A citation-based method for searching scientific literature

Yamini V Virkud, Richard D Todd, Anna M Abbacchi, Yi Zhang, John N Constantino. Am J Med Genet B Neuropsychiatr Genet 2009
Times Cited: 139







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



Times Cited
  Times     Co-cited
Similarity


Sibling recurrence and the genetic epidemiology of autism.
John N Constantino, Yi Zhang, Thomas Frazier, Anna M Abbacchi, Paul Law. Am J Psychiatry 2010
262
41


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
34

Autistic traits in the general population: a twin study.
John N Constantino, Richard D Todd. Arch Gen Psychiatry 2003
714
33

Defining key features of the broad autism phenotype: a comparison across parents of multiple- and single-incidence autism families.
Molly Losh, Debra Childress, Kristen Lam, Joseph Piven. Am J Med Genet B Neuropsychiatr Genet 2008
168
23


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
568
22

Broader autism phenotype: evidence from a family history study of multiple-incidence autism families.
J Piven, P Palmer, D Jacobi, D Childress, S Arndt. Am J Psychiatry 1997
453
21

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
256
21


Validation of a brief quantitative measure of autistic traits: comparison of the social responsiveness scale with the autism diagnostic interview-revised.
John N Constantino, Sandra A Davis, Richard D Todd, Matthew K Schindler, Maggie M Gross, Susan L Brophy, Lisa M Metzger, Christiana S Shoushtari, Reagan Splinter, Wendy Reich. J Autism Dev Disord 2003
872
19

Advances in autism genetics: on the threshold of a new neurobiology.
Brett S Abrahams, Daniel H Geschwind. Nat Rev Genet 2008
18

Can family affectedness inform infant sibling outcomes of autism spectrum disorders?
A J Schwichtenberg, G S Young, M Sigman, T Hutman, S Ozonoff. J Child Psychol Psychiatry 2010
37
48

Parental social responsiveness and risk of autism spectrum disorder in offspring.
Kristen Lyall, John N Constantino, Marc G Weisskopf, Andrea L Roberts, Alberto Ascherio, Susan L Santangelo. JAMA Psychiatry 2014
55
32

Autistic social impairment in the siblings of children with pervasive developmental disorders.
John N Constantino, Clara Lajonchere, Marin Lutz, Teddi Gray, Anna Abbacchi, Kathleen McKenna, Deepti Singh, Richard D Todd. Am J Psychiatry 2006
178
17

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
16


Recurrence risk for autism spectrum disorders: a Baby Siblings Research Consortium study.
Sally Ozonoff, Gregory S Young, Alice Carter, Daniel Messinger, Nurit Yirmiya, Lonnie Zwaigenbaum, Susan Bryson, Leslie J Carver, John N Constantino, Karen Dobkins,[...]. Pediatrics 2011
697
15

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
994
15

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
15

The broader autism phenotype in simplex and multiplex families.
Jennifer A Gerdts, Raphael Bernier, Geraldine Dawson, Annette Estes. J Autism Dev Disord 2013
32
46

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
15

A case-control family history study of autism.
P Bolton, H Macdonald, A Pickles, P Rios, S Goode, M Crowson, A Bailey, M Rutter. J Child Psychol Psychiatry 1994
653
14

The factor structure of autistic traits.
John N Constantino, Christian P Gruber, Sandra Davis, Stephanie Hayes, Natalie Passanante, Thomas Przybeck. J Child Psychol Psychiatry 2004
222
14

Confirmatory factor analytic structure and measurement invariance of quantitative autistic traits measured by the social responsiveness scale-2.
Thomas W Frazier, Kristin R Ratliff, Chris Gruber, Yi Zhang, Paul A Law, John N Constantino. Autism 2014
116
14

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
13

Reciprocal social behavior in children with and without pervasive developmental disorders.
J N Constantino, T Przybeck, D Friesen, R D Todd. J Dev Behav Pediatr 2000
250
13

Personality and language characteristics in parents from multiple-incidence autism families.
J Piven, P Palmer, R Landa, S Santangelo, D Jacobi, D Childress. Am J Med Genet 1997
175
13

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
13


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
12

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
12

The familial risk of autism.
Sven Sandin, Paul Lichtenstein, Ralf Kuja-Halkola, Henrik Larsson, Christina M Hultman, Abraham Reichenberg. JAMA 2014
497
12

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
11

Rapid quantitative assessment of autistic social impairment by classroom teachers.
John N Constantino, Patricia D Lavesser, Yi Zhang, Anna M Abbacchi, Teddi Gray, Richard D Todd. J Am Acad Child Adolesc Psychiatry 2007
88
12

Evidence for broader autism phenotype characteristics in parents from multiple-incidence autism families.
Raphael Bernier, Jennifer Gerdts, Jeff Munson, Geraldine Dawson, Annette Estes. Autism Res 2012
44
25

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
815
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
11

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
196
11

The broad autism phenotype questionnaire.
Robert S E Hurley, Molly Losh, Morgan Parlier, J Steven Reznick, Joseph Piven. J Autism Dev Disord 2007
254
10

Defining the broader, medium and narrow autism phenotype among parents using the Autism Spectrum Quotient (AQ).
Sally Wheelwright, Bonnie Auyeung, Carrie Allison, Simon Baron-Cohen. Mol Autism 2010
159
10

Infantile autism: a genetic study of 21 twin pairs.
S Folstein, M Rutter. J Child Psychol Psychiatry 1977
767
10

The familial aggregation of the lesser variant in biological and nonbiological relatives of PDD probands: a family history study.
P Szatmari, J E MacLean, M B Jones, S E Bryson, L Zwaigenbaum, G Bartolucci, W J Mahoney, L Tuff. J Child Psychol Psychiatry 2000
91
10

A genome-wide linkage and association scan reveals novel loci for autism.
Lauren A Weiss, Dan E Arking, Mark J Daly, Aravinda Chakravarti. Nature 2009
417
10

Quantitative autism traits in first degree relatives: evidence for the broader autism phenotype in fathers, but not in mothers and siblings.
Wouter De la Marche, Ilse Noens, Jan Luts, Evert Scholte, Sabine Van Huffel, Jean Steyaert. Autism 2012
27
37

Evidence that autistic traits show the same etiology in the general population and at the quantitative extremes (5%, 2.5%, and 1%).
Elise B Robinson, Karestan C Koenen, Marie C McCormick, Kerim Munir, Victoria Hallett, Francesca HappĂ©, Robert Plomin, Angelica Ronald. Arch Gen Psychiatry 2011
179
10

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
447
10

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
10

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
539
10

The role of de novo mutations in the genetics of autism spectrum disorders.
Michael Ronemus, Ivan Iossifov, Dan Levy, Michael Wigler. Nat Rev Genet 2014
204
10


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.