| Year |
Citation |
Score |
| 2021 |
Hagerman RJ, Hagerman PJ. Fragile X Syndrome: Lessons Learned and What New Treatment Avenues Are on the Horizon. Annual Review of Pharmacology and Toxicology. PMID 34499526 DOI: 10.1146/annurev-pharmtox-052120-090147 |
0.321 |
|
| 2021 |
Tassanakijpanich N, McKenzie F, McLennan YA, Makhoul E, Tassone F, Jasoliya MJ, Romney C, Petrasic IC, Napalinga K, Buchanan CB, Hagerman P, Hagerman R, Casanova EL. Hypermobile Ehlers-Danlos syndrome (hEDS) phenotype in fragile X premutation carriers: case series. Journal of Medical Genetics. PMID 34193467 DOI: 10.1136/jmedgenet-2020-107609 |
0.326 |
|
| 2021 |
Hagerman PJ, Hagerman R. Fragile X syndrome. Current Biology : Cb. 31: R273-R275. PMID 33756134 DOI: 10.1016/j.cub.2021.01.043 |
0.328 |
|
| 2020 |
Schneider A, Summers S, Tassone F, Seritan A, Hessl D, Hagerman P, Hagerman R. Women with Fragile X-associated Tremor/Ataxia Syndrome. Movement Disorders Clinical Practice. 7: 910-919. PMID 33163562 DOI: 10.1002/Mdc3.13084 |
0.448 |
|
| 2020 |
Schneider A, Winarni TI, Cabal-Herrera AM, Bacalman S, Gane L, Hagerman P, Tassone F, Hagerman R. Elevated FMR1-mRNA and lowered FMRP - A double-hit mechanism for psychiatric features in men with FMR1 premutations. Translational Psychiatry. 10: 205. PMID 32576818 DOI: 10.1038/S41398-020-00863-W |
0.498 |
|
| 2020 |
Ma L, Hagerman PJ. Autofluorescence-based analyses of intranuclear inclusions of Fragile X-associated tremor/ataxia syndrome. Biotechniques. PMID 32486839 DOI: 10.2144/Btn-2019-0144 |
0.372 |
|
| 2020 |
Santos E, Emeka-Nwonovo C, Wang JY, Schneider A, Tassone F, Hagerman P, Hagerman R. Developmental aspects of FXAND in a man with the FMR1 premutation. Molecular Genetics & Genomic Medicine. e1050. PMID 31899609 DOI: 10.1002/Mgg3.1050 |
0.389 |
|
| 2019 |
Kim K, Hessl D, Randol JL, Espinal GM, Schneider A, Protic D, Aydin EY, Hagerman RJ, Hagerman PJ. Association between IQ and FMR1 protein (FMRP) across the spectrum of CGG repeat expansions. Plos One. 14: e0226811. PMID 31891607 DOI: 10.1371/Journal.Pone.0226811 |
0.462 |
|
| 2019 |
Ma L, Herren AW, Espinal G, Randol J, McLaughlin B, Martinez-Cerdeño V, Pessah IN, Hagerman RJ, Hagerman PJ. Composition of the Intranuclear Inclusions of Fragile X-associated Tremor/Ataxia Syndrome. Acta Neuropathologica Communications. 7: 143. PMID 31481131 DOI: 10.1186/S40478-019-0796-1 |
0.425 |
|
| 2019 |
Wenzel HJ, Murray KD, Haify SN, Hunsaker MR, Schwartzer JJ, Kim K, La Spada AR, Sopher BL, Hagerman PJ, Raske C, Severijnen LWFM, Willemsen R, Hukema RK, Berman RF. Astroglial-targeted expression of the fragile X CGG repeat premutation in mice yields RAN translation, motor deficits and possible evidence for cell-to-cell propagation of FXTAS pathology. Acta Neuropathologica Communications. 7: 27. PMID 30808398 DOI: 10.1186/S40478-019-0677-7 |
0.439 |
|
| 2018 |
Martínez Cerdeño V, Hong T, Amina S, Lechpammer M, Ariza J, Tassone F, Noctor SC, Hagerman P, Hagerman R. Microglial cell activation and senescence are characteristic of the pathology FXTAS. Movement Disorders : Official Journal of the Movement Disorder Society. PMID 30537011 DOI: 10.1002/Mds.27553 |
0.479 |
|
| 2018 |
Ramírez-Cheyne JA, Duque GA, Ayala-Zapata S, Saldarriaga-Gil W, Hagerman P, Hagerman R, Payán-Gómez C. FRAGILE X SYNDROME AND CONNECTIVE TISSUE CONNECTIVE TISSUE DEFICITS IN FRAGILE X SYNDROME. Clinical Genetics. PMID 30414172 DOI: 10.1111/Cge.13469 |
0.407 |
|
| 2017 |
Jiraanont P, Sweha SR, AlOlaby RR, Silva M, Tang HT, Durbin-Johnson B, Schneider A, Espinal GM, Hagerman PJ, Rivera SM, Hessl D, Hagerman RJ, Chutabhakdikul N, Tassone F. Clinical and molecular correlates in fragile X premutation females. Eneurologicalsci. 7: 49-56. PMID 28971146 DOI: 10.1016/J.Ensci.2017.04.003 |
0.395 |
|
| 2017 |
Hagerman RJ, Berry-Kravis E, Hazlett HC, Bailey DB, Moine H, Kooy RF, Tassone F, Gantois I, Sonenberg N, Mandel JL, Hagerman PJ. Fragile X syndrome. Nature Reviews. Disease Primers. 3: 17065. PMID 28960184 DOI: 10.1038/nrdp.2017.65 |
0.369 |
|
| 2017 |
Jiraanont P, Kumar M, Tang HT, Espinal G, Hagerman PJ, Hagerman RJ, Chutabhakdikul N, Tassone F. Size and methylation mosaicism in males with Fragile X syndrome. Expert Review of Molecular Diagnostics. PMID 28929824 DOI: 10.1080/14737159.2017.1377612 |
0.424 |
|
| 2017 |
Lechpammer M, Martínez Cerdeńo V, Hunsaker MR, Hah M, Gonzales H, Tisch S, Joffe R, Pamphlett R, Tassone F, Hagerman PJ, Bolitho SJ, Hagerman RJ. Concomitant occurrence of FXTAS and clinically defined sporadic inclusion body myositis: report of two cases. Croatian Medical Journal. 58: 310-315. PMID 28857524 DOI: 10.3325/Cmj.2017.58.310 |
0.376 |
|
| 2017 |
Martínez-Cerdeño V, Lechpammer M, Noctor S, Ariza J, Hagerman P, Hagerman R. FMR1 premutation with Prader-Willi phenotype and fragile X-associated tremor/ataxia syndrome. Clinical Case Reports. 5: 625-629. PMID 28469864 DOI: 10.1002/Ccr3.834 |
0.421 |
|
| 2017 |
Robin G, López JR, Espinal GM, Hulsizer S, Hagerman PJ, Pessah IN. Calcium dysregulation and Cdk5-ATM pathway involved in a mouse model of Fragile X-associated tremor-ataxia syndrome. Human Molecular Genetics. PMID 28444183 DOI: 10.1093/Hmg/Ddx148 |
0.398 |
|
| 2017 |
Ariza J, Rogers H, Hartvigsen A, Snell M, Dill M, Judd D, Hagerman P, Martínez-Cerdeño V. Iron accumulation and dysregulation in the putamen in fragile X-associated tremor/ataxia syndrome. Movement Disorders : Official Journal of the Movement Disorder Society. PMID 28233916 DOI: 10.1002/Mds.26902 |
0.413 |
|
| 2016 |
Hagerman RJ, Hagerman P. Fragile X-associated tremor/ataxia syndrome - features, mechanisms and management. Nature Reviews. Neurology. 12: 403-12. PMID 27340021 DOI: 10.1038/Nrneurol.2016.82 |
0.471 |
|
| 2016 |
Kashima R, Roy S, Ascano M, Martinez-Cerdeno V, Ariza-Torres J, Kim S, Louie J, Lu Y, Leyton P, Bloch KD, Kornberg TB, Hagerman PJ, Hagerman R, Lagna G, Hata A. Augmented noncanonical BMP type II receptor signaling mediates the synaptic abnormality of fragile X syndrome. Science Signaling. 9: ra58. PMID 27273096 DOI: 10.1126/Scisignal.Aaf6060 |
0.423 |
|
| 2016 |
Ariza J, Rogers H, Monterrubio A, Reyes-Miranda A, Hagerman PJ, Martínez-Cerdeño V. A Majority of FXTAS Cases Present with Intranuclear Inclusions Within Purkinje Cells. Cerebellum (London, England). PMID 27108270 DOI: 10.1007/S12311-016-0776-Y |
0.355 |
|
| 2016 |
Pham TT, Yin J, Eid JS, Adams E, Lam R, Turner SW, Loomis EW, Wang JY, Hagerman PJ, Hanes JW. Single-locus enrichment without amplification for sequencing and direct detection of epigenetic modifications. Molecular Genetics and Genomics : Mgg. PMID 26825750 DOI: 10.1007/S00438-016-1167-2 |
0.79 |
|
| 2016 |
Robin G, López JR, Hulsizer S, Hagerman PJ, Pessah IN. Fragile X-Associated Tremor-Ataxia Syndrome: Linking Ca2+ Dysregulation and DNA Damage Responses Biophysical Journal. 110: 319a-320a. DOI: 10.1016/J.Bpj.2015.11.1715 |
0.361 |
|
| 2015 |
Hukema RK, Buijsen RA, Schonewille M, Raske C, Severijnen LA, Nieuwenhuizen-Bakker I, Verhagen RF, van Dessel L, Maas A, Charlet-Berguerand N, De Zeeuw CI, Hagerman PJ, Berman RF, Willemsen R. Reversibility of neuropathology and motor deficits in an inducible mouse model for FXTAS. Human Molecular Genetics. PMID 26060190 DOI: 10.1093/Hmg/Ddv216 |
0.417 |
|
| 2015 |
Hagerman PJ, Hagerman RJ. Fragile X-associated tremor/ataxia syndrome. Annals of the New York Academy of Sciences. 1338: 58-70. PMID 25622649 DOI: 10.1111/Nyas.12693 |
0.512 |
|
| 2015 |
Ariza J, Steward C, Rueckert F, Widdison M, Coffman R, Afjei A, Noctor SC, Hagerman R, Hagerman P, Martínez-Cerdeño V. Dysregulated iron metabolism in the choroid plexus in fragile X-associated tremor/ataxia syndrome. Brain Research. 1598: 88-96. PMID 25498860 DOI: 10.1016/J.Brainres.2014.11.058 |
0.367 |
|
| 2015 |
Pretto DI, Eid JS, Yrigollen CM, Tang HT, Loomis EW, Raske C, Durbin-Johnson B, Hagerman PJ, Tassone F. Differential increases of specific FMR1 mRNA isoforms in premutation carriers. Journal of Medical Genetics. 52: 42-52. PMID 25358671 DOI: 10.1136/Jmedgenet-2014-102593 |
0.816 |
|
| 2014 |
Hukema RK, Buijsen RA, Raske C, Severijnen LA, Nieuwenhuizen-Bakker I, Minneboo M, Maas A, de Crom R, Kros JM, Hagerman PJ, Berman RF, Willemsen R. Induced expression of expanded CGG RNA causes mitochondrial dysfunction in vivo. Cell Cycle (Georgetown, Tex.). 13: 2600-8. PMID 25486200 DOI: 10.4161/15384101.2014.943112 |
0.394 |
|
| 2014 |
Pretto D, Yrigollen CM, Tang HT, Williamson J, Espinal G, Iwahashi CK, Durbin-Johnson B, Hagerman RJ, Hagerman PJ, Tassone F. Clinical and molecular implications of mosaicism in FMR1 full mutations. Frontiers in Genetics. 5: 318. PMID 25278957 DOI: 10.3389/Fgene.2014.00318 |
0.383 |
|
| 2014 |
Tassone F, Hagerman PJ, Hagerman RJ. Fragile x premutation. Journal of Neurodevelopmental Disorders. 6: 22. PMID 25170346 DOI: 10.1186/1866-1955-6-22 |
0.453 |
|
| 2014 |
Yang JC, Chi L, Teichholtz S, Schneider A, Nanakul R, Nowacki R, Seritan A, Reed B, DeCarli C, Iragui VJ, Kutas M, Hagerman PJ, Hagerman RJ, Olichney JM. ERP abnormalities elicited by word repetition in fragile X-associated tremor/ataxia syndrome (FXTAS) and amnestic MCI. Neuropsychologia. 63: 34-42. PMID 25111034 DOI: 10.1016/J.Neuropsychologia.2014.08.001 |
0.419 |
|
| 2014 |
Yang JC, Niu YQ, Simon C, Seritan AL, Chen L, Schneider A, Moghaddam ST, Hagerman PJ, Hagerman RJ, Olichney JM. Memantine effects on verbal memory in fragile X-associated tremor/ataxia syndrome (FXTAS): a double-blind brain potential study. Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology. 39: 2760-8. PMID 24871547 DOI: 10.1038/Npp.2014.122 |
0.315 |
|
| 2014 |
Juang BT, Ludwig AL, Benedetti KL, Gu C, Collins K, Morales C, Asundi A, Wittmann T, L'Etoile N, Hagerman PJ. Expression of an expanded CGG-repeat RNA in a single pair of primary sensory neurons impairs olfactory adaptation in Caenorhabditis elegans. Human Molecular Genetics. 23: 4945-59. PMID 24821701 DOI: 10.1093/Hmg/Ddu210 |
0.757 |
|
| 2014 |
Loomis EW, Sanz LA, Chédin F, Hagerman PJ. Transcription-associated R-loop formation across the human FMR1 CGG-repeat region. Plos Genetics. 10: e1004294. PMID 24743386 DOI: 10.1371/Journal.Pgen.1004294 |
0.802 |
|
| 2014 |
Ludwig AL, Espinal GM, Pretto DI, Jamal AL, Arque G, Tassone F, Berman RF, Hagerman PJ. CNS expression of murine fragile X protein (FMRP) as a function of CGG-repeat size. Human Molecular Genetics. 23: 3228-38. PMID 24463622 DOI: 10.1093/Hmg/Ddu032 |
0.789 |
|
| 2014 |
Seritan AL, Nguyen DV, Mu Y, Tassone F, Bourgeois JA, Schneider A, Cogswell JB, Cook KR, Leehey MA, Grigsby J, Olichney JM, Adams PE, Legg W, Zhang L, Hagerman PJ, et al. Memantine for fragile X-associated tremor/ataxia syndrome: a randomized, double-blind, placebo-controlled trial. The Journal of Clinical Psychiatry. 75: 264-71. PMID 24345444 DOI: 10.4088/Jcp.13M08546 |
0.302 |
|
| 2014 |
Yang JC, Simon C, Schneider A, Seritan AL, Hamilton L, Hagerman PJ, Hagerman RJ, Olichney JM. Abnormal semantic processing in females with fragile X-associated tremor/ataxia syndrome. Genes, Brain, and Behavior. 13: 152-62. PMID 24299169 DOI: 10.1111/Gbb.12114 |
0.349 |
|
| 2013 |
Hagerman R, Hagerman P. Advances in clinical and molecular understanding of the FMR1 premutation and fragile X-associated tremor/ataxia syndrome. The Lancet. Neurology. 12: 786-98. PMID 23867198 DOI: 10.1016/S1474-4422(13)70125-X |
0.491 |
|
| 2013 |
Hagerman PJ. Fragile X-associated tremor/ataxia syndrome (FXTAS): Pathology and mechanisms Acta Neuropathologica. 126: 1-19. PMID 23793382 DOI: 10.1007/S00401-013-1138-1 |
0.441 |
|
| 2013 |
Pretto DI, Hunsaker MR, Cunningham CL, Greco CM, Hagerman RJ, Noctor SC, Hall DA, Hagerman PJ, Tassone F. Intranuclear inclusions in a fragile X mosaic male. Translational Neurodegeneration. 2: 10. PMID 23692864 DOI: 10.1186/2047-9158-2-10 |
0.505 |
|
| 2013 |
Yang JC, Simon C, Niu YQ, Bogost M, Schneider A, Tassone F, Seritan A, Grigsby J, Hagerman PJ, Hagerman RJ, Olichney JM. Phenotypes of hypofrontality in older female fragile X premutation carriers. Annals of Neurology. 74: 275-83. PMID 23686745 DOI: 10.1002/Ana.23933 |
0.367 |
|
| 2013 |
Cao Z, Hulsizer S, Cui Y, Pretto DL, Kim KH, Hagerman PJ, Tassone F, Pessah IN. Enhanced asynchronous Ca(2+) oscillations associated with impaired glutamate transport in cortical astrocytes expressing Fmr1 gene premutation expansion. The Journal of Biological Chemistry. 288: 13831-41. PMID 23553633 DOI: 10.1074/Jbc.M112.441055 |
0.353 |
|
| 2013 |
Sellier C, Freyermuth F, Tabet R, Tran T, He F, Ruffenach F, Alunni V, Moine H, Thibault C, Page A, Tassone F, Willemsen R, Disney MD, Hagerman PJ, Todd PK, et al. Sequestration of DROSHA and DGCR8 by expanded CGG RNA repeats alters microRNA processing in fragile X-associated tremor/ataxia syndrome. Cell Reports. 3: 869-80. PMID 23478018 DOI: 10.1016/J.Celrep.2013.02.004 |
0.421 |
|
| 2013 |
Loomis EW, Eid JS, Peluso P, Yin J, Hickey L, Rank D, McCalmon S, Hagerman RJ, Tassone F, Hagerman PJ. Sequencing the unsequenceable: expanded CGG-repeat alleles of the fragile X gene. Genome Research. 23: 121-8. PMID 23064752 DOI: 10.1101/Gr.141705.112 |
0.809 |
|
| 2013 |
Wang JY, Hessl D, Iwahashi C, Cheung K, Schneider A, Hagerman RJ, Hagerman PJ, Rivera SM. Influence of the fragile X mental retardation (FMR1) gene on the brain and working memory in men with normal FMR1 alleles. Neuroimage. 65: 288-98. PMID 23063447 DOI: 10.1016/J.Neuroimage.2012.09.075 |
0.319 |
|
| 2013 |
Yang JC, Chan SH, Khan S, Schneider A, Nanakul R, Teichholtz S, Niu YQ, Seritan A, Tassone F, Grigsby J, Hagerman PJ, Hagerman RJ, Olichney JM. Neural substrates of executive dysfunction in fragile X-associated tremor/ataxia syndrome (FXTAS): a brain potential study. Cerebral Cortex (New York, N.Y. : 1991). 23: 2657-66. PMID 22918986 DOI: 10.1093/Cercor/Bhs251 |
0.355 |
|
| 2013 |
Hagerman PJ, Eid J, Peluso P, Rank D, Yin J, Hickey L, Tassone F, Loomis E. Sequencing the Unsequenceable: Expanded CGG Repeats in the Human FMR1 Gene Biophysical Journal. 104: 377a. DOI: 10.1016/J.Bpj.2012.11.2097 |
0.808 |
|
| 2012 |
Wang JM, Koldewyn K, Hashimoto R, Schneider A, Le L, Tassone F, Cheung K, Hagerman P, Hessl D, Rivera SM. Male carriers of the FMR1 premutation show altered hippocampal-prefrontal function during memory encoding. Frontiers in Human Neuroscience. 6: 297. PMID 23115550 DOI: 10.3389/Fnhum.2012.00297 |
0.327 |
|
| 2012 |
Kaplan ES, Cao Z, Hulsizer S, Tassone F, Berman RF, Hagerman PJ, Pessah IN. Early mitochondrial abnormalities in hippocampal neurons cultured from Fmr1 pre-mutation mouse model. Journal of Neurochemistry. 123: 613-21. PMID 22924671 DOI: 10.1111/J.1471-4159.2012.07936.X |
0.448 |
|
| 2012 |
Liu J, Koscielska KA, Cao Z, Hulsizer S, Grace N, Mitchell G, Nacey C, Githinji J, McGee J, Garcia-Arocena D, Hagerman RJ, Nolta J, Pessah IN, Hagerman PJ. Signaling defects in iPSC-derived fragile X premutation neurons. Human Molecular Genetics. 21: 3795-805. PMID 22641815 DOI: 10.1093/Hmg/Dds207 |
0.753 |
|
| 2012 |
Yrigollen CM, Durbin-Johnson B, Gane L, Nelson DL, Hagerman R, Hagerman PJ, Tassone F. AGG interruptions within the maternal FMR1 gene reduce the risk of offspring with fragile X syndrome. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 14: 729-36. PMID 22498846 DOI: 10.1038/Gim.2012.34 |
0.408 |
|
| 2012 |
Jenkins EC, Tassone F, Ye L, Hoogeveen AT, Brown WT, Hagerman RJ, Hagerman PJ. Reduced telomere length in individuals with FMR1 premutations and full mutations. American Journal of Medical Genetics. Part A. 158: 1060-5. PMID 22489017 DOI: 10.1002/Ajmg.A.35275 |
0.368 |
|
| 2012 |
Cao Z, Hulsizer S, Tassone F, Tang HT, Hagerman RJ, Rogawski MA, Hagerman PJ, Pessah IN. Clustered burst firing in FMR1 premutation hippocampal neurons: amelioration with allopregnanolone. Human Molecular Genetics. 21: 2923-35. PMID 22466801 DOI: 10.1093/Hmg/Dds118 |
0.357 |
|
| 2012 |
Tassone F, Greco CM, Hunsaker MR, Seritan AL, Berman RF, Gane LW, Jacquemont S, Basuta K, Jin LW, Hagerman PJ, Hagerman RJ. Neuropathological, clinical and molecular pathology in female fragile X premutation carriers with and without FXTAS. Genes, Brain, and Behavior. 11: 577-85. PMID 22463693 DOI: 10.1111/J.1601-183X.2012.00779.X |
0.4 |
|
| 2012 |
Leehey MA, Hagerman PJ. Fragile X-associated tremor/ataxia syndrome. Handbook of Clinical Neurology. 103: 373-86. PMID 21827901 DOI: 10.1016/B978-0-444-51892-7.00023-1 |
0.498 |
|
| 2011 |
Narcisa V, Aguilar D, Nguyen DV, Campos L, Brodovsky J, White S, Adams P, Tassone F, Hagerman PJ, Hagerman RJ. A Quantitative Assessment of Tremor and Ataxia in Female FMR1 Premutation Carriers Using CATSYS. Current Gerontology and Geriatrics Research. 2011: 484713. PMID 23008705 DOI: 10.1155/2011/484713 |
0.337 |
|
| 2011 |
Stöger R, Genereux DP, Hagerman RJ, Hagerman PJ, Tassone F, Laird CD. Testing the FMR1 promoter for mosaicism in DNA methylation among CpG sites, strands, and cells in FMR1-expressing males with fragile X syndrome. Plos One. 6: e23648. PMID 21909353 DOI: 10.1371/Journal.Pone.0023648 |
0.402 |
|
| 2011 |
Selmeczy D, Koldewyn K, Wang JM, Lee A, Harvey D, Hessl DR, Tassone F, Adams P, Hagerman RJ, Hagerman PJ, Rivera SM. Investigation of amygdala volume in men with the fragile X premutation. Brain Imaging and Behavior. 5: 285-94. PMID 21786216 DOI: 10.1007/S11682-011-9132-5 |
0.421 |
|
| 2011 |
Hunsaker MR, Greco CM, Spath MA, Smits AP, Navarro CS, Tassone F, Kros JM, Severijnen LA, Berry-Kravis EM, Berman RF, Hagerman PJ, Willemsen R, Hagerman RJ, Hukema RK. Widespread non-central nervous system organ pathology in fragile X premutation carriers with fragile X-associated tremor/ataxia syndrome and CGG knock-in mice. Acta Neuropathologica. 122: 467-79. PMID 21785977 DOI: 10.1007/S00401-011-0860-9 |
0.394 |
|
| 2011 |
Hessl D, Wang JM, Schneider A, Koldewyn K, Le L, Iwahashi C, Cheung K, Tassone F, Hagerman PJ, Rivera SM. Decreased fragile X mental retardation protein expression underlies amygdala dysfunction in carriers of the fragile X premutation. Biological Psychiatry. 70: 859-65. PMID 21783174 DOI: 10.1016/J.Biopsych.2011.05.033 |
0.446 |
|
| 2011 |
Hagerman R, Au J, Hagerman P. FMR1 premutation and full mutation molecular mechanisms related to autism. Journal of Neurodevelopmental Disorders. 3: 211-24. PMID 21617890 DOI: 10.1007/S11689-011-9084-5 |
0.497 |
|
| 2011 |
Hunsaker MR, Greco CM, Tassone F, Berman RF, Willemsen R, Hagerman RJ, Hagerman PJ. Rare intranuclear inclusions in the brains of 3 older adult males with fragile x syndrome: implications for the spectrum of fragile x-associated disorders. Journal of Neuropathology and Experimental Neurology. 70: 462-9. PMID 21572337 DOI: 10.1097/Nen.0B013E31821D3194 |
0.509 |
|
| 2011 |
Hall DA, Berry-Kravis E, Zhang W, Tassone F, Spector E, Zerbe G, Hagerman PJ, Ouyang B, Leehey MA. FMR1 gray-zone alleles: association with Parkinson's disease in women? Movement Disorders : Official Journal of the Movement Disorder Society. 26: 1900-6. PMID 21567456 DOI: 10.1002/Mds.23755 |
0.436 |
|
| 2011 |
Napoli E, Ross-Inta C, Wong S, Omanska-Klusek A, Barrow C, Iwahashi C, Garcia-Arocena D, Sakaguchi D, Berry-Kravis E, Hagerman R, Hagerman PJ, Giulivi C. Altered zinc transport disrupts mitochondrial protein processing/import in fragile X-associated tremor/ataxia syndrome. Human Molecular Genetics. 20: 3079-92. PMID 21558427 DOI: 10.1093/Hmg/Ddr211 |
0.389 |
|
| 2011 |
Tassone F, De Rubeis S, Carosi C, La Fata G, Serpa G, Raske C, Willemsen R, Hagerman PJ, Bagni C. Differential usage of transcriptional start sites and polyadenylation sites in FMR1 premutation alleles. Nucleic Acids Research. 39: 6172-85. PMID 21478165 DOI: 10.1093/Nar/Gkr100 |
0.481 |
|
| 2011 |
Chen L, Hadd AG, Sah S, Houghton JF, Filipovic-Sadic S, Zhang W, Hagerman PJ, Tassone F, Latham GJ. High-resolution methylation polymerase chain reaction for fragile X analysis: evidence for novel FMR1 methylation patterns undetected in Southern blot analyses. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 13: 528-38. PMID 21430544 DOI: 10.1097/Gim.0B013E31820A780F |
0.326 |
|
| 2011 |
Hoem G, Raske CR, Garcia-Arocena D, Tassone F, Sanchez E, Ludwig AL, Iwahashi CK, Kumar M, Yang JE, Hagerman PJ. CGG-repeat length threshold for FMR1 RNA pathogenesis in a cellular model for FXTAS. Human Molecular Genetics. 20: 2161-70. PMID 21389081 DOI: 10.1093/Hmg/Ddr101 |
0.782 |
|
| 2011 |
Greco CM, Navarro CS, Hunsaker MR, Maezawa I, Shuler JF, Tassone F, Delany M, Au JW, Berman RF, Jin LW, Schumann C, Hagerman PJ, Hagerman RJ. Neuropathologic features in the hippocampus and cerebellum of three older men with fragile X syndrome. Molecular Autism. 2: 2. PMID 21303513 DOI: 10.1186/2040-2392-2-2 |
0.396 |
|
| 2011 |
Ludwig AL, Hershey JW, Hagerman PJ. Initiation of translation of the FMR1 mRNA Occurs predominantly through 5'-end-dependent ribosomal scanning. Journal of Molecular Biology. 407: 21-34. PMID 21237174 DOI: 10.1016/J.Jmb.2011.01.006 |
0.762 |
|
| 2011 |
Cunningham CL, Martínez Cerdeño V, Navarro Porras E, Prakash AN, Angelastro JM, Willemsen R, Hagerman PJ, Pessah IN, Berman RF, Noctor SC. Premutation CGG-repeat expansion of the Fmr1 gene impairs mouse neocortical development. Human Molecular Genetics. 20: 64-79. PMID 20935171 DOI: 10.1093/Hmg/Ddq432 |
0.454 |
|
| 2010 |
Hagerman R, Hoem G, Hagerman P. Fragile X and autism: Intertwined at the molecular level leading to targeted treatments. Molecular Autism. 1: 12. PMID 20858229 DOI: 10.1186/2040-2392-1-12 |
0.506 |
|
| 2010 |
Chen L, Hadd A, Sah S, Filipovic-Sadic S, Krosting J, Sekinger E, Pan R, Hagerman PJ, Stenzel TT, Tassone F, Latham GJ. An information-rich CGG repeat primed PCR that detects the full range of fragile X expanded alleles and minimizes the need for southern blot analysis. The Journal of Molecular Diagnostics : Jmd. 12: 589-600. PMID 20616364 DOI: 10.2353/Jmoldx.2010.090227 |
0.427 |
|
| 2010 |
Ross-Inta C, Omanska-Klusek A, Wong S, Barrow C, Garcia-Arocena D, Iwahashi C, Berry-Kravis E, Hagerman RJ, Hagerman PJ, Giulivi C. Evidence of mitochondrial dysfunction in fragile X-associated tremor/ataxia syndrome. The Biochemical Journal. 429: 545-52. PMID 20513237 DOI: 10.1042/Bj20091960 |
0.457 |
|
| 2010 |
Paul R, Pessah IN, Gane L, Ono M, Hagerman PJ, Brunberg JA, Tassone F, Bourgeois JA, Adams PE, Nguyen DV, Hagerman R. Early onset of neurological symptoms in fragile X premutation carriers exposed to neurotoxins. Neurotoxicology. 31: 399-402. PMID 20466021 DOI: 10.1016/J.Neuro.2010.04.002 |
0.379 |
|
| 2010 |
Garcia-Arocena D, Hagerman PJ. Advances in understanding the molecular basis of FXTAS. Human Molecular Genetics. 19: R83-9. PMID 20430935 DOI: 10.1093/Hmg/Ddq166 |
0.458 |
|
| 2010 |
Sellier C, Rau F, Liu Y, Tassone F, Hukema RK, Gattoni R, Schneider A, Richard S, Willemsen R, Elliott DJ, Hagerman PJ, Charlet-Berguerand N. Sam68 sequestration and partial loss of function are associated with splicing alterations in FXTAS patients. The Embo Journal. 29: 1248-61. PMID 20186122 DOI: 10.1038/Emboj.2010.21 |
0.415 |
|
| 2010 |
Filipovic-Sadic S, Sah S, Chen L, Krosting J, Sekinger E, Zhang W, Hagerman PJ, Stenzel TT, Hadd AG, Latham GJ, Tassone F. A novel FMR1 PCR method for the routine detection of low abundance expanded alleles and full mutations in fragile X syndrome. Clinical Chemistry. 56: 399-408. PMID 20056738 DOI: 10.1373/Clinchem.2009.136101 |
0.412 |
|
| 2010 |
Adams PE, Adams JS, Nguyen DV, Hessl D, Brunberg JA, Tassone F, Zhang W, Koldewyn K, Rivera SM, Grigsby J, Zhang L, Decarli C, Hagerman PJ, Hagerman RJ. Psychological symptoms correlate with reduced hippocampal volume in fragile X premutation carriers. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 153: 775-85. PMID 19908235 DOI: 10.1002/Ajmg.B.31046 |
0.337 |
|
| 2010 |
Garcia-Arocena D, Yang JE, Brouwer JR, Tassone F, Iwahashi C, Berry-Kravis EM, Goetz CG, Sumis AM, Zhou L, Nguyen DV, Campos L, Howell E, Ludwig A, Greco C, Willemsen R, ... ... Hagerman PJ, et al. Fibroblast phenotype in male carriers of FMR1 premutation alleles. Human Molecular Genetics. 19: 299-312. PMID 19864489 DOI: 10.1093/Hmg/Ddp497 |
0.787 |
|
| 2010 |
Chen Y, Tassone F, Berman RF, Hagerman PJ, Hagerman RJ, Willemsen R, Pessah IN. Murine hippocampal neurons expressing Fmr1 gene premutations show early developmental deficits and late degeneration. Human Molecular Genetics. 19: 196-208. PMID 19846466 DOI: 10.1093/Hmg/Ddp479 |
0.408 |
|
| 2010 |
Stafstrom CE, Hagerman PJ, Pessah IN. Epilepsy in autism spectrum disorders Epilepsia. 51: 78. DOI: 10.1111/J.1528-1167.2010.02864.X |
0.352 |
|
| 2010 |
Tassone F, Hagerman PJ. The molecular biology of FXTAS The Fragile X-Associated Tremor Ataxia Syndrome (Fxtas). 77-93. DOI: 10.1007/978-1-4419-5805-1_6 |
0.402 |
|
| 2009 |
Raske C, Hagerman PJ. Molecular pathogenesis of fragile X-associated tremor/ataxia syndrome. Journal of Investigative Medicine : the Official Publication of the American Federation For Clinical Research. 57: 825-9. PMID 19794313 DOI: 10.2310/Jim.0B013E3181Be329A |
0.521 |
|
| 2009 |
Ludwig AL, Raske C, Tassone F, Garcia-Arocena D, Hershey JW, Hagerman PJ. Translation of the FMR1 mRNA is not influenced by AGG interruptions. Nucleic Acids Research. 37: 6896-904. PMID 19752155 DOI: 10.1093/Nar/Gkp713 |
0.772 |
|
| 2009 |
Hagerman PJ, Stafstrom CE. Origins of epilepsy in fragile X syndrome. Epilepsy Currents / American Epilepsy Society. 9: 108-12. PMID 19693328 DOI: 10.1111/J.1535-7511.2009.01309.X |
0.425 |
|
| 2009 |
Zhang L, Coffey S, Lua LL, Greco CM, Schafer JA, Brunberg J, Borodyanskaya M, Agius MA, Apperson M, Leehey M, Tartaglia N, Tassone F, Hagerman PJ, Hagerman RJ. FMR1 premutation in females diagnosed with multiple sclerosis. Journal of Neurology, Neurosurgery, and Psychiatry. 80: 812-4. PMID 19531693 DOI: 10.1136/Jnnp.2008.160960 |
0.36 |
|
| 2009 |
Fernandez-Carvajal I, Lopez Posadas B, Pan R, Raske C, Hagerman PJ, Tassone F. Expansion of an FMR1 grey-zone allele to a full mutation in two generations. The Journal of Molecular Diagnostics : Jmd. 11: 306-10. PMID 19525339 DOI: 10.2353/Jmoldx.2009.080174 |
0.375 |
|
| 2009 |
Dodds ED, Tassone F, Hagerman PJ, Lebrilla CB. Polymerase chain reaction, nuclease digestion, and mass spectrometry based assay for the trinucleotide repeat status of the fragile X mental retardation 1 gene Analytical Chemistry. 81: 5533-5540. PMID 19514725 DOI: 10.1021/Ac9008918 |
0.471 |
|
| 2009 |
Fernandez-Carvajal I, Walichiewicz P, Xiaosen X, Pan R, Hagerman PJ, Tassone F. Screening for expanded alleles of the FMR1 gene in blood spots from newborn males in a Spanish population. The Journal of Molecular Diagnostics : Jmd. 11: 324-9. PMID 19460941 DOI: 10.2353/Jmoldx.2009.080173 |
0.369 |
|
| 2009 |
Iwahashi C, Tassone F, Hagerman RJ, Yasui D, Parrott G, Nguyen D, Mayeur G, Hagerman PJ. A quantitative ELISA assay for the fragile x mental retardation 1 protein. The Journal of Molecular Diagnostics : Jmd. 11: 281-9. PMID 19460937 DOI: 10.2353/Jmoldx.2009.080118 |
0.448 |
|
| 2009 |
Bourgeois JA, Coffey SM, Rivera SM, Hessl D, Gane LW, Tassone F, Greco C, Finucane B, Nelson L, Berry-Kravis E, Grigsby J, Hagerman PJ, Hagerman RJ. A review of fragile X premutation disorders: expanding the psychiatric perspective. The Journal of Clinical Psychiatry. 70: 852-62. PMID 19422761 DOI: 10.4088/Jcp.08M04476 |
0.445 |
|
| 2009 |
Brega AG, Reynolds A, Bennett RE, Leehey MA, Bounds LS, Cogswell JB, Hagerman RJ, Hagerman PJ, Grigsby J. Functional status of men with the fragile X premutation, with and without the tremor/ataxia syndrome (FXTAS). International Journal of Geriatric Psychiatry. 24: 1101-9. PMID 19404994 DOI: 10.1002/Gps.2231 |
0.471 |
|
| 2009 |
Hagerman PJ. Incomplete financial disclosure in a commentary on testing for fragile X gene mutations throughout the life span. Jama. 301: 601-2. PMID 19211466 DOI: 10.1001/Jama.2009.79 |
0.336 |
|
| 2009 |
Cilia R, Kraff J, Canesi M, Pezzoli G, Goldwurm S, Amiri K, Tang HT, Pan R, Hagerman PJ, Tassone F. Screening for the presence of FMR1 premutation alleles in women with parkinsonism. Archives of Neurology. 66: 244-9. PMID 19204162 DOI: 10.1001/Archneurol.2008.548 |
0.405 |
|
| 2009 |
Sentürk D, Nguyen DV, Tassone F, Hagerman RJ, Carroll RJ, Hagerman PJ. Covariate adjusted correlation analysis with application to FMR1 premutation female carrier data. Biometrics. 65: 781-92. PMID 19173699 DOI: 10.1111/J.1541-0420.2008.01169.X |
0.373 |
|
| 2008 |
Koldewyn K, Hessl D, Adams J, Tassone F, Hagerman PJ, Hagerman RJ, Rivera SM. Reduced Hippocampal Activation During Recall is Associated with Elevated FMR1 mRNA and Psychiatric Symptoms in Men with the Fragile X Premutation. Brain Imaging and Behavior. 2: 105-116. PMID 19430586 DOI: 10.1007/S11682-008-9020-9 |
0.365 |
|
| 2008 |
Harris SW, Hessl D, Goodlin-Jones B, Ferranti J, Bacalman S, Barbato I, Tassone F, Hagerman PJ, Herman H, Hagerman RJ. Autism profiles of males with fragile X syndrome. American Journal of Mental Retardation : Ajmr. 113: 427-38. PMID 19127654 DOI: 10.1352/2008.113:427-438 |
0.42 |
|
| 2008 |
Hagerman RJ, Hagerman PJ. Testing for fragile X gene mutations throughout the life span. Jama. 300: 2419-21. PMID 19033593 DOI: 10.1001/Jama.2008.684 |
0.478 |
|
| 2008 |
Greco CM, Tassone F, Garcia-Arocena D, Tartaglia N, Coffey SM, Vartanian TK, Brunberg JA, Hagerman PJ, Hagerman RJ. Clinical and neuropathologic findings in a woman with the FMR1 premutation and multiple sclerosis. Archives of Neurology. 65: 1114-6. PMID 18695063 DOI: 10.1001/Archneur.65.8.1114 |
0.347 |
|
| 2008 |
Hagerman RJ, Hall DA, Coffey S, Leehey M, Bourgeois J, Gould J, Zhang L, Seritan A, Berry-Kravis E, Olichney J, Miller JW, Fong AL, Carpenter R, Bodine C, Gane LW, ... ... Hagerman PJ, et al. Treatment of fragile X-associated tremor ataxia syndrome (FXTAS) and related neurological problems. Clinical Interventions in Aging. 3: 251-62. PMID 18686748 DOI: 10.2147/Cia.S1794 |
0.434 |
|
| 2008 |
Brega AG, Goodrich G, Bennett RE, Hessl D, Engle K, Leehey MA, Bounds LS, Paulich MJ, Hagerman RJ, Hagerman PJ, Cogswell JB, Tassone F, Reynolds A, Kooken R, Kenny M, et al. The primary cognitive deficit among males with fragile X-associated tremor/ataxia syndrome (FXTAS) is a dysexecutive syndrome. Journal of Clinical and Experimental Neuropsychology. 30: 853-69. PMID 18608667 DOI: 10.1080/13803390701819044 |
0.398 |
|
| 2008 |
Jenkins EC, Tassone F, Ye L, Gu H, Xi M, Velinov M, Brown WT, Hagerman RJ, Hagerman PJ. Reduced telomere length in older men with premutation alleles of the fragile X mental retardation 1 gene. American Journal of Medical Genetics. Part A. 146: 1543-6. PMID 18478592 DOI: 10.1002/Ajmg.A.32342 |
0.418 |
|
| 2008 |
Cornish KM, Li L, Kogan CS, Jacquemont S, Turk J, Dalton A, Hagerman RJ, Hagerman PJ. Age-dependent cognitive changes in carriers of the fragile X syndrome. Cortex; a Journal Devoted to the Study of the Nervous System and Behavior. 44: 628-36. PMID 18472033 DOI: 10.1016/J.Cortex.2006.11.002 |
0.422 |
|
| 2008 |
Soontarapornchai K, Maselli R, Fenton-Farrell G, Tassone F, Hagerman PJ, Hessl D, Hagerman RJ. Abnormal nerve conduction features in fragile X premutation carriers. Archives of Neurology. 65: 495-8. PMID 18413472 DOI: 10.1001/Archneur.65.4.495 |
0.342 |
|
| 2008 |
Hagerman PJ. The fragile X prevalence paradox. Journal of Medical Genetics. 45: 498-9. PMID 18413371 DOI: 10.1136/Jmg.2008.059055 |
0.301 |
|
| 2008 |
Coffey SM, Cook K, Tartaglia N, Tassone F, Nguyen DV, Pan R, Bronsky HE, Yuhas J, Borodyanskaya M, Grigsby J, Doerflinger M, Hagerman PJ, Hagerman RJ. Expanded clinical phenotype of women with the FMR1 premutation. American Journal of Medical Genetics. Part A. 146: 1009-16. PMID 18348275 DOI: 10.1002/Ajmg.A.32060 |
0.353 |
|
| 2008 |
Aguilar D, Sigford KE, Soontarapornchai K, Nguyen DV, Adams PE, Yuhas JM, Tassone F, Hagerman PJ, Hagerman RJ. A quantitative assessment of tremor and ataxia in FMR1 premutation carriers using CATSYS. American Journal of Medical Genetics. Part A. 146: 629-35. PMID 18241072 DOI: 10.1002/Ajmg.A.32211 |
0.306 |
|
| 2008 |
Grigsby J, Brega AG, Engle K, Leehey MA, Hagerman RJ, Tassone F, Hessl D, Hagerman PJ, Cogswell JB, Bennett RE, Cook K, Hall DA, Bounds LS, Paulich MJ, Reynolds A. Cognitive profile of fragile X premutation carriers with and without fragile X-associated tremor/ataxia syndrome. Neuropsychology. 22: 48-60. PMID 18211155 DOI: 10.1037/0894-4105.22.1.48 |
0.367 |
|
| 2008 |
Amiri K, Hagerman RJ, Hagerman PJ. Fragile X-associated tremor/ataxia syndrome: an aging face of the fragile X gene. Archives of Neurology. 65: 19-25. PMID 18195136 DOI: 10.1001/Archneurol.2007.30 |
0.522 |
|
| 2008 |
Tassone F, Pan R, Amiri K, Taylor AK, Hagerman PJ. A rapid polymerase chain reaction-based screening method for identification of all expanded alleles of the fragile X (FMR1) gene in newborn and high-risk populations. The Journal of Molecular Diagnostics : Jmd. 10: 43-9. PMID 18165273 DOI: 10.2353/Jmoldx.2008.070073 |
0.406 |
|
| 2008 |
Leehey MA, Berry-Kravis E, Goetz CG, Zhang L, Hall DA, Li L, Rice CD, Lara R, Cogswell J, Reynolds A, Gane L, Jacquemont S, Tassone F, Grigsby J, Hagerman RJ, ... Hagerman PJ, et al. FMR1 CGG repeat length predicts motor dysfunction in premutation carriers. Neurology. 70: 1397-402. PMID 18057320 DOI: 10.1212/01.Wnl.0000281692.98200.F5 |
0.444 |
|
| 2008 |
Hagerman RJ, Rivera SM, Hagerman PJ. The fragile X family of disorders: A model for autism and targeted treatments Current Pediatric Reviews. 4: 40-52. DOI: 10.2174/157339608783565770 |
0.482 |
|
| 2008 |
Tassone F, Hagerman PJ, Hagerman RJ. Newborn screening in Fragile X syndrome Journal of Intellectual Disability Research. 52: 814-814. DOI: 10.1111/J.1365-2788.2008.01119_10.X |
0.325 |
|
| 2007 |
Zumwalt M, Ludwig A, Hagerman PJ, Dieckmann T. Secondary structure and dynamics of the r(CGG) repeat in the mRNA of the fragile X mental retardation 1 (FMR1) gene. Rna Biology. 4: 93-100. PMID 17962727 DOI: 10.4161/Rna.4.2.5039 |
0.78 |
|
| 2007 |
Hagerman RJ, Coffey SM, Maselli R, Soontarapornchai K, Brunberg JA, Leehey MA, Zhang L, Gane LW, Fenton-Farrell G, Tassone F, Hagerman PJ. Neuropathy as a presenting feature in fragile X-associated tremor/ataxia syndrome. American Journal of Medical Genetics. Part A. 143: 2256-60. PMID 17726686 DOI: 10.1002/Ajmg.A.31920 |
0.401 |
|
| 2007 |
Adams JS, Adams PE, Nguyen D, Brunberg JA, Tassone F, Zhang W, Koldewyn K, Rivera SM, Grigsby J, Zhang L, DeCarli C, Hagerman PJ, Hagerman RJ. Volumetric brain changes in females with fragile X-associated tremor/ataxia syndrome (FXTAS). Neurology. 69: 851-9. PMID 17724287 DOI: 10.1212/01.Wnl.0000269781.10417.7B |
0.393 |
|
| 2007 |
Kraff J, Tang HT, Cilia R, Canesi M, Pezzoli G, Goldwurm S, Hagerman PJ, Tassone F. Screen for excess FMR1 premutation alleles among males with parkinsonism. Archives of Neurology. 64: 1002-6. PMID 17620491 DOI: 10.1001/Archneur.64.7.1002 |
0.409 |
|
| 2007 |
Berry-Kravis E, Abrams L, Coffey SM, Hall DA, Greco C, Gane LW, Grigsby J, Bourgeois JA, Finucane B, Jacquemont S, Brunberg JA, Zhang L, Lin J, Tassone F, Hagerman PJ, et al. Fragile X-associated tremor/ataxia syndrome: clinical features, genetics, and testing guidelines. Movement Disorders : Official Journal of the Movement Disorder Society. 22: 2018-30, quiz 2140. PMID 17618523 DOI: 10.1002/Mds.21493 |
0.495 |
|
| 2007 |
Tassone F, Adams J, Berry-Kravis EM, Cohen SS, Brusco A, Leehey MA, Li L, Hagerman RJ, Hagerman PJ. CGG repeat length correlates with age of onset of motor signs of the fragile X-associated tremor/ataxia syndrome (FXTAS). American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 144: 566-9. PMID 17427188 DOI: 10.1002/Ajmg.B.30482 |
0.409 |
|
| 2007 |
Greco CM, Soontrapornchai K, Wirojanan J, Gould JE, Hagerman PJ, Hagerman RJ. Testicular and pituitary inclusion formation in fragile X associated tremor/ataxia syndrome. The Journal of Urology. 177: 1434-7. PMID 17382748 DOI: 10.1016/J.Juro.2006.11.097 |
0.491 |
|
| 2007 |
Leehey MA, Hagerman RJ, Hagerman PJ. Fragile X syndrome vs fragile X-associated tremor/ataxia syndrome. Archives of Neurology. 64: 289; author reply 28. PMID 17296852 DOI: 10.1001/Archneur.64.2.289-A |
0.434 |
|
| 2007 |
Tassone F, Beilina A, Carosi C, Albertosi S, Bagni C, Li L, Glover K, Bentley D, Hagerman PJ. Elevated FMR1 mRNA in premutation carriers is due to increased transcription. Rna (New York, N.Y.). 13: 555-62. PMID 17283214 DOI: 10.1261/Rna.280807 |
0.451 |
|
| 2007 |
Hagerman PJ, Hagerman RJ. Fragile X-associated tremor/ataxia syndrome--an older face of the fragile X gene. Nature Clinical Practice. Neurology. 3: 107-12. PMID 17279084 DOI: 10.1038/Ncpneuro0373 |
0.352 |
|
| 2007 |
Grigsby J, Brega AG, Leehey MA, Goodrich GK, Jacquemont S, Loesch DZ, Cogswell JB, Epstein J, Wilson R, Jardini T, Gould E, Bennett RE, Hessl D, Cohen S, Cook K, ... ... Hagerman PJ, et al. Impairment of executive cognitive functioning in males with fragile X-associated tremor/ataxia syndrome. Movement Disorders : Official Journal of the Movement Disorder Society. 22: 645-50. PMID 17266074 DOI: 10.1002/Mds.21359 |
0.377 |
|
| 2007 |
Hessl D, Rivera S, Koldewyn K, Cordeiro L, Adams J, Tassone F, Hagerman PJ, Hagerman RJ. Amygdala dysfunction in men with the fragile X premutation. Brain : a Journal of Neurology. 130: 404-16. PMID 17166860 DOI: 10.1093/Brain/Awl338 |
0.395 |
|
| 2007 |
Jacquemont S, Hagerman RJ, Hagerman PJ, Leehey MA. Fragile-X syndrome and fragile X-associated tremor/ataxia syndrome: two faces of FMR1. The Lancet. Neurology. 6: 45-55. PMID 17166801 DOI: 10.1016/S1474-4422(06)70676-7 |
0.499 |
|
| 2007 |
Berry-Kravis E, Goetz CG, Leehey MA, Hagerman RJ, Zhang L, Li L, Nguyen D, Hall DA, Tartaglia N, Cogswell J, Tassone F, Hagerman PJ. Neuropathic features in fragile X premutation carriers. American Journal of Medical Genetics. Part A. 143: 19-26. PMID 17152065 DOI: 10.1002/Ajmg.A.31559 |
0.449 |
|
| 2007 |
Leehey MA, Berry-Kravis E, Min SJ, Hall DA, Rice CD, Zhang L, Grigsby J, Greco CM, Reynolds A, Lara R, Cogswell J, Jacquemont S, Hessl DR, Tassone F, Hagerman R, ... Hagerman PJ, et al. Progression of tremor and ataxia in male carriers of the FMR1 premutation. Movement Disorders : Official Journal of the Movement Disorder Society. 22: 203-6. PMID 17133502 DOI: 10.1002/Mds.21252 |
0.4 |
|
| 2007 |
Hagerman PJ. RNA-based disorders of muscle and brain Neurobiology of Disease. 125-133. DOI: 10.1016/B978-012088592-3/50013-X |
0.47 |
|
| 2006 |
Cohen S, Masyn K, Adams J, Hessl D, Rivera S, Tassone F, Brunberg J, DeCarli C, Zhang L, Cogswell J, Loesch D, Leehey M, Grigsby J, Hagerman PJ, Hagerman R. Molecular and imaging correlates of the fragile X-associated tremor/ataxia syndrome. Neurology. 67: 1426-31. PMID 17060569 DOI: 10.1212/01.Wnl.0000239837.57475.3A |
0.393 |
|
| 2006 |
Grigsby J, Leehey MA, Jacquemont S, Brunberg JA, Hagerman RJ, Wilson R, Epstein JH, Greco CM, Tassone F, Hagerman PJ. Cognitive impairment in a 65-year-old male with the fragile X-associated tremor-ataxia syndrome (FXTAS). Cognitive and Behavioral Neurology : Official Journal of the Society For Behavioral and Cognitive Neurology. 19: 165-71. PMID 16957495 DOI: 10.1097/01.Wnn.0000213906.57148.01 |
0.361 |
|
| 2006 |
Hagerman RJ, Hagerman PJ. X inactivation and cellular mosaicism. Jama. 296: 930-1; author reply . PMID 16926349 DOI: 10.1001/Jama.296.8.930-C |
0.363 |
|
| 2006 |
Grigsby J, Brega AG, Jacquemont S, Loesch DZ, Leehey MA, Goodrich GK, Hagerman RJ, Epstein J, Wilson R, Cogswell JB, Jardini T, Tassone F, Hagerman PJ. Impairment in the cognitive functioning of men with fragile X-associated tremor/ataxia syndrome (FXTAS). Journal of the Neurological Sciences. 248: 227-33. PMID 16780889 DOI: 10.1016/J.Jns.2006.05.016 |
0.373 |
|
| 2006 |
Hall DA, Berry-Kravis E, Hagerman RJ, Hagerman PJ, Rice CD, Leehey MA. Symptomatic treatment in the fragile X-associated tremor/ataxia syndrome. Movement Disorders : Official Journal of the Movement Disorder Society. 21: 1741-4. PMID 16773616 DOI: 10.1002/Mds.21001 |
0.316 |
|
| 2006 |
Jacquemont S, Leehey MA, Hagerman RJ, Beckett LA, Hagerman PJ. Size bias of fragile X premutation alleles in late-onset movement disorders. Journal of Medical Genetics. 43: 804-9. PMID 16723388 DOI: 10.1136/Jmg.2006.042374 |
0.449 |
|
| 2006 |
Bourgeois JA, Farzin F, Brunberg JA, Tassone F, Hagerman P, Zhang L, Hessl D, Hagerman R. Dementia with mood symptoms in a fragile X premutation carrier with the fragile X-associated tremor/ataxia syndrome: clinical intervention with donepezil and venlafaxine. The Journal of Neuropsychiatry and Clinical Neurosciences. 18: 171-7. PMID 16720793 DOI: 10.1176/Appi.Neuropsych.18.2.171 |
0.403 |
|
| 2006 |
Farzin F, Perry H, Hessl D, Loesch D, Cohen J, Bacalman S, Gane L, Tassone F, Hagerman P, Hagerman R. Autism spectrum disorders and attention-deficit/hyperactivity disorder in boys with the fragile X premutation. Journal of Developmental and Behavioral Pediatrics : Jdbp. 27: S137-44. PMID 16685180 DOI: 10.1097/00004703-200604002-00012 |
0.342 |
|
| 2006 |
Hall DA, Hagerman RJ, Hagerman PJ, Jacquemont S, Leehey MA. Prevalence of FMR1 repeat expansions in movement disorders. A systematic review. Neuroepidemiology. 26: 151-5. PMID 16493202 DOI: 10.1159/000091656 |
0.337 |
|
| 2006 |
Greco CM, Berman RF, Martin RM, Tassone F, Schwartz PH, Chang A, Trapp BD, Iwahashi C, Brunberg J, Grigsby J, Hessl D, Becker EJ, Papazian J, Leehey MA, Hagerman RJ, ... Hagerman PJ, et al. Neuropathology of fragile X-associated tremor/ataxia syndrome (FXTAS). Brain : a Journal of Neurology. 129: 243-55. PMID 16332642 DOI: 10.1093/Brain/Awh683 |
0.409 |
|
| 2006 |
Iwahashi CK, Yasui DH, An HJ, Greco CM, Tassone F, Nannen K, Babineau B, Lebrilla CB, Hagerman RJ, Hagerman PJ. Protein composition of the intranuclear inclusions of FXTAS. Brain : a Journal of Neurology. 129: 256-71. PMID 16246864 DOI: 10.1093/Brain/Awh650 |
0.388 |
|
| 2006 |
Hagerman RJ, Hagerman PJ. Fragile X syndrome and fragile X-associated tremor/ataxia syndrome Genetic Instabilities and Neurological Diseases, Second Edition. 165-174. DOI: 10.1016/B978-012369462-1/50011-9 |
0.325 |
|
| 2005 |
Hagerman RJ, Ono MY, Hagerman PJ. Recent advances in fragile X: a model for autism and neurodegeneration. Current Opinion in Psychiatry. 18: 490-6. PMID 16639106 DOI: 10.1097/01.Yco.0000179485.39520.B0 |
0.428 |
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| 2005 |
Saluto A, Brussino A, Tassone F, Arduino C, Cagnoli C, Pappi P, Hagerman PJ, Migone N, Brusco A. An Enhanced Polymerase Chain Reaction Assay to Detect Pre- and Full Mutation Alleles of the Fragile X Mental Retardation 1 Gene The Journal of Molecular Diagnostics. 7: 605-612. PMID 16258159 DOI: 10.1016/S1525-1578(10)60594-6 |
0.4 |
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| 2005 |
Arocena DG, Iwahashi CK, Won N, Beilina A, Ludwig AL, Tassone F, Schwartz PH, Hagerman PJ. Induction of inclusion formation and disruption of lamin A/C structure by premutation CGG-repeat RNA in human cultured neural cells. Human Molecular Genetics. 14: 3661-71. PMID 16239243 DOI: 10.1093/Hmg/Ddi394 |
0.782 |
|
| 2005 |
Hessl D, Tassone F, Loesch DZ, Berry-Kravis E, Leehey MA, Gane LW, Barbato I, Rice C, Gould E, Hall DA, Grigsby J, Wegelin JA, Harris S, Lewin F, Weinberg D, ... Hagerman PJ, et al. Abnormal elevation of FMR1 mRNA is associated with psychological symptoms in individuals with the fragile X premutation. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 139: 115-21. PMID 16184602 DOI: 10.1002/Ajmg.B.30241 |
0.406 |
|
| 2005 |
Hall DA, Berry-Kravis E, Jacquemont S, Rice CD, Cogswell J, Zhang L, Hagerman RJ, Hagerman PJ, Leehey MA. Initial diagnoses given to persons with the fragile X associated tremor/ataxia syndrome (FXTAS). Neurology. 65: 299-301. PMID 16043804 DOI: 10.1212/01.Wnl.0000168900.86323.9C |
0.465 |
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| 2005 |
Jacquemont S, Orrico A, Galli L, Sahota PK, Brunberg JA, Anichini C, Leehey M, Schaeffer S, Hagerman RJ, Hagerman PJ, Tassone F. Spastic paraparesis, cerebellar ataxia, and intention tremor: a severe variant of FXTAS? Journal of Medical Genetics.. 42: e14. PMID 15689437 DOI: 10.1136/Jmg.2004.024190 |
0.434 |
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| 2005 |
Schwartz PH, Tassone F, Greco CM, Nethercott HE, Ziaeian B, Hagerman RJ, Hagerman PJ. Neural progenitor cells from an adult patient with fragile X syndrome. Bmc Medical Genetics. 6: 2. PMID 15649335 DOI: 10.1186/1471-2350-6-2 |
0.427 |
|
| 2004 |
Tassone F, Iwahashi C, Hagerman PJ. FMR1 RNA within the intranuclear inclusions of fragile X-associated tremor/ataxia syndrome (FXTAS). Rna Biology. 1: 103-5. PMID 17179750 DOI: 10.4161/Rna.1.2.1035 |
0.501 |
|
| 2004 |
Moore CJ, Daly EM, Tassone F, Tysoe C, Schmitz N, Ng V, Chitnis X, McGuire P, Suckling J, Davies KE, Hagerman RJ, Hagerman PJ, Murphy KC, Murphy DG. The effect of pre-mutation of X chromosome CGG trinucleotide repeats on brain anatomy. Brain : a Journal of Neurology. 127: 2672-81. PMID 15483045 DOI: 10.1093/Brain/Awh256 |
0.424 |
|
| 2004 |
Moore CJ, Daly EM, Schmitz N, Tassone F, Tysoe C, Hagerman RJ, Hagerman PJ, Morris RG, Murphy KC, Murphy DG. A neuropsychological investigation of male premutation carriers of fragile X syndrome. Neuropsychologia. 42: 1934-47. PMID 15381024 DOI: 10.1016/J.Neuropsychologia.2004.05.002 |
0.429 |
|
| 2004 |
Garcia Arocena D, Louis ED, Tassone F, Gilliam TC, Ottman R, Jacquemont S, Hagerman PJ. Screen for expanded FMR1 alleles in patients with essential tremor. Movement Disorders : Official Journal of the Movement Disorder Society. 19: 930-3. PMID 15300658 DOI: 10.1002/Mds.20043 |
0.424 |
|
| 2004 |
Mills JB, Hagerman PJ. Origin of the intrinsic rigidity of DNA Nucleic Acids Research. 32: 4055-4059. PMID 15289578 DOI: 10.1093/Nar/Gkh740 |
0.313 |
|
| 2004 |
Hagerman RJ, Leavitt BR, Farzin F, Jacquemont S, Greco CM, Brunberg JA, Tassone F, Hessl D, Harris SW, Zhang L, Jardini T, Gane LW, Ferranti J, Ruiz L, Leehey MA, ... ... Hagerman PJ, et al. Fragile-X-associated tremor/ataxia syndrome (FXTAS) in females with the FMR1 premutation. American Journal of Human Genetics. 74: 1051-6. PMID 15065016 DOI: 10.1086/420700 |
0.383 |
|
| 2004 |
Tassone F, Hagerman RJ, Garcia-Arocena D, Khandjian EW, Greco CM, Hagerman PJ. Intranuclear inclusions in neural cells with premutation alleles in fragile X associated tremor/ataxia syndrome. Journal of Medical Genetics. 41: e43. PMID 15060119 DOI: 10.1136/Jmg.2003.012518 |
0.518 |
|
| 2004 |
Hagerman PJ, Hagerman RJ. The Fragile-X Premutation: A Maturing Perspective American Journal of Human Genetics. 74: 805-816. PMID 15052536 DOI: 10.1086/386296 |
0.462 |
|
| 2004 |
Jacquemont S, Farzin F, Hall D, Leehey M, Tassone F, Gane L, Zhang L, Grigsby J, Jardini T, Lewin F, Berry-Kravis E, Hagerman PJ, Hagerman RJ. Aging in individuals with the FMR1 mutation. American Journal of Mental Retardation : Ajmr. 109: 154-64. PMID 15000674 DOI: 10.1352/0895-8017(2004)109<154:Aiiwtf>2.0.Co;2 |
0.482 |
|
| 2004 |
Hagerman PJ, Hagerman RJ. Fragile X-Associated, Tremor/Ataxia Syndrome (FXTAS) Mental Retardation and Developmental Disabilities Research Reviews. 10: 25-30. PMID 14994285 DOI: 10.1002/Mrdd.20005 |
0.519 |
|
| 2004 |
Jacquemont S, Hagerman RJ, Leehey MA, Hall DA, Levine RA, Brunberg JA, Zhang L, Jardini T, Gane LW, Harris SW, Herman K, Grigsby J, Greco CM, Berry-Kravis E, Tassone F, ... Hagerman PJ, et al. Penetrance of the fragile X-associated tremor/ataxia syndrome in a premutation carrier population. Jama. 291: 460-9. PMID 14747503 DOI: 10.1001/Jama.291.4.460 |
0.434 |
|
| 2004 |
Beilina A, Tassone F, Schwartz PH, Sahota P, Hagerman PJ. Redistribution of transcription start sites within the FMR1 promoter region with expansion of the downstream CGG-repeat element. Human Molecular Genetics. 13: 543-9. PMID 14722156 DOI: 10.1093/Hmg/Ddh053 |
0.383 |
|
| 2004 |
Nowicki ST, Jacquemont S, Li L, Nguyen DV, Gregg JP, Hagerman RJ, Hagerman PJ, Institute MI. 127 AN APPROACH TO IDENTIFY EPISTATIC GENES INVOLVED IN THE DEVELOPMENT OF AUTISM SPECTRUM DISORDER IN PATIENTS WITH FRAGILE X SYNDROME. Journal of Investigative Medicine. 52: S101.2-S101. DOI: 10.1136/Jim-52-Suppl1-127 |
0.418 |
|
| 2003 |
Hagerman PJ, Greco CM, Hagerman RJ. A cerebellar tremor/ataxia syndrome among fragile X premutation carriers. Cytogenetic and Genome Research. 100: 206-12. PMID 14526182 DOI: 10.1159/000072856 |
0.514 |
|
| 2003 |
Tassone F, Hagerman PJ. Expression of the FMR1 gene Cytogenetic and Genome Research. 100: 124-128. PMID 14526172 DOI: 10.1159/000072846 |
0.493 |
|
| 2003 |
Chen LS, Tassone F, Sahota P, Hagerman PJ. The (CGG)n repeat element within the 5' untranslated region of the FMR1 message provides both positive and negative cis effects on in vivo translation of a downstream reporter. Human Molecular Genetics. 12: 3067-74. PMID 14519687 DOI: 10.1093/Hmg/Ddg331 |
0.475 |
|
| 2003 |
Arocena DG, Breece KE, Hagerman PJ. Distribution of CGG repeat sizes within the fragile X mental retardation 1 (FMR1) homologue in a non-human primate population Human Genetics. 113: 371-376. PMID 12905066 DOI: 10.1007/S00439-003-0982-9 |
0.447 |
|
| 2003 |
Berry-Kravis E, Lewin F, Wuu J, Leehey M, Hagerman R, Hagerman P, Goetz CG. Tremor and ataxia in fragile X premutation carriers: Blinded videotape study Annals of Neurology. 53: 616-623. PMID 12730995 DOI: 10.1002/Ana.10522 |
0.419 |
|
| 2003 |
Willemsen R, Hoogeveen-Westerveld M, Reis S, Holstege J, Severijnen LA, Nieuwenhuizen IM, Schrier M, van Unen L, Tassone F, Hoogeveen AT, Hagerman PJ, Mientjes EJ, Oostra BA. The FMR1 CGG repeat mouse displays ubiquitin-positive intranuclear neuronal inclusions; implications for the cerebellar tremor/ataxia syndrome. Human Molecular Genetics. 12: 949-59. PMID 12700164 DOI: 10.1093/Hmg/Ddg114 |
0.447 |
|
| 2003 |
Jacquemont S, Hagerman RJ, Leehey M, Grigsby J, Zhang L, Brunberg JA, Greco C, Des Portes V, Jardini T, Levine R, Berry-Kravis E, Brown WT, Schaeffer S, Kissel J, Tassone F, ... Hagerman PJ, et al. Fragile X premutation tremor/ataxia syndrome: molecular, clinical, and neuroimaging correlates. American Journal of Human Genetics. 72: 869-78. PMID 12638084 DOI: 10.1086/374321 |
0.459 |
|
| 2003 |
Leehey MA, Munhoz RP, Lang AE, Brunberg JA, Grigsby J, Greco C, Jacquemont S, Tassone F, Lozano AM, Hagerman PJ, Hagerman RJ. The fragile X premutation presenting as essential tremor. Archives of Neurology. 60: 117-21. PMID 12533098 DOI: 10.1001/Archneur.60.1.117 |
0.387 |
|
| 2002 |
Primerano B, Tassone F, Hagerman RJ, Hagerman P, Amaldi F, Bagni C. Reduced FMR1 mRNA translation efficiency in fragile X patients with premutations. Rna (New York, N.Y.). 8: 1482-8. PMID 12515381 DOI: 10.1017/S1355838202020642 |
0.435 |
|
| 2002 |
Greco CM, Hagerman RJ, Tassone F, Chudley AE, Del Bigio MR, Jacquemont S, Leehey M, Hagerman PJ. Neuronal intranuclear inclusions in a new cerebellar tremor/ataxia syndrome among fragile X carriers. Brain : a Journal of Neurology. 125: 1760-71. PMID 12135967 DOI: 10.1093/Brain/Awf184 |
0.459 |
|
| 2002 |
Hagerman RJ, Hagerman PJ. The fragile X premutation: Into the phenotypic fold Current Opinion in Genetics and Development. 12: 278-283. PMID 12076670 DOI: 10.1016/S0959-437X(02)00299-X |
0.48 |
|
| 2002 |
Leehey MA, Hagerman RJ, Landau WM, Grigsby J, Tassone F, Hagerman PJ. Tremor/ataxia syndrome in fragile X carrier males Movement Disorders. 17: 744-745. DOI: 10.1002/Mds.10208 |
0.428 |
|
| 2001 |
Hagerman RJ, Hagerman PJ. Fragile x syndrome: A model of gene-brain-behavior relationships Molecular Genetics and Metabolism. 74: 89-97. PMID 11592806 DOI: 10.1006/Mgme.2001.3225 |
0.378 |
|
| 2001 |
Chiang PW, Carpenter LE, Hagerman PJ. The 5′-Untranslated Region of the FMR1 Message Facilitates Translation by Internal Ribosome Entry Journal of Biological Chemistry. 276: 37916-37921. PMID 11489899 DOI: 10.1074/Jbc.M105584200 |
0.399 |
|
| 2001 |
Hagerman RJ, Leehey M, Heinrichs W, Tassone F, Wilson R, Hills J, Grigsby J, Gage B, Hagerman PJ. Intention tremor, parkinsonism, and generalized brain atrophy in male carriers of fragile X. Neurology. 57: 127-30. PMID 11445641 DOI: 10.1212/Wnl.57.1.127 |
0.459 |
|
| 2001 |
Tassone F, Hagerman RJ, Taylor AK, Hagerman PJ. A majority of fragile X males with methylated, full mutation alleles have significant levels of FMR1 messenger RNA Journal of Medical Genetics. 38: 453-456. PMID 11432964 DOI: 10.1136/Jmg.38.7.453 |
0.403 |
|
| 2001 |
Hagerman PJ, Hagerman RJ. El síndrome X frágil: un modelo de la relación gen-cerebro-conducta Revista De NeurologíA. 33: 51. DOI: 10.33588/Rn.33S1.2001352 |
0.339 |
|
| 2000 |
Tassone F, Hagerman RJ, Chamberlain WD, Hagerman PJ. Transcription of the FMR1 gene in individuals with fragile X syndrome American Journal of Medical Genetics - Seminars in Medical Genetics. 97: 195-203. PMID 11449488 DOI: 10.1002/1096-8628(200023)97:3<195::Aid-Ajmg1037>3.0.Co;2-R |
0.492 |
|
| 2000 |
Tassone F, Hagerman RJ, Loesch DZ, Lachiewicz A, Taylor AK, Hagerman PJ. Fragile X males with unmethylated, full mutation trinucleotide repeat expansions have elevated levels of FMR1 messenger RNA American Journal of Medical Genetics. 94: 232-236. PMID 10995510 DOI: 10.1002/1096-8628(20000918)94:3<232::Aid-Ajmg9>3.0.Co;2-H |
0.464 |
|
| 2000 |
Hagerman PJ. Transient electric birefringence for determining global conformations of nonhelix elements and protein-induced bends in RNA Methods in Enzymology. 317: 440-453. PMID 10829294 DOI: 10.1016/S0076-6879(00)17028-4 |
0.305 |
|
| 2000 |
Tassone F, Hagerman RJ, Taylor AK, Mills JB, Harris SW, Gane LW, Hagerman P. Clinical involvement and protein expression in individuals with the FMR1 premutation American Journal of Medical Genetics. 91: 144-152. PMID 10748416 DOI: 10.1002/(Sici)1096-8628(20000313)91:2<144::Aid-Ajmg14>3.0.Co;2-V |
0.413 |
|
| 2000 |
Tassone F, Hagerman RJ, Taylor AK, Gane LW, Godfrey TE, Hagerman PJ. Elevated levels of FMR1 mRNA carrier males: A new mechanism of involvement in the fragile-X syndrome American Journal of Human Genetics. 66: 6-15. PMID 10631132 DOI: 10.1086/302720 |
0.506 |
|
| 1999 |
Mills JB, Vacano E, Hagerman PJ. Flexibility of single-stranded DNA: Use of gapped duplex helices to determine the persistence lengths of Poly(dT) and Poly(dA) Journal of Molecular Biology. 285: 245-257. PMID 9878403 DOI: 10.1006/Jmbi.1998.2287 |
0.338 |
|
| 1998 |
Friederich MW, Vacano E, Hagerman PJ. Global flexibility of tertiary structure in RNA: Yeast tRNA(Phe) as a model system Proceedings of the National Academy of Sciences of the United States of America. 95: 3572-3577. PMID 9520407 DOI: 10.1073/Pnas.95.7.3572 |
0.343 |
|
| 1997 |
Hagerman PJ. Flexibility of RNA Annual Review of Biophysics and Biomolecular Structure. 26: 139-156. PMID 9241416 DOI: 10.1146/Annurev.Biophys.26.1.139 |
0.312 |
|
| 1996 |
Zacharias M, Hagerman PJ. The influence of symmetric internal loops on the flexibility of RNA Journal of Molecular Biology. 257: 276-289. PMID 8609623 DOI: 10.1006/Jmbi.1996.0162 |
0.315 |
|
| 1995 |
Hodges-Garcia Y, Hagerman PJ. Investigation of the influence of cytosine methylation on DNA flexibility Journal of Biological Chemistry. 270: 197-201. PMID 7814373 DOI: 10.1074/Jbc.270.1.197 |
0.304 |
|
| 1995 |
Zacharias M, Hagerman PJ. The bend in RNA created by the trans-activation response element bulge of human immunodeficiency virus is straightened by arginine and by Tat-derived peptide Proceedings of the National Academy of Sciences of the United States of America. 92: 6052-6056. PMID 7597079 DOI: 10.1073/Pnas.92.13.6052 |
0.302 |
|
| 1995 |
Zacharias M, Hagerman PJ. Bulge-Induced Bends in RNA: Quantification by Transient Electric Birefringence Journal of Molecular Biology. 247: 486-500. PMID 7536250 DOI: 10.1006/Jmbi.1995.0155 |
0.324 |
|
| 1995 |
Kebbekus P, Draper DE, Hagerman P. Persistence length of RNA. Biochemistry. 34: 4354-7. PMID 7535562 DOI: 10.1021/Bi00013A026 |
0.33 |
|
| 1994 |
Mills JB, Cooper JP, Hagerman PJ. Electrophoretic evidence that single-stranded regions of one or more nucleotides dramatically increase the flexibility of DNA. Biochemistry. 33: 1797-803. PMID 8110781 DOI: 10.1021/Bi00173A024 |
0.318 |
|
| 1994 |
Olmsted MC, Hagerman PJ. Excess counterion accumulation around branched nucleic acids Journal of Molecular Biology. 243: 919-929. PMID 7525974 DOI: 10.1006/Jmbi.1994.1692 |
0.314 |
|
| 1994 |
Shen Z, Hagerman PJ. Conformation of the central, three-helix junction of the 5 S ribosomal RNA of Sulfolobus acidocaldarius Journal of Molecular Biology. 241: 415-430. PMID 7520504 DOI: 10.1006/Jmbi.1994.1517 |
0.3 |
|
| 1991 |
Hagerman PJ. Electrophoretic and hydrodynamic properties of duplex ribonucleic acid molecules transcribed in vitro: Evidence that a-tracts do not generate curvature in RNA Biochemistry. 30: 4268-4277. PMID 2021619 DOI: 10.1021/Bi00231A024 |
0.332 |
|
| 1990 |
Taylor WH, Hagerman PJ. Application of the method of phage T4 DNA ligase-catalyzed ring-closure to the study of DNA structure. II. NaCl-dependence of DNA flexibility and helical repeat. Journal of Molecular Biology. 212: 363-76. PMID 2319604 DOI: 10.1016/0022-2836(90)90131-5 |
0.331 |
|
| 1990 |
Hagerman PJ, Ramadevi VA. Application of the method of phage T4 DNA ligase-catalyzed ring-closure to the study of DNA structure. I. Computational analysis Journal of Molecular Biology. 212: 351-362. PMID 2319603 DOI: 10.1016/0022-2836(90)90130-E |
0.3 |
|
| 1990 |
Hagerman PJ. Sequence-directed curvature of DNA Annual Review of Biochemistry. 59: 755-781. PMID 2197990 DOI: 10.1146/Annurev.Bi.59.070190.003543 |
0.302 |
|
| 1989 |
Cooper JP, Hagerman PJ. Geometry of a branched DNA structure in solution. Proceedings of the National Academy of Sciences of the United States of America. 86: 7336-40. PMID 2798413 DOI: 10.1073/Pnas.86.19.7336 |
0.315 |
|
| 1984 |
Hagerman PJ. Evidence for the existence of stable curvature of DNA in solution Proceedings of the National Academy of Sciences of the United States of America. 81: 4632-4636. PMID 6087336 DOI: 10.1073/Pnas.81.15.4632 |
0.302 |
|
| 1983 |
Hagerman RJ, McBOGG P, Hagerman PJ. The fragile x syndrome: History, diagnosis, and treatment Journal of Developmental and Behavioral Pediatrics. 4: 122-130. PMID 6348096 DOI: 10.1097/00004703-198306000-00009 |
0.434 |
|
| 1981 |
Hagerman PJ. Investigation of the flexibility of DNA using transient electric birefringence Biopolymers - Peptide Science Section. 20: 1503-1535. PMID 7023566 DOI: 10.1002/Bip.1981.360200710 |
0.313 |
|
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