Ken‐Shiung Chen

Homologous recombination of a flanking repeat gene cluster is a mechanism for a common contiguous gene deletion syndrome

Ken‐Shiung Chen, Prasad Manian, Thearith Koeuth et al. · Nature Genetics · 1997 · 384 citations

Genetic Disorder, Homologous Recombination, Genetics +8

Novel mutations of MYO15A associated with profound deafness in consanguineous families and moderately severe hearing loss in a patient with Smith-Magenis syndrome

Nikki Liburd, Manju Ghosh, Saima Riazuddin et al. · Human Genetics · 2001 · 148 citations · Full text

Mendelian Disorder, Genetic Disorder, Novel Mutations +6

Fliih, a Gelsolin-Related Cytoskeletal Regulator Essential for Early Mammalian Embryonic Development

Hugh D. Campbell, Shelley Fountain, Ian S. McLennan et al. · Molecular and Cellular Biology · 2002 · 87 citations · Full text

Oocyte, Developmental Biology, Human Flii Gene +15

NMDA receptor activation enhances inhibitory GABAergic transmission onto hippocampal pyramidal neurons via presynaptic and postsynaptic mechanisms

Jiu-Gang Xue, Takayoshi Masuoka, Xian-Di Gong et al. · Journal of Neurophysiology · 2011 · 73 citations

DNA Rearrangements on Both Homologues of Chromosome 17 in a Mildly Delayed Individual with a Family History of Autosomal Dominant Carpal Tunnel Syndrome

Lorraine Potocki, Ken‐Shiung Chen, Thearith Koeuth et al. · The American Journal of Human Genetics · 1999 · 69 citations · Full text

Chromatin, Chromosome Dynamics, Mendelian Disorder +14