Author

Tara Schmidlen

Invitae (United States)ORCID 0000-0002-9749-112XUnclaimed 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· 2 Approach:statistical model· 2 Research Focus:benchmarking· 1 Research Focus:database / resource· 1 Research Focus:polygenic risk· 1 Research Focus:software / tool· 1 Assay:whole-exome sequencing· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Adam Gordon· 1 shared Allison Hazell· 1 shared Altovise T. EwingiD· 1 shared Amit V. KheraiD· 1 shared Amy L. McGuireiD· 1 shared Amy McGuire· 1 shared Anthony Johnson· 1 shared Atlas KhaniD· 1 shared

Activity by Year

2023-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Adam Gordon

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Author profile →

2 papers

Recent·Most cited

Elective genomic sequencing for adults in research, clinical and commercial contexts

Michael D. Linderman, Sophia M. Adelson, Tala M. Berro, Jennifer L. Anderson, Scott D. Crawford, Tshaka J. Cunningham, Edward D. Esplin, Altovise T. Ewing, Daiva E. Nielsen, Stacey Pereira, Tara Schmidlen, Heather Andrighetti, Steven B. Bleyl, George McDonald Church, Eden V. Haverfield, , Anthony Johnson

The paper examines motivations and outcomes of elective genomic sequencing across research, clinical, and commercial contexts, finding most participants found results medically important but few shared them with healthcare providers.

BMC Medical Genomics · Jul 3, 2026Peer-reviewedGenetic & Genomic Medicine

Selection, optimization, and validation of ten chronic disease polygenic risk scores for clinical implementation in diverse populations

Niall J. Lennon, Leah Claire Kottyan, C. Kachulis, Noura S. Abul‐Husn, Josh Arias, Gillian M. Belbin, Jennifer Elizabeth Below, Sonja I. Berndt, Wendy K. Chung, James J. Cimino, Ellen Wright Clayton, John J. Connolly, David R. Crosslin, Ozan Dikilitas, Digna R. Velez Edwards, , Eimear E. Kenny

The paper selects and validates ten polygenic risk scores for clinical use in diverse populations, focusing on chronic diseases and addressing disparities in predictive performance.

medRxiv · May 25, 2023 · PreprintGenetic & Genomic Medicine