A citation-based method for searching scientific literature

L D'Abate, S Walker, R K C Yuen, K Tammimies, J A Buchanan, R W Davies, B Thiruvahindrapuram, J Wei, J Brian, S E Bryson, K Dobkins, J Howe, R Landa, J Leef, D Messinger, S Ozonoff, I M Smith, W L Stone, Z E Warren, G Young, L Zwaigenbaum, S W Scherer. Nat Commun 2019
Times Cited: 9







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



Times Cited
  Times     Co-cited
Similarity


Identification of common genetic risk variants for autism spectrum disorder.
Jakob Grove, Stephan Ripke, Thomas D Als, Manuel Mattheisen, Raymond K Walters, Hyejung Won, Jonatan Pallesen, Esben Agerbo, Ole A Andreassen, Richard Anney,[...]. Nat Genet 2019
437
44

Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders.
Daniel J Weiner, Emilie M Wigdor, Stephan Ripke, Raymond K Walters, Jack A Kosmicki, Jakob Grove, Kaitlin E Samocha, Jacqueline I Goldstein, Aysu Okbay, Jonas Bybjerg-Grauholm,[...]. Nat Genet 2017
182
33

Methylomic analysis of monozygotic twins discordant for autism spectrum disorder and related behavioural traits.
C C Y Wong, E L Meaburn, A Ronald, T S Price, A R Jeffries, L C Schalkwyk, R Plomin, J Mill. Mol Psychiatry 2014
172
22

Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism.
F Kyle Satterstrom, Jack A Kosmicki, Jiebiao Wang, Michael S Breen, Silvia De Rubeis, Joon-Yong An, Minshi Peng, Ryan Collins, Jakob Grove, Lambertus Klei,[...]. Cell 2020
310
22

The autism diagnostic observation schedule-generic: a standard measure of social and communication deficits associated with the spectrum of autism.
C Lord, S Risi, L Lambrecht, E H Cook, B L Leventhal, P C DiLavore, A Pickles, M Rutter. J Autism Dev Disord 2000
22


The genetics of autism spectrum disorders and related neuropsychiatric disorders in childhood.
Paul Lichtenstein, Eva Carlström, Maria Råstam, Christopher Gillberg, Henrik Anckarsäter. Am J Psychiatry 2010
388
22

Whole-genome sequencing in a family with twin boys with autism and intellectual disability suggests multimodal polygenic risk.
Brooke McKenna, Tanner Koomar, Kevin Vervier, Jamie Kremsreiter, Jacob J Michaelson. Cold Spring Harb Mol Case Stud 2018
5
40

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
22

Genomic Patterns of De Novo Mutation in Simplex Autism.
Tychele N Turner, Bradley P Coe, Diane E Dickel, Kendra Hoekzema, Bradley J Nelson, Michael C Zody, Zev N Kronenberg, Fereydoun Hormozdiari, Archana Raja, Len A Pennacchio,[...]. Cell 2017
135
22

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
22

Insufficient Evidence for "Autism-Specific" Genes.
Scott M Myers, Thomas D Challman, Raphael Bernier, Thomas Bourgeron, Wendy K Chung, John N Constantino, Evan E Eichler, Sebastien Jacquemont, David T Miller, Kevin J Mitchell,[...]. Am J Hum Genet 2020
24
22

Mapping autism risk loci using genetic linkage and chromosomal rearrangements.
Peter Szatmari, Andrew D Paterson, Lonnie Zwaigenbaum, Wendy Roberts, Jessica Brian, Xiao-Qing Liu, John B Vincent, Jennifer L Skaug, Ann P Thompson, Lili Senman,[...]. Nat Genet 2007
948
22

A large data resource of genomic copy number variation across neurodevelopmental disorders.
Mehdi Zarrei, Christie L Burton, Worrawat Engchuan, Edwin J Young, Edward J Higginbotham, Jeffrey R MacDonald, Brett Trost, Ada J S Chan, Susan Walker, Sylvia Lamoureux,[...]. NPJ Genom Med 2019
31
22

The Heritability of Autism Spectrum Disorder.
Sven Sandin, Paul Lichtenstein, Ralf Kuja-Halkola, Christina Hultman, Henrik Larsson, Abraham Reichenberg. JAMA 2017
183
22

Rare de novo and transmitted copy-number variation in autistic spectrum disorders.
Dan Levy, Michael Ronemus, Boris Yamrom, Yoon-ha Lee, Anthony Leotta, Jude Kendall, Steven Marks, B Lakshmi, Deepa Pai, Kenny Ye,[...]. Neuron 2011
434
22

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
802
22

Heritability of autism spectrum disorders: a meta-analysis of twin studies.
Beata Tick, Patrick Bolton, Francesca Happé, Michael Rutter, Frühling Rijsdijk. J Child Psychol Psychiatry 2016
262
22

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
22

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
22

Strong association of de novo copy number mutations with autism.
Jonathan Sebat, B Lakshmi, Dheeraj Malhotra, Jennifer Troge, Christa Lese-Martin, Tom Walsh, Boris Yamrom, Seungtai Yoon, Alex Krasnitz, Jude Kendall,[...]. Science 2007
22

Paternally inherited cis-regulatory structural variants are associated with autism.
William M Brandler, Danny Antaki, Madhusudan Gujral, Morgan L Kleiber, Joe Whitney, Michelle S Maile, Oanh Hong, Timothy R Chapman, Shirley Tan, Prateek Tandon,[...]. Science 2018
70
22

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
250
22

Prevalence of disorders of the autism spectrum in a population cohort of children in South Thames: the Special Needs and Autism Project (SNAP).
Gillian Baird, Emily Simonoff, Andrew Pickles, Susie Chandler, Tom Loucas, David Meldrum, Tony Charman. Lancet 2006
987
22

Psychiatric disorders from childhood to adulthood in 22q11.2 deletion syndrome: results from the International Consortium on Brain and Behavior in 22q11.2 Deletion Syndrome.
Maude Schneider, Martin Debbané, Anne S Bassett, Eva W C Chow, Wai Lun Alan Fung, Marianne van den Bree, Michael Owen, Kieran C Murphy, Maria Niarchou, Wendy R Kates,[...]. Am J Psychiatry 2014
386
22


Genotype-phenotype associations in children with copy number variants associated with high neuropsychiatric risk in the UK (IMAGINE-ID): a case-control cohort study.
Samuel J R A Chawner, Michael J Owen, Peter Holmans, F Lucy Raymond, David Skuse, Jeremy Hall, Marianne B M van den Bree. Lancet Psychiatry 2019
32
22

Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies.
David T Miller, Margaret P Adam, Swaroop Aradhya, Leslie G Biesecker, Arthur R Brothman, Nigel P Carter, Deanna M Church, John A Crolla, Evan E Eichler, Charles J Epstein,[...]. Am J Hum Genet 2010
22

The phenotypic manifestations of rare genic CNVs in autism spectrum disorder.
A K Merikangas, R Segurado, E A Heron, R J L Anney, A D Paterson, E H Cook, D Pinto, S W Scherer, P Szatmari, M Gill,[...]. Mol Psychiatry 2015
23
22

Autism genetics: opportunities and challenges for clinical translation.
Jacob A S Vorstman, Jeremy R Parr, Daniel Moreno-De-Luca, Richard J L Anney, John I Nurnberger, Joachim F Hallmayer. Nat Rev Genet 2017
165
22

Analysis of shared heritability in common disorders of the brain.
Verneri Anttila, Brendan Bulik-Sullivan, Hilary K Finucane, Raymond K Walters, Jose Bras, Laramie Duncan, Valentina Escott-Price, Guido J Falcone, Padhraig Gormley, Rainer Malik,[...]. Science 2018
622
22


Infant social attention: an endophenotype of ASD-related traits?
Emily J H Jones, Kaitlin Venema, Rachel K Earl, Rachel Lowy, Sara J Webb. J Child Psychol Psychiatry 2017
16
22

EEG Analytics for Early Detection of Autism Spectrum Disorder: A data-driven approach.
William J Bosl, Helen Tager-Flusberg, Charles A Nelson. Sci Rep 2018
70
22

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
547
22


Longitudinal EEG power in the first postnatal year differentiates autism outcomes.
Laurel J Gabard-Durnam, Carol Wilkinson, Kush Kapur, Helen Tager-Flusberg, April R Levin, Charles A Nelson. Nat Commun 2019
28
22

Developmental pathways to autism: a review of prospective studies of infants at risk.
Emily J H Jones, Teodora Gliga, Rachael Bedford, Tony Charman, Mark H Johnson. Neurosci Biobehav Rev 2014
255
22

Early brain development in infants at high risk for autism spectrum disorder.
Heather Cody Hazlett, Hongbin Gu, Brent C Munsell, Sun Hyung Kim, Martin Styner, Jason J Wolff, Jed T Elison, Meghan R Swanson, Hongtu Zhu, Kelly N Botteron,[...]. Nature 2017
357
22




Mutations in the gene encoding CADM1 are associated with autism spectrum disorder.
Yu Zhiling, Eriko Fujita, Yuko Tanabe, Takanori Yamagata, Takashi Momoi, Mariko Y Momoi. Biochem Biophys Res Commun 2008
73
11


Predictors of outcomes in autism early intervention: why don't we know more?
Giacomo Vivanti, Margot Prior, Katrina Williams, Cheryl Dissanayake. Front Pediatr 2014
68
11

Systems biology and gene networks in neurodevelopmental and neurodegenerative disorders.
Neelroop N Parikshak, Michael J Gandal, Daniel H Geschwind. Nat Rev Genet 2015
208
11

SynCAMs organize synapses through heterophilic adhesion.
Adam I Fogel, Michael R Akins, Alexander J Krupp, Massimiliano Stagi, Valentin Stein, Thomas Biederer. J Neurosci 2007
139
11


FARP-1 deletion is associated with lack of response to autism treatment by early start denver model in a multiplex family.
Francesca Cucinotta, Arianna Ricciardello, Laura Turriziani, Giorgia Calabrese, Marilena Briguglio, Maria Boncoddo, Fabiana Bellomo, Pasquale Tomaiuolo, Silvia Martines, Marianna Bruschetta,[...]. Mol Genet Genomic Med 2020
1
100



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.