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Author Details

Carla Marquez-Luna
2014
17
9
PMIDPaper TitleJournal TitlePublished Year
36988189Phenome-wide Mendelian randomization study of plasma triglyceride levels and 2600 disease traits.Elife2023
36563696Machine learning-based marker for coronary artery disease: derivation and validation in two longitudinal cohorts.Lancet2023
37042260Machine Learning Identifies Plasma Metabolites Associated With Heart Failure in Underrepresented Populations With the <i>TTR</i> V122I Variant.J Am Heart Assoc2023
35331410Coronary Risk Estimation Based on Clinical Data in Electronic Health Records.J Am Coll Cardiol2022
35526571Genome-first recall of healthy individuals by polygenic risk score reveals differences in coronary artery calcium.Am Heart J2022
35862132Polygenic Risk Scores for Cardiovascular Disease: A Scientific Statement From the American Heart Association.Circulation2022
36788979Short-term prediction of coronary artery disease using serum metabolomic patterns.Am Heart J Plus2022
33947393Correction to: Genetic architecture of cardiometabolic risks in people living with HIV.BMC Med2021
36017067Neuropsychiatric Genetics of Psychosis in the Mexican Population: A Genome-Wide Association Study Protocol for Schizophrenia, Schizoaffective, and Bipolar Disorder Patients and Controls.Complex Psychiatry2021
33704450Genome-wide polygenic risk score for retinopathy of type 2 diabetes.Hum Mol Genet2021
33109212Genetic architecture of cardiometabolic risks in people living with HIV.BMC Med2020
33199916Functionally informed fine-mapping and polygenic localization of complex trait heritability.Nat Genet2020
33288751Improving the informativeness of Mendelian disease-derived pathogenicity scores for common disease.Nature Communications2020
31285579Reconciling S-LDSC and LDAK functional enrichment estimates.Nature Genetics2019
29110330Multiethnic polygenic risk scores improve risk prediction in diverse populations.Genet Epidemiol2017
24374739Founder effect and ancestral origin of the spinocerebellar ataxia type 7 (SCA7) mutation in Mexican families.Neurogenetics2014
24390345Sequence variants in SLC16A11 are a common risk factor for type 2 diabetes in Mexico.Nature2014
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