A citation-based method for searching scientific literature

Yoshitsugu Aoki, Raquel Manzano, Yi Lee, Ruxandra Dafinca, Misako Aoki, Andrew G L Douglas, Miguel A Varela, Chaitra Sathyaprakash, Jakub Scaber, Paola Barbagallo, Pieter Vader, Imre Mäger, Kariem Ezzat, Martin R Turner, Naoki Ito, Samanta Gasco, Norihiko Ohbayashi, Samir El Andaloussi, Shin'ichi Takeda, Mitsunori Fukuda, Kevin Talbot, Matthew J A Wood. Brain 2017
Times Cited: 98







List of co-cited articles
1772 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


Direct conversion of patient fibroblasts demonstrates non-cell autonomous toxicity of astrocytes to motor neurons in familial and sporadic ALS.
Kathrin Meyer, Laura Ferraiuolo, Carlos J Miranda, Shibi Likhite, Sohyun McElroy, Samantha Renusch, Dara Ditsworth, Clotilde Lagier-Tourenne, Richard A Smith, John Ravits,[...]. Proc Natl Acad Sci U S A 2014
232
8

Poly(GR) impairs protein translation and stress granule dynamics in C9orf72-associated frontotemporal dementia and amyotrophic lateral sclerosis.
Yong-Jie Zhang, Tania F Gendron, Mark T W Ebbert, Aliesha D O'Raw, Mei Yue, Karen Jansen-West, Xu Zhang, Mercedes Prudencio, Jeannie Chew, Casey N Cook,[...]. Nat Med 2018
159
8

C9orf72 intermediate repeats are associated with corticobasal degeneration, increased C9orf72 expression and disruption of autophagy.
Christopher P Cali, Maribel Patino, Yee Kit Tai, Wan Yun Ho, Catriona A McLean, Christopher M Morris, William W Seeley, Bruce L Miller, Carles Gaig, Jean Paul G Vonsattel,[...]. Acta Neuropathol 2019
38
21

C9orf72 associates with inactive Rag GTPases and regulates mTORC1-mediated autophagosomal and lysosomal biogenesis.
Mingmei Wang, Hongfeng Wang, Zhouteng Tao, Qin Xia, Zongbing Hao, Jochen H M Prehn, Xuechu Zhen, Guanghui Wang, Zheng Ying. Aging Cell 2020
19
42

Mutation in VPS35 associated with Parkinson's disease impairs WASH complex association and inhibits autophagy.
Eszter Zavodszky, Matthew N J Seaman, Kevin Moreau, Maria Jimenez-Sanchez, Sophia Y Breusegem, Michael E Harbour, David C Rubinsztein. Nat Commun 2014
290
7

Progranulin Deficiency Promotes Circuit-Specific Synaptic Pruning by Microglia via Complement Activation.
Hansen Lui, Jiasheng Zhang, Stefanie R Makinson, Michelle K Cahill, Kevin W Kelley, Hsin-Yi Huang, Yulei Shang, Michael C Oldham, Lauren Herl Martens, Fuying Gao,[...]. Cell 2016
390
7

Amyotrophic Lateral Sclerosis.
Robert H Brown, Ammar Al-Chalabi. N Engl J Med 2017
824
7

Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis.
Wouter van Rheenen, Aleksey Shatunov, Annelot M Dekker, Russell L McLaughlin, Frank P Diekstra, Sara L Pulit, Rick A A van der Spek, Urmo Võsa, Simone de Jong, Matthew R Robinson,[...]. Nat Genet 2016
326
7

Quantitative analysis and clinico-pathological correlations of different dipeptide repeat protein pathologies in C9ORF72 mutation carriers.
Ian R A Mackenzie, Petra Frick, Friedrich A Grässer, Tania F Gendron, Leonard Petrucelli, Neil R Cashman, Dieter Edbauer, Elisabeth Kremmer, Johannes Prudlo, Dirk Troost,[...]. Acta Neuropathol 2015
159
7

Exosome secretion is a key pathway for clearance of pathological TDP-43.
Yohei Iguchi, Lara Eid, Martin Parent, Geneviève Soucy, Christine Bareil, Yuichi Riku, Kaori Kawai, Shinnosuke Takagi, Mari Yoshida, Masahisa Katsuno,[...]. Brain 2016
188
7

Defective recognition of LC3B by mutant SQSTM1/p62 implicates impairment of autophagy as a pathogenic mechanism in ALS-FTLD.
Alice Goode, Kevin Butler, Jed Long, James Cavey, Daniel Scott, Barry Shaw, Jill Sollenberger, Christopher Gell, Terje Johansen, Neil J Oldham,[...]. Autophagy 2016
94
7

SQSTM1 mutations in frontotemporal lobar degeneration and amyotrophic lateral sclerosis.
Elisa Rubino, Innocenzo Rainero, Adriano Chiò, Ekaterina Rogaeva, Daniela Galimberti, Pierpaola Fenoglio, Yakov Grinberg, Giancarlo Isaia, Andrea Calvo, Salvatore Gentile,[...]. Neurology 2012
208
7

Mutations in SQSTM1 encoding p62 in amyotrophic lateral sclerosis: genetics and neuropathology.
Elisa Teyssou, Takahiro Takeda, Vincent Lebon, Séverine Boillée, Brahima Doukouré, Guillaume Bataillon, Véronique Sazdovitch, Cécile Cazeneuve, Vincent Meininger, Eric LeGuern,[...]. Acta Neuropathol 2013
156
7

TBK1: a new player in ALS linking autophagy and neuroinflammation.
James A Oakes, Maria C Davies, Mark O Collins. Mol Brain 2017
169
7

p62/SQSTM1 binds directly to Atg8/LC3 to facilitate degradation of ubiquitinated protein aggregates by autophagy.
Serhiy Pankiv, Terje Høyvarde Clausen, Trond Lamark, Andreas Brech, Jack-Ansgar Bruun, Heidi Outzen, Aud Øvervatn, Geir Bjørkøy, Terje Johansen. J Biol Chem 2007
7


Nucleolar stress and impaired stress granule formation contribute to C9orf72 RAN translation-induced cytotoxicity.
Zhouteng Tao, Hongfeng Wang, Qin Xia, Ke Li, Kai Li, Xiaogang Jiang, Guoqiang Xu, Guanghui Wang, Zheng Ying. Hum Mol Genet 2015
163
7

Autophagy regulates amyotrophic lateral sclerosis-linked fused in sarcoma-positive stress granules in neurons.
Hyun-Hee Ryu, Mi-Hee Jun, Kyung-Jin Min, Deok-Jin Jang, Yong-Seok Lee, Hyong Kyu Kim, Jin-A Lee. Neurobiol Aging 2014
85
8

VCP/p97 is essential for maturation of ubiquitin-containing autophagosomes and this function is impaired by mutations that cause IBMPFD.
Emilie Tresse, Florian A Salomons, Jouni Vesa, Laura C Bott, Virginia Kimonis, Tso-Pang Yao, Nico P Dantuma, J Paul Taylor. Autophagy 2010
324
7

Valosin-containing protein (VCP) is required for autophagy and is disrupted in VCP disease.
Jeong-Sun Ju, Rodrigo A Fuentealba, Sara E Miller, Erin Jackson, David Piwnica-Worms, Robert H Baloh, Conrad C Weihl. J Cell Biol 2009
377
7

Rapamycin treatment augments motor neuron degeneration in SOD1(G93A) mouse model of amyotrophic lateral sclerosis.
Xiaojie Zhang, Liang Li, Sheng Chen, Dehua Yang, Yi Wang, Xin Zhang, Zheng Wang, Weidong Le. Autophagy 2011
274
7

Defects in optineurin- and myosin VI-mediated cellular trafficking in amyotrophic lateral sclerosis.
Vinod Sundaramoorthy, Adam K Walker, Vanessa Tan, Jennifer A Fifita, Emily P Mccann, Kelly L Williams, Ian P Blair, Gilles J Guillemin, Manal A Farg, Julie D Atkin. Hum Mol Genet 2015
55
12

TFEB links autophagy to lysosomal biogenesis.
Carmine Settembre, Chiara Di Malta, Vinicia Assunta Polito, Moises Garcia Arencibia, Francesco Vetrini, Serkan Erdin, Serpil Uckac Erdin, Tuong Huynh, Diego Medina, Pasqualina Colella,[...]. Science 2011
7

Distribution of dipeptide repeat proteins in cellular models and C9orf72 mutation cases suggests link to transcriptional silencing.
Martin H Schludi, Stephanie May, Friedrich A Grässer, Kristin Rentzsch, Elisabeth Kremmer, Clemens Küpper, Thomas Klopstock, Thomas Arzberger, Dieter Edbauer. Acta Neuropathol 2015
132
7

Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosis.
Janel O Johnson, Erik P Pioro, Ashley Boehringer, Ruth Chia, Howard Feit, Alan E Renton, Hannah A Pliner, Yevgeniya Abramzon, Giuseppe Marangi, Brett J Winborn,[...]. Nat Neurosci 2014
318
7

An antisense oligonucleotide against SOD1 delivered intrathecally for patients with SOD1 familial amyotrophic lateral sclerosis: a phase 1, randomised, first-in-man study.
Timothy M Miller, Alan Pestronk, William David, Jeffrey Rothstein, Ericka Simpson, Stanley H Appel, Patricia L Andres, Katy Mahoney, Peggy Allred, Katie Alexander,[...]. Lancet Neurol 2013
421
7

Glycine-alanine dipeptide repeat protein contributes to toxicity in a zebrafish model of C9orf72 associated neurodegeneration.
Yu Ohki, Andrea Wenninger-Weinzierl, Alexander Hruscha, Kazuhide Asakawa, Koichi Kawakami, Christian Haass, Dieter Edbauer, Bettina Schmid. Mol Neurodegener 2017
46
15

Characterization of the dipeptide repeat protein in the molecular pathogenesis of c9FTD/ALS.
Mai Yamakawa, Daisuke Ito, Takao Honda, Ken-ichiro Kubo, Mariko Noda, Kazunori Nakajima, Norihiro Suzuki. Hum Mol Genet 2015
107
7

In Situ Structure of Neuronal C9orf72 Poly-GA Aggregates Reveals Proteasome Recruitment.
Qiang Guo, Carina Lehmer, Antonio Martínez-Sánchez, Till Rudack, Florian Beck, Hannelore Hartmann, Manuela Pérez-Berlanga, Frédéric Frottin, Mark S Hipp, F Ulrich Hartl,[...]. Cell 2018
205
7

Gene-specific mitochondria dysfunctions in human TARDBP and C9ORF72 fibroblasts.
Elisa Onesto, Claudia Colombrita, Valentina Gumina, Maria Orietta Borghi, Sabrina Dusi, Alberto Doretti, Gigliola Fagiolari, Federica Invernizzi, Maurizio Moggio, Valeria Tiranti,[...]. Acta Neuropathol Commun 2016
104
7

CRISPR-Cas9 screens in human cells and primary neurons identify modifiers of C9ORF72 dipeptide-repeat-protein toxicity.
Nicholas J Kramer, Michael S Haney, David W Morgens, Ana Jovičić, Julien Couthouis, Amy Li, James Ousey, Rosanna Ma, Gregor Bieri, C Kimberly Tsui,[...]. Nat Genet 2018
116
7

The changing scene of amyotrophic lateral sclerosis.
Wim Robberecht, Thomas Philips. Nat Rev Neurosci 2013
682
7

Lack of C9ORF72 coding mutations supports a gain of function for repeat expansions in amyotrophic lateral sclerosis.
Matthew B Harms, Janet Cady, Craig Zaidman, Paul Cooper, Taha Bali, Peggy Allred, Carlos Cruchaga, Michael Baughn, Ryan T Libby, Alan Pestronk,[...]. Neurobiol Aging 2013
50
14

The expanding biology of the C9orf72 nucleotide repeat expansion in neurodegenerative disease.
Aaron R Haeusler, Christopher J Donnelly, Jeffrey D Rothstein. Nat Rev Neurosci 2016
125
7

ALS Genes in the Genomic Era and their Implications for FTD.
Hung Phuoc Nguyen, Christine Van Broeckhoven, Julie van der Zee. Trends Genet 2018
163
7

The phenotypic variability of amyotrophic lateral sclerosis.
Bart Swinnen, Wim Robberecht. Nat Rev Neurol 2014
325
7

Hot-spot KIF5A mutations cause familial ALS.
David Brenner, Rüstem Yilmaz, Kathrin Müller, Torsten Grehl, Susanne Petri, Thomas Meyer, Julian Grosskreutz, Patrick Weydt, Wolfgang Ruf, Christoph Neuwirth,[...]. Brain 2018
117
7

Clinico-pathological features in amyotrophic lateral sclerosis with expansions in C9ORF72.
Johnathan Cooper-Knock, Christopher Hewitt, J Robin Highley, Alice Brockington, Antonio Milano, Somai Man, Joanne Martindale, Judith Hartley, Theresa Walsh, Catherine Gelsthorpe,[...]. Brain 2012
233
7

Amyotrophic lateral sclerosis patient iPSC-derived astrocytes impair autophagy via non-cell autonomous mechanisms.
Martin Madill, Katya McDonagh, Jun Ma, Alice Vajda, Paul McLoughlin, Timothy O'Brien, Orla Hardiman, Sanbing Shen. Mol Brain 2017
77
9

A C9orf72-CARM1 axis regulates lipid metabolism under glucose starvation-induced nutrient stress.
Yang Liu, Tao Wang, Yon Ju Ji, Kenji Johnson, Honghe Liu, Kaitlin Johnson, Scott Bailey, Yongwon Suk, Yu-Ning Lu, Mingming Liu,[...]. Genes Dev 2018
39
17


Extensive transcriptomic study emphasizes importance of vesicular transport in C9orf72 expansion carriers.
Dennis W Dickson, Matthew C Baker, Jazmyne L Jackson, Mariely DeJesus-Hernandez, NiCole A Finch, Shulan Tian, Michael G Heckman, Cyril Pottier, Tania F Gendron, Melissa E Murray,[...]. Acta Neuropathol Commun 2019
24
29

Implementation of an antibody characterization procedure and application to the major ALS/FTD disease gene C9ORF72.
Carl Laflamme, Paul M McKeever, Rahul Kumar, Julie Schwartz, Mahshad Kolahdouzan, Carol X Chen, Zhipeng You, Faiza Benaliouad, Opher Gileadi, Heidi M McBride,[...]. Elife 2019
26
26

Synaptic localization of C9orf72 regulates post-synaptic glutamate receptor 1 levels.
Shangxi Xiao, Paul M McKeever, Agnes Lau, Janice Robertson. Acta Neuropathol Commun 2019
24
29

Knocking out C9ORF72 Exacerbates Axonal Trafficking Defects Associated with Hexanucleotide Repeat Expansion and Reduces Levels of Heat Shock Proteins.
Masin Abo-Rady, Norman Kalmbach, Arun Pal, Carina Schludi, Antje Janosch, Tanja Richter, Petra Freitag, Marc Bickle, Anne-Karin Kahlert, Susanne Petri,[...]. Stem Cell Reports 2020
31
22

Spt4 selectively regulates the expression of C9orf72 sense and antisense mutant transcripts.
Nicholas J Kramer, Yari Carlomagno, Yong-Jie Zhang, Sandra Almeida, Casey N Cook, Tania F Gendron, Mercedes Prudencio, Marka Van Blitterswijk, Veronique Belzil, Julien Couthouis,[...]. Science 2016
92
6

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
595
6

ANG mutations segregate with familial and 'sporadic' amyotrophic lateral sclerosis.
Matthew J Greenway, Peter M Andersen, Carsten Russ, Sean Ennis, Susan Cashman, Colette Donaghy, Victor Patterson, Robert Swingler, Dairin Kieran, Jochen Prehn,[...]. Nat Genet 2006
510
6

Ubiquitin-independent function of optineurin in autophagic clearance of protein aggregates.
Jelena Korac, Veronique Schaeffer, Igor Kovacevic, Albrecht M Clement, Benno Jungblut, Christian Behl, Janos Terzic, Ivan Dikic. J Cell Sci 2013
223
6

Regulation of autophagy by the Rab GTPase network.
X Ao, L Zou, Y Wu. Cell Death Differ 2014
238
6


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.