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Brian H Shirts

Showing results (51-60 of 113) with videos related to

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Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 9, 2020
Systematic misclassification of missense variants in BRCA1 and BRCA2 "coldspots"Jennifer N Dines, Brian H Shirts, Thomas P Slavin, et al.
Plos One|September 30, 2020
Effects of germline and somatic events in candidate BRCA-like genes on breast-tumor signaturesWeston R Bodily, Brian H Shirts, Tom Walsh, et al.
American Journal of Clinical Pathology|April 29, 2016
Applying Ancestry and Sex Computation as a Quality Control Tool in Targeted Next-Generation SequencingPatrick C Mathias, Emily H Turner, Sheena M Scroggins, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 6, 2015
Development of clinical decision support alerts for pharmacogenomic incidental findings from exome sequencingAdam A Nishimura, Brian H Shirts, Michael O Dorschner, et al.
Genetics|October 15, 2024
A maternal germline mutator phenotype in a family affected by heritable colorectal cancerCandice L Young, Annabel C Beichman, David Mas-Ponte, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 31, 2018
Outcomes of 92 patient-driven family studies for reclassification of variants of uncertain significanceGinger J Tsai, John Michael O Rañola, Christina Smith, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 1, 2024
Primary care provider practices, attitudes, and confidence with hereditary cancer risk assessment and testing: A mixed methods studySarah Conner, Tesla Theoryn, Emerson Dusic, et al.
Medrxiv : the Preprint Server for Health Sciences|January 10, 2024
A maternal germline mutator phenotype in a family affected by heritable colorectal cancerCandice L Young, Annabel C Beichman, David Mas-Ponte, et al.
Journal of the American Medical Directors Association|February 24, 2009
Provider management of and satisfaction with laboratory testing in the nursing home setting: results of a national internet-based surveyBrian H Shirts, Subashan Perera, Joseph T Hanlon, et al.
American Journal of Human Genetics|December 16, 2023
ClinGen guidance for use of the PP1/BS4 co-segregation and PP4 phenotype specificity criteria for sequence variant pathogenicity classificationLeslie G Biesecker, Alicia B Byrne, Steven M Harrison, et al.
Pageof 12

Showing results (51-60 of 113) with videos related to

Sort By:
Pageof 12
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 9, 2020
Systematic misclassification of missense variants in BRCA1 and BRCA2 "coldspots"Jennifer N Dines, Brian H Shirts, Thomas P Slavin, et al.
Plos One|September 30, 2020
Effects of germline and somatic events in candidate BRCA-like genes on breast-tumor signaturesWeston R Bodily, Brian H Shirts, Tom Walsh, et al.
American Journal of Clinical Pathology|April 29, 2016
Applying Ancestry and Sex Computation as a Quality Control Tool in Targeted Next-Generation SequencingPatrick C Mathias, Emily H Turner, Sheena M Scroggins, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 6, 2015
Development of clinical decision support alerts for pharmacogenomic incidental findings from exome sequencingAdam A Nishimura, Brian H Shirts, Michael O Dorschner, et al.
Genetics|October 15, 2024
A maternal germline mutator phenotype in a family affected by heritable colorectal cancerCandice L Young, Annabel C Beichman, David Mas-Ponte, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 31, 2018
Outcomes of 92 patient-driven family studies for reclassification of variants of uncertain significanceGinger J Tsai, John Michael O Rañola, Christina Smith, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 1, 2024
Primary care provider practices, attitudes, and confidence with hereditary cancer risk assessment and testing: A mixed methods studySarah Conner, Tesla Theoryn, Emerson Dusic, et al.
Medrxiv : the Preprint Server for Health Sciences|January 10, 2024
A maternal germline mutator phenotype in a family affected by heritable colorectal cancerCandice L Young, Annabel C Beichman, David Mas-Ponte, et al.
Journal of the American Medical Directors Association|February 24, 2009
Provider management of and satisfaction with laboratory testing in the nursing home setting: results of a national internet-based surveyBrian H Shirts, Subashan Perera, Joseph T Hanlon, et al.
American Journal of Human Genetics|December 16, 2023
ClinGen guidance for use of the PP1/BS4 co-segregation and PP4 phenotype specificity criteria for sequence variant pathogenicity classificationLeslie G Biesecker, Alicia B Byrne, Steven M Harrison, et al.
Pageof 12