Author details

Full Name

Khanh K Thai

Affiliation

ORCID

Career Start Year

2012

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
36852680	Practice Patterns and Outcomes Associated With Anticoagulation Use Following Sepsis Hospitalizations With New-Onset Atrial Fibrillation.	Circ Cardiovasc Qual Outcomes	2023
36122170	Predicting Cardiovascular Events after Sepsis withÂ Death as a Competing Risk.	Ann Am Thorac Soc	2023
36930723	Development and Validation of a Diabetic Retinopathy Risk Stratification Algorithm.	Diabetes Care	2023
36199081	Assessment of genetic susceptibility to multiple primary cancers through whole-exome sequencing in two large multi-ancestry studies.	BMC Med	2022
35425904	Prognostic Accuracy of Presepsis and Intrasepsis Characteristics for Prediction of Cardiovascular Events After a Sepsis Hospitalization.	Crit Care Explor	2022
36477530	Genetic diversity fuels gene discovery for tobacco and alcohol use.	Nature	2022
36409498	Trends and Risk Factors for Venous Thromboembolism Among Hospitalized Medical Patients.	JAMA Netw Open	2022
34038701	Association between Troponin I Levels during Sepsis and Postsepsis Cardiovascular Complications.	Am J Respir Crit Care Med	2021
33674754	Correction: Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder.	Mol Psychiatry	2021
33579919	Cross-cancer evaluation of polygenic risk scores for 16 cancer types in two large cohorts.	Nat Commun	2021
34312202	Development of a healthcare system COVID Hotspotting Score in California: an observational study with prospective validation.	BMJ Open	2021
32216088	Associations of CYP2C9 and CYP2C19 Pharmacogenetic Variation with Phenytoin-Induced Cutaneous Adverse Drug Reactions.	Clin Transl Sci	2020
32887889	Pan-cancer study detects genetic risk variants and shared genetic basis in two large cohorts.	Nat Commun	2020
32732251	Pathway Analysis of Renal Cell Carcinoma Genome-Wide Association Studies Identifies Novel Associations.	Cancer Epidemiol Biomarkers Prev	2020
32605384	Meta-Analysis of 26 638 Individuals Identifies Two Genetic Loci Associated With Left Ventricular Ejection Fraction.	Circ Genom Precis Med	2020
32231278	Meta-analysis of 542,934 subjects of European ancestry identifies new genes and mechanisms predisposing to refractive error and myopia.	Nat Genet	2020
31461080	Assessing the clinical impact of CYP2C9 pharmacogenetic variation on phenytoin prescribing practice and patient response in an integrated health system.	Pharmacogenet Genomics	2019
30755537	Reply to Liu et al.: Tissue specificity of <i>SIM1</i> gene expression and erectile dysfunction.	Proc Natl Acad Sci U S A	2019
29891935	A multiethnic genome-wide association study of primary open-angle glaucoma identifies novel risk loci.	Nature Communications	2018
30297428	Genetic variation in the <i>SIM1</i> locus is associated with erectile dysfunction.	Proc Natl Acad Sci U S A	2018
29235454	A large multi-ethnic genome-wide association study identifies novel genetic loci for intraocular pressure.	Nature Communications	2017
28485404	Genetic contributors to variation in alcohol consumption vary by race/ethnicity in a large multi-ethnic genome-wide association study.	Mol Psychiatry	2017
27170569	Population-based risks for cancer in patients with ALS.	Neurology	2016
26086378	Repeat Associated Non-AUG Translation (RAN Translation) Dependent on Sequence Downstream of the ATXN2 CAG Repeat.	PLoS ONE	2015
25285812	Amyotrophic lateral sclerosis risk for spinocerebellar ataxia type 2 ATXN2 CAG repeat alleles: a meta-analysis.	JAMA Neurology	2014
22914732	ETS1 regulates the expression of ATXN2.	Human Molecular Genetics	2012