Author

Foram N. Ashar

Johns Hopkins University

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Genetics· 2

Signature Assays, Organisms & Methods

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Research Focus:GWAS / association mapping· 2 Organism:human· 2 Approach:statistical model· 2 Assay:GWAS summary statistics· 1

Frequent Co-Authors

Dan E. ArkingiD· 2 shared Heikki V. HuikuriiD· 2 shared Jennifer A. BrodyiD· 2 shared John David RiouxiD· 2 shared Juhani M. JunttilaiD· 2 shared Nona SotoodehniaiD· 2 shared Philippe Goyette· 2 shared Rebecca N. Mitchell· 2 shared

Activity by Year

2018-2019 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersGenetics

Dan E. ArkingORCID

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2 papers

Recent·Most cited

The effect of sex and underlying disease on the genetic association of QT interval and sudden cardiac death

Rebecca N. Mitchell, Foram N. Ashar, Marjo‐Riitta Järvelin, Philippe Froguel, Nona Sotoodehnia, Jennifer A. Brody, Sylvain P Sebert, Heikki V. Huikuri, John David Rioux, Philippe Goyette, Charles Newcomb, Juhani M. Junttila, Dan E. Arking

The paper examines how sex and underlying disease influence the genetic link between prolonged QT interval and sudden cardiac death risk using logistic regression and Mendelian randomization.

Journal of the American Heart Association · Nov 21, 2019Peer-reviewedGenetics

A Comprehensive Evaluation of the Genetic Architecture of Sudden Cardiac Arrest

Foram N. Ashar, Rebecca N. Mitchell, Christine M. Albert, Christopher Newton‐Cheh, Jennifer A. Brody, Martina Müller‐Nurasyid, Anna Moes, Thomas Meitinger, Angel C. Y. Mak, Heikki V. Huikuri, Juhani M. Junttila, Philippe Goyette, Sara L. Pulit, Raha Pazoki, Michael W.T. Tanck, , Nona Sotoodehnia

This study evaluates the genetic architecture of sudden cardiac arrest through GWAS and Mendelian randomization, finding genetic correlations with CAD, height, BMI, and electrical instability traits.

European Heart Journal · Jul 20, 2018Peer-reviewedGenetics