A citation-based method for searching scientific literature

John Mitchell, Praveen Paul, Han-Jou Chen, Alex Morris, Miles Payling, Mario Falchi, James Habgood, Stefania Panoutsou, Sabine Winkler, Veronica Tisato, Amin Hajitou, Bradley Smith, Caroline Vance, Christopher Shaw, Nicholas D Mazarakis, Jacqueline de Belleroche. Proc Natl Acad Sci U S A 2010
Times Cited: 165







List of co-cited articles
1688 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


D-amino acid oxidase controls motoneuron degeneration through D-serine.
Jumpei Sasabe, Yurika Miyoshi, Masataka Suzuki, Masashi Mita, Ryuichi Konno, Masaaki Matsuoka, Kenji Hamase, Sadakazu Aiso. Proc Natl Acad Sci U S A 2012
122
39

D-serine is a key determinant of glutamate toxicity in amyotrophic lateral sclerosis.
Jumpei Sasabe, Tomohiro Chiba, Marina Yamada, Koichi Okamoto, Ikuo Nishimoto, Masaaki Matsuoka, Sadakazu Aiso. EMBO J 2007
188
34

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
31

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
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
31

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
30

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
30

D-serine is an endogenous ligand for the glycine site of the N-methyl-D-aspartate receptor.
J P Mothet, A T Parent, H Wolosker, R O Brady, D J Linden, C D Ferris, M A Rogawski, S H Snyder. Proc Natl Acad Sci U S A 2000
827
29

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
27

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
27

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
761
26

Exome sequencing reveals VCP mutations as a cause of familial ALS.
Janel O Johnson, Jessica Mandrioli, Michael Benatar, Yevgeniya Abramzon, Vivianna M Van Deerlin, John Q Trojanowski, J Raphael Gibbs, Maura Brunetti, Susan Gronka, Joanne Wuu,[...]. Neuron 2010
838
26

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

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
367
24

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
835
24

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
848
24

SQSTM1 mutations in familial and sporadic amyotrophic lateral sclerosis.
Faisal Fecto, Jianhua Yan, S Pavan Vemula, Erdong Liu, Yi Yang, Wenjie Chen, Jian Guo Zheng, Yong Shi, Nailah Siddique, Hasan Arrat,[...]. Arch Neurol 2011
420
22

A mutation in the vesicle-trafficking protein VAPB causes late-onset spinal muscular atrophy and amyotrophic lateral sclerosis.
Agnes L Nishimura, Miguel Mitne-Neto, Helga C A Silva, Antônio Richieri-Costa, Susan Middleton, Duilio Cascio, Fernando Kok, João R M Oliveira, Tom Gillingwater, Jeanette Webb,[...]. Am J Hum Genet 2004
658
22

Deleterious variants of FIG4, a phosphoinositide phosphatase, in patients with ALS.
Clement Y Chow, John E Landers, Sarah K Bergren, Peter C Sapp, Adrienne E Grant, Julie M Jones, Lesley Everett, Guy M Lenk, Diane M McKenna-Yasek, Lois S Weisman,[...]. Am J Hum Genet 2009
273
21

ANG mutations segregate with familial and 'sporadic' amyotrophic lateral sclerosis.
Matthew J Greenway, Peter M Andersen, Carsten Russ, Sean Ennis, Susan Cashman, Colette Donaghy, Victor Patterson, Robert Swingler, Dairin Kieran, Jochen Prehn,[...]. Nat Genet 2006
490
21

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
287
21

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
21

DNA/RNA helicase gene mutations in a form of juvenile amyotrophic lateral sclerosis (ALS4).
Ying-Zhang Chen, Craig L Bennett, Huy M Huynh, Ian P Blair, Imke Puls, Joy Irobi, Ines Dierick, Annette Abel, Marina L Kennerson, Bruce A Rabin,[...]. Am J Hum Genet 2004
551
20

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
18

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
258
17

The gene encoding alsin, a protein with three guanine-nucleotide exchange factor domains, is mutated in a form of recessive amyotrophic lateral sclerosis.
Y Yang, A Hentati, H X Deng, O Dabbagh, T Sasaki, M Hirano, W Y Hung, K Ouahchi, J Yan, A C Azim,[...]. Nat Genet 2001
547
16

A mutation in sigma-1 receptor causes juvenile amyotrophic lateral sclerosis.
Amr Al-Saif, Futwan Al-Mohanna, Saeed Bohlega. Ann Neurol 2011
272
16

Point mutations of the p150 subunit of dynactin (DCTN1) gene in ALS.
C Münch, R Sedlmeier, T Meyer, V Homberg, A D Sperfeld, A Kurt, J Prudlo, G Peraus, C O Hanemann, G Stumm,[...]. Neurology 2004
295
16

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
199
16

Physiological functions of D-amino acid oxidases: from yeast to humans.
L Pollegioni, L Piubelli, S Sacchi, M S Pilone, G Molla. Cell Mol Life Sci 2007
216
15

The neurobiology of D-amino acid oxidase and its involvement in schizophrenia.
L Verrall, P W J Burnet, J F Betts, P J Harrison. Mol Psychiatry 2010
108
15

A gene encoding a putative GTPase regulator is mutated in familial amyotrophic lateral sclerosis 2.
S Hadano, C K Hand, H Osuga, Y Yanagisawa, A Otomo, R S Devon, N Miyamoto, J Showguchi-Miyata, Y Okada, R Singaraja,[...]. Nat Genet 2001
484
15

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
15

SPATACSIN mutations cause autosomal recessive juvenile amyotrophic lateral sclerosis.
Antonio Orlacchio, Carla Babalini, Antonella Borreca, Clarice Patrono, Roberto Massa, Sarenur Basaran, Renato P Munhoz, Ekaterina A Rogaeva, Peter H St George-Hyslop, Giorgio Bernardi,[...]. Brain 2010
157
15

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
283
15

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
15

Mutational analysis reveals the FUS homolog TAF15 as a candidate gene for familial amyotrophic lateral sclerosis.
N Ticozzi, C Vance, A L Leclerc, P Keagle, J D Glass, D McKenna-Yasek, P C Sapp, V Silani, D A Bosco, C E Shaw,[...]. Am J Med Genet B Neuropsychiatr Genet 2011
117
14

Evaluating the role of the FUS/TLS-related gene EWSR1 in amyotrophic lateral sclerosis.
Julien Couthouis, Michael P Hart, Renske Erion, Oliver D King, Zamia Diaz, Tadashi Nakaya, Fadia Ibrahim, Hyung-Jun Kim, Jelena Mojsilovic-Petrovic, Saarene Panossian,[...]. Hum Mol Genet 2012
188
14

Purification of serine racemase: biosynthesis of the neuromodulator D-serine.
H Wolosker, K N Sheth, M Takahashi, J P Mothet, R O Brady, C D Ferris, S H Snyder. Proc Natl Acad Sci U S A 1999
381
14

d-Amino acid oxidase and serine racemase in human brain: normal distribution and altered expression in schizophrenia.
Louise Verrall, Mary Walker, Nancy Rawlings, Isabel Benzel, James N C Kew, Paul J Harrison, Philip W J Burnet. Eur J Neurosci 2007
136
13



Glia-derived D-serine controls NMDA receptor activity and synaptic memory.
Aude Panatier, Dionysia T Theodosis, Jean-Pierre Mothet, Bastien Touquet, Loredano Pollegioni, Dominique A Poulain, Stéphane H R Oliet. Cell 2006
590
13

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
13

A yeast functional screen predicts new candidate ALS disease genes.
Julien Couthouis, Michael P Hart, James Shorter, Mariely DeJesus-Hernandez, Renske Erion, Rachel Oristano, Annie X Liu, Daniel Ramos, Niti Jethava, Divya Hosangadi,[...]. Proc Natl Acad Sci U S A 2011
277
13

Variants of the heavy neurofilament subunit are associated with the development of amyotrophic lateral sclerosis.
D A Figlewicz, A Krizus, M G Martinoli, V Meininger, M Dib, G A Rouleau, J P Julien. Hum Mol Genet 1994
371
13

Pathogenic effects of amyotrophic lateral sclerosis-linked mutation in D-amino acid oxidase are mediated by D-serine.
Praveen Paul, Tytus Murphy, Zainab Oseni, Suganthinie Sivalokanathan, Jacqueline S de Belleroche. Neurobiol Aging 2014
19
68

Genetic and physiological data implicating the new human gene G72 and the gene for D-amino acid oxidase in schizophrenia.
Ilya Chumakov, Marta Blumenfeld, Oxana Guerassimenko, Laurent Cavarec, Marta Palicio, Hadi Abderrahim, Lydie Bougueleret, Caroline Barry, Hiroaki Tanaka, Philippe La Rosa,[...]. Proc Natl Acad Sci U S A 2002
624
13

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
13

CCNF mutations in amyotrophic lateral sclerosis and frontotemporal dementia.
Kelly L Williams, Simon Topp, Shu Yang, Bradley Smith, Jennifer A Fifita, Sadaf T Warraich, Katharine Y Zhang, Natalie Farrawell, Caroline Vance, Xun Hu,[...]. Nat Commun 2016
106
13


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.