A citation-based method for searching scientific literature

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, Dominic B Rowe, Kelly L Williams, Ian P Blair. J Med Genet 2020
Times Cited: 12







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



Times Cited
  Times     Co-cited
Similarity


El Escorial revisited: revised criteria for the diagnosis of amyotrophic lateral sclerosis.
B R Brooks, R G Miller, M Swash, T L Munsat. Amyotroph Lateral Scler Other Motor Neuron Disord 2000
50

State of play in amyotrophic lateral sclerosis genetics.
Alan E Renton, Adriano Chiò, Bryan J Traynor. Nat Neurosci 2014
890
50

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
50

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
50

Evidence for an oligogenic basis of amyotrophic lateral sclerosis.
Marka van Blitterswijk, Michael A van Es, Eric A M Hennekam, Dennis Dooijes, Wouter van Rheenen, Jelena Medic, Pierre R Bourque, Helenius J Schelhaas, Anneke J van der Kooi, Marianne de Visser,[...]. Hum Mol Genet 2012
227
41

A comprehensive analysis of rare genetic variation in amyotrophic lateral sclerosis in the UK.
Sarah Morgan, Aleksey Shatunov, William Sproviero, Ashley R Jones, Maryam Shoai, Deborah Hughes, Ahmad Al Khleifat, Andrea Malaspina, Karen E Morrison, Pamela J Shaw,[...]. Brain 2017
40
41

Amyotrophic lateral sclerosis.
L P Rowland, N A Shneider. N Engl J Med 2001
33

Analysis of amyotrophic lateral sclerosis as a multistep process: a population-based modelling study.
Ammar Al-Chalabi, Andrea Calvo, Adriano Chio, Shuna Colville, Cathy M Ellis, Orla Hardiman, Mark Heverin, Robin S Howard, Mark H B Huisman, Noa Keren,[...]. Lancet Neurol 2014
173
33

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
33

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
33

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
33

Mutations in UBQLN2 cause dominant X-linked juvenile and adult-onset ALS and ALS/dementia.
Han-Xiang Deng, Wenjie Chen, Seong-Tshool Hong, Kym M Boycott, George H Gorrie, Nailah Siddique, Yi Yang, Faisal Fecto, Yong Shi, Hong Zhai,[...]. Nature 2011
770
33

Mutations in the profilin 1 gene cause familial amyotrophic lateral sclerosis.
Chi-Hong Wu, Claudia Fallini, Nicola Ticozzi, Pamela J Keagle, Peter C Sapp, Katarzyna Piotrowska, Patrick Lowe, Max Koppers, Diane McKenna-Yasek, Desiree M Baron,[...]. Nature 2012
371
33

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.
Sue Richards, Nazneen Aziz, Sherri Bale, David Bick, Soma Das, Julie Gastier-Foster, Wayne W Grody, Madhuri Hegde, Elaine Lyon, Elaine Spector,[...]. Genet Med 2015
33

The genotype-phenotype landscape of familial amyotrophic lateral sclerosis in Australia.
E P McCann, K L Williams, J A Fifita, I S Tarr, J O'Connor, D B Rowe, G A Nicholson, I P Blair. Clin Genet 2017
25
25

ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data.
Kai Wang, Mingyao Li, Hakon Hakonarson. Nucleic Acids Res 2010
25

An estimate of amyotrophic lateral sclerosis heritability using twin data.
A Al-Chalabi, F Fang, M F Hanby, P N Leigh, C E Shaw, W Ye, F Rijsdijk. J Neurol Neurosurg Psychiatry 2010
166
25

Lifetime Risk and Heritability of Amyotrophic Lateral Sclerosis.
Marie Ryan, Mark Heverin, Russell L McLaughlin, Orla Hardiman. JAMA Neurol 2019
31
25

Gene discovery in amyotrophic lateral sclerosis: implications for clinical management.
Ammar Al-Chalabi, Leonard H van den Berg, Jan Veldink. Nat Rev Neurol 2017
139
25

Amyotrophic lateral sclerosis.
Matthew C Kiernan, Steve Vucic, Benjamin C Cheah, Martin R Turner, Andrew Eisen, Orla Hardiman, James R Burrell, Margaret C Zoing. Lancet 2011
25

Amyotrophic lateral sclerosis onset is influenced by the burden of rare variants in known amyotrophic lateral sclerosis genes.
Janet Cady, Peggy Allred, Taha Bali, Alan Pestronk, Alison Goate, Timothy M Miller, Robi D Mitra, John Ravits, Matthew B Harms, Robert H Baloh. Ann Neurol 2015
122
25


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
25

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
25

Mutations of optineurin in amyotrophic lateral sclerosis.
Hirofumi Maruyama, Hiroyuki Morino, Hidefumi Ito, Yuishin Izumi, Hidemasa Kato, Yasuhito Watanabe, Yoshimi Kinoshita, Masaki Kamada, Hiroyuki Nodera, Hidenori Suzuki,[...]. Nature 2010
844
25

TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis.
Jemeen Sreedharan, Ian P Blair, Vineeta B Tripathi, Xun Hu, Caroline Vance, Boris Rogelj, Steven Ackerley, Jennifer C Durnall, Kelly L Williams, Emanuele Buratti,[...]. Science 2008
25

NEK1 variants confer susceptibility to amyotrophic lateral sclerosis.
Kevin P Kenna, Perry T C van Doormaal, Annelot M Dekker, Nicola Ticozzi, Brendan J Kenna, Frank P Diekstra, Wouter van Rheenen, Kristel R van Eijk, Ashley R Jones, Pamela Keagle,[...]. Nat Genet 2016
126
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

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
25

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
25

The multistep hypothesis of ALS revisited: The role of genetic mutations.
Adriano Chiò, Letizia Mazzini, Sandra D'Alfonso, Lucia Corrado, Antonio Canosa, Cristina Moglia, Umberto Manera, Enrica Bersano, Maura Brunetti, Marco Barberis,[...]. Neurology 2018
67
25

ALS Genes in the Genomic Era and their Implications for FTD.
Hung Phuoc Nguyen, Christine Van Broeckhoven, Julie van der Zee. Trends Genet 2018
125
25

ALS Genetics, Mechanisms, and Therapeutics: Where Are We Now?
Rita Mejzini, Loren L Flynn, Ianthe L Pitout, Sue Fletcher, Steve D Wilton, P Anthony Akkari. Front Neurosci 2019
147
25

Recessive amyotrophic lateral sclerosis families with the D90A SOD1 mutation share a common founder: evidence for a linked protective factor.
A Al-Chalabi, P M Andersen, B Chioza, C Shaw, P C Sham, W Robberecht, G Matthijs, W Camu, S L Marklund, L Forsgren,[...]. Hum Mol Genet 1998
123
16


Genetics of motor neuron disorders: new insights into pathogenic mechanisms.
Patrick A Dion, Hussein Daoud, Guy A Rouleau. Nat Rev Genet 2009
205
16

D90A-SOD1 mediated amyotrophic lateral sclerosis: a single founder for all cases with evidence for a Cis-acting disease modifier in the recessive haplotype.
Matthew J Parton, Wendy Broom, Peter M Andersen, Ammar Al-Chalabi, P Nigel Leigh, John F Powell, Christopher E Shaw. Hum Mutat 2002
73
16

Age and founder effect of SOD1 A4V mutation causing ALS.
M Saeed, Y Yang, H-X Deng, W-Y Hung, N Siddique, L Dellefave, C Gellera, P M Andersen, T Siddique. Neurology 2009
47
16

The Genome Analysis Toolkit: a MapReduce framework for analyzing next-generation DNA sequencing data.
Aaron McKenna, Matthew Hanna, Eric Banks, Andrey Sivachenko, Kristian Cibulskis, Andrew Kernytsky, Kiran Garimella, David Altshuler, Stacey Gabriel, Mark Daly,[...]. Genome Res 2010
16

TIA1 Mutations in Amyotrophic Lateral Sclerosis and Frontotemporal Dementia Promote Phase Separation and Alter Stress Granule Dynamics.
Ian R Mackenzie, Alexandra M Nicholson, Mohona Sarkar, James Messing, Maria D Purice, Cyril Pottier, Kavya Annu, Matt Baker, Ralph B Perkerson, Aishe Kurti,[...]. Neuron 2017
285
16


ALS phenotypes with mutations in CHMP2B (charged multivesicular body protein 2B).
N Parkinson, P G Ince, M O Smith, R Highley, G Skibinski, P M Andersen, K E Morrison, H S Pall, O Hardiman, J Collinge,[...]. Neurology 2006
285
16

Delineating the genetic heterogeneity of ALS using targeted high-throughput sequencing.
Kevin P Kenna, Russell L McLaughlin, Susan Byrne, Marwa Elamin, Mark Heverin, Elaine M Kenny, Paul Cormican, Derek W Morris, Colette G Donaghy, Daniel G Bradley,[...]. J Med Genet 2013
115
16

ATXN1 intermediate-length polyglutamine expansions are associated with amyotrophic lateral sclerosis.
Serena Lattante, Maria Grazia Pomponi, Amelia Conte, Giuseppe Marangi, Giulia Bisogni, Agata Katia Patanella, Emiliana Meleo, Christian Lunetta, Nilo Riva, Lorena Mosca,[...]. Neurobiol Aging 2018
23
16

SPG7 mutations in amyotrophic lateral sclerosis: a genetic link to hereditary spastic paraplegia.
Alma Osmanovic, Maylin Widjaja, Alisa Förster, Julia Weder, Mike P Wattjes, Inken Lange, Anastasia Sarikidi, Bernd Auber, Peter Raab, Anne Christians,[...]. J Neurol 2020
4
50

Exome-wide rare variant analysis identifies TUBA4A mutations associated with familial ALS.
Bradley N Smith, Nicola Ticozzi, Claudia Fallini, Athina Soragia Gkazi, Simon Topp, Kevin P Kenna, Emma L Scotter, Jason Kost, Pamela Keagle, Jack W Miller,[...]. Neuron 2014
203
16

A mitochondrial origin for frontotemporal dementia and amyotrophic lateral sclerosis through CHCHD10 involvement.
Sylvie Bannwarth, Samira Ait-El-Mkadem, Annabelle Chaussenot, Emmanuelle C Genin, Sandra Lacas-Gervais, Konstantina Fragaki, Laetitia Berg-Alonso, Yusuke Kageyama, Valérie Serre, David G Moore,[...]. Brain 2014
264
16

ALS-associated missense and nonsense TBK1 mutations can both cause loss of kinase function.
Martina de Majo, Simon D Topp, Bradley N Smith, Agnes L Nishimura, Han-Jou Chen, Athina Soragia Gkazi, Jack Miller, Chun Hao Wong, Caroline Vance, Frank Baas,[...]. Neurobiol Aging 2018
40
16

Deletions of the heavy neurofilament subunit tail in amyotrophic lateral sclerosis.
A Al-Chalabi, P M Andersen, P Nilsson, B Chioza, J L Andersson, C Russ, C E Shaw, J F Powell, P N Leigh. Hum Mol Genet 1999
262
16

Four familial ALS pedigrees discordant for two SOD1 mutations: are all SOD1 mutations pathogenic?
Ansgar Felbecker, William Camu, Paul N Valdmanis, Anne-Dorte Sperfeld, Stefan Waibel, Peter Steinbach, Guy A Rouleau, Albert C Ludolph, Peter M Andersen. J Neurol Neurosurg Psychiatry 2010
50
16


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.