A citation-based method for searching scientific literature

Dina Vojinovic, Nathalie Brison, Shahzad Ahmad, Ilse Noens, Irene Pappa, Lennart C Karssen, Henning Tiemeier, Cornelia M van Duijn, Hilde Peeters, Najaf Amin. Eur J Hum Genet 2017
Times Cited: 2







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



Times Cited
  Times     Co-cited
Similarity


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
376
100

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
649
100

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
428
100

Common genetic variants on 1p13.2 associate with risk of autism.
K Xia, H Guo, Z Hu, G Xun, L Zuo, Y Peng, K Wang, Y He, Z Xiong, L Sun,[...]. Mol Psychiatry 2014
60
100

Autism Spectrum Disorder and Amplified Pain.
Ciaran Clarke. Case Rep Psychiatry 2015
24
50


Genome-wide association analyses of chronotype in 697,828 individuals provides insights into circadian rhythms.
Samuel E Jones, Jacqueline M Lane, Andrew R Wood, Vincent T van Hees, Jessica Tyrrell, Robin N Beaumont, Aaron R Jeffries, Hassan S Dashti, Melvyn Hillsdon, Katherine S Ruth,[...]. Nat Commun 2019
228
50

Evidence for shared genetic risk between methamphetamine-induced psychosis and schizophrenia.
Masashi Ikeda, Yuko Okahisa, Branko Aleksic, Mujun Won, Naoki Kondo, Nobuya Naruse, Kumi Aoyama-Uehara, Ichiro Sora, Masaomi Iyo, Ryota Hashimoto,[...]. Neuropsychopharmacology 2013
42
50

Association between a high-risk autism locus on 5p14 and social communication spectrum phenotypes in the general population.
Beate St Pourcain, Kai Wang, Joseph T Glessner, Jean Golding, Colin Steer, Susan M Ring, David H Skuse, Struan F A Grant, Hakon Hakonarson, George Davey Smith. Am J Psychiatry 2010
43
50

Genome-Wide Association Studies of the Human Gut Microbiota.
Emily R Davenport, Darren A Cusanovich, Katelyn Michelini, Luis B Barreiro, Carole Ober, Yoav Gilad. PLoS One 2015
153
50

Diagnostic exome sequencing provides a molecular diagnosis for a significant proportion of patients with epilepsy.
Katherine L Helbig, Kelly D Farwell Hagman, Deepali N Shinde, Cameron Mroske, Zöe Powis, Shuwei Li, Sha Tang, Ingo Helbig. Genet Med 2016
206
50

A combined analysis of genetically correlated traits identifies 187 loci and a role for neurogenesis and myelination in intelligence.
W D Hill, R E Marioni, O Maghzian, S J Ritchie, S P Hagenaars, A M McIntosh, C R Gale, G Davies, I J Deary. Mol Psychiatry 2019
123
50

Genome-wide association meta-analysis of neuropathologic features of Alzheimer's disease and related dementias.
Gary W Beecham, Kara Hamilton, Adam C Naj, Eden R Martin, Matt Huentelman, Amanda J Myers, Jason J Corneveaux, John Hardy, Jean-Paul Vonsattel, Steven G Younkin,[...]. PLoS Genet 2014
221
50


Depression and Anxiety Symptoms in Children and Adolescents with Autism Spectrum Disorders without Intellectual Disability.
John F Strang, Lauren Kenworthy, Peter Daniolos, Laura Case, Meagan C Wills, Alex Martin, Gregory L Wallace. Res Autism Spectr Disord 2012
130
50

Shared genetic influences between dimensional ASD and ADHD symptoms during child and adolescent development.
Evie Stergiakouli, George Davey Smith, Joanna Martin, David H Skuse, Wolfgang Viechtbauer, Susan M Ring, Angelica Ronald, David E Evans, Simon E Fisher, Anita Thapar,[...]. Mol Autism 2017
57
50



Aggressive behaviors and treatable risk factors of preschool children with autism spectrum disorder.
Chen Chen, Yi-Dong Shen, Guang-Lei Xun, Wei-Xiong Cai, Li-Juan Shi, Lu Xiao, Ren-Rong Wu, Jing-Ping Zhao, Jian-Jun Ou. Autism Res 2017
8
50

Variants in the 1q21 risk region are associated with a visual endophenotype of autism and schizophrenia.
P T Goodbourn, J M Bosten, G Bargary, R E Hogg, A J Lawrance-Owen, J D Mollon. Genes Brain Behav 2014
29
50

Associations Among Symptoms of Autism, Symptoms of Depression and Executive Functions in Children with High-Functioning Autism: A 2 Year Follow-Up Study.
Per Normann Andersen, Erik Winther Skogli, Kjell Tore Hovik, Jens Egeland, Merete Øie. J Autism Dev Disord 2015
22
50

Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function.
Gail Davies, Max Lam, Sarah E Harris, Joey W Trampush, Michelle Luciano, W David Hill, Saskia P Hagenaars, Stuart J Ritchie, Riccardo E Marioni, Chloe Fawns-Ritchie,[...]. Nat Commun 2018
260
50

Prevalence of Autism Spectrum Disorder Among US Children and Adolescents, 2014-2016.
Guifeng Xu, Lane Strathearn, Buyun Liu, Wei Bao. JAMA 2018
162
50

Genome-wide association study of depression phenotypes in UK Biobank identifies variants in excitatory synaptic pathways.
David M Howard, Mark J Adams, Masoud Shirali, Toni-Kim Clarke, Riccardo E Marioni, Gail Davies, Jonathan R I Coleman, Clara Alloza, Xueyi Shen, Miruna C Barbu,[...]. Nat Commun 2018
216
50

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
50


Genome-Wide Association Study of Loneliness Demonstrates a Role for Common Variation.
Jianjun Gao, Lea K Davis, Amy B Hart, Sandra Sanchez-Roige, Lide Han, John T Cacioppo, Abraham A Palmer. Neuropsychopharmacology 2017
48
50

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
50

Heightened brain response to pain anticipation in high-functioning adults with autism spectrum disorder.
Xiaosi Gu, Thomas J Zhou, Evdokia Anagnostou, Latha Soorya, Alexander Kolevzon, Patrick R Hof, Jin Fan. Eur J Neurosci 2018
19
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
98
50

Depression in persons with autism: implications for research and clinical care.
Mohammad Ghaziuddin, Neera Ghaziuddin, John Greden. J Autism Dev Disord 2002
235
50

KCNH2-3.1 expression impairs cognition and alters neuronal function in a model of molecular pathology associated with schizophrenia.
Gregory V Carr, Jingshan Chen, Feng Yang, Ming Ren, Peixiong Yuan, Qingjun Tian, Audrey Bebensee, Grace Y Zhang, Jing Du, Paul Glineburg,[...]. Mol Psychiatry 2016
19
50

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
242
50

Neuroscience. The emerging biology of autism spectrum disorders.
Matthew W State, Nenad Šestan. Science 2012
103
50

Genome-wide pharmacogenomic study of citalopram-induced side effects in STAR*D.
D E Adkins, S L Clark, K Åberg, J M Hettema, J Bukszár, J L McClay, R P Souza, E J C G van den Oord. Transl Psychiatry 2012
31
50

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
184
50

Family-based association analyses of imputed genotypes reveal genome-wide significant association of Alzheimer's disease with OSBPL6, PTPRG, and PDCL3.
C Herold, B V Hooli, K Mullin, T Liu, J T Roehr, M Mattheisen, A R Parrado, L Bertram, C Lange, R E Tanzi. Mol Psychiatry 2016
52
50

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
50

Association analysis in over 329,000 individuals identifies 116 independent variants influencing neuroticism.
Michelle Luciano, Saskia P Hagenaars, Gail Davies, W David Hill, Toni-Kim Clarke, Masoud Shirali, Sarah E Harris, Riccardo E Marioni, David C Liewald, Chloe Fawns-Ritchie,[...]. Nat Genet 2018
154
50

Autism genome-wide copy number variation reveals ubiquitin and neuronal genes.
Joseph T Glessner, Kai Wang, Guiqing Cai, Olena Korvatska, Cecilia E Kim, Shawn Wood, Haitao Zhang, Annette Estes, Camille W Brune, Jonathan P Bradfield,[...]. Nature 2009
971
50

A genome-wide scan for common alleles affecting risk for autism.
Richard Anney, Lambertus Klei, Dalila Pinto, Regina Regan, Judith Conroy, Tiago R Magalhaes, Catarina Correia, Brett S Abrahams, Nuala Sykes, Alistair T Pagnamenta,[...]. Hum Mol Genet 2010
418
50

GeneCards Version 3: the human gene integrator.
Marilyn Safran, Irina Dalah, Justin Alexander, Naomi Rosen, Tsippi Iny Stein, Michael Shmoish, Noam Nativ, Iris Bahir, Tirza Doniger, Hagit Krug,[...]. Database (Oxford) 2010
793
50

Genome-wide association study in a Swedish population yields support for greater CNV and MHC involvement in schizophrenia compared with bipolar disorder.
S E Bergen, C T O'Dushlaine, S Ripke, P H Lee, D M Ruderfer, S Akterin, J L Moran, K D Chambert, R E Handsaker, L Backlund,[...]. Mol Psychiatry 2012
169
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
261
50

A primate-specific, brain isoform of KCNH2 affects cortical physiology, cognition, neuronal repolarization and risk of schizophrenia.
Stephen J Huffaker, Jingshan Chen, Kristin K Nicodemus, Fabio Sambataro, Feng Yang, Venkata Mattay, Barbara K Lipska, Thomas M Hyde, Jian Song, Dan Rujescu,[...]. Nat Med 2009
190
50

Genome-wide copy number variation analysis in a Chinese autism spectrum disorder cohort.
Hui Guo, Yu Peng, Zhengmao Hu, Ying Li, Guanglei Xun, Jianjun Ou, Liangdan Sun, Zhimin Xiong, Yanling Liu, Tianyun Wang,[...]. Sci Rep 2017
34
50

Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals.
James J Lee, Robbee Wedow, Aysu Okbay, Edward Kong, Omeed Maghzian, Meghan Zacher, Tuan Anh Nguyen-Viet, Peter Bowers, Julia Sidorenko, Richard Karlsson Linnér,[...]. Nat Genet 2018
830
50

New evidences on the altered gut microbiota in autism spectrum disorders.
Francesco Strati, Duccio Cavalieri, Davide Albanese, Claudio De Felice, Claudio Donati, Joussef Hayek, Olivier Jousson, Silvia Leoncini, Daniela Renzi, Antonio Calabrò,[...]. Microbiome 2017
419
50

Genome-wide association study of schizophrenia in Ashkenazi Jews.
Fernando S Goes, John McGrath, Dimitrios Avramopoulos, Paula Wolyniec, Mehdi Pirooznia, Ingo Ruczinski, Gerald Nestadt, Eimear E Kenny, Vladimir Vacic, Inga Peters,[...]. Am J Med Genet B Neuropsychiatr Genet 2015
123
50

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
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.