A citation-based method for searching scientific literature

Manon Boivin, Nicolas Charlet-Berguerand. Front Genet 2022
Times Cited: 2







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



Times Cited
  Times     Co-cited
Similarity


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
100

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
100

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
61
100

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
100

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
100

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
100

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
100

Molecular mechanisms underlying nucleotide repeat expansion disorders.
Indranil Malik, Chase P Kelley, Eric T Wang, Peter K Todd. Nat Rev Mol Cell Biol 2021
42
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
25
100

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
40
100

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
100


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
100


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
18
100

Upstream open reading frame with NOTCH2NLC GGC expansion generates polyglycine aggregates and disrupts nucleocytoplasmic transport: implications for polyglycine diseases.
Shaoping Zhong, Yangye Lian, Wenyi Luo, Rongkui Luo, Xiaoling Wu, Jun Ji, Yuan Ji, Jing Ding, Xin Wang. Acta Neuropathol 2021
10
100

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
26
100

Human-Specific NOTCH2NL Genes Expand Cortical Neurogenesis through Delta/Notch Regulation.
Ikuo K Suzuki, David Gacquer, Roxane Van Heurck, Devesh Kumar, Marta Wojno, Angéline Bilheu, Adèle Herpoel, Nelle Lambert, Julian Cheron, Franck Polleux,[...]. Cell 2018
172
100

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
16
100

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
100

Neuronal intranuclear inclusion disease showing intranuclear inclusions in renal biopsy 12 years earlier.
Mikiko Motoki, Hideto Nakajima, Tomoe Sato, Mari Tada, Akiyoshi Kakita, Shigeki Arawaka. Neurology 2018
17
100

Neuronal intranuclear inclusion disease cases with leukoencephalopathy diagnosed via skin biopsy.
Jun Sone, Naoyuki Kitagawa, Eriko Sugawara, Masaaki Iguchi, Ryoichi Nakamura, Haruki Koike, Yasushi Iwasaki, Mari Yoshida, Tatsuya Takahashi, Susumu Chiba,[...]. J Neurol Neurosurg Psychiatry 2014
77
100

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
100

Identification of expanded repeats in NOTCH2NLC in neurodegenerative dementias.
Bin Jiao, Lu Zhou, Yafang Zhou, Ling Weng, Xinxin Liao, Yun Tian, Lina Guo, Xixi Liu, Zhenhua Yuan, Xuewen Xiao,[...]. Neurobiol Aging 2020
37
100

Repeat expansion disease: progress and puzzles in disease pathogenesis.
Albert R La Spada, J Paul Taylor. Nat Rev Genet 2010
308
100

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
223
100

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
100

The Phenotypes and Mechanisms of NOTCH2NLC-Related GGC Repeat Expansion Disorders: a Comprehensive Review.
Xiu-Rong Huang, Bei-Sha Tang, Peng Jin, Ji-Feng Guo. Mol Neurobiol 2022
9
100

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
50

Neurodegenerative disease: RNA repeats put a freeze on cells.
David W Sanders, Clifford P Brangwynne. Nature 2017
3
50

Neuronal intranuclear inclusion disease: report on a case originally diagnosed as dopa-responsive dystonia with Lewy bodies.
Dominic C Paviour, Tamas Revesz, Janice L Holton, Andrew Evans, Jan-Edvin Olsson, Andrew J Lees. Mov Disord 2005
20
50

Interrelated Pathogenesis? Neuronal Intranuclear Inclusion Disease Combining With Hemiplegic Migraine.
Rongfei Wang, Xiting Nie, Shiyang Xu, Mingjie Zhang, Zhao Dong, Shengyuan Yu. Headache 2020
11
50

Adult-onset neuronal intranuclear inclusion disease presented transient global amnesia-a case report.
Jun Takeshita, Hiromitsu Kobayashi, Yutaka Shimoe, Jun Sone, Gen Sobue, Masaru Kuriyama. Rinsho Shinkeigaku 2017
4
50

A familial neuronal disease presenting as intestinal pseudoobstruction.
M D Schuffler, T D Bird, S M Sumi, A Cook. Gastroenterology 1978
186
50


Neuronal intranuclear inclusion disease. Clinical ophthalmological features and ophthalmic pathology.
M Haltia, A Tarkkanen, H Somer, J Palo, H Karli. Acta Ophthalmol (Copenh) 1986
15
50


2
50

Fragile X-associated tremor/ataxia syndrome: pathophysiology and management.
Randi Hagerman, Paul Hagerman. Curr Opin Neurol 2021
10
50

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
50

Neuronal intranuclear inclusion disease showing blepharoptosis and positive serum anti-acetylcholine receptor antibody without myasthenia gravis.
Koji Hayashi, Tsuyoshi Hamaguchi, Kenji Sakai, Keiko Nakamura, Koichi Wakabayashi, Hiroe Shirasaki, Masahito Yamada. J Neurol Sci 2019
2
50


A multimodal imaging features of the brain in adult-onset neuronal intranuclear inclusion disease.
Yajing Liu, Jiancong Lu, Kai Li, Hai Zhao, Yanyun Feng, Zaiqiang Zhang, Lang Hu, Guode Li, Yan Shao, Yukai Wang. Neurol Sci 2019
6
50

Neuropathology of RAN translation proteins in fragile X-associated tremor/ataxia syndrome.
Amy Krans, Geena Skariah, Yuan Zhang, Bryana Bayly, Peter K Todd. Acta Neuropathol Commun 2019
26
50

Activation of the ubiquitin-proteasome system contributes to oculopharyngeal muscular dystrophy through muscle atrophy.
Cécile Ribot, Cédric Soler, Aymeric Chartier, Sandy Al Hayek, Rima Naït-Saïdi, Nicolas Barbezier, Olivier Coux, Martine Simonelig. PLoS Genet 2022
4
50

Coexistence of neuronal intranuclear inclusion disease and amyotrophic lateral sclerosis: an autopsy case.
Atsuhiko Sugiyama, Takahiro Takeda, Mizuho Koide, Hajime Yokota, Hiroki Mukai, Yoshihisa Kitayama, Kazumoto Shibuya, Nobuyuki Araki, Ai Ishikawa, Sagiri Isose,[...]. BMC Neurol 2021
6
50

Skin biopsy is useful for the antemortem diagnosis of neuronal intranuclear inclusion disease.
J Sone, F Tanaka, H Koike, A Inukai, M Katsuno, M Yoshida, H Watanabe, G Sobue. Neurology 2011
104
50

Repeat-associated non-ATG (RAN) translation.
John Douglas Cleary, Amrutha Pattamatta, Laura P W Ranum. J Biol Chem 2018
54
50

Neuronal intranuclear inclusion disease: two cases of dopa-responsive juvenile parkinsonism with drug-induced dyskinesia.
Szu-Chia Lai, Shih-Ming Jung, Padraic Grattan-Smith, Ella Sugo, Yen-Wen Lin, Rou-Shayn Chen, Chiung-Chu Chen, Yah-Huei Wu-Chou, Anthony E Lang, Chin-Song Lu. Mov Disord 2010
13
50

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
6
50


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.