Shinya Yamamoto

Affiliations: 
Baylor College of Medicine, Houston, TX 
Area:
Genetics, Drosophila, Rare and Undiagnosed Diseases, Neurological and Psychiatric Disorders, Developmental Biology
Website:
https://www.bcm.edu/people-search/shinya-yamamoto-33456
Google:
"Shinya Yamamoto"
Bio:

https://nri.texaschildrens.org/faculty/shinya-yamamoto-dvm-phd
https://www.researchgate.net/profile/Shinya_Yamamoto3
https://scholar.google.com/citations?user=GCbIDKwAAAAJ&hl=en

Cross-listing: Neurotree - FlyTree

Parents

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Kazuhiko Imakawa research assistant 2002-2005 The University of Tokyo (Japan) (Neurotree)
 (D.V.M. thesis project)
Hugo J. Bellen grad student 2005-2012 Baylor College of Medicine
 (Ph.D. student)

Children

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Jasmine O. Brown research assistant 2023- Baylor College of Medicine (Neurotree)
Samantha L. Deal grad student Baylor College of Medicine (Neurotree)
Shelley B. Gibson grad student Baylor College of Medicine (Neurotree)
Harim Delgado-Seo grad student 2022- Baylor College of Medicine (FlyTree)
J. Michael Harnish grad student 2021 Baylor College of Medicine (Neurotree)
Jose L. Salazar grad student 2021 Baylor College of Medicine (Neurotree)
Jung Wan Mok post-doc 2021- Baylor College of Medicine (FlyTree)
Hirokazu Hashimoto post-doc 2022- Baylor College of Medicine (FlyTree)
Mikiko Oka post-doc 2022- Baylor College of Medicine (Neurotree)
Rei Yasuda post-doc 2022- (FlyTree)
Sheng-An Yang post-doc 2022 Baylor College of Medicine (Neurotree)
BETA: Related publications

Publications

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Dutta D, Kanca O, Shridharan RV, et al. (2024) Loss of the endoplasmic reticulum protein Tmem208 affects cell polarity, development, and viability. Proceedings of the National Academy of Sciences of the United States of America. 121: e2322582121
Ma M, Zheng Y, Lu S, et al. (2024) variants in are associated with hearing impairment, ocular pathology, and cardiac defects. Medrxiv : the Preprint Server For Health Sciences
Link N, Harnish JM, Hull B, et al. (2024) A Zika virus protein expression screen in Drosophila to investigate targeted host pathways during development. Disease Models & Mechanisms
Pan X, Alvarez AN, Ma M, et al. (2023) Allelic strengths of encephalopathy-associated variants correlate between in vivo and in vitro assays. Elife. 12
Nil Z, Deshwar AR, Huang Y, et al. (2023) Rare de novo gain-of-function missense variants in DOT1L are associated with developmental delay and congenital anomalies. American Journal of Human Genetics
Pan X, Alvarez AN, Ma M, et al. (2023) Allelic strengths of encephalopathy-associated variants correlate between and assays. Medrxiv : the Preprint Server For Health Sciences
Yamamoto S, Kanca O, Wangler MF, et al. (2023) Integrating non-mammalian model organisms in the diagnosis of rare genetic diseases in humans. Nature Reviews. Genetics
Guichard A, Lu S, Kanca O, et al. (2023) A comprehensive Drosophila resource to identify key functional interactions between SARS-CoV-2 factors and host proteins. Cell Reports. 42: 112842
Jangam SV, Briere LC, Jay KL, et al. (2023) A de novo missense variant in EZH1 associated with developmental delay exhibits functional deficits in Drosophila melanogaster. Genetics
Link N, Harnish JM, Hull B, et al. (2023) A Zika virus protein expression screen in to investigate targeted host pathways during development. Biorxiv : the Preprint Server For Biology
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