Marguerite R. Irvin - Concepedia

Author

Marguerite R. Irvin

University of Alabama at Birmingham ORCID

Also Known As

Aslibekyan, Stella, Blanca Himes, Boerwinkle, Eric, Borecki, Ingrid B., Bressler, Jan, Cashell Jaquish, Chen, Ming-Huei, Chen, Wei-Min, Chen, Yii-Der Ida, Chii Min Hwu

448

Publications

24.4K

Citations

H-Index

159

Concepts

All Affiliations

University of Alabama at Birmingham University of Washington University of Kentucky Harvard University The University of Texas Health Science Center at Houston

About

Marguerite R. Irvin is an author at University of Alabama at Birmingham specializing in medicine, public health, and genetic epidemiology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	27	47	4.1K
2	Health Sciences	4	5	255
3	Engineering	3	3	784
4	Education	1	1	83
5	Nursing	1	1	29

Marguerite R. Irvin

162

Publications

13.4K

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
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
Genetic diversity fuels gene discovery for tobacco and alcohol use Gretchen Saunders, Xingyan Wang, Fang Chen, Nature	2022	470
Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program Daniel Taliun, Daniel Harris, Michael D. Kessler, EngineeringGeneticsGenomicsHigh Throughput SequencingTopmed Goals	2019	422
Association of Body Mass Index with DNA Methylation and Gene Expression in Blood Cells and Relations to Cardiometabolic Disease: A Mendelian Randomization Approach Michael Mendelson, Riccardo E. Marioni, Roby Joehanes, PLoS Medicine	2017	383
Epigenome-wide association study (EWAS) of BMI, BMI change and waist circumference in African American adults identifies multiple replicated loci Ellen W. Demerath, Weihua Guan, Megan L. Grove, Human Molecular Genetics Metabolic DisorderDna MethylationGenetic EpidemiologyHuman PolymorphismEpigenetics	2015	372
Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixed African and Hispanic/Latino populations Madeline H. Kowalski, Huijun Qian, Ziyi Hou, PLoS Genetics	2019	308
Systematic Error Removal Using Random Forest for Normalizing Large-Scale Untargeted Lipidomics Data Sili Fan, Tobias Kind, Tomáš Čajka, Analytical Chemistry Normalization MethodsEngineeringData ScienceCardiovascular DiseaseBiomedical Data Science	2019	301
Dynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole-genome sequencing studies at scale Xihao Li, Zilin Li, Hufeng Zhou, Nature Genetics Genome-wide Association StudyDynamic IncorporationVariant Association AnalysisAllelic VariantFunctional Genomics	2020	280
Loci associated with ischaemic stroke and its subtypes (SiGN): a genome-wide association study Sara L. Pulit, Patrick F. McArdle, Quenna Wong, The Lancet Neurology Genome-wide Association StudyThrombosisEpidemiologyIschemic StrokeMedicine	2015	260

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