Chuan Tan

X-exome sequencing of 405 unresolved families identifies seven novel intellectual disability genes

Hao Hu, Stefan A. Haas, Jamel Chelly et al. · Molecular Psychiatry · 2015 · 299 citations · Full text

Mutations of protocadherin 19 in female epilepsy (PCDH19-FE) lead to allopregnanolone deficiency

Chuan Tan, Chloé Shard, Enzo Ranieri et al. · Human Molecular Genetics · 2015 · 100 citations · Full text

Molecular Neuroscience, Developmental Biology, Syndromic Autism +13

THOC2 Mutations Implicate mRNA-Export Pathway in X-Linked Intellectual Disability

Raman Kumar, Mark Corbett, Bregje W.M. van Bon et al. · The American Journal of Human Genetics · 2015 · 77 citations · Full text

Genetic Disorder, Genetics, Fragile X Spectrum +4

PCDH19 regulation of neural progenitor cell differentiation suggests asynchrony of neurogenesis as a mechanism contributing to PCDH19 Girls Clustering Epilepsy

Claire C. Homan, Stephen Pederson, Thu-Hien To et al. · Neurobiology of Disease · 2018 · 49 citations · Full text

Developmental Biology, Ependyma, Neuroanatomy +8

Homozygous mutation of <i>STXBP5L</i> explains an autosomal recessive infantile-onset neurodegenerative disorder

Raman Kumar, Mark Corbett, Nicholas Smith et al. · Human Molecular Genetics · 2014 · 34 citations · Full text