A citation-based method for searching scientific literature

Chantal Sellier, Frédérique Rau, Yilei Liu, Flora Tassone, Renate K Hukema, Renata Gattoni, Anne Schneider, Stéphane Richard, Rob Willemsen, David J Elliott, Paul J Hagerman, Nicolas Charlet-Berguerand. EMBO J 2010
Times Cited: 236







List of co-cited articles
1474 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
270
57

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
142
48

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
230
38

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
217
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
102
35

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
517
34

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
239
33

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
346
28

Intention tremor, parkinsonism, and generalized brain atrophy in male carriers of fragile X.
R J Hagerman, M Leehey, W Heinrichs, F Tassone, R Wilson, J Hills, J Grigsby, B Gage, P J Hagerman. Neurology 2001
637
25

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
50
50


The FMR1 CGG repeat mouse displays ubiquitin-positive intranuclear neuronal inclusions; implications for the cerebellar tremor/ataxia syndrome.
Rob Willemsen, Marianne Hoogeveen-Westerveld, Surya Reis, Joan Holstege, Lies-Anne W F M Severijnen, Ingeborg M Nieuwenhuizen, Mariette Schrier, Leontine van Unen, Flora Tassone, Andre T Hoogeveen,[...]. Hum Mol Genet 2003
205
24


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
584
22

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
42
52

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
22

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
372
22

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
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
41
51

Unconventional translation of C9ORF72 GGGGCC expansion generates insoluble polypeptides specific to c9FTD/ALS.
Peter E A Ash, Kevin F Bieniek, Tania F Gendron, Thomas Caulfield, Wen-Lang Lin, Mariely Dejesus-Hernandez, Marka M van Blitterswijk, Karen Jansen-West, Joseph W Paul, Rosa Rademakers,[...]. Neuron 2013
658
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
116
17

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

CGG Repeat-Associated Non-AUG Translation Utilizes a Cap-Dependent Scanning Mechanism of Initiation to Produce Toxic Proteins.
Michael G Kearse, Katelyn M Green, Amy Krans, Caitlin M Rodriguez, Alexander E Linsalata, Aaron C Goldstrohm, Peter K Todd. Mol Cell 2016
73
23

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
27
59

Elevated FMR1 mRNA in premutation carriers is due to increased transcription.
Flora Tassone, Alexandra Beilina, Chiara Carosi, Serena Albertosi, Claudia Bagni, Lexin Li, Kira Glover, David Bentley, Paul J Hagerman. RNA 2007
128
16

A small molecule that targets r(CGG)(exp) and improves defects in fragile X-associated tremor ataxia syndrome.
Matthew D Disney, Biao Liu, Wang-Yong Yang, Chantal Sellier, Tuan Tran, Nicolas Charlet-Berguerand, Jessica L Childs-Disney. ACS Chem Biol 2012
67
23

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
496
16

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
16


RNA phase transitions in repeat expansion disorders.
Ankur Jain, Ronald D Vale. Nature 2017
280
16


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
34
44

Early mitochondrial abnormalities in hippocampal neurons cultured from Fmr1 pre-mutation mouse model.
Eitan S Kaplan, Zhengyu Cao, Susan Hulsizer, Flora Tassone, Robert F Berman, Paul J Hagerman, Isaac N Pessah. J Neurochem 2012
51
29

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
111
15

Myotonic dystrophy type 2 caused by a CCTG expansion in intron 1 of ZNF9.
C L Liquori, K Ricker, M L Moseley, J F Jacobsen, W Kress, S L Naylor, J W Day, L P Ranum. Science 2001
798
15

The C9orf72 repeat expansion disrupts nucleocytoplasmic transport.
Ke Zhang, Christopher J Donnelly, Aaron R Haeusler, Jonathan C Grima, James B Machamer, Peter Steinwald, Elizabeth L Daley, Sean J Miller, Kathleen M Cunningham, Svetlana Vidensky,[...]. Nature 2015
514
15

The C9orf72 GGGGCC repeat is translated into aggregating dipeptide-repeat proteins in FTLD/ALS.
Kohji Mori, Shih-Ming Weng, Thomas Arzberger, Stephanie May, Kristin Rentzsch, Elisabeth Kremmer, Bettina Schmid, Hans A Kretzschmar, Marc Cruts, Christine Van Broeckhoven,[...]. Science 2013
738
14

Altered zinc transport disrupts mitochondrial protein processing/import in fragile X-associated tremor/ataxia syndrome.
Eleonora Napoli, Catherine Ross-Inta, Sarah Wong, Alicja Omanska-Klusek, Cedrick Barrow, Christine Iwahashi, Dolores Garcia-Arocena, Danielle Sakaguchi, Elizabeth Berry-Kravis, Randi Hagerman,[...]. Hum Mol Genet 2011
71
19

Fragile X-associated tremor/ataxia syndrome.
Paul J Hagerman, Randi J Hagerman. Ann N Y Acad Sci 2015
86
16

Mouse models of the fragile X premutation and fragile X-associated tremor/ataxia syndrome.
Robert F Berman, Ronald Am Buijsen, Karen Usdin, Elizabeth Pintado, Frank Kooy, Dalyir Pretto, Isaac N Pessah, David L Nelson, Zachary Zalewski, Nicholas Charlet-Bergeurand,[...]. J Neurodev Disord 2014
34
38

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
210
13

Trinucleotide repeat disorders.
Harry T Orr, Huda Y Zoghbi. Annu Rev Neurosci 2007
951
13

Hexanucleotide repeats in ALS/FTD form length-dependent RNA foci, sequester RNA binding proteins, and are neurotoxic.
Youn-Bok Lee, Han-Jou Chen, João N Peres, Jorge Gomez-Deza, Jan Attig, Maja Stalekar, Claire Troakes, Agnes L Nishimura, Emma L Scotter, Caroline Vance,[...]. Cell Rep 2013
283
13

RAN proteins and RNA foci from antisense transcripts in C9ORF72 ALS and frontotemporal dementia.
Tao Zu, Yuanjing Liu, Monica Bañez-Coronel, Tammy Reid, Olga Pletnikova, Jada Lewis, Timothy M Miller, Matthew B Harms, Annet E Falchook, S H Subramony,[...]. Proc Natl Acad Sci U S A 2013
439
13

Loss of MBNL leads to disruption of developmentally regulated alternative polyadenylation in RNA-mediated disease.
Ranjan Batra, Konstantinos Charizanis, Mini Manchanda, Apoorva Mohan, Moyi Li, Dustin J Finn, Marianne Goodwin, Chaolin Zhang, Krzysztof Sobczak, Charles A Thornton,[...]. Mol Cell 2014
149
13

GGGGCC repeat expansion in C9orf72 compromises nucleocytoplasmic transport.
Brian D Freibaum, Yubing Lu, Rodrigo Lopez-Gonzalez, Nam Chul Kim, Sandra Almeida, Kyung-Ha Lee, Nisha Badders, Marc Valentine, Bruce L Miller, Philip C Wong,[...]. Nature 2015
440
13

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
418
13

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
160
12

DNA methylation represses FMR-1 transcription in fragile X syndrome.
J S Sutcliffe, D L Nelson, F Zhang, M Pieretti, C T Caskey, D Saxe, S T Warren. Hum Mol Genet 1992
469
12

Targeting the r(CGG) repeats that cause FXTAS with modularly assembled small molecules and oligonucleotides.
Tuan Tran, Jessica L Childs-Disney, Biao Liu, Lirui Guan, Suzanne Rzuczek, Matthew D Disney. ACS Chem Biol 2014
36
33


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.