| Year |
Citation |
Score |
| 2023 |
Purcell RH, Sefik E, Werner E, King AT, Mosley TJ, Merritt-Garza ME, Chopra P, McEachin ZT, Karne S, Raj N, Vaglio BJ, Sullivan D, Firestein BL, Tilahun K, Robinette MI, ... Warren ST, et al. Cross-species analysis identifies mitochondrial dysregulation as a functional consequence of the schizophrenia-associated 3q29 deletion. Science Advances. 9: eadh0558. PMID 37585521 DOI: 10.1126/sciadv.adh0558 |
0.756 |
|
| 2023 |
Purcell RH, Sefik E, Werner E, King AT, Mosley TJ, Merritt-Garza ME, Chopra P, McEachin ZT, Karne S, Raj N, Tilahun K, Robinette M, Warren ST, Wen Z, Faundez V, et al. Cross-species transcriptomic analysis identifies mitochondrial dysregulation as a functional consequence of the schizophrenia-associated 3q29 deletion. Biorxiv : the Preprint Server For Biology. PMID 36747819 DOI: 10.1101/2023.01.27.525748 |
0.766 |
|
| 2022 |
Kozlova A, Zhang S, Kotlar AV, Jamison B, Zhang H, Shi S, Forrest MP, McDaid J, Cutler DJ, Epstein MP, Zwick ME, Pang ZP, Sanders AR, Warren ST, Gejman PV, et al. Loss of function of OTUD7A in the schizophrenia- associated 15q13.3 deletion impairs synapse development and function in human neurons. American Journal of Human Genetics. 109: 1500-1519. PMID 35931052 DOI: 10.1016/j.ajhg.2022.07.001 |
0.629 |
|
| 2022 |
Albizua I, Charen K, Shubeck L, Talboy A, Berry-Kravis E, Kaufmann WE, Stallworth JL, Drazba KT, Erickson CA, Sweeney JA, Tartaglia N, Warren SF, Hagerman R, Sherman SL, Warren ST, et al. Descriptive analysis of seizures and comorbidities associated with fragile X syndrome. Molecular Genetics & Genomic Medicine. e2001. PMID 35852003 DOI: 10.1002/mgg3.2001 |
0.414 |
|
| 2022 |
Kong HE, Lim J, Linsalata A, Kang Y, Malik I, Allen EG, Cao Y, Shubeck L, Johnston R, Huang Y, Gu Y, Guo X, Zwick ME, Qin Z, Wingo TS, ... ... Warren ST, et al. Identification of as a genetic modifier of fragile X-associated tremor/ataxia syndrome. Proceedings of the National Academy of Sciences of the United States of America. 119: e2118124119. PMID 35617426 DOI: 10.1073/pnas.2118124119 |
0.484 |
|
| 2022 |
Pollak RM, Purcell RH, Rutkowski TP, Malone T, Pachura KJ, Bassell GJ, Epstein MP, Dawson PA, Smith MR, Jones DP, Zwick ME, Warren ST, Caspary T, Weinshenker D, Mulle JG. Metabolic effects of the schizophrenia-associated 3q29 deletion. Translational Psychiatry. 12: 66. PMID 35177588 DOI: 10.1038/s41398-022-01824-1 |
0.574 |
|
| 2021 |
Kang Y, Zhou Y, Li Y, Han Y, Xu J, Niu W, Li Z, Liu S, Feng H, Huang W, Duan R, Xu T, Raj N, Zhang F, Dou J, ... ... Warren ST, et al. A human forebrain organoid model of fragile X syndrome exhibits altered neurogenesis and highlights new treatment strategies. Nature Neuroscience. PMID 34413513 DOI: 10.1038/s41593-021-00913-6 |
0.668 |
|
| 2021 |
Trevino CE, Rounds JC, Charen K, Shubeck L, Hipp HS, Spencer JB, Johnston HR, Cutler DJ, Zwick ME, Epstein MP, Murray A, Macpherson JN, Mila M, Rodriguez-Revenga L, Berry-Kravis E, ... ... Warren ST, et al. Identifying susceptibility genes for primary ovarian insufficiency on the high-risk genetic background of a fragile X premutation. Fertility and Sterility. PMID 34016428 DOI: 10.1016/j.fertnstert.2021.04.021 |
0.417 |
|
| 2021 |
Raj N, McEachin ZT, Harousseau W, Zhou Y, Zhang F, Merritt-Garza ME, Taliaferro JM, Kalinowska M, Marro SG, Hales CM, Berry-Kravis E, Wolf-Ochoa MW, Martinez-Cerdeño V, Wernig M, Chen L, ... ... Warren ST, et al. Cell-type-specific profiling of human cellular models of fragile X syndrome reveal PI3K-dependent defects in translation and neurogenesis. Cell Reports. 35: 108991. PMID 33852833 DOI: 10.1016/j.celrep.2021.108991 |
0.464 |
|
| 2020 |
Cleynen I, Engchuan W, Hestand MS, Heung T, Holleman AM, Johnston HR, Monfeuga T, McDonald-McGinn DM, Gur RE, Morrow BE, Swillen A, Vorstman JAS, Bearden CE, Chow EWC, van den Bree M, ... ... Warren ST, et al. Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion. Molecular Psychiatry. PMID 32015465 DOI: 10.1038/S41380-020-0654-3 |
0.621 |
|
| 2019 |
Graef JD, Wu H, Ng C, Sun C, Villegas V, Qadir D, Jesseman K, Warren ST, Jaenisch R, Cacace A, Wallace O. Partial FMRP expression is sufficient to normalize neuronal hyperactivity in Fragile X neurons. The European Journal of Neuroscience. PMID 31880363 DOI: 10.1111/Ejn.14660 |
0.378 |
|
| 2019 |
Albizua I, Chopra P, Sherman SL, Gambello MJ, Warren ST. Analysis of the genomic expression profile in trisomy 18: insight into possible genes involved in the associated phenotypes. Human Molecular Genetics. PMID 31813999 DOI: 10.1093/Hmg/Ddz279 |
0.367 |
|
| 2019 |
Rutkowski TP, Purcell RH, Pollak RM, Grewenow SM, Gafford GM, Malone T, Khan UA, Schroeder JP, Epstein MP, Bassell GJ, Warren ST, Weinshenker D, Caspary T, Mulle JG. Behavioral changes and growth deficits in a CRISPR engineered mouse model of the schizophrenia-associated 3q29 deletion. Molecular Psychiatry. PMID 30976085 DOI: 10.1038/S41380-019-0413-5 |
0.636 |
|
| 2019 |
Pollak R, Purcell R, Rutkowski T, Malone T, Pachura K, Bassell GJ, Epstein MP, Caspary T, Dawson PA, Jones DP, Warren ST, Weinshenker D, Zwick ME, Mulle JG. T11Metabolic Dysfunction As A Contributor To Phenotypes Of The Schizophrenia-Associated 3Q29 Deletion European Neuropsychopharmacology. 29. DOI: 10.1016/J.Euroneuro.2019.08.210 |
0.596 |
|
| 2019 |
Monfeuga T, Epstein MP, Holleman AM, Cleynen I, Johnston H, Zhao Y, McDonald-McGinn DM, Gur RE, Warren ST, Vermeesch J, Emanuel BS, Morrow BE, Bassett AS, Williams N. 7Schizophrenia Polygenic Risk Score Analysis In 22Q11.2 Deletion Syndrome European Neuropsychopharmacology. 29. DOI: 10.1016/J.Euroneuro.2018.08.014 |
0.3 |
|
| 2018 |
Deng PY, Carlin D, Mi Oh Y, Myrick LK, Warren ST, Cavalli V, Klyachko VA. Voltage-Independent SK Channel Dysfunction Causes Neuronal Hyperexcitability in the Hippocampus of KO mice. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. PMID 30389838 DOI: 10.1523/Jneurosci.1593-18.2018 |
0.774 |
|
| 2018 |
Andrews SV, Sheppard B, Windham GC, Schieve LA, Schendel DE, Croen LA, Chopra P, Alisch RS, Newschaffer CJ, Warren ST, Feinberg AP, Fallin MD, Ladd-Acosta C. Case-control meta-analysis of blood DNA methylation and autism spectrum disorder. Molecular Autism. 9: 40. PMID 29988321 DOI: 10.1186/S13229-018-0224-6 |
0.657 |
|
| 2018 |
Rutkowski T, Schroeder J, Gafford G, Grewenow S, Malone T, Warren S, Mulle J, Weinshenker D, Caspary T. T224. A Mouse Model of the 3q29 Deletion Biological Psychiatry. 83: S215. DOI: 10.1016/J.Biopsych.2018.02.561 |
0.583 |
|
| 2017 |
Johnston HR, Chopra P, Wingo TS, Patel V, Epstein MP, Mulle JG, Warren ST, Zwick ME, Cutler DJ. Reply to Plüss et al.: The strength of PEMapper/PECaller lies in unbiased calling using large sample sizes. Proceedings of the National Academy of Sciences of the United States of America. PMID 28916730 DOI: 10.1073/Pnas.1714535114 |
0.565 |
|
| 2017 |
Bienkowski RS, Banerjee A, Rounds JC, Rha J, Omotade OF, Gross C, Morris KJ, Leung SW, Pak C, Jones SK, Santoro MR, Warren ST, Zheng JQ, Bassell GJ, Corbett AH, et al. The Conserved, Disease-Associated RNA Binding Protein dNab2 Interacts with the Fragile X Protein Ortholog in Drosophila Neurons. Cell Reports. 20: 1372-1384. PMID 28793261 DOI: 10.1016/J.Celrep.2017.07.038 |
0.788 |
|
| 2017 |
Gur RE, Bassett AS, McDonald-McGinn DM, Bearden CE, Chow E, Emanuel BS, Owen M, Swillen A, Van den Bree M, Vermeesch J, Vorstman JAS, Warren S, Lehner T, Morrow B. A neurogenetic model for the study of schizophrenia spectrum disorders: the International 22q11.2 Deletion Syndrome Brain Behavior Consortium. Molecular Psychiatry. PMID 28761081 DOI: 10.1038/Mp.2017.161 |
0.333 |
|
| 2017 |
Johnston HR, Chopra P, Wingo TS, Patel V, Epstein MP, Mulle JG, Warren ST, Zwick ME, Cutler DJ. PEMapper and PECaller provide a simplified approach to whole-genome sequencing. Proceedings of the National Academy of Sciences of the United States of America. PMID 28223510 DOI: 10.1073/Pnas.1618065114 |
0.574 |
|
| 2016 |
Rutkowski TP, Schroeder JP, Gafford GM, Warren ST, Weinshenker D, Caspary T, Mulle JG. Unraveling the genetic architecture of copy number variants associated with schizophrenia and other neuropsychiatric disorders. Journal of Neuroscience Research. PMID 27859486 DOI: 10.1002/Jnr.23970 |
0.628 |
|
| 2016 |
Xie N, Gong H, Suhl JA, Chopra P, Wang T, Warren ST. Reactivation of FMR1 by CRISPR/Cas9-Mediated Deletion of the Expanded CGG-Repeat of the Fragile X Chromosome. Plos One. 11: e0165499. PMID 27768763 DOI: 10.1371/Journal.Pone.0165499 |
0.818 |
|
| 2016 |
Anderson BR, Chopra P, Suhl JA, Warren ST, Bassell GJ. Identification of consensus binding sites clarifies FMRP binding determinants. Nucleic Acids Research. PMID 27378784 DOI: 10.1093/Nar/Gkw593 |
0.788 |
|
| 2016 |
Hestand MS, Nowakowska BA, Vergaelen E, Van Houdt J, Dehaspe L, Suhl JA, Del-Favero J, Mortier G, Zackai E, Swillen A, Devriendt K, Gur RE, McDonald-McGinn DM, Warren ST, Emanuel BS, et al. A catalog of hemizygous variation in 127 22q11 deletion patients. Human Genome Variation. 3: 15065. PMID 27274857 DOI: 10.1038/Hgv.2015.65 |
0.804 |
|
| 2015 |
Suhl JA, Warren ST. Single-Nucleotide Mutations in FMR1 Reveal Novel Functions and Regulatory Mechanisms of the Fragile X Syndrome Protein FMRP. Journal of Experimental Neuroscience. 9: 35-41. PMID 26819560 DOI: 10.4137/Jen.S25524 |
0.82 |
|
| 2015 |
Suhl JA, Muddashetty RS, Anderson BR, Ifrim MF, Visootsak J, Bassell GJ, Warren ST. A 3' untranslated region variant in FMR1 eliminates neuronal activity-dependent translation of FMRP by disrupting binding of the RNA-binding protein HuR. Proceedings of the National Academy of Sciences of the United States of America. PMID 26554012 DOI: 10.1073/Pnas.1514260112 |
0.827 |
|
| 2015 |
Goes FS, McGrath J, Avramopoulos D, Wolyniec P, Pirooznia M, Ruczinski I, Nestadt G, Kenny EE, Vacic V, Peters I, Lencz T, Darvasi A, Mulle JG, Warren ST, Pulver AE. Genome-wide association study of schizophrenia in Ashkenazi Jews. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 168: 649-59. PMID 26198764 DOI: 10.1002/Ajmg.B.32349 |
0.614 |
|
| 2015 |
Myrick LK, Deng PY, Hashimoto H, Oh YM, Cho Y, Poidevin MJ, Suhl JA, Visootsak J, Cavalli V, Jin P, Cheng X, Warren ST, Klyachko VA. Independent role for presynaptic FMRP revealed by an FMR1 missense mutation associated with intellectual disability and seizures. Proceedings of the National Academy of Sciences of the United States of America. 112: 949-56. PMID 25561520 DOI: 10.1073/Pnas.1423094112 |
0.809 |
|
| 2015 |
Myrick LK, Hashimoto H, Cheng X, Warren ST. Human FMRP contains an integral tandem Agenet (Tudor) and KH motif in the amino terminal domain. Human Molecular Genetics. 24: 1733-40. PMID 25416280 DOI: 10.1093/Hmg/Ddu586 |
0.812 |
|
| 2014 |
Suhl JA, Chopra P, Anderson BR, Bassell GJ, Warren ST. Analysis of FMRP mRNA target datasets reveals highly associated mRNAs mediated by G-quadruplex structures formed via clustered WGGA sequences. Human Molecular Genetics. 23: 5479-91. PMID 24876161 DOI: 10.1093/Hmg/Ddu272 |
0.807 |
|
| 2014 |
Alpatov R, Lesch BJ, Nakamoto-Kinoshita M, Blanco A, Chen S, Stützer A, Armache KJ, Simon MD, Xu C, Ali M, Murn J, Prisic S, Kutateladze TG, Vakoc CR, Min J, ... ... Warren ST, et al. A chromatin-dependent role of the fragile X mental retardation protein FMRP in the DNA damage response. Cell. 157: 869-81. PMID 24813610 DOI: 10.1016/J.Cell.2014.03.040 |
0.445 |
|
| 2014 |
Zhu G, Li Y, Zhu F, Wang T, Jin W, Mu W, Lin W, Tan W, Li W, Street RC, Peng S, Zhang J, Feng Y, Warren ST, Sun Q, et al. Coordination of engineered factors with TET1/2 promotes early-stage epigenetic modification during somatic cell reprogramming. Stem Cell Reports. 2: 253-61. PMID 24672749 DOI: 10.1016/J.Stemcr.2014.01.012 |
0.655 |
|
| 2014 |
Chopra P, Papale LA, White AT, Hatch A, Brown RM, Garthwaite MA, Roseboom PH, Golos TG, Warren ST, Alisch RS. Array-based assay detects genome-wide 5-mC and 5-hmC in the brains of humans, non-human primates, and mice. Bmc Genomics. 15: 131. PMID 24524199 DOI: 10.1186/1471-2164-15-131 |
0.675 |
|
| 2014 |
Satten GA, Allen AS, Ikeda M, Mulle JG, Warren ST. Robust regression analysis of copy number variation data based on a univariate score. Plos One. 9: e86272. PMID 24516529 DOI: 10.1371/Journal.Pone.0086272 |
0.755 |
|
| 2014 |
Myrick LK, Nakamoto-Kinoshita M, Lindor NM, Kirmani S, Cheng X, Warren ST. Fragile X syndrome due to a missense mutation. European Journal of Human Genetics : Ejhg. 22: 1185-9. PMID 24448548 DOI: 10.1038/Ejhg.2013.311 |
0.814 |
|
| 2014 |
Mulle JG, Pulver AE, McGrath JA, Wolyniec PS, Dodd AF, Cutler DJ, Sebat J, Malhotra D, Nestadt G, Conrad DF, Hurles M, Barnes CP, Ikeda M, Iwata N, Levinson DF, ... ... Warren ST, et al. Reciprocal duplication of the Williams-Beuren syndrome deletion on chromosome 7q11.23 is associated with schizophrenia. Biological Psychiatry. 75: 371-7. PMID 23871472 DOI: 10.1016/J.Biopsych.2013.05.040 |
0.64 |
|
| 2013 |
Wang T, Warren ST, Jin P. Toward pluripotency by reprogramming: mechanisms and application. Protein & Cell. 4: 820-32. PMID 24078387 DOI: 10.1007/S13238-013-3074-1 |
0.477 |
|
| 2013 |
Wang T, Wu H, Li Y, Szulwach KE, Lin L, Li X, Chen IP, Goldlust IS, Chamberlain SJ, Dodd A, Gong H, Ananiev G, Han JW, Yoon YS, Rudd MK, ... ... Warren ST, et al. Subtelomeric hotspots of aberrant 5-hydroxymethylcytosine-mediated epigenetic modifications during reprogramming to pluripotency. Nature Cell Biology. 15: 700-11. PMID 23685628 DOI: 10.1038/Ncb2748 |
0.719 |
|
| 2013 |
Nelson DL, Orr HT, Warren ST. The unstable repeats--three evolving faces of neurological disease. Neuron. 77: 825-43. PMID 23473314 DOI: 10.1016/J.Neuron.2013.02.022 |
0.359 |
|
| 2013 |
Alisch RS, Wang T, Chopra P, Visootsak J, Conneely KN, Warren ST. Genome-wide analysis validates aberrant methylation in fragile X syndrome is specific to the FMR1 locus. Bmc Medical Genetics. 14: 18. PMID 23356558 DOI: 10.1186/1471-2350-14-18 |
0.715 |
|
| 2013 |
McDonald-McGinn DM, Fahiminiya S, Revil T, Nowakowska BA, Suhl J, Bailey A, Mlynarski E, Lynch DR, Yan AC, Bilaniuk LT, Sullivan KE, Warren ST, Emanuel BS, Vermeesch JR, Zackai EH, et al. Hemizygous mutations in SNAP29 unmask autosomal recessive conditions and contribute to atypical findings in patients with 22q11.2DS. Journal of Medical Genetics. 50: 80-90. PMID 23231787 DOI: 10.1136/Jmedgenet-2012-101320 |
0.794 |
|
| 2012 |
Wang T, Pan Q, Lin L, Szulwach KE, Song CX, He C, Wu H, Warren ST, Jin P, Duan R, Li X. Genome-wide DNA hydroxymethylation changes are associated with neurodevelopmental genes in the developing human cerebellum. Human Molecular Genetics. 21: 5500-10. PMID 23042784 DOI: 10.1093/Hmg/Dds394 |
0.558 |
|
| 2012 |
Henderson C, Wijetunge L, Kinoshita MN, Shumway M, Hammond RS, Postma FR, Brynczka C, Rush R, Thomas A, Paylor R, Warren ST, Vanderklish PW, Kind PC, Carpenter RL, Bear MF, et al. Reversal of disease-related pathologies in the fragile X mouse model by selective activation of GABAB receptors with arbaclofen. Science Translational Medicine. 4: 152ra128. PMID 22993295 DOI: 10.1126/Scitranslmed.3004218 |
0.796 |
|
| 2012 |
Kenny EE, Pe'er I, Karban A, Ozelius L, Mitchell AA, Ng SM, Erazo M, Ostrer H, Abraham C, Abreu MT, Atzmon G, Barzilai N, Brant SR, Bressman S, Burns ER, ... ... Warren ST, et al. A genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility loci. Plos Genetics. 8: e1002559. PMID 22412388 DOI: 10.1371/Journal.Pgen.1002559 |
0.6 |
|
| 2012 |
Wang T, Bray SM, Warren ST. New perspectives on the biology of fragile X syndrome. Current Opinion in Genetics & Development. 22: 256-63. PMID 22382129 DOI: 10.1016/J.Gde.2012.02.002 |
0.624 |
|
| 2012 |
Mulle JG, Warren ST. Genomic tics in tourette syndrome. Biological Psychiatry. 71: 390-1. PMID 22310325 DOI: 10.1016/J.Biopsych.2011.12.017 |
0.659 |
|
| 2012 |
Alisch RS, Barwick BG, Chopra P, Myrick LK, Satten GA, Conneely KN, Warren ST. Age-associated DNA methylation in pediatric populations. Genome Research. 22: 623-32. PMID 22300631 DOI: 10.1101/Gr.125187.111 |
0.765 |
|
| 2012 |
Santoro MR, Bray SM, Warren ST. Molecular mechanisms of fragile X syndrome: a twenty-year perspective. Annual Review of Pathology. 7: 219-45. PMID 22017584 DOI: 10.1146/Annurev-Pathol-011811-132457 |
0.823 |
|
| 2011 |
Girirajan S, Brkanac Z, Coe BP, Baker C, Vives L, Vu TH, Shafer N, Bernier R, Ferrero GB, Silengo M, Warren ST, Moreno CS, Fichera M, Romano C, Raskind WH, et al. Relative burden of large CNVs on a range of neurodevelopmental phenotypes. Plos Genetics. 7: e1002334. PMID 22102821 DOI: 10.1371/Journal.Pgen.1002334 |
0.346 |
|
| 2011 |
Liu-Yesucevitz L, Bassell GJ, Gitler AD, Hart AC, Klann E, Richter JD, Warren ST, Wolozin B. Local RNA translation at the synapse and in disease. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 31: 16086-93. PMID 22072660 DOI: 10.1523/Jneurosci.4105-11.2011 |
0.38 |
|
| 2011 |
Kaminsky EB, Kaul V, Paschall J, Church DM, Bunke B, Kunig D, Moreno-De-Luca D, Moreno-De-Luca A, Mulle JG, Warren ST, Richard G, Compton JG, Fuller AE, Gliem TJ, Huang S, et al. An evidence-based approach to establish the functional and clinical significance of copy number variants in intellectual and developmental disabilities. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 13: 777-84. PMID 21844811 DOI: 10.1097/Gim.0B013E31822C79F9 |
0.618 |
|
| 2011 |
Moreno-De-Luca D, Mulle JG, Kaminsky EB, Sanders SJ, Myers SM, Adam MP, Pakula AT, Eisenhauer NJ, Uhas K, Weik L, Guy L, Care ME, Morel CF, Boni C, Salbert BA, ... ... Warren ST, et al. Erratum: Deletion 17q12 is a recurrent copy number variant that confers high risk of autism and schizophrenia (The American Journal of Human Genetics (2010) 87 (618-630)) American Journal of Human Genetics. 88. DOI: 10.1016/J.Ajhg.2010.12.005 |
0.599 |
|
| 2010 |
Moreno-De-Luca D, Mulle JG, Kaminsky EB, Sanders SJ, Myers SM, Adam MP, Pakula AT, Eisenhauer NJ, Uhas K, Weik L, Guy L, Care ME, ... ... Warren ST, et al. Deletion 17q12 is a recurrent copy number variant that confers high risk of autism and schizophrenia. American Journal of Human Genetics. 87: 618-30. PMID 21055719 DOI: 10.1016/J.Ajhg.2010.10.004 |
0.636 |
|
| 2010 |
Zoghbi HY, Warren ST. Neurogenetics: advancing the "next-generation" of brain research. Neuron. 68: 165-73. PMID 20955921 DOI: 10.1016/J.Neuron.2010.10.015 |
0.319 |
|
| 2010 |
Collins SC, Bray SM, Suhl JA, Cutler DJ, Coffee B, Zwick ME, Warren ST. Identification of novel FMR1 variants by massively parallel sequencing in developmentally delayed males. American Journal of Medical Genetics. Part A. 152: 2512-20. PMID 20799337 DOI: 10.1002/Ajmg.A.33626 |
0.797 |
|
| 2010 |
Bray SM, Mulle JG, Dodd AF, Pulver AE, Wooding S, Warren ST. Signatures of founder effects, admixture, and selection in the Ashkenazi Jewish population. Proceedings of the National Academy of Sciences of the United States of America. 107: 16222-7. PMID 20798349 DOI: 10.1073/Pnas.1004381107 |
0.657 |
|
| 2010 |
Gross C, Nakamoto M, Yao X, Chan CB, Yim SY, Ye K, Warren ST, Bassell GJ. Excess phosphoinositide 3-kinase subunit synthesis and activity as a novel therapeutic target in fragile X syndrome. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 30: 10624-38. PMID 20702695 DOI: 10.1523/Jneurosci.0402-10.2010 |
0.372 |
|
| 2010 |
Mulle JG, Dodd AF, McGrath JA, Wolyniec PS, Mitchell AA, Shetty AC, Sobreira NL, Valle D, Rudd MK, Satten G, Cutler DJ, Pulver AE, Warren ST. Microdeletions of 3q29 confer high risk for schizophrenia. American Journal of Human Genetics. 87: 229-36. PMID 20691406 DOI: 10.1016/J.Ajhg.2010.07.013 |
0.646 |
|
| 2010 |
Mulle JG, Patel VC, Warren ST, Hegde MR, Cutler DJ, Zwick ME. Empirical evaluation of oligonucleotide probe selection for DNA microarrays. Plos One. 5: e9921. PMID 20360966 DOI: 10.1371/Journal.Pone.0009921 |
0.594 |
|
| 2010 |
Collins SC, Coffee B, Benke PJ, Berry-Kravis E, Gilbert F, Oostra B, Halley D, Zwick ME, Cutler DJ, Warren ST. Array-based FMR1 sequencing and deletion analysis in patients with a fragile X syndrome-like phenotype. Plos One. 5: e9476. PMID 20221430 DOI: 10.1371/Journal.Pone.0009476 |
0.611 |
|
| 2009 |
Coffee B, Keith K, Albizua I, Malone T, Mowrey J, Sherman SL, Warren ST. Incidence of fragile X syndrome by newborn screening for methylated FMR1 DNA. American Journal of Human Genetics. 85: 503-14. PMID 19804849 DOI: 10.1016/J.Ajhg.2009.09.007 |
0.348 |
|
| 2009 |
Arlt MF, Mulle JG, Schaibley VM, Ragland RL, Durkin SG, Warren ST, Glover TW. Replication Stress Induces Genome-wide Copy Number Changes in Human Cells that Resemble Polymorphic and Pathogenic Variants American Journal of Human Genetics. 84: 339-350. PMID 19232554 DOI: 10.1016/J.Ajhg.2009.01.024 |
0.621 |
|
| 2008 |
Bassell GJ, Warren ST. Fragile X syndrome: loss of local mRNA regulation alters synaptic development and function. Neuron. 60: 201-14. PMID 18957214 DOI: 10.1016/J.Neuron.2008.10.004 |
0.435 |
|
| 2008 |
Hegde MR, Chin EL, Mulle JG, Okou DT, Warren ST, Zwick ME. Microarray-based mutation detection in the dystrophin gene. Human Mutation. 29: 1091-9. PMID 18663755 DOI: 10.1002/Humu.20831 |
0.635 |
|
| 2008 |
Narayanan U, Nalavadi V, Nakamoto M, Thomas G, Ceman S, Bassell GJ, Warren ST. 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. 283: 18478-82. PMID 18474609 DOI: 10.1074/Jbc.C800055200 |
0.802 |
|
| 2008 |
Coffee B, Ikeda M, Budimirovic DB, Hjelm LN, Kaufmann WE, Warren ST. 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. 146: 1358-67. PMID 18412117 DOI: 10.1002/Ajmg.A.32261 |
0.822 |
|
| 2008 |
Garber KB, Visootsak J, Warren ST. Fragile X syndrome. European Journal of Human Genetics : Ejhg. 16: 666-72. PMID 18398441 DOI: 10.1038/Ejhg.2008.61 |
0.485 |
|
| 2008 |
Chang S, Bray SM, Li Z, Zarnescu DC, He C, Jin P, Warren ST. Identification of small molecules rescuing fragile X syndrome phenotypes in Drosophila. Nature Chemical Biology. 4: 256-63. PMID 18327252 DOI: 10.1038/Nchembio.78 |
0.759 |
|
| 2008 |
Durkin SG, Ragland RL, Arlt MF, Mulle JG, Warren ST, Glover TW. Replication stress induces tumor-like microdeletions in FHIT/FRA3B Proceedings of the National Academy of Sciences of the United States of America. 105: 246-251. PMID 18162546 DOI: 10.1073/Pnas.0708097105 |
0.631 |
|
| 2007 |
Warren ST. The Epigenetics of Fragile X Syndrome Cell Stem Cell. 1: 488-489. PMID 18938744 DOI: 10.1016/J.Stem.2007.10.017 |
0.369 |
|
| 2007 |
Alisch RS, Jin P, Epstein M, Caspary T, Warren ST. Argonaute2 is essential for mammalian gastrulation and proper mesoderm formation. Plos Genetics. 3: e227. PMID 18166081 DOI: 10.1371/Journal.Pgen.0030227 |
0.713 |
|
| 2007 |
Narayanan U, Nalavadi V, Nakamoto M, Pallas DC, Ceman S, Bassell GJ, Warren ST. 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. 27: 14349-57. PMID 18160642 DOI: 10.1523/Jneurosci.2969-07.2007 |
0.804 |
|
| 2007 |
Friedman MJ, Shah AG, Fang ZH, Ward EG, Warren ST, Li S, Li XJ. Polyglutamine domain modulates the TBP-TFIIB interaction: implications for its normal function and neurodegeneration. Nature Neuroscience. 10: 1519-28. PMID 17994014 DOI: 10.1038/Nn2011 |
0.329 |
|
| 2007 |
Nakamoto M, Nalavadi V, Epstein MP, Narayanan U, Bassell GJ, Warren ST. 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. 104: 15537-42. PMID 17881561 DOI: 10.1073/Pnas.0707484104 |
0.787 |
|
| 2007 |
Jin P, Duan R, Qurashi A, Qin Y, Tian D, Rosser TC, Liu H, Feng Y, Warren ST. Pur α Binds to rCGG Repeats and Modulates Repeat-Mediated Neurodegeneration in a Drosophila Model of Fragile X Tremor/Ataxia Syndrome Neuron. 55: 556-564. PMID 17698009 DOI: 10.1016/J.Neuron.2007.07.020 |
0.803 |
|
| 2007 |
Nishimura Y, Martin CL, Vazquez-Lopez A, Spence SJ, Alvarez-Retuerto AI, Sigman M, Steindler C, Pellegrini S, Schanen NC, Warren ST, Geschwind DH. Genome-wide expression profiling of lymphoblastoid cell lines distinguishes different forms of autism and reveals shared pathways. Human Molecular Genetics. 16: 1682-98. PMID 17519220 DOI: 10.1093/Hmg/Ddm116 |
0.413 |
|
| 2007 |
Penagarikano O, Mulle JG, Warren ST. The pathophysiology of fragile X syndrome Annual Review of Genomics and Human Genetics. 8: 109-129. PMID 17477822 DOI: 10.1146/Annurev.Genom.8.080706.092249 |
0.835 |
|
| 2007 |
Mulle J, Penagarikano O, Warren ST. Path to understanding the pathophysiology of fragile X syndrome Future Neurology. 2: 567-575. DOI: 10.2217/14796708.2.5.567 |
0.642 |
|
| 2006 |
Khachidze M, Buil A, Viel KR, Porter S, Warren D, Machiah DK, Soria JM, Souto JC, Ameri A, Lathrop M, Blangero J, Fontcuberta J, Warren ST, Almasy L, Howard TE. 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. 4: 1537-1545. PMID 16839351 DOI: 10.1111/J.1538-7836.2006.02024.X |
0.301 |
|
| 2006 |
Garber K, Smith KT, Reines D, Warren ST. Transcription, translation and fragile X syndrome. Current Opinion in Genetics & Development. 16: 270-5. PMID 16647847 DOI: 10.1016/J.Gde.2006.04.010 |
0.451 |
|
| 2006 |
Alisch RS, Caspary T, Warren ST. Disruption of the microRNA pathway by the targeted loss of eIF2C2 results in aberrant primitive streak formation Developmental Biology. 295: 380. DOI: 10.1016/J.Ydbio.2006.04.166 |
0.655 |
|
| 2005 |
Nakamoto M, Jin P, O'Donnell WT, Warren ST. Physiological identification of human transcripts translationally regulated by a specific microRNA. Human Molecular Genetics. 14: 3813-21. PMID 16239240 DOI: 10.1093/Hmg/Ddi397 |
0.765 |
|
| 2005 |
Zarnescu DC, Shan G, Warren ST, Jin P. Come FLY with us: toward understanding fragile X syndrome. Genes, Brain, and Behavior. 4: 385-92. PMID 16098136 DOI: 10.1111/J.1601-183X.2005.00136.X |
0.405 |
|
| 2005 |
Visootsak J, Warren ST, Anido A, Graham JM. Fragile X syndrome: An update and review for the primary pediatrician Clinical Pediatrics. 44: 371-381. PMID 15965543 DOI: 10.1177/000992280504400501 |
0.339 |
|
| 2005 |
Zarnescu DC, Jin P, Betschinger J, Nakamoto M, Wang Y, Dockendorff TC, Feng Y, Jongens TA, Sisson JC, Knoblich JA, Warren ST, Moses K. Fragile X protein functions with lgl and the par complex in flies and mice. Developmental Cell. 8: 43-52. PMID 15621528 DOI: 10.1016/J.Devcel.2004.10.020 |
0.649 |
|
| 2004 |
Jin P, Alisch RS, Warren ST. RNA and microRNAs in fragile X mental retardation Nature Cell Biology. 6: 1048-1053. PMID 15516998 DOI: 10.1038/Ncb1104-1048 |
0.762 |
|
| 2004 |
Lu R, Wang H, Liang Z, Ku L, O'donnell WT, Li W, Warren ST, Feng Y. 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. 101: 15201-6. PMID 15475576 DOI: 10.1073/Pnas.0404995101 |
0.816 |
|
| 2004 |
Bear MF, Huber KM, Warren ST. The mGluR theory of fragile X mental retardation. Trends in Neurosciences. 27: 370-7. PMID 15219735 DOI: 10.1016/J.Tins.2004.04.009 |
0.442 |
|
| 2004 |
Kaytor MD, Wilkinson KD, Warren ST. Modulating huntingtin half-life alters polyglutamine-dependent aggregate formation and cell toxicity. Journal of Neurochemistry. 89: 962-73. PMID 15140195 DOI: 10.1111/J.1471-4159.2004.02376.X |
0.726 |
|
| 2004 |
Darnell JC, Warren ST, Darnell RB. The Fragile X Mental Retardation Protein, FMRP, Recognizes G-Quartets Mental Retardation and Developmental Disabilities Research Reviews. 10: 49-52. PMID 14994288 DOI: 10.1002/Mrdd.20008 |
0.396 |
|
| 2004 |
Jin P, Zarnescu DC, Ceman S, Nakamoto M, Mowrey J, Jongens TA, Nelson DL, Moses K, Warren ST. Biochemical and genetic interaction between the fragile X mental retardation protein and the microRNA pathway. Nature Neuroscience. 7: 113-7. PMID 14703574 DOI: 10.1038/Nn1174 |
0.774 |
|
| 2003 |
Ceman S, O'Donnell WT, Reed M, Patton S, Pohl J, Warren ST. Phosphorylation influences the translation state of FMRP-associated polyribosomes. Human Molecular Genetics. 12: 3295-305. PMID 14570712 DOI: 10.1093/Hmg/Ddg350 |
0.793 |
|
| 2003 |
Jin P, Zarnescu DC, Zhang F, Pearson CE, Lucchesi JC, Moses K, Warren ST. RNA-mediated neurodegeneration caused by the fragile X premutation rCGG repeats in Drosophila. Neuron. 39: 739-47. PMID 12948442 DOI: 10.1016/S0896-6273(03)00533-6 |
0.576 |
|
| 2003 |
Jin P, Warren ST. New insights into fragile X syndrome: From molecules to neurobehaviors Trends in Biochemical Sciences. 28: 152-158. PMID 12633995 DOI: 10.1016/S0968-0004(03)00033-1 |
0.57 |
|
| 2003 |
Ceman S, Zhang F, Johnson T, Warren ST. Development and characterization of antibodies that immunoprecipitate the FMR1 protein. Methods in Molecular Biology (Clifton, N.J.). 217: 345-54. PMID 12491946 DOI: 10.1385/1-59259-330-5:345 |
0.666 |
|
| 2002 |
D'Agata V, Warren ST, Zhao W, Torre ER, Alkon DL, Cavallaro S. Gene expression profiles in a transgenic animal model of fragile X syndrome. Neurobiology of Disease. 10: 211-8. PMID 12270684 DOI: 10.1006/Nbdi.2002.0506 |
0.436 |
|
| 2002 |
Coffee B, Zhang F, Ceman S, Warren ST, Reines D. Histone modifications depict an aberrantly heterochromatinized FMR1 gene in fragile x syndrome. American Journal of Human Genetics. 71: 923-32. PMID 12232854 DOI: 10.1086/342931 |
0.686 |
|
| 2002 |
O'Donnell WT, Warren ST. A decade of molecular studies of fragile X syndrome. Annual Review of Neuroscience. 25: 315-38. PMID 12052912 DOI: 10.1146/Annurev.Neuro.25.112701.142909 |
0.815 |
|
| 2002 |
Huber KM, Gallagher SM, Warren ST, Bear MF. 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. 99: 7746-50. PMID 12032354 DOI: 10.1073/Pnas.122205699 |
0.464 |
|
| 2002 |
Tarleton J, Kenneson A, Taylor AK, Crandall K, Fletcher R, Casey R, Hart PS, Hatton D, Fisch G, Warren ST. A single base alteration in the CGG repeat region of FMR1: Possible effects on gene expression and phenotype [4] Journal of Medical Genetics. 39: 196-200. PMID 11897823 DOI: 10.1136/Jmg.39.3.196 |
0.435 |
|
| 2001 |
Darnell JC, Jensen KB, Jin P, Brown V, Warren ST, Darnell RB. Fragile X mental retardation protein targets G quartet mRNAs important for neuronal function Cell. 107: 489-499. PMID 11719189 DOI: 10.1016/S0092-8674(01)00566-9 |
0.446 |
|
| 2001 |
Brown V, Jin P, Ceman S, Darnell JC, O'Donnell WT, Tenenbaum SA, Jin X, Feng Y, Wilkinson KD, Keene JD, Darnell RB, Warren ST. Microarray identification of FMRP-associated brain mRNAs and altered mRNA translational profiles in fragile X syndrome. Cell. 107: 477-87. PMID 11719188 DOI: 10.1016/S0092-8674(01)00568-2 |
0.807 |
|
| 2001 |
Hegde MR, Chong B, Fawkner M, Lambiris N, Peters H, Kenneson A, Warren ST, Love DR, McGaughran J. Microdeletion in the FMR-1 gene: An apparent null allele using routine clinical PCR amplification [5] Journal of Medical Genetics. 38: 624-629. PMID 11565550 DOI: 10.1136/Jmg.38.9.624 |
0.458 |
|
| 2001 |
Kenneson A, Warren ST. The female and the fragile X reviewed Seminars in Reproductive Medicine. 19: 159-165. PMID 11480913 DOI: 10.1055/S-2001-15401 |
0.409 |
|
| 2001 |
Kenneson A, Zhang F, Hagedorn CH, Warren ST. Reduced FMRP and increased FMR1 transcription is proportionally associated with CGG repeat number in intermediate-length and premutation carriers. Human Molecular Genetics. 10: 1449-54. PMID 11448936 DOI: 10.1093/Hmg/10.14.1449 |
0.45 |
|
| 2001 |
Li Z, Zhang Y, Ku L, Wilkinson KD, Warren ST, Feng Y. The fragile X mental retardation protein inhibits translation via interacting with mRNA Nucleic Acids Research. 29: 2276-2283. PMID 11376146 DOI: 10.1093/Nar/29.11.2276 |
0.411 |
|
| 2000 |
Ceman S, Nelson R, Warren ST. Identification of mouse YB1/p50 as a component of the FMRP-associated mRNP particle Biochemical and Biophysical Research Communications. 279: 904-908. PMID 11162447 DOI: 10.1006/Bbrc.2000.4035 |
0.716 |
|
| 2000 |
Crawford DC, Zhang F, Wilson B, Warren ST, Sherman SL. Fragile X CGG repeat structures among African-Americans: Identification of a novel factor responsible for repeat instability Human Molecular Genetics. 9: 1759-1769. PMID 10915764 DOI: 10.1093/Hmg/9.12.1759 |
0.37 |
|
| 2000 |
Tsui S, Dai T, Warren ST, Salido EC, Yen PH. Association of the mouse infertility factor DAZL1 with actively translating polyribosomes Biology of Reproduction. 62: 1655-1660. PMID 10819768 DOI: 10.1095/Biolreprod62.6.1655 |
0.42 |
|
| 2000 |
Peier AM, McIlwain KL, Kenneson A, Warren ST, Paylor R, Nelson DL. (Over)correction of FMR1 deficiency with YAC transgenics: behavioral and physical features. Human Molecular Genetics. 9: 1145-59. PMID 10767339 DOI: 10.1093/Hmg/9.8.1145 |
0.424 |
|
| 2000 |
Jin P, Warren ST. Understanding the molecular basis of fragile X syndrome Human Molecular Genetics. 9: 901-908. PMID 10767313 DOI: 10.1093/Hmg/9.6.901 |
0.478 |
|
| 2000 |
Crawford DC, Schwartz CE, Meadows KL, Newman JL, Taft LF, Gunter C, Brown WT, Carpenter NJ, Howard-Peebles PN, Monaghan KG, Nolin SL, Reiss AL, Feldman GL, Rohlfs EM, Warren ST, et al. 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. 66: 480-93. PMID 10677308 DOI: 10.1086/302762 |
0.67 |
|
| 1999 |
Zacharias AS, Wagener ME, Warren ST, Hopkins LC. Emery-Dreifuss muscular dystrophy. Seminars in Neurology. 19: 67-79. PMID 10711990 DOI: 10.1055/S-2008-1040827 |
0.361 |
|
| 1999 |
Paradee W, Melikian HE, Rasmussen DL, Kenneson A, Conn PJ, Warren ST. Fragile X mouse: strain effects of knockout phenotype and evidence suggesting deficient amygdala function. Neuroscience. 94: 185-92. PMID 10613508 DOI: 10.1016/S0306-4522(99)00285-7 |
0.728 |
|
| 1999 |
Ceman S, Brown V, Warren ST. 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. 19: 7925-7932. PMID 10567518 DOI: 10.1128/Mcb.19.12.7925 |
0.736 |
|
| 1999 |
Coffee B, Zhang F, Warren ST, Reines D. Acetylated histones are associated with FMR1 in normal but not fragile X-syndrome cells Nature Genetics. 22: 98-101. PMID 10319871 DOI: 10.1038/8807 |
0.335 |
|
| 1998 |
Gunter C, Paradee W, Crawford DC, Meadows KA, Newman J, Kunst CB, Nelson DL, Schwartz C, Murray A, Macpherson JN, Sherman SL, Warren ST. Re-examination of factors associated with expansion of CGG repeats using a single nucleotide polymorphism in FMR1. Human Molecular Genetics. 7: 1935-46. PMID 9811938 DOI: 10.1093/Hmg/7.12.1935 |
0.694 |
|
| 1998 |
Gunter C, Warren ST. Polymorphism in the FMR1 gene [1] Human Genetics. 103: 365-366. PMID 9799094 DOI: 10.1007/S004390050830 |
0.629 |
|
| 1998 |
Chou HH, Takematsu H, Diaz S, Iber J, Nickerson E, Wright KL, Muchmore EA, Nelson DL, Warren ST, 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. 95: 11751-6. PMID 9751737 DOI: 10.1073/Pnas.95.20.11751 |
0.327 |
|
| 1998 |
Brown V, Small K, Lakkis L, Feng Y, Gunter C, Wilkinson KD, Warren ST. Purified recombinant Fmrp exhibits selective RNA binding as an intrinsic property of the fragile X mental retardation protein Journal of Biological Chemistry. 273: 15521-15527. PMID 9624140 DOI: 10.1074/Jbc.273.25.15521 |
0.69 |
|
| 1998 |
Small K, Warren ST. Emerin deletions occurring on both Xq28 inversion backgrounds Human Molecular Genetics. 7: 135-139. PMID 9384614 DOI: 10.1093/Hmg/7.1.135 |
0.427 |
|
| 1997 |
Feng Y, Absher D, Eberhart DE, Brown V, Malter HE, Warren ST. FMRP associates with polyribosomes as an mRNP, and the I304N mutation of severe fragile X syndrome abolishes this association Molecular Cell. 1: 109-118. PMID 9659908 DOI: 10.1016/S1097-2765(00)80012-X |
0.435 |
|
| 1997 |
Kenneson A, Cramer DW, Warren ST. Fragile X premutations are not a major cause of early menopause American Journal of Human Genetics. 61: 1362-1369. PMID 9399905 DOI: 10.1086/301647 |
0.361 |
|
| 1997 |
Losekoot M, Hoogendoorn E, Olmer R, Jansen CC, Oosterwijk JC, van den Ouweland AM, Halley DJ, Warren ST, Willemsen R, Oostra BA, 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. 34: 924-6. PMID 9391887 DOI: 10.1136/Jmg.34.11.924 |
0.459 |
|
| 1997 |
Kunst CB, Leeflang EP, Iber JC, Arnheim N, Warren ST. The effect of FMR1 CGG repeat interruptions on mutation frequency as measured by sperm typing Journal of Medical Genetics. 34: 627-631. PMID 9279752 DOI: 10.1136/Jmg.34.8.627 |
0.367 |
|
| 1997 |
Small K, Iber J, Warren ST. Emerin deletion reveals a common X-chromosome inversion mediated by inverted repeats Nature Genetics. 16: 96-99. PMID 9140403 DOI: 10.1038/Ng0597-96 |
0.412 |
|
| 1997 |
Warren ST, Timmie WP. Trinucleotide repetition and fragile X syndrome Hospital Practice. 32: 73-98. PMID 9109809 DOI: 10.1080/21548331.1997.11443466 |
0.396 |
|
| 1997 |
Small K, Wagener M, Warren ST. Isolation and characterization of the complete mouse emerin gene Mammalian Genome. 8: 337-341. PMID 9107678 DOI: 10.1007/S003359900435 |
0.374 |
|
| 1997 |
Feng Y, Gutekunst CA, Eberhart DE, Yi H, Warren ST, Hersch SM. Fragile X mental retardation protein: nucleocytoplasmic shuttling and association with somatodendritic ribosomes. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 17: 1539-47. PMID 9030614 DOI: 10.1523/Jneurosci.17-05-01539.1997 |
0.431 |
|
| 1997 |
Malter HE, Iber JC, Willemsen R, De Graaff E, Tarleton JC, Leisti J, Warren ST, Oostra BA. Characterization of the full fragile X syndrome mutation in fetal gametes Nature Genetics. 15: 165-169. PMID 9020841 DOI: 10.1038/Ng0297-165 |
0.387 |
|
| 1996 |
Eberhart DE, Warren ST. Nuclease sensitivity of permeabilized cells confirms altered chromatin formation at the fragile X locus Somatic Cell and Molecular Genetics. 22: 435-441. PMID 9131013 DOI: 10.1007/Bf02369435 |
0.436 |
|
| 1996 |
Lachiewicz AM, Spiridigliozzi GA, McConkie-Rosell A, Burgess D, Feng Y, Warren ST, 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. 64: 278-282. PMID 8844065 DOI: 10.1002/(Sici)1096-8628(19960809)64:2<278::Aid-Ajmg9>3.0.Co;2-Q |
0.431 |
|
| 1996 |
Eberhart DE, Malter HE, Feng Y, Warren ST. The fragile X mental retardation protein is a ribonucleoprotein containing both nuclear localization and nuclear export signals Human Molecular Genetics. 5: 1083-1091. PMID 8842725 DOI: 10.1093/Hmg/5.8.1083 |
0.43 |
|
| 1996 |
DiMarco SP, Glover TW, Miller DE, Reines D, Warren ST. Transcription elongation factor SII (TCEA) maps to human chromosome 3p22 → p21.3 Genomics. 36: 185-188. PMID 8812434 DOI: 10.1006/Geno.1996.0443 |
0.323 |
|
| 1996 |
Price DK, Zhang F, Ashley CT, Warren ST. The chicken FMR1 gene is highly conserved with a CCT 5′-untranslated repeat and encodes an RNA-binding protein Genomics. 31: 3-12. PMID 8808273 DOI: 10.1006/Geno.1996.0002 |
0.442 |
|
| 1996 |
Eberhart DE, Warren ST. The Molecular Basis Of Fragile X Syndrome Cold Spring Harbor Symposia On Quantitative Biology. 61: 679-687. DOI: 10.1101/Sqb.1996.061.01.068 |
0.382 |
|
| 1995 |
Kirchgessner CU, Warren ST, Willard HF. X inactivation of the FMR1 fragile X mental retardation gene Journal of Medical Genetics. 32: 925-929. PMID 8825916 DOI: 10.1136/Jmg.32.12.925 |
0.63 |
|
| 1995 |
Ashley CT, Warren ST. Trinucleotide repeat expansion and human disease Annual Review of Genetics. 29: 703-728. PMID 8825491 DOI: 10.1146/Annurev.Ge.29.120195.003415 |
0.381 |
|
| 1995 |
Feng Y, Zhang F, Lokey LK, Chastain JL, Lakkis L, Eberhart D, Warren ST. Translational suppression by trinucleotide repeat expansion at FMR1 Science. 268: 731-734. PMID 7732383 DOI: 10.1126/Science.7732383 |
0.417 |
|
| 1995 |
Warren ST, Ashley CT. Triplet repeat expansion mutations: The example of fragile X syndrome Annual Review of Neuroscience. 18: 77-99. PMID 7605075 DOI: 10.1146/Annurev.Ne.18.030195.000453 |
0.379 |
|
| 1995 |
Eichler EE, Kunst CB, Lugenbeel KA, Ryder OA, Davison D, Warren ST, Nelson DL. Evolution of the cryptic FMR1 CGG repeat. Nature Genetics. 11: 301-8. PMID 7581454 DOI: 10.1038/Ng1195-301 |
0.317 |
|
| 1995 |
Small K, Warren ST. Analysis of FMRP, the protein deficient in fragile X syndrome Mental Retardation and Developmental Disabilities Research Reviews. 1: 245-250. DOI: 10.1002/Mrdd.1410010404 |
0.476 |
|
| 1994 |
Riggins GJ, Zhang F, Warren ST. Lack of imprinting of BCR Nature Genetics. 6: 226. PMID 8012382 DOI: 10.1038/Ng0394-226 |
0.542 |
|
| 1994 |
Kunst CB, Warren ST. Cryptic and polar variation of the fragile X repeat could result in predisposing normal alleles Cell. 77: 853-861. PMID 7911740 DOI: 10.1016/0092-8674(94)90134-1 |
0.411 |
|
| 1994 |
Ouweland AMwVD, Deelen WH, Kunst CB, Uzielli MLG, Nelson DL, Warren ST, Oostra BA, Halley DJJ. Loss of mutation at the FMR1 locus through multiple exchanges between maternal X chromosomes Human Molecular Genetics. 3: 1823-1827. PMID 7849707 DOI: 10.1093/Hmg/3.10.1823 |
0.446 |
|
| 1994 |
Riggins GJ, Sherman SL, Phillips CN, Stock W, Westbrook CA, Warren ST. CGG-repeat polymorphism of the BCR gene rules out predisposing alleles leading to the Philadelphia chromosome. Genes, Chromosomes & Cancer. 9: 141-4. PMID 7513545 DOI: 10.1002/Gcc.2870090211 |
0.57 |
|
| 1994 |
Warren ST, Nelson DL. Advances in Molecular Analysis of Fragile X Syndrome Jama: the Journal of the American Medical Association. 271: 536-542. DOI: 10.1001/Jama.1994.03510310066040 |
0.461 |
|
| 1993 |
Hinds HL, Ashley CT, Sutcliffe JS, Nelson DL, Warren ST, Housman DE, Schalling M. Tissue specific expression of FMR-1 provides evidence for a functional role in fragile X syndrome. Nature Genetics. 3: 36-43. PMID 8490651 DOI: 10.1038/Ng0193-36 |
0.623 |
|
| 1993 |
Smits APT, Dreesen JCFM, Post JG, Smeets DFCM, De Die-Smulders C, Spaans-Van Der Bijl T, Govaerts LCP, Warren ST, Oostra BA, Van Oost BA. The fragile X syndrome: No evidence for any recent mutations Journal of Medical Genetics. 30: 94-96. PMID 8445628 DOI: 10.1136/Jmg.30.2.94 |
0.417 |
|
| 1993 |
Gorlin JB, Henske E, Warren ST, Kunst CB, D'Urso M, Palmieri G, Hartwig JH, Bruns G, Kwiatkowski DJ. Actin-Binding Protein (ABP-280) Filamin Gene (FLN) Maps Telomeric to the Color Vision Locus (R/GCP) and Centromeric to G6PD in Xq28 Genomics. 17: 496-498. PMID 8406501 DOI: 10.1006/Geno.1993.1354 |
0.303 |
|
| 1993 |
Ashley CT, Sutcliffe JS, Kunst CB, Leiner HA, Eichler EE, Nelson DL, Warren ST. Human and murine FMR-1: alternative splicing and translational initiation downstream of the CGG-repeat. Nature Genetics. 4: 244-51. PMID 8358432 DOI: 10.1038/Ng0793-244 |
0.629 |
|
| 1993 |
Hornstra LK, Nelson DL, Warren ST, Yang TP. High resolution methylation analysis of the FMR1 gene trinucleotide repeat region in fragile X syndrome Human Molecular Genetics. 2: 1659-1665. PMID 8268919 DOI: 10.1093/hmg/2.10.1659 |
0.347 |
|
| 1993 |
Warren ST, Nelson DL. Trinucleotide repeat expansions in neurological disease Current Opinion in Neurobiology. 3: 752-759. PMID 8260825 DOI: 10.1016/0959-4388(93)90149-S |
0.336 |
|
| 1993 |
Ashley CT, Wilkinson KD, Reines D, Warren ST. FMR1 protein: Conserved RNP family domains and selective RNA binding Science. 262: 563-566. PMID 7692601 DOI: 10.1126/Science.7692601 |
0.421 |
|
| 1993 |
Hinds HL, Ashley CT, Sutcliffe JS, Nelson DL, Warren ST, Housman DE, Schalling M. Erratum: Corrigendum: Tissue specific expression of FMR–1 provides evidence for a functional role in fragile X syndrome Nature Genetics. 5: 312-312. DOI: 10.1038/Ng1193-312B |
0.615 |
|
| 1993 |
Riggins GJ, Lokey LK, Chastain JL, Leiner HA, Sherman SL, Wilkinson KD, Warren ST. Erratum: Corrigendum: Human genes containing polymorphic trinucleotide repeats Nature Genetics. 3: 273-273. DOI: 10.1038/Ng0393-273B |
0.559 |
|
| 1992 |
Traupe H, van den Ouweland AMW, van Oost BA, Vogel W, Vetter U, Warren ST, Rocchi M, Darlison MG, Ropers HH. Fine mapping of the human biglycan (BGN) gene within the Xq28 region employing a hybrid cell panel Genomics. 13: 481-483. PMID 1612609 DOI: 10.1016/0888-7543(92)90279-2 |
0.36 |
|
| 1992 |
Riggins GJ, Sherman SL, Oostra BA, Sutcliffe JS, Feitell D, Nelson DL, Van Oost BA, Smits APT, Ramos FJ, Pfendner E, Kuhl DPA, Caskey CT, Warren ST. Characterization of a highly polymorphic dinucleotide repeat 150 kb proximal to the fragile X site American Journal of Medical Genetics. 43: 237-243. PMID 1605197 DOI: 10.1002/Ajmg.1320430138 |
0.745 |
|
| 1992 |
Verkerk AJ, deVries BB, Niermeijer MF, Fu YH, Nelson DL, Warren ST, Majoor-Krakauer DF, Halley DJ, Oostra BA. Intragenic probe used for diagnostics in fragile X families. American Journal of Medical Genetics. 43: 192-6. PMID 1605192 DOI: 10.1002/Ajmg.1320430132 |
0.326 |
|
| 1992 |
Consalez GG, Stayton CL, Freimer NB, Goonewardena P, Brown WT, Gilliam TC, Warren ST. Isolation and characterization of a highly polymorphic human locus (DXS455) in proximal Xq28 Genomics. 12: 710-714. PMID 1572645 DOI: 10.1016/0888-7543(92)90299-8 |
0.351 |
|
| 1992 |
Sutcliffe JS, Zhang F, Caskey CT, Nelson DL, Warren ST. PCR amplification and analysis of yeast artificial chromosomes. Genomics. 13: 1303-6. PMID 1380485 DOI: 10.1016/0888-7543(92)90051-S |
0.595 |
|
| 1992 |
Riggins GJ, Lokey LK, Chastain JL, Leiner HA, Sherman SL, Wilkinson KD, Warren ST. Human genes containing polymorphic trinucleotide repeats Nature Genetics. 2: 186-191. PMID 1345166 DOI: 10.1038/Ng1192-186 |
0.61 |
|
| 1992 |
Riggins GJ, Lokey LK, Warren ST. CCG repeat polymorphism at the c-Ha-ras oncogene locus Human Molecular Genetics. 1: 775. PMID 1302617 DOI: 10.1093/Hmg/1.9.775 |
0.509 |
|
| 1992 |
Sutcliffe JS, Nelson DL, Zhang F, Pieretti M, Caskey CT, Saxe D, Warren ST. DNA methylation represses FMR-1 transcription in fragile X syndrome. Human Molecular Genetics. 1: 397-400. PMID 1301913 DOI: 10.1093/hmg/1.6.397 |
0.635 |
|
| 1991 |
Yu S, Pritchard M, Kremer E, Lynch M, Nancarrow J, Baker E, Holman K, Mulley JC, Warren ST, Schlessinger D. Fragile X genotype characterized by an unstable region of DNA. Science (New York, N.Y.). 252: 1179-81. PMID 2031189 DOI: 10.1126/Science.252.5009.1179 |
0.38 |
|
| 1991 |
Poustka A, Dietrich A, Langenstein G, Toniolo D, Warren ST, 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. 88: 8302-8306. PMID 1924290 DOI: 10.1073/Pnas.88.19.8302 |
0.373 |
|
| 1991 |
Pieretti M, Zhang FP, Fu YH, Warren ST, Oostra BA, Caskey CT, Nelson DL. Absence of expression of the FMR-1 gene in fragile X syndrome. Cell. 66: 817-22. PMID 1878973 DOI: 10.1016/0092-8674(91)90125-I |
0.432 |
|
| 1991 |
Fu YH, Kuhl DP, Pizzuti A, Pieretti M, Sutcliffe JS, Richards S, Verkerk AJ, Holden JJ, Fenwick RG, Warren ST. Variation of the CGG repeat at the fragile X site results in genetic instability: resolution of the Sherman paradox. Cell. 67: 1047-58. PMID 1760838 DOI: 10.1016/0092-8674(91)90283-5 |
0.638 |
|
| 1991 |
Kremer EJ, Pritchard M, Lynch M, Yu S, Holman K, Baker E, Warren ST, Schlessinger D, Sutherland GR, Richards RI. Mapping of DNA instability at the fragile X to a trinucleotide repeat sequence p(CCG)n. Science (New York, N.Y.). 252: 1711-4. PMID 1675488 DOI: 10.1126/Science.1675488 |
0.354 |
|
| 1990 |
Warren ST, Knight SJL, Peters JF, Stayton CL, Consalez GG, Zhang F. 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. 87: 3856-3860. PMID 2339126 DOI: 10.1073/Pnas.87.10.3856 |
0.39 |
|
| 1990 |
Ledbetter SA, Nelson DL, Warren ST, Ledbetter DH. Rapid isolation of DNA probes within specific chromosome regions by interspersed repetitive sequence polymerase chain reaction Genomics. 6: 475-481. PMID 2328990 DOI: 10.1016/0888-7543(90)90477-C |
0.343 |
|
| 1990 |
Willems PJ, Dijkstra I, Van der Auwera BJ, Vits L, Coucke P, Raeymaekers P, Van Broeckhoven C, Consalez GG, Freeman SB, Warren ST, Brouwer OF, Brunner HG, Renier WO, Van Elsen AF, Dumon JE. Assignment of X-linked hydrocephalus to Xq28 by linkage analysis Genomics. 8: 367-370. PMID 1979056 DOI: 10.1016/0888-7543(90)90294-5 |
0.354 |
|
| 1989 |
El-Fouly MH, Trosko JE, Chang CC, Warren ST. Potential role of the human Ha-ras oncogene in the inhibition of gap junctional intercellular communication Molecular Carcinogenesis. 2: 131-135. PMID 2675903 DOI: 10.1002/Mc.2940020305 |
0.486 |
|
| 1988 |
Warren ST. Fragile X syndrome: A hypothesis regarding the molecular mechanism of the phenotype American Journal of Medical Genetics. 30: 681-688. PMID 3177478 DOI: 10.1002/Ajmg.1320300169 |
0.449 |
|
| 1988 |
Warren ST, Zhang F, Sutcliffe JS, Peters JF. Strategy for molecular cloning of the fragile X site DNA American Journal of Medical Genetics. 30: 613-623. PMID 3177473 DOI: 10.1002/Ajmg.1320300162 |
0.638 |
|
| 1987 |
Warren ST, Zhang F, Licameli GR, Peters JF. The fragile X site in somatic cell hybrids: An approach for molecular cloning of fragile sites Science. 237: 420-423. PMID 3603029 DOI: 10.1126/Science.3603029 |
0.399 |
|
| 1985 |
Warren ST, Glover TW, Davidson RL, Jagadeeswaran P. Linkage and recombination between fragile X-linked mental retardation and the factor IX gene. Human Genetics. 69: 44-6. PMID 3967889 DOI: 10.1007/Bf00295528 |
0.637 |
|
| 1985 |
Smith GF, Warren ST. The biology of Down syndrome. Annals of the New York Academy of Sciences. 450: 1-9. PMID 2990308 DOI: 10.1111/J.1749-6632.1985.Tb21478.X |
0.373 |
|
| 1984 |
Warren ST, Davidson RL. Expression of fragile X chromosome in human-rodent somatic cell hybrids. Somatic Cell and Molecular Genetics. 10: 409-13. PMID 6589793 DOI: 10.1007/Bf01535636 |
0.64 |
|
| 1984 |
Jagadeeswaran P, Lavelle DE, Kaul R, Mohandas T, Warren ST. Isolation and characterization of human factor IX cDNA: Identification of Taq I polymorphism and regional assignment Somatic Cell and Molecular Genetics. 10: 465-473. PMID 6089357 DOI: 10.1007/Bf01534851 |
0.33 |
|
| 1982 |
Warren ST, Dolittle DJ, Chang Cc, Goodman JI, Trosko JE. Evaluation of the carcinogenic potential of 2,4-dinitrofluorobenzene and its implications regarding mutagenicity testing Carcinogenesis. 3: 139-145. PMID 7039854 DOI: 10.1093/Carcin/3.2.139 |
0.503 |
|
| 1982 |
Chang CC, Boezi JA, Warren ST, Sabourin CLK, Liu PK, Glatzer L, Trosko JE. Isolation and characterization of a UV-sensitive hypermutable aphidicolin-resistant Chinese hamster cell line Somatic Cell Genetics. 7: 235-253. PMID 6794164 DOI: 10.1007/Bf01567660 |
0.473 |
|
| 1981 |
Warren ST, Yotti LP, Moskal JR, Chang CC, Trosko JE. Metabolic cooperation in CHO and V79 cells following treatment with a tumor promoter Experimental Cell Research. 131: 427-430. PMID 7202544 DOI: 10.1016/0014-4827(81)90250-0 |
0.477 |
|
| 1981 |
Warren ST, Schultz RA, Chang CC, Wade MH, Trosko JE. Elevated spontaneous mutation rate in Bloom syndrome fibroblasts Proceedings of the National Academy of Sciences of the United States of America. 78: 3133-3137. PMID 6942420 DOI: 10.1073/Pnas.78.5.3133 |
0.556 |
|
| 1980 |
Toriello HV, Warren ST, Lindstrom JA. Possible X-linked anencephaly and spina bifida: Report of a kindred American Journal of Medical Genetics. 6: 119-121. PMID 7004185 DOI: 10.1002/Ajmg.1320060205 |
0.343 |
|
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