Yuya Kobayashi
Affiliations: | 2008-2012 | Genetics | Stanford University, Palo Alto, CA |
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"Yuya Kobayashi"
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Padigepati SR, Stafford DA, Tan CA, et al. (2024) Scalable approaches for generating, validating and incorporating data from high-throughput functional assays to improve clinical variant classification. Human Genetics |
Yang S, Lincoln SE, Kobayashi Y, et al. (2017) Sources of discordance among germ-line variant classifications in ClinVar. Genetics in Medicine : Official Journal of the American College of Medical Genetics |
Nykamp K, Anderson M, Powers M, et al. (2017) Sherloc: a comprehensive refinement of the ACMG-AMP variant classification criteria. Genetics in Medicine : Official Journal of the American College of Medical Genetics |
Kobayashi Y, Yang S, Nykamp K, et al. (2017) Pathogenic variant burden in the ExAC database: an empirical approach to evaluating population data for clinical variant interpretation. Genome Medicine. 9: 13 |
Lincoln SE, Cline M, Yang S, et al. (2016) Variant classifications in BRCA1 and BRCA2: A systematic analysis of interlaboratory concordance Journal of Clinical Oncology. 34: 1592-1592 |
Lincoln S, Nykamp K, Kobayashi Y, et al. (2016) Abstract P2-09-11: Consistency of pathogenicity determinations for hereditary cancer gene mutations Cancer Research. 76 |
Desmond A, Kurian AW, Gabree M, et al. (2015) Clinical Actionability of Multigene Panel Testing for Hereditary Breast and Ovarian Cancer Risk Assessment. Jama Oncology |
Lincoln SE, Kobayashi Y, Anderson MJ, et al. (2015) A Systematic Comparison of Traditional and Multigene Panel Testing for Hereditary Breast and Ovarian Cancer Genes in More Than 1000 Patients. The Journal of Molecular Diagnostics : Jmd. 17: 533-44 |
Ellisen L, Kurian A, Lincoln S, et al. (2015) Abstract P4-12-04: Clinical evaluation of multigene testing for hereditary breast and ovarian cancer Cancer Research. 75 |
Ellisen LW, Lincoln SE, Kurian AW, et al. (2015) MG-114 Clinical actionability of multi-gene panel tests for hereditary breast and ovarian cancer (HBOC) Journal of Medical Genetics. 52: A6.1-A6 |