A citation-based method for searching scientific literature

Keqin Xu, Yujing Li, Emily G Allen, Peng Jin. Front Cell Neurosci 2021
Times Cited: 5







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



Times Cited
  Times     Co-cited
Similarity


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
23
80

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
147
80

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
112
80

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
24
80

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
21
80

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
159
80

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
122
80

CGG expansion in NOTCH2NLC is associated with oculopharyngodistal myopathy with neurological manifestations.
Masashi Ogasawara, Aritoshi Iida, Theerawat Kumutpongpanich, Ayami Ozaki, Yasushi Oya, Hirofumi Konishi, Akinori Nakamura, Ryuta Abe, Hiroshi Takai, Ritsuko Hanajima,[...]. Acta Neuropathol Commun 2020
24
80

NOTCH2NLC Intermediate-Length Repeat Expansions Are Associated with Parkinson Disease.
Chang-He Shi, Yu Fan, Jing Yang, Yan-Peng Yuan, Si Shen, Fen Liu, Cheng-Yuan Mao, Han Liu, Shuo Zhang, Zheng-Wei Hu,[...]. Ann Neurol 2021
18
80


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
246
60

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
310
60

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
125
60

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
161
60

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
233
60

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
19
60

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
27
60

GGC Repeat Expansion of NOTCH2NLC in Adult Patients with Leukoencephalopathy.
Masaki Okubo, Hiroshi Doi, Ryoko Fukai, Atsushi Fujita, Satomi Mitsuhashi, Shunta Hashiguchi, Hitaru Kishida, Naohisa Ueda, Keisuke Morihara, Akihiro Ogasawara,[...]. Ann Neurol 2019
49
60

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
72
60

Neuronal intranuclear (hyaline) inclusion disease and fragile X-associated tremor/ataxia syndrome: a morphological and molecular dilemma.
Ellen Gelpi, Teresa Botta-Orfila, Laia Bodi, Stefanie Marti, Gabor Kovacs, Oriol Grau-Rivera, Manuel Lozano, Raquel Sánchez-Valle, Esteban Muñoz, Francesc Valldeoriola,[...]. Brain 2017
30
60

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
31
60

Genetic origin of sporadic cases and RNA toxicity in neuronal intranuclear inclusion disease.
Jianwen Deng, Binbin Zhou, Jiaxi Yu, Xiaochen Han, Jianhui Fu, Xiaobin Li, Xufang Xie, Min Zhu, Yilei Zheng, Xueyu Guo,[...]. J Med Genet 2022
9
60

Intracellular FMRpolyG-Hsp70 complex in fibroblast cells from a patient affected by fragile X tremor ataxia syndrome.
Giuseppe Bonapace, Rosa Gullace, Daniela Concolino, Grazia Iannello, Radha Procopio, Monica Gagliardi, Gennarina Arabia, Gaetano Barbagallo, Angela Lupo, Lucia Ilaria Manfredini,[...]. Heliyon 2019
6
40

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
55
40

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
77
40

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
41
40

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
64
40

An Integrative Study of Protein-RNA Condensates Identifies Scaffolding RNAs and Reveals Players in Fragile X-Associated Tremor/Ataxia Syndrome.
Fernando Cid-Samper, Mariona Gelabert-Baldrich, Benjamin Lang, Nieves Lorenzo-Gotor, Riccardo Delli Ponti, Lies-Anne W F M Severijnen, Benedetta Bolognesi, Ellen Gelpi, Renate K Hukema, Teresa Botta-Orfila,[...]. Cell Rep 2018
38
40

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
249
40

RNA toxicity in non-coding repeat expansion disorders.
Bart Swinnen, Wim Robberecht, Ludo Van Den Bosch. EMBO J 2020
83
40

Induction of inclusion formation and disruption of lamin A/C structure by premutation CGG-repeat RNA in human cultured neural cells.
Dolores Garcia Arocena, Christine K Iwahashi, Nelly Won, Alexandra Beilina, Anna L Ludwig, Flora Tassone, Philip H Schwartz, Paul J Hagerman. Hum Mol Genet 2005
122
40

FMRpolyG alters mitochondrial transcripts level and respiratory chain complex assembly in Fragile X associated tremor/ataxia syndrome [FXTAS].
Dhruv Gohel, Lakshmi Sripada, Paresh Prajapati, Kritarth Singh, Milton Roy, Darshan Kotadia, Flora Tassone, Nicolas Charlet-Berguerand, Rajesh Singh. Biochim Biophys Acta Mol Basis Dis 2019
14
40

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
31
40



The FMRpolyGlycine Protein Mediates Aggregate Formation and Toxicity Independent of the CGG mRNA Hairpin in a Cellular Model for FXTAS.
Gry Hoem, Kenneth Bowitz Larsen, Aud Øvervatn, Andreas Brech, Trond Lamark, Eva Sjøttem, Terje Johansen. Front Genet 2019
12
40

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
608
40

Neuropathology of FMR1-premutation carriers presenting with dementia and neuropsychiatric symptoms.
Anke A Dijkstra, Saif N Haify, Niek A Verwey, Niels D Prins, Esmay C van der Toorn, Annemieke J M Rozemuller, Marianna Bugiani, Wilfred F A den Dunnen, Peter K Todd, Nicolas Charlet-Berguerand,[...]. Brain Commun 2021
3
66

NOTCH2NLC-linked neuronal intranuclear inclusion body disease and fragile X-associated tremor/ataxia syndrome.
Adeline S L Ng, Zheyu Xu, Zhiyong Chen, Yi Jayne Tan, Weng Khong Lim, Simon K S Ting, Wai Yung Yu, Qian Hui Cheng, Jia Nee Foo, Eng King Tan,[...]. Brain 2020
2
100

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
15
40

Analysis of NOTCH2NLC GGC repeat expansion in Taiwanese patients with amyotrophic lateral sclerosis.
Kang-Yang Jih, Ying-Tsen Chou, Pei-Chien Tsai, Yi-Chu Liao, Yi-Chung Lee. Neurobiol Aging 2021
3
66

Clinical Characteristics of Neuronal Intranuclear Inclusion Disease-Related Retinopathy With CGG Repeat Expansions in the NOTCH2NLC Gene.
Natsuko Nakamura, Kazushige Tsunoda, Akihiko Mitsutake, Shota Shibata, Tatsuo Mano, Yu Nagashima, Hiroyuki Ishiura, Atsushi Iwata, Tatsushi Toda, Shoji Tsuji,[...]. Invest Ophthalmol Vis Sci 2020
9
40


GGC repeat expansions in NOTCH2NLC causing a phenotype of distal motor neuropathy and myopathy.
Jiaxi Yu, Xing-Hua Luan, Meng Yu, Wei Zhang, He Lv, Li Cao, Lingchao Meng, Min Zhu, Binbin Zhou, Xiao-Rong Wu,[...]. Ann Clin Transl Neurol 2021
9
40

Adult-onset neuronal intranuclear inclusion disease mimicking Fragile X-associated tremor-ataxia syndrome in ethnic Chinese patients.
Shen-Yang Lim, Hiroyuki Ishiura, Norlisah Ramli, Shota Shibata, M Asem Almansour, Ai Huey Tan, Henry Houlden, Anthony E Lang, Shoji Tsuji. Parkinsonism Relat Disord 2020
7
40

Re-defining the clinicopathological spectrum of neuronal intranuclear inclusion disease.
Hao Chen, Likui Lu, Bin Wang, Guiyun Cui, Xingqi Wang, Yujing Wang, Hafiz Khuram Raza, Yan Min, Keke Li, Yingying Cui,[...]. Ann Clin Transl Neurol 2020
11
40


Clinicopathological features of neuronal intranuclear inclusion disease diagnosed by skin biopsy.
Gao-Jia Zhang, Di Wu, Yi-Xin Zhu, Hai-Feng Ni, Zhi-Jun Zhang. Neurol Sci 2022
3
66

NOTCH2NLC GGC Repeat Expansions Are Associated with Sporadic Essential Tremor: Variable Disease Expressivity on Long-Term Follow-up.
Adeline S L Ng, Weng Khong Lim, Zheyu Xu, Helen L Ong, Yi Jayne Tan, Wei Ying Sim, Ebonne Y L Ng, Jing Xian Teo, Jia Nee Foo, Tchoyoson C C Lim,[...]. Ann Neurol 2020
20
40

Human-Specific NOTCH2NL Genes Affect Notch Signaling and Cortical Neurogenesis.
Ian T Fiddes, Gerrald A Lodewijk, Meghan Mooring, Colleen M Bosworth, Adam D Ewing, Gary L Mantalas, Adam M Novak, Anouk van den Bout, Alex Bishara, Jimi L Rosenkrantz,[...]. Cell 2018
205
40


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.