A citation-based method for searching scientific literature

Ellen Gelpi, Teresa Botta-Orfila, Laia Bodi, Stefanie Marti, Gabor Kovacs, Oriol Grau-Rivera, Manuel Lozano, Raquel Sánchez-Valle, Esteban Muñoz, Francesc Valldeoriola, Javier Pagonabarraga, Gian-Gaetano Tartaglia, Montserrat Milà. Brain 2017
Times Cited: 30







List of co-cited articles
244 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
147
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
76

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
66

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
60

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
95
50

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
68
40

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
40

Neuronal intranuclear hyaline inclusion disease.
Junko Takahashi-Fujigasaki. Neuropathology 2003
89
36

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
36

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
48
36

MR Imaging Features of the Cerebellum in Adult-Onset Neuronal Intranuclear Inclusion Disease: 8 Cases.
A Sugiyama, N Sato, Y Kimura, T Maekawa, M Enokizono, Y Saito, Y Takahashi, H Matsuda, S Kuwabara. AJNR Am J Neuroradiol 2017
34
33

Neuronal intranuclear hyaline inclusion disease showing motor-sensory and autonomic neuropathy.
J Sone, N Hishikawa, H Koike, N Hattori, M Hirayama, M Nagamatsu, M Yamamoto, F Tanaka, M Yoshida, Y Hashizume,[...]. Neurology 2005
43
30

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
30


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
30

Neuropathology of fragile X-associated tremor/ataxia syndrome (FXTAS).
C M Greco, R F Berman, R M Martin, F Tassone, P H Schwartz, A Chang, B D Trapp, C Iwahashi, J Brunberg, J Grigsby,[...]. Brain 2006
362
26

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
669
26

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
29

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
33

Inclusion-positive cell types in adult-onset intranuclear inclusion body disease: implications for clinical diagnosis.
Ying Liu, Maya Mimuro, Mari Yoshida, Yoshio Hashizume, Hisayoshi Niwa, Shinichi Miyao, Nobuko Ujihira, Hiroyasu Akatsu. Acta Neuropathol 2008
28
25

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
159
23

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
23

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
23

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
29
24

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
29

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
23

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
33

Reversibility of neuropathology and motor deficits in an inducible mouse model for FXTAS.
Renate K Hukema, Ronald A M Buijsen, Martijn Schonewille, Chris Raske, Lies-Anne W F M Severijnen, Ingeborg Nieuwenhuizen-Bakker, Rob F M Verhagen, Lisanne van Dessel, Alex Maas, Nicolas Charlet-Berguerand,[...]. Hum Mol Genet 2015
34
20

Familial neuronal intranuclear inclusion disease with ubiquitin positive inclusions.
T E Kimber, P C Blumbergs, J P Rice, J F Hallpike, R Edis, P D Thompson, G Suthers. J Neurol Sci 1998
47
20

Reply: Neuronal intranuclear (hyaline) inclusion disease and fragile X-associated tremor/ataxia syndrome: a morphological and molecular dilemma.
Jun Sone, Tomohiko Nakamura, Haruki Koike, Masahisa Katsuno, Fumiaki Tanaka, Yasushi Iwasaki, Mari Yoshida, Gen Sobue. Brain 2017
9
66

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
20

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
95
20

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
20

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
27
22

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
31


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
521
16

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
444
16

Memory Loss and Frontal Cognitive Dysfunction in a Patient with Adult-onset Neuronal Intranuclear Inclusion Disease.
Kunihiko Araki, Jun Sone, Yusuke Fujioka, Michihito Masuda, Reiko Ohdake, Yasuhiro Tanaka, Tomohiko Nakamura, Hirohisa Watanabe, Gen Sobue. Intern Med 2016
15
33

Adult-onset neuronal intranuclear hyaline inclusion disease is not rare in older adults.
Junko Takahashi-Fujigasaki, Yuta Nakano, Akiko Uchino, Shigeo Murayama. Geriatr Gerontol Int 2016
35
16

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
257
16

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
16

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
12
41

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
18
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
20
25

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
27

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
21

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
578
16

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
71

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
13


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.