Publications by authors named "Stephen T Warren"

90Publications

Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion.

Authors:
Isabelle Cleynen Worrawat Engchuan Matthew S Hestand Tracy Heung Aaron M Holleman H Richard Johnston Thomas Monfeuga Donna M McDonald-McGinn Raquel E Gur Bernice E Morrow Ann Swillen Jacob A S Vorstman Carrie E Bearden Eva W C Chow Marianne van den Bree Beverly S Emanuel Joris R Vermeesch Stephen T Warren Michael J Owen Pankaj Chopra David J Cutler Richard Duncan Alex V Kotlar Jennifer G Mulle Anna J Voss Michael E Zwick Alexander Diacou Aaron Golden Tingwei Guo Jhih-Rong Lin Tao Wang Zhengdong Zhang Yingjie Zhao Christian Marshall Daniele Merico Andrea Jin Brenna Lilley Harold I Salmons Oanh Tran Peter Holmans Antonio Pardinas James T R Walters Wolfram Demaerel Erik Boot Nancy J Butcher Gregory A Costain Chelsea Lowther Rens Evers Therese A M J van Amelsvoort Esther van Duin Claudia Vingerhoets Jeroen Breckpot Koen Devriendt Elfi Vergaelen Annick Vogels T Blaine Crowley Daniel E McGinn Edward M Moss Robert J Sharkus Marta Unolt Elaine H Zackai Monica E Calkins Robert S Gallagher Ruben C Gur Sunny X Tang Rosemarie Fritsch Claudia Ornstein Gabriela M Repetto Elemi Breetvelt Sasja N Duijff Ania Fiksinski Hayley Moss Maria Niarchou Kieran C Murphy Sarah E Prasad Eileen M Daly Maria Gudbrandsen Clodagh M Murphy Declan G Murphy Antonio Buzzanca Fabio Di Fabio Maria C Digilio Maria Pontillo Bruno Marino Stefano Vicari Karlene Coleman Joseph F Cubells Opal Y Ousley Miri Carmel Doron Gothelf Ehud Mekori-Domachevsky Elena Michaelovsky Ronnie Weinberger Abraham Weizman Leila Kushan Maria Jalbrzikowski Marco Armando Stéphan Eliez Corrado Sandini Maude Schneider Frédérique Sloan Béna Kevin M Antshel Wanda Fremont Wendy R Kates Raoul Belzeaux Tiffany Busa Nicole Philip Linda E Campbell Kathryn L McCabe Stephen R Hooper Kelly Schoch Vandana Shashi Tony J Simon Flora Tassone Celso Arango David Fraguas Sixto García-Miñaúr Jaume Morey-Canyelles Jordi Rosell Damià H Suñer Jasna Raventos-Simic Michael P Epstein Nigel M Williams Anne S Bassett

Mol Psychiatry 2020 Feb 3. Epub 2020 Feb 3.

Clinical Genetics Research Program, Centre for Addiction and Mental Health, Toronto, ON, Canada.

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http://dx.doi.org/10.1038/s41380-020-0654-3DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7396297PMC
February 2020

Analysis of the genomic expression profile in trisomy 18: insight into possible genes involved in the associated phenotypes.

Hum Mol Genet 2020 01;29(2):238-247

Department of Human Genetics, Emory University School of Medicine, Atlanta, 30322, USA.

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http://dx.doi.org/10.1093/hmg/ddz279DOI Listing
January 2020

Reply to Plüss et al.: The strength of PEMapper/PECaller lies in unbiased calling using large sample sizes.

Proc Natl Acad Sci U S A 2017 10 15;114(40):E8323. Epub 2017 Sep 15.

Department of Human Genetics, Emory University School of Medicine, Atlanta, GA 30322;

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http://dx.doi.org/10.1073/pnas.1714535114DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5635938PMC
October 2017

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

Proc Natl Acad Sci U S A 2017 03 21;114(10):E1923-E1932. Epub 2017 Feb 21.

Department of Human Genetics, Emory University School of Medicine, Atlanta, GA 30322;

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http://dx.doi.org/10.1073/pnas.1618065114DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5347547PMC
March 2017

Reactivation of FMR1 by CRISPR/Cas9-Mediated Deletion of the Expanded CGG-Repeat of the Fragile X Chromosome.

PLoS One 2016 21;11(10):e0165499. Epub 2016 Oct 21.

Department of Human Genetics, Emory University School of Medicine, Atlanta, Georgia, United States of America.

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0165499PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5074572PMC
June 2017

Identification of consensus binding sites clarifies FMRP binding determinants.

Nucleic Acids Res 2016 08 4;44(14):6649-59. Epub 2016 Jul 4.

Department of Cell Biology, Emory University School of Medicine, Atlanta, GA, USA Department of Neurology, Emory University School of Medicine, Atlanta, GA 30322, USA

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http://dx.doi.org/10.1093/nar/gkw593DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5001617PMC
August 2016

Single-Nucleotide Mutations in FMR1 Reveal Novel Functions and Regulatory Mechanisms of the Fragile X Syndrome Protein FMRP.

J Exp Neurosci 2015 8;9(Suppl 2):35-41. Epub 2015 Dec 8.

Department of Human Genetics, Emory University School of Medicine, Atlanta, GA, USA.; Department of Biochemistry, Emory University School of Medicine, Atlanta, GA, USA.; Department of Pediatrics, Emory University School of Medicine, Atlanta, GA, USA.

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http://dx.doi.org/10.4137/JEN.S25524DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4720182PMC
January 2016

A 3' untranslated region variant in FMR1 eliminates neuronal activity-dependent translation of FMRP by disrupting binding of the RNA-binding protein HuR.

Proc Natl Acad Sci U S A 2015 Nov 9;112(47):E6553-61. Epub 2015 Nov 9.

Department of Human Genetics, Emory University, Atlanta, GA 30322; Department of Biochemistry, Emory University, Atlanta, GA 30322; Department of Pediatrics, Emory University, Atlanta, GA 30322

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http://dx.doi.org/10.1073/pnas.1514260112DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4664359PMC
November 2015

Genome-wide association study of schizophrenia in Ashkenazi Jews.

Am J Med Genet B Neuropsychiatr Genet 2015 Dec 21;168(8):649-59. Epub 2015 Jul 21.

Department of Psychiatry and Behavioral Sciences, Johns Hopkins University School of Medicine, Baltimore, Maryland.

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http://dx.doi.org/10.1002/ajmg.b.32349DOI Listing
December 2015

Human FMRP contains an integral tandem Agenet (Tudor) and KH motif in the amino terminal domain.

Hum Mol Genet 2015 Mar 20;24(6):1733-40. Epub 2014 Nov 20.

Department of Human Genetics, Department of Biochemistry Department of Pediatrics, Emory University School of Medicine, Atlanta, GA 30322, USA

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http://dx.doi.org/10.1093/hmg/ddu586DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4381759PMC
March 2015

Analysis of FMRP mRNA target datasets reveals highly associated mRNAs mediated by G-quadruplex structures formed via clustered WGGA sequences.

Hum Mol Genet 2014 Oct 29;23(20):5479-91. Epub 2014 May 29.

Department of Human Genetics, Departments of Biochemistry and Pediatrics, Emory University School of Medicine, Atlanta, GA, USA

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http://dx.doi.org/10.1093/hmg/ddu272DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4168832PMC
October 2014

Array-based assay detects genome-wide 5-mC and 5-hmC in the brains of humans, non-human primates, and mice.

BMC Genomics 2014 Feb 13;15:131. Epub 2014 Feb 13.

Department of Psychiatry, University of Wisconsin-Madison, 6001 Research Park Blvd,, Madison, Wisconsin 53719, USA.

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http://dx.doi.org/10.1186/1471-2164-15-131DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3930898PMC
February 2014

Robust regression analysis of copy number variation data based on a univariate score.

PLoS One 2014 7;9(2):e86272. Epub 2014 Feb 7.

Department of Epidemiology, Emory University, Atlanta, Georgia, United States of America.

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0086272PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3917847PMC
May 2015

Fragile X syndrome due to a missense mutation.

Eur J Hum Genet 2014 Oct 22;22(10):1185-9. Epub 2014 Jan 22.

1] Department of Human Genetics, Emory University School of Medicine, Atlanta, GA, USA [2] Department of Biochemistry, Emory University, Atlanta, GA, USA [3] Department of Pediatrics, Emory University, Atlanta, GA, USA.

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https://genetics.emory.edu/documents/Warren%20Publications/M
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http://www.nature.com/doifinder/10.1038/ejhg.2013.311
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http://dx.doi.org/10.1038/ejhg.2013.311DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4169535PMC
October 2014

Toward pluripotency by reprogramming: mechanisms and application.

Protein Cell 2013 Nov;4(11):820-32

Department of Human Genetics, Emory University, Atlanta, GA 30322, USA; Genetics and Molecular Biology Graduate Program, Emory University, Atlanta, GA 30322, USA.

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http://dx.doi.org/10.1007/s13238-013-3074-1DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4875451PMC
November 2013

The unstable repeats--three evolving faces of neurological disease.

Neuron 2013 Mar;77(5):825-43

Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA.

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https://linkinghub.elsevier.com/retrieve/pii/S08966273130018
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http://dx.doi.org/10.1016/j.neuron.2013.02.022DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3608403PMC
March 2013

Genome-wide analysis validates aberrant methylation in fragile X syndrome is specific to the FMR1 locus.

BMC Med Genet 2013 Jan 29;14:18. Epub 2013 Jan 29.

Departments of Human Genetics, Emory University School of Medicine, 615 Michael Street, Atlanta, GA 30322, USA.

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http://bmcmedgenet.biomedcentral.com/articles/10.1186/1471-2
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http://dx.doi.org/10.1186/1471-2350-14-18DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3599197PMC
January 2013

The human genome: a diamond in the rough.

Curr Opin Genet Dev 2012 Jun 18;22(3):189-90. Epub 2012 May 18.

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http://dx.doi.org/10.1016/j.gde.2012.04.005DOI Listing
June 2012

New perspectives on the biology of fragile X syndrome.

Curr Opin Genet Dev 2012 Jun 28;22(3):256-63. Epub 2012 Feb 28.

Genetics and Molecular Biology Graduate Program, Emory University, Atlanta, GA 30322, USA.

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http://dx.doi.org/10.1016/j.gde.2012.02.002DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3653273PMC
June 2012

Genomic tics in tourette syndrome.

Biol Psychiatry 2012 Mar;71(5):390-1

Department of Epidemiology, Rollins School of Public Health, Emory University, Atlanta, Georgia 30322, USA.

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http://dx.doi.org/10.1016/j.biopsych.2011.12.017DOI Listing
March 2012

Age-associated DNA methylation in pediatric populations.

Genome Res 2012 Apr 1;22(4):623-32. Epub 2012 Feb 1.

Department of Human Genetics, Emory University School of Medicine, Atlanta, Georgia 30322, USA.

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http://dx.doi.org/10.1101/gr.125187.111DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3317145PMC
April 2012

Local RNA translation at the synapse and in disease.

J Neurosci 2011 Nov;31(45):16086-93

Department of Pharmacology, Boston University School of Medicine, Boston, Massachusetts 02118, USA.

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http://dx.doi.org/10.1523/JNEUROSCI.4105-11.2011DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3241995PMC
November 2011

Molecular mechanisms of fragile X syndrome: a twenty-year perspective.

Annu Rev Pathol 2012 10;7:219-45. Epub 2011 Oct 10.

Department of Human Genetics, Emory University School of Medicine, Atlanta, Georgia 30322, USA.

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http://dx.doi.org/10.1146/annurev-pathol-011811-132457DOI Listing
April 2013

Neurogenetics: advancing the "next-generation" of brain research.

Neuron 2010 Oct;68(2):165-73

Department of Molecular and Human Genetics, Howard Hughes Medical Institute, Baylor College of Medicine, Houston, TX 77030, USA.

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http://dx.doi.org/10.1016/j.neuron.2010.10.015DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2982747PMC
October 2010

Signatures of founder effects, admixture, and selection in the Ashkenazi Jewish population.

Proc Natl Acad Sci U S A 2010 Sep 26;107(37):16222-7. Epub 2010 Aug 26.

Department of Human Genetics, Emory University School of Medicine, Atlanta, GA 30322, USA.

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http://www.pnas.org/cgi/doi/10.1073/pnas.1004381107
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http://dx.doi.org/10.1073/pnas.1004381107DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2941333PMC
September 2010

Empirical evaluation of oligonucleotide probe selection for DNA microarrays.

PLoS One 2010 Mar 29;5(3):e9921. Epub 2010 Mar 29.

Department of Human Genetics, Emory University School of Medicine, Atlanta, Georgia, United States of America.

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0009921PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2847945PMC
March 2010

Incidence of fragile X syndrome by newborn screening for methylated FMR1 DNA.

Am J Hum Genet 2009 Oct;85(4):503-14

Department of Human Genetics, Emory University School of Medicine, Atlanta, GA 30322, USA.

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http://dx.doi.org/10.1016/j.ajhg.2009.09.007DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2756550PMC
October 2009

Fragile X syndrome: loss of local mRNA regulation alters synaptic development and function.

Neuron 2008 Oct;60(2):201-14

Department of Cell Biology and Neurology, Emory University School of Medicine, Atlanta, GA 30322, USA.

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https://linkinghub.elsevier.com/retrieve/pii/S08966273080084
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http://dx.doi.org/10.1016/j.neuron.2008.10.004DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3691995PMC
October 2008

The epigenetics of fragile X syndrome.

Authors:
Stephen T Warren

Cell Stem Cell 2007 Nov;1(5):488-9

Department of Human Genetics, Emory University School of Medicine, Atlanta, GA 30322, USA.

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http://dx.doi.org/10.1016/j.stem.2007.10.017DOI Listing
November 2007

Neuroscience: fragile dopamine.

Nature 2008 Oct;455(7213):607-8

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http://www.nature.com/doifinder/10.1038/455607a
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http://dx.doi.org/10.1038/455607aDOI Listing
October 2008

Microarray-based mutation detection in the dystrophin gene.

Hum Mutat 2008 Sep;29(9):1091-9

Department of Human Genetics, Emory University School of Medicine, Atlanta, Georgia 30322, USA.

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http://dx.doi.org/10.1002/humu.20831DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2574813PMC
September 2008

Fragile X syndrome.

Eur J Hum Genet 2008 Jun 9;16(6):666-72. Epub 2008 Apr 9.

Department of Human Genetics, Emory University School of Medicine, 615 Michael Street, Atlanta, GA 30322, USA.

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http://www.nature.com/articles/ejhg200861
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http://dx.doi.org/10.1038/ejhg.2008.61DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4369150PMC
June 2008

Identification of small molecules rescuing fragile X syndrome phenotypes in Drosophila.

Nat Chem Biol 2008 Apr 9;4(4):256-63. Epub 2008 Mar 9.

Department of Human Genetics, Emory University School of Medicine, 615 Michael Street Suite 300, Atlanta, Georgia 30322, USA.

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http://dx.doi.org/10.1038/nchembio.78DOI Listing
April 2008

Argonaute2 is essential for mammalian gastrulation and proper mesoderm formation.

PLoS Genet 2007 Dec;3(12):e227

Department of Human Genetics, Emory University School of Medicine, Atlanta, Georgia, United States of America.

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http://dx.doi.org/10.1371/journal.pgen.0030227DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2323323PMC
December 2007

Replication stress induces tumor-like microdeletions in FHIT/FRA3B.

Proc Natl Acad Sci U S A 2008 Jan 27;105(1):246-51. Epub 2007 Dec 27.

Department of Human Genetics, University of Michigan, Ann Arbor, MI 48109-5618, USA.

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http://dx.doi.org/10.1073/pnas.0708097105DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2224195PMC
January 2008

Polyglutamine domain modulates the TBP-TFIIB interaction: implications for its normal function and neurodegeneration.

Nat Neurosci 2007 Dec 11;10(12):1519-28. Epub 2007 Nov 11.

Department of Human Genetics, Emory University School of Medicine, 615 Michael Street, Atlanta, Georgia 30322, USA.

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http://dx.doi.org/10.1038/nn2011DOI Listing
December 2007

2006 ASHG Presidential Address. Our society and the scientist-citizen.

Authors:
Stephen T Warren

Am J Hum Genet 2007 Oct;81(4):642-5

Departments of Human Genetics, Biochemistry, and Pediatrics, Emory University School of Medicine, Atlanta, USA.

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http://dx.doi.org/10.1086/521404DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2227911PMC
October 2007

Fragile X mental retardation protein deficiency leads to excessive mGluR5-dependent internalization of AMPA receptors.

Proc Natl Acad Sci U S A 2007 Sep 19;104(39):15537-42. Epub 2007 Sep 19.

Department of Human Genetics, Emory University School of Medicine, 615 Michael Street, Whitehead Biomedical Research Building, Atlanta, GA 30322, USA.

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http://www.pnas.org/cgi/doi/10.1073/pnas.0707484104
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http://dx.doi.org/10.1073/pnas.0707484104DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2000537PMC
September 2007

Genome-wide expression profiling of lymphoblastoid cell lines distinguishes different forms of autism and reveals shared pathways.

Hum Mol Genet 2007 Jul 21;16(14):1682-98. Epub 2007 May 21.

Center for Autism Research and Treatment, Semel Institute for Neuroscience and Human Behavior, David Geffen School of Medicine, University of California Los Angeles, Los Angeles, CA 90095, USA.

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http://dx.doi.org/10.1093/hmg/ddm116DOI Listing
July 2007

The pathophysiology of fragile x syndrome.

Annu Rev Genomics Hum Genet 2007 ;8:109-29

Department of Human Genetics, Emory University School of Medicine, Atlanta, Georgia 30322, USA.

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http://dx.doi.org/10.1146/annurev.genom.8.080706.092249DOI Listing
December 2007

Molecular diagnosis of Beckwith-Wiedemann syndrome using quantitative methylation-sensitive polymerase chain reaction.

Genet Med 2006 Oct;8(10):628-34

Department of Human Genetics, Emory University School of Medicine, Atlanta, Georgia 30322, USA.

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http://dx.doi.org/10.1097/01.gim.0000237770.42442.ccDOI Listing
October 2006

Transcription, translation and fragile X syndrome.

Curr Opin Genet Dev 2006 Jun 2;16(3):270-5. Epub 2006 May 2.

Department of Human Genetics, 615 Michael Street, Room 300, Emory University, Atlanta, GA 30322, USA.

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http://dx.doi.org/10.1016/j.gde.2006.04.010DOI Listing
June 2006

Physiological identification of human transcripts translationally regulated by a specific microRNA.

Hum Mol Genet 2005 Dec 20;14(24):3813-21. Epub 2005 Oct 20.

Department of Human Genetics, Emory University School of Medicine, Atlanta, GA 30322, USA.

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http://dx.doi.org/10.1093/hmg/ddi397DOI Listing
December 2005

Fragile X syndrome: an update and review for the primary pediatrician.

Clin Pediatr (Phila) 2005 Jun;44(5):371-81

Departments of Human Genetics and Pediatrics, Emory University School of Medicine, Atlanta, GA, USA.

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https://genetics.emory.edu/documents/labs/warren/Clin_Pediat
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http://dx.doi.org/10.1177/000992280504400501DOI Listing
June 2005

RNA and microRNAs in fragile X mental retardation.

Nat Cell Biol 2004 Nov;6(11):1048-53

Department of Human Genetics, Emory University School of Medicine, Atlanta, GA 30322, USA.

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http://www.nature.com/articles/ncb1104-1048
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http://dx.doi.org/10.1038/ncb1104-1048DOI Listing
November 2004

The fragile X protein controls microtubule-associated protein 1B translation and microtubule stability in brain neuron development.

Proc Natl Acad Sci U S A 2004 Oct 8;101(42):15201-6. Epub 2004 Oct 8.

Department of Pharmacology, Emory University School of Medicine, Atlanta, GA 30322, USA.

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http://dx.doi.org/10.1073/pnas.0404995101DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC524058PMC
October 2004

The mGluR theory of fragile X mental retardation.

Trends Neurosci 2004 Jul;27(7):370-7

The Picower Center for Learning and Memory, Howard Hughes Medical Institute and Department of Brain and Cognitive Sciences, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.

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http://dx.doi.org/10.1016/j.tins.2004.04.009DOI Listing
July 2004

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

J Neurochem 2004 May;89(4):962-73

Department of Human Genetics, Emory University School of Medicine, Atlanta, Georgia, USA.

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http://dx.doi.org/10.1111/j.1471-4159.2004.02376.xDOI Listing
May 2004

The fragile X mental retardation protein, FMRP, recognizes G-quartets.

Ment Retard Dev Disabil Res Rev 2004 ;10(1):49-52

The Rockefeller University, Laboratory of Molecular Neuro-Oncology New York, New York 10021, USA.

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http://dx.doi.org/10.1002/mrdd.20008DOI Listing
July 2004

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

Nat Neurosci 2004 Feb 4;7(2):113-7. Epub 2004 Jan 4.

Department of Human Genetics, Emory University, 615 Michael Street, Atlanta, Georgia 30322, USA.

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http://dx.doi.org/10.1038/nn1174DOI Listing
February 2004

Phosphorylation influences the translation state of FMRP-associated polyribosomes.

Hum Mol Genet 2003 Dec 21;12(24):3295-305. Epub 2003 Oct 21.

Department of Human Genetics,Emory University School of Medicine, Atlanta, GA 30322, USA.

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http://dx.doi.org/10.1093/hmg/ddg350DOI Listing
December 2003

RNA-mediated neurodegeneration caused by the fragile X premutation rCGG repeats in Drosophila.

Neuron 2003 Aug;39(5):739-47

Department of Human Genetics, Emory University, Atlanta, GA 30322, USA.

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http://dx.doi.org/10.1016/s0896-6273(03)00533-6DOI Listing
August 2003

New insights into fragile X syndrome: from molecules to neurobehaviors.

Trends Biochem Sci 2003 Mar;28(3):152-8

Department of Human Genetics, Emory University School of Medicine, Atlanta, GA 30322, USA.

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http://dx.doi.org/10.1016/S0968-0004(03)00033-1DOI Listing
March 2003

Development and characterization of antibodies that immunoprecipitate the FMR1 protein.

Methods Mol Biol 2003 ;217:345-54

Howard Hughes Medical Institute, Emory School of Medicine, Atlanta, GA, USA.

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http://dx.doi.org/10.1385/1-59259-330-5:345DOI Listing
April 2003

Gene expression profiles in a transgenic animal model of fragile X syndrome.

Neurobiol Dis 2002 Aug;10(3):211-8

Blanchette Rockefeller Neurosciences Institute, West Virginia University, Rockville, MD 20850, USA.

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http://dx.doi.org/10.1006/nbdi.2002.0506DOI Listing
August 2002

Histone modifications depict an aberrantly heterochromatinized FMR1 gene in fragile x syndrome.

Am J Hum Genet 2002 Oct 13;71(4):923-32. Epub 2002 Sep 13.

Department of Biochemistry, Emory University School of Medicine, Atlanta, GA 30322, USA.

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http://dx.doi.org/10.1086/342931DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC378545PMC
October 2002

A decade of molecular studies of fragile X syndrome.

Annu Rev Neurosci 2002 20;25:315-38. Epub 2002 Mar 20.

Howard Hughes Medical Institute and Department of Human Genetics, Emory University School of Medicine, Atlanta, Georgia 30322, USA.

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http://dx.doi.org/10.1146/annurev.neuro.25.112701.142909DOI Listing
October 2002

Altered synaptic plasticity in a mouse model of fragile X mental retardation.

Proc Natl Acad Sci U S A 2002 May;99(11):7746-50

Department of Neuroscience, Howard Hughes Medical Institute, Brown University, Providence, RI 02912, USA.

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http://www.pnas.org/cgi/doi/10.1073/pnas.122205699
Publisher Site
http://dx.doi.org/10.1073/pnas.122205699DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC124340PMC
May 2002