A citation-based method for searching scientific literature

Jeffrey W Hofmann, William W Seeley, Eric J Huang. Annu Rev Pathol 2019
Times Cited: 12







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



Times Cited
  Times     Co-cited
Similarity


Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis.
Manuela Neumann, Deepak M Sampathu, Linda K Kwong, Adam C Truax, Matthew C Micsenyi, Thomas T Chou, Jennifer Bruce, Theresa Schuck, Murray Grossman, Christopher M Clark,[...]. Science 2006
25

Phase separation by low complexity domains promotes stress granule assembly and drives pathological fibrillization.
Amandine Molliex, Jamshid Temirov, Jihun Lee, Maura Coughlin, Anderson P Kanagaraj, Hong Joo Kim, Tanja Mittag, J Paul Taylor. Cell 2015
25


The frontotemporal dementia-motor neuron disease continuum.
James R Burrell, Glenda M Halliday, Jillian J Kril, Lars M Ittner, Jürgen Götz, Matthew C Kiernan, John R Hodges. Lancet 2016
168
25

Atomic structures of low-complexity protein segments reveal kinked β sheets that assemble networks.
Michael P Hughes, Michael R Sawaya, David R Boyer, Lukasz Goldschmidt, Jose A Rodriguez, Duilio Cascio, Lisa Chong, Tamir Gonen, David S Eisenberg. Science 2018
169
16

ALS/FTD Mutation-Induced Phase Transition of FUS Liquid Droplets and Reversible Hydrogels into Irreversible Hydrogels Impairs RNP Granule Function.
Tetsuro Murakami, Seema Qamar, Julie Qiaojin Lin, Gabriele S Kaminski Schierle, Eric Rees, Akinori Miyashita, Ana R Costa, Roger B Dodd, Fiona T S Chan, Claire H Michel,[...]. Neuron 2015
421
16

Phosphorylation of the FUS low-complexity domain disrupts phase separation, aggregation, and toxicity.
Zachary Monahan, Veronica H Ryan, Abigail M Janke, Kathleen A Burke, Shannon N Rhoads, Gül H Zerze, Robert O'Meally, Gregory L Dignon, Alexander E Conicella, Wenwei Zheng,[...]. EMBO J 2017
289
16

Cytoplasmic TDP-43 De-mixing Independent of Stress Granules Drives Inhibition of Nuclear Import, Loss of Nuclear TDP-43, and Cell Death.
Fatima Gasset-Rosa, Shan Lu, Haiyang Yu, Cong Chen, Ze'ev Melamed, Lin Guo, James Shorter, Sandrine Da Cruz, Don W Cleveland. Neuron 2019
139
16

RNA seeds higher-order assembly of FUS protein.
Jacob C Schwartz, Xueyin Wang, Elaine R Podell, Thomas R Cech. Cell Rep 2013
185
16

Germline P granules are liquid droplets that localize by controlled dissolution/condensation.
Clifford P Brangwynne, Christian R Eckmann, David S Courson, Agata Rybarska, Carsten Hoege, Jöbin Gharakhani, Frank Jülicher, Anthony A Hyman. Science 2009
16

Structure of FUS Protein Fibrils and Its Relevance to Self-Assembly and Phase Separation of Low-Complexity Domains.
Dylan T Murray, Masato Kato, Yi Lin, Kent R Thurber, Ivan Hung, Steven L McKnight, Robert Tycko. Cell 2017
295
16

A Liquid-to-Solid Phase Transition of the ALS Protein FUS Accelerated by Disease Mutation.
Avinash Patel, Hyun O Lee, Louise Jawerth, Shovamayee Maharana, Marcus Jahnel, Marco Y Hein, Stoyno Stoynov, Julia Mahamid, Shambaditya Saha, Titus M Franzmann,[...]. Cell 2015
16

TDP-43 is a component of ubiquitin-positive tau-negative inclusions in frontotemporal lobar degeneration and amyotrophic lateral sclerosis.
Tetsuaki Arai, Masato Hasegawa, Haruhiko Akiyama, Kenji Ikeda, Takashi Nonaka, Hiroshi Mori, David Mann, Kuniaki Tsuchiya, Mari Yoshida, Yoshio Hashizume,[...]. Biochem Biophys Res Commun 2006
16

Liquid phase condensation in cell physiology and disease.
Yongdae Shin, Clifford P Brangwynne. Science 2017
16

ALS Mutations Disrupt Phase Separation Mediated by α-Helical Structure in the TDP-43 Low-Complexity C-Terminal Domain.
Alexander E Conicella, Gül H Zerze, Jeetain Mittal, Nicolas L Fawzi. Structure 2016
324
16

Residue-by-Residue View of In Vitro FUS Granules that Bind the C-Terminal Domain of RNA Polymerase II.
Kathleen A Burke, Abigail M Janke, Christy L Rhine, Nicolas L Fawzi. Mol Cell 2015
397
16

Mechanistic View of hnRNPA2 Low-Complexity Domain Structure, Interactions, and Phase Separation Altered by Mutation and Arginine Methylation.
Veronica H Ryan, Gregory L Dignon, Gül H Zerze, Charlene V Chabata, Rute Silva, Alexander E Conicella, Joshua Amaya, Kathleen A Burke, Jeetain Mittal, Nicolas L Fawzi. Mol Cell 2018
163
16

The role of FUS gene variants in neurodegenerative diseases.
Hao Deng, Kai Gao, Joseph Jankovic. Nat Rev Neurol 2014
151
16

RNA-Binding Proteins in Amyotrophic Lateral Sclerosis.
Melody Zhao, Jihye Rachel Kim, Rebekah van Bruggen, Jeehye Park. Mol Cells 2018
46
16

Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways.
Elizabeth T Cirulli, Brittany N Lasseigne, Slavé Petrovski, Peter C Sapp, Patrick A Dion, Claire S Leblond, Julien Couthouis, Yi-Fan Lu, Quanli Wang, Brian J Krueger,[...]. Science 2015
572
16

Haploinsufficiency of TBK1 causes familial ALS and fronto-temporal dementia.
Axel Freischmidt, Thomas Wieland, Benjamin Richter, Wolfgang Ruf, Veronique Schaeffer, Kathrin Müller, Nicolai Marroquin, Frida Nordin, Annemarie Hübers, Patrick Weydt,[...]. Nat Neurosci 2015
474
16


Mutations in the endosomal ESCRTIII-complex subunit CHMP2B in frontotemporal dementia.
Gaia Skibinski, Nicholas J Parkinson, Jeremy M Brown, Lisa Chakrabarti, Sarah L Lloyd, Holger Hummerich, Jørgen E Nielsen, John R Hodges, Maria Grazia Spillantini, Tove Thusgaard,[...]. Nat Genet 2005
578
16


A harmonized classification system for FTLD-TDP pathology.
Ian R A Mackenzie, Manuela Neumann, Atik Baborie, Deepak M Sampathu, Daniel Du Plessis, Evelyn Jaros, Robert H Perry, John Q Trojanowski, David M A Mann, Virginia M Y Lee. Acta Neuropathol 2011
584
16

Sensitivity of revised diagnostic criteria for the behavioural variant of frontotemporal dementia.
Katya Rascovsky, John R Hodges, David Knopman, Mario F Mendez, Joel H Kramer, John Neuhaus, John C van Swieten, Harro Seelaar, Elise G P Dopper, Chiadi U Onyike,[...]. Brain 2011
16

Classification of primary progressive aphasia and its variants.
M L Gorno-Tempini, A E Hillis, S Weintraub, A Kertesz, M Mendez, S F Cappa, J M Ogar, J D Rohrer, S Black, B F Boeve,[...]. Neurology 2011
16

Amyotrophic lateral sclerosis - frontotemporal spectrum disorder (ALS-FTSD): Revised diagnostic criteria.
Michael J Strong, Sharon Abrahams, Laura H Goldstein, Susan Woolley, Paula Mclaughlin, Julie Snowden, Eneida Mioshi, Angie Roberts-South, Michael Benatar, Tibor HortobáGyi,[...]. Amyotroph Lateral Scler Frontotemporal Degener 2017
316
16

An overview of autophagy: morphology, mechanism, and regulation.
Katherine R Parzych, Daniel J Klionsky. Antioxid Redox Signal 2014
818
8

VCP-dependent muscle degeneration is linked to defects in a dynamic tubular lysosomal network in vivo.
Alyssa E Johnson, Huidy Shu, Anna G Hauswirth, Amy Tong, Graeme W Davis. Elife 2015
43
8

Familial distal myopathy with rimmed vacuole and lamellar (myeloid) body formation.
I Nonaka, N Sunohara, S Ishiura, E Satoyoshi. J Neurol Sci 1981
228
8

The emerging phenotype of late-onset Pompe disease: A systematic literature review.
Justin Chan, Ankit K Desai, Zoheb B Kazi, Kaitlyn Corey, Stephanie Austin, Lisa D Hobson-Webb, Laura E Case, Harrison N Jones, Priya S Kishnani. Mol Genet Metab 2017
84
8



Satellite cells maintain regenerative capacity but fail to repair disease-associated muscle damage in mice with Pompe disease.
Gerben J Schaaf, Tom J M van Gestel, Stijn L M In 't Groen, Bart de Jong, Björn Boomaars, Antonietta Tarallo, Monica Cardone, Giancarlo Parenti, Ans T van der Ploeg, W W M Pim Pijnappel. Acta Neuropathol Commun 2018
16
8

Risk of Colchicine-Associated Myopathy in Gout: Influence of Concomitant Use of Statin.
Oh Chan Kwon, Seokchan Hong, Byeongzu Ghang, Yong-Gil Kim, Chang-Keun Lee, Bin Yoo. Am J Med 2017
13
8

When more is less: excess and deficiency of autophagy coexist in skeletal muscle in Pompe disease.
Nina Raben, Rebecca Baum, Cynthia Schreiner, Shoichi Takikita, Noboru Mizushima, Evelyn Ralston, Paul Plotz. Autophagy 2009
41
8

Genotype-phenotype study in patients with valosin-containing protein mutations associated with multisystem proteinopathy.
E Al-Obeidi, S Al-Tahan, A Surampalli, N Goyal, A K Wang, A Hermann, M Omizo, C Smith, T Mozaffar, V Kimonis. Clin Genet 2018
40
8

A knock-in/knock-out mouse model of HSPB8-associated distal hereditary motor neuropathy and myopathy reveals toxic gain-of-function of mutant Hspb8.
Delphine Bouhy, Manisha Juneja, Istvan Katona, Anne Holmgren, Bob Asselbergh, Vicky De Winter, Tino Hochepied, Steven Goossens, Jody J Haigh, Claude Libert,[...]. Acta Neuropathol 2018
32
8

Induction of lysosomal dilatation, arrested autophagy, and cell death by chloroquine in cultured ARPE-19 cells.
Young Hee Yoon, Kyung Sook Cho, Jung Jin Hwang, Sook-Jeong Lee, Jeong A Choi, Jae-Young Koh. Invest Ophthalmol Vis Sci 2010
153
8


Colchicine myopathy and neuropathy.
R W Kuncl, G Duncan, D Watson, K Alderson, M A Rogawski, M Peper. N Engl J Med 1987
304
8

Autophagy as a new therapeutic target in Duchenne muscular dystrophy.
C De Palma, F Morisi, S Cheli, S Pambianco, V Cappello, M Vezzoli, P Rovere-Querini, M Moggio, M Ripolone, M Francolini,[...]. Cell Death Dis 2012
150
8


Prophylactic treatment with sialic acid metabolites precludes the development of the myopathic phenotype in the DMRV-hIBM mouse model.
May Christine V Malicdan, Satoru Noguchi, Yukiko K Hayashi, Ikuya Nonaka, Ichizo Nishino. Nat Med 2009
111
8

Satellite cells fail to contribute to muscle repair but are functional in Pompe disease (glycogenosis type II).
Lydie Lagalice, Julien Pichon, Eliot Gougeon, Salwa Soussi, Johan Deniaud, Mireille Ledevin, Virginie Maurier, Isabelle Leroux, Sylvie Durand, Carine Ciron,[...]. Acta Neuropathol Commun 2018
14
8

Inhibition of lysosomal function in red and white skeletal muscles by chloroquine.
W T Stauber, A M Hedge, J J Trout, B A Schottelius. Exp Neurol 1981
61
8

Clinical and molecular studies in a unique family with autosomal dominant limb-girdle muscular dystrophy and Paget disease of bone.
V E Kimonis, M J Kovach, B Waggoner, S Leal, A Salam, L Rimer, K Davis, R Khardori, D Gelber. Genet Med 2000
90
8

Clinical utility of LC3 and p62 immunohistochemistry in diagnosis of drug-induced autophagic vacuolar myopathies: a case-control study.
Han S Lee, Brianne H Daniels, Eduardo Salas, Andrew W Bollen, Jayanta Debnath, Marta Margeta. PLoS One 2012
53
8

Autophagy is defective in collagen VI muscular dystrophies, and its reactivation rescues myofiber degeneration.
Paolo Grumati, Luisa Coletto, Patrizia Sabatelli, Matilde Cescon, Alessia Angelin, Enrico Bertaggia, Bert Blaauw, Anna Urciuolo, Tania Tiepolo, Luciano Merlini,[...]. Nat Med 2010
365
8


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.