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



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  Times     Co-cited
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Short antisense oligonucleotides alleviate the pleiotropic toxicity of RNA harboring expanded CGG repeats.
Magdalena Derbis, Emre Kul, Daria Niewiadomska, Michał Sekrecki, Agnieszka Piasecka, Katarzyna Taylor, Renate K Hukema, Oliver Stork, Krzysztof Sobczak. Nat Commun 2021
13
50

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
50

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
133
50

Association of NOTCH2NLC Repeat Expansions With Parkinson Disease.
Dongrui Ma, Yi Jayne Tan, Adeline S L Ng, Helen L Ong, Weiying Sim, Weng Khong Lim, Jing Xian Teo, Ebonne Y L Ng, Ee-Chien Lim, Ee-Wei Lim,[...]. JAMA Neurol 2020
36
50

Expansion of GGC repeat in the human-specific NOTCH2NLC gene is associated with essential tremor.
Qi-Ying Sun, Qian Xu, Yun Tian, Zheng-Mao Hu, Li-Xia Qin, Jin-Xia Yang, Wen Huang, Jin Xue, Jin-Chen Li, Sheng Zeng,[...]. Brain 2020
89
50

Long-read sequencing identified repeat expansions in the 5'UTR of the NOTCH2NLC gene from Chinese patients with neuronal intranuclear inclusion disease.
Jianwen Deng, Muliang Gu, Yu Miao, Sheng Yao, Min Zhu, Pu Fang, Xuefan Yu, Pidong Li, Yanan Su, Jian Huang,[...]. J Med Genet 2019
62
50

Long-read sequencing identifies GGC repeat expansions in NOTCH2NLC associated with neuronal intranuclear inclusion disease.
Jun Sone, Satomi Mitsuhashi, Atsushi Fujita, Takeshi Mizuguchi, Kohei Hamanaka, Keiko Mori, Haruki Koike, Akihiro Hashiguchi, Hiroshi Takashima, Hiroshi Sugiyama,[...]. Nat Genet 2019
190
50

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
148
50

Expansion of Human-Specific GGC Repeat in Neuronal Intranuclear Inclusion Disease-Related Disorders.
Yun Tian, Jun-Ling Wang, Wen Huang, Sheng Zeng, Bin Jiao, Zhen Liu, Zhao Chen, Yujing Li, Ying Wang, Hao-Xuan Min,[...]. Am J Hum Genet 2019
129
50

Repeat expansion scanning of the NOTCH2NLC gene in patients with multiple system atrophy.
Pu Fang, Yanyan Yu, Sheng Yao, Shuyun Chen, Min Zhu, Yunqing Chen, Keji Zou, Lulu Wang, Huan Wang, Ling Xin,[...]. Ann Clin Transl Neurol 2020
42
50

Therapeutic Development for CGG Repeat Expansion-Associated Neurodegeneration.
Keqin Xu, Yujing Li, Emily G Allen, Peng Jin. Front Cell Neurosci 2021
9
50

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
133
50

Timing of the absence of FMR1 expression in full mutation chorionic villi.
Rob Willemsen, Carola J M Bontekoe, Lies-Anne Severijnen, Ben A Oostra. Hum Genet 2002
80
33

Regional FMRP deficits and large repeat expansions into the full mutation range in a new Fragile X premutation mouse model.
Ali Entezam, Rea Biacsi, Bonnie Orrison, Tapas Saha, Gloria E Hoffman, Ed Grabczyk, Robert L Nussbaum, Karen Usdin. Gene 2007
146
33

Somatic expansion in mouse and human carriers of fragile X premutation alleles.
Rachel Adihe Lokanga, Ali Entezam, Daman Kumari, Dmitry Yudkin, Mei Qin, Carolyn Beebe Smith, Karen Usdin. Hum Mutat 2013
59
33


Mutsβ generates both expansions and contractions in a mouse model of the Fragile X-associated disorders.
Xiao-Nan Zhao, Daman Kumari, Shikha Gupta, Di Wu, Maya Evanitsky, Wei Yang, Karen Usdin. Hum Mol Genet 2015
43
33

Calcium dysregulation and Cdk5-ATM pathway involved in a mouse model of fragile X-associated tremor/ataxia syndrome.
Gaëlle Robin, José R López, Glenda M Espinal, Susan Hulsizer, Paul J Hagerman, Isaac N Pessah. Hum Mol Genet 2017
39
33

AGG interruptions and maternal age affect FMR1 CGG repeat allele stability during transmission.
Carolyn M Yrigollen, Loreto Martorell, Blythe Durbin-Johnson, Montserrat Naudo, Jordi Genoves, Alessandra Murgia, Roberta Polli, Lili Zhou, Deborah Barbouth, Abigail Rupchock,[...]. J Neurodev Disord 2014
67
33

The fragile-X premutation: a maturing perspective.
Paul J Hagerman, Randi J Hagerman. Am J Hum Genet 2004
355
33

Heterozygosity for a hypomorphic Polβ mutation reduces the expansion frequency in a mouse model of the Fragile X-related disorders.
Rachel Adihe Lokanga, Alireza Ghodsi Senejani, Joann Balazs Sweasy, Karen Usdin. PLoS Genet 2015
31
33

Double-strand break repair plays a role in repeat instability in a fragile X mouse model.
Inbal Gazy, Bruce Hayward, Svetlana Potapova, Xiaonan Zhao, Karen Usdin. DNA Repair (Amst) 2019
14
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
78
33

Repeat-associated non-AUG (RAN) translation and other molecular mechanisms in Fragile X Tremor Ataxia Syndrome.
M Rebecca Glineburg, Peter K Todd, Nicolas Charlet-Berguerand, Chantal Sellier. Brain Res 2018
44
33

Expansions and contractions of the FMR1 CGG repeat in 5,508 transmissions of normal, intermediate, and premutation alleles.
Sarah L Nolin, Anne Glicksman, Nicole Tortora, Emily Allen, James Macpherson, Montserrat Mila, Angela M Vianna-Morgante, Stephanie L Sherman, Carl Dobkin, Gary J Latham,[...]. Am J Med Genet A 2019
25
33

Curcumin Regulates the r(CGG)exp RNA Hairpin Structure and Ameliorate Defects in Fragile X-Associated Tremor Ataxia Syndrome.
Arun Kumar Verma, Eshan Khan, Subodh Kumar Mishra, Amit Mishra, Nicolas Charlet-Berguerand, Amit Kumar. Front Neurosci 2020
10
33

MutLγ promotes repeat expansion in a Fragile X mouse model while EXO1 is protective.
Xiaonan Zhao, Yongwei Zhang, Kenneth Wilkins, Winfried Edelmann, Karen Usdin. PLoS Genet 2018
31
33


The DNA replication program is altered at the FMR1 locus in fragile X embryonic stem cells.
Jeannine Gerhardt, Mark J Tomishima, Nikica Zaninovic, Dilek Colak, Zi Yan, Qiansheng Zhan, Zev Rosenwaks, Samie R Jaffrey, Carl L Schildkraut. Mol Cell 2014
74
33


A MutSβ-Dependent Contribution of MutSα to Repeat Expansions in Fragile X Premutation Mice?
Xiao-Nan Zhao, Rachel Lokanga, Kimaada Allette, Inbal Gazy, Di Wu, Karen Usdin. PLoS Genet 2016
32
33

Association of fragile X syndrome with delayed replication of the FMR1 gene.
R S Hansen, T K Canfield, M M Lamb, S M Gartler, C D Laird. Cell 1993
218
33

Hairpins are formed by the single DNA strands of the fragile X triplet repeats: structure and biological implications.
X Chen, S V Mariappan, P Catasti, R Ratliff, R K Moyzis, A Laayoun, S S Smith, E M Bradbury, G Gupta. Proc Natl Acad Sci U S A 1995
210
33




Replication Stress Induces Global Chromosome Breakage in the Fragile X Genome.
Arijita Chakraborty, Piroon Jenjaroenpun, Jing Li, Sami El Hilali, Andrew McCulley, Brian Haarer, Elizabeth A Hoffman, Aimee Belak, Audrey Thorland, Heidi Hehnly,[...]. Cell Rep 2020
16
33

CGG repeats associated with fragile X chromosome form left-handed Z-DNA structure.
Daniel Renčiuk, Jaroslav Kypr, Michaela Vorlíčková. Biopolymers 2011
22
33

Neuronal intranuclear inclusion disease is genetically heterogeneous.
Zhongbo Chen, Wai Yan Yau, Zane Jaunmuktane, Arianna Tucci, Prasanth Sivakumar, Sarah A Gagliano Taliun, Chris Turner, Stephanie Efthymiou, Kristina Ibáñez, Roisin Sullivan,[...]. Ann Clin Transl Neurol 2020
23
33

The GGC repeat expansion in NOTCH2NLC is associated with oculopharyngodistal myopathy type 3.
Jiaxi Yu, Jianwen Deng, Xueyu Guo, Jingli Shan, Xinghua Luan, Li Cao, Juan Zhao, Meng Yu, Wei Zhang, He Lv,[...]. Brain 2021
38
33

Clinicopathological features of adult-onset neuronal intranuclear inclusion disease.
Jun Sone, Keiko Mori, Tomonori Inagaki, Ryu Katsumata, Shinnosuke Takagi, Satoshi Yokoi, Kunihiko Araki, Toshiyasu Kato, Tomohiko Nakamura, Haruki Koike,[...]. Brain 2016
169
33



Neuronal intranuclear inclusion disease without polyglutamine inclusions in a child.
Kathryn McFadden, Ronald L Hamilton, Sam J Insalaco, Lawrence Lavine, Majeed Al-Mateen, Guoji Wang, Clayton A Wiley. J Neuropathol Exp Neurol 2005
29
33

Identification of GGC repeat expansion in the NOTCH2NLC gene in amyotrophic lateral sclerosis.
Yanchun Yuan, Zhen Liu, Xuan Hou, Wanzhen Li, Jie Ni, Ling Huang, Yiting Hu, Pan Liu, Xiaorong Hou, Jin Xue,[...]. Neurology 2020
33
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
23
33

Translation of GGC repeat expansions into a toxic polyglycine protein in NIID defines a novel class of human genetic disorders: The polyG diseases.
Manon Boivin, Jianwen Deng, Véronique Pfister, Erwan Grandgirard, Mustapha Oulad-Abdelghani, Bastien Morlet, Frank Ruffenach, Luc Negroni, Pascale Koebel, Hugues Jacob,[...]. Neuron 2021
29
33

Clinical and pathological features in adult-onset NIID patients with cortical enhancement.
Huiting Liang, Bo Wang, Qing Li, Jianwen Deng, Lulu Wang, Huan Wang, Xiaobin Li, Min Zhu, Yu Cai, Zhaoxia Wang,[...]. J Neurol 2020
25
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.