Jamee M. Bomar
Max Planck Research Unit for Neurogenetics(DE)
Publications by Year
Research Areas
Genetics and Neurodevelopmental Disorders, Mitochondrial Function and Pathology, Chromosomal and Genetic Variations, RNA and protein synthesis mechanisms, Genetic Neurodegenerative Diseases
Most-Cited Works
- → Linkage, Association, and Gene-Expression Analyses Identify CNTNAP2 as an Autism-Susceptibility Gene(2008)822 cited
- → X-linked protocadherin 19 mutations cause female-limited epilepsy and cognitive impairment(2008)444 cited
- → Human-specific transcriptional regulation of CNS development genes by FOXP2(2009)394 cited
- → Identification of the Transcriptional Targets of FOXP2, a Gene Linked to Speech and Language, in Developing Human Brain(2007)294 cited
- → Mutations in a novel gene encoding a CRAL-TRIO domain cause human Cayman ataxia and ataxia/dystonia in the jittery mouse(2003)152 cited
- → Characterization of a mutagenic B1 retrotransposon insertion in the jittery mouse(2004)26 cited
- → Erratum: Corrigendum: Mutations in a novel gene encoding a CRAL-TRIO domain cause human Cayman ataxia and ataxia/dystonia in the jittery mouse(2005)3 cited
- Characterization of a mutagenic B1 retrotransposon insertion in the jittery mouse Communicated by Haig H. Kazazian(2004)