A citation-based method for searching scientific literature

Jessica Root, Paola Merino, Austin Nuckols, Michelle Johnson, Thomas Kukar. Neurobiol Dis 2021
Times Cited: 9







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



Times Cited
  Times     Co-cited
Similarity


C9ORF72, implicated in amytrophic lateral sclerosis and frontotemporal dementia, regulates endosomal trafficking.
Manal A Farg, Vinod Sundaramoorthy, Jessica M Sultana, Shu Yang, Rachel A K Atkinson, Vita Levina, Mark A Halloran, Paul A Gleeson, Ian P Blair, Kai Y Soo,[...]. Hum Mol Genet 2014
290
44

Haploinsufficiency leads to neurodegeneration in C9ORF72 ALS/FTD human induced motor neurons.
Yingxiao Shi, Shaoyu Lin, Kim A Staats, Yichen Li, Wen-Hsuan Chang, Shu-Ting Hung, Eric Hendricks, Gabriel R Linares, Yaoming Wang, Esther Y Son,[...]. Nat Med 2018
230
33

The C9orf72 protein interacts with Rab1a and the ULK1 complex to regulate initiation of autophagy.
Christopher P Webster, Emma F Smith, Claudia S Bauer, Annekathrin Moller, Guillaume M Hautbergue, Laura Ferraiuolo, Monika A Myszczynska, Adrian Higginbottom, Matthew J Walsh, Alexander J Whitworth,[...]. EMBO J 2016
213
33

C9orf72 expansion within astrocytes reduces metabolic flexibility in amyotrophic lateral sclerosis.
Scott P Allen, Benjamin Hall, Ryan Woof, Laura Francis, Noemi Gatto, Allan C Shaw, Monika Myszczynska, Jordan Hemingway, Ian Coldicott, Amelia Willcock,[...]. Brain 2019
25
33

Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17.
Matt Baker, Ian R Mackenzie, Stuart M Pickering-Brown, Jennifer Gass, Rosa Rademakers, Caroline Lindholm, Julie Snowden, Jennifer Adamson, A Dessa Sadovnick, Sara Rollinson,[...]. Nature 2006
33

Network analysis of the progranulin-deficient mouse brain proteome reveals pathogenic mechanisms shared in human frontotemporal dementia caused by GRN mutations.
Meixiang Huang, Erica Modeste, Eric Dammer, Paola Merino, Georgia Taylor, Duc M Duong, Qiudong Deng, Christopher J Holler, Marla Gearing, Dennis Dickson,[...]. Acta Neuropathol Commun 2020
10
33

Inflammation in ALS/FTD pathogenesis.
Madelyn E McCauley, Robert H Baloh. Acta Neuropathol 2019
78
33

A C9ORF72/SMCR8-containing complex regulates ULK1 and plays a dual role in autophagy.
Mei Yang, Chen Liang, Kunchithapadam Swaminathan, Stephanie Herrlinger, Fan Lai, Ramin Shiekhattar, Jian-Fu Chen. Sci Adv 2016
135
22


The ALS/FTLD associated protein C9orf72 associates with SMCR8 and WDR41 to regulate the autophagy-lysosome pathway.
Peter M Sullivan, Xiaolai Zhou, Adam M Robins, Daniel H Paushter, Dongsung Kim, Marcus B Smolka, Fenghua Hu. Acta Neuropathol Commun 2016
164
22

A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD.
Alan E Renton, Elisa Majounie, Adrian Waite, Javier Simón-Sánchez, Sara Rollinson, J Raphael Gibbs, Jennifer C Schymick, Hannu Laaksovirta, John C van Swieten, Liisa Myllykangas,[...]. Neuron 2011
22

Loss of C9ORF72 impairs autophagy and synergizes with polyQ Ataxin-2 to induce motor neuron dysfunction and cell death.
Chantal Sellier, Maria-Letizia Campanari, Camille Julie Corbier, Angeline Gaucherot, Isabelle Kolb-Cheynel, Mustapha Oulad-Abdelghani, Frank Ruffenach, Adeline Page, Sorana Ciura, Edor Kabashi,[...]. EMBO J 2016
233
22


A gene network regulating lysosomal biogenesis and function.
Marco Sardiello, Michela Palmieri, Alberto di Ronza, Diego Luis Medina, Marta Valenza, Vincenzo Alessandro Gennarino, Chiara Di Malta, Francesca Donaudy, Valerio Embrione, Roman S Polishchuk,[...]. Science 2009
22

The endosomal-lysosomal system: from acidification and cargo sorting to neurodegeneration.
Yong-Bo Hu, Eric B Dammer, Ru-Jing Ren, Gang Wang. Transl Neurodegener 2015
206
22

C9orf72 ALS-FTD: recent evidence for dysregulation of the autophagy-lysosome pathway at multiple levels.
Jimmy Beckers, Arun Kumar Tharkeshwar, Philip Van Damme. Autophagy 2021
4
50

The genetic architecture of Parkinson's disease.
Cornelis Blauwendraat, Mike A Nalls, Andrew B Singleton. Lancet Neurol 2020
172
22

Amyotrophic Lateral Sclerosis.
Robert H Brown, Ammar Al-Chalabi. N Engl J Med 2017
592
22

Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis.
D R Rosen, T Siddique, D Patterson, D A Figlewicz, P Sapp, A Hentati, D Donaldson, J Goto, J P O'Regan, H X Deng. Nature 1993
22


Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions.
Vivianna M Van Deerlin, Patrick M A Sleiman, Maria Martinez-Lage, Alice Chen-Plotkin, Li-San Wang, Neill R Graff-Radford, Dennis W Dickson, Rosa Rademakers, Bradley F Boeve, Murray Grossman,[...]. Nat Genet 2010
327
22

Review: Neuropathology of non-tau frontotemporal lobar degeneration.
M Neumann, I R A Mackenzie. Neuropathol Appl Neurobiol 2019
47
22

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
328
22

Long pre-mRNA depletion and RNA missplicing contribute to neuronal vulnerability from loss of TDP-43.
Magdalini Polymenidou, Clotilde Lagier-Tourenne, Kasey R Hutt, Stephanie C Huelga, Jacqueline Moran, Tiffany Y Liang, Shuo-Chien Ling, Eveline Sun, Edward Wancewicz, Curt Mazur,[...]. Nat Neurosci 2011
743
22

C9orf72 is required for proper macrophage and microglial function in mice.
J G O'Rourke, L Bogdanik, A Yáñez, D Lall, A J Wolf, A K M G Muhammad, R Ho, S Carmona, J P Vit, J Zarrow,[...]. Science 2016
289
22

The lysosomal function of progranulin, a guardian against neurodegeneration.
Daniel H Paushter, Huan Du, Tuancheng Feng, Fenghua Hu. Acta Neuropathol 2018
65
22

Converging mechanisms in ALS and FTD: disrupted RNA and protein homeostasis.
Shuo-Chien Ling, Magdalini Polymenidou, Don W Cleveland. Neuron 2013
907
22


Plasma glial fibrillary acidic protein is raised in progranulin-associated frontotemporal dementia.
Carolin Heller, Martha S Foiani, Katrina Moore, Rhian Convery, Martina Bocchetta, Mollie Neason, David M Cash, David Thomas, Caroline V Greaves, Ione Oc Woollacott,[...]. J Neurol Neurosurg Psychiatry 2020
31
22


TDP-43 regulation of stress granule dynamics in neurodegenerative disease-relevant cell types.
Yousra Khalfallah, Rachel Kuta, Camille Grasmuck, Alexandre Prat, Heather D Durham, Christine Vande Velde. Sci Rep 2018
56
22

Progranulin regulates lysosomal function and biogenesis through acidification of lysosomes.
Yoshinori Tanaka, Genjiro Suzuki, Takashi Matsuwaki, Masato Hosokawa, Geidy Serrano, Thomas G Beach, Keitaro Yamanouchi, Masato Hasegawa, Masugi Nishihara. Hum Mol Genet 2017
78
22

Gene Expression Profile in Frontal Cortex in Sporadic Frontotemporal Lobar Degeneration-TDP.
Pol Andrés-Benito, Ellen Gelpi, Mónica Povedano, Gabriel Santpere, Isidro Ferrer. J Neuropathol Exp Neurol 2018
9
22

TDP-43 controls lysosomal pathways thereby determining its own clearance and cytotoxicity.
Christine Leibiger, Jana Deisel, Andreas Aufschnaiter, Stefanie Ambros, Maria Tereshchenko, Bert M Verheijen, Sabrina Büttner, Ralf J Braun. Hum Mol Genet 2018
30
22

TDP-43 interacts with mitochondrial proteins critical for mitophagy and mitochondrial dynamics.
Stephani A Davis, Sheed Itaman, Christopher M Khalid-Janney, Justin A Sherard, James A Dowell, Nigel J Cairns, Michael A Gitcho. Neurosci Lett 2018
63
22

Neuroanatomical Quantitative Proteomics Reveals Common Pathogenic Biological Routes between Amyotrophic Lateral Sclerosis (ALS) and Frontotemporal Dementia (FTD).
Marina Oaia Iridoy, Irene Zubiri, María Victoria Zelaya, Leyre Martinez, Karina Ausín, Mercedes Lachen-Montes, Enrique Santamaría, Joaquín Fernandez-Irigoyen, Ivonne Jericó. Int J Mol Sci 2018
18
22

C9orf72 ablation causes immune dysregulation characterized by leukocyte expansion, autoantibody production, and glomerulonephropathy in mice.
Amanda Atanasio, Vilma Decman, Derek White, Meg Ramos, Burcin Ikiz, Hoi-Ching Lee, Chia-Jen Siao, Susannah Brydges, Elizabeth LaRosa, Yu Bai,[...]. Sci Rep 2016
147
22

Progranulin-mediated deficiency of cathepsin D results in FTD and NCL-like phenotypes in neurons derived from FTD patients.
Clarissa Valdez, Yvette C Wong, Michael Schwake, Guojun Bu, Zbigniew K Wszolek, Dimitri Krainc. Hum Mol Genet 2017
50
22

Loss-of-function mutations in the C9ORF72 mouse ortholog cause fatal autoimmune disease.
Aaron Burberry, Naoki Suzuki, Jin-Yuan Wang, Rob Moccia, Daniel A Mordes, Morag H Stewart, Satomi Suzuki-Uematsu, Sulagna Ghosh, Ajay Singh, Florian T Merkle,[...]. Sci Transl Med 2016
140
22

Whole-genome sequencing reveals important role for TBK1 and OPTN mutations in frontotemporal lobar degeneration without motor neuron disease.
Cyril Pottier, Kevin F Bieniek, NiCole Finch, Maartje van de Vorst, Matt Baker, Ralph Perkersen, Patricia Brown, Thomas Ravenscroft, Marka van Blitterswijk, Alexandra M Nicholson,[...]. Acta Neuropathol 2015
204
22

Lipidomic and Transcriptomic Basis of Lysosomal Dysfunction in Progranulin Deficiency.
Bret M Evers, Carlos Rodriguez-Navas, Rachel J Tesla, Janine Prange-Kiel, Catherine R Wasser, Kyoung Shin Yoo, Jeffrey McDonald, Basar Cenik, Thomas A Ravenscroft, Florian Plattner,[...]. Cell Rep 2017
54
22

Development of disease-modifying drugs for frontotemporal dementia spectrum disorders.
Francesco Panza, Madia Lozupone, Davide Seripa, Antonio Daniele, Mark Watling, Gianluigi Giannelli, Bruno P Imbimbo. Nat Rev Neurol 2020
23
22

Genetics and molecular mechanisms of frontotemporal lobar degeneration: an update and future avenues.
Raffaele Ferrari, Claudia Manzoni, John Hardy. Neurobiol Aging 2019
20
22

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
22

Progranulin deficiency causes impairment of autophagy and TDP-43 accumulation.
Michael C Chang, Karpagam Srinivasan, Brad A Friedman, Eric Suto, Zora Modrusan, Wyne P Lee, Joshua S Kaminker, David V Hansen, Morgan Sheng. J Exp Med 2017
60
22

C9orf72-mediated ALS and FTD: multiple pathways to disease.
Rubika Balendra, Adrian M Isaacs. Nat Rev Neurol 2018
210
22

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
22

TDP-43 knockdown causes innate immune activation via protein kinase R in astrocytes.
Thomas J LaRocca, Andrea Mariani, Linda R Watkins, Christopher D Link. Neurobiol Dis 2019
17
22

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
22

Extracellular TDP-43 aggregates target MAPK/MAK/MRK overlapping kinase (MOK) and trigger caspase-3/IL-18 signaling in microglia.
María M Leal-Lasarte, Jaime M Franco, Adahir Labrador-Garrido, David Pozo, Cintia Roodveldt. FASEB J 2017
25
22


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.