Stephen T. Warren

Biochemistry, Genetics and Molecular Biology · Life Sciences

86h-index35.6kcitations267works0.02yr avg
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Research Topics

Genetics and Neurodevelopmental Disorders(152), Autism Spectrum Disorder Research(57), Genomic variations and chromosomal abnormalities(51), RNA modifications and cancer(45), Congenital heart defects research(38)

Publications266 total

Review by Stephen Warren
2025Open Access
Cross-species analysis identifies mitochondrial dysregulation as a functional consequence of the schizophrenia-associated 3q29 deletion
Science Advances·2023· 19 citedOpen Access
Cross-species transcriptomic analysis identifies mitochondrial dysregulation as a functional consequence of the schizophrenia-associated 3q29 deletion
2023· 2 citedOpen Access
Fragile X Syndrome Patient–Derived Neurons Developing in the Mouse Brain Show FMR1-Dependent Phenotypes
Biological Psychiatry·2022· 2 cited
Loss of function of OTUD7A in the schizophrenia- associated 15q13.3 deletion impairs synapse development and function in human neurons
The American Journal of Human Genetics·2022· 20 citedOpen Access
Descriptive analysis of seizures and comorbidities associated with fragile X syndrome
Molecular Genetics & Genomic Medicine·2022· 8 citedOpen Access
Identification of <i>PSMB5</i> as a genetic modifier of fragile X–associated tremor/ataxia syndrome
Proceedings of the National Academy of Sciences·2022· 12 citedOpen Access
Metabolic effects of the schizophrenia-associated 3q29 deletion
Translational Psychiatry·2022· 7 citedOpen Access
Loss-of-function of <i>OTUD7A</i> in the schizophrenia-associated 15q13.3 deletion impairs synapse development and function in human neurons
2022Open Access
Fragile X syndrome patient-derived neurons developing in the mouse brain show <i>FMR1</i> -dependent phenotypes
2021Open Access
57. MODELING THE LOSS-OF-FUNCTION MUTATION OF OTUD7A WITHIN THE SCHIZOPHRENIA-ASSOCIATED 15Q13.3 MICRODELETION IN HUMAN NEURONS
European Neuropsychopharmacology·2021
A human forebrain organoid model of fragile X syndrome exhibits altered neurogenesis and highlights new treatment strategies
Nature Neuroscience·2021· 162 citedOpen Access
Convergent and distributed effects of the 3q29 deletion on the human neural transcriptome
Translational Psychiatry·2021· 16 citedOpen Access
Identifying susceptibility genes for primary ovarian insufficiency on the high-risk genetic background of a fragile X premutation
Fertility and Sterility·2021· 6 citedOpen Access
Faculty Opinions recommendation of Taking an antiracist posture in scientific publications in human genetics and genomics.
Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature·2021
Cell-type-specific profiling of human cellular models of fragile X syndrome reveal PI3K-dependent defects in translation and neurogenesis
Cell Reports·2021· 55 citedOpen Access
A normative chart for cognitive development in a genetically selected population
Neuropsychopharmacology·2021· 24 citedOpen Access
Deep phenotyping in 3q29 deletion syndrome: recommendations for clinical care
Genetics in Medicine·2021· 46 citedOpen Access
Survey of the Fragile X Syndrome CGG Repeat and the Short-Tandem-Repeat and Single-Nucleotide-Polymorphism Haplotypes in an African American Population
UNC Libraries·2020Open Access
Reciprocal Duplication of the Williams-Beuren Syndrome Deletion on Chromosome 7q11.23 Is Associated with Schizophrenia
UNC Libraries·2020Open Access
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Frequent Co-authors

Peng Jin(8), David L. Nelson(7), Gary J. Bassell(7), Stephanie Ceman(6), Yue Feng(6), Fuping Zhang(5), M. Nakamoto(5), Jennifer G. Mullé(5), James S. Sutcliffe(4), William T. O'Donnell(4), Claude T. Ashley(4), Vijayalaxmi Nalavadi(4), Ben A. Oostra(3), Mark F. Bear(3), Victoria Brown(3), Daniel Reines(3), Daniela C. Zarnescu(3), Derek E. Eberhart(3), Alastair J. Martin(3), Bradford Coffee(3)