Déborah Morris-Rosendahl

The core <i>FOXG1</i> syndrome phenotype consists of postnatal microcephaly, severe mental retardation, absent language, dyskinesia, and corpus callosum hypogenesis

Fanny Kortüm, Soma Das, M. Flindt et al. · Journal of Medical Genetics · 2011 · 246 citations · Full text

Isolation of a novel potassium channel gene hSKCa3 containing a polymorphic CAG repeat: a candidate for schizophrenia and bipolar disorder?

K. George Chandy, Emmanuelle Fantino, Oliver H. Wittekindt et al. · Molecular Psychiatry · 1998 · 208 citations

Molecular Neuroscience, Signal Transduction, Hyperpolarization (Biology) +8

De Novo Mutations in FOXJ1 Result in a Motile Ciliopathy with Hydrocephalus and Randomization of Left/Right Body Asymmetry

Julia Wallmeier, Diana Frank, Amelia Shoemark et al. · The American Journal of Human Genetics · 2019 · 201 citations · Full text

Developmental Biology, Genetic Disorder, Genetics +7

Loss-of-Function Mutations in TBC1D20 Cause Cataracts and Male Infertility in blind sterile Mice and Warburg Micro Syndrome in Humans

Ryan P. Liegel, Mark T. Handley, Adam Ronchetti et al. · The American Journal of Human Genetics · 2013 · 132 citations · Full text

Genetic Disorder, Genetics, Pathogenesis +8

Brief research communication: serotonin transporter (5-HTT) gene polymorphisms are not associated with susceptibility to mood disorders

Margret R. Hoehe, Birgit Wendel, Ingrid Grunewald et al. · American Journal of Medical Genetics · 1998 · 123 citations · Full text

Psychiatric Disorders, Genetics, Genetic Epidemiology +22