A citation-based method for searching scientific literature

Xiaoming Yang, Yanan Ji, Wei Wang, Lilei Zhang, Zehao Chen, Miaomei Yu, Yuntian Shen, Fei Ding, Xiaosong Gu, Hualin Sun. Antioxidants (Basel) 2021
Times Cited: 2







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



Times Cited
  Times     Co-cited
Similarity


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
100

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
100

Polymyositis and dermatomyositis in adults.
P Hudgson. Clin Rheum Dis 1984
16
50

Study of 962 patients indicates progressive muscular atrophy is a form of ALS.
W-K Kim, X Liu, J Sandner, M Pasmantier, J Andrews, L P Rowland, H Mitsumoto. Neurology 2009
111
50

Genetics insight into the amyotrophic lateral sclerosis/frontotemporal dementia spectrum.
Ai-Ling Ji, Xia Zhang, Wei-Wei Chen, Wen-Juan Huang. J Med Genet 2017
47
50

p62 positive, TDP-43 negative, neuronal cytoplasmic and intranuclear inclusions in the cerebellum and hippocampus define the pathology of C9orf72-linked FTLD and MND/ALS.
Safa Al-Sarraj, Andrew King, Claire Troakes, Bradley Smith, Satomi Maekawa, Istvan Bodi, Boris Rogelj, Ammar Al-Chalabi, Tibor Hortobágyi, Christopher E Shaw. Acta Neuropathol 2011
347
50

Atypical, slowly progressive behavioural variant frontotemporal dementia associated with C9ORF72 hexanucleotide expansion.
Baber K Khan, Jennifer S Yokoyama, Leonel T Takada, Sharon J Sha, Nicola J Rutherford, Jamie C Fong, Anna M Karydas, Teresa Wu, Robin S Ketelle, Matthew C Baker,[...]. J Neurol Neurosurg Psychiatry 2012
140
50

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
50

Familial ALS with extreme phenotypic variability due to the I113T SOD1 mutation.
Glenn Lopate, Robert H Baloh, Muhammad T Al-Lozi, Timothy M Miller, J Americo Fernandes Filho, Oliver Ni, Alison Leston, Julaine Florence, Jeanine Schierbecker, Peggy Allred. Amyotroph Lateral Scler 2010
27
50

Evidence for polygenic and oligogenic basis of Australian sporadic amyotrophic lateral sclerosis.
Emily P McCann, Lyndal Henden, Jennifer A Fifita, Katharine Y Zhang, Natalie Grima, Denis C Bauer, Sandrine Chan Moi Fat, Natalie A Twine, Roger Pamphlett, Matthew C Kiernan,[...]. J Med Genet 2020
12
50


Genetics of amyotrophic lateral sclerosis: an update.
Sheng Chen, Pavani Sayana, Xiaojie Zhang, Weidong Le. Mol Neurodegener 2013
186
50

TDP-43 as a potential biomarker for amyotrophic lateral sclerosis: a systematic review and meta-analysis.
Vivek Majumder, Jenna M Gregory, Marcelo A Barria, Alison Green, Suvankar Pal. BMC Neurol 2018
34
50

Spinal Muscular Atrophy in the Treatment Era.
Megan A Waldrop, Bakri H Elsheikh. Neurol Clin 2020
6
50


Inclusion body myositis mimicking motor neuron disease.
R Dabby, D J Lange, W Trojaborg, A P Hays, R E Lovelace, T H Brannagan, L P Rowland. Arch Neurol 2001
52
50

Neuropathology of ALS: an overview.
A Hirano. Neurology 1996
102
50


Analysis of ALS-related proteins during herpes simplex virus-2 latent infection.
Jorge Rubén Cabrera, Ignacio Rodríguez-Izquierdo, José Luis Jiménez, María Ángeles Muñoz-Fernández. J Neuroinflammation 2020
3
50

Motor neuron disease of paraneoplastic origin: a rare but treatable condition.
Nicolas Mélé, Giulia Berzero, Thierry Maisonobe, François Salachas, Guillaume Nicolas, Nicolas Weiss, Guillemette Beaudonnet, Francois Ducray, Dimitri Psimaras, Timothée Lenglet. J Neurol 2018
17
50

Genetic analysis of amyotrophic lateral sclerosis identifies contributing pathways and cell types.
Sara Saez-Atienzar, Sara Bandres-Ciga, Rebekah G Langston, Jonggeol J Kim, Shing Wan Choi, Regina H Reynolds, Yevgeniya Abramzon, Ramita Dewan, Sarah Ahmed, John E Landers,[...]. Sci Adv 2021
12
50

Sporadic Parkinson disease and amyotrophic lateral sclerosis complex (Brait-Fahn-Schwartz disease).
Concetta Manno, Alessio Lipari, Valeria Bono, Alfonsa Claudia Taiello, Vincenzo La Bella. J Neurol Sci 2013
12
50

Neurofilament light chain in serum for the diagnosis of amyotrophic lateral sclerosis.
Federico Verde, Petra Steinacker, Jochen H Weishaupt, Jan Kassubek, Patrick Oeckl, Steffen Halbgebauer, Hayrettin Tumani, Christine A F von Arnim, Johannes Dorst, Emily Feneberg,[...]. J Neurol Neurosurg Psychiatry 2019
94
50

[Progressive bulbar palsy (Fazio-Londe disease): case report].
Bianca Helena Brum Batista, Andrea Garcia Almeida, Magda Lahorgue Nunes, Paulo Márcio Condessa Pitrez, João Arthur Ehlers. Arq Neuropsiquiatr 2002
2
50

Phenotype difference between ALS patients with expanded repeats in C9ORF72 and patients with mutations in other ALS-related genes.
Stéphanie Millecamps, Séverine Boillée, Isabelle Le Ber, Danielle Seilhean, Elisa Teyssou, Marine Giraudeau, Carine Moigneu, Nadia Vandenberghe, Véronique Danel-Brunaud, Philippe Corcia,[...]. J Med Genet 2012
115
50

Cognitive and Behavioral Manifestations in ALS: Beyond Motor System Involvement.
Robert Rusina, Rik Vandenberghe, Rose Bruffaerts. Diagnostics (Basel) 2021
3
50

Sporadic and familial parkinsonism and motor neuron disease.
K Brait, S Fahn, G A Schwarz. Neurology 1973
61
50


Spinal Muscular Atrophy.
Stephen J Kolb, John T Kissel. Neurol Clin 2015
176
50

Amyotrophic lateral sclerosis.
Lokesh C Wijesekera, P Nigel Leigh. Orphanet J Rare Dis 2009
566
50

A revision of the El Escorial criteria - 2015.
Albert Ludolph, Vivian Drory, Orla Hardiman, Imaharu Nakano, John Ravits, Wim Robberecht, Jeremy Shefner. Amyotroph Lateral Scler Frontotemporal Degener 2015
230
50

Stages of pTDP-43 pathology in amyotrophic lateral sclerosis.
Johannes Brettschneider, Kelly Del Tredici, Jon B Toledo, John L Robinson, David J Irwin, Murray Grossman, EunRan Suh, Vivianna M Van Deerlin, Elisabeth M Wood, Young Baek,[...]. Ann Neurol 2013
524
50

Cognitive function in bulbar- and spinal-onset amyotrophic lateral sclerosis. A longitudinal study in 52 patients.
Herbert Schreiber, Tanja Gaigalat, Ursula Wiedemuth-Catrinescu, Michael Graf, Ingo Uttner, Rainer Muche, Albert Christian Ludolph. J Neurol 2005
125
50

Cerebrospinal Fluid TDP-43 in Frontotemporal Lobar Degeneration and Amyotrophic Lateral Sclerosis Patients with and without the C9ORF72 Hexanucleotide Expansion.
Anna Junttila, Mari Kuvaja, Päivi Hartikainen, Maritta Siloaho, Seppo Helisalmi, Virpi Moilanen, Anna Kiviharju, Lilja Jansson, Pentti J Tienari, Anne Marja Remes,[...]. Dement Geriatr Cogn Dis Extra 2016
27
50

Tau protein as a diagnostic and prognostic biomarker in amyotrophic lateral sclerosis.
Luisa Agnello, Tiziana Colletti, Bruna Lo Sasso, Matteo Vidali, Rossella Spataro, Caterina Maria Gambino, Rosaria Vincenza Giglio, Tommaso Piccoli, Giulia Bivona, Vincenzo La Bella,[...]. Eur J Neurol 2021
3
50

Effects of gender in amyotrophic lateral sclerosis.
Pamela A McCombe, Robert D Henderson. Gend Med 2010
170
50

Recommended diagnostic criteria for paraneoplastic neurological syndromes.
F Graus, J Y Delattre, J C Antoine, J Dalmau, B Giometto, W Grisold, J Honnorat, P Sillevis Smitt, Ch Vedeler, J J G M Verschuuren,[...]. J Neurol Neurosurg Psychiatry 2004
980
50

p62- and ubiquitin-dependent stress-induced autophagy of the mammalian 26S proteasome.
Victoria Cohen-Kaplan, Ido Livneh, Noa Avni, Bertrand Fabre, Tamar Ziv, Yong Tae Kwon, Aaron Ciechanover. Proc Natl Acad Sci U S A 2016
130
50

Syringomyelia simulating amyotrophic lateral sclerosis.
J Rafalowska, B Wasowicz. Pol Med J 1968
2
50

Differential involvement of optineurin in amyotrophic lateral sclerosis with or without SOD1 mutations.
Han-Xiang Deng, Eileen H Bigio, Hong Zhai, Faisal Fecto, Kaouther Ajroud, Yong Shi, Jianhua Yan, Manjari Mishra, Senda Ajroud-Driss, Scott Heller,[...]. Arch Neurol 2011
51
50

Amyotrophic Lateral Sclerosis.
Robert H Brown, Ammar Al-Chalabi. N Engl J Med 2017
592
50

SOD1 in neurotoxicity and its controversial roles in SOD1 mutation-negative ALS.
Yuki Hayashi, Kengo Homma, Hidenori Ichijo. Adv Biol Regul 2016
59
50


Monomelic amyotrophy with proximal upper limb involvement: a case report.
Eman Al-Ghawi, Talal Al-Harbi, Adnan Al-Sarawi, Mohamed Binfalah. J Med Case Rep 2016
6
50

Amyotrophic lateral sclerosis mimic syndromes.
Majid Ghasemi. Iran J Neurol 2016
16
50

Pathological characterization of astrocytic hyaline inclusions in familial amyotrophic lateral sclerosis.
S Kato, H Hayashi, K Nakashima, E Nanba, M Kato, A Hirano, I Nakano, K Asayama, E Ohama. Am J Pathol 1997
90
50

The patient experience of fatigue in motor neurone disease.
Chris J Gibbons, Everard W Thornton, Carolyn A Young. Front Psychol 2013
17
50

Prognostic factors in ALS: A critical review.
Adriano Chiò, Giancarlo Logroscino, Orla Hardiman, Robert Swingler, Douglas Mitchell, Ettore Beghi, Bryan G Traynor. Amyotroph Lateral Scler 2009
531
50

Alterations in Tau Metabolism in ALS and ALS-FTSD.
Michael J Strong, Neil S Donison, Kathryn Volkening. Front Neurol 2020
5
50



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.