S. T. Warren

Loss-of-function of OTUD7A in the schizophrenia-associated 15q13.3 deletion impairs synapse development and function in human neurons

Alex V. Kotlar, D. Cutler, J. Duan, 2022, bioRxiv.

Identification of PSMB5 as a genetic modifier of fragile X–associated tremor/ataxia syndrome

Peter K. Todd, D. Cutler, P. Jin, 2022, Proceedings of the National Academy of Sciences of the United States of America.

PEMapper and PECaller provide a simplified approach to whole-genome sequencing

Viren Patel, Pankaj Chopra, H. Richard Johnston, 2017, Proceedings of the National Academy of Sciences.

Genome‐wide association study of schizophrenia in Ashkenazi Jews

Vladimir Vacic, Ingo Ruczinski, Mehdi Pirooznia, 2015, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Genetic determinants of normal variation in coagulation factor (F) IX levels: genome‐wide scan and examination of the FIX structural gene

L. Almasy, A. Buil, M. Lathrop, 2006, Journal of thrombosis and haemostasis : JTH.

Identification of novel FMR1 variants by massively parallel sequencing in developmentally delayed males

D. Cutler, S. Warren, M. Zwick, 2010, American journal of medical genetics. Part A.

Unraveling the genetic architecture of copy number variants associated with schizophrenia and other neuropsychiatric disorders

G. Gafford, J. Mulle, D. Weinshenker, 2017, Journal of neuroscience research.

Mosaic FMR1 deletion causes fragile X syndrome and can lead to molecular misdiagnosis: A case report and review of the literature

S. Warren, W. Kaufmann, M. Ikeda, 2008, American journal of medical genetics. Part A.

Modulating huntingtin half‐life alters polyglutamine‐dependent aggregate formation and cell toxicity

K. Wilkinson, M. D. Kaytor, S. T. Warren, 2004, Journal of neurochemistry.

Cross-species transcriptomic analysis identifies mitochondrial dysregulation as a functional consequence of the schizophrenia-associated 3q29 deletion

S. Sloan, P. Chopra, V. Faundez, 2023, bioRxiv.

Deep phenotyping in 3q29 deletion syndrome: recommendations for clinical care

Steven E. Sloan, E. Walker, P. Dawson, 2021, Genetics in Medicine.

Cross-species transcriptomic analysis identifies mitochondrial dysregulation as a functional consequence of the schizophrenia-associated 3q29 deletion

S. Sloan, P. Chopra, B. Firestein, 2023, bioRxiv.

Descriptive analysis of seizures and comorbidities associated with fragile X syndrome

S. Warren, J. Sweeney, W. Kaufmann, 2022, Molecular genetics & genomic medicine.