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Brian H Shirts

Showing results (71-80 of 113) with videos related to

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American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|March 12, 2014
Refining the structure and content of clinical genomic reportsMichael O Dorschner, Laura M Amendola, Brian H Shirts, et al.
Journal of Genetic Counseling|December 6, 2015
Next Generation Sequencing in the Clinic: a Patterns of Care Study in a Retrospective Cohort of Subjects Referred to a Genetic Medicine Clinic for Suspected Lynch SyndromeCarlos J Gallego, Matthew L Perez, Amber Burt, et al.
Schizophrenia Research|February 9, 2010
Grey matter changes associated with host genetic variation and exposure to Herpes Simplex Virus 1 (HSV1) in first episode schizophreniaKonasale M Prasad, Mikhil N Bamne, Brian H Shirts, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 29, 2014
Deep sequencing with intronic capture enables identification of an APC exon 10 inversion in a patient with polyposisBrian H Shirts, Stephen J Salipante, Silvia Casadei, et al.
Translational Behavioral Medicine|June 25, 2020
Relationship between genetic knowledge and familial communication of CRC risk and intent to communicate CRCP genetic information: insights from FamilyTalk eMERGE IIISukh Makhnoon, Deborah J Bowen, Brian H Shirts, et al.
Medrxiv : the Preprint Server for Health Sciences|February 20, 2025
Insights on improving accessibility and usability of functional data to unlock its potential for variant interpretationMin Seon Park, Runjun D Kumar, Cristian Ovadiuc, et al.
Journal of Biomedical Informatics|January 19, 2016
The genomic CDS sandbox: An assessment among domain expertsAyesha Aziz, Kensaku Kawamoto, Karen Eilbeck, et al.
American Journal of Human Genetics|November 18, 2021
Closing the gap: Systematic integration of multiplexed functional data resolves variants of uncertain significance in BRCA1, TP53, and PTENShawn Fayer, Carrie Horton, Jennifer N Dines, et al.
Cancer Medicine|November 25, 2022
A multicenter study of clinical impact of variant of uncertain significance reclassification in breast, ovarian and colorectal cancer susceptibility genesSukh Makhnoon, Brooke Levin, Megan Ensinger, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 27, 2023
Laboratory perspectives in the development of polygenic risk scores for disease: A points to consider statement of the American College of Medical Genetics and Genomics (ACMG)Honey V Reddi, Hannah Wand, Birgit Funke, et al.
Pageof 12

Showing results (71-80 of 113) with videos related to

Sort By:
Pageof 12
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|March 12, 2014
Refining the structure and content of clinical genomic reportsMichael O Dorschner, Laura M Amendola, Brian H Shirts, et al.
Journal of Genetic Counseling|December 6, 2015
Next Generation Sequencing in the Clinic: a Patterns of Care Study in a Retrospective Cohort of Subjects Referred to a Genetic Medicine Clinic for Suspected Lynch SyndromeCarlos J Gallego, Matthew L Perez, Amber Burt, et al.
Schizophrenia Research|February 9, 2010
Grey matter changes associated with host genetic variation and exposure to Herpes Simplex Virus 1 (HSV1) in first episode schizophreniaKonasale M Prasad, Mikhil N Bamne, Brian H Shirts, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 29, 2014
Deep sequencing with intronic capture enables identification of an APC exon 10 inversion in a patient with polyposisBrian H Shirts, Stephen J Salipante, Silvia Casadei, et al.
Translational Behavioral Medicine|June 25, 2020
Relationship between genetic knowledge and familial communication of CRC risk and intent to communicate CRCP genetic information: insights from FamilyTalk eMERGE IIISukh Makhnoon, Deborah J Bowen, Brian H Shirts, et al.
Medrxiv : the Preprint Server for Health Sciences|February 20, 2025
Insights on improving accessibility and usability of functional data to unlock its potential for variant interpretationMin Seon Park, Runjun D Kumar, Cristian Ovadiuc, et al.
Journal of Biomedical Informatics|January 19, 2016
The genomic CDS sandbox: An assessment among domain expertsAyesha Aziz, Kensaku Kawamoto, Karen Eilbeck, et al.
American Journal of Human Genetics|November 18, 2021
Closing the gap: Systematic integration of multiplexed functional data resolves variants of uncertain significance in BRCA1, TP53, and PTENShawn Fayer, Carrie Horton, Jennifer N Dines, et al.
Cancer Medicine|November 25, 2022
A multicenter study of clinical impact of variant of uncertain significance reclassification in breast, ovarian and colorectal cancer susceptibility genesSukh Makhnoon, Brooke Levin, Megan Ensinger, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 27, 2023
Laboratory perspectives in the development of polygenic risk scores for disease: A points to consider statement of the American College of Medical Genetics and Genomics (ACMG)Honey V Reddi, Hannah Wand, Birgit Funke, et al.
Pageof 12