Author

Abigail S. Baldridge

Northwestern UniversityORCID 0000-0002-1573-0554Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Organism:human· 3 Approach:statistical model· 3 Assay:whole-genome sequencing· 3 Research Focus:gene regulatory network inference· 1 Research Focus:GWAS / association mapping· 1 Research Focus:variant effect prediction· 1

Frequent Co-Authors

Adolfo CorreaiD· 3 shared Alain Gerald BertoniiD· 3 shared Alanna C. MorrisoniD· 3 shared Alex P. ReineriD· 3 shared Álvaro AlonsoiD· 3 shared Bertha HidalgoiD· 3 shared Bruce M. PsatyiD· 3 shared Charles L KooperbergiD· 3 shared

Activity by Year

2020-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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3 shared papersGenetic & Genomic Medicine

Adolfo CorreaORCID

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3 papers

Recent·Most cited

Genetic & Genomic MedicineDiabetesPeer-reviewedFeb 15, 2023

Investigating gene-diet interactions impacting the association between macronutrient intake and glycemic traits

Kenneth E. Westerman, Maura E. Walker, Sheila M. Gaynor…·Alisa Knodle Manning

The paper identifies a gene-diet interaction modifying the association between macronutrient intake and glycemic traits, highlighting challenges in detecting such interactions due to measurement error and sample size.

16 citations

humanwhole-genome sequencing

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Genetic & Genomic MedicineCommunications BiologyPeer-reviewedJul 28, 2022

Whole Genome Sequence Association Analysis of Fasting Glucose and Fasting Insulin Levels in Diverse Cohorts from the NHLBI TOPMed Program

DANIEL A. DICORPO, Sheila M. Gaynor, Emily M. Russell…·Alisa Knodle Manning

The paper performs whole genome sequence association analysis of fasting glucose and insulin levels in diverse cohorts, identifying 22 significant variants across 16 gene regions, including rare variants.

22 citations

humanwhole-genome sequencing

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Genetic & Genomic MedicinemedRxivPreprintNov 13, 2020

Rare Non-coding Variation Identified by Large Scale Whole Genome Sequencing Reveals Unexplained Heritability of Type 2 Diabetes: Trans-Omics for Precision Medicine (TOPMed) Program

Jennifer Wessel, Timothy D. Majarian, Heather M. Highland…·José C. Florez

The paper identifies rare non-coding variants from whole genome sequencing in the TOPMed program, showing they contribute significantly to type 2 diabetes heritability.

12 citations

humanwhole-genome sequencing

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