Ellen M. Schmidt - Concepedia

Author

Ellen M. Schmidt

Also Known As

Beckmann, Jacques S, Boomsma, Dorret I., Buchkovich, Martin L., Chen, Jin, Christensen, Henry, Christopher Scheller, Cristen J Willer , E M S Schmidt, E Schmidt, E. Schmidt

103

Publications

24.1K

Citations

H-Index

Concepts

All Affiliations

University of Michigan Icahn School of Medicine at Mount Sinai University of North Carolina at Chapel Hill Stanford University Broad Institute

About

Ellen M. Schmidt is an author at University of Michigan specializing in medicine, genetics, and genomics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	17	19	6.1K
2	Public Health	12	13	3K
3	Engineering	3	3	1.2K
4	Arts	1	1	20
5	Behavioral Sciences	1	1	133

Ellen M. Schmidt

Publications

10.3K

Citations

H-Index

Page 1

	Year	Citations
Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program Daniel Taliun, Daniel Harris, Michael D. Kessler, Nature	2021	2.2K
Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps Anubha Mahajan, Daniel Taliun, Matthias Thurner, Nature Genetics Genome-wide Association StudyAllelic VariantGenetic DeterminantSingle-variant ResolutionVariant Interpretation	2018	1.9K
Biobank-driven genomic discovery yields new insight into atrial fibrillation biology Jonas B. Nielsen, Rósa B. Þórólfsdóttir, Lars G. Fritsche, Nature Genetics CardiomyopathyFunctional GenomicsEngineeringTranslational BioinformaticsGenetics	2018	900
Common variants associated with plasma triglycerides and risk for coronary artery disease Ron Do, Cristen J. Willer, Ellen M. Schmidt, Nature Genetics Metabolic SyndromeCardiovascular EpidemiologyCardiovascular DiseaseGenetic EpidemiologyCardiovascular Genetics	2013	890
Inherited causes of clonal haematopoiesis in 97,691 whole genomes Alexander G. Bick, Joshua S. Weinstock, Satish K. Nandakumar, Nature Genetic DisorderGeneticsHematologyInherited CausesChromosomal Rearrangement	2020	698
Open Targets Genetics: systematic identification of trait-associated genes using large-scale genetics and functional genomics Maya Ghoussaini, Edward Mountjoy, Miguel Carmona, Nucleic Acids Research BioinformaticsGenetic AnalysisSystematic IdentificationGenome-wide Association StudyBioinformatics Database	2020	666
An open approach to systematically prioritize causal variants and genes at all published human GWAS trait-associated loci Edward Mountjoy, Ellen M. Schmidt, Miguel Carmona, Nature Genetics	2021	601
Rare variant in scavenger receptor BI raises HDL cholesterol and increases risk of coronary heart disease Paolo Zanoni, Sumeet A. Khetarpal, Daniel B. Larach, Science Metabolic SyndromeScavenger Receptor BiCardiovascular DiseaseMedicineSr-bi Knockout Mice	2016	539
Systematic evaluation of coding variation identifies a candidate causal variant in TM6SF2 influencing total cholesterol and myocardial infarction risk Oddgeir L. Holmen, He Zhang, Yanbo Fan, Nature Genetics EpidemiologyCardiovascular DiseaseMyocardial Infarction RiskGenetic EpidemiologyCandidate Causal Variant	2014	307
Whole-Exome Sequencing Identifies Rare and Low-Frequency Coding Variants Associated with LDL Cholesterol Leslie A. Lange, Youna Hu, He Zhang, The American Journal of Human Genetics Genome-wide Association StudyAllelic VariantEngineeringMedicineGenetics	2014	214

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