Michael E. Talkowski, Ph.D.
Affiliations: | 2008 | University of Pittsburgh, Pittsburgh, PA, United States |
Area:
Genetics, Epidemiology, Neuroscience BiologyGoogle:
"Michael Talkowski"Parents
Sign in to add mentor| Vishwajit L. Nimgaonkar | grad student | 2008 | University of Pittsburgh | |
| (The dopaminergic network and genetic susceptibility to schizophrenia.) | ||||
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Publications
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| Ansari M, Faour KNW, Shimamura A, et al. (2024) Heterozygous loss-of-function SMC3 variants are associated with variable growth and developmental features. Hgg Advances. 100273 |
| Ansari M, Faour KNW, Shimamura A, et al. (2023) Heterozygous loss-of-function variants are associated with variable and incompletely penetrant growth and developmental features. Medrxiv : the Preprint Server For Health Sciences |
| Liao C, Moyses-Oliveira M, De Esch CEF, et al. (2023) Convergent coexpression of autism-associated genes suggests some novel risk genes may not be detectable in large-scale genetic studies. Cell Genomics. 3: 100277 |
| Weiner DJ, Ling E, Erdin S, et al. (2022) Statistical and functional convergence of common and rare genetic influences on autism at chromosome 16p. Nature Genetics |
| Fu JM, Satterstrom FK, Peng M, et al. (2022) Rare coding variation provides insight into the genetic architecture and phenotypic context of autism. Nature Genetics |
| Chen H, Victor AK, Klein J, et al. (2020) Loss of MAGEL2 in Prader-Willi syndrome leads to decreased secretory granule and neuropeptide production. Jci Insight. 5 |
| Moyses-Oliveira M, Yadav R, Erdin S, et al. (2020) New gene discoveries highlight functional convergence in autism and related neurodevelopmental disorders. Current Opinion in Genetics & Development. 65: 195-206 |
| Hu S, Vich Vila A, Gacesa R, et al. (2020) Whole exome sequencing analyses reveal gene-microbiota interactions in the context of IBD. Gut |
| Han L, Zhao X, Benton ML, et al. (2020) Functional annotation of rare structural variation in the human brain. Nature Communications. 11: 2990 |
| Seabra CM, Aneichyk T, Erdin S, et al. (2020) Transcriptional consequences of MBD5 disruption in mouse brain and CRISPR-derived neurons. Molecular Autism. 11: 45 |