A citation-based method for searching scientific literature

R J Hagerman, M Leehey, W Heinrichs, F Tassone, R Wilson, J Hills, J Grigsby, B Gage, P J Hagerman. Neurology 2001
Times Cited: 642







List of co-cited articles
975 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


CGG repeat-associated translation mediates neurodegeneration in fragile X tremor ataxia syndrome.
Peter K Todd, Seok Yoon Oh, Amy Krans, Fang He, Chantal Sellier, Michelle Frazer, Abigail J Renoux, Kai-chun Chen, K Matthew Scaglione, Venkatesha Basrur,[...]. Neuron 2013
274
40

Fragile X premutation tremor/ataxia syndrome: molecular, clinical, and neuroimaging correlates.
Sébastien Jacquemont, Randi J Hagerman, Maureen Leehey, Jim Grigsby, Lin Zhang, James A Brunberg, Claudia Greco, Vincent Des Portes, Tristan Jardini, Richard Levine,[...]. Am J Hum Genet 2003
499
38

Translation of Expanded CGG Repeats into FMRpolyG Is Pathogenic and May Contribute to Fragile X Tremor Ataxia Syndrome.
Chantal Sellier, Ronald A M Buijsen, Fang He, Sam Natla, Laura Jung, Philippe Tropel, Angeline Gaucherot, Hugues Jacobs, Hamid Meziane, Alexandre Vincent,[...]. Neuron 2017
106
32

Penetrance of the fragile X-associated tremor/ataxia syndrome in a premutation carrier population.
Sébastien Jacquemont, Randi J Hagerman, Maureen A Leehey, Deborah A Hall, Richard A Levine, James A Brunberg, Lin Zhang, Tristan Jardini, Louise W Gane, Susan W Harris,[...]. JAMA 2004
421
31

Neuropathology of fragile X-associated tremor/ataxia syndrome (FXTAS).
C M Greco, R F Berman, R M Martin, F Tassone, P H Schwartz, A Chang, B D Trapp, C Iwahashi, J Brunberg, J Grigsby,[...]. Brain 2006
348
28

Non-ATG-initiated translation directed by microsatellite expansions.
Tao Zu, Brian Gibbens, Noelle S Doty, Mário Gomes-Pereira, Aline Huguet, Matthew D Stone, Jamie Margolis, Mark Peterson, Todd W Markowski, Melissa A C Ingram,[...]. Proc Natl Acad Sci U S A 2011
521
25

Neuronal intranuclear inclusions in a new cerebellar tremor/ataxia syndrome among fragile X carriers.
C M Greco, R J Hagerman, F Tassone, A E Chudley, M R Del Bigio, S Jacquemont, M Leehey, P J Hagerman. Brain 2002
374
25

Protein composition of the intranuclear inclusions of FXTAS.
C K Iwahashi, D H Yasui, H-J An, C M Greco, F Tassone, K Nannen, B Babineau, C B Lebrilla, R J Hagerman, P J Hagerman. Brain 2006
241
24

RNA-binding proteins hnRNP A2/B1 and CUGBP1 suppress fragile X CGG premutation repeat-induced neurodegeneration in a Drosophila model of FXTAS.
Oyinkan A Sofola, Peng Jin, Yunlong Qin, Ranhui Duan, Huijie Liu, Maria de Haro, David L Nelson, Juan Botas. Neuron 2007
232
23

Elevated levels of FMR1 mRNA in carrier males: a new mechanism of involvement in the fragile-X syndrome.
F Tassone, R J Hagerman, A K Taylor, L W Gane, T E Godfrey, P J Hagerman. Am J Hum Genet 2000
586
23

Pur alpha binds to rCGG repeats and modulates repeat-mediated neurodegeneration in a Drosophila model of fragile X tremor/ataxia syndrome.
Peng Jin, Ranhui Duan, Abrar Qurashi, Yunlong Qin, Donghua Tian, Tracie C Rosser, Huijie Liu, Yue Feng, Stephen T Warren. Neuron 2007
219
22


Presence of inclusions positive for polyglycine containing protein, FMRpolyG, indicates that repeat-associated non-AUG translation plays a role in fragile X-associated primary ovarian insufficiency.
R A M Buijsen, J A Visser, P Kramer, E A W F M Severijnen, M Gearing, N Charlet-Berguerand, S L Sherman, R F Berman, R Willemsen, R K Hukema. Hum Reprod 2016
44
43

Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome.
A J Verkerk, M Pieretti, J S Sutcliffe, Y H Fu, D P Kuhl, A Pizzuti, O Reiner, S Richards, M F Victoria, F P Zhang. Cell 1991
18

Sequestration of DROSHA and DGCR8 by expanded CGG RNA repeats alters microRNA processing in fragile X-associated tremor/ataxia syndrome.
Chantal Sellier, Fernande Freyermuth, Ricardos Tabet, Tuan Tran, Fang He, Frank Ruffenach, Violaine Alunni, Herve Moine, Christelle Thibault, Adeline Page,[...]. Cell Rep 2013
145
18

Sam68 sequestration and partial loss of function are associated with splicing alterations in FXTAS patients.
Chantal Sellier, Frédérique Rau, Yilei Liu, Flora Tassone, Renate K Hukema, Renata Gattoni, Anne Schneider, Stéphane Richard, Rob Willemsen, David J Elliott,[...]. EMBO J 2010
238
18

Fragile X-associated tremor/ataxia syndrome: clinical features, genetics, and testing guidelines.
Elizabeth Berry-Kravis, Liane Abrams, Sarah M Coffey, Deborah A Hall, Claudia Greco, Louise W Gane, Jim Grigsby, James A Bourgeois, Brenda Finucane, Sebastien Jacquemont,[...]. Mov Disord 2007
219
18

Penetrance of FMR1 premutation associated pathologies in fragile X syndrome families.
Laia Rodriguez-Revenga, Irene Madrigal, Javier Pagonabarraga, Mar Xunclà, Celia Badenas, Jaime Kulisevsky, Beatriz Gomez, Montserrat Milà. Eur J Hum Genet 2009
192
18


A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD.
Alan E Renton, Elisa Majounie, Adrian Waite, Javier Simón-Sánchez, Sara Rollinson, J Raphael Gibbs, Jennifer C Schymick, Hannu Laaksovirta, John C van Swieten, Liisa Myllykangas,[...]. Neuron 2011
17

Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS.
Mariely DeJesus-Hernandez, Ian R Mackenzie, Bradley F Boeve, Adam L Boxer, Matt Baker, Nicola J Rutherford, Alexandra M Nicholson, NiCole A Finch, Heather Flynn, Jennifer Adamson,[...]. Neuron 2011
17


Evidence of mitochondrial dysfunction in fragile X-associated tremor/ataxia syndrome.
Catherine Ross-Inta, Alicja Omanska-Klusek, Sarah Wong, Cedrick Barrow, Dolores Garcia-Arocena, Christine Iwahashi, Elizabeth Berry-Kravis, Randi J Hagerman, Paul J Hagerman, Cecilia Giulivi. Biochem J 2010
117
14

FMRpolyG-positive inclusions in CNS and non-CNS organs of a fragile X premutation carrier with fragile X-associated tremor/ataxia syndrome.
Ronald A M Buijsen, Chantal Sellier, Lies-Anne W F M Severijnen, Mustapha Oulad-Abdelghani, Rob F M Verhagen, Robert F Berman, Nicolas Charlet-Berguerand, Rob Willemsen, Renate K Hukema. Acta Neuropathol Commun 2014
45
31

Fragile X premutation carriers: characteristic MR imaging findings of adult male patients with progressive cerebellar and cognitive dysfunction.
James A Brunberg, Sebastien Jacquemont, Randi J Hagerman, Elizabeth M Berry-Kravis, Jim Grigsby, Maureen A Leehey, Flora Tassone, W Ted Brown, Claudia M Greco, Paul J Hagerman. AJNR Am J Neuroradiol 2002
269
14


RNA-mediated neurodegeneration caused by the fragile X premutation rCGG repeats in Drosophila.
Peng Jin, Daniela C Zarnescu, Fuping Zhang, Christopher E Pearson, John C Lucchesi, Kevin Moses, Stephen T Warren. Neuron 2003
250
13

Variation of the CGG repeat at the fragile X site results in genetic instability: resolution of the Sherman paradox.
Y H Fu, D P Kuhl, A Pizzuti, M Pieretti, J S Sutcliffe, S Richards, A J Verkerk, J J Holden, R G Fenwick, S T Warren. Cell 1991
13

Widespread non-central nervous system organ pathology in fragile X premutation carriers with fragile X-associated tremor/ataxia syndrome and CGG knock-in mice.
Michael R Hunsaker, Claudia M Greco, Marian A Spath, Arie P T Smits, Celestine S Navarro, Flora Tassone, Johan M Kros, Lies-Anne Severijnen, Elizabeth M Berry-Kravis, Robert F Berman,[...]. Acta Neuropathol 2011
69
18

FXTAS: new insights and the need for revised diagnostic criteria.
Emmanuelle Apartis, Anne Blancher, Wassilios G Meissner, Lucie Guyant-Maréchal, David Maltête, Thomas De Broucker, André-Pierre Legrand, Hichem Bouzenada, Hung Tran Thanh, Magali Sallansonnet-Froment,[...]. Neurology 2012
96
13

Expanded clinical phenotype of women with the FMR1 premutation.
Sarah M Coffey, Kylee Cook, Nicole Tartaglia, Flora Tassone, Danh V Nguyen, Ruiqin Pan, Hannah E Bronsky, Jennifer Yuhas, Mariya Borodyanskaya, Jim Grigsby,[...]. Am J Med Genet A 2008
211
13

New clinical findings in the fragile X-associated tremor ataxia syndrome (FXTAS).
Jorge L Juncos, Joash T Lazarus, Emily Graves-Allen, Lisa Shubeck, Michelle Rusin, Gloria Novak, Deborah Hamilton, Julia Rohr, Stephanie L Sherman. Neurogenetics 2011
49
26

A novel FMR1 PCR method for the routine detection of low abundance expanded alleles and full mutations in fragile X syndrome.
Stela Filipovic-Sadic, Sachin Sah, Liangjing Chen, Julie Krosting, Edward Sekinger, Wenting Zhang, Paul J Hagerman, Timothy T Stenzel, Andrew G Hadd, Gary J Latham,[...]. Clin Chem 2010
169
13


Impaired Mitochondrial Function and Dynamics in the Pathogenesis of FXTAS.
M I Alvarez-Mora, L Rodriguez-Revenga, I Madrigal, M Guitart-Mampel, G Garrabou, M Milà. Mol Neurobiol 2017
27
44

Induced expression of expanded CGG RNA causes mitochondrial dysfunction in vivo.
Renate K Hukema, Ronald A M Buijsen, Chris Raske, Lies Anne Severijnen, Ingeborg Nieuwenhuizen-Bakker, Michelle Minneboo, Alex Maas, Rini de Crom, Johan M Kros, Paul J Hagerman,[...]. Cell Cycle 2014
35
34

CGG repeat length correlates with age of onset of motor signs of the fragile X-associated tremor/ataxia syndrome (FXTAS).
Flora Tassone, John Adams, Elizabeth M Berry-Kravis, Susannah S Cohen, Alfredo Brusco, Maureen A Leehey, Lexin Li, Randi J Hagerman, Paul J Hagerman. Am J Med Genet B Neuropsychiatr Genet 2007
104
12

FMR1 CGG repeat length predicts motor dysfunction in premutation carriers.
M A Leehey, E Berry-Kravis, C G Goetz, L Zhang, D A Hall, L Li, C D Rice, R Lara, J Cogswell, A Reynolds,[...]. Neurology 2008
118
12

Association of FMR1 repeat size with ovarian dysfunction.
A K Sullivan, M Marcus, M P Epstein, E G Allen, A E Anido, J J Paquin, M Yadav-Shah, S L Sherman. Hum Reprod 2005
291
11


FMR1 CGG allele size and prevalence ascertained through newborn screening in the United States.
Flora Tassone, Ka Pou Iong, Tzu-Han Tong, Joyce Lo, Louise W Gane, Elizabeth Berry-Kravis, Danh Nguyen, Lisa Y Mu, Jennifer Laffin, Don B Bailey,[...]. Genome Med 2012
162
11

Reversibility of neuropathology and motor deficits in an inducible mouse model for FXTAS.
Renate K Hukema, Ronald A M Buijsen, Martijn Schonewille, Chris Raske, Lies-Anne W F M Severijnen, Ingeborg Nieuwenhuizen-Bakker, Rob F M Verhagen, Lisanne van Dessel, Alex Maas, Nicolas Charlet-Berguerand,[...]. Hum Mol Genet 2015
29
37

Epidemiology of fragile X syndrome: a systematic review and meta-analysis.
Jessica Hunter, Oliver Rivero-Arias, Angel Angelov, Edward Kim, Iain Fotheringham, Jose Leal. Am J Med Genet A 2014
138
11

RAN translation at CGG repeats induces ubiquitin proteasome system impairment in models of fragile X-associated tremor ataxia syndrome.
Seok Yoon Oh, Fang He, Amy Krans, Michelle Frazer, J Paul Taylor, Henry L Paulson, Peter K Todd. Hum Mol Genet 2015
51
21

Examination of reproductive aging milestones among women who carry the FMR1 premutation.
E G Allen, A K Sullivan, M Marcus, C Small, C Dominguez, M P Epstein, K Charen, W He, K C Taylor, S L Sherman. Hum Reprod 2007
137
11

Progression of tremor and ataxia in male carriers of the FMR1 premutation.
Maureen A Leehey, Elizabeth Berry-Kravis, Sung-Joon Min, Deborah A Hall, Cathlin D Rice, Lin Zhang, Jim Grigsby, Claudia M Greco, Ann Reynolds, Rebecca Lara,[...]. Mov Disord 2007
86
12

Neuropathological, clinical and molecular pathology in female fragile X premutation carriers with and without FXTAS.
F Tassone, C M Greco, M R Hunsaker, A L Seritan, R F Berman, L W Gane, S Jacquemont, K Basuta, L-W Jin, P J Hagerman,[...]. Genes Brain Behav 2012
91
12

Fragile X premutation is a significant risk factor for premature ovarian failure: the International Collaborative POF in Fragile X study--preliminary data.
D J Allingham-Hawkins, R Babul-Hirji, D Chitayat, J J Holden, K T Yang, C Lee, R Hudson, H Gorwill, S L Nolin, A Glicksman,[...]. Am J Med Genet 1999
281
10

Transcription-associated R-loop formation across the human FMR1 CGG-repeat region.
Erick W Loomis, Lionel A Sanz, Frédéric Chédin, Paul J Hagerman. PLoS Genet 2014
113
10

Friedreich's ataxia: autosomal recessive disease caused by an intronic GAA triplet repeat expansion.
V Campuzano, L Montermini, M D Moltò, L Pianese, M Cossée, F Cavalcanti, E Monros, F Rodius, F Duclos, A Monticelli,[...]. Science 1996
10


Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.