Risk Score in Colorectal Cancer Risk.
Am J Hum Genet
; 107(3): 432-444, 2020 09 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-32758450
4.
Returning integrated genomic risk and clinical recommendations: The eMERGE study.
Genet Med
; 25(4): 100006, 2023 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-36621880
5.
Evaluating construct validity of computable acute respiratory distress syndrome definitions in adults hospitalized with COVID-19: an electronic health records based approach.
BMC Pulm Med
; 23(1): 292, 2023 Aug 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-37559024
6.
Loci identified by a genome-wide association study of carotid artery stenosis in the eMERGE network.
Genet Epidemiol
; 45(1): 4-15, 2021 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-32964493
7.
Uterine fibroid polygenic risk score (PRS) associates and predicts risk for uterine fibroid.
Hum Genet
; 141(11): 1739-1748, 2022 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-35226188
8.
Rates of Actionable Genetic Findings in Individuals with Colorectal Cancer or Polyps Ascertained from a Community Medical Setting.
Am J Hum Genet
; 105(3): 526-533, 2019 09 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-31422818
9.
The reckoning: The return of genomic results to 1444 participants across the eMERGE3 Network.
Genet Med
; 24(5): 1130-1138, 2022 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-35216901
10.
Medical Records-Based Genetic Studies of the Complement System.
J Am Soc Nephrol
; 32(8): 2031-2047, 2021 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-33941608
11.
Evaluation of the MC4R gene across eMERGE network identifies many unreported obesity-associated variants.
Int J Obes (Lond)
; 45(1): 155-169, 2021 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32952152
12.
The FamilyTalk randomized controlled trial: patient-reported outcomes in clinical genetic sequencing for colorectal cancer.
Cancer Causes Control
; 32(5): 483-492, 2021 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-33591484
13.
Genomic considerations for FHIR®; eMERGE implementation lessons.
J Biomed Inform
; 118: 103795, 2021 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-33930535
14.
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
15.
A genome-wide association study of polycystic ovary syndrome identified from electronic health records.
Am J Obstet Gynecol
; 223(4): 559.e1-559.e21, 2020 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-32289280
16.
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
17.
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
18.
Probing the Virtual Proteome to Identify Novel Disease Biomarkers.
Circulation
; 138(22): 2469-2481, 2018 11 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-30571344
19.
LPA Variants Are Associated With Residual Cardiovascular Risk in Patients Receiving Statins.
Circulation
; 138(17): 1839-1849, 2018 10 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-29703846
20.
Platelet-Related Variants Identified by Exomechip Meta-analysis in 157,293 Individuals.
Am J Hum Genet
; 99(1): 40-55, 2016 Jul 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-27346686