A citation-based method for searching scientific literature

Arun Kumar Verma, Eshan Khan, Subodh Kumar Mishra, Neha Jain, Amit Kumar. ACS Chem Neurosci 2019
Times Cited: 9







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



Times Cited
  Times     Co-cited
Similarity


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
643
55

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
242
55

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
279
55

Trinucleotide repeat disorders.
Harry T Orr, Huda Y Zoghbi. Annu Rev Neurosci 2007
961
44

Myricetin Reduces Toxic Level of CAG Repeats RNA in Huntington's Disease (HD) and Spino Cerebellar Ataxia (SCAs).
Eshan Khan, Arpita Tawani, Subodh Kumar Mishra, Arun Kumar Verma, Arun Upadhyay, Mohit Kumar, Rajat Sandhir, Amit Mishra, Amit Kumar. ACS Chem Biol 2018
17
44

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
524
44

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
146
44

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
241
44

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
109
44

R-loops associated with triplet repeat expansions promote gene silencing in Friedreich ataxia and fragile X syndrome.
Matthias Groh, Michele M P Lufino, Richard Wade-Martins, Natalia Gromak. PLoS Genet 2014
185
33

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
423
33

Rationally designed small molecules targeting toxic CAG repeat RNA that causes Huntington's disease (HD) and spinocerebellar ataxia (SCAs).
Eshan Khan, Soumen Biswas, Subodh Kumar Mishra, Ribhav Mishra, Sampak Samanta, Amit Mishra, Arpita Tawani, Amit Kumar. Biochimie 2019
9
33

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
33

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
68
33

Precise small-molecule cleavage of an r(CUG) repeat expansion in a myotonic dystrophy mouse model.
Alicia J Angelbello, Suzanne G Rzuczek, Kendra K Mckee, Jonathan L Chen, Hailey Olafson, Michael D Cameron, Walter N Moss, Eric T Wang, Matthew D Disney. Proc Natl Acad Sci U S A 2019
43
33

Chemical screen reveals small molecules suppressing fragile X premutation rCGG repeat-mediated neurodegeneration in Drosophila.
Abrar Qurashi, Huijie Liu, Laurie Ray, David L Nelson, Ranhui Duan, Peng Jin. Hum Mol Genet 2012
28
33

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
37
33

Chemical correction of pre-mRNA splicing defects associated with sequestration of muscleblind-like 1 protein by expanded r(CAG)-containing transcripts.
Amit Kumar, Raman Parkesh, Lukasz J Sznajder, Jessica L Childs-Disney, Krzysztof Sobczak, Matthew D Disney. ACS Chem Biol 2012
59
33

Small Molecule Recognition and Tools to Study Modulation of r(CGG)(exp) in Fragile X-Associated Tremor Ataxia Syndrome.
Wang-Yong Yang, Fang He, Rita L Strack, Seok Yoon Oh, Michelle Frazer, Samie R Jaffrey, Peter K Todd, Matthew D Disney. ACS Chem Biol 2016
28
33

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
118
33

Expandable DNA repeats and human disease.
Sergei M Mirkin. Nature 2007
581
33

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
33


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
233
33


A small molecule regulates hairpin structures in d(CGG) trinucleotide repeats.
Masaki Hagihara, Hanping He, Maki Kimura, Kazuhiko Nakatani. Bioorg Med Chem Lett 2012
20
22


The P42 peptide and Peptide-based therapies for Huntington's disease.
Cecilia Marelli, Florence Maschat. Orphanet J Rare Dis 2016
12
22

Polyglutamine expansion as a pathological epitope in Huntington's disease and four dominant cerebellar ataxias.
Y Trottier, Y Lutz, G Stevanin, G Imbert, D Devys, G Cancel, F Saudou, C Weber, G David, L Tora. Nature 1995
539
22

FMR1 gene premutation is a frequent genetic cause of late-onset sporadic cerebellar ataxia.
A Brussino, C Gellera, A Saluto, C Mariotti, C Arduino, B Castellotti, M Camerlingo, V de Angelis, L Orsi, P Tosca,[...]. Neurology 2005
59
22

Trinucleotide repeat amplification and hypermethylation of a CpG island in FRAXE mental retardation.
S J Knight, A V Flannery, M C Hirst, L Campbell, Z Christodoulou, S R Phelps, J Pointon, H R Middleton-Price, A Barnicoat, M E Pembrey. Cell 1993
487
22



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
504
22

Identification of the gene FMR2, associated with FRAXE mental retardation.
J Gecz, A K Gedeon, G R Sutherland, J C Mulley. Nat Genet 1996
244
22

A Huntingtin-based peptide inhibitor of caspase-6 provides protection from mutant Huntingtin-induced motor and behavioral deficits.
Israel Aharony, Dagmar E Ehrnhoefer, Adi Shruster, Xiaofan Qiu, Sonia Franciosi, Michael R Hayden, Daniel Offen. Hum Mol Genet 2015
34
22

Screening for FMR-1 premutations in 122 older Flemish males presenting with ataxia.
Hilde Van Esch, Rene Dom, Dorien Bex, Ivo Salden, Jo Caeckebeke, Alain Wibail, Martine Borghgraef, Eric Legius, Jean-Pierre Fryns, Gert Matthijs. Eur J Hum Genet 2005
46
22

Naphthyridine-Benzoazaquinolone: Evaluation of a Tricyclic System for the Binding to (CAG)n Repeat DNA and RNA.
Jinxing Li, Akihiro Sakata, Hanping He, Li-Ping Bai, Asako Murata, Chikara Dohno, Kazuhiko Nakatani. Chem Asian J 2016
10
22

Precise small-molecule recognition of a toxic CUG RNA repeat expansion.
Suzanne G Rzuczek, Lesley A Colgan, Yoshio Nakai, Michael D Cameron, Denis Furling, Ryohei Yasuda, Matthew D Disney. Nat Chem Biol 2017
101
22

Green tea (-)-epigallocatechin-gallate modulates early events in huntingtin misfolding and reduces toxicity in Huntington's disease models.
Dagmar E Ehrnhoefer, Martin Duennwald, Phoebe Markovic, Jennifer L Wacker, Sabine Engemann, Margaret Roark, Justin Legleiter, J Lawrence Marsh, Leslie M Thompson, Susan Lindquist,[...]. Hum Mol Genet 2006
258
22

Small-molecule ligand induces nucleotide flipping in (CAG)n trinucleotide repeats.
Kazuhiko Nakatani, Shinya Hagihara, Yuki Goto, Akio Kobori, Masaki Hagihara, Gosuke Hayashi, Motoki Kyo, Makoto Nomura, Masaki Mishima, Chojiro Kojima. Nat Chem Biol 2005
99
22

Piperine ameliorates SCA17 neuropathology by reducing ER stress.
Jifeng Guo, Yiting Cui, Qiong Liu, Yang Yang, Yujing Li, Ling Weng, Beisha Tang, Peng Jin, Xiao-Jiang Li, Su Yang,[...]. Mol Neurodegener 2018
19
22

Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy.
A R La Spada, E M Wilson, D B Lubahn, A E Harding, K H Fischbeck. Nature 1991
22

Reducing Mutant Huntingtin Protein Expression in Living Cells by a Newly Identified RNA CAG Binder.
Frank Matthes, Serena Massari, Anna Bochicchio, Kenji Schorpp, Judith Schilling, Stephanie Weber, Nina Offermann, Jenny Desantis, Erich Wanker, Paolo Carloni,[...]. ACS Chem Neurosci 2018
11
22


Neuroprotective effects of curcumin.
Greg M Cole, Bruce Teter, Sally A Frautschy. Adv Exp Med Biol 2007
267
22

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
162
22

Design of a bioactive small molecule that targets the myotonic dystrophy type 1 RNA via an RNA motif-ligand database and chemical similarity searching.
Raman Parkesh, Jessica L Childs-Disney, Masayuki Nakamori, Amit Kumar, Eric Wang, Thomas Wang, Jason Hoskins, Tuan Tran, David Housman, Charles A Thornton,[...]. J Am Chem Soc 2012
99
22

TDP-43 suppresses CGG repeat-induced neurotoxicity through interactions with HnRNP A2/B1.
Fang He, Amy Krans, Brian D Freibaum, J Paul Taylor, Peter K Todd. Hum Mol Genet 2014
33
22

Repeat-associated non-ATG (RAN) translation.
John Douglas Cleary, Amrutha Pattamatta, Laura P W Ranum. J Biol Chem 2018
36
22


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.