Hsiao-Tuan Chao

Department of Molecular and Human Genetics, Baylor College of Medicine

Affiliated withBaylor College of Medicine Texas Children's Hospital

Research Area

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JoVE Journal Publications

ArticleTotal : 1	Year
Publication title Cited by 43	2019

Other Publications

Article	Year
Distinct domains of complexin I differentially regulate neurotransmitter release. Nature structural & molecular biology\| PubMed ID: 17828276	2007
MeCP2 controls excitatory synaptic strength by regulating glutamatergic synapse number. Neuron\| PubMed ID: 17920015	2007
A partial loss of function allele of methyl-CpG-binding protein 2 predicts a human neurodevelopmental syndrome. Human molecular genetics\| PubMed ID: 18321864	2008
Deletion of Mecp2 in Sim1-expressing neurons reveals a critical role for MeCP2 in feeding behavior, aggression, and the response to stress. Neuron\| PubMed ID: 18817733	2008
The yin and yang of MeCP2 phosphorylation. Proceedings of the National Academy of Sciences of the United States of America\| PubMed ID: 19293386	2009
Math1 is essential for the development of hindbrain neurons critical for perinatal breathing. Neuron\| PubMed ID: 19914183	2009
Loss of MeCP2 in aminergic neurons causes cell-autonomous defects in neurotransmitter synthesis and specific behavioral abnormalities. Proceedings of the National Academy of Sciences of the United States of America\| PubMed ID: 20007372	2009
Binding of the complexin N terminus to the SNARE complex potentiates synaptic-vesicle fusogenicity. Nature structural & molecular biology\| PubMed ID: 20400951	2010
Dysfunction in GABA signalling mediates autism-like stereotypies and Rett syndrome phenotypes. Nature\| PubMed ID: 21068835	2010
Etiology of a genetically complex seizure disorder in Celf4 mutant mice. Genes, brain, and behavior\| PubMed ID: 21745337	2011
Dendritic arborization and spine dynamics are abnormal in the mouse model of MECP2 duplication syndrome. The Journal of neuroscience : the official journal of the Society for Neuroscience\| PubMed ID: 24336718	2013
Investigation of synapse formation and function in a glutamatergic-GABAergic two-neuron microcircuit. The Journal of neuroscience : the official journal of the Society for Neuroscience\| PubMed ID: 24431444	2014
A Syndromic Neurodevelopmental Disorder Caused by De Novo Variants in EBF3. American journal of human genetics\| PubMed ID: 28017372	2017
MARRVEL: Integration of Human and Model Organism Genetic Resources to Facilitate Functional Annotation of the Human Genome. American journal of human genetics\| PubMed ID: 28502612	2017
Building dialogues between clinical and biomedical research through cross-species collaborations. Seminars in cell & developmental biology\| PubMed ID: 28579453	2017
Clinical and molecular characterization of de novo loss of function variants in HNRNPU. American journal of medical genetics. Part A\| PubMed ID: 28815871	2017
Model Organisms Facilitate Rare Disease Diagnosis and Therapeutic Research. Genetics\| PubMed ID: 28874452	2017
Identification of novel candidate disease genes from de novo exonic copy number variants. Genome medicine\| PubMed ID: 28934986	2017
Recurrent mosaic MTOR c.5930C > T (p.Thr1977Ile) variant causing megalencephaly, asymmetric polymicrogyria, and cutaneous pigmentary mosaicism: Case report and review of the literature. American journal of medical genetics. Part A\| PubMed ID: 30569621	2019
DYRK1A-related intellectual disability: a syndrome associated with congenital anomalies of the kidney and urinary tract. Genetics in medicine : official journal of the American College of Medical Genetics\| PubMed ID: 31263215	2019