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Birgit Funke

Showing results (11-20 of 56) with videos related to

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Schizophrenia Research|November 1, 2006
DTNBP1 genotype influences cognitive decline in schizophreniaKatherine E Burdick, Terry E Goldberg, Birgit Funke, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 1, 2019
Considerations for clinical curation, classification, and reporting of low-penetrance and low effect size variants associated with disease riskOzlem Senol-Cosar, Ryan J Schmidt, Emily Qian, et al.
The Journal of Molecular Diagnostics : JMD|February 25, 2020
Design and Reporting Considerations for Genetic Screening TestsJill Hagenkord, Birgit Funke, Emily Qian, et al.
The Journal of Molecular Diagnostics : JMD|August 13, 2021
Creation of an Expert Curated Variant List for Clinical Genomic Test Development and Validation: A ClinGen and GeT-RM Collaborative ProjectEmma Wilcox, Steven M Harrison, Edward Lockhart, et al.
American Journal of Human Genetics|September 14, 2004
Association of the DTNBP1 locus with schizophrenia in a U.S. populationBirgit Funke, Christine T Finn, Alex M Plocik, et al.
The American Journal of Psychiatry|March 4, 2006
Dysbindin genotype and negative symptoms in schizophreniaPamela DeRosse, Birgit Funke, Katherine E Burdick, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 21, 2005
A 200-kb region of human chromosome 22q11.2 confers antipsychotic-responsive behavioral abnormalities in miceNoboru Hiroi, Hongwen Zhu, Moonsook Lee, et al.
Schizophrenia Research|July 11, 2006
COMT genotype and manic symptoms in schizophreniaPamela DeRosse, Birgit Funke, Katherine E Burdick, et al.
Human Molecular Genetics|January 18, 2006
Genetic variation in DTNBP1 influences general cognitive abilityKatherine E Burdick, Todd Lencz, Birgit Funke, et al.
Archives of Pathology & Laboratory Medicine|March 22, 2017
Development and Validation of Targeted Next-Generation Sequencing Panels for Detection of Germline Variants in Inherited DiseasesAvni Santani, Jill Murrell, Birgit Funke, et al.
Pageof 6

Showing results (11-20 of 56) with videos related to

Sort By:
Pageof 6
Schizophrenia Research|November 1, 2006
DTNBP1 genotype influences cognitive decline in schizophreniaKatherine E Burdick, Terry E Goldberg, Birgit Funke, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 1, 2019
Considerations for clinical curation, classification, and reporting of low-penetrance and low effect size variants associated with disease riskOzlem Senol-Cosar, Ryan J Schmidt, Emily Qian, et al.
The Journal of Molecular Diagnostics : JMD|February 25, 2020
Design and Reporting Considerations for Genetic Screening TestsJill Hagenkord, Birgit Funke, Emily Qian, et al.
The Journal of Molecular Diagnostics : JMD|August 13, 2021
Creation of an Expert Curated Variant List for Clinical Genomic Test Development and Validation: A ClinGen and GeT-RM Collaborative ProjectEmma Wilcox, Steven M Harrison, Edward Lockhart, et al.
American Journal of Human Genetics|September 14, 2004
Association of the DTNBP1 locus with schizophrenia in a U.S. populationBirgit Funke, Christine T Finn, Alex M Plocik, et al.
The American Journal of Psychiatry|March 4, 2006
Dysbindin genotype and negative symptoms in schizophreniaPamela DeRosse, Birgit Funke, Katherine E Burdick, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 21, 2005
A 200-kb region of human chromosome 22q11.2 confers antipsychotic-responsive behavioral abnormalities in miceNoboru Hiroi, Hongwen Zhu, Moonsook Lee, et al.
Schizophrenia Research|July 11, 2006
COMT genotype and manic symptoms in schizophreniaPamela DeRosse, Birgit Funke, Katherine E Burdick, et al.
Human Molecular Genetics|January 18, 2006
Genetic variation in DTNBP1 influences general cognitive abilityKatherine E Burdick, Todd Lencz, Birgit Funke, et al.
Archives of Pathology & Laboratory Medicine|March 22, 2017
Development and Validation of Targeted Next-Generation Sequencing Panels for Detection of Germline Variants in Inherited DiseasesAvni Santani, Jill Murrell, Birgit Funke, et al.
Pageof 6