A citation-based method for searching scientific literature

Fengping Dong, Joanna Jiang, Colleen McSweeney, Donghua Zou, Long Liu, Yingwei Mao. Hum Mol Genet 2016
Times Cited: 35







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



Times Cited
  Times     Co-cited
Similarity


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
45

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
773
34

Chd8 mediates cortical neurogenesis via transcriptional regulation of cell cycle and Wnt signaling.
Omer Durak, Fan Gao, Yea Jin Kaeser-Woo, Richard Rueda, Anthony J Martorell, Alexi Nott, Carol Y Liu, L Ashley Watson, Li-Huei Tsai. Nat Neurosci 2016
108
34

A de novo convergence of autism genetics and molecular neuroscience.
Niklas Krumm, Brian J O'Roak, Jay Shendure, Evan E Eichler. Trends Neurosci 2014
272
34

Wnt signaling networks in autism spectrum disorder and intellectual disability.
Vickie Kwan, Brianna K Unda, Karun K Singh. J Neurodev Disord 2016
45
31

De novo mutations in beta-catenin (CTNNB1) appear to be a frequent cause of intellectual disability: expanding the mutational and clinical spectrum.
Alma Kuechler, Marjolein H Willemsen, Beate Albrecht, Carlos A Bacino, Dennis W Bartholomew, Hans van Bokhoven, Marie Jose H van den Boogaard, Nuria Bramswig, Christian Büttner, Kirsten Cremer,[...]. Hum Genet 2015
48
28


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
28


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
25

Adenomatous polyposis coli protein deletion leads to cognitive and autism-like disabilities.
J L Mohn, J Alexander, A Pirone, C D Palka, S-Y Lee, L Mebane, P G Haydon, M H Jacob. Mol Psychiatry 2014
45
25

Diagnostic exome sequencing in persons with severe intellectual disability.
Joep de Ligt, Marjolein H Willemsen, Bregje W M van Bon, Tjitske Kleefstra, Helger G Yntema, Thessa Kroes, Anneke T Vulto-van Silfhout, David A Koolen, Petra de Vries, Christian Gilissen,[...]. N Engl J Med 2012
961
22

A new intellectual disability syndrome caused by CTNNB1 haploinsufficiency.
Estelle Dubruc, Audrey Putoux, Audrey Labalme, Christelle Rougeot, Damien Sanlaville, Patrick Edery. Am J Med Genet A 2014
30
26

Dominant β-catenin mutations cause intellectual disability with recognizable syndromic features.
Valter Tucci, Tjitske Kleefstra, Andrea Hardy, Ines Heise, Silvia Maggi, Marjolein H Willemsen, Helen Hilton, Chris Esapa, Michelle Simon, Maria-Teresa Buenavista,[...]. J Clin Invest 2014
73
22

A rare WNT1 missense variant overrepresented in ASD leads to increased Wnt signal pathway activation.
P-M Martin, X Yang, N Robin, E Lam, J S Rabinowitz, C A Erdman, J Quinn, L A Weiss, S P Hamilton, P-Y Kwok,[...]. Transl Psychiatry 2013
22
36

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
20

Synaptic Wnt/GSK3β Signaling Hub in Autism.
Mario O Caracci, Miguel E Ávila, Giancarlo V De Ferrari. Neural Plast 2016
37
20

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
601
20


Inactivation of the beta-catenin gene by Wnt1-Cre-mediated deletion results in dramatic brain malformation and failure of craniofacial development.
V Brault, R Moore, S Kutsch, M Ishibashi, D H Rowitch, A P McMahon, L Sommer, O Boussadia, R Kemler. Development 2001
831
17

Pten Mutations Alter Brain Growth Trajectory and Allocation of Cell Types through Elevated β-Catenin Signaling.
Youjun Chen, Wen-Chin Huang, Julien Séjourné, Amy E Clipperton-Allen, Damon T Page. J Neurosci 2015
60
17

DIXDC1 contributes to psychiatric susceptibility by regulating dendritic spine and glutamatergic synapse density via GSK3 and Wnt/β-catenin signaling.
P-M Martin, R E Stanley, A P Ross, A E Freitas, C E Moyer, A C Brumback, J Iafrati, K S Stapornwongkul, S Dominguez, S Kivimäe,[...]. Mol Psychiatry 2018
28
21

Disruption of the non-canonical Wnt gene PRICKLE2 leads to autism-like behaviors with evidence for hippocampal synaptic dysfunction.
L P Sowers, L Loo, Y Wu, E Campbell, J D Ulrich, S Wu, L Paemka, T Wassink, K Meyer, X Bing,[...]. Mol Psychiatry 2013
47
17

Disruptive CHD8 mutations define a subtype of autism early in development.
Raphael Bernier, Christelle Golzio, Bo Xiong, Holly A Stessman, Bradley P Coe, Osnat Penn, Kali Witherspoon, Jennifer Gerdts, Carl Baker, Anneke T Vulto-van Silfhout,[...]. Cell 2014
382
17

Deletion of PTEN produces autism-like behavioral deficits and alterations in synaptic proteins.
Joaquin N Lugo, Gregory D Smith, Erin P Arbuckle, Jessika White, Andrew J Holley, Crina M Floruta, Nowrin Ahmed, Maribel C Gomez, Obi Okonkwo. Front Mol Neurosci 2014
86
17

Wnt/β-catenin signaling and disease.
Hans Clevers, Roel Nusse. Cell 2012
17

Rare de novo variants associated with autism implicate a large functional network of genes involved in formation and function of synapses.
Sarah R Gilman, Ivan Iossifov, Dan Levy, Michael Ronemus, Michael Wigler, Dennis Vitkup. Neuron 2011
426
17

Wnt/beta-catenin signaling: components, mechanisms, and diseases.
Bryan T MacDonald, Keiko Tamai, Xi He. Dev Cell 2009
17

Beta-catenin is critical for dendritic morphogenesis.
Xiang Yu, Robert C Malenka. Nat Neurosci 2003
373
17


Lack of parvalbumin in mice leads to behavioral deficits relevant to all human autism core symptoms and related neural morphofunctional abnormalities.
M Wöhr, D Orduz, P Gregory, H Moreno, U Khan, K J Vörckel, D P Wolfer, H Welzl, D Gall, S N Schiffmann,[...]. Transl Psychiatry 2015
130
17

Impaired neurodevelopmental pathways in autism spectrum disorder: a review of signaling mechanisms and crosstalk.
Santosh Kumar, Kurt Reynolds, Yu Ji, Ran Gu, Sunil Rai, Chengji J Zhou. J Neurodev Disord 2019
29
20

A de novo CTNNB1 nonsense mutation associated with syndromic atypical hyperekplexia, microcephaly and intellectual disability: a case report.
Anna Winczewska-Wiktor, Magdalena Badura-Stronka, Anna Monies-Nowicka, Michal Maciej Nowicki, Barbara Steinborn, Anna Latos-Bieleńska, Dorota Monies. BMC Neurol 2016
14
35

GSK3 influences social preference and anxiety-related behaviors during social interaction in a mouse model of fragile X syndrome and autism.
Marjelo A Mines, Christopher J Yuskaitis, Margaret K King, Eleonore Beurel, Richard S Jope. PLoS One 2010
144
14

Association of adenomatous polyposis coli (APC) gene polymorphisms with autism spectrum disorder (ASD).
Xiao-Lei Zhou, MaiBritt Giacobini, Britt-Marie Anderlid, Henrik Anckarsäter, Davood Omrani, Christopher Gillberg, Magnus Nordenskjöld, Annika Lindblom. Am J Med Genet B Neuropsychiatr Genet 2007
25
20

Synaptic Wnt signaling-a contributor to major psychiatric disorders?
Nathan D Okerlund, Benjamin N R Cheyette. J Neurodev Disord 2011
90
14

Functionally distinct groups of inherited PTEN mutations in autism and tumour syndromes.
Laura Spinelli, Fiona M Black, Jonathan N Berg, Britta J Eickholt, Nicholas R Leslie. J Med Genet 2015
58
14

Molecular and phenotypic abnormalities in individuals with germline heterozygous PTEN mutations and autism.
T W Frazier, R Embacher, A K Tilot, K Koenig, J Mester, C Eng. Mol Psychiatry 2015
82
14

Pten regulates neuronal arborization and social interaction in mice.
Chang-Hyuk Kwon, Bryan W Luikart, Craig M Powell, Jing Zhou, Sharon A Matheny, Wei Zhang, Yanjiao Li, Suzanne J Baker, Luis F Parada. Neuron 2006
653
14

Most genetic risk for autism resides with common variation.
Trent Gaugler, Lambertus Klei, Stephan J Sanders, Corneliu A Bodea, Arthur P Goldberg, Ann B Lee, Milind Mahajan, Dina Manaa, Yudi Pawitan, Jennifer Reichert,[...]. Nat Genet 2014
537
14

Evidence supporting WNT2 as an autism susceptibility gene.
T H Wassink, J Piven, V J Vieland, J Huang, R E Swiderski, J Pietila, T Braun, G Beck, S E Folstein, J L Haines,[...]. Am J Med Genet 2001
142
14

Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations.
Brian J O'Roak, Pelagia Deriziotis, Choli Lee, Laura Vives, Jerrod J Schwartz, Santhosh Girirajan, Emre Karakoc, Alexandra P Mackenzie, Sarah B Ng, Carl Baker,[...]. Nat Genet 2011
760
14

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
14

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
14

Autistic-like behaviour in Scn1a+/- mice and rescue by enhanced GABA-mediated neurotransmission.
Sung Han, Chao Tai, Ruth E Westenbroek, Frank H Yu, Christine S Cheah, Gregory B Potter, John L Rubenstein, Todd Scheuer, Horacio O de la Iglesia, William A Catterall. Nature 2012
363
14

Meta-analysis of SHANK Mutations in Autism Spectrum Disorders: a gradient of severity in cognitive impairments.
Claire S Leblond, Caroline Nava, Anne Polge, Julie Gauthier, Guillaume Huguet, Serge Lumbroso, Fabienne Giuliano, Coline Stordeur, Christel Depienne, Kevin Mouzat,[...]. PLoS Genet 2014
280
14

Dysfunction in GABA signalling mediates autism-like stereotypies and Rett syndrome phenotypes.
Hsiao-Tuan Chao, Hongmei Chen, Rodney C Samaco, Mingshan Xue, Maria Chahrour, Jong Yoo, Jeffrey L Neul, Shiaoching Gong, Hui-Chen Lu, Nathaniel Heintz,[...]. Nature 2010
733
14

Neocortical excitation/inhibition balance in information processing and social dysfunction.
Ofer Yizhar, Lief E Fenno, Matthias Prigge, Franziska Schneider, Thomas J Davidson, Daniel J O'Shea, Vikaas S Sohal, Inbal Goshen, Joel Finkelstein, Jeanne T Paz,[...]. Nature 2011
14

The Number of Parvalbumin-Expressing Interneurons Is Decreased in the Prefrontal Cortex in Autism.
Ezzat Hashemi, Jeanelle Ariza, Haille Rogers, Stephen C Noctor, Verónica Martínez-Cerdeño. Cereb Cortex 2017
146
14

Chd8 Mutation Leads to Autistic-like Behaviors and Impaired Striatal Circuits.
Randall J Platt, Yang Zhou, Ian M Slaymaker, Ashwin S Shetty, Niels R Weisbach, Jin-Ah Kim, Jitendra Sharma, Mitul Desai, Sabina Sood, Hannah R Kempton,[...]. Cell Rep 2017
86
14


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.