Author details

Full Name

Marijana Vujkovic

Affiliation

ORCID

Career Start Year

2007

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
37034649	Multi-ancestry genome-wide study in >2.5 million individuals reveals heterogeneity in mechanistic pathways of type 2 diabetes and complications.	medRxiv	2023
37599905	Large-scale identification of undiagnosed hepatic steatosis using natural language processing.	EClinicalMedicine	2023
37417779	Mendelian randomization study of diabetes and dementia in the Million Veteran Program.	Alzheimers Dement	2023
37399599	A genetically supported drug repurposing pipeline for diabetes treatment using electronic health records.	EBioMedicine	2023
36945581	Mendelian randomization study of diabetes and dementia in the Million Veteran Program.	medRxiv	2023
37248657	A coding variant in the microsomal triglyceride transfer protein reduces both hepatic steatosis and plasma lipids.		2023
36865344	Comparison of the structure-function properties of wild-type human apoA-V and a C-terminal truncation associated with elevated plasma triglycerides.		2023
36540995	Session Introduction: SALUD: Scalable Applications of cLinical risk Utility and preDiction.	Pac Symp Biocomput	2023
37358849	Association of Statin Use With Risk of Liver Disease, Hepatocellular Carcinoma, and Liver-Related Mortality.	JAMA Netw Open	2023
35325778	Lipid traits and type 2 diabetes risk in African ancestry individuals: A Mendelian Randomization study.	EBioMedicine	2022
35654975	A multiancestry genome-wide association study of unexplained chronic ALT elevation as a proxy for nonalcoholic fatty liver disease with histological and radiological validation.	Nat Genet	2022
35654908	Transferability of genetic risk scores in African populations.	Nature Medicine	2022
35654591	The Potential of Genetic Data for Prioritizing Drug Repurposing Efforts.	Neurology	2022
35393509	Identification of genetic effects underlying type 2 diabetes in South Asian and European populations.	Commun Biol	2022
36041056	A Diabetes Genetic Risk Score Is Associated With All-Cause Dementia and Clinically Diagnosed Vascular Dementia in the Million Veteran Program.	Diabetes Care	2022
35513483	Author Correction: Identification of genetic effects underlying type 2 diabetes in South Asian and European populations.	Commun Biol	2022
35500537	Using Mendelian randomisation to identify opportunities for type 2 diabetes prevention by repurposing medications used for lipid management.	EBioMedicine	2022
35551307	Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation.	Nat Genet	2022
35482673	A Phenome-Wide Association Study of genes associated with COVID-19 severity reveals shared genetics with complex diseases in the Million Veteran Program.	PLoS Genet	2022
35915156	Large-scale genome-wide association study of coronary artery disease in genetically diverse populations.	Nat Med	2022
36936593	Effects of metabolic traits, lifestyle factors, and pharmacological interventions on liver fat: mendelian randomisation study.	BMJ Med	2022
35288522	Dietary Vitamin E Intake Is Associated With a Reduced Risk of Developing Digestive Diseases and Nonalcoholic Fatty Liver Disease.	American Journal of Gastroenterology	2022
35186008	Multi-Trait Genome-Wide Association Study of Atherosclerosis Detects Novel Pleiotropic Loci.	Front Genet	2022
35129650	Separating the direct effects of traits on atherosclerotic cardiovascular disease from those mediated by type 2 diabetes.	Diabetologia	2022
34505161	Leveraging human genetic data to investigate the cardiometabolic effects of glucose-dependent insulinotropic polypeptide signalling.	Diabetologia	2021
34078102	Metabolic Traits and Stroke Risk in Individuals of African Ancestry: Mendelian Randomization Analysis.	Stroke	2021
33745059	Genome-first approach to rare EYA4 variants and cardio-auditory phenotypes in adults.	Hum Genet	2021
33576413	Quantification of abdominal fat from computed tomography using deep learning and its association with electronic health records in an academic biobank.	J Am Med Inform Assoc	2021
33837377	Actionable druggable genome-wide Mendelian randomization identifies repurposing opportunities for COVID-19.	Nat Med	2021
34258604	A genome-first approach to mortality and metabolic phenotypes in p.Ala165Thr (rs2642438) heterozygotes and homozygotes.	Med	2021
33822779	Correction: A missense variant in Mitochondrial Amidoxime Reducing Component 1 gene and protection against liver disease.	PLoS Genet	2021
34184541	Genetic Evidence for Repurposing of GLP1R (Glucagon-Like Peptide-1 Receptor) Agonists to Prevent Heart Failure.	J Am Heart Assoc	2021
33813844	Relationship Between Blood Pressure and Incident Cardiovascular Disease: Linear and Nonlinear Mendelian Randomization Analyses.	Hypertension	2021
32833022	Genetic determinants of increased body mass index mediate the effect of smoking on increased risk for type 2 diabetes but not coronary artery disease.	Hum Mol Genet	2020
33031386	Genetics of height and risk of atrial fibrillation: A Mendelian randomization study.	PLoS Med	2020
32841307	Validating a non-invasive, ALT-based non-alcoholic fatty liver phenotype in the million veteran program.	PLoS One	2020
31118516	Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls.	Nature	2019
30168000	Impact of Efavirenz Metabolism on Loss to Care in Older HIV+ Africans.	Eur J Drug Metab Pharmacokinet	2019
31285632	Genome-wide association study of peripheral artery disease in the Million Veteran Program.	Nat Med	2019
30275531	Genetics of blood lipids among ~300,000 multi-ethnic participants of the Million Veteran Program.	Nat Genet	2018
30371334	Genetic Variants Associated With Plasma Lipids Are Associated With the Lipid Response to Niacin.	J Am Heart Assoc	2018
29855606	Polymorphisms in cytochrome P450 are associated with extensive efavirenz pharmacokinetics and CNS toxicities in an HIV cohort in Botswana.	Pharmacogenomics J	2018
28481785	Brief Report: CYP2B6 516G>T Minor Allele Protective of Late Virologic Failure in Efavirenz-Treated HIV-Infected Patients in Botswana.	J Acquir Immune Defic Syndr	2017
28692529	CYP2B6 genotypes and early efavirenz-based HIV treatment outcomes in Botswana.	AIDS	2017
28411282	Genomic architecture and treatment outcome in pediatric acute myeloid leukemia: a Children's Oncology Group report.	Blood	2017
27547214	Comparing Analytic Methods for Longitudinal GWAS and a Case-Study Evaluating Chemotherapy Course Length in Pediatric AML. A Report from the Children's Oncology Group.	Front Genet	2016
26163103	Concordance of copy number alterations using a common analytic pipeline for genome-wide analysis of Illumina and Affymetrix genotyping data: a report from the Children's Oncology Group.	Cancer Genet	2015
26605150	Associations between genetic variants in folate and drug metabolizing pathways and relapse risk in pediatric acute lymphoid leukemia on CCG-1952.	Leuk Res Rep	2015
24737678	TPMT and MTHFR genotype is not associated with altered risk of thioguanine-related sinusoidal obstruction syndrome in pediatric acute lymphoblastic leukemia: a report from the Children's Oncology Group.	Pediatr Blood Cancer	2014
25465053	Validity of a questionnaire measuring the world health organization concept of health system responsiveness with respect to perinatal services in the Dutch obstetric care system.	BMC Health Services Research	2014