A citation-based method for searching scientific literature

D A Solomon, J C Mitchell, M-T Salcher-Konrad, C A Vance, S Mizielinska. Neuropathol Appl Neurobiol 2019
Times Cited: 8







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



Times Cited
  Times     Co-cited
Similarity


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
62

Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS.
Mariely DeJesus-Hernandez, Ian R Mackenzie, Bradley F Boeve, Adam L Boxer, Matt Baker, Nicola J Rutherford, Alexandra M Nicholson, NiCole A Finch, Heather Flynn, Jennifer Adamson,[...]. Neuron 2011
62

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
62

Mutations in FUS, an RNA processing protein, cause familial amyotrophic lateral sclerosis type 6.
Caroline Vance, Boris Rogelj, Tibor Hortobágyi, Kurt J De Vos, Agnes Lumi Nishimura, Jemeen Sreedharan, Xun Hu, Bradley Smith, Deborah Ruddy, Paul Wright,[...]. Science 2009
50

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
50

Review: Neuropathology of non-tau frontotemporal lobar degeneration.
M Neumann, I R A Mackenzie. Neuropathol Appl Neurobiol 2019
47
37

Review: Molecular pathology of frontotemporal lobar degenerations.
B Borroni, A Alberici, E Buratti. Neuropathol Appl Neurobiol 2019
8
37

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
37

Frontotemporal Dementia.
Nicholas T Olney, Salvatore Spina, Bruce L Miller. Neurol Clin 2017
128
37

C9orf72-mediated ALS and FTD: multiple pathways to disease.
Rubika Balendra, Adrian M Isaacs. Nat Rev Neurol 2018
210
37

Mutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosis.
T J Kwiatkowski, D A Bosco, A L Leclerc, E Tamrazian, C R Vanderburg, C Russ, A Davis, J Gilchrist, E J Kasarskis, T Munsat,[...]. Science 2009
37


Ataxin-2 intermediate-length polyglutamine expansions are associated with increased risk for ALS.
Andrew C Elden, Hyung-Jun Kim, Michael P Hart, Alice S Chen-Plotkin, Brian S Johnson, Xiaodong Fang, Maria Armakola, Felix Geser, Robert Greene, Min Min Lu,[...]. Nature 2010
770
37

Divergent roles of ALS-linked proteins FUS/TLS and TDP-43 intersect in processing long pre-mRNAs.
Clotilde Lagier-Tourenne, Magdalini Polymenidou, Kasey R Hutt, Anthony Q Vu, Michael Baughn, Stephanie C Huelga, Kevin M Clutario, Shuo-Chien Ling, Tiffany Y Liang, Curt Mazur,[...]. Nat Neurosci 2012
444
37

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
37


Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21.
Marc Cruts, Ilse Gijselinck, Julie van der Zee, Sebastiaan Engelborghs, Hans Wils, Daniel Pirici, Rosa Rademakers, Rik Vandenberghe, Bart Dermaut, Jean-Jacques Martin,[...]. Nature 2006
25

Review: an update on clinical, genetic and pathological aspects of frontotemporal lobar degenerations.
Tammaryn Lashley, Jonathan D Rohrer, Simon Mead, Tamas Revesz. Neuropathol Appl Neurobiol 2015
116
25

Review: Fluid biomarkers for frontotemporal dementias.
H Zetterberg, J C van Swieten, A L Boxer, J D Rohrer. Neuropathol Appl Neurobiol 2019
20
25

Review: Clinical, genetic and neuroimaging features of frontotemporal dementia.
R Convery, S Mead, J D Rohrer. Neuropathol Appl Neurobiol 2019
13
25

The behavioural variant frontotemporal dementia (bvFTD) syndrome in psychiatry.
Serggio C Lanata, Bruce L Miller. J Neurol Neurosurg Psychiatry 2016
59
25

Frontotemporal dementia.
Jee Bang, Salvatore Spina, Bruce L Miller. Lancet 2015
350
25

Intrafamilial variable phenotype including corticobasal syndrome in a family with p.P301L mutation in the MAPT gene: first report in South America.
Emilia M Gatto, Ricardo F Allegri, Gustavo Da Prat, Patricio Chrem Mendez, David S Hanna, Michael O Dorschner, Ezequiel I Surace, Cyrus P Zabetian, Ignacio F Mata. Neurobiol Aging 2017
6
33

Cerebrospinal fluid and blood biomarkers for neurodegenerative dementias: An update of the Consensus of the Task Force on Biological Markers in Psychiatry of the World Federation of Societies of Biological Psychiatry.
Piotr Lewczuk, Peter Riederer, Sid E O'Bryant, Marcel M Verbeek, Bruno Dubois, Pieter Jelle Visser, Kurt A Jellinger, Sebastiaan Engelborghs, Alfredo Ramirez, Lucilla Parnetti,[...]. World J Biol Psychiatry 2018
125
25

Cellular ageing, increased mortality and FTLD-TDP-associated neuropathology in progranulin knockout mice.
Hans Wils, Gernot Kleinberger, Sandra Pereson, Jonathan Janssens, Anja Capell, Debby Van Dam, Ivy Cuijt, Geert Joris, Peter P De Deyn, Christian Haass,[...]. J Pathol 2012
87
25

Recent advances in the molecular genetics of frontotemporal lobar degeneration.
Innocenzo Rainero, E Rubino, A Michelerio, F D'Agata, Salvatore Gentile, Lorenzo Pinessi. Funct Neurol 2017
23
25

Phenotypes and malignancy risk of different FUS mutations in genetic amyotrophic lateral sclerosis.
Marcel Naumann, Kevin Peikert, Rene Günther, Anneke J van der Kooi, Eleonora Aronica, Annemarie Hübers, Veronique Danel, Philippe Corcia, Francisco Pan-Montojo, Sebahattin Cirak,[...]. Ann Clin Transl Neurol 2019
22
25

Therapeutic modulation of eIF2α phosphorylation rescues TDP-43 toxicity in amyotrophic lateral sclerosis disease models.
Hyung-Jun Kim, Alya R Raphael, Eva S LaDow, Leeanne McGurk, Ross A Weber, John Q Trojanowski, Virginia M-Y Lee, Steven Finkbeiner, Aaron D Gitler, Nancy M Bonini. Nat Genet 2014
238
25

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
292
25


The genetics of amyotrophic lateral sclerosis: current insights.
Afnan A Alsultan, Rachel Waller, Paul R Heath, Janine Kirby. Degener Neurol Neuromuscul Dis 2016
39
25

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
25

TDP-43 gains function due to perturbed autoregulation in a Tardbp knock-in mouse model of ALS-FTD.
Matthew A White, Eosu Kim, Amanda Duffy, Robert Adalbert, Benjamin U Phillips, Owen M Peters, Jodie Stephenson, Sujeong Yang, Francesca Massenzio, Ziqiang Lin,[...]. Nat Neurosci 2018
92
25

Misregulation of human sortilin splicing leads to the generation of a nonfunctional progranulin receptor.
Mercedes Prudencio, Karen R Jansen-West, Wing C Lee, Tania F Gendron, Yong-Jie Zhang, Ya-Fei Xu, Jennifer Gass, Cristiana Stuani, Caroline Stetler, Rosa Rademakers,[...]. Proc Natl Acad Sci U S A 2012
52
25

TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis.
Edor Kabashi, Paul N Valdmanis, Patrick Dion, Dan Spiegelman, Brendan J McConkey, Christine Vande Velde, Jean-Pierre Bouchard, Lucette Lacomblez, Ksenia Pochigaeva, Francois Salachas,[...]. Nat Genet 2008
25

Therapeutic reduction of ataxin-2 extends lifespan and reduces pathology in TDP-43 mice.
Lindsay A Becker, Brenda Huang, Gregor Bieri, Rosanna Ma, David A Knowles, Paymaan Jafar-Nejad, James Messing, Hong Joo Kim, Armand Soriano, Georg Auburger,[...]. Nature 2017
233
25


TDP-43 in the ubiquitin pathology of frontotemporal dementia with VCP gene mutations.
Manuela Neumann, Ian R Mackenzie, Nigel J Cairns, Philip J Boyer, William R Markesbery, Charles D Smith, J Paul Taylor, Hans A Kretzschmar, Virginia E Kimonis, Mark S Forman. J Neuropathol Exp Neurol 2007
244
25

Genetics of FTLD: overview and what else we can expect from genetic studies.
Cyril Pottier, Thomas A Ravenscroft, Monica Sanchez-Contreras, Rosa Rademakers. J Neurochem 2016
82
25

Disease-modifying effects of metabolic perturbations in ALS/FTLD.
Ali Jawaid, Romesa Khan, Magdalini Polymenidou, Paul E Schulz. Mol Neurodegener 2018
16
25

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
539
25

TDP-43 affects splicing profiles and isoform production of genes involved in the apoptotic and mitotic cellular pathways.
Laura De Conti, Maureen V Akinyi, Ramiro Mendoza-Maldonado, Maurizio Romano, Marco Baralle, Emanuele Buratti. Nucleic Acids Res 2015
39
25

Acetylation-induced TDP-43 pathology is suppressed by an HSF1-dependent chaperone program.
Ping Wang, Connor M Wander, Chao-Xing Yuan, Michael S Bereman, Todd J Cohen. Nat Commun 2017
31
25

Molecular Mechanisms of TDP-43 Misfolding and Pathology in Amyotrophic Lateral Sclerosis.
Archana Prasad, Vidhya Bharathi, Vishwanath Sivalingam, Amandeep Girdhar, Basant K Patel. Front Mol Neurosci 2019
165
25

Decoding ALS: from genes to mechanism.
J Paul Taylor, Robert H Brown, Don W Cleveland. Nature 2016
903
25

Mechanisms of disease in frontotemporal lobar degeneration: gain of function versus loss of function effects.
Glenda Halliday, Eileen H Bigio, Nigel J Cairns, Manuela Neumann, Ian R A Mackenzie, David M A Mann. Acta Neuropathol 2012
58
25


The C9orf72 repeat expansion disrupts nucleocytoplasmic transport.
Ke Zhang, Christopher J Donnelly, Aaron R Haeusler, Jonathan C Grima, James B Machamer, Peter Steinwald, Elizabeth L Daley, Sean J Miller, Kathleen M Cunningham, Svetlana Vidensky,[...]. Nature 2015
566
25

Sortilin-mediated endocytosis determines levels of the frontotemporal dementia protein, progranulin.
Fenghua Hu, Thihan Padukkavidana, Christian B Vægter, Owen A Brady, Yanqiu Zheng, Ian R Mackenzie, Howard H Feldman, Anders Nykjaer, Stephen M Strittmatter. Neuron 2010
336
25

Mutations in prion-like domains in hnRNPA2B1 and hnRNPA1 cause multisystem proteinopathy and ALS.
Hong Joo Kim, Nam Chul Kim, Yong-Dong Wang, Emily A Scarborough, Jennifer Moore, Zamia Diaz, Kyle S MacLea, Brian Freibaum, Songqing Li, Amandine Molliex,[...]. Nature 2013
865
25


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.