A citation-based method for searching scientific literature

Matthew Jensen, Corrine Smolen, Santhosh Girirajan. J Med Genet 2020
Times Cited: 2







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



Times Cited
  Times     Co-cited
Similarity


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
50

Medicine. Brain disorders? Precisely.
Thomas R Insel, Bruce N Cuthbert. Science 2015
286
50

Rare variants in the genetic background modulate cognitive and developmental phenotypes in individuals carrying disease-associated variants.
Lucilla Pizzo, Matthew Jensen, Andrew Polyak, Jill A Rosenfeld, Katrin Mannik, Arjun Krishnan, Elizabeth McCready, Olivier Pichon, Cedric Le Caignec, Anke Van Dijck,[...]. Genet Med 2019
53
50

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
50

Mutations in HECW2 are associated with intellectual disability and epilepsy.
Jonatan Halvardson, Jin J Zhao, Ammar Zaghlool, Christian Wentzel, Patrik Georgii-Hemming, Else Månsson, Helena Ederth Sävmarker, Göran Brandberg, Cecilia Soussi Zander, Ann-Charlotte Thuresson,[...]. J Med Genet 2016
30
50

The reliability and validity of discrete and continuous measures of psychopathology: a quantitative review.
Kristian E Markon, Michael Chmielewski, Christopher J Miller. Psychol Bull 2011
224
50

Prevalence of intellectual disability: a meta-analysis of population-based studies.
Pallab K Maulik, Maya N Mascarenhas, Colin D Mathers, Tarun Dua, Shekhar Saxena. Res Dev Disabil 2011
560
50

The familial risk of autism.
Sven Sandin, Paul Lichtenstein, Ralf Kuja-Halkola, Henrik Larsson, Christina M Hultman, Abraham Reichenberg. JAMA 2014
482
50

Common alleles contribute to schizophrenia in CNV carriers.
K E Tansey, E Rees, D E Linden, S Ripke, K D Chambert, J L Moran, S A McCarroll, P Holmans, G Kirov, J Walters,[...]. Mol Psychiatry 2016
47
50

Social and non-social autism symptoms and trait domains are genetically dissociable.
Varun Warrier, Roberto Toro, Hyejung Won, Claire S Leblond, Freddy Cliquet, Richard Delorme, Ward De Witte, Janita Bralten, Bhismadev Chakrabarti, Anders D Børglum,[...]. Commun Biol 2019
16
50

Common genetic variants contribute to risk of rare severe neurodevelopmental disorders.
Mari E K Niemi, Hilary C Martin, Daniel L Rice, Giuseppe Gallone, Scott Gordon, Martin Kelemen, Kerrie McAloney, Jeremy McRae, Elizabeth J Radford, Sui Yu,[...]. Nature 2018
101
50


A shifting view of neurodevelopmental disability.
The Lancet Neurology. Lancet Neurol 2013
1
100

Autism spectrum disorder and attention deficit hyperactivity disorder have a similar burden of rare protein-truncating variants.
F Kyle Satterstrom, Raymond K Walters, Tarjinder Singh, Emilie M Wigdor, Francesco Lescai, Ditte Demontis, Jack A Kosmicki, Jakob Grove, Christine Stevens, Jonas Bybjerg-Grauholm,[...]. Nat Neurosci 2019
37
50

Measuring and Estimating the Effect Sizes of Copy Number Variants on General Intelligence in Community-Based Samples.
Guillaume Huguet, Catherine Schramm, Elise Douard, Lai Jiang, Aurélie Labbe, Frédérique Tihy, Géraldine Mathonnet, Sonia Nizard, Emmanuelle Lemyre, Alexandre Mathieu,[...]. JAMA Psychiatry 2018
36
50

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
50

State of the Field: Differentiating Intellectual Disability From Autism Spectrum Disorder.
Audrey Thurm, Cristan Farmer, Emma Salzman, Catherine Lord, Somer Bishop. Front Psychiatry 2019
32
50

Neurodevelopmental disease genes implicated by de novo mutation and copy number variation morbidity.
Bradley P Coe, Holly A F Stessman, Arvis Sulovari, Madeleine R Geisheker, Trygve E Bakken, Allison M Lake, Joseph D Dougherty, Ed S Lein, Fereydoun Hormozdiari, Raphael A Bernier,[...]. Nat Genet 2019
95
50

Meta-analysis and multidisciplinary consensus statement: exome sequencing is a first-tier clinical diagnostic test for individuals with neurodevelopmental disorders.
Siddharth Srivastava, Jamie A Love-Nichols, Kira A Dies, David H Ledbetter, Christa L Martin, Wendy K Chung, Helen V Firth, Thomas Frazier, Robin L Hansen, Lisa Prock,[...]. Genet Med 2019
98
50

Targeted sequencing identifies 91 neurodevelopmental-disorder risk genes with autism and developmental-disability biases.
Holly A F Stessman, Bo Xiong, Bradley P Coe, Tianyun Wang, Kendra Hoekzema, Michaela Fenckova, Malin Kvarnung, Jennifer Gerdts, Sandy Trinh, Nele Cosemans,[...]. Nat Genet 2017
219
50

A Cross-Disorder Method to Identify Novel Candidate Genes for Developmental Brain Disorders.
Andrea J Gonzalez-Mantilla, Andres Moreno-De-Luca, David H Ledbetter, Christa Lese Martin. JAMA Psychiatry 2016
59
50

Limited genetic covariance between autistic traits and intelligence: findings from a longitudinal twin study.
Rosa A Hoekstra, Francesca Happé, Simon Baron-Cohen, Angelica Ronald. Am J Med Genet B Neuropsychiatr Genet 2010
24
50

Quantifying the Impact of Rare and Ultra-rare Coding Variation across the Phenotypic Spectrum.
Andrea Ganna, F Kyle Satterstrom, Seyedeh M Zekavat, Indraniel Das, Mitja I Kurki, Claire Churchhouse, Jessica Alfoldi, Alicia R Martin, Aki S Havulinna, Andrea Byrnes,[...]. Am J Hum Genet 2018
39
50

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
50

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
78
50

Effect Sizes of Deletions and Duplications on Autism Risk Across the Genome.
Elise Douard, Abderrahim Zeribi, Catherine Schramm, Petra Tamer, Mor Absa Loum, Sabrina Nowak, Zohra Saci, Marie-Pier Lord, Borja Rodríguez-Herreros, Martineau Jean-Louis,[...]. Am J Psychiatry 2021
6
50



The Problem of Non-Shared Environment in Behavioral Genetics.
Oleg N Tikhodeyev, Оlga V Shcherbakova. Behav Genet 2019
10
50

The clinical presentation caused by truncating CHD8 variants.
Sofia Douzgou, Hui Wen Liang, Kay Metcalfe, Suresh Somarathi, Marc Tischkowitz, Wafik Mohamed, Usha Kini, Shane McKee, Laura Yates, Marta Bertoli,[...]. Clin Genet 2019
15
50

Genome sequencing identifies major causes of severe intellectual disability.
Christian Gilissen, Jayne Y Hehir-Kwa, Djie Tjwan Thung, Maartje van de Vorst, Bregje W M van Bon, Marjolein H Willemsen, Michael Kwint, Irene M Janssen, Alexander Hoischen, Annette Schenck,[...]. Nature 2014
619
50

Association of Genetic and Environmental Factors With Autism in a 5-Country Cohort.
Dan Bai, Benjamin Hon Kei Yip, Gayle C Windham, Andre Sourander, Richard Francis, Rinat Yoffe, Emma Glasson, Behrang Mahjani, Auli Suominen, Helen Leonard,[...]. JAMA Psychiatry 2019
98
50

Heterogeneity in clinical sequencing tests marketed for autism spectrum disorders.
Ny Hoang, Janet A Buchanan, Stephen W Scherer. NPJ Genom Med 2018
12
50


Molecular subtyping and improved treatment of neurodevelopmental disease.
Holly A F Stessman, Tychele N Turner, Evan E Eichler. Genome Med 2016
12
50


Meta-analysis of 2,104 trios provides support for 10 new genes for intellectual disability.
Stefan H Lelieveld, Margot R F Reijnders, Rolph Pfundt, Helger G Yntema, Erik-Jan Kamsteeg, Petra de Vries, Bert B A de Vries, Marjolein H Willemsen, Tjitske Kleefstra, Katharina Löhner,[...]. Nat Neurosci 2016
219
50


An autism-linked missense mutation in SHANK3 reveals the modularity of Shank3 function.
Li Wang, Kaifang Pang, Kihoon Han, Carolyn J Adamski, Wei Wang, Lingjie He, Jason K Lai, Vitaliy V Bondar, Joseph G Duman, Ronald Richman,[...]. Mol Psychiatry 2020
18
50

Getting to the Cores of Autism.
Lilia M Iakoucheva, Alysson R Muotri, Jonathan Sebat. Cell 2019
56
50

The diagnosis of mental disorders: the problem of reification.
Steven E Hyman. Annu Rev Clin Psychol 2010
380
50

Developmental brain dysfunction: revival and expansion of old concepts based on new genetic evidence.
Andres Moreno-De-Luca, Scott M Myers, Thomas D Challman, Daniel Moreno-De-Luca, David W Evans, David H Ledbetter. Lancet Neurol 2013
169
50

Inherited and multiple de novo mutations in autism/developmental delay risk genes suggest a multifactorial model.
Hui Guo, Tianyun Wang, Huidan Wu, Min Long, Bradley P Coe, Honghui Li, Guanglei Xun, Jianjun Ou, Biyuan Chen, Guiqin Duan,[...]. Mol Autism 2018
41
50

A framework for the investigation of rare genetic disorders in neuropsychiatry.
Stephan J Sanders, Mustafa Sahin, Joseph Hostyk, Audrey Thurm, Sebastien Jacquemont, Paul Avillach, Elise Douard, Christa L Martin, Meera E Modi, Andres Moreno-De-Luca,[...]. Nat Med 2019
28
50

Joint Contributions of Rare Copy Number Variants and Common SNPs to Risk for Schizophrenia.
Sarah E Bergen, Alexander Ploner, Daniel Howrigan, Michael C O'Donovan, Jordan W Smoller, Patrick F Sullivan, Jonathan Sebat, Benjamin Neale, Kenneth S Kendler. Am J Psychiatry 2019
41
50

Clashing Diagnostic Approaches: DSM-ICD Versus RDoC.
Scott O Lilienfeld, Michael T Treadway. Annu Rev Clin Psychol 2016
67
50

Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study.
Anita Rauch, Dagmar Wieczorek, Elisabeth Graf, Thomas Wieland, Sabine Endele, Thomas Schwarzmayr, Beate Albrecht, Deborah Bartholdi, Jasmin Beygo, Nataliya Di Donato,[...]. Lancet 2012
657
50


The role of parental cognitive, behavioral, and motor profiles in clinical variability in individuals with chromosome 16p11.2 deletions.
Andres Moreno-De-Luca, David W Evans, K B Boomer, Ellen Hanson, Raphael Bernier, Robin P Goin-Kochel, Scott M Myers, Thomas D Challman, Daniel Moreno-De-Luca, Mylissa M Slane,[...]. JAMA Psychiatry 2015
86
50

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
50


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.