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Archives of Pathology & Laboratory Medicine
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September 29, 2024
Harnessing the Power of Generative Artificial Intelligence in Pathology Education: Opportunities, Challenges, and Future Directions
Matthew J Cecchini, Michael J Borowitz, Eric F Glassy, et al.
Cancer Research
|
July 14, 2022
Genetic Risk of Second Primary Cancer in Breast Cancer Survivors: The Multiethnic Cohort Study
Fei Chen, Sungshim L Park, Lynne R Wilkens, et al.
Human Mutation
|
May 23, 2020
Mutation prevalence tables for hereditary cancer derived from multigene panel testing
Steven N Hart, Eric C Polley, Amal Yussuf, et al.
Journal of the National Cancer Institute
|
February 25, 2020
The Contribution of Germline Predisposition Gene Mutations to Clinical Subtypes of Invasive Breast Cancer From a Clinical Genetic Testing Cohort
Chunling Hu, Eric C Polley, Siddhartha Yadav, et al.
American Journal of Clinical Pathology
|
May 11, 2026
The CARE framework for AI dataset documentation in clinical laboratories: a comprehensive checklist and data lineage methodology
Christopher A Garcia, Katelyn A Reed, Eric Lantz, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
December 20, 2019
Classification of variants of uncertain significance in BRCA1 and BRCA2 using personal and family history of cancer from individuals in a large hereditary cancer multigene panel testing cohort
Hongyan Li, Holly LaDuca, Tina Pesaran, et al.
Archives of Pathology & Laboratory Medicine
|
April 22, 2024
Democratizing Artificial Intelligence in Anatomic Pathology
Thomas J Flotte, Stephanie A Derauf, Rachel K Byrd, et al.
JAMA Oncology
|
May 27, 2021
Comparison of the Prevalence of Pathogenic Variants in Cancer Susceptibility Genes in Black Women and Non-Hispanic White Women With Breast Cancer in the United States
Susan M Domchek, Song Yao, Fei Chen, et al.
Briefings in Bioinformatics
|
September 12, 2015
Collaborative science in the next-generation sequencing era: a viewpoint on how to combine exome sequencing data across sites to identify novel disease susceptibility genes
Steven N Hart, Kara N Maxwell, Tinu Thomas, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
June 10, 2018
Comprehensive annotation of BRCA1 and BRCA2 missense variants by functionally validated sequence-based computational prediction models
Steven N Hart, Tanya Hoskin, Hermela Shimelis, et al.
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Search research articles
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Showing results (41-50 of 124) with videos related to
Sort By:
Page
of 13
Archives of Pathology & Laboratory Medicine
|
September 29, 2024
Harnessing the Power of Generative Artificial Intelligence in Pathology Education: Opportunities, Challenges, and Future Directions
Matthew J Cecchini, Michael J Borowitz, Eric F Glassy, et al.
Cancer Research
|
July 14, 2022
Genetic Risk of Second Primary Cancer in Breast Cancer Survivors: The Multiethnic Cohort Study
Fei Chen, Sungshim L Park, Lynne R Wilkens, et al.
Human Mutation
|
May 23, 2020
Mutation prevalence tables for hereditary cancer derived from multigene panel testing
Steven N Hart, Eric C Polley, Amal Yussuf, et al.
Journal of the National Cancer Institute
|
February 25, 2020
The Contribution of Germline Predisposition Gene Mutations to Clinical Subtypes of Invasive Breast Cancer From a Clinical Genetic Testing Cohort
Chunling Hu, Eric C Polley, Siddhartha Yadav, et al.
American Journal of Clinical Pathology
|
May 11, 2026
The CARE framework for AI dataset documentation in clinical laboratories: a comprehensive checklist and data lineage methodology
Christopher A Garcia, Katelyn A Reed, Eric Lantz, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
December 20, 2019
Classification of variants of uncertain significance in BRCA1 and BRCA2 using personal and family history of cancer from individuals in a large hereditary cancer multigene panel testing cohort
Hongyan Li, Holly LaDuca, Tina Pesaran, et al.
Archives of Pathology & Laboratory Medicine
|
April 22, 2024
Democratizing Artificial Intelligence in Anatomic Pathology
Thomas J Flotte, Stephanie A Derauf, Rachel K Byrd, et al.
JAMA Oncology
|
May 27, 2021
Comparison of the Prevalence of Pathogenic Variants in Cancer Susceptibility Genes in Black Women and Non-Hispanic White Women With Breast Cancer in the United States
Susan M Domchek, Song Yao, Fei Chen, et al.
Briefings in Bioinformatics
|
September 12, 2015
Collaborative science in the next-generation sequencing era: a viewpoint on how to combine exome sequencing data across sites to identify novel disease susceptibility genes
Steven N Hart, Kara N Maxwell, Tinu Thomas, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
June 10, 2018
Comprehensive annotation of BRCA1 and BRCA2 missense variants by functionally validated sequence-based computational prediction models
Steven N Hart, Tanya Hoskin, Hermela Shimelis, et al.
Page
of 13