A citation-based method for searching scientific literature

O Mercati, G Huguet, A Danckaert, G André-Leroux, A Maruani, M Bellinzoni, T Rolland, L Gouder, A Mathieu, J Buratti, F Amsellem, M Benabou, J Van-Gils, A Beggiato, M Konyukh, J-P Bourgeois, M J Gazzellone, R K C Yuen, S Walker, M Delépine, A Boland, B Régnault, M Francois, T Van Den Abbeele, A L Mosca-Boidron, L Faivre, Y Shimoda, K Watanabe, D Bonneau, M Rastam, M Leboyer, S W Scherer, C Gillberg, R Delorme, I Cloëz-Tayarani, T Bourgeron. Mol Psychiatry 2017
Times Cited: 38







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



Times Cited
  Times     Co-cited
Similarity


CNTN6 copy number variations in 14 patients: a possible candidate gene for neurodevelopmental and neuropsychiatric disorders.
Jie Hu, Jun Liao, Malini Sathanoori, Sally Kochmar, Jessica Sebastian, Svetlana A Yatsenko, Urvashi Surti. J Neurodev Disord 2015
48
39

A current view on contactin-4, -5, and -6: Implications in neurodevelopmental disorders.
Asami Oguro-Ando, Amila Zuko, Kristel T E Kleijer, J Peter H Burbach. Mol Cell Neurosci 2017
44
28

Social Responsiveness Scale-aided analysis of the clinical impact of copy number variations in autism.
Emma van Daalen, Chantal Kemner, Nienke E Verbeek, Bert van der Zwaag, Trijnie Dijkhuizen, Patrick Rump, Renske Houben, Ruben van 't Slot, Maretha V de Jonge, Wouter G Staal,[...]. Neurogenetics 2011
58
26

Rare Copy Number Variants in NRXN1 and CNTN6 Increase Risk for Tourette Syndrome.
Alden Y Huang, Dongmei Yu, Lea K Davis, Jae Hoon Sul, Fotis Tsetsos, Vasily Ramensky, Ivette Zelaya, Eliana Marisa Ramos, Lisa Osiecki, Jason A Chen,[...]. Neuron 2017
86
26

Single gene microdeletions and microduplication of 3p26.3 in three unrelated families: CNTN6 as a new candidate gene for intellectual disability.
Anna A Kashevarova, Lyudmila P Nazarenko, Soren Schultz-Pedersen, Nikolay A Skryabin, Olga A Salyukova, Nataliya N Chechetkina, Ekaterina N Tolmacheva, Aleksey A Rudko, Pamela Magini, Claudio Graziano,[...]. Mol Cytogenet 2014
39
23

Contribution of the neural cell recognition molecule NB-3 to synapse formation between parallel fibers and Purkinje cells in mouse.
Kunie Sakurai, Manabu Toyoshima, Hidehiro Ueda, Kota Matsubara, Yasuo Takeda, Domna Karagogeos, Yasushi Shimoda, Kazutada Watanabe. Dev Neurobiol 2009
50
23

Contactins in the neurobiology of autism.
Amila Zuko, Kristel T E Kleijer, Asami Oguro-Ando, Martien J H Kas, Emma van Daalen, Bert van der Zwaag, J Peter H Burbach. Eur J Pharmacol 2013
73
23

Neural recognition molecules CHL1 and NB-3 regulate apical dendrite orientation in the neocortex via PTP alpha.
Haihong Ye, Yen Ling Jessie Tan, Sathivel Ponniah, Yasuo Takeda, Shi-Qiang Wang, Melitta Schachner, Kazutada Watanabe, Catherine J Pallen, Zhi-Cheng Xiao. EMBO J 2008
68
21


Contactin 4, -5 and -6 differentially regulate neuritogenesis while they display identical PTPRG binding sites.
Oriane Mercati, Anne Danckaert, Gwénaëlle André-Leroux, Marco Bellinzoni, Laura Gouder, Kazutada Watanabe, Yasushi Shimoda, Régis Grailhe, Fabrice De Chaumont, Thomas Bourgeron,[...]. Biol Open 2013
31
22


Impaired motor coordination in mice lacking neural recognition molecule NB-3 of the contactin/F3 subgroup.
Yasuo Takeda, Keiko Akasaka, Suni Lee, Satoru Kobayashi, Hitoshi Kawano, Shigeo Murayama, Naoki Takahashi, Kouichi Hashimoto, Masanobu Kano, Masahide Asano,[...]. J Neurobiol 2003
58
15

Prospective diagnostic analysis of copy number variants using SNP microarrays in individuals with autism spectrum disorders.
Caroline Nava, Boris Keren, Cyril Mignot, Agnès Rastetter, Sandra Chantot-Bastaraud, Anne Faudet, Eric Fonteneau, Claire Amiet, Claudine Laurent, Aurélia Jacquette,[...]. Eur J Hum Genet 2014
47
15


Developmental role of the cell adhesion molecule Contactin-6 in the cerebral cortex and hippocampus.
Amila Zuko, Asami Oguro-Ando, Roland van Dijk, Sara Gregorio-Jordan, Bert van der Zwaag, J Peter H Burbach. Cell Adh Migr 2016
14
42

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
15


Rare copy number variation discovery and cross-disorder comparisons identify risk genes for ADHD.
Anath C Lionel, Jennifer Crosbie, Nicole Barbosa, Tara Goodale, Bhooma Thiruvahindrapuram, Jessica Rickaby, Matthew Gazzellone, Andrew R Carson, Jennifer L Howe, Zhuozhi Wang,[...]. Sci Transl Med 2011
241
13


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
966
13

No evidence for association of autism with rare heterozygous point mutations in Contactin-Associated Protein-Like 2 (CNTNAP2), or in Other Contactin-Associated Proteins or Contactins.
John D Murdoch, Abha R Gupta, Stephan J Sanders, Michael F Walker, John Keaney, Thomas V Fernandez, Michael T Murtha, Samuel Anyanwu, Gordon T Ober, Melanie J Raubeson,[...]. PLoS Genet 2015
40
13

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
13

Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder.
Ryan K C Yuen, Daniele Merico, Matt Bookman, Jennifer L Howe, Bhooma Thiruvahindrapuram, Rohan V Patel, Joe Whitney, Nicole Deflaux, Jonathan Bingham, Zhuozhi Wang,[...]. Nat Neurosci 2017
421
13

Whole-genome sequencing of quartet families with autism spectrum disorder.
Ryan K C Yuen, Bhooma Thiruvahindrapuram, Daniele Merico, Susan Walker, Kristiina Tammimies, Ny Hoang, Christina Chrysler, Thomas Nalpathamkalam, Giovanna Pellecchia, Yi Liu,[...]. Nat Med 2015
325
13

Autism and hearing loss.
U Rosenhall, V Nordin, M Sandström, G Ahlsén, C Gillberg. J Autism Dev Disord 1999
207
13

Structural Characterization of the Extracellular Domain of CASPR2 and Insights into Its Association with the Novel Ligand Contactin1.
Eva N Rubio-Marrero, Gabriele Vincelli, Cy M Jeffries, Tanvir R Shaikh, Irene S Pakos, Fanomezana M Ranaivoson, Sventja von Daake, Borries Demeler, Antonella De Jaco, Guy Perkins,[...]. J Biol Chem 2016
23
17

Expression and regulation of a gene encoding neural recognition molecule NB-3 of the contactin/F3 subgroup in mouse brain.
S Lee, Y Takeda, H Kawano, H Hosoya, M Nomoto, D Fujimoto, N Takahashi, K Watanabe. Gene 2000
46
10

BIG-2 mediates olfactory axon convergence to target glomeruli.
Tomomi Kaneko-Goto, Sei-Ichi Yoshihara, Haruko Miyazaki, Yoshihiro Yoshihara. Neuron 2008
122
10

cDNA cloning and chromosomal localization of neural adhesion molecule NB-3 in human.
Y Kamei, O Tsutsumi, Y Taketani, K Watanabe. J Neurosci Res 1998
22
18

NB-3/Notch1 pathway via Deltex1 promotes neural progenitor cell differentiation into oligodendrocytes.
Xiao-Ying Cui, Qi-Dong Hu, Meriem Tekaya, Yasushi Shimoda, Beng-Ti Ang, Du-Yu Nie, Li Sun, Wei-Ping Hu, Meliha Karsak, Tanya Duka,[...]. J Biol Chem 2004
105
10

Disruption of contactin 4 (CNTN4) results in developmental delay and other features of 3p deletion syndrome.
Thomas Fernandez, Thomas Morgan, Nicole Davis, Ami Klin, Ashley Morris, Anita Farhi, Richard P Lifton, Matthew W State. Am J Hum Genet 2004
125
10

Limited impact of Cntn4 mutation on autism-related traits in developing and adult C57BL/6J mice.
Remco T Molenhuis, Hilgo Bruining, Esther Remmelink, Leonie de Visser, Maarten Loos, J Peter H Burbach, Martien J H Kas. J Neurodev Disord 2016
13
30


Disruption of Contactin 4 in two subjects with autism in Chinese population.
Hui Guo, Guanglei Xun, Yu Peng, Xinying Xiang, Zhimin Xiong, Lusi Zhang, Yiqun He, Xiaojuan Xu, Yalan Liu, Lina Lu,[...]. Gene 2012
21
19

Aberrant responses to acoustic stimuli in mice deficient for neural recognition molecule NB-2.
Hong Li, Yasuo Takeda, Hiroaki Niki, Junko Ogawa, Satoru Kobayashi, Nobuyuki Kai, Keiko Akasaka, Masahide Asano, Katsuko Sudo, Yoichiro Iwakura,[...]. Eur J Neurosci 2003
32
12

Contactin 4 as an autism susceptibility locus.
Catherine E Cottrell, Natalie Bir, Elizabeth Varga, Carlos E Alvarez, Samuel Bouyain, Randall Zernzach, Devon L Thrush, Johnna Evans, Michael Trimarchi, Eric M Butter,[...]. Autism Res 2011
48
10

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
852
10

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
586
10

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
10

Microduplication of 3p26.3 implicated in cognitive development.
Leah Te Weehi, Raj Maikoo, Adrian Mc Cormack, Roberto Mazzaschi, Fern Ashton, Liangtao Zhang, Alice M George, Donald R Love. Case Rep Genet 2014
14
28

A Subset of Autism-Associated Genes Regulate the Structural Stability of Neurons.
Yu-Chih Lin, Jeannine A Frei, Michaela B C Kilander, Wenjuan Shen, Gene J Blatt. Front Cell Neurosci 2016
56
10

Clinical and Molecular Characterization of Two Patients with CNTN6 Copy Number Variations.
Elisa Tassano, Sara Uccella, Thea Giacomini, Mariasavina Severino, Patrizia Fiorio, Giorgio Gimelli, Patrizia Ronchetto. Cytogenet Genome Res 2018
5
80

Efferent inhibition strength is a physiological correlate of hyperacusis in children with autism spectrum disorder.
Uzma S Wilson, Kate M Sadler, Kenneth E Hancock, John J Guinan, Jeffery T Lichtenhan. J Neurophysiol 2017
31
12

Auditory hypersensitivity in the autistic spectrum disorder.
Erissandra Gomes, Fleming Salvador Pedroso, Mário Bernardes Wagner. Pro Fono 2008
74
10

Tinnitus and hyperacusis in autism spectrum disorders with emphasis on high functioning individuals diagnosed with Asperger's Syndrome.
Ali A Danesh, Dustin Lang, Wafaa Kaf, William D Andreassen, Jack Scott, Adrien A Eshraghi. Int J Pediatr Otorhinolaryngol 2015
29
13


Allele-biased expression in differentiating human neurons: implications for neuropsychiatric disorders.
Mingyan Lin, Anastasia Hrabovsky, Erika Pedrosa, Tao Wang, Deyou Zheng, Herbert M Lachman. PLoS One 2012
54
7

Characterization of molecular and cellular phenotypes associated with a heterozygous CNTNAP2 deletion using patient-derived hiPSC neural cells.
Inkyu S Lee, Claudia M B Carvalho, Panagiotis Douvaras, Seok-Man Ho, Brigham J Hartley, Luciana W Zuccherato, Ian G Ladran, Arthur J Siegel, Shane McCarthy, Dheeraj Malhotra,[...]. NPJ Schizophr 2015
39
7

Exogenous and evoked oxytocin restores social behavior in the Cntnap2 mouse model of autism.
Olga Peñagarikano, María T Lázaro, Xiao-Hong Lu, Aaron Gordon, Hongmei Dong, Hoa A Lam, Elior Peles, Nigel T Maidment, Niall P Murphy, X William Yang,[...]. Sci Transl Med 2015
220
7

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
564
7


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.