Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Brian H Shirts

Showing results (41-50 of 113) with videos related to

Pageof 12
Sort By:
Journal of Genetic Counseling|January 10, 2020
Exploring relatives' perceptions of participation, ethics, and communication in a patient-driven study for hereditary cancer variant reclassificationGinger J Tsai, Annie T Chen, Lauren T Garrett, et al.
Schizophrenia Research|March 1, 2006
A comprehensive genetic association and functional study of TNF in schizophrenia riskBrian H Shirts, Mikhil Bamne, Jung Jin Kim, et al.
The Consultant Pharmacist : the Journal of the American Society of Consultant Pharmacists|June 11, 2008
Frequency of laboratory monitoring of chronic medications administered to nursing facility residents: results of a national Internet-based studySteven M Handler, Brian H Shirts, Subashan Perera, et al.
The Journal of Molecular Diagnostics : JMD|May 25, 2018
Efficient Detection of Copy Number Mutations in PMS2 Exons with a Close HomologDaniel S Herman, Christina Smith, Chang Liu, et al.
Schizophrenia Research|September 20, 2008
Antibodies to cytomegalovirus and Herpes Simplex Virus 1 associated with cognitive function in schizophreniaBrian H Shirts, Konasale M Prasad, Michael F Pogue-Geile, et al.
Journal of Genetic Counseling|July 17, 2016
Family Studies for Classification of Variants of Uncertain Classification: Current Laboratory Clinical Practice and a New Web-Based Educational ToolLauren T Garrett, Nathan Hickman, Angela Jacobson, et al.
Genetics|April 13, 2021
Multiplexing mutation rate assessment: determining pathogenicity of Msh2 variants in Saccharomyces cerevisiaeAnja R Ollodart, Chiann-Ling C Yeh, Aaron W Miller, et al.
The Pharmacogenomics Journal|April 2, 2022
Implementation of pharmacogenomic clinical decision support for health systems: a cost-utility analysisShangqing Jiang, Patrick C Mathias, Nathaniel Hendrix, et al.
Schizophrenia Research|June 15, 2007
Polymorphisms in MICB are associated with human herpes virus seropositivity and schizophrenia riskBrian H Shirts, Jung Jin Kim, Shani Reich, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 6, 2016
CADD score has limited clinical validity for the identification of pathogenic variants in noncoding regions in a hereditary cancer panelCheryl A Mather, Sean D Mooney, Stephen J Salipante, et al.
Pageof 12

Showing results (41-50 of 113) with videos related to

Sort By:
Pageof 12
Journal of Genetic Counseling|January 10, 2020
Exploring relatives' perceptions of participation, ethics, and communication in a patient-driven study for hereditary cancer variant reclassificationGinger J Tsai, Annie T Chen, Lauren T Garrett, et al.
Schizophrenia Research|March 1, 2006
A comprehensive genetic association and functional study of TNF in schizophrenia riskBrian H Shirts, Mikhil Bamne, Jung Jin Kim, et al.
The Consultant Pharmacist : the Journal of the American Society of Consultant Pharmacists|June 11, 2008
Frequency of laboratory monitoring of chronic medications administered to nursing facility residents: results of a national Internet-based studySteven M Handler, Brian H Shirts, Subashan Perera, et al.
The Journal of Molecular Diagnostics : JMD|May 25, 2018
Efficient Detection of Copy Number Mutations in PMS2 Exons with a Close HomologDaniel S Herman, Christina Smith, Chang Liu, et al.
Schizophrenia Research|September 20, 2008
Antibodies to cytomegalovirus and Herpes Simplex Virus 1 associated with cognitive function in schizophreniaBrian H Shirts, Konasale M Prasad, Michael F Pogue-Geile, et al.
Journal of Genetic Counseling|July 17, 2016
Family Studies for Classification of Variants of Uncertain Classification: Current Laboratory Clinical Practice and a New Web-Based Educational ToolLauren T Garrett, Nathan Hickman, Angela Jacobson, et al.
Genetics|April 13, 2021
Multiplexing mutation rate assessment: determining pathogenicity of Msh2 variants in Saccharomyces cerevisiaeAnja R Ollodart, Chiann-Ling C Yeh, Aaron W Miller, et al.
The Pharmacogenomics Journal|April 2, 2022
Implementation of pharmacogenomic clinical decision support for health systems: a cost-utility analysisShangqing Jiang, Patrick C Mathias, Nathaniel Hendrix, et al.
Schizophrenia Research|June 15, 2007
Polymorphisms in MICB are associated with human herpes virus seropositivity and schizophrenia riskBrian H Shirts, Jung Jin Kim, Shani Reich, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 6, 2016
CADD score has limited clinical validity for the identification of pathogenic variants in noncoding regions in a hereditary cancer panelCheryl A Mather, Sean D Mooney, Stephen J Salipante, et al.
Pageof 12