A citation-based method for searching scientific literature


List of co-cited articles
1184 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


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


Transcriptomic analysis of autistic brain reveals convergent molecular pathology.
Irina Voineagu, Xinchen Wang, Patrick Johnston, Jennifer K Lowe, Yuan Tian, Steve Horvath, Jonathan Mill, Rita M Cantor, Benjamin J Blencowe, Daniel H Geschwind. Nature 2011
13


Disruption of cerebral cortex MET signaling in autism spectrum disorder.
Daniel B Campbell, Rosanna D'Oronzio, Krassi Garbett, Philip J Ebert, Karoly Mirnics, Pat Levitt, Antonio M Persico. Ann Neurol 2007
140
12

A genetic variant that disrupts MET transcription is associated with autism.
Daniel B Campbell, James S Sutcliffe, Philip J Ebert, Roberto Militerni, Carmela Bravaccio, Simona Trillo, Maurizio Elia, Cindy Schneider, Raun Melmed, Roberto Sacco,[...]. Proc Natl Acad Sci U S A 2006
291
11

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
695
11

Autism-associated promoter variant in MET impacts functional and structural brain networks.
Jeffrey D Rudie, Leanna M Hernandez, Jesse A Brown, Devora Beck-Pancer, Natalie L Colich, Philip Gorrindo, Paul M Thompson, Daniel H Geschwind, Susan Y Bookheimer, Pat Levitt,[...]. Neuron 2012
110
11

Autism spectrum disorders: developmental disconnection syndromes.
Daniel H Geschwind, Pat Levitt. Curr Opin Neurobiol 2007
889
11

A synaptic trek to autism.
Thomas Bourgeron. Curr Opin Neurobiol 2009
447
11

Neuroglial activation and neuroinflammation in the brain of patients with autism.
Diana L Vargas, Caterina Nascimbene, Chitra Krishnan, Andrew W Zimmerman, Carlos A Pardo. Ann Neurol 2005
11

Association between microdeletion and microduplication at 16p11.2 and autism.
Lauren A Weiss, Yiping Shen, Joshua M Korn, Dan E Arking, David T Miller, Ragnheidur Fossdal, Evald Saemundsen, Hreinn Stefansson, Manuel A R Ferreira, Todd Green,[...]. N Engl J Med 2008
10

Reversal of learning deficits in a Tsc2+/- mouse model of tuberous sclerosis.
Dan Ehninger, Sangyeul Han, Carrie Shilyansky, Yu Zhou, Weidong Li, David J Kwiatkowski, Vijaya Ramesh, Alcino J Silva. Nat Med 2008
592
10

Neuroanatomy of autism.
David G Amaral, Cynthia Mills Schumann, Christine Wu Nordahl. Trends Neurosci 2008
878
10

Advances in autism genetics: on the threshold of a new neurobiology.
Brett S Abrahams, Daniel H Geschwind. Nat Rev Genet 2008
10



Subset of individuals with autism spectrum disorders and extreme macrocephaly associated with germline PTEN tumour suppressor gene mutations.
M G Butler, M J Dasouki, X-P Zhou, Z Talebizadeh, M Brown, T N Takahashi, J H Miles, C H Wang, R Stratton, R Pilarski,[...]. J Med Genet 2005
522
9

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
9

The autistic neuron: troubled translation?
Raymond J Kelleher, Mark F Bear. Cell 2008
417
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
893
9

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
9

Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2.
R E Amir, I B Van den Veyver, M Wan, C Q Tran, U Francke, H Y Zoghbi. Nat Genet 1999
9

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
532
9


SFARI Gene 2.0: a community-driven knowledgebase for the autism spectrum disorders (ASDs).
Brett S Abrahams, Dan E Arking, Daniel B Campbell, Heather C Mefford, Eric M Morrow, Lauren A Weiss, Idan Menashe, Tim Wadkins, Sharmila Banerjee-Basu, Alan Packer. Mol Autism 2013
333
9

Dynamic gene and protein expression patterns of the autism-associated met receptor tyrosine kinase in the developing mouse forebrain.
Matthew C Judson, Mica Y Bergman, Daniel B Campbell, Kathie L Eagleson, Pat Levitt. J Comp Neurol 2009
62
14

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
9

Dysregulation of mTOR signaling in fragile X syndrome.
Ali Sharma, Charles A Hoeffer, Yukihiro Takayasu, Takahiro Miyawaki, Sean M McBride, Eric Klann, R Suzanne Zukin. J Neurosci 2010
408
8

Correction of fragile X syndrome in mice.
Gül Dölen, Emily Osterweil, B S Shankaranarayana Rao, Gordon B Smith, Benjamin D Auerbach, Sumantra Chattarji, Mark F Bear. Neuron 2007
702
8


Genetics of autism spectrum disorders.
Daniel H Geschwind. Trends Cogn Sci 2011
342
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
8

Autism as a strongly genetic disorder: evidence from a British twin study.
A Bailey, A Le Couteur, I Gottesman, P Bolton, E Simonoff, E Yuzda, M Rutter. Psychol Med 1995
8

Neuronal connectivity as a convergent target of gene × environment interactions that confer risk for Autism Spectrum Disorders.
Marianna Stamou, Karin M Streifel, Paula E Goines, Pamela J Lein. Neurotoxicol Teratol 2013
82
9

Autism-like behavioral phenotypes in BTBR T+tf/J mice.
H G McFarlane, G K Kusek, M Yang, J L Phoenix, V J Bolivar, J N Crawley. Genes Brain Behav 2008
526
8

Coexpression networks implicate human midfetal deep cortical projection neurons in the pathogenesis of autism.
A Jeremy Willsey, Stephan J Sanders, Mingfeng Li, Shan Dong, Andrew T Tebbenkamp, Rebecca A Muhle, Steven K Reilly, Leon Lin, Sofia Fertuzinhos, Jeremy A Miller,[...]. Cell 2013
536
8

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
604
8

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
581
8

MAP'ing CNS development and cognition: an ERKsome process.
Ivy S Samuels, Sulagna C Saitta, Gary E Landreth. Neuron 2009
136
8

Autism traits in the RASopathies.
Brigid Adviento, Iris L Corbin, Felicia Widjaja, Guillaume Desachy, Nicole Enrique, Tena Rosser, Susan Risi, Elysa J Marco, Robert L Hendren, Carrie E Bearden,[...]. J Med Genet 2014
97
8



Autism genetics: searching for specificity and convergence.
Jamee M Berg, Daniel H Geschwind. Genome Biol 2012
122
8

Regulation of MET by FOXP2, genes implicated in higher cognitive dysfunction and autism risk.
Zohar Mukamel, Genevieve Konopka, Eric Wexler, Gregory E Osborn, Hongmei Dong, Mica Y Bergman, Pat Levitt, Daniel H Geschwind. J Neurosci 2011
70
11


Recurrent 16p11.2 microdeletions in autism.
Ravinesh A Kumar, Samer KaraMohamed, Jyotsna Sudi, Donald F Conrad, Camille Brune, Judith A Badner, T Conrad Gilliam, Norma J Nowak, Edwin H Cook, William B Dobyns,[...]. Hum Mol Genet 2008
475
7

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
661
7

Residential proximity to freeways and autism in the CHARGE study.
Heather E Volk, Irva Hertz-Picciotto, Lora Delwiche, Fred Lurmann, Rob McConnell. Environ Health Perspect 2011
202
7

Genetic heritability and shared environmental factors among twin pairs with autism.
Joachim Hallmayer, Sue Cleveland, Andrea Torres, Jennifer Phillips, Brianne Cohen, Tiffany Torigoe, Janet Miller, Angie Fedele, Jack Collins, Karen Smith,[...]. Arch Gen Psychiatry 2011
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.