Christoph Redies, Nicole Hertel, Christian A Hübner. Brain Res 2012
Times Cited: 161
Times Cited: 161
Times Cited
Times Co-cited
Similarity
Cadherins in brain morphogenesis and wiring.
Shinji Hirano, Masatoshi Takeichi. Physiol Rev 2012
Shinji Hirano, Masatoshi Takeichi. Physiol Rev 2012
23
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
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
17
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
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
16
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
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
11
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
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
11
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
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
10
Protocadherin-19 and N-cadherin interact to control cell movements during anterior neurulation.
Sayantanee Biswas, Michelle R Emond, James D Jontes. J Cell Biol 2010
Sayantanee Biswas, Michelle R Emond, James D Jontes. J Cell Biol 2010
15
Spatiotemporal expression pattern of non-clustered protocadherin family members in the developing rat brain.
S-Y Kim, H Sun Chung, W Sun, H Kim. Neuroscience 2007
S-Y Kim, H Sun Chung, W Sun, H Kim. Neuroscience 2007
9
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
João Peça, Cátia Feliciano, Jonathan T Ting, Wenting Wang, Michael F Wells, Talaignair N Venkatraman, Christopher D Lascola, Zhanyan Fu, Guoping Feng. Nature 2011
9
X-linked protocadherin 19 mutations cause female-limited epilepsy and cognitive impairment.
Leanne M Dibbens, Patrick S Tarpey, Kim Hynes, Marta A Bayly, Ingrid E Scheffer, Raffaella Smith, Jamee Bomar, Edwina Sutton, Lucianne Vandeleur, Cheryl Shoubridge,[...]. Nat Genet 2008
Leanne M Dibbens, Patrick S Tarpey, Kim Hynes, Marta A Bayly, Ingrid E Scheffer, Raffaella Smith, Jamee Bomar, Edwina Sutton, Lucianne Vandeleur, Cheryl Shoubridge,[...]. Nat Genet 2008
9
PCDH19-related infantile epileptic encephalopathy: an unusual X-linked inheritance disorder.
Christel Depienne, Eric LeGuern. Hum Mutat 2012
Christel Depienne, Eric LeGuern. Hum Mutat 2012
11
Sporadic infantile epileptic encephalopathy caused by mutations in PCDH19 resembles Dravet syndrome but mainly affects females.
Christel Depienne, Delphine Bouteiller, Boris Keren, Emmanuel Cheuret, Karine Poirier, Oriane Trouillard, Baya Benyahia, Chloé Quelin, Wassila Carpentier, Sophie Julia,[...]. PLoS Genet 2009
Christel Depienne, Delphine Bouteiller, Boris Keren, Emmanuel Cheuret, Karine Poirier, Oriane Trouillard, Baya Benyahia, Chloé Quelin, Wassila Carpentier, Sophie Julia,[...]. PLoS Genet 2009
9
Structural determinants of adhesion by Protocadherin-19 and implications for its role in epilepsy.
Sharon R Cooper, James D Jontes, Marcos Sotomayor. Elife 2016
Sharon R Cooper, James D Jontes, Marcos Sotomayor. Elife 2016
18
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
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
11
Neuroligins and neurexins link synaptic function to cognitive disease.
Thomas C Südhof. Nature 2008
Thomas C Südhof. Nature 2008
8
Chemoaffinity revisited: dscams, protocadherins, and neural circuit assembly.
S Lawrence Zipursky, Joshua R Sanes. Cell 2010
S Lawrence Zipursky, Joshua R Sanes. Cell 2010
8
Non-clustered protocadherin.
Soo-Young Kim, Shin Yasuda, Hidekazu Tanaka, Kanato Yamagata, Hyun Kim. Cell Adh Migr 2011
Soo-Young Kim, Shin Yasuda, Hidekazu Tanaka, Kanato Yamagata, Hyun Kim. Cell Adh Migr 2011
8
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
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
8
Synaptic dysfunction in neurodevelopmental disorders associated with autism and intellectual disabilities.
Huda Y Zoghbi, Mark F Bear. Cold Spring Harb Perspect Biol 2012
Huda Y Zoghbi, Mark F Bear. Cold Spring Harb Perspect Biol 2012
8
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
Stéphane Jamain, Hélène Quach, Catalina Betancur, Maria Råstam, Catherine Colineaux, I Carina Gillberg, Henrik Soderstrom, Bruno Giros, Marion Leboyer, Christopher Gillberg,[...]. Nat Genet 2003
8
Molecular evolution of the cadherin superfamily.
Paco Hulpiau, Frans van Roy. Int J Biochem Cell Biol 2009
Paco Hulpiau, Frans van Roy. Int J Biochem Cell Biol 2009
8
Cadherin expression in the somatosensory cortex: evidence for a combinatorial molecular code at the single-cell level.
K Krishna-K, N Hertel, C Redies. Neuroscience 2011
K Krishna-K, N Hertel, C Redies. Neuroscience 2011
14
The cadherin superfamily in neuronal connections and interactions.
Masatoshi Takeichi. Nat Rev Neurosci 2007
Masatoshi Takeichi. Nat Rev Neurosci 2007
7
Combinatorial homophilic interaction between gamma-protocadherin multimers greatly expands the molecular diversity of cell adhesion.
Dietmar Schreiner, Joshua A Weiner. Proc Natl Acad Sci U S A 2010
Dietmar Schreiner, Joshua A Weiner. Proc Natl Acad Sci U S A 2010
7
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
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
7
A complex of Protocadherin-19 and N-cadherin mediates a novel mechanism of cell adhesion.
Michelle R Emond, Sayantanee Biswas, Cheasequah J Blevins, James D Jontes. J Cell Biol 2011
Michelle R Emond, Sayantanee Biswas, Cheasequah J Blevins, James D Jontes. J Cell Biol 2011
10
Protocadherins control the modular assembly of neuronal columns in the zebrafish optic tectum.
Sharon R Cooper, Michelle R Emond, Phan Q Duy, Brandon G Liebau, Marc A Wolman, James D Jontes. J Cell Biol 2015
Sharon R Cooper, Michelle R Emond, Phan Q Duy, Brandon G Liebau, Marc A Wolman, James D Jontes. J Cell Biol 2015
18
delta-Protocadherins: a gene family expressed differentially in the mouse brain.
K Vanhalst, P Kools, K Staes, F van Roy, C Redies. Cell Mol Life Sci 2005
K Vanhalst, P Kools, K Staes, F van Roy, C Redies. Cell Mol Life Sci 2005
7
Single-cell identity generated by combinatorial homophilic interactions between α, β, and γ protocadherins.
Chan Aye Thu, Weisheng V Chen, Rotem Rubinstein, Maxime Chevee, Holly N Wolcott, Klara O Felsovalyi, Juan Carlos Tapia, Lawrence Shapiro, Barry Honig, Tom Maniatis. Cell 2014
Chan Aye Thu, Weisheng V Chen, Rotem Rubinstein, Maxime Chevee, Holly N Wolcott, Klara O Felsovalyi, Juan Carlos Tapia, Lawrence Shapiro, Barry Honig, Tom Maniatis. Cell 2014
6
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
Ethan R Graf, XueZhao Zhang, Shan-Xue Jin, Michael W Linhoff, Ann Marie Craig. Cell 2004
6
Protocadherins, not prototypical: a complex tale of their interactions, expression, and functions.
Joshua A Weiner, James D Jontes. Front Mol Neurosci 2013
Joshua A Weiner, James D Jontes. Front Mol Neurosci 2013
13
Protocadherins mediate dendritic self-avoidance in the mammalian nervous system.
Julie L Lefebvre, Dimitar Kostadinov, Weisheng V Chen, Tom Maniatis, Joshua R Sanes. Nature 2012
Julie L Lefebvre, Dimitar Kostadinov, Weisheng V Chen, Tom Maniatis, Joshua R Sanes. Nature 2012
6
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
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
6
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
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
6
From the genetic architecture to synaptic plasticity in autism spectrum disorder.
Thomas Bourgeron. Nat Rev Neurosci 2015
Thomas Bourgeron. Nat Rev Neurosci 2015
6
Model of autism: increased ratio of excitation/inhibition in key neural systems.
J L R Rubenstein, M M Merzenich. Genes Brain Behav 2003
J L R Rubenstein, M M Merzenich. Genes Brain Behav 2003
6
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
Katsuhiko Tabuchi, Jacqueline Blundell, Mark R Etherton, Robert E Hammer, Xinran Liu, Craig M Powell, Thomas C Südhof. Science 2007
6
Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis.
. Lancet 2013
. Lancet 2013
6
Structural Basis of Diverse Homophilic Recognition by Clustered α- and β-Protocadherins.
Kerry Marie Goodman, Rotem Rubinstein, Chan Aye Thu, Fabiana Bahna, Seetha Mannepalli, Göran Ahlsén, Chelsea Rittenhouse, Tom Maniatis, Barry Honig, Lawrence Shapiro. Neuron 2016
Kerry Marie Goodman, Rotem Rubinstein, Chan Aye Thu, Fabiana Bahna, Seetha Mannepalli, Göran Ahlsén, Chelsea Rittenhouse, Tom Maniatis, Barry Honig, Lawrence Shapiro. Neuron 2016
11
Loss of function of PCDH12 underlies recessive microcephaly mimicking intrauterine infection.
Adi Aran, Nuphar Rosenfeld, Ranit Jaron, Paul Renbaum, Shachar Zuckerman, Hila Fridman, Sharon Zeligson, Reeval Segel, Yoav Kohn, Lara Kamal,[...]. Neurology 2016
Adi Aran, Nuphar Rosenfeld, Ranit Jaron, Paul Renbaum, Shachar Zuckerman, Hila Fridman, Sharon Zeligson, Reeval Segel, Yoav Kohn, Lara Kamal,[...]. Neurology 2016
25
Thinking outside the cell: how cadherins drive adhesion.
Julia Brasch, Oliver J Harrison, Barry Honig, Lawrence Shapiro. Trends Cell Biol 2012
Julia Brasch, Oliver J Harrison, Barry Honig, Lawrence Shapiro. Trends Cell Biol 2012
6
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
Mark R Etherton, Cory A Blaiss, Craig M Powell, Thomas C Südhof. Proc Natl Acad Sci U S A 2009
6
Sociability Deficits and Altered Amygdala Circuits in Mice Lacking Pcdh10, an Autism Associated Gene.
Hannah Schoch, Arati S Kreibich, Sarah L Ferri, Rachel S White, Dominique Bohorquez, Anamika Banerjee, Russell G Port, Holly C Dow, Lucero Cordero, Ashley A Pallathra,[...]. Biol Psychiatry 2017
Hannah Schoch, Arati S Kreibich, Sarah L Ferri, Rachel S White, Dominique Bohorquez, Anamika Banerjee, Russell G Port, Holly C Dow, Lucero Cordero, Ashley A Pallathra,[...]. Biol Psychiatry 2017
16
Cadherin-6 mediates axon-target matching in a non-image-forming visual circuit.
Jessica A Osterhout, Nicko Josten, Jena Yamada, Feng Pan, Shaw-wen Wu, Phong L Nguyen, Georgia Panagiotakos, Yukiko U Inoue, Saki F Egusa, Bela Volgyi,[...]. Neuron 2011
Jessica A Osterhout, Nicko Josten, Jena Yamada, Feng Pan, Shaw-wen Wu, Phong L Nguyen, Georgia Panagiotakos, Yukiko U Inoue, Saki F Egusa, Bela Volgyi,[...]. Neuron 2011
5
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
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
5
Association of CDH11 with non-syndromic ASD.
An Crepel, Veerle De Wolf, Nathalie Brison, Berten Ceulemans, Didier Walleghem, Gilian Peuteman, Diether Lambrechts, Jean Steyaert, Ilse Noens, Koen Devriendt,[...]. Am J Med Genet B Neuropsychiatr Genet 2014
An Crepel, Veerle De Wolf, Nathalie Brison, Berten Ceulemans, Didier Walleghem, Gilian Peuteman, Diether Lambrechts, Jean Steyaert, Ilse Noens, Koen Devriendt,[...]. Am J Med Genet B Neuropsychiatr Genet 2014
41
Identification and localization of multiple classic cadherins in developing rat limbic system.
I H Bekirov, L A Needleman, W Zhang, D L Benson. Neuroscience 2002
I H Bekirov, L A Needleman, W Zhang, D L Benson. Neuroscience 2002
7
γ-protocadherins control cortical dendrite arborization by regulating the activity of a FAK/PKC/MARCKS signaling pathway.
Andrew M Garrett, Dietmar Schreiner, Mark A Lobas, Joshua A Weiner. Neuron 2012
Andrew M Garrett, Dietmar Schreiner, Mark A Lobas, Joshua A Weiner. Neuron 2012
5
Control of excitatory and inhibitory synapse formation by neuroligins.
Ben Chih, Holly Engelman, Peter Scheiffele. Science 2005
Ben Chih, Holly Engelman, Peter Scheiffele. Science 2005
5
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.