2020 - Fellow of the American Association for the Advancement of Science (AAAS)
2015 - Fellow of the American Academy of Arts and Sciences
2011 - Member of the National Academy of Sciences
Stephen T. Warren mainly focuses on Fragile X syndrome, Genetics, FMR1, Molecular biology and Messenger RNA. His Fragile X syndrome research integrates issues from Synaptic plasticity, DNA methylation, Polysome, Translation and Neuroscience. Stephen T. Warren studies Fragile X-associated tremor/ataxia syndrome which is a part of FMR1.
He has researched Fragile X-associated tremor/ataxia syndrome in several fields, including Sherman paradox and Fragile X Tremor/Ataxia Syndrome. His work deals with themes such as Gene expression, HDAC4, Exon, RNA-binding protein and CpG site, which intersect with Molecular biology. The various areas that Stephen T. Warren examines in his Messenger RNA study include RNA and microRNA.
His scientific interests lie mostly in Genetics, Fragile X syndrome, Molecular biology, FMR1 and Gene. His study in Allele, X chromosome, Trinucleotide repeat expansion, Chromosomal fragile site and Locus falls within the category of Genetics. His biological study spans a wide range of topics, including Neuroscience, Metabotropic glutamate receptor, Phenotype and Messenger RNA, RNA-binding protein.
His work carried out in the field of Messenger RNA brings together such families of science as RNA and Polysome. As a part of the same scientific study, he usually deals with the Molecular biology, concentrating on Methylation and frequently concerns with CpG site. His study in FMR1 focuses on Fragile X-associated tremor/ataxia syndrome in particular.
The scientist’s investigation covers issues in Genetics, Fragile X syndrome, Gene, FMR1 and DNA methylation. His Genetics study frequently involves adjacent topics like Schizophrenia. The study incorporates disciplines such as DNA damage, Trinucleotide repeat expansion, Mutation, RNA and Intellectual disability in addition to Fragile X syndrome.
The Gene study combines topics in areas such as Disease and Bioinformatics. His research in FMR1 intersects with topics in Missense mutation, Metabotropic glutamate receptor, Molecular biology, Untranslated region and Neuroscience. His research in DNA methylation tackles topics such as X chromosome which are related to areas like X-linked intellectual disability, Intellectual development, Gene expression profiling, Chromosomal fragile site and Cas9.
His main research concerns Genetics, Fragile X syndrome, FMR1, Gene and DNA methylation. His Genetics research incorporates themes from Odds ratio and Disease. His Fragile X syndrome research incorporates elements of Trinucleotide repeat expansion, Mutation, Chromatin, Gene silencing and Gene product.
His FMR1 research is multidisciplinary, incorporating elements of Missense mutation, Metabotropic glutamate receptor, Psychiatry, Molecular biology and Neuroscience. His Molecular biology research includes themes of Autism spectrum disorder, Intellectual disability and Chromosome abnormality. Stephen T. Warren usually deals with DNA methylation and limits it to topics linked to Epigenetics and CpG site, Human genome, X chromosome, Reprogramming and 5-Hydroxymethylcytosine.
Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome
Annemiske J.M.H. Verkerk;Maura Pieretti;James S. Sutcliffe;Ying-Hui Fu.
Variation of the CGG repeat at the fragile X site results in genetic instability: resolution of the Sherman paradox.
Ying-Hui Fu;Derek P.A. Kuhl;Antonio Pizzuti;Maura Pieretti.
The mGluR theory of fragile X mental retardation
Mark F Bear;Kimberly M Huber;Stephen T Warren.
Trends in Neurosciences (2004)
Absence of expression of the FMR-1 gene in fragile X syndrome.
Maura Pieretti;Fuping Zhang;Ying-Hui Fu;Stephen T. Warren.
Altered synaptic plasticity in a mouse model of fragile X mental retardation
Kimberly M. Huber;Kimberly M. Huber;Sean M. Gallagher;Stephen T. Warren;Mark F. Bear.
Proceedings of the National Academy of Sciences of the United States of America (2002)
Microarray Identification of FMRP-Associated Brain mRNAs and Altered mRNA Translational Profiles in Fragile X Syndrome
Victoria Brown;Victoria Brown;Peng Jin;Peng Jin;Stephanie Ceman;Stephanie Ceman;Jennifer C. Darnell.
Fragile X Syndrome: Loss of Local mRNA Regulation Alters Synaptic Development and Function
Gary J. Bassell;Stephen T. Warren.
Mapping of DNA instability at the fragile X to a trinucleotide repeat sequence p(CCG)n.
EJ Kremer;M Pritchard;M Lynch;S Yu.
Fragile X Mental Retardation Protein Targets G Quartet mRNAs Important for Neuronal Function
Jennifer C. Darnell;Kirk B. Jensen;Peng Jin;Victoria Brown.
Fragile X genotype characterized by an unstable region of DNA
S. Yu;M. Pritchard;E. Kremer;M. Lynch.
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