Hsiao-Tuan Chao
Affiliations: | Baylor College of Medicine, Houston, TX |
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"Hsiao-Tuan Chao"Mean distance: 13.89 (cluster 11) | S | N | B | C | P |
Cross-listing: BCM Tree
Parents
Sign in to add mentor| 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
Sign in to add trainee| 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 |
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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 |