Author

Anjali D. Zimmer

Color (United States)ORCID 0000-0002-8644-2963Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

Click to filter author papers

Genetic & Genomic Medicine· 1 Genetics· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

Organism:human· 2 Research Focus:benchmarking· 1 Research Focus:database / resource· 1 Assay:GWAS summary statistics· 1 Approach:statistical model· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Adam Matsil· 1 shared Alicia Yiran ZhouiD· 1 shared Amy A. LemkeiD· 1 shared Cynthia L. NebeniD· 1 shared Hannah WilliamsiD· 1 shared Henry Mark DunnenbergeriD· 1 shared Huy Hong· 1 shared Jeremy GinsbergiD· 1 shared

Activity by Year

2020-2021 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

1 shared paperGenetic & Genomic Medicine

Adam Matsil

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

Implementing Primary Care Mediated Population Genetic Screening within an Integrated Health System

Sean P. David, Henry Mark Dunnenberger, Raabiah Ali, Adam Matsil, Amy A. Lemke, Lavisha Singh, Anjali D. Zimmer, Peter J. Hulick

This study evaluates a population genetic screening program mediated by primary care physicians, finding actionable variants in nearly 8% of patients and suggesting its potential to improve preventative care.

The Journal of the American Board of Family Medicine · Jul 1, 2021Peer-reviewedGenetic & Genomic Medicine

Color Data v2: a user-friendly, open-access database with hereditary cancer and hereditary cardiovascular conditions datasets

Mark J. Berger, Hannah Williams, Ryan Barrett, Anjali D. Zimmer, Wendy McKennon, Huy Hong, Jeremy Ginsberg, Alicia Yiran Zhou, Cynthia L. Neben

Color Data v2 provides an updated open-access database with genetic and phenotypic data on hereditary cancer and cardiovascular conditions, including polygenic risk scores and clinical risk models.

Database · Jan 1, 2020Peer-reviewedGenetics