A citation-based method for searching scientific literature

Julie Gauthier, Tabrez J Siddiqui, Peng Huashan, Daisaku Yokomaku, Fadi F Hamdan, Nathalie Champagne, Mathieu Lapointe, Dan Spiegelman, Anne Noreau, Ronald G Lafrenière, Ferid Fathalli, Ridha Joober, Marie-Odile Krebs, Lynn E DeLisi, Laurent Mottron, Eric Fombonne, Jacques L Michaud, Pierre Drapeau, Salvatore Carbonetto, Ann Marie Craig, Guy A Rouleau. Hum Genet 2011
Times Cited: 171







List of co-cited articles
1509 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity



Mouse neurexin-1alpha deletion causes correlated electrophysiological and behavioral changes consistent with cognitive impairments.
Mark R Etherton, Cory A Blaiss, Craig M Powell, Thomas C Südhof. Proc Natl Acad Sci U S A 2009
279
30

Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism.
Stéphane Jamain, Hélène Quach, Catalina Betancur, Maria Råstam, Catherine Colineaux, I Carina Gillberg, Henrik Soderstrom, Bruno Giros, Marion Leboyer, Christopher Gillberg,[...]. Nat Genet 2003
29

Alpha-neurexins couple Ca2+ channels to synaptic vesicle exocytosis.
Markus Missler, Weiqi Zhang, Astrid Rohlmann, Gunnar Kattenstroth, Robert E Hammer, Kurt Gottmann, Thomas C Südhof. Nature 2003
446
28

Rare deletions at the neurexin 3 locus in autism spectrum disorder.
Andrea K Vaags, Anath C Lionel, Daisuke Sato, McKinsey Goodenberger, Quinn P Stein, Sarah Curran, Caroline Ogilvie, Joo Wook Ahn, Irene Drmic, Lili Senman,[...]. Am J Hum Genet 2012
134
27

High frequency of neurexin 1beta signal peptide structural variants in patients with autism.
Jinong Feng, Richard Schroer, Jin Yan, Wenjia Song, Chunmei Yang, Anke Bockholt, Edwin H Cook, Cindy Skinner, Charles E Schwartz, Steve S Sommer. Neurosci Lett 2006
221
25

Deletion of α-neurexin II results in autism-related behaviors in mice.
J Dachtler, J Glasper, R N Cohen, J L Ivorra, D J Swiffen, A J Jackson, M K Harte, R J Rodgers, S J Clapcote. Transl Psychiatry 2014
53
43

Mapping autism risk loci using genetic linkage and chromosomal rearrangements.
Peter Szatmari, Andrew D Paterson, Lonnie Zwaigenbaum, Wendy Roberts, Jessica Brian, Xiao-Qing Liu, John B Vincent, Jennifer L Skaug, Ann P Thompson, Lili Senman,[...]. Nat Genet 2007
948
21

Autism genome-wide copy number variation reveals ubiquitin and neuronal genes.
Joseph T Glessner, Kai Wang, Guiqing Cai, Olena Korvatska, Cecilia E Kim, Shawn Wood, Haitao Zhang, Annette Estes, Camille W Brune, Jonathan P Bradfield,[...]. Nature 2009
922
20

Disruption of the neurexin 1 gene is associated with schizophrenia.
Dan Rujescu, Andres Ingason, Sven Cichon, Olli P H Pietiläinen, Michael R Barnes, Timothea Toulopoulou, Marco Picchioni, Evangelos Vassos, Ulrich Ettinger, Elvira Bramon,[...]. Hum Mol Genet 2009
334
20

Disruption of neurexin 1 associated with autism spectrum disorder.
Hyung-Goo Kim, Shotaro Kishikawa, Anne W Higgins, Ihn-Sik Seong, Diana J Donovan, Yiping Shen, Eric Lally, Lauren A Weiss, Juliane Najm, Kerstin Kutsche,[...]. Am J Hum Genet 2008
398
19

Altered social behaviours in neurexin 1α knockout mice resemble core symptoms in neurodevelopmental disorders.
Hannah Mary Grayton, Markus Missler, David Andrew Collier, Cathy Fernandes. PLoS One 2013
92
20

Deletions of NRXN1 (neurexin-1) predispose to a wide spectrum of developmental disorders.
Michael S L Ching, Yiping Shen, Wen-Hann Tan, Shafali S Jeste, Eric M Morrow, Xiaoli Chen, Nahit M Mukaddes, Seung-Yun Yoo, Ellen Hanson, Rachel Hundley,[...]. Am J Med Genet B Neuropsychiatr Genet 2010
194
19

A neuroligin-3 mutation implicated in autism increases inhibitory synaptic transmission in mice.
Katsuhiko Tabuchi, Jacqueline Blundell, Mark R Etherton, Robert E Hammer, Xinran Liu, Craig M Powell, Thomas C Südhof. Science 2007
622
18

Functional impact of global rare copy number variation in autism spectrum disorders.
Dalila Pinto, Alistair T Pagnamenta, Lambertus Klei, Richard Anney, Daniele Merico, Regina Regan, Judith Conroy, Tiago R Magalhaes, Catarina Correia, Brett S Abrahams,[...]. Nature 2010
18

Neuroligins determine synapse maturation and function.
Frédérique Varoqueaux, Gayane Aramuni, Randi L Rawson, Ralf Mohrmann, Markus Missler, Kurt Gottmann, Weiqi Zhang, Thomas C Südhof, Nils Brose. Neuron 2006
528
17

Shank3 mutant mice display autistic-like behaviours and striatal dysfunction.
João Peça, Cátia Feliciano, Jonathan T Ting, Wenting Wang, Michael F Wells, Talaignair N Venkatraman, Christopher D Lascola, Zhanyan Fu, Guoping Feng. Nature 2011
784
17



Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism.
Stephan J Sanders, A Gulhan Ercan-Sencicek, Vanessa Hus, Rui Luo, Michael T Murtha, Daniel Moreno-De-Luca, Su H Chu, Michael P Moreau, Abha R Gupta, Susanne A Thomson,[...]. Neuron 2011
802
16


Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders.
Christelle M Durand, Catalina Betancur, Tobias M Boeckers, Juergen Bockmann, Pauline Chaste, Fabien Fauchereau, Gudrun Nygren, Maria Rastam, I Carina Gillberg, Henrik Anckarsäter,[...]. Nat Genet 2007
933
16

Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations.
Brian J O'Roak, Laura Vives, Santhosh Girirajan, Emre Karakoc, Niklas Krumm, Bradley P Coe, Roie Levy, Arthur Ko, Choli Lee, Joshua D Smith,[...]. Nature 2012
16

Cartography of neurexin alternative splicing mapped by single-molecule long-read mRNA sequencing.
Barbara Treutlein, Ozgun Gokce, Stephen R Quake, Thomas C Südhof. Proc Natl Acad Sci U S A 2014
155
15


Mutations in the SHANK2 synaptic scaffolding gene in autism spectrum disorder and mental retardation.
Simone Berkel, Christian R Marshall, Birgit Weiss, Jennifer Howe, Ralph Roeth, Ute Moog, Volker Endris, Wendy Roberts, Peter Szatmari, Dalila Pinto,[...]. Nat Genet 2010
341
14

SHANK1 Deletions in Males with Autism Spectrum Disorder.
Daisuke Sato, Anath C Lionel, Claire S Leblond, Aparna Prasad, Dalila Pinto, Susan Walker, Irene O'Connor, Carolyn Russell, Irene E Drmic, Fadi F Hamdan,[...]. Am J Hum Genet 2012
204
14

Presynaptic neurexin-3 alternative splicing trans-synaptically controls postsynaptic AMPA receptor trafficking.
Jason Aoto, David C Martinelli, Robert C Malenka, Katsuhiko Tabuchi, Thomas C Südhof. Cell 2013
171
14

Structural variation of chromosomes in autism spectrum disorder.
Christian R Marshall, Abdul Noor, John B Vincent, Anath C Lionel, Lars Feuk, Jennifer Skaug, Mary Shago, Rainald Moessner, Dalila Pinto, Yan Ren,[...]. Am J Hum Genet 2008
14

Reduced social interaction and ultrasonic communication in a mouse model of monogenic heritable autism.
Stephane Jamain, Konstantin Radyushkin, Kurt Hammerschmidt, Sylvie Granon, Susann Boretius, Frederique Varoqueaux, Nelina Ramanantsoa, Jorge Gallego, Anja Ronnenberg, Dorina Winter,[...]. Proc Natl Acad Sci U S A 2008
361
13

Neuroligin-1 deletion results in impaired spatial memory and increased repetitive behavior.
Jacqueline Blundell, Cory A Blaiss, Mark R Etherton, Felipe Espinosa, Katsuhiko Tabuchi, Christopher Walz, Marc F Bolliger, Thomas C Südhof, Craig M Powell. J Neurosci 2010
289
13

Trans-synaptic interaction of GluRdelta2 and Neurexin through Cbln1 mediates synapse formation in the cerebellum.
Takeshi Uemura, Sung-Jin Lee, Misato Yasumura, Tomonori Takeuchi, Tomoyuki Yoshida, Moonjin Ra, Ryo Taguchi, Kenji Sakimura, Masayoshi Mishina. Cell 2010
308
13

LRRTMs and neuroligins bind neurexins with a differential code to cooperate in glutamate synapse development.
Tabrez J Siddiqui, Raika Pancaroglu, Yunhee Kang, Amanda Rooyakkers, Ann Marie Craig. J Neurosci 2010
190
13

De novo mutations revealed by whole-exome sequencing are strongly associated with autism.
Stephan J Sanders, Michael T Murtha, Abha R Gupta, John D Murdoch, Melanie J Raubeson, A Jeremy Willsey, A Gulhan Ercan-Sencicek, Nicholas M DiLullo, Neelroop N Parikshak, Jason L Stein,[...]. Nature 2012
13

Mutations in NRXN1 in a family multiply affected with brain disorders: NRXN1 mutations and brain disorders.
Linh Duong, Laura L Klitten, Rikke S Møller, Andrés Ingason, Klaus D Jakobsen, Celina Skjødt, Michael Didriksen, Helle Hjalgrim, Thomas Werge, Niels Tommerup. Am J Med Genet B Neuropsychiatr Genet 2012
49
24

Neurexins induce differentiation of GABA and glutamate postsynaptic specializations via neuroligins.
Ethan R Graf, XueZhao Zhang, Shan-Xue Jin, Michael W Linhoff, Ann Marie Craig. Cell 2004
659
12

Neuroligin 1: a splice site-specific ligand for beta-neurexins.
K Ichtchenko, Y Hata, T Nguyen, B Ullrich, M Missler, C Moomaw, T C Südhof. Cell 1995
520
12

A splice code for trans-synaptic cell adhesion mediated by binding of neuroligin 1 to alpha- and beta-neurexins.
Antony A Boucard, Alexander A Chubykin, Davide Comoletti, Palmer Taylor, Thomas C Südhof. Neuron 2005
330
12

Neurexins.
Carsten Reissner, Fabian Runkel, Markus Missler. Genome Biol 2013
100
12

LRRTM2 interacts with Neurexin1 and regulates excitatory synapse formation.
Joris de Wit, Emily Sylwestrak, Matthew L O'Sullivan, Stefanie Otto, Katie Tiglio, Jeffrey N Savas, John R Yates, Davide Comoletti, Palmer Taylor, Anirvan Ghosh. Neuron 2009
258
12

Mutation analysis of the NRXN1 gene in a Chinese autism cohort.
Yalan Liu, Zhengmao Hu, Guanglei Xun, Yu Peng, Lina Lu, Xiaojuan Xu, Zhimin Xiong, Lu Xia, Deyuan Liu, Wei Li,[...]. J Psychiatr Res 2012
24
50

Neurexins: synaptic cell surface proteins related to the alpha-latrotoxin receptor and laminin.
Y A Ushkaryov, A G Petrenko, M Geppert, T C Südhof. Science 1992
525
12

Synaptic, transcriptional and chromatin genes disrupted in autism.
Silvia De Rubeis, Xin He, Arthur P Goldberg, Christopher S Poultney, Kaitlin Samocha, A Erucment Cicek, Yan Kou, Li Liu, Menachem Fromer, Susan Walker,[...]. Nature 2014
12

The contribution of de novo coding mutations to autism spectrum disorder.
Ivan Iossifov, Brian J O'Roak, Stephan J Sanders, Michael Ronemus, Niklas Krumm, Dan Levy, Holly A Stessman, Kali T Witherspoon, Laura Vives, Karynne E Patterson,[...]. Nature 2014
12

Convergence of genes and cellular pathways dysregulated in autism spectrum disorders.
Dalila Pinto, Elsa Delaby, Daniele Merico, Mafalda Barbosa, Alison Merikangas, Lambertus Klei, Bhooma Thiruvahindrapuram, Xiao Xu, Robert Ziman, Zhuozhi Wang,[...]. Am J Hum Genet 2014
516
12

Genetic targeting of NRXN2 in mice unveils role in excitatory cortical synapse function and social behaviors.
Gesche Born, Hannah M Grayton, Hanna Langhorst, Irina Dudanova, Astrid Rohlmann, Benjamin W Woodward, David A Collier, Cathy Fernandes, Markus Missler. Front Synaptic Neurosci 2015
37
32

Investigation of NRXN1 deletions: clinical and molecular characterization.
Mindy Preston Dabell, Jill A Rosenfeld, Patricia Bader, Luis F Escobar, Dima El-Khechen, Stephanie E Vallee, Mary Beth Palko Dinulos, Cynthia Curry, Jamie Fisher, Raymond Tervo,[...]. Am J Med Genet A 2013
69
15

Phenotypic spectrum and genotype-phenotype correlations of NRXN1 exon deletions.
Christian P Schaaf, Philip M Boone, Srirangan Sampath, Charles Williams, Patricia I Bader, Jennifer M Mueller, Oleg A Shchelochkov, Chester W Brown, Heather P Crawford, James A Phalen,[...]. Eur J Hum Genet 2012
70
15

CNTNAP2 and NRXN1 are mutated in autosomal-recessive Pitt-Hopkins-like mental retardation and determine the level of a common synaptic protein in Drosophila.
Christiane Zweier, Eiko K de Jong, Markus Zweier, Alfredo Orrico, Lilian B Ousager, Amanda L Collins, Emilia K Bijlsma, Merel A W Oortveld, Arif B Ekici, André Reis,[...]. Am J Hum Genet 2009
227
11

Linkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility gene.
Maricela Alarcón, Brett S Abrahams, Jennifer L Stone, Jacqueline A Duvall, Julia V Perederiy, Jamee M Bomar, Jonathan Sebat, Michael Wigler, Christa L Martin, David H Ledbetter,[...]. Am J Hum Genet 2008
535
11


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.