A citation-based method for searching scientific literature

An Crepel, Veerle De Wolf, Nathalie Brison, Berten Ceulemans, Didier Walleghem, Gilian Peuteman, Diether Lambrechts, Jean Steyaert, Ilse Noens, Koen Devriendt, Hilde Peeters. Am J Med Genet B Neuropsychiatr Genet 2014
Times Cited: 12







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



Times Cited
  Times     Co-cited
Similarity


Common genetic variants on 5p14.1 associate with autism spectrum disorders.
Kai Wang, Haitao Zhang, Deqiong Ma, Maja Bucan, Joseph T Glessner, Brett S Abrahams, Daria Salyakina, Marcin Imielinski, Jonathan P Bradfield, Patrick M A Sleiman,[...]. Nature 2009
689
75

Rare familial 16q21 microdeletions under a linkage peak implicate cadherin 8 (CDH8) in susceptibility to autism and learning disability.
Alistair T Pagnamenta, Hameed Khan, Susan Walker, Dianne Gerrelli, Kirsty Wing, Maria Clara Bonaglia, Roberto Giorda, Tom Berney, Elisa Mani, Massimo Molteni,[...]. J Med Genet 2011
74
66

Cadherins in brain morphogenesis and wiring.
Shinji Hirano, Masatoshi Takeichi. Physiol Rev 2012
193
50

Cadherins and neuropsychiatric disorders.
Christoph Redies, Nicole Hertel, Christian A Hübner. Brain Res 2012
171
41

Loss of cadherin-11 adhesion receptor enhances plastic changes in hippocampal synapses and modifies behavioral responses.
T Manabe, H Togashi, N Uchida, S C Suzuki, Y Hayakawa, M Yamamoto, H Yoda, T Miyakawa, M Takeichi, O Chisaka. Mol Cell Neurosci 2000
132
41

Cadherins and catenins in dendrite and synapse morphogenesis.
Eunju Seong, Li Yuan, Jyothi Arikkath. Cell Adh Migr 2015
56
41

Autistic-like behaviour and cerebellar dysfunction in Purkinje cell Tsc1 mutant mice.
Peter T Tsai, Court Hull, YunXiang Chu, Emily Greene-Colozzi, Abbey R Sadowski, Jarrett M Leech, Jason Steinberg, Jacqueline N Crawley, Wade G Regehr, Mustafa Sahin. Nature 2012
544
33

Patterns and rates of exonic de novo mutations in autism spectrum disorders.
Benjamin M Neale, Yan Kou, Li Liu, Avi Ma'ayan, Kaitlin E Samocha, Aniko Sabo, Chiao-Feng Lin, Christine Stevens, Li-San Wang, Vladimir Makarov,[...]. Nature 2012
33

Cadherin-9 regulates synapse-specific differentiation in the developing hippocampus.
Megan E Williams, Scott A Wilke, Anthony Daggett, Elizabeth Davis, Stefanie Otto, Deepak Ravi, Beth Ripley, Eric A Bushong, Mark H Ellisman, Gerd Klein,[...]. Neuron 2011
151
33

Clinical and genetic aspects of PCDH19-related epilepsy syndromes and the possible role of PCDH19 mutations in males with autism spectrum disorders.
J J T van Harssel, S Weckhuysen, M J A van Kempen, K Hardies, N E Verbeek, C G F de Kovel, W B Gunning, E van Daalen, M V de Jonge, A C Jansen,[...]. Neurogenetics 2013
50
33

Synaptic proteins and receptors defects in autism spectrum disorders.
Jianling Chen, Shunying Yu, Yingmei Fu, Xiaohong Li. Front Cell Neurosci 2014
101
33

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
33

Cadherin-8 expression, synaptic localization, and molecular control of neuronal form in prefrontal corticostriatal circuits.
Lauren G Friedman, Fréderike W Riemslagh, Josefa M Sullivan, Roxana Mesias, Frances M Williams, George W Huntley, Deanna L Benson. J Comp Neurol 2015
19
33

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
859
33

A noise-reduction GWAS analysis implicates altered regulation of neurite outgrowth and guidance in autism.
John P Hussman, Ren-Hua Chung, Anthony J Griswold, James M Jaworski, Daria Salyakina, Deqiong Ma, Ioanna Konidari, Patrice L Whitehead, Jeffery M Vance, Eden R Martin,[...]. Mol Autism 2011
128
33


Multiplex targeted sequencing identifies recurrently mutated genes in autism spectrum disorders.
Brian J O'Roak, Laura Vives, Wenqing Fu, Jarrett D Egertson, Ian B Stanaway, Ian G Phelps, Gemma Carvill, Akash Kumar, Choli Lee, Katy Ankenman,[...]. Science 2012
861
25

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
25


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
25

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
25

Absence of CNTNAP2 leads to epilepsy, neuronal migration abnormalities, and core autism-related deficits.
Olga Peñagarikano, Brett S Abrahams, Edward I Herman, Kellen D Winden, Amos Gdalyahu, Hongmei Dong, Lisa I Sonnenblick, Robin Gruver, Joel Almajano, Anatol Bragin,[...]. Cell 2011
643
25

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
971
25

Loss of Tsc2 in Purkinje cells is associated with autistic-like behavior in a mouse model of tuberous sclerosis complex.
R Michelle Reith, James McKenna, Henry Wu, S Shahrukh Hashmi, Seo-Hee Cho, Pramod K Dash, Michael J Gambello. Neurobiol Dis 2013
124
25

Neuroligin 1 is a postsynaptic cell-adhesion molecule of excitatory synapses.
J Y Song, K Ichtchenko, T C Südhof, N Brose. Proc Natl Acad Sci U S A 1999
503
25

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
310
25

X-linked mental retardation and autism are associated with a mutation in the NLGN4 gene, a member of the neuroligin family.
Frédéric Laumonnier, Frédérique Bonnet-Brilhault, Marie Gomot, Romuald Blanc, Albert David, Marie-Pierre Moizard, Martine Raynaud, Nathalie Ronce, Eric Lemonnier, Patrick Calvas,[...]. Am J Hum Genet 2004
531
25

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
25

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
595
25

Integrative functional genomic analyses implicate specific molecular pathways and circuits in autism.
Neelroop N Parikshak, Rui Luo, Alice Zhang, Hyejung Won, Jennifer K Lowe, Vijayendran Chandran, Steve Horvath, Daniel H Geschwind. Cell 2013
632
25

A synaptic trek to autism.
Thomas Bourgeron. Curr Opin Neurobiol 2009
451
25

Excess of rare, inherited truncating mutations in autism.
Niklas Krumm, Tychele N Turner, Carl Baker, Laura Vives, Kiana Mohajeri, Kali Witherspoon, Archana Raja, Bradley P Coe, Holly A Stessman, Zong-Xiao He,[...]. Nat Genet 2015
346
25

Contribution of SHANK3 mutations to autism spectrum disorder.
Rainald Moessner, Christian R Marshall, James S Sutcliffe, Jennifer Skaug, Dalila Pinto, John Vincent, Lonnie Zwaigenbaum, Bridget Fernandez, Wendy Roberts, Peter Szatmari,[...]. Am J Hum Genet 2007
457
25

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
25

N-cadherin mediates cortical organization in the mouse brain.
Masakazu Kadowaki, Shoko Nakamura, Ondrej Machon, Stefan Krauss, Glenn L Radice, Masatoshi Takeichi. Dev Biol 2007
226
25


Rab GTPases-dependent endocytic pathways regulate neuronal migration and maturation through N-cadherin trafficking.
Takeshi Kawauchi, Katsutoshi Sekine, Mima Shikanai, Kaori Chihama, Kenji Tomita, Ken-ichiro Kubo, Kazunori Nakajima, Yo-Ichi Nabeshima, Mikio Hoshino. Neuron 2010
238
25


Cadherin-13, a risk gene for ADHD and comorbid disorders, impacts GABAergic function in hippocampus and cognition.
O Rivero, M M Selten, S Sich, S Popp, L Bacmeister, E Amendola, M Negwer, D Schubert, F Proft, D Kiser,[...]. Transl Psychiatry 2015
60
25

Molecular evolution of the cadherin superfamily.
Paco Hulpiau, Frans van Roy. Int J Biochem Cell Biol 2009
295
25

Cadherin regulates dendritic spine morphogenesis.
Hideru Togashi, Kentaro Abe, Akira Mizoguchi, Kanna Takaoka, Osamu Chisaka, Masatoshi Takeichi. Neuron 2002
407
25

Cognitive and behavioral profile in females with epilepsy with PDCH19 mutation: two novel mutations and review of the literature.
Ana Camacho, Rogelio Simón, Raúl Sanz, Antonio Viñuela, Antonio Martínez-Salio, Fernando Mateos. Epilepsy Behav 2012
29
25


The classic cadherins in synaptic specificity.
Raunak Basu, Matthew R Taylor, Megan E Williams. Cell Adh Migr 2015
35
25

Identifying autism loci and genes by tracing recent shared ancestry.
Eric M Morrow, Seung-Yun Yoo, Steven W Flavell, Tae-Kyung Kim, Yingxi Lin, Robert Sean Hill, Nahit M Mukaddes, Soher Balkhy, Generoso Gascon, Asif Hashmi,[...]. Science 2008
518
25

Genome-scan for IQ discrepancy in autism: evidence for loci on chromosomes 10 and 16.
Nicola H Chapman, Annette Estes, Jeff Munson, Raphael Bernier, Sara J Webb, Joseph H Rothstein, Nancy J Minshew, Geraldine Dawson, Gerard D Schellenberg, Ellen M Wijsman. Hum Genet 2011
32
25

An RNAi-based approach identifies molecules required for glutamatergic and GABAergic synapse development.
Suzanne Paradis, Dana B Harrar, Yingxi Lin, Alex C Koon, Jessica L Hauser, Eric C Griffith, Li Zhu, Lawrence F Brass, Chinfei Chen, Michael E Greenberg. Neuron 2007
175
25

Cadherin-8 and N-cadherin differentially regulate pre- and postsynaptic development of the hippocampal mossy fiber pathway.
Iddil H Bekirov, Vanja Nagy, Alexandra Svoronos, George W Huntley, Deanna L Benson. Hippocampus 2008
48
25

Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci.
Stephan J Sanders, Xin He, A Jeremy Willsey, A Gulhan Ercan-Sencicek, Kaitlin E Samocha, A Ercument Cicek, Michael T Murtha, Vanessa H Bal, Somer L Bishop, Shan Dong,[...]. Neuron 2015
755
25

Exome sequencing of extended families with autism reveals genes shared across neurodevelopmental and neuropsychiatric disorders.
Holly N Cukier, Nicole D Dueker, Susan H Slifer, Joycelyn M Lee, Patrice L Whitehead, Eminisha Lalanne, Natalia Leyva, Ioanna Konidari, Ryan C Gentry, William F Hulme,[...]. Mol Autism 2014
147
25


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.