Author

Nauder R. Faraday

Johns Hopkins UniversityORCID 0000-0002-7397-9980Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 2 Genetics· 1 Genomics· 1

Signature Assays, Organisms & Methods

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Organism:human· 4 Approach:statistical model· 4 Assay:whole-genome sequencing· 4 Research Focus:GWAS / association mapping· 3 Research Focus:differential expression· 1 Research Focus:fine-mapping· 1 Research Focus:imputation· 1 Approach:matrix factorization· 1

Frequent Co-Authors

Lisa R. YanekiD· 4 shared Charles L KooperbergiD· 3 shared Jerome I. RotteriD· 3 shared Joshua P. LewisiD· 3 shared Laura M. RaffieldiD· 3 shared Lewis C. BeckeriD· 3 shared Nathan PankratziD· 3 shared Paul Livermore AueriD· 3 shared

Activity by Year

2019-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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4 shared papersGenetic & Genomic Medicine

Lisa R. YanekORCID

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Author profile →

4 papers

Recent·Most cited

A genome-wide meta-analysis identifies a sex-specific genetic effect for platelet aggregation in response to agonists

Julius Suh Ngwa, Ming‐Huei Chen, Gaynor Brady, Lisa R. Yanek, Kai Kammers, Kanika Kanchan, Margaret A. Taub, Yuzheng Dun, Nilanjan Chatterjee, Kathleen A. Ryan, Lewis C. Becker, Rasika A. Mathias, Joshua P. Lewis, Andrew D. Johnson, Nauder R. Faraday, Ingo Ruczinski

This study identifies a sex-specific genetic variant affecting platelet aggregation in response to low-dose epinephrine across multiple cohorts.

medRxiv · May 18, 2026 · PreprintGenetic & Genomic Medicine

Whole genome analysis of plasma fibrinogen reveals population-differentiated genetic regulators with putative liver roles.

Jennifer E. Huffman, Jayna C. Nicholas, Julie M. Hahn, Adam S. Heath, Laura M. Raffield, Lisa R. Yanek, Jennifer A. Brody, Florian Thibord, Laura A. Almasy, Traci M. Bartz, Lawrence F. Bielak, Russell Paul Bowler, Germán D. Carrasquilla, Daniel I. Chasman, Ming‐Huei Chen, , Yoav Ben‐Shlomo

This study uses whole genome sequencing to identify 18 novel genetic loci associated with plasma fibrinogen levels, including variants more common in African populations and linked to liver-related traits and disease.

Blood · Sep 3, 2024Peer-reviewedGenetic & Genomic Medicine

Whole Genome Sequencing Based Analysis of Inflammation Biomarkers in the Trans-Omics for Precision Medicine (TOPMed) Consortium

Min-Zhi Jiang, Sheila M. Gaynor, Xihao Li, Eric Van Buren, A.M. Stilp, Erin Buth, Fei Fei Wang, Regina Manansala, Stephanie M. Gogarten, Zilin Li, Linda M. Polfus, Shabnam Salimi, Joshua C. Bis, Nathan Pankratz, Lisa R. Yanek, , TOPMed Inflammation Working Group

The paper analyzes inflammation biomarkers using whole-genome sequencing from the TOPMed consortium, identifying both single-variant and rare variant associations with inflammatory traits.

bioRxiv · Sep 10, 2023 · PreprintGenetics

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, Jonathan D. Rosen, Amanda L. Tapia, Yue Shan, Deepti Jain, Maria Argos, Donna K. Arnett, Christy L. Avery, Kathleen C. Barnes, Lewis C. Becker, Stephanie A. Bien, Joshua C. Bis, John Blangero, , Yun Li

This study uses TOPMed whole genome sequences to improve imputation quality and detect rare variant associations in admixed African and Hispanic/Latino populations, identifying two novel associations with hematological traits.

PLoS Genetics · Dec 23, 2019Peer-reviewedGenomics