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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.
Bipolar Disorders|June 6, 2007
COMT genotype increases risk for bipolar I disorder and influences neurocognitive performanceKatherine E Burdick, Birgit Funke, Joseph F Goldberg, 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.
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 Mutation|July 29, 2020
Fitting a naturally scaled point system to the ACMG/AMP variant classification guidelinesSean V Tavtigian, Steven M Harrison, Kenneth M Boucher, 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.
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