Stephen T. Warren
Affiliations: | Emory University School of Medicine, Atlanta, GA, United States |
Area:
human geneticsGoogle:
"Stephen Warren"Mean distance: (not calculated yet)
Parents
Sign in to add mentor| James E. Trosko | grad student | Michigan State (Cell Biology Tree) | |
| Richard L. Davidson | post-doc | UIC College of Medicine |
Children
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Publications
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| Purcell RH, Sefik E, Werner E, et al. (2023) Cross-species analysis identifies mitochondrial dysregulation as a functional consequence of the schizophrenia-associated 3q29 deletion. Science Advances. 9: eadh0558 |
| Purcell RH, Sefik E, Werner E, et al. (2023) Cross-species transcriptomic analysis identifies mitochondrial dysregulation as a functional consequence of the schizophrenia-associated 3q29 deletion. Biorxiv : the Preprint Server For Biology |
| Kozlova A, Zhang S, Kotlar AV, et al. (2022) Loss of function of OTUD7A in the schizophrenia- associated 15q13.3 deletion impairs synapse development and function in human neurons. American Journal of Human Genetics. 109: 1500-1519 |
| Albizua I, Charen K, Shubeck L, et al. (2022) Descriptive analysis of seizures and comorbidities associated with fragile X syndrome. Molecular Genetics & Genomic Medicine. e2001 |
| Kong HE, Lim J, Linsalata A, et al. (2022) Identification of as a genetic modifier of fragile X-associated tremor/ataxia syndrome. Proceedings of the National Academy of Sciences of the United States of America. 119: e2118124119 |
| Pollak RM, Purcell RH, Rutkowski TP, et al. (2022) Metabolic effects of the schizophrenia-associated 3q29 deletion. Translational Psychiatry. 12: 66 |
| Kang Y, Zhou Y, Li Y, et al. (2021) A human forebrain organoid model of fragile X syndrome exhibits altered neurogenesis and highlights new treatment strategies. Nature Neuroscience |
| Trevino CE, Rounds JC, Charen K, et al. (2021) Identifying susceptibility genes for primary ovarian insufficiency on the high-risk genetic background of a fragile X premutation. Fertility and Sterility |
| Raj N, McEachin ZT, Harousseau W, et al. (2021) Cell-type-specific profiling of human cellular models of fragile X syndrome reveal PI3K-dependent defects in translation and neurogenesis. Cell Reports. 35: 108991 |
| Cleynen I, Engchuan W, Hestand MS, et al. (2020) Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion. Molecular Psychiatry |