Lisa Bastarache

Biomedical Informatics Vanderbilt University School of Medicine, Nashville, TN, United States 
"Lisa Bastarache"
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Schlueter DJ, Sulieman L, Mo H, et al. (2023) Systematic replication of smoking disease associations using survey responses and EHR data in the All of Us Research Program. Journal of the American Medical Informatics Association : Jamia
Schuler BA, Bastarache L, Wang J, et al. (2023) Population genetic testing and SERPINA1 sequencing identifies unidentified alpha-1 antitrypsin deficiency alleles and gene-environment interaction with hepatitis C infection. Plos One. 18: e0286469
Cassini T, Bastarache L, Zeng C, et al. (2023) A Test of Automated Use of Electronic Health Records to Aid in Diagnosis of Genetic Disease. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 100966
Bastarache L, Delozier S, Pandit A, et al. (2023) The phenotype-genotype reference map: Improving biobank data science through replication. American Journal of Human Genetics
Allaire P, He J, Mayer J, et al. (2023) Genetic and clinical determinants of telomere length. Hgg Advances. 4: 100201
Robinson JR, Carroll RJ, Bastarache L, et al. (2022) Quantifying the phenome-wide disease burden of obesity using electronic health records and genomics. Obesity (Silver Spring, Md.)
Aref L, Bastarache L, Hughey JJ. (2022) The phers R package: using phenotype risk scores based on electronic health records to study Mendelian disease and rare genetic variants. Bioinformatics (Oxford, England)
Zeng C, Bastarache LA, Tao R, et al. (2022) Association of Pathogenic Variants in Hereditary Cancer Genes With Multiple Diseases. Jama Oncology
Irlmeier R, Hughey JJ, Bastarache L, et al. (2022) Cox Regression is Robust to Inaccurate EHR-extracted Event Time-an Application to EHR-based GWAS. Bioinformatics (Oxford, England)
Bastarache L, Denny JC, Roden DM. (2022) Phenome-Wide Association Studies. Jama. 327: 75-76
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