Eric Venner
Human Genome Sciences (United States)(US)Baylor College of Medicine(US)
Publications by Year
Research Areas
Genomics and Rare Diseases, Cancer Genomics and Diagnostics, Genetic Associations and Epidemiology, BRCA gene mutations in cancer, Genomic variations and chromosomal abnormalities
Most-Cited Works
- → A large-scale evaluation of computational protein function prediction(2013)1,078 cited
- → Genomic data in the All of Us Research Program(2024)647 cited
- → Improving reporting standards for polygenic scores in risk prediction studies(2021)476 cited
- → Best practices for the interpretation and reporting of clinical whole genome sequencing(2022)144 cited
- → Novel Genetic Triggers and Genotype–Phenotype Correlations in Patients With Left Ventricular Noncompaction(2017)130 cited
- → Frequency of genomic secondary findings among 21,915 eMERGE network participants(2020)117 cited
- → Harmonizing Clinical Sequencing and Interpretation for the eMERGE III Network(2019)115 cited
- → Variant Classification Concordance using the ACMG-AMP Variant Interpretation Guidelines across Nine Genomic Implementation Research Studies(2020)100 cited
- → Implementation of preemptive DNA sequence–based pharmacogenomics testing across a large academic medical center: The Mayo-Baylor RIGHT 10K Study(2022)65 cited
- → Exome variant discrepancies due to reference-genome differences(2021)63 cited