A citation-based method for searching scientific literature


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



Times Cited
  Times     Co-cited
Similarity


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
33

Diagnosing young children with autism.
Johnny L Matson, Rachel L Goldin. Int J Dev Neurosci 2014
12
33

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

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
436
25

Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs.
S Hong Lee, Stephan Ripke, Benjamin M Neale, Stephen V Faraone, Shaun M Purcell, Roy H Perlis, Bryan J Mowry, Anita Thapar, Michael E Goddard, John S Witte,[...]. Nat Genet 2013
25

The health status of adults on the autism spectrum.
Lisa A Croen, Ousseny Zerbo, Yinge Qian, Maria L Massolo, Steve Rich, Stephen Sidney, Clarissa Kripke. Autism 2015
397
25


Discovering schizophrenia endophenotypes in randomly ascertained pedigrees.
David C Glahn, Jeff T Williams, D Reese McKay, Emma E Knowles, Emma Sprooten, Samuel R Mathias, Joanne E Curran, Jack W Kent, Melanie A Carless, Harald H H Göring,[...]. Biol Psychiatry 2015
25
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
852
16

Linkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility gene.
Maricela Alarcón, Brett S Abrahams, Jennifer L Stone, Jacqueline A Duvall, Julia V Perederiy, Jamee M Bomar, Jonathan Sebat, Michael Wigler, Christa L Martin, David H Ledbetter,[...]. Am J Hum Genet 2008
564
16


An integrated map of genetic variation from 1,092 human genomes.
Goncalo R Abecasis, Adam Auton, Lisa D Brooks, Mark A DePristo, Richard M Durbin, Robert E Handsaker, Hyun Min Kang, Gabor T Marth, Gil A McVean. Nature 2012
16

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
16

Individual common variants exert weak effects on the risk for autism spectrum disorders.
Richard Anney, Lambertus Klei, Dalila Pinto, Joana Almeida, Elena Bacchelli, Gillian Baird, Nadia Bolshakova, Sven Bölte, Patrick F Bolton, Thomas Bourgeron,[...]. Hum Mol Genet 2012
239
16

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
16

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
972
16

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
16

A genome-wide association study of autism using the Simons Simplex Collection: Does reducing phenotypic heterogeneity in autism increase genetic homogeneity?
Pauline Chaste, Lambertus Klei, Stephan J Sanders, Vanessa Hus, Michael T Murtha, Jennifer K Lowe, A Jeremy Willsey, Daniel Moreno-De-Luca, Timothy W Yu, Eric Fombonne,[...]. Biol Psychiatry 2015
95
16

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
455
16

Advances in autism genetics: on the threshold of a new neurobiology.
Brett S Abrahams, Daniel H Geschwind. Nat Rev Genet 2008
16

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
16

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
635
16

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
640
16

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
16

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
16

Autism: many genes, common pathways?
Daniel H Geschwind. Cell 2008
207
16

Common genetic variants, acting additively, are a major source of risk for autism.
Lambertus Klei, Stephan J Sanders, Michael T Murtha, Vanessa Hus, Jennifer K Lowe, A Jeremy Willsey, Daniel Moreno-De-Luca, Timothy W Yu, Eric Fombonne, Daniel Geschwind,[...]. Mol Autism 2012
267
16

Whole-genome sequencing of quartet families with autism spectrum disorder.
Ryan K C Yuen, Bhooma Thiruvahindrapuram, Daniele Merico, Susan Walker, Kristiina Tammimies, Ny Hoang, Christina Chrysler, Thomas Nalpathamkalam, Giovanna Pellecchia, Yi Liu,[...]. Nat Med 2015
325
16

Validation of electronic health record phenotyping of bipolar disorder cases and controls.
Victor M Castro, Jessica Minnier, Shawn N Murphy, Isaac Kohane, Susanne E Churchill, Vivian Gainer, Tianxi Cai, Alison G Hoffnagle, Yael Dai, Stefanie Block,[...]. Am J Psychiatry 2015
78
16

Common polygenic risk for autism spectrum disorder (ASD) is associated with cognitive ability in the general population.
T-K Clarke, M K Lupton, A M Fernandez-Pujals, J Starr, G Davies, S Cox, A Pattie, D C Liewald, L S Hall, D J MacIntyre,[...]. Mol Psychiatry 2016
97
16

Using electronic medical records to enable large-scale studies in psychiatry: treatment resistant depression as a model.
R H Perlis, D V Iosifescu, V M Castro, S N Murphy, V S Gainer, J Minnier, T Cai, S Goryachev, Q Zeng, P J Gallagher,[...]. Psychol Med 2012
110
16

QT interval and antidepressant use: a cross sectional study of electronic health records.
Victor M Castro, Caitlin C Clements, Shawn N Murphy, Vivian S Gainer, Maurizio Fava, Jeffrey B Weilburg, Jane L Erb, Susanne E Churchill, Isaac S Kohane, Dan V Iosifescu,[...]. BMJ 2013
167
16

Identifying phenotypic signatures of neuropsychiatric disorders from electronic medical records.
Svetlana Lyalina, Bethany Percha, Paea LePendu, Srinivasan V Iyer, Russ B Altman, Nigam H Shah. J Am Med Inform Assoc 2013
40
16

Predicting the risk of suicide by analyzing the text of clinical notes.
Chris Poulin, Brian Shiner, Paul Thompson, Linas Vepstas, Yinong Young-Xu, Benjamin Goertzel, Bradley Watts, Laura Flashman, Thomas McAllister. PLoS One 2014
71
16

Mining electronic health records: towards better research applications and clinical care.
Peter B Jensen, Lars J Jensen, Søren Brunak. Nat Rev Genet 2012
608
16

Toward personalizing treatment for depression: predicting diagnosis and severity.
Sandy H Huang, Paea LePendu, Srinivasan V Iyer, Ming Tai-Seale, David Carrell, Nigam H Shah. J Am Med Inform Assoc 2014
47
16

Asthma and Allergies in Children With Autism Spectrum Disorders: Results From the CHARGE Study.
Kristen Lyall, Judy Van de Water, Paul Ashwood, Irva Hertz-Picciotto. Autism Res 2015
50
16

Immune mediated conditions in autism spectrum disorders.
Ousseny Zerbo, Albin Leong, Lisa Barcellos, Pilar Bernal, Bruce Fireman, Lisa A Croen. Brain Behav Immun 2015
82
16

Alterations of the intestinal barrier in patients with autism spectrum disorders and in their first-degree relatives.
Laura de Magistris, Valeria Familiari, Antonio Pascotto, Anna Sapone, Alessandro Frolli, Patrizia Iardino, Maria Carteni, Mario De Rosa, Ruggiero Francavilla, Gabriele Riegler,[...]. J Pediatr Gastroenterol Nutr 2010
295
16

Behavioral and Neuroanatomical Phenotypes in Mouse Models of Autism.
Jacob Ellegood, Jacqueline N Crawley. Neurotherapeutics 2015
67
16

Children with autism show reduced somatosensory response: an MEG study.
Elysa J Marco, Kasra Khatibi, Susanna S Hill, Bryna Siegel, Monica S Arroyo, Anne F Dowling, John M Neuhaus, Elliott H Sherr, Leighton N B Hinkley, Srikantan S Nagarajan. Autism Res 2012
60
16


The role of immune dysfunction in the pathophysiology of autism.
Charity Onore, Milo Careaga, Paul Ashwood. Brain Behav Immun 2012
385
16

Autistic-like behavioural and neurochemical changes in a mouse model of food allergy.
Caroline G M de Theije, Jiangbo Wu, Pim J Koelink, Gerdien A H Korte-Bouws, Yuliya Borre, Martien J H Kas, Sofia Lopes da Silva, S Mechiel Korte, Berend Olivier, Johan Garssen,[...]. Behav Brain Res 2014
41
16

Pathways underlying the gut-to-brain connection in autism spectrum disorders as future targets for disease management.
Caroline G M de Theije, Jiangbo Wu, Sofia Lopes da Silva, Patrick J Kamphuis, Johan Garssen, S Mechiel Korte, Aletta D Kraneveld. Eur J Pharmacol 2011
103
16

Autism spectrum disorder in the genetics clinic: a review.
M T Carter, S W Scherer. Clin Genet 2013
111
16

Gastrointestinal symptoms in autism spectrum disorder: a meta-analysis.
Barbara O McElhanon, Courtney McCracken, Saul Karpen, William G Sharp. Pediatrics 2014
343
16

Brief Report: Whole Blood Serotonin Levels and Gastrointestinal Symptoms in Autism Spectrum Disorder.
Sarah Marler, Bradley J Ferguson, Evon Batey Lee, Brittany Peters, Kent C Williams, Erin McDonnell, Eric A Macklin, Pat Levitt, Catherine Hagan Gillespie, George M Anderson,[...]. J Autism Dev Disord 2016
46
16

Accelerated maturation of white matter in young children with autism: a high b value DWI study.
Dafna Ben Bashat, Vered Kronfeld-Duenias, Ditza A Zachor, Perla M Ekstein, Talma Hendler, Ricardo Tarrasch, Ariela Even, Yonata Levy, Liat Ben Sira. Neuroimage 2007
211
16



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.