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Stephen Warren

This is a preview profile on BiomedExperts - the first literature-based scientific social network. It brings the right researchers together and allows them to collaborate online. Collexis and Dell provide the BiomedExperts network of +1.5 Million pre-calculated profiles free of charge to researchers worldwide.

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Coffee Bradford; Keith Krayton; Albizua Igor; Malone Tamika; Mowrey Julie; Sherman Stephanie L; Warren Stephen T
Incidence of fragile X syndrome by newborn screening for methylated FMR1 DNA.
Tesla Catherine; Korf Bruce R; Holt Lynn; Prucka Sandra; Robin Nathaniel H; Descartes Maria; Lose Edward; Stembridge Adrya; Epstein Michael; Warren Stephen
AsktheGeneticist: five years of online experience.
Arlt Martin F; Mulle Jennifer G; Schaibley Valerie M; Ragland Ryan L; Durkin Sandra G; Warren Stephen T; Glover Thomas W
Replication stress induces genome-wide copy number changes in human cells that resemble polymorphic and pathogenic variants.

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All Publications

2009: Coffee Bradford; Keith Krayton; Albizua Igor; Malone Tamika; Mowrey Julie; Sherman Stephanie L; Warren Stephen T
Incidence of fragile X syndrome by newborn screening for methylated FMR1 DNA.
American journal of human genetics 2009;85(4):503-14.
2009: Tesla Catherine; Korf Bruce R; Holt Lynn; Prucka Sandra; Robin Nathaniel H; Descartes Maria; Lose Edward; Stembridge Adrya; Epstein Michael; Warren Stephen
AsktheGeneticist: five years of online experience.
Genetics in medicine : official journal of the American College of Medical Genetics 2009;11(4):294-304.
2009: Arlt Martin F; Mulle Jennifer G; Schaibley Valerie M; Ragland Ryan L; Durkin Sandra G; Warren Stephen T; Glover Thomas W
Replication stress induces genome-wide copy number changes in human cells that resemble polymorphic and pathogenic variants.
American journal of human genetics 2009;84(3):339-50.
2008: Bassell Gary J; Warren Stephen T
Fragile X syndrome: loss of local mRNA regulation alters synaptic development and function.
Neuron 2008;60(2):201-14.
2008: Weinshenker David; Warren Stephen T
Neuroscience: fragile dopamine.
Nature 2008;455(7213):607-8.
2008: Hegde Madhuri R; Chin Ephrem L H; Mulle Jennifer G; Okou David T; Warren Stephen T; Zwick Michael E
Microarray-based mutation detection in the dystrophin gene.
Human mutation 2008;29(9):1091-9.
2008: Narayanan Usha; Nalavadi Vijayalaxmi; Nakamoto Mika; Thomas George; Ceman Stephanie; Bassell Gary J; Warren Stephen T
S6K1 phosphorylates and regulates fragile X mental retardation protein (FMRP) with the neuronal protein synthesis-dependent mammalian target of rapamycin (mTOR) signaling cascade.
The Journal of biological chemistry 2008;283(27):18478-82.
2008: Garber Kathryn B; Visootsak Jeannie; Warren Stephen T
Fragile X syndrome.
European journal of human genetics : EJHG 2008;16(6):666-72.
2008: Coffee Bradford; Ikeda Morna; Budimirovic Dejan B; Hjelm Lawrence N; Kaufmann Walter E; Warren Stephen T
Mosaic FMR1 deletion causes fragile X syndrome and can lead to molecular misdiagnosis: a case report and review of the literature.
American journal of medical genetics. Part A 2008;146A(10):1358-67.
2008: Chang Shuang; Bray Steven M; Li Zigang; Zarnescu Daniela C; He Chuan; Jin Peng; Warren Stephen T
Identification of small molecules rescuing fragile X syndrome phenotypes in Drosophila.
Nature chemical biology 2008;4(4):256-63.
2008: Durkin Sandra G; Ragland Ryan L; Arlt Martin F; Mulle Jennifer G; Warren Stephen T; Glover Thomas W
Replication stress induces tumor-like microdeletions in FHIT/FRA3B.
Proceedings of the National Academy of Sciences of the United States of America 2008;105(1):246-51.
2007: Alisch Reid S; Jin Peng; Epstein Michael; Caspary Tamara; Warren Stephen T
Argonaute2 is essential for mammalian gastrulation and proper mesoderm formation.
PLoS genetics 2007;3(12):e227.
2007: Narayanan Usha; Nalavadi Vijayalaxmi; Nakamoto Mika; Pallas David C; Ceman Stephanie; Bassell Gary J; Warren Stephen T
FMRP phosphorylation reveals an immediate-early signaling pathway triggered by group I mGluR and mediated by PP2A.
The Journal of neuroscience : the official journal of the Society for Neuroscience 2007;27(52):14349-57.
2007: Friedman Meyer J; Shah Anjali G; Fang Zhi-Hui; Ward Elizabeth G; Warren Stephen T; Li Shihua; Li Xiao-Jiang
Polyglutamine domain modulates the TBP-TFIIB interaction: implications for its normal function and neurodegeneration.
Nature neuroscience 2007;10(12):1519-28.
2007: Warren Stephen T
The epigenetics of fragile X syndrome.
Cell stem cell 2007;1(5):488-9.
2007: Nakamoto Mika; Nalavadi Vijayalaxmi; Epstein Michael P; Narayanan Usha; Bassell Gary J; Warren Stephen T
Fragile X mental retardation protein deficiency leads to excessive mGluR5-dependent internalization of AMPA receptors.
Proceedings of the National Academy of Sciences of the United States of America 2007;104(39):15537-42.
2007: Jin Peng; Duan Ranhui; Qurashi Abrar; Qin Yunlong; Tian Donghua; Rosser Tracie C; Liu Huijie; Feng Yue; Warren Stephen T
Pur alpha binds to rCGG repeats and modulates repeat-mediated neurodegeneration in a Drosophila model of fragile X tremor/ataxia syndrome.
Neuron 2007;55(4):556-64.
2007: Nishimura Yuhei; Martin Christa L; Vazquez-Lopez Araceli; Spence Sarah J; Alvarez-Retuerto Ana Isabel; Sigman Marian; Steindler Corinna; Pellegrini Sandra; Schanen N Carolyn; Warren Stephen T; Geschwind Daniel H
Genome-wide expression profiling of lymphoblastoid cell lines distinguishes different forms of autism and reveals shared pathways.
Human molecular genetics 2007;16(14):1682-98.
2007: Viel Kevin R; Machiah Deepa K; Warren Diane M; Khachidze Manana; Buil Alfonso; Fernstrom Karl; Souto Juan C; Peralta Juan M; Smith Todd; Blangero John; Porter Sandra; Warren Stephen T; Fontcuberta Jordi; Soria Jose M; Flanders W Dana; Almasy Laura; Howard Tom E
A sequence variation scan of the coagulation factor VIII (FVIII) structural gene and associations with plasma FVIII activity levels.
Blood 2007;109(9):3713-24.
2007: Penagarikano Olga; Mulle Jennifer G; Warren Stephen T
The pathophysiology of fragile x syndrome.
Annual review of genomics and human genetics 2007;8():109-29.
2006: Coffee Bradford; Muralidharan Kasinathan; Highsmith William E; Lapunzina Pablo; Warren Stephen T
Molecular diagnosis of Beckwith-Wiedemann syndrome using quantitative methylation-sensitive polymerase chain reaction.
Genetics in medicine : official journal of the American College of Medical Genetics 2006;8(10):628-34.
2006: Khachidze M; Buil A; Viel K R; Porter S; Warren D; Machiah D K; Soria J M; Souto J C; Ameri A; Lathrop M; Blangero J; Fontcuberta J; Warren S T; Almasy L; Howard T E
Genetic determinants of normal variation in coagulation factor (F) IX levels: genome-wide scan and examination of the FIX structural gene.
Journal of thrombosis and haemostasis : JTH 2006;4(7):1537-45.
2006: Garber Kathryn; Smith Karen T; Reines Danny; Warren Stephen T
Transcription, translation and fragile X syndrome.
Current opinion in genetics & development 2006;16(3):270-5.
2005: Nakamoto Mika; Jin Peng; O'Donnell William T; Warren Stephen T
Physiological identification of human transcripts translationally regulated by a specific microRNA.
Human molecular genetics 2005;14(24):3813-21.
2005: Zarnescu D C; Shan G; Warren S T; Jin P
Come FLY with us: toward understanding fragile X syndrome.
Genes, brain, and behavior 2005;4(6):385-92.
2005: Visootsak Jeannie; Warren Stephen T; Anido Aimee; Graham John M
Fragile X syndrome: an update and review for the primary pediatrician.
Clinical pediatrics 2005;44(5):371-81.
2005: Zarnescu Daniela C; Jin Peng; Betschinger Joerg; Nakamoto Mika; Wang Yan; Dockendorff Thomas C; Feng Yue; Jongens Thomas A; Sisson John C; Knoblich Juergen A; Warren Stephen T; Moses Kevin
Fragile X protein functions with lgl and the par complex in flies and mice.
Developmental cell 2005;8(1):43-52.
2004: Jin Peng; Alisch Reid S; Warren Stephen T
RNA and microRNAs in fragile X mental retardation.
Nature cell biology 2004;6(11):1048-53.
2004: Lu Robert; Wang Houping; Liang Zhe; Ku Li; O'donnell William T; Li Wen; Warren Stephen T; Feng Yue
The fragile X protein controls microtubule-associated protein 1B translation and microtubule stability in brain neuron development.
Proceedings of the National Academy of Sciences of the United States of America 2004;101(42):15201-6.
2004: Bear Mark F; Huber Kimberly M; Warren Stephen T
The mGluR theory of fragile X mental retardation.
Trends in neurosciences 2004;27(7):370-7.
2004: Kaytor Michael D; Wilkinson Keith D; Warren Stephen T
Modulating huntingtin half-life alters polyglutamine-dependent aggregate formation and cell toxicity.
Journal of neurochemistry 2004;89(4):962-73.
2004: Jin Peng; Zarnescu Daniela C; Ceman Stephanie; Nakamoto Mika; Mowrey Julie; Jongens Thomas A; Nelson David L; Moses Kevin; Warren Stephen T
Biochemical and genetic interaction between the fragile X mental retardation protein and the microRNA pathway.
Nature neuroscience 2004;7(2):113-7.
2004: Darnell Jennifer C; Warren Stephen T; Darnell Robert B
The fragile X mental retardation protein, FMRP, recognizes G-quartets.
Mental retardation and developmental disabilities research reviews 2004;10(1):49-52.
2003: Ceman Stephanie; O'Donnell William T; Reed Matt; Patton Stephana; Pohl Jan; Warren Stephen T
Phosphorylation influences the translation state of FMRP-associated polyribosomes.
Human molecular genetics 2003;12(24):3295-305.
2003: Jin Peng; Zarnescu Daniela C; Zhang Fuping; Pearson Christopher E; Lucchesi John C; Moses Kevin; Warren Stephen T
RNA-mediated neurodegeneration caused by the fragile X premutation rCGG repeats in Drosophila.
Neuron 2003;39(5):739-47.
2003: Warren Stephen T
Minimum description length block finder, a method to identify haplotype blocks and to compare the strength of block boundaries.
American journal of human genetics 2003;73(2):444.
2003: Jin Peng; Warren Stephen T
New insights into fragile X syndrome: from molecules to neurobehaviors.
Trends in biochemical sciences 2003;28(3):152-8.
2003: Ceman Stephanie; Zhang Fuping; Johnson Tamika; Warren Stephen T
Development and characterization of antibodies that immunoprecipitate the FMR1 protein.
Methods in molecular biology (Clifton, N.J.) 2003;217():345-54.
2002: Coffee Bradford; Zhang Fuping; Ceman Stephanie; Warren Stephen T; Reines Daniel
Histone modifications depict an aberrantly heterochromatinized FMR1 gene in fragile x syndrome.
American journal of human genetics 2002;71(4):923-32.
2002: D'Agata Velia; Warren Stephen T; Zhao Weiqin; Torre Enrique R; Alkon Daniel L; Cavallaro Sebastiano
Gene expression profiles in a transgenic animal model of fragile X syndrome.
Neurobiology of disease 2002;10(3):211-8.
2002: Huber Kimberly M; Gallagher Sean M; Warren Stephen T; Bear Mark F
Altered synaptic plasticity in a mouse model of fragile X mental retardation.
Proceedings of the National Academy of Sciences of the United States of America 2002;99(11):7746-50.
2002: Tarleton J; Kenneson A; Taylor A K; Crandall K; Fletcher R; Casey R; Hart P S; Hatton D; Fisch G; Warren S T
A single base alteration in the CGG repeat region of FMR1: possible effects on gene expression and phenotype.
Journal of medical genetics 2002;39(3):196-200.
2002: O'Donnell William T; Warren Stephen T
A decade of molecular studies of fragile X syndrome.
Annual review of neuroscience 2002;25():315-38.
2001: Darnell J C; Jensen K B; Jin P; Brown V; Warren S T; Darnell R B
Fragile X mental retardation protein targets G quartet mRNAs important for neuronal function.
Cell 2001;107(4):489-99.
2001: Brown V; Jin P; Ceman S; Darnell J C; O'Donnell W T; Tenenbaum S A; Jin X; Feng Y; Wilkinson K D; Keene J D; Darnell R B; Warren S T
Microarray identification of FMRP-associated brain mRNAs and altered mRNA translational profiles in fragile X syndrome.
Cell 2001;107(4):477-87.
2001: Hegde M R; Chong B; Fawkner M; Lambiris N; Peters H; Kenneson A; Warren S T; Love D R; McGaughran J
Microdeletion in the FMR-1 gene: an apparent null allele using routine clinical PCR amplification.
Journal of medical genetics 2001;38(9):624-9.
2001: Kenneson A; Zhang F; Hagedorn C H; Warren S T
Reduced FMRP and increased FMR1 transcription is proportionally associated with CGG repeat number in intermediate-length and premutation carriers.
Human molecular genetics 2001;10(14):1449-54.
2001: Kenneson A; Warren S T
The female and the fragile X reviewed.
Seminars in reproductive medicine 2001;19(2):159-65.
2001: Li Z; Zhang Y; Ku L; Wilkinson K D; Warren S T; Feng Y
The fragile X mental retardation protein inhibits translation via interacting with mRNA.
Nucleic acids research 2001;29(11):2276-83.
2000: Ceman S; Nelson R; Warren S T
Identification of mouse YB1/p50 as a component of the FMRP-associated mRNP particle.
Biochemical and biophysical research communications 2000;279(3):904-8.
2000: Conway K E; McConnell B B; Bowring C E; Donald C D; Warren S T; Vertino P M
TMS1, a novel proapoptotic caspase recruitment domain protein, is a target of methylation-induced gene silencing in human breast cancers.
Cancer research 2000;60(22):6236-42.
2000: Crawford D C; Zhang F; Wilson B; Warren S T; Sherman S L
Fragile X CGG repeat structures among African-Americans: identification of a novel factor responsible for repeat instability.
Human molecular genetics 2000;9(12):1759-69.
2000: Tsui S; Dai T; Warren S T; Salido E C; Yen P H
Association of the mouse infertility factor DAZL1 with actively translating polyribosomes.
Biology of reproduction 2000;62(6):1655-60.
2000: Peier A M; McIlwain K L; Kenneson A; Warren S T; Paylor R; Nelson D L
(Over)correction of FMR1 deficiency with YAC transgenics: behavioral and physical features.
Human molecular genetics 2000;9(8):1145-59.
2000: Jin P; Warren S T
Understanding the molecular basis of fragile X syndrome.
Human molecular genetics 2000;9(6):901-8.
2000: Crawford D C; Schwartz C E; Meadows K L; Newman J L; Taft L F; Gunter C; Brown W T; Carpenter N J; Howard-Peebles P N; Monaghan K G; Nolin S L; Reiss A L; Feldman G L; Rohlfs E M; Warren S T; Sherman S L
Survey of the fragile X syndrome CGG repeat and the short-tandem-repeat and single-nucleotide-polymorphism haplotypes in an African American population.
American journal of human genetics 2000;66(2):480-93.
2000: Ping D; Boekhoudt G; Zhang F; Morris A; Philipsen S; Warren S T; Boss J M
Sp1 binding is critical for promoter assembly and activation of the MCP-1 gene by tumor necrosis factor.
The Journal of biological chemistry 2000;275(3):1708-14.
2000: Warren S T
A new millennium and a new editor.
American journal of human genetics 2000;66(1):3-5.
1999: Kaytor M D; Warren S T
Aberrant protein deposition and neurological disease.
The Journal of biological chemistry 1999;274(53):37507-10.
1999: Ceman S; Brown V; Warren S T
Isolation of an FMRP-associated messenger ribonucleoprotein particle and identification of nucleolin and the fragile X-related proteins as components of the complex.
Molecular and cellular biology 1999;19(12):7925-32.
1999: Coffee B; Zhang F; Warren S T; Reines D
Acetylated histones are associated with FMR1 in normal but not fragile X-syndrome cells.
Nature genetics 1999;22(1):98-101.
1999: Zacharias A S; Wagener M E; Warren S T; Hopkins L C
Emery-Dreifuss muscular dystrophy.
Seminars in neurology 1999;19(1):67-79.
1999: Paradee W; Melikian H E; Rasmussen D L; Kenneson A; Conn P J; Warren S T
Fragile X mouse: strain effects of knockout phenotype and evidence suggesting deficient amygdala function.
Neuroscience 1999;94(1):185-92.
1998: Gunter C; Paradee W; Crawford D C; Meadows K A; Newman J; Kunst C B; Nelson D L; Schwartz C; Murray A; Macpherson J N; Sherman S L; Warren S T
Re-examination of factors associated with expansion of CGG repeats using a single nucleotide polymorphism in FMR1.
Human molecular genetics 1998;7(12):1935-46.
1998: Gunter C; Warren S T
Polymorphism in the FMR1 gene.
Human genetics 1998;103(3):365-6.
1998: Chou H H; Takematsu H; Diaz S; Iber J; Nickerson E; Wright K L; Muchmore E A; Nelson D L; Warren S T; Varki A
A mutation in human CMP-sialic acid hydroxylase occurred after the Homo-Pan divergence.
Proceedings of the National Academy of Sciences of the United States of America 1998;95(20):11751-6.
1998: Brown V; Small K; Lakkis L; Feng Y; Gunter C; Wilkinson K D; Warren S T
Purified recombinant Fmrp exhibits selective RNA binding as an intrinsic property of the fragile X mental retardation protein.
The Journal of biological chemistry 1998;273(25):15521-7.
1998: Small K; Warren S T
Emerin deletions occurring on both Xq28 inversion backgrounds.
Human molecular genetics 1998;7(1):135-9.
1997: Feng Y; Absher D; Eberhart D E; Brown V; Malter H E; Warren S T
FMRP associates with polyribosomes as an mRNP, and the I304N mutation of severe fragile X syndrome abolishes this association.
Molecular cell 1997;1(1):109-18.
1997: Kenneson A; Cramer D W; Warren S T
Fragile X premutations are not a major cause of early menopause.
American journal of human genetics 1997;61(6):1362-9.
1997: Losekoot M; Hoogendoorn E; Olmer R; Jansen C C; Oosterwijk J C; van den Ouweland A M; Halley D J; Warren S T; Willemsen R; Oostra B A; Bakker E
Prenatal diagnosis of the fragile X syndrome: loss of mutation owing to a double recombinant or gene conversion event at the FMR1 locus.
Journal of medical genetics 1997;34(11):924-6.
1997: Kunst C B; Leeflang E P; Iber J C; Arnheim N; Warren S T
The effect of FMR1 CGG repeat interruptions on mutation frequency as measured by sperm typing.
Journal of medical genetics 1997;34(8):627-31.
1997: Small K; Iber J; Warren S T
Emerin deletion reveals a common X-chromosome inversion mediated by inverted repeats.
Nature genetics 1997;16(1):96-9.
1997: Small K; Wagener M; Warren S T
Isolation and characterization of the complete mouse emerin gene.
Mammalian genome : official journal of the International Mammalian Genome Society 1997;8(5):337-41.
1997: Warren S T
Trinucleotide repetition and fragile X syndrome.
Hospital practice (1995) 1997;32(4):73-6, 81-5, 90-2 passim.
1997: Feng Y; Gutekunst C A; Eberhart D E; Yi H; Warren S T; Hersch S M
Fragile X mental retardation protein: nucleocytoplasmic shuttling and association with somatodendritic ribosomes.
The Journal of neuroscience : the official journal of the Society for Neuroscience 1997;17(5):1539-47.
1997: Malter H E; Iber J C; Willemsen R; de Graaff E; Tarleton J C; Leisti J; Warren S T; Oostra B A
Characterization of the full fragile X syndrome mutation in fetal gametes.
Nature genetics 1997;15(2):165-9.
1997: Warren S T
Polyalanine expansion in synpolydactyly might result from unequal crossing-over of HOXD13.
Science (New York, N.Y.) 1997;275(5298):408-9.
1996: Eberhart D E; Warren S T
Nuclease sensitivity of permeabilized cells confirms altered chromatin formation at the fragile X locus.
Somatic cell and molecular genetics 1996;22(6):435-41.
1996: Lachiewicz A M; Spiridigliozzi G A; McConkie-Rosell A; Burgess D; Feng Y; Warren S T; Tarleton J
A fragile X male with a broad smear on Southern blot analysis representing 100-500 CGG repeats and no methylation at the EagI site of the FMR-1 gene.
American journal of medical genetics 1996;64(2):278-82.
1996: Eberhart D E; Malter H E; Feng Y; Warren S T
The fragile X mental retardation protein is a ribonucleoprotein containing both nuclear localization and nuclear export signals.
Human molecular genetics 1996;5(8):1083-91.
1996: DiMarco S P; Glover T W; Miller D E; Reines D; Warren S T
Transcription elongation factor SII (TCEA) maps to human chromosome 3p22 --> p21.3.
Genomics 1996;36(1):185-8.
1996: Kunst C B; Zerylnick C; Karickhoff L; Eichler E; Bullard J; Chalifoux M; Holden J J; Torroni A; Nelson D L; Warren S T
FMR1 in global populations.
American journal of human genetics 1996;58(3):513-22.
1996: Warren S T
The expanding world of trinucleotide repeats.
Science (New York, N.Y.) 1996;271(5254):1374-5.
1996: Price D K; Zhang F; Ashley C T; Warren S T
The chicken FMR1 gene is highly conserved with a CCT 5'-untranslated repeat and encodes an RNA-binding protein.
Genomics 1996;31(1):3-12.
1996: Eberhart D E; Warren S T
The molecular basis of fragile X syndrome.
Cold Spring Harbor symposia on quantitative biology 1996;61():679-87.
1995: Kirchgessner C U; Warren S T; Willard H F
X inactivation of the FMR1 fragile X mental retardation gene.
Journal of medical genetics 1995;32(12):925-9.
1995: Eichler E E; Kunst C B; Lugenbeel K A; Ryder O A; Davison D; Warren S T; Nelson D L
Evolution of the cryptic FMR1 CGG repeat.
Nature genetics 1995;11(3):301-8.
1995: Bione S; Small K; Aksmanovic V M; D'Urso M; Ciccodicola A; Merlini L; Morandi L; Kress W; Yates J R; Warren S T
Identification of new mutations in the Emery-Dreifuss muscular dystrophy gene and evidence for genetic heterogeneity of the disease.
Human molecular genetics 1995;4(10):1859-63.
1995: Feng Y; Zhang F; Lokey L K; Chastain J L; Lakkis L; Eberhart D; Warren S T
Translational suppression by trinucleotide repeat expansion at FMR1.
Science (New York, N.Y.) 1995;268(5211):731-4.
1995: Zerylnick C; Torroni A; Sherman S L; Warren S T
Normal variation at the myotonic dystrophy locus in global human populations.
American journal of human genetics 1995;56(1):123-30.
1995: Feng Y; Lakkis L; Devys D; Warren S T
Quantitative comparison of FMR1 gene expression in normal and premutation alleles.
American journal of human genetics 1995;56(1):106-13.
1995: Gregor P; Nash S R; Caron M G; Seldin M F; Warren S T
Assignment of the creatine transporter gene (SLC6A8) to human chromosome Xq28 telomeric to G6PD.
Genomics 1995;25(1):332-3.
1995: Ashley C T; Warren S T
Trinucleotide repeat expansion and human disease.
Annual review of genetics 1995;29():703-28.
1995: Andersson B; Lu F; Muzny D M; Warren S T; Gibbs R A
Complete sequence of a 38.4-kb human cosmid insert containing the polymorphic marker DXS455 from Xq28.
DNA sequence : the journal of DNA sequencing and mapping 1995;5(4):219-23.
1995: Warren S T; Ashley C T
Triplet repeat expansion mutations: the example of fragile X syndrome.
Annual review of neuroscience 1995;18():77-99.
1994: van den Ouweland A M; Deelen W H; Kunst C B; Uzielli M L; Nelson D L; Warren S T; Oostra B A; Halley D J
Loss of mutation at the FMR1 locus through multiple exchanges between maternal X chromosomes.
Human molecular genetics 1994;3(10):1823-7.
1994: Kunst C B; Warren S T
Cryptic and polar variation of the fragile X repeat could result in predisposing normal alleles.
Cell 1994;77(6):853-61.
1994: Riggins G J; Zhang F; Warren S T
Lack of imprinting of BCR.
Nature genetics 1994;6(3):226.
1994: Warren S T; Nelson D L
Advances in molecular analysis of fragile X syndrome.
JAMA : the journal of the American Medical Association 1994;271(7):536-42.
1994: Riggins G J; Sherman S L; Phillips C N; Stock W; Westbrook C A; Warren S T
CGG-repeat polymorphism of the BCR gene rules out predisposing alleles leading to the Philadelphia chromosome.
Genes, chromosomes & cancer 1994;9(2):141-4.
1993: Hornstra I K; Nelson D L; Warren S T; Yang T P
High resolution methylation analysis of the FMR1 gene trinucleotide repeat region in fragile X syndrome.
Human molecular genetics 1993;2(10):1659-65.
1993: Warren S T; Nelson D L
Trinucleotide repeat expansions in neurological disease.
Current opinion in neurobiology 1993;3(5):752-9.
1993: Ashley C T; Wilkinson K D; Reines D; Warren S T
FMR1 protein: conserved RNP family domains and selective RNA binding.
Science (New York, N.Y.) 1993;262(5133):563-6.
1993: Gorlin J B; Henske E; Warren S T; Kunst C B; D'Urso M; Palmieri G; Hartwig J H; Bruns G; Kwiatkowski D J
Actin-binding protein (ABP-280) filamin gene (FLN) maps telomeric to the color vision locus (R/GCP) and centromeric to G6PD in Xq28.
Genomics 1993;17(2):496-8.
1993: Ashley C T; Sutcliffe J S; Kunst C B; Leiner H A; Eichler E E; Nelson D L; Warren S T
Human and murine FMR-1: alternative splicing and translational initiation downstream of the CGG-repeat.
Nature genetics 1993;4(3):244-51.
1993: Nelson D L; Warren S T
Trinucleotide repeat instability: when and where?
Nature genetics 1993;4(2):107-8.
1993: Smits A P; Dreesen J C; Post J G; Smeets D F; de Die-Smulders C; Spaans-van der Bijl T; Govaerts L C; Warren S T; Oostra B A; van Oost B A
The fragile X syndrome: no evidence for any recent mutations.
Journal of medical genetics 1993;30(2):94-6.
1993: Hinds H L; Ashley C T; Sutcliffe J S; Nelson D L; Warren S T; Housman D E; Schalling M
Tissue specific expression of FMR-1 provides evidence for a functional role in fragile X syndrome.
Nature genetics 1993;3(1):36-43.
1993: Kaneko K; Warren S T; Miyatake T; Tsuji S
Isolation of 353 NotI-linking clones and 62 DNA markers (DXS607-DXS668) from human chromosome Xq24-->qter.
Cytogenetics and cell genetics 1993;64(1):5-8.
1992: Riggins G J; Lokey L K; Warren S T
CGG repeat polymorphism at the c-Ha-ras oncogene locus.
Human molecular genetics 1992;1(9):775.
1992: Riggins G J; Lokey L K; Chastain J L; Leiner H A; Sherman S L; Wilkinson K D; Warren S T
Human genes containing polymorphic trinucleotide repeats.
Nature genetics 1992;2(3):186-91.
1992: Sutcliffe J S; Nelson D L; Zhang F; Pieretti M; Caskey C T; Saxe D; Warren S T
DNA methylation represses FMR-1 transcription in fragile X syndrome.
Human molecular genetics 1992;1(6):397-400.
1992: Willems P J; Vits L; Raeymaekers P; Beuten J; Coucke P; Holden J J; Van Broeckhoven C; Warren S T; Sagi M; Robinson D
Further localization of X-linked hydrocephalus in the chromosomal region Xq28.
American journal of human genetics 1992;51(2):307-15.
1992: Sutcliffe J S; Zhang F; Caskey C T; Nelson D L; Warren S T
PCR amplification and analysis of yeast artificial chromosomes.
Genomics 1992;13(4):1303-6.
1992: van den Ouweland A M; Knoop M T; Knoers V V; Markslag P W; Rocchi M; Warren S T; Ropers H H; Fahrenholz F; Monnens L A; van Oost B A
Colocalization of the gene for nephrogenic diabetes insipidus (DIR) and the vasopressin type 2 receptor gene (AVPR2) in the Xq28 region.
Genomics 1992;13(4):1350-2.
1992: Traupe H; van den Ouweland A M; van Oost B A; Vogel W; Vetter U; Warren S T; Rocchi M; Darlison M G; Ropers H H
Fine mapping of the human biglycan (BGN) gene within the Xq28 region employing a hybrid cell panel.
Genomics 1992;13(2):481-3.
1992: Verkerk A J; deVries B B; Niermeijer M F; Fu Y H; Nelson D L; Warren S T; Majoor-Krakauer D F; Halley D J; Oostra B A
Intragenic probe used for diagnostics in fragile X families.
American journal of medical genetics 1992;43(1-2):192-6.
1992: Consalez G G; Stayton C L; Freimer N B; Goonewardena P; Brown W T; Gilliam T C; Warren S T
Isolation and characterization of a highly polymorphic human locus (DXS455) in proximal Xq28.
Genomics 1992;12(4):710-4.
1991: Fu Y H; Kuhl D P; Pizzuti A; Pieretti M; Sutcliffe J S; Richards S; Verkerk A J; Holden J J; Fenwick R G; Warren S T
Variation of the CGG repeat at the fragile X site results in genetic instability: resolution of the Sherman paradox.
Cell 1991;67(6):1047-58.
1991: Poustka A; Dietrich A; Langenstein G; Toniolo D; Warren S T; Lehrach H
Physical map of human Xq27-qter: localizing the region of the fragile X mutation.
Proceedings of the National Academy of Sciences of the United States of America 1991;88(19):8302-6.
1991: Pieretti M; Zhang F P; Fu Y H; Warren S T; Oostra B A; Caskey C T; Nelson D L
Absence of expression of the FMR-1 gene in fragile X syndrome.
Cell 1991;66(4):817-22.
1991: Kremer E J; Pritchard M; Lynch M; Yu S; Holman K; Baker E; Warren S T; Schlessinger D; Sutherland G R; Richards R I
Mapping of DNA instability at the fragile X to a trinucleotide repeat sequence p(CCG)n.
Science (New York, N.Y.) 1991;252(5013):1711-4.
1991: Yu S; Pritchard M; Kremer E; Lynch M; Nancarrow J; Baker E; Holman K; Mulley J C; Warren S T; Schlessinger D
Fragile X genotype characterized by an unstable region of DNA.
Science (New York, N.Y.) 1991;252(5010):1179-81.
1991: Consalez G G; Thomas N S; Stayton C L; Knight S J; Johnson M; Hopkins L C; Harper P S; Elsas L J; Warren S T
Assignment of Emery-Dreifuss muscular dystrophy to the distal region of Xq28: the results of a collaborative study.
American journal of human genetics 1991;48(3):468-80.
1991: Rousseau F; Vincent A; Rivella S; Heitz D; Triboli C; Maestrini E; Warren S T; Suthers G K; Goodfellow P; Mandel J L
Four chromosomal breakpoints and four new probes mark out a 10-cM region encompassing the fragile-X locus (FRAXA).
American journal of human genetics 1991;48(1):108-16.
1990: Willems P J; Dijkstra I; Van der Auwera B J; Vits L; Coucke P; Raeymaekers P; Van Broeckhoven C; Consalez G G; Freeman S B; Warren S T
Assignment of X-linked hydrocephalus to Xq28 by linkage analysis.
Genomics 1990;8(2):367-70.
1990: Warren S T; Knight S J; Peters J F; Stayton C L; Consalez G G; Zhang F P
Isolation of the human chromosomal band Xq28 within somatic cell hybrids by fragile X site breakage.
Proceedings of the National Academy of Sciences of the United States of America 1990;87(10):3856-60.
1990: Ledbetter S A; Nelson D L; Warren S T; Ledbetter D H
Rapid isolation of DNA probes within specific chromosome regions by interspersed repetitive sequence polymerase chain reaction.
Genomics 1990;6(3):475-81.
1989: el-Fouly M H; Trosko J E; Chang C C; Warren S T
Potential role of the human Ha-ras oncogene in the inhibition of gap junctional intercellular communication.
Molecular carcinogenesis 1989;2(3):131-5.
1988: Priest J H; Blackston R D; Pearse L A; Warren S T
Molecular evidence for true isochromosome 21q.
Human genetics 1988;81(1):1-3.
1988: Warren S T
Fragile X syndrome: a hypothesis regarding the molecular mechanism of the phenotype.
American journal of medical genetics 1988;30(1-2):681-8.
1988: Warren S T; Zhang F P; Sutcliffe J S; Peters J F
Strategy for molecular cloning of the fragile X site DNA.
American journal of medical genetics 1988;30(1-2):613-23.
1987: Warren S T; Zhang F; Licameli G R; Peters J F
The fragile X site in somatic cell hybrids: an approach for molecular cloning of fragile sites.
Science (New York, N.Y.) 1987;237(4813):420-3.
1985: Warren S T; Glover T W; Davidson R L; Jagadeeswaran P
Linkage and recombination between fragile X-linked mental retardation and the factor IX gene.
Human genetics 1985;69(1):44-6.
1985: Smith G F; Warren S T
The biology of Down syndrome.
Annals of the New York Academy of Sciences 1985;450():1-9.
1984: Jagadeeswaran P; Lavelle D E; Kaul R; Mohandas T; Warren S T
Isolation and characterization of human factor IX cDNA: identification of Taq I polymorphism and regional assignment.
Somatic cell and molecular genetics 1984;10(5):465-73.
1984: Warren S T; Davidson R L
Expression of fragile X chromosome in human-rodent somatic cell hybrids.
Somatic cell and molecular genetics 1984;10(4):409-13.
1982: Warren S T; Doolittle D J; Chang C C; Goodmann J I; Trosko J E
Evaluation of the carcinogenic potential of 2,4-dinitrofluorobenzene and its implications regarding mutagenicity testing.
Carcinogenesis 1982;3(2):139-45.
1982: Trosko J E; Yotti L P; Warren S T; Tsushimoto G; Chang C
Inhibition of cell-cell communication by tumor promoters.
Carcinogenesis; a comprehensive survey 1982;7():565-85.
1981: Scott-Emuakpor A B; Warren S T; Kapur S; Quiachon E B; Higgins J V
Familial occurrence of congenital pulmonary lymphangiectasis. Genetic implications.
American journal of diseases of children (1960) 1981;135(6):532-4.
1981: Warren S T; Schultz R A; Chang C C; Wade M H; Trosko J E
Elevated spontaneous mutation rate in Bloom syndrome fibroblasts.
Proceedings of the National Academy of Sciences of the United States of America 1981;78(5):3133-7.
1981: Warren S T
Allelism in human oculocutaneous albinism.
American journal of human genetics 1981;33(3):479-80.
1981: Chang C C; Boezi J A; Warren S T; Sabourin C L; Liu P K; Glatzer L; Trosko J E
Isolation and characterization of a UV-sensitive hypermutable aphidicolin-resistant Chinese hamster cell line.
Somatic cell genetics 1981;7(2):235-53.
1981: Warren S T; Yotti L P; Moskal J R; Chang C C; Trosko J E
Metabolic cooperation in CHO and V79 cells following treatment with a tumor promoter.
Experimental cell research 1981;131(2):427-30.
1980: Toriello H V; Warren S T; Lindstrom J A
Brief communication: possible X-linked anencephaly and spina bifida--report of a kindred.
American journal of medical genetics 1980;6(2):119-21.
1978: Chang C C; Trosko J E; Warren S T
In vitro assay for tumor promoters and anti-promoters.
Journal of environmental pathology and toxicology 1978;2(1):43-64.
1975: Scott-Emuakpor A B; Uviovo J E; Warren S T
Genetic variation in Nigeria. I. The genetics of phenylthiourea tasting ability.
Human heredity 1975;25(5):360-9.

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