A citation-based method for searching scientific literature

Hiroyuki Ishiura, Shota Shibata, Jun Yoshimura, Yuta Suzuki, Wei Qu, Koichiro Doi, M Asem Almansour, Junko Kanda Kikuchi, Makiko Taira, Jun Mitsui, Yuji Takahashi, Yaeko Ichikawa, Tatsuo Mano, Atsushi Iwata, Yasuo Harigaya, Miho Kawabe Matsukawa, Takashi Matsukawa, Masaki Tanaka, Yuichiro Shirota, Ryo Ohtomo, Hisatomo Kowa, Hidetoshi Date, Aki Mitsue, Hiroyuki Hatsuta, Satoru Morimoto, Shigeo Murayama, Yasushi Shiio, Yuko Saito, Akihiko Mitsutake, Mizuho Kawai, Takuya Sasaki, Yusuke Sugiyama, Masashi Hamada, Gaku Ohtomo, Yasuo Terao, Yoshihiko Nakazato, Akitoshi Takeda, Yoshio Sakiyama, Yumi Umeda-Kameyama, Jun Shinmi, Katsuhisa Ogata, Yutaka Kohno, Shen-Yang Lim, Ai Huey Tan, Jun Shimizu, Jun Goto, Ichizo Nishino, Tatsushi Toda, Shinichi Morishita, Shoji Tsuji. Nat Genet 2019
Times Cited: 122



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, Zhenhong Nan, Colleen Forster, Walter C Low, Benedikt Schoser, Nikunj V Somia, H Brent Clark, Stephen Schmechel, Peter B Bitterman, Geneviève Gourdon, Maurice S Swanson, Melinda Moseley, Laura P W Ranum. Proc Natl Acad Sci U S A 2011
Times Cited: 578




List of shared articles



Times cited


The molecular pathogenesis of repeat expansion diseases.
Yuzo Fujino, Yoshitaka Nagai. Biochem Soc Trans 2022
0

Advancing genomic technologies and clinical awareness accelerates discovery of disease-associated tandem repeat sequences.
Terence Gall-Duncan, Nozomu Sato, Ryan K C Yuen, Christopher E Pearson. Genome Res 2022
1

Molecular Mechanisms in Pentanucleotide Repeat Diseases.
Joana R Loureiro, Ana F Castro, Ana S Figueiredo, Isabel Silveira. Cells 2022
1

Hornerin deposits in neuronal intranuclear inclusion disease: direct identification of proteins with compositionally biased regions in inclusions.
Hongsun Park, Tomoyuki Yamanaka, Yumiko Toyama, Atsushi Fujita, Hiroshi Doi, Takashi Nirasawa, Shigeo Murayama, Naomichi Matsumoto, Tomomi Shimogori, Masaya Ikegawa,[...]. Acta Neuropathol Commun 2022
0

Trinucleotide CGG Repeat Diseases: An Expanding Field of Polyglycine Proteins?
Manon Boivin, Nicolas Charlet-Berguerand. Front Genet 2022
0

Identification of PSMB5 as a genetic modifier of fragile X-associated tremor/ataxia syndrome.
Ha Eun Kong, Junghwa Lim, Alexander Linsalata, Yunhee Kang, Indranil Malik, Emily G Allen, Yiqu Cao, Lisa Shubeck, Rich Johnston, Yanting Huang,[...]. Proc Natl Acad Sci U S A 2022
0

The polyG diseases: a new disease entity.
Tongling Liufu, Yilei Zheng, Jiaxi Yu, Yun Yuan, Zhaoxia Wang, Jianwen Deng, Daojun Hong. Acta Neuropathol Commun 2022
0

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


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

Therapeutic Development for CGG Repeat Expansion-Associated Neurodegeneration.
Keqin Xu, Yujing Li, Emily G Allen, Peng Jin. Front Cell Neurosci 2021
5

Molecular mechanisms underlying nucleotide repeat expansion disorders.
Indranil Malik, Chase P Kelley, Eric T Wang, Peter K Todd. Nat Rev Mol Cell Biol 2021
22

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