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Michael Wangler, MD

Affiliations: 
Genetics Baylor College of Medicine, Houston, TX 
Area:
Peroxisomes
Google:
"Wangler, Michael"
Bio:

postdoc in the Bellen lab
Assisatant Professor, Dept. of Molecular and Human Genetics, BCM

Cross-listing: Neurotree - GenetiTree

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Parents

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Hugo J. Bellen post-doc Baylor College of Medicine

Children

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Jonathan Andrews post-doc Baylor College of Medicine (Neurotree)

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Publications

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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
Tepe B, Macke EL, Niceta M, et al. (2023) Bi-allelic variants in INTS11 are associated with a complex neurological disorder. American Journal of Human Genetics
Andrews JC, Mok JW, Kanca O, et al. (2023) De Novo Variants in MRTFB have gain of function activity in Drosophila and are associated with a novel neurodevelopmental phenotype with dysmorphic features. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 100833
Jangam S, Briere LC, Jay K, et al. (2023) A missense variant in associated with developmental delay exhibits functional deficits in . Medrxiv : the Preprint Server For Health Sciences
Huang Y, Lemire G, Briere LC, et al. (2022) The recurrent de novo c.2011C>T missense variant in MTSS2 causes syndromic intellectual disability. American Journal of Human Genetics. 109: 2092
Lu S, Ma M, Mao X, et al. (2022) De novo variants in FRMD5 are associated with developmental delay, intellectual disability, ataxia, and abnormalities of eye movement. American Journal of Human Genetics. 109: 1932-1943
Gofin Y, Zhao X, Gerard A, et al. (2022) Evidence for an association between Coffin-Siris syndrome and congenital diaphragmatic hernia. American Journal of Medical Genetics. Part A
Barish S, Senturk M, Schoch K, et al. (2022) The microRNA processor DROSHA is a candidate gene for a severe progressive neurological disorder. Human Molecular Genetics
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