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Anticancer Research|October 15, 2010
Sporadic breast carcinomas with somatic BRCA1 gene deletions share genotype/phenotype features with familial breast carcinomasKerstin Rhiem, Unda Todt, Barbara Wappenschmidt, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|December 22, 2006
Adult index patient with Currarino syndrome due to a novel HLXB9 mutation, c.336dupG (p.P113fsX224), presenting with Hirschsprung's disease, cephalgia, and lumbodyniaAlexander Volk, Mohsen Karbasiyan, Alexander Semmler, et al.
Human Genetics|January 20, 2009
New genetic evidence for involvement of the dopamine system in migraine with auraUnda Todt, Christian Netzer, Mohammad Toliat, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|March 2, 2006
Haplotype-based systematic association studies of ATP1A2 in migraine with auraChristian Netzer, Unda Todt, Axel Heinze, et al.
Genomics|May 6, 2008
Replication study of the insulin receptor gene in migraine with auraChristian Netzer, Jan Freudenberg, Axel Heinze, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|August 8, 2007
Genetic association studies of the chromosome 15 GABA-A receptor cluster in migraine with auraChristian Netzer, Jan Freudenberg, Mohammad R Toliat, et al.
Human Molecular Genetics|May 5, 2007
Severe mental retardation with breathing abnormalities (Pitt-Hopkins syndrome) is caused by haploinsufficiency of the neuronal bHLH transcription factor TCF4Antje Brockschmidt, Unda Todt, Soojin Ryu, et al.
Human Mutation|August 20, 2005
Rare missense variants in ATP1A2 in families with clustering of common forms of migraineUnda Todt, Martin Dichgans, Karin Jurkat-Rott, et al.
Human Mutation|April 18, 2007
Aberrant splicing is a common mutational mechanism in MKS1, a key player in Meckel-Gruber syndromeValeska Frank, Nadina Ortiz Brüchle, Silke Mager, et al.
Human Molecular Genetics|August 5, 2008
A high-density association screen of 155 ion transport genes for involvement with common migraineDale R Nyholt, K Steven LaForge, Mikko Kallela, et al.
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