World's Best Scientists 2026 revealed!
Stephen T. Warren

Stephen T. Warren

D-Index & Metrics

Genetics

D-Index
101
Citations
51432
World Ranking
716
National Ranking
364

Medicine

D-Index
101
Citations
51469
World Ranking
7828
National Ranking
4079

Research.com Recognitions

  • 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

Overview

Stephen T. Warren was affiliated with Emory University in the United States. Their research primarily focused on biochemistry, genetics, and molecular biology, with a significant emphasis on genetics and neurodevelopmental disorders. They contributed to several subfields including genetics, molecular biology, cognitive neuroscience, plant science, and cell biology.

The scientist's work covered a range of topics such as genetics and neurodevelopmental disorders, congenital heart defects research, genomic variations and chromosomal abnormalities, autism spectrum disorder research, epigenetics and DNA methylation, genetic associations and epidemiology, and chromosomal and genetic variations.

Frequent coauthors included Michael E. Zwick, Jennifer G. Mullé, Gary J. Bassell, David J. Cutler, and Michael P. Epstein.

Stephen T. Warren's publications were often found in the following venues:

  • bioRxiv (Cold Spring Harbor Laboratory)
  • UNC Libraries
  • Translational Psychiatry
  • Faculty Opinions - Post-Publication Peer Review of the Biomedical Literature
  • Nature Neuroscience

Notable recent papers by Stephen T. Warren included:

  • A human forebrain organoid model of fragile X syndrome exhibits altered neurogenesis and highlights new treatment strategies, 2021, Nature Neuroscience
  • Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion, 2020, Molecular Psychiatry
  • Cell-type-specific profiling of human cellular models of fragile X syndrome reveal PI3K-dependent defects in translation and neurogenesis, 2021, Cell Reports
  • Deep phenotyping in 3q29 deletion syndrome: recommendations for clinical care, 2021, Genetics in Medicine
  • A normative chart for cognitive development in a genetically selected population, 2021, Neuropsychopharmacology

Throughout their career, Stephen T. Warren received several honors including:

  • Fellow of the American Association for the Advancement of Science (AAAS), 2020
  • Fellow of the American Academy of Arts and Sciences, 2015
  • Member of the National Academy of Sciences, 2011

Best Publications

  • 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

  • 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

  • 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

  • FMR1 protein: conserved RNP family domains and selective RNA binding

    Claude T. Ashley;Keith D. Wilkinson;Daniel Reines;Stephen T. Warren

  • DNA methylation represses FMR-1 transcription in fragile X syndrome

    Sutcliffe Js;Nelson Dl;Zhang F;Pieretti M

  • Biochemical and genetic interaction between the fragile X mental retardation protein and the microRNA pathway

    Peng Jin;Daniela C Zarnescu;Stephanie Ceman;Stephanie Ceman;Mika Nakamoto

  • A mutation in human CMP-sialic acid hydroxylase occurred after the Homo-Pan divergence

    Hsun Hua Chou;Hiromu Takematsu;Sandra Diaz;Jane Iber

  • Molecular Mechanisms of Fragile X Syndrome: A Twenty-Year Perspective

    Michael R. Santoro;Steven M. Bray;Stephen T. Warren

  • Fragile X Mental Retardation Protein: Nucleocytoplasmic Shuttling and Association with Somatodendritic Ribosomes

    Yue Feng;Claire-Anne Gutekunst;Derek E. Eberhart;Hong Yi

  • FMRP Associates with Polyribosomes as an mRNP, and the I304N Mutation of Severe Fragile X Syndrome Abolishes This Association

    Yue Feng;Devin Absher;Derek E Eberhart;Victoria Brown

  • Reduced FMRP and increased FMR1 transcription is proportionally associated with CGG repeat number in intermediate-length and premutation carriers

    Aileen Kenneson;Fuping Zhang;Curt H. Hagedorn;Stephen T. Warren

  • A decade of molecular studies of fragile X syndrome.

    William T. O'Donnell;Stephen T. Warren

  • TRINUCLEOTIDE REPEAT EXPANSION AND HUMAN DISEASE

    Claude T. Ashley;Stephen T. Warren

Frequent Co-Authors

David L. Nelson
David L. Nelson Baylor College of Medicine
Peng Jin
Peng Jin Emory University
Gary J. Bassell
Gary J. Bassell Emory University
Michael P. Epstein
Michael P. Epstein Emory University
James S. Sutcliffe
James S. Sutcliffe Vanderbilt University
Stephanie L. Sherman
Stephanie L. Sherman Emory University
Ben A. Oostra
Ben A. Oostra Erasmus University Rotterdam
Beverly S. Emanuel
Beverly S. Emanuel Children's Hospital of Philadelphia
David J. Cutler
David J. Cutler Emory University

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