A citation-based method for searching scientific literature

Rita Barone, Mariangela Gulisano, Renata Amore, Carla Domini, Maria Chiara Milana, Sabrina Giglio, Francesca Madia, Teresa Mattina, Antonino Casabona, Marco Fichera, Renata Rizzo. Int J Dev Neurosci 2020
Times Cited: 3

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

Times Cited
  Times     Co-cited

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

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

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

Molecular Diagnostic Yield of Chromosomal Microarray Analysis and Whole-Exome Sequencing in Children With Autism Spectrum Disorder.
Kristiina Tammimies, Christian R Marshall, Susan Walker, Gaganjot Kaur, Bhooma Thiruvahindrapuram, Anath C Lionel, Ryan K C Yuen, Mohammed Uddin, Wendy Roberts, Rosanna Weksberg,[...]. JAMA 2015

Prevalence of Autism Spectrum Disorder Among Children Aged 8 Years - Autism and Developmental Disabilities Monitoring Network, 11 Sites, United States, 2014.
Jon Baio, Lisa Wiggins, Deborah L Christensen, Matthew J Maenner, Julie Daniels, Zachary Warren, Margaret Kurzius-Spencer, Walter Zahorodny, Cordelia Robinson Rosenberg, Tiffany White,[...]. MMWR Surveill Summ 2018

Prevalence of Autism Spectrum Disorder Among Children Aged 8 Years - Autism and Developmental Disabilities Monitoring Network, 11 Sites, United States, 2016.
Matthew J Maenner, Kelly A Shaw, Jon Baio, Anita Washington, Mary Patrick, Monica DiRienzo, Deborah L Christensen, Lisa D Wiggins, Sydney Pettygrove, Jennifer G Andrews,[...]. MMWR Surveill Summ 2020

High density SNP association study of a major autism linkage region on chromosome 17.
Jennifer L Stone, Barry Merriman, Rita M Cantor, Daniel H Geschwind, Stanley F Nelson. Hum Mol Genet 2007

Epilepsy in autism is associated with intellectual disability and gender: evidence from a meta-analysis.
Claire Amiet, Isabelle Gourfinkel-An, Anissa Bouzamondo, Sylvie Tordjman, Michel Baulac, Philippe Lechat, Laurent Mottron, David Cohen. Biol Psychiatry 2008

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

Gender and age differences in the core triad of impairments in autism spectrum disorders: a systematic review and meta-analysis.
Patricia J M Van Wijngaarden-Cremers, Evelien van Eeten, Wouter B Groen, Patricia A Van Deurzen, Iris J Oosterling, Rutger Jan Van der Gaag. J Autism Dev Disord 2014

Next-generation sequencing of duplication CNVs reveals that most are tandem and some create fusion genes at breakpoints.
Scott Newman, Karen E Hermetz, Brooke Weckselblatt, M Katharine Rudd. Am J Hum Genet 2015

The social behavioral phenotype in boys and girls with an extra X chromosome (Klinefelter syndrome and Trisomy X): a comparison with autism spectrum disorder.
Sophie van Rijn, Lex Stockmann, Martine Borghgraef, Hilgo Bruining, Conny van Ravenswaaij-Arts, Lutgarde Govaerts, Kerstin Hansson, Hanna Swaab. J Autism Dev Disord 2014

Longitudinal comparison between male and female preschool children with autism spectrum disorder.
Valentina Postorino, Laura Maria Fatta, Lavinia De Peppo, Giulia Giovagnoli, Marco Armando, Stefano Vicari, Luigi Mazzone. J Autism Dev Disord 2015

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

Increased female autosomal burden of rare copy number variants in human populations and in autism families.
G Desachy, L A Croen, A R Torres, M Kharrazi, G N Delorenze, G C Windham, C K Yoshida, L A Weiss. Mol Psychiatry 2015

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

Xp22.3 interstitial deletion: a recognizable chromosomal abnormality encompassing VCX3A and STS genes in a patient with X-linked ichthyosis and mental retardation.
Hela Ben Khelifa, Najla Soyah, Inesse Ben-Abdallah-Bouhjar, Ryma Gritly, Damien Sanlaville, Hatem Elghezal, Ali Saad, Soumaya Mougou-Zerelli. Gene 2013

Autism spectrum disorders: sex differences in autistic behaviour domains and coexisting psychopathology.
Martin Holtmann, Sven Bölte, Fritz Poustka. Dev Med Child Neurol 2007

New gene discoveries highlight functional convergence in autism and related neurodevelopmental disorders.
Mariana Moyses-Oliveira, Rachita Yadav, Serkan Erdin, Michael E Talkowski. Curr Opin Genet Dev 2020

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

Development and validation of a CGH microarray for clinical cytogenetic diagnosis.
Sau W Cheung, Chad A Shaw, Wei Yu, Jiangzham Li, Zhishuo Ou, Ankita Patel, Svetlana A Yatsenko, Mitchell L Cooper, Patti Furman, Pawel Stankiewicz,[...]. Genet Med 2005

Autism, language and communication in children with sex chromosome trisomies.
Dorothy V M Bishop, Patricia A Jacobs, Katherine Lachlan, Diana Wellesley, Angela Barnicoat, Patricia A Boyd, Alan Fryer, Prisca Middlemiss, Sarah Smithson, Kay Metcalfe,[...]. Arch Dis Child 2011

Array-CGH Analysis in a Cohort of Phenotypically Well-Characterized Individuals with "Essential" Autism Spectrum Disorders.
Eleonora Napoli, Serena Russo, Laura Casula, Viola Alesi, Filomena Alessandra Amendola, Adriano Angioni, Antonio Novelli, Giovanni Valeri, Deny Menghini, Stefano Vicari. J Autism Dev Disord 2018

Gene expression in human brain implicates sexually dimorphic pathways in autism spectrum disorders.
Donna M Werling, Neelroop N Parikshak, Daniel H Geschwind. Nat Commun 2016

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

A higher mutational burden in females supports a "female protective model" in neurodevelopmental disorders.
Sébastien Jacquemont, Bradley P Coe, Micha Hersch, Michael H Duyzend, Niklas Krumm, Sven Bergmann, Jacques S Beckmann, Jill A Rosenfeld, Evan E Eichler. Am J Hum Genet 2014

Practice parameter for the assessment and treatment of children and adolescents with autism spectrum disorder.
Fred Volkmar, Matthew Siegel, Marc Woodbury-Smith, Bryan King, James McCracken, Matthew State. J Am Acad Child Adolesc Psychiatry 2014

De novo gene disruptions in children on the autistic spectrum.
Ivan Iossifov, Michael Ronemus, Dan Levy, Zihua Wang, Inessa Hakker, Julie Rosenbaum, Boris Yamrom, Yoon-Ha Lee, Giuseppe Narzisi, Anthony Leotta,[...]. Neuron 2012

A dual-mode single-molecule fluorescence assay for the detection of expanded CGG repeats in Fragile X syndrome.
Brian Cannon, Cynthia Pan, Liangjing Chen, Andrew G Hadd, Rick Russell. Mol Biotechnol 2013

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

16p13 microduplication without CREBBP involvement: Moving toward a phenotype delineation.
Claudia Ciaccio, Arianna Tucci, Giulietta Scuvera, Margherita Estienne, Susanna Esposito, Donatella Milani. Eur J Med Genet 2017

Pathogenic variants in USP7 cause a neurodevelopmental disorder with speech delays, altered behavior, and neurologic anomalies.
Michael D Fountain, David S Oleson, Megan E Rech, Lara Segebrecht, Jill V Hunter, John M McCarthy, Philip J Lupo, Manuel Holtgrewe, Rocio Moran, Jill A Rosenfeld,[...]. Genet Med 2019

Psychiatric disorders in children with 16p11.2 deletion and duplication.
Maria Niarchou, Samuel J R A Chawner, Joanne L Doherty, Anne M Maillard, Sébastien Jacquemont, Wendy K Chung, LeeAnne Green-Snyder, Raphael A Bernier, Robin P Goin-Kochel, Ellen Hanson,[...]. Transl Psychiatry 2019

The EU-AIMS Longitudinal European Autism Project (LEAP): clinical characterisation.
Tony Charman, Eva Loth, Julian Tillmann, Daisy Crawley, Caroline Wooldridge, David Goyard, Jumana Ahmad, Bonnie Auyeung, Sara Ambrosino, Tobias Banaschewski,[...]. Mol Autism 2017

E3 ligase Nedd4 promotes axon branching by downregulating PTEN.
Jovana Drinjakovic, Hosung Jung, Douglas S Campbell, Laure Strochlic, Asha Dwivedy, Christine E Holt. Neuron 2010

Pleiotropic Mechanisms Indicated for Sex Differences in Autism.
Ileena Mitra, Kathryn Tsang, Christine Ladd-Acosta, Lisa A Croen, Kimberly A Aldinger, Robert L Hendren, Michela Traglia, Alinoë Lavillaureix, Noah Zaitlen, Michael C Oldham,[...]. PLoS Genet 2016

Convergence of Sex Differences and the Neuroimmune System in Autism Spectrum Disorder.
Margaret M McCarthy, Christopher L Wright. Biol Psychiatry 2017

Early sex differences are not autism-specific: A Baby Siblings Research Consortium (BSRC) study.
Daniel S Messinger, Gregory S Young, Sara Jane Webb, Sally Ozonoff, Susan E Bryson, Alice Carter, Leslie Carver, Tony Charman, Katarzyna Chawarska, Suzanne Curtin,[...]. Mol Autism 2015

Sex differences in children with autism spectrum disorder identified within a high-risk infant cohort.
Lonnie Zwaigenbaum, Susan E Bryson, Peter Szatmari, Jessica Brian, Isabel M Smith, Wendy Roberts, Tracy Vaillancourt, Caroline Roncadin. J Autism Dev Disord 2012

Essential versus complex autism: definition of fundamental prognostic subtypes.
J H Miles, T N Takahashi, S Bagby, P K Sahota, D F Vaslow, C H Wang, R E Hillman, J E Farmer. Am J Med Genet A 2005

An integrated analysis of rare CNV and exome variation in Autism Spectrum Disorder using the Infinium PsychArray.
Elena Bacchelli, Cinzia Cameli, Marta Viggiano, Roberta Igliozzi, Alice Mancini, Raffaella Tancredi, Agatino Battaglia, Elena Maestrini. Sci Rep 2020

Genomic Deletion Involving the IMMP2L Gene in Two Cases of Autism Spectrum Disorder.
Federica Baldan, Chiara Gnan, Alessandra Franzoni, Lucia Ferino, Lorenzo Allegri, Nadia Passon, Giuseppe Damante. Cytogenet Genome Res 2018

Environmental risk factors and biomarkers for autism spectrum disorder: an umbrella review of the evidence.
Jong Yeob Kim, Min Ji Son, Chei Yun Son, Joaquim Radua, Michael Eisenhut, Florence Gressier, Ai Koyanagi, Andre F Carvalho, Brendon Stubbs, Marco Solmi,[...]. Lancet Psychiatry 2019

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.