Hsiao-Tuan Chao

Affiliations: 
Baylor College of Medicine, Houston, TX 
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"Hsiao-Tuan Chao"
Mean distance: 13.89 (cluster 11)
 
SNBCP
Cross-listing: BCM Tree

Parents

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Christian Rosenmund grad student 2004-2009 Baylor
Huda Y. Zoghbi grad student 2004-2009 Baylor
Hugo J. Bellen post-doc 2016-2019 Baylor College of Medicine/Jan and Dan Duncan Neurological Research Institute
John W. Swann post-doc 2017-2019 Baylor
 (Post-doc Co-Mentor)

Children

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Harim Delgado-Seo research assistant 2020-2021 Baylor
Vanesa Lerma research assistant 2020-2022 Baylor
John Thomas Gebert grad student 2020- Baylor
Christina Magyar grad student 2021- Baylor
Brooke Horist grad student 2022- Baylor
Maimuna Paul post-doc 2019- Baylor
Kailin Mao post-doc 2022- Baylor
BETA: Related publications

Publications

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Keehan L, Haviland I, Gofin Y, et al. (2022) Wide range of phenotypic severity in individuals with late truncations unique to the predominant CDKL5 transcript in the brain. American Journal of Medical Genetics. Part A
Thomas AX, Link N, Robak LA, et al. (2022) ANKLE2-related microcephaly: A variable microcephaly syndrome resembling Zika infection. Annals of Clinical and Translational Neurology
Deisseroth CA, Lerma VC, Magyar CL, et al. (2022) An integrated phenotypic and genotypic approach reveals a high-risk subtype association for EBF3 missense variants affecting the zinc finger domain. Annals of Neurology
Marcogliese PC, Deal SL, Andrews J, et al. (2022) Drosophila functional screening of de novo variants in autism uncovers damaging variants and facilitates discovery of rare neurodevelopmental diseases. Cell Reports. 38: 110517
Magyar CL, Murdock DR, Burrage LC, et al. (2022) PRUNE1 c.933G>A synonymous variant induces exon 7 skipping, disrupts the DHHA2 domain, and leads to an atypical NMIHBA syndrome presentation: Case report and review of the literature. American Journal of Medical Genetics. Part A
Murdock DR, Dai H, Burrage LC, et al. (2020) Transcriptome-directed analysis for Mendelian disease diagnosis overcomes limitations of conventional genomic testing. The Journal of Clinical Investigation
Chung HL, Mao X, Wang H, et al. (2020) De Novo Variants in CDK19 Are Associated with a Syndrome Involving Intellectual Disability and Epileptic Encephalopathy. American Journal of Human Genetics
Mao D, Reuter CM, Ruzhnikov MRZ, et al. (2020) De novo EIF2AK1 and EIF2AK2 Variants Are Associated with Developmental Delay, Leukoencephalopathy, and Neurologic Decompensation. American Journal of Human Genetics
Chen W, Cai ZL, Chao ES, et al. (2020) haploinsufficiency impairs inhibition and mediates key neurological features of encephalopathy. Elife. 9
Chen W, Cai Z, Chao ES, et al. (2020) Author response: Stxbp1/Munc18-1 haploinsufficiency impairs inhibition and mediates key neurological features of STXBP1 encephalopathy Elife
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