A citation-based method for searching scientific literature

Manon Boivin, Jianwen Deng, Véronique Pfister, Erwan Grandgirard, Mustapha Oulad-Abdelghani, Bastien Morlet, Frank Ruffenach, Luc Negroni, Pascale Koebel, Hugues Jacob, Fabrice Riet, Anke A Dijkstra, Kathryn McFadden, Wiley A Clayton, Daojun Hong, Hiroaki Miyahara, Yasushi Iwasaki, Jun Sone, Zhaoxia Wang, Nicolas Charlet-Berguerand. Neuron 2021
Times Cited: 18







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



Times Cited
  Times     Co-cited
Similarity


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
116
83

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
147
83

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
100
66

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
19
55

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
19
55

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
139
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
63
50

Expansion of GGC Repeat in GIPC1 Is Associated with Oculopharyngodistal Myopathy.
Jianwen Deng, Jiaxi Yu, Pidong Li, Xinghua Luan, Li Cao, Juan Zhao, Meng Yu, Wei Zhang, He Lv, Zhiying Xie,[...]. Am J Hum Genet 2020
24
44

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
21
38

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
26
33

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
123
33

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
562
33

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
304
33

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
27
33

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
97
33

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
43
33

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
14
42

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
25
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
18
33

CUG initiation and frameshifting enable production of dipeptide repeat proteins from ALS/FTD C9ORF72 transcripts.
Ricardos Tabet, Laure Schaeffer, Fernande Freyermuth, Melanie Jambeau, Michael Workman, Chao-Zong Lee, Chun-Chia Lin, Jie Jiang, Karen Jansen-West, Hussein Abou-Hamdan,[...]. Nat Commun 2018
73
27

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
89
27

CGG repeat RNA G-quadruplexes interact with FMRpolyG to cause neuronal dysfunction in fragile X-related tremor/ataxia syndrome.
Sefan Asamitsu, Yasushi Yabuki, Susumu Ikenoshita, Kosuke Kawakubo, Moe Kawasaki, Shingo Usuki, Yuji Nakayama, Kaori Adachi, Hiroyuki Kugoh, Kazuhiro Ishii,[...]. Sci Adv 2021
17
29

Modifiers of C9orf72 dipeptide repeat toxicity connect nucleocytoplasmic transport defects to FTD/ALS.
Ana Jovičić, Jerome Mertens, Steven Boeynaems, Elke Bogaert, Noori Chai, Shizuka B Yamada, Joseph W Paul, Shuying Sun, Joseph R Herdy, Gregor Bieri,[...]. Nat Neurosci 2015
383
27

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
30
27

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
158
27

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
229
27

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
6
83

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
43
27

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
28
27

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
18
27

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
195
27

5' UTR CGG repeat expansion in GIPC1 is associated with oculopharyngodistal myopathy.
Jianying Xi, Xilu Wang, Dongyue Yue, Tonghai Dou, Qunfeng Wu, Jun Lu, Yiqi Liu, Wenbo Yu, Kai Qiao, Jie Lin,[...]. Brain 2021
16
31

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
7
57

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
243
22


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
62
22

Polyglutamine Repeats in Neurodegenerative Diseases.
Andrew P Lieberman, Vikram G Shakkottai, Roger L Albin. Annu Rev Pathol 2019
92
22

Repeat-associated non-ATG (RAN) translation.
John Douglas Cleary, Amrutha Pattamatta, Laura P W Ranum. J Biol Chem 2018
45
22

Repeat expansion diseases.
Henry Paulson. Handb Clin Neurol 2018
130
22

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
87
22

Myotonic dystrophy type 2 caused by a CCTG expansion in intron 1 of ZNF9.
C L Liquori, K Ricker, M L Moseley, J F Jacobsen, W Kress, S L Naylor, J W Day, L P Ranum. Science 2001
836
22

Unconventional translation of C9ORF72 GGGGCC expansion generates insoluble polypeptides specific to c9FTD/ALS.
Peter E A Ash, Kevin F Bieniek, Tania F Gendron, Thomas Caulfield, Wen-Lang Lin, Mariely Dejesus-Hernandez, Marka M van Blitterswijk, Karen Jansen-West, Joseph W Paul, Rosa Rademakers,[...]. Neuron 2013
724
22

Neuronal intranuclear hyaline inclusion disease.
Junko Takahashi-Fujigasaki. Neuropathology 2003
88
22

Clinicopathologic Features of Oculopharyngodistal Myopathy With LRP12 CGG Repeat Expansions Compared With Other Oculopharyngodistal Myopathy Subtypes.
Theerawat Kumutpongpanich, Masashi Ogasawara, Ayami Ozaki, Hiroyuki Ishiura, Shoji Tsuji, Narihiro Minami, Shinichiro Hayashi, Satoru Noguchi, Aritoshi Iida, Ichizo Nishino,[...]. JAMA Neurol 2021
4
100


Oculopharyngodistal myopathy with coexisting histology of systemic neuronal intranuclear inclusion disease: Clinicopathologic features of an autopsied patient harboring CGG repeat expansions in LRP12.
Rie Saito, Hiroshi Shimizu, Takeshi Miura, Norikazu Hara, Naomi Mezaki, Yo Higuchi, Akinori Miyashita, Izumi Kawachi, Kazuhiro Sanpei, Yoshiaki Honma,[...]. Acta Neuropathol Commun 2020
9
44


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
91
22

Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS.
Mariely DeJesus-Hernandez, Ian R Mackenzie, Bradley F Boeve, Adam L Boxer, Matt Baker, Nicola J Rutherford, Alexandra M Nicholson, NiCole A Finch, Heather Flynn, Jennifer Adamson,[...]. Neuron 2011
22

Oculopharyngodistal myopathy is a distinct entity: clinical and genetic features of 47 patients.
H Durmus, S H Laval, F Deymeer, Y Parman, E Kiyan, M Gokyigiti, C Ertekin, I Ercan, S Solakoglu, V Karcagi,[...]. Neurology 2011
40
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.