A citation-based method for searching scientific literature


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



Times Cited
  Times     Co-cited
Similarity


Genome-wide Analyses Identify KIF5A as a Novel ALS Gene.
Aude Nicolas, Kevin P Kenna, Alan E Renton, Nicola Ticozzi, Faraz Faghri, Ruth Chia, Janice A Dominov, Brendan J Kenna, Mike A Nalls, Pamela Keagle,[...]. Neuron 2018
209
31

Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis.
Wouter van Rheenen, Aleksey Shatunov, Annelot M Dekker, Russell L McLaughlin, Frank P Diekstra, Sara L Pulit, Rick A A van der Spek, Urmo Võsa, Simone de Jong, Matthew R Robinson,[...]. Nat Genet 2016
253
31

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
29

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
27

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
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
564
21

State of play in amyotrophic lateral sclerosis genetics.
Alan E Renton, Adriano Chiò, Bryan J Traynor. Nat Neurosci 2014
878
21

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
19

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
164
19

Gene discovery in amyotrophic lateral sclerosis: implications for clinical management.
Ammar Al-Chalabi, Leonard H van den Berg, Jan Veldink. Nat Rev Neurol 2017
134
17

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
17

PLINK: a tool set for whole-genome association and population-based linkage analyses.
Shaun Purcell, Benjamin Neale, Kathe Todd-Brown, Lori Thomas, Manuel A R Ferreira, David Bender, Julian Maller, Pamela Sklar, Paul I W de Bakker, Mark J Daly,[...]. Am J Hum Genet 2007
17

ALSoD: A user-friendly online bioinformatics tool for amyotrophic lateral sclerosis genetics.
Olubunmi Abel, John F Powell, Peter M Andersen, Ammar Al-Chalabi. Hum Mutat 2012
167
17

Amyotrophic Lateral Sclerosis.
Robert H Brown, Ammar Al-Chalabi. N Engl J Med 2017
565
17

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
17

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
168
17

Detection of long repeat expansions from PCR-free whole-genome sequence data.
Egor Dolzhenko, Joke J F A van Vugt, Richard J Shaw, Mitchell A Bekritsky, Marka van Blitterswijk, Giuseppe Narzisi, Subramanian S Ajay, Vani Rajan, Bryan R Lajoie, Nathan H Johnson,[...]. Genome Res 2017
116
15

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
122
15

The project MinE databrowser: bringing large-scale whole-genome sequencing in ALS to researchers and the public.
Rick A A van der Spek, Wouter van Rheenen, Sara L Pulit, Kevin P Kenna, Leonard H van den Berg, Jan H Veldink. Amyotroph Lateral Scler Frontotemporal Degener 2019
23
34

Amyotrophic lateral sclerosis.
Michael A van Es, Orla Hardiman, Adriano Chio, Ammar Al-Chalabi, R Jeroen Pasterkamp, Jan H Veldink, Leonard H van den Berg. Lancet 2017
374
13

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
465
13



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
66
13

Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study.
Elisa Majounie, Alan E Renton, Kin Mok, Elise G P Dopper, Adrian Waite, Sara Rollinson, Adriano Chiò, Gabriella Restagno, Nayia Nicolaou, Javier Simon-Sanchez,[...]. Lancet Neurol 2012
741
13

Cognitive and clinical characteristics of patients with amyotrophic lateral sclerosis carrying a C9orf72 repeat expansion: a population-based cohort study.
Susan Byrne, Marwa Elamin, Peter Bede, Aleksey Shatunov, Cathal Walsh, Bernie Corr, Mark Heverin, Norah Jordan, Kevin Kenna, Catherine Lynch,[...]. Lancet Neurol 2012
313
13

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
758
11

Clinical genetics of amyotrophic lateral sclerosis: what do we really know?
Peter M Andersen, Ammar Al-Chalabi. Nat Rev Neurol 2011
447
11

ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data.
Kai Wang, Mingyao Li, Hakon Hakonarson. Nucleic Acids Res 2010
11

A method and server for predicting damaging missense mutations.
Ivan A Adzhubei, Steffen Schmidt, Leonid Peshkin, Vasily E Ramensky, Anna Gerasimova, Peer Bork, Alexey S Kondrashov, Shamil R Sunyaev. Nat Methods 2010
11

Analysis of protein-coding genetic variation in 60,706 humans.
Monkol Lek, Konrad J Karczewski, Eric V Minikel, Kaitlin E Samocha, Eric Banks, Timothy Fennell, Anne H O'Donnell-Luria, James S Ware, Andrew J Hill, Beryl B Cummings,[...]. Nature 2016
11

The epidemiology of ALS: a conspiracy of genes, environment and time.
Ammar Al-Chalabi, Orla Hardiman. Nat Rev Neurol 2013
393
11

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
512
11

Tracking a Fast-Moving Disease: Longitudinal Markers, Monitoring, and Clinical Trial Endpoints in ALS.
Rangariroyashe Hannah Chipika, Eoin Finegan, Stacey Li Hi Shing, Orla Hardiman, Peter Bede. Front Neurol 2019
45
13

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
121
11

Isaac: ultra-fast whole-genome secondary analysis on Illumina sequencing platforms.
Come Raczy, Roman Petrovski, Christopher T Saunders, Ilya Chorny, Semyon Kruglyak, Elliott H Margulies, Han-Yu Chuang, Morten Källberg, Swathi A Kumar, Arnold Liao,[...]. Bioinformatics 2013
169
11

ALS Genes in the Genomic Era and their Implications for FTD.
Hung Phuoc Nguyen, Christine Van Broeckhoven, Julie van der Zee. Trends Genet 2018
121
11

Lifetime Risk and Heritability of Amyotrophic Lateral Sclerosis.
Marie Ryan, Mark Heverin, Russell L McLaughlin, Orla Hardiman. JAMA Neurol 2019
28
21

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
224
11

Hot-spot KIF5A mutations cause familial ALS.
David Brenner, Rüstem Yilmaz, Kathrin Müller, Torsten Grehl, Susanne Petri, Thomas Meyer, Julian Grosskreutz, Patrick Weydt, Wolfgang Ruf, Christoph Neuwirth,[...]. Brain 2018
88
9

Genetic correlation between amyotrophic lateral sclerosis and schizophrenia.
Russell L McLaughlin, Dick Schijven, Wouter van Rheenen, Kristel R van Eijk, Margaret O'Brien, René S Kahn, Roel A Ophoff, An Goris, Daniel G Bradley, Ammar Al-Chalabi,[...]. Nat Commun 2017
67
9

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
9

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
39
12

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
9

Screening for cognition and behaviour changes in ALS.
Sharon Abrahams, Judith Newton, Elaine Niven, Jennifer Foley, Thomas H Bak. Amyotroph Lateral Scler Frontotemporal Degener 2014
265
9

The Sequence Alignment/Map format and SAMtools.
Heng Li, Bob Handsaker, Alec Wysoker, Tim Fennell, Jue Ruan, Nils Homer, Gabor Marth, Goncalo Abecasis, Richard Durbin. Bioinformatics 2009
9



The natural history of primary lateral sclerosis.
P H Gordon, B Cheng, I B Katz, M Pinto, A P Hays, H Mitsumoto, L P Rowland. Neurology 2006
216
9



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.