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S. Warren · SciRah

Researcher profile · Semantic Scholar

S. Warren

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S. Warren — researcher profile on SciRah

h-index: 83
Works: 205
Citations: 32K

Most-cited papers

Fragile X Syndrome: Loss of Local mRNA Regulation Alters Synaptic Development and Function
G. Bassell, S. Warren
2008Neuron1,065 citations Open access
Semantic Scholar
Molecular mechanisms of fragile X syndrome: a twenty-year perspective.
Michael R. Santoro, Steven M Bray, S. Warren
2012Annual Review of Pathology539 citations
Semantic Scholar
An evidence-based approach to establish the functional and clinical significance of CNVs in intellectual and developmental disabilities
E. B. Kaminsky, V. Kaul, J. Paschall, D. Church +30 more
2011Genetics in Medicine412 citations Open access
Semantic Scholar
The pathophysiology of fragile x syndrome.
O. Peñagarikano, J. Mulle, S. Warren
2007Annual review of genomics and human genetics (Print)405 citations
Semantic Scholar
Incidence of fragile X syndrome by newborn screening for methylated FMR1 DNA.
Bradford Coffee, K. Keith, Igor Albizua, Tamika Malone +3 more
2009American Journal of Human Genetics392 citations Open access
Semantic Scholar
Age-associated DNA methylation in pediatric populations.
Reid S. Alisch, B. Barwick, P. Chopra, L. K. Myrick +3 more
2012Genome Research372 citations Open access
Semantic Scholar
Reversible inhibition of PSD-95 mRNA translation by miR-125a, FMRP phosphorylation and mGluR signaling
Ravi S. Muddashetty, Vijayalaxmi C. Nalavadi, C. Gross, Xiaodi Yao +4 more
2011Molecules and Cells369 citations Open access
Semantic Scholar
Deletion 17q12 is a recurrent copy number variant that confers high risk of autism and schizophrenia.
D. Moreno-De-Luca, J. Mulle, E. B. Kaminsky, Stephan J Sanders +31 more
2010American Journal of Human Genetics341 citations Open access
Semantic Scholar
Relative Burden of Large CNVs on a Range of Neurodevelopmental Phenotypes
S. Girirajan, Z. Brkanac, Bradley P. Coe, C. Baker +12 more
2011PLoS Genetics327 citations Open access
Semantic Scholar
Local RNA Translation at the Synapse and in Disease
L. Liu‐Yesucevitz, G. Bassell, A. Gitler, A. Hart +4 more
2011Journal of Neuroscience315 citations Open access
Semantic Scholar
Pur α binds to rCGG repeats and modulates repeat-mediated neurodegeneration in a Drosophila model of Fragile X Tremor/Ataxia Syndrome
P. Jin, R. Duan, A. Qurashi, Yun-Long Qin +5 more
2007297 citations Open access
Semantic Scholar
Genome-wide expression profiling of lymphoblastoid cell lines distinguishes different forms of autism and reveals shared pathways.
Y. Nishimura, C. Martin, A. Vázquez-López, Sarah J. Spence +7 more
2007Human Molecular Genetics280 citations
Semantic Scholar
Identification of small molecules rescuing fragile X syndrome phenotypes in Drosophila.
Shuang Chang, Steven M Bray, Zi-Gang Li, D. Zarnescu +3 more
2008Nature Chemical Biology273 citations
Semantic Scholar
Reversal of Disease-Related Pathologies in the Fragile X Mouse Model by Selective Activation of GABAB Receptors with Arbaclofen
Chris Henderson, Lasani S. Wijetunge, M. Kinoshita, Matthew J. Shumway +12 more
2012Science Translational Medicine256 citations Open access
Semantic Scholar
Fragile X mental retardation protein deficiency leads to excessive mGluR5-dependent internalization of AMPA receptors
Mika Nakamoto, Vijayalaxmi C. Nalavadi, Michael P. Epstein, U. Narayanan +2 more
2007Proceedings of the National Academy of Sciences of the United States of America250 citations Open access
Semantic Scholar
FMRP Phosphorylation Reveals an Immediate-Early Signaling Pathway Triggered by Group I mGluR and Mediated by PP2A
U. Narayanan, Vijayalaxmi C. Nalavadi, Mika Nakamoto, D. Pallas +3 more
2007Journal of Neuroscience243 citations Open access
Semantic Scholar
Excess PI3K subunit synthesis and activity as a novel therapeutic target in Fragile X Syndrome
C. Gross, Mika Nakamoto, Xiaodi Yao, Chi Chan +4 more
2010Journal of Neuroscience236 citations Open access
Semantic Scholar
Microdeletions of 3q29 confer high risk for schizophrenia.
J. Mulle, Anne F. Dodd, J. McGrath, P. Wolyniec +9 more
2010American Journal of Human Genetics229 citations Open access
Semantic Scholar
S6K1 Phosphorylates and Regulates Fragile X Mental Retardation Protein (FMRP) with the Neuronal Protein Synthesis-dependent Mammalian Target of Rapamycin (mTOR) Signaling Cascade*
U. Narayanan, Vijayalaxmi C. Nalavadi, Mika Nakamoto, G. Thomas +3 more
2008Journal of Biological Chemistry220 citations Open access
Semantic Scholar
The Unstable Repeats - Three Evolving Faces of Neurological Disease
D. Nelson, H. Orr, S. Warren
2013Neuron200 citations Open access
Semantic Scholar
Polyglutamine domain modulates the TBP-TFIIB interaction: implications for its normal function and neurodegeneration
M. Friedman, Anjali G Shah, Zhi-Hui Fang, Elizabeth G Ward +3 more
2007Nature Neuroscience172 citations
Semantic Scholar
Genome-wide DNA hydroxymethylation changes are associated with neurodevelopmental genes in the developing human cerebellum.
Tao Wang, Q. Pan, Li Lin, Keith E. Szulwach +7 more
2012Human Molecular Genetics167 citations Open access
Semantic Scholar
A chromatin-dependent role of the fragile X mental retardation protein FMRP in the DNA damage response
Roman Alpatov, Bluma J. Lesch, Mika Nakamoto-Kinoshita, A. Blanco +16 more
2014Cell159 citations Open access
Semantic Scholar
A Genome-Wide Scan of Ashkenazi Jewish Crohn's Disease Suggests Novel Susceptibility Loci
E. Kenny, I. Pe'er, A. Karban, L. Ozelius +39 more
2012PLoS Genetics155 citations Open access
Semantic Scholar
Transcription, translation and fragile X syndrome.
Kathryn B. Garber, Karen T. Smith, D. Reines, S. Warren
2006Current Opinion in Genetics and Development149 citations
Semantic Scholar
Replication stress induces genome-wide copy number changes in human cells that resemble polymorphic and pathogenic variants.
Martin F. Arlt, J. Mulle, Valerie Schaibley, Ryan L. Ragland +3 more
2009American Journal of Human Genetics148 citations Open access
Semantic Scholar
A human forebrain organoid model of fragile X syndrome exhibits altered neurogenesis and highlights new treatment strategies
Yunhee Kang, Ying Zhou, Yu-Jing Li, Yanfei Han +18 more
2021Nature Neuroscience146 citations Open access
Semantic Scholar
Independent role for presynaptic FMRP revealed by an FMR1 missense mutation associated with intellectual disability and seizures
L. K. Myrick, Pan-Yue Deng, H. Hashimoto, Young Mi Oh +9 more
2015Proceedings of the National Academy of Sciences of the United States of America131 citations Open access
Semantic Scholar
Replication stress induces tumor-like microdeletions in FHIT/FRA3B
Sandra G. Durkin, Ryan L. Ragland, Martin F. Arlt, J. Mulle +2 more
2008Proceedings of the National Academy of Sciences of the United States of America128 citations Open access
Semantic Scholar
Signatures of founder effects, admixture, and selection in the Ashkenazi Jewish population
Steven M Bray, J. Mulle, Anne F. Dodd, A. Pulver +2 more
2010Proceedings of the National Academy of Sciences of the United States of America118 citations Open access
Semantic Scholar
Reactivation of FMR1 by CRISPR/Cas9-Mediated Deletion of the Expanded CGG-Repeat of the Fragile X Chromosome
Nina Xie, He Gong, Joshua A. Suhl, P. Chopra +2 more
2016PLoS ONE117 citations Open access
Semantic Scholar
New Perspectives on the Biology of Fragile X Syndrome
Tao Wang, Steven M Bray, S. Warren
2012Current Opinion in Genetics and Development116 citations Open access
Semantic Scholar
Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion
I. Cleynen, W. Engchuan, M. Hestand, Tracy Heung +120 more
2020Molecular Psychiatry113 citations Open access
Semantic Scholar
Human FMRP contains an integral tandem Agenet (Tudor) and KH motif in the amino terminal domain.
L. K. Myrick, H. Hashimoto, Xiaodong Cheng, S. Warren
2015Human Molecular Genetics110 citations Open access
Semantic Scholar
Hemizygous mutations in SNAP29 unmask autosomal recessive conditions and contribute to atypical findings in patients with 22q11.2DS
D. McDonald-McGinn, S. Fahiminiya, T. Revil, B. Nowakowska +12 more
2012Journal of Medical Genetics109 citations Open access
Semantic Scholar
A sequence variation scan of the coagulation factor VIII (FVIII) structural gene and associations with plasma FVIII activity levels.
K. Viel, D. Machiah, Diane M. Warren, M. Khachidze +13 more
2007Blood101 citations Open access
Semantic Scholar
Fragile X syndrome due to a missense mutation
L. K. Myrick, Mika Nakamoto-Kinoshita, N. Lindor, S. Kirmani +2 more
2014European Journal of Human Genetics96 citations Open access
Semantic Scholar
Subtelomeric hotspots of aberrant 5-hydroxymethylcytosine-mediated epigenetic modifications during reprogramming to pluripotency
Tao Wang, Hao Wu, Yu-Jing Li, Keith E. Szulwach +17 more
2013Nature Cell Biology90 citations Open access
Semantic Scholar
Case-control meta-analysis of blood DNA methylation and autism spectrum disorder
Shan V. Andrews, Brooke K. Sheppard, G. Windham, L. Schieve +9 more
2018Molecular Autism89 citations Open access
Semantic Scholar
Analysis of FMRP mRNA target datasets reveals highly associated mRNAs mediated by G-quadruplex structures formed via clustered WGGA sequences.
Joshua A. Suhl, P. Chopra, Bart R. Anderson, G. Bassell +1 more
2014Human Molecular Genetics78 citations Open access
Semantic Scholar
Reciprocal duplication of the Williams-Beuren syndrome deletion on chromosome 7q11.23 is associated with schizophrenia
J. Mulle, A. Pulver, J. McGrath, P. Wolyniec +26 more
2013Biological Psychiatry76 citations Open access
Semantic Scholar
Identification of consensus binding sites clarifies FMRP binding determinants
Bart R. Anderson, P. Chopra, Joshua A. Suhl, S. Warren +1 more
2016Nucleic Acids Research55 citations Open access
Semantic Scholar
Argonaute2 Is Essential for Mammalian Gastrulation and Proper Mesoderm Formation
Reid S. Alisch, P. Jin, Michael P. Epstein, T. Caspary +1 more
2007PLoS Genetics54 citations Open access
Semantic Scholar
Cell-type-specific profiling of human cellular models of fragile X syndrome reveal PI3K-dependent defects in translation and neurogenesis
N. Raj, Zachary T. McEachin, William Harousseau, Ying Zhou +16 more
2021Cell Reports50 citations Open access
Semantic Scholar
Voltage-Independent SK-Channel Dysfunction Causes Neuronal Hyperexcitability in the Hippocampus of Fmr1 Knock-Out Mice
Pan-Yue Deng, Dan Carlin, Young Mi Oh, L. K. Myrick +3 more
2018Journal of Neuroscience49 citations Open access
Semantic Scholar
Genome-wide analysis validates aberrant methylation in fragile X syndrome is specific to the FMR1 locus
Reid S. Alisch, Tao Wang, P. Chopra, J. Visootsak +2 more
2013BMC Medical Genetics49 citations Open access
Semantic Scholar
Behavioral changes and growth deficits in a CRISPR engineered mouse model of the schizophrenia-associated 3q29 deletion
Timothy P. Rutkowski, Ryan H. Purcell, R. Pollak, Stephanie M. Grewenow +10 more
2018bioRxiv47 citations Open access
Semantic Scholar
Neurogenetics: Advancing the “Next-Generation” of Brain Research
H. Zoghbi, S. Warren
2010Neuron47 citations Open access
Semantic Scholar
Single-Nucleotide Mutations in FMR1 Reveal Novel Functions and Regulatory Mechanisms of the Fragile X Syndrome Protein FMRP
Joshua A. Suhl, S. Warren
2015Journal of Experimental Neuroscience44 citations Open access
Semantic Scholar
Partial FMRP expression is sufficient to normalize neuronal hyperactivity in Fragile X neurons
J. Graef, Hao Wu, Carrie Ng, Chicheng Sun +7 more
2019bioRxiv36 citations Open access
Semantic Scholar

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