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1.
Transcriptional Dysregulation Underlies Both Monogenic Arrhythmia Syndrome and Common Modifiers of Cardiac Repolarization.
Circulation
; 147(10): 824-840, 2023 03 07.
Article
in English
| MEDLINE | ID: mdl-36524479
2.
Interactive network-based clustering and investigation of multimorbidity association matrices with associationSubgraphs.
Bioinformatics
; 39(1)2023 01 01.
Article
in English
| MEDLINE | ID: mdl-36472455
3.
Next-generation phenotyping: introducing phecodeX for enhanced discovery research in medical phenomics.
Bioinformatics
; 39(11)2023 11 01.
Article
in English
| MEDLINE | ID: mdl-37930895
4.
ABO O blood group as a risk factor for platelet reactivity in heparin-induced thrombocytopenia.
Blood
; 140(3): 274-284, 2022 07 21.
Article
in English
| MEDLINE | ID: mdl-35377938
5.
High-throughput framework for genetic analyses of adverse drug reactions using electronic health records.
PLoS Genet
; 17(6): e1009593, 2021 06.
Article
in English
| MEDLINE | ID: mdl-34061827
6.
Common Ancestry-Specific Ion Channel Variants Predispose to Drug-Induced Arrhythmias.
Circulation
; 145(4): 299-308, 2022 01 25.
Article
in English
| MEDLINE | ID: mdl-34994586
7.
Arrhythmia Variant Associations and Reclassifications in the eMERGE-III Sequencing Study.
Circulation
; 145(12): 877-891, 2022 03 22.
Article
in English
| MEDLINE | ID: mdl-34930020
8.
High-Throughput Reclassification of SCN5A Variants.
Am J Hum Genet
; 107(1): 111-123, 2020 07 02.
Article
in English
| MEDLINE | ID: mdl-32533946
9.
Genome-wide Study Identifies Association between HLA-B∗55:01 and Self-Reported Penicillin Allergy.
Am J Hum Genet
; 107(4): 612-621, 2020 10 01.
Article
in English
| MEDLINE | ID: mdl-32888428
10.
Continuous Bayesian variant interpretation accounts for incomplete penetrance among Mendelian cardiac channelopathies.
Genet Med
; 25(3): 100355, 2023 03.
Article
in English
| MEDLINE | ID: mdl-36496179
11.
A Bayesian method to estimate variant-induced disease penetrance.
PLoS Genet
; 16(6): e1008862, 2020 06.
Article
in English
| MEDLINE | ID: mdl-32569262
12.
Polygenic risk score for ACE-inhibitor-associated cough based on the discovery of new genetic loci.
Eur Heart J
; 43(45): 4707-4718, 2022 12 01.
Article
in English
| MEDLINE | ID: mdl-35751511
13.
Frequency of benign neutropenia among Black versus White individuals undergoing a bone marrow assessment.
J Cell Mol Med
; 26(13): 3628-3635, 2022 07.
Article
in English
| MEDLINE | ID: mdl-35642720
14.
GRIK5 Genetically Regulated Expression Associated with Eye and Vascular Phenomes: Discovery through Iteration among Biobanks, Electronic Health Records, and Zebrafish.
Am J Hum Genet
; 104(3): 503-519, 2019 03 07.
Article
in English
| MEDLINE | ID: mdl-30827500
15.
Dominant negative effects of SCN5A missense variants.
Genet Med
; 24(6): 1238-1248, 2022 06.
Article
in English
| MEDLINE | ID: mdl-35305865
16.
Molecular characterization and investigation of the role of genetic variation in phenotypic variability and response to treatment in a large pediatric Marfan syndrome cohort.
Genet Med
; 24(5): 1045-1053, 2022 05.
Article
in English
| MEDLINE | ID: mdl-35058154
17.
The reckoning: The return of genomic results to 1444 participants across the eMERGE3 Network.
Genet Med
; 24(5): 1130-1138, 2022 05.
Article
in English
| MEDLINE | ID: mdl-35216901
18.
How Will Genetics Inform the Clinical Care of Atrial Fibrillation?
Circ Res
; 127(1): 111-127, 2020 06 19.
Article
in English
| MEDLINE | ID: mdl-32716712
19.
Anticancer drug-induced life-threatening ventricular arrhythmias: a World Health Organization pharmacovigilance study.
Eur Heart J
; 42(38): 3915-3928, 2021 10 07.
Article
in English
| MEDLINE | ID: mdl-34370839
20.
Deep learning analysis of electrocardiogram for risk prediction of drug-induced arrhythmias and diagnosis of long QT syndrome.
Eur Heart J
; 42(38): 3948-3961, 2021 10 07.
Article
in English
| MEDLINE | ID: mdl-34468739