A citation-based method for searching scientific literature

Haloom Rafehi, David J Szmulewicz, Kate Pope, Mathew Wallis, John Christodoulou, Susan M White, Martin B Delatycki, Paul J Lockhart, Melanie Bahlo. Mov Disord 2020
Times Cited: 1







List of co-cited articles
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
122
100

ExpansionHunter: a sequence-graph-based tool to analyze variation in short tandem repeat regions.
Egor Dolzhenko, Viraj Deshpande, Felix Schlesinger, Peter Krusche, Roman Petrovski, Sai Chen, Dorothea Emig-Agius, Andrew Gross, Giuseppe Narzisi, Brett Bowman,[...]. Bioinformatics 2019
42
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
82
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
119
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
95
100


STRetch: detecting and discovering pathogenic short tandem repeat expansions.
Harriet Dashnow, Monkol Lek, Belinda Phipson, Andreas Halman, Simon Sadedin, Andrew Lonsdale, Mark Davis, Phillipa Lamont, Joshua S Clayton, Nigel G Laing,[...]. Genome Biol 2018
47
100

Consensus Statement on the classification of tremors. from the task force on tremor of the International Parkinson and Movement Disorder Society.
Kailash P Bhatia, Peter Bain, Nin Bajaj, Rodger J Elble, Mark Hallett, Elan D Louis, Jan Raethjen, Maria Stamelou, Claudia M Testa, Guenther Deuschl. Mov Disord 2018
374
100

Second consensus statement on the diagnosis of multiple system atrophy.
S Gilman, G K Wenning, P A Low, D J Brooks, C J Mathias, J Q Trojanowski, N W Wood, C Colosimo, A Dürr, C J Fowler,[...]. Neurology 2008
100

Interrogating the "unsequenceable" genomic trinucleotide repeat disorders by long-read sequencing.
Qian Liu, Peng Zhang, Depeng Wang, Weihong Gu, Kai Wang. Genome Med 2017
35
100

Essential tremor with ubiquitinated Purkinje cell intranuclear inclusions.
Elan D Louis, Cordelia Erickson-Davis, Rajesh Pahwa, Kelly E Lyons, Anthony Garber, Carol B Moskowitz, Arlene Lawton, Phyllis L Faust, Jean-Paul G Vonsattel. Acta Neuropathol 2010
11
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
51
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
20
100

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
84
100

MDS clinical diagnostic criteria for Parkinson's disease.
Ronald B Postuma, Daniela Berg, Matthew Stern, Werner Poewe, C Warren Olanow, Wolfgang Oertel, José Obeso, Kenneth Marek, Irene Litvan, Anthony E Lang,[...]. Mov Disord 2015
100

Integrative genomics viewer.
James T Robinson, Helga Thorvaldsdóttir, Wendy Winckler, Mitchell Guttman, Eric S Lander, Gad Getz, Jill P Mesirov. Nat Biotechnol 2011
100

Essential tremor as the early symptom of NOTCH2NLC gene-related repeat expansion disorder.
Hao Chen, Likui Lu, Bin Wang, Xiaodong Hua, Bo Wan, Miao Sun, Xingshun Xu. Brain 2020
15
100

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
12
100


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.