A citation-based method for searching scientific literature

M Rebecca Glineburg, Peter K Todd, Nicolas Charlet-Berguerand, Chantal Sellier. Brain Res 2018
Times Cited: 32







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



Times Cited
  Times     Co-cited
Similarity


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
112
59

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
283
56

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
245
37

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
150
34

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
378
34

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
49
34

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
591
34

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
56
28

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
243
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
528
28

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
29
31

Fragile X syndrome.
Randi J Hagerman, Elizabeth Berry-Kravis, Heather Cody Hazlett, Donald B Bailey, Herve Moine, R Frank Kooy, Flora Tassone, Ilse Gantois, Nahum Sonenberg, Jean Louis Mandel,[...]. Nat Rev Dis Primers 2017
172
25

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
352
25

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
507
21

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
222
21

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
45
18

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
79
18

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
148
18

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
425
18

Fragile X-Associated Tremor/Ataxia Syndrome: From Molecular Pathogenesis to Development of Therapeutics.
Ha Eun Kong, Juan Zhao, Shunliang Xu, Peng Jin, Yan Jin. Front Cell Neurosci 2017
23
26

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
253
18

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
235
18

The fragile-X premutation: a maturing perspective.
Paul J Hagerman, Randi J Hagerman. Am J Hum Genet 2004
346
18


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
120
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
218
18

Composition of the Intranuclear Inclusions of Fragile X-associated Tremor/Ataxia Syndrome.
Lisa Ma, Anthony W Herren, Glenda Espinal, Jamie Randol, Bridget McLaughlin, Veronica Martinez-Cerdeño, Isaac N Pessah, Randi J Hagerman, Paul J Hagerman. Acta Neuropathol Commun 2019
21
28

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
118
18

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
30
16

RAN translation-What makes it run?
Katelyn M Green, Alexander E Linsalata, Peter K Todd. Brain Res 2016
59
15

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
645
15

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
15

RAN Translation in Huntington Disease.
Monica Bañez-Coronel, Fatma Ayhan, Alex D Tarabochia, Tao Zu, Barbara A Perez, Solaleh Khoramian Tusi, Olga Pletnikova, David R Borchelt, Christopher A Ross, Russell L Margolis,[...]. Neuron 2015
164
15

C9ORF72 GGGGCC repeat-associated non-AUG translation is upregulated by stress through eIF2α phosphorylation.
Weiwei Cheng, Shaopeng Wang, Alexander A Mestre, Chenglai Fu, Andres Makarem, Fengfan Xian, Lindsey R Hayes, Rodrigo Lopez-Gonzalez, Kevin Drenner, Jie Jiang,[...]. Nat Commun 2018
69
15

Fragile X-associated tremor/ataxia syndrome.
Paul J Hagerman, Randi J Hagerman. Ann N Y Acad Sci 2015
88
15

RAN translation at C9orf72-associated repeat expansions is selectively enhanced by the integrated stress response.
Katelyn M Green, M Rebecca Glineburg, Michael G Kearse, Brittany N Flores, Alexander E Linsalata, Stephen J Fedak, Aaron C Goldstrohm, Sami J Barmada, Peter K Todd. Nat Commun 2017
78
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
759
15

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
54
15

Altered redox mitochondrial biology in the neurodegenerative disorder fragile X-tremor/ataxia syndrome: use of antioxidants in precision medicine.
Gyu Song, Eleonora Napoli, Sarah Wong, Randi Hagerman, Siming Liu, Flora Tassone, Cecilia Giulivi. Mol Med 2016
30
16

Intranuclear inclusions in neural cells with premutation alleles in fragile X associated tremor/ataxia syndrome.
F Tassone, R J Hagerman, D Garcia-Arocena, E W Khandjian, C M Greco, P J Hagerman. J Med Genet 2004
119
15

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
36
15

Fragile X-Associated Neuropsychiatric Disorders (FXAND).
Randi J Hagerman, Dragana Protic, Akash Rajaratnam, Maria J Salcedo-Arellano, Elber Yuksel Aydin, Andrea Schneider. Front Psychiatry 2018
56
15

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
195
15

Noncoding CGG repeat expansions in neuronal intranuclear inclusion disease, oculopharyngodistal myopathy and an overlapping disease.
Hiroyuki Ishiura, Shota Shibata, Jun Yoshimura, Yuta Suzuki, Wei Qu, Koichiro Doi, M Asem Almansour, Junko Kanda Kikuchi, Makiko Taira, Jun Mitsui,[...]. Nat Genet 2019
87
15

The unstable repeats--three evolving faces of neurological disease.
David L Nelson, Harry T Orr, Stephen T Warren. Neuron 2013
116
12

New developments in RAN translation: insights from multiple diseases.
John Douglas Cleary, Laura Pw Ranum. Curr Opin Genet Dev 2017
49
12

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
165
12


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.