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All papers authored by Eric Venner

This paper was not found in any repository; the policy of its publisher is unknown or unclear.

2024 Moez Dawood, Shawn Fayer, Sriram Pendyala, Mason Post, Divya Kalra, Karynne Patterson, Eric Venner

ORCID

, Lara A. Muffley, Douglas M. Fowler, Alan F. Rubin, Jennifer E. Posey, Sharon E. Plon, James R. Lupski, Richard A. Gibbs, Lea M. Starita and 3 other authors

Defining and Reducing Variant Classification Disparities

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Lele Li

ORCID

, Xia Tian, Vaughan Woodzell, Richard A. Gibbs, Bo Yuan, Eric Venner

ORCID

Tracking updates in clinical databases increases efficiency for variant reanalysis

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This paper was not found in any repository; the policy of its publisher is unknown or unclear.

2022 Alicia Zhou, Stephan Zuchner, Eric Venner

ORCID

, Joshua D. Smith, Karynne Patterson, Philip E. Empey, Lee Lichtenstein, Divya Kalra, Richard A. Gibbs, Brian Ahmedani, Marsha M. Wheeler, Christine D. Cole Johnson, Habib Ahsan, Hoda Anton-Culver, Eric Topol and 173 other authors

The frequency of pathogenic variation in the All of Us cohort reveals ancestry-driven disparities

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This paper is made freely available by the publisher.

Eric Venner

ORCID

, Donna Muzny, Joshua D. Smith, Kimberly Walker, Cynthia L. Neben, Christina M. Lockwood, Phillip E. Empey, Ginger A. Metcalf, Chris Kachulis, Sana Mian, Anjene Musick, Heidi L. Rehm, Steven Harrison, Stacey Gabriel, Richard A. Gibbs and 6 other authors

Whole-genome sequencing as an investigational device for return of hereditary disease risk and pharmacogenomic results as part of the All of Us Research Program

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This paper is made freely available by the publisher.

Chayakrit Krittanawong, Kipp W. Johnson

ORCID

, Edward Choi, Scott Kaplin

ORCID

, Eric Venner

ORCID

, Mullai Murugan, Zhen Wang, Benjamin S. Glicksberg

ORCID

, Christopher I. Amos

ORCID

, Michael C. Schatz

ORCID

, W. H. Wilson Tang

ORCID

Artificial Intelligence and Cardiovascular Genetics

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This paper was not found in any repository, but could be made available legally by the author.

2021 Mullai Murugan

ORCID

, Lawrence J. Babb, Casey Overby Taylor, Luke V. Rasmussen, Robert R. Freimuth, Eric Venner

ORCID

, Fei Yan, Victoria Yi, Stephen J. Granite, Hana Zouk, Samuel J. Aronson, Kevin Power, Alex Fedotov, David R. Crosslin, David Fasel and 11 other authors

Genomic considerations for FHIR®; eMERGE implementation lessons

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This paper is made freely available by the publisher.

Elena Valeryevna Feofanova

ORCID

, Guo-Qiang Zhang

ORCID

, Samden Lhatoo

ORCID

, Ginger A. Metcalf

ORCID

, Eric Boerwinkle

ORCID

, Eric Venner

ORCID

The Implementation Science for Genomic Health Translation (INSIGHT) Study in Epilepsy: Protocol for a Learning Health Care System

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This paper was not found in any repository; the policy of its publisher is unknown or unclear.

Chenjie Zeng, Lisa A. Bastarache

ORCID

, Ran Tao, Eric Venner

ORCID

, Scott Hebbring, Justin D. Andujar, Sarah T. Bland, David R. Crosslin, Siddharth Pratap, Ayorinde Cooley

ORCID

, Jennifer A. Pacheco, Kurt D. Christensen, Emma Perez, Carrie L. Blout Zawatsky, Leora Witkowski and 18 other authors

A scalable EHR-based approach for phenotype discovery and variant interpretation for hereditary cancer genes

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This paper was not found in any repository; the policy of its publisher is unknown or unclear.

2020 Elena Valeryevna Feofanova, Guo-Qiang Zhang, Samden Lhatoo, Ginger A. Metcalf, Eric Boerwinkle, Eric Venner

ORCID

The Implementation Science for Genomic Health Translation (INSIGHT) Study in Epilepsy: Protocol for a Learning Health Care System (Preprint)

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