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Author Details

Eric Venner
Baylor College of Medicine
2009
29
15
PMIDPaper TitleJournal TitlePublished Year
37071725Familial Hypercholesterolemia in the Electronic Medical Records and Genomics Network: Prevalence, Penetrance, Cardiovascular Risk, and Outcomes After Return of Results.Circ Genom Precis Med2023
37790445Genetic Sex Validation for Sample Tracking in Clinical Testing.Res Sq2023
34923710Harmonizing variant classification for return of results in the All of Us Research Program.Hum Mutat2022
35346344Whole-genome sequencing as an investigational device for return of hereditary disease risk and pharmacogenomic results as part of the All of Us Research Program.Genome Med2022
35395838Best practices for the interpretation and reporting of clinical whole genome sequencing.NPJ Genom Med2022
35446370Association of Pathogenic Variants in Hereditary Cancer Genes With Multiple Diseases.JAMA Oncol2022
35331649Implementation of preemptive DNA sequence-based pharmacogenomics testing across a large academic medical center: The Mayo-Baylor RIGHT 10K Study.Genet Med2022
35207566Artificial Intelligence and Cardiovascular Genetics.Life (Basel)2022
34257418Neptune: an environment for the delivery of genomic medicine.Genet Med2021
33769305The Implementation Science for Genomic Health Translation (INSIGHT) Study in Epilepsy: Protocol for a Learning Health Care System.JMIR Res Protoc2021
33930535Genomic considerations for FHIR®; eMERGE implementation lessons.J Biomed Inform2021
34129815Exome variant discrepancies due to reference-genome differences.Am J Hum Genet2021
34363016Genetic testing in ambulatory cardiology clinics reveals high rate of findings with clinical management implications.Genet Med2021
31378813Cohort Profile: The Right Drug, Right Dose, Right Time: Using Genomic Data to Individualize Treatment Protocol (RIGHT Protocol).Int J Epidemiol2020
31971667Genome sequencing analysis of a family with a child displaying severe abdominal distention and recurrent hypoglycemia.Mol Genet Genomic Med2020
33108757Variant Classification Concordance using the ACMG-AMP Variant Interpretation Guidelines across Nine Genomic Implementation Research Studies.Am J Hum Genet2020
30890783Atlas-CNV: a validated approach to call single-exon CNVs in the eMERGESeq gene panel.Genet Med2019
31241152ARBoR: an identity and security solution for clinical reporting.J Am Med Inform Assoc2019
30392543The Return of Actionable Variants Empirical (RAVE) Study, a Mayo Clinic Genomic Medicine Implementation Study: Design and Initial Results.Mayo Clin Proc2018
29860405Empowering genomic medicine by establishing critical sequencing result data flows: the eMERGE example.J Am Med Inform Assoc2018
28798025Novel Genetic Triggers and Genotype-Phenotype Correlations in Patients With Left Ventricular Noncompaction.Circ Cardiovasc Genet2017
26590254UET: a database of evolutionarily-predicted functional determinants of protein sequences that cluster as functional sites in protein structures.Nucleic Acids Res2016
23353650A large-scale evaluation of computational protein function prediction.Nat Methods2013
24021383Accounting for epistatic interactions improves the functional analysis of protein structures.Bioinformatics2013
23514548Function prediction from networks of local evolutionary similarity in protein structure.BMC Bioinformatics2013
22689386ETAscape: analyzing protein networks to predict enzymatic function and substrates in Cytoscape.Bioinformatics2012
20036248Evolutionary trace annotation of protein function in the structural proteome.J Mol Biol2010
21179190Accurate protein structure annotation through competitive diffusion of enzymatic functions over a network of local evolutionary similarities.PLoS One2010
19307237Evolutionary Trace Annotation Server: automated enzyme function prediction in protein structures using 3D templates.Bioinformatics2009
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Collaborators

Richard A Gibbs
Baylor College of Medicine
Co-authored papers 16
Olivier Lichtarge
Baylor College of Medicine
Co-authored papers 8
Heidi L Rehm
The Broad Institute of MIT and Harvard
Co-authored papers 8
Donna M Muzny
Baylor College of Medicine
Co-authored papers 8
Gail P Jarvik
University of Washington Medical Center
Co-authored papers 8
Mullai Murugan
Baylor College of Medicine
Co-authored papers 7
Jianhong Hu
Co-authored papers 6
Eric Boerwinkle
Baylor College of Medicine
Co-authored papers 6
Pedro J Caraballo
Mayo Clinic
Co-authored papers 5
Robert R Freimuth
Center for Individualized Medicine, Mayo Clinic
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Christie L Kovar
Baylor College of Medicine
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Iftikhar J Kullo
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Richard R Sharp
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David R Crosslin
University of Washington Medical Center
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Viktoriya Korchina
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Josh F Peterson
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Niall J Lennon
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Marc S Williams
University of Washington Medical Center
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Hakon Hakonarson
The Center for Applied Genomics, Children's Hospital of Philadelphia
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Ken Wiley
National Human Genome Research Institute.
Co-authored papers 3
Wendy K Chung
Boston Children's Hospital, Harvard Medical School
Co-authored papers 3
Ginger A Metcalf
Co-authored papers 3
Aniko Sabo
Co-authored papers 3
Janet E Olson
Mayo Clinic
Co-authored papers 3
Carolyn R Rohrer Vitek
Center for Individualized Medicine, College of Medicine, Mayo Clinic
Co-authored papers 2
Joel E Pacyna
Biomedical Ethics Program, Mayo Clinic
Co-authored papers 2
Harshavardhan Doddapaneni
Baylor College of Medicine
Co-authored papers 2
Shalini N Jhangiani
Baylor College of Medicine
Co-authored papers 2
Matthew A Hathcock
Mayo Clinic
Co-authored papers 2
Samuel J Aronson
Georgetown University.
Co-authored papers 2
Release 1.2