A citation-based method for searching scientific literature

Kate Baker, Rory T Devine, Elise Ng-Cordell, F Lucy Raymond, Claire Hughes. Br J Psychiatry 2020
Times Cited: 7







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



Times Cited
  Times     Co-cited
Similarity


Sex/gender differences and autism: setting the scene for future research.
Meng-Chuan Lai, Michael V Lombardo, Bonnie Auyeung, Bhismadev Chakrabarti, Simon Baron-Cohen. J Am Acad Child Adolesc Psychiatry 2015
331
28

16p11.2 deletion and duplication: Characterizing neurologic phenotypes in a large clinically ascertained cohort.
Kyle J Steinman, Sarah J Spence, Melissa B Ramocki, Monica B Proud, Sudha K Kessler, Elysa J Marco, LeeAnne Green Snyder, Debra D'Angelo, Qixuan Chen, Wendy K Chung,[...]. Am J Med Genet A 2016
70
28

Defining the Effect of the 16p11.2 Duplication on Cognition, Behavior, and Medical Comorbidities.
Debra D'Angelo, Sébastien Lebon, Qixuan Chen, Sandra Martin-Brevet, LeeAnne Green Snyder, Loyse Hippolyte, Ellen Hanson, Anne M Maillard, W Andrew Faucett, Aurélien Macé,[...]. JAMA Psychiatry 2016
104
28

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
43
28

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
28

Mental health of parents of children with a developmental disability in British Columbia, Canada.
Sandra Maureen Marquis, Kimberlyn McGrail, Michael Hayes. J Epidemiol Community Health 2020
7
28

Global services and support for children with developmental delays and disabilities: Bridging research and policy gaps.
Pamela Y Collins, Beverly Pringle, Charlee Alexander, Gary L Darmstadt, Jody Heymann, Gillian Huebner, Vesna Kutlesic, Cheryl Polk, Lorraine Sherr, Andy Shih,[...]. PLoS Med 2017
20
28


Health coaching for parents of children with developmental disabilities: a systematic review.
Tatiana Ogourtsova, Maureen O'Donnell, Wagner De Souza Silva, Annette Majnemer. Dev Med Child Neurol 2019
10
28

Psychopathology in parents of children with autism spectrum disorder: A systematic review and meta-analysis of prevalence.
Alexandra Schnabel, George J Youssef, David J Hallford, Eliza J Hartley, Jane A McGillivray, Michelle Stewart, David Forbes, David W Austin. Autism 2020
13
28

Caregiving process and caregiver burden: conceptual models to guide research and practice.
Parminder Raina, Maureen O'Donnell, Heidi Schwellnus, Peter Rosenbaum, Gillian King, Jamie Brehaut, Dianne Russell, Marilyn Swinton, Susanne King, Micheline Wong,[...]. BMC Pediatr 2004
179
28


Fathers' contributions to the management of their child's long-term medical condition: a narrative review of the literature.
Veronica Swallow, Ann Macfadyen, Sheila J Santacroce, Heather Lambert. Health Expect 2012
54
28


Prenatal and Perinatal Factors Related to Autism, IQ, and Adaptive Functioning.
Kristin Perrone-McGovern, Stephanie Simon-Dack, Lindsay Niccolai. J Genet Psychol 2015
9
14

A recurrent 16p12.1 microdeletion supports a two-hit model for severe developmental delay.
Santhosh Girirajan, Jill A Rosenfeld, Gregory M Cooper, Francesca Antonacci, Priscillia Siswara, Andy Itsara, Laura Vives, Tom Walsh, Shane E McCarthy, Carl Baker,[...]. Nat Genet 2010
411
14

Genic intolerance to functional variation and the interpretation of personal genomes.
Slavé Petrovski, Quanli Wang, Erin L Heinzen, Andrew S Allen, David B Goldstein. PLoS Genet 2013
561
14

Examining and interpreting the female protective effect against autistic behavior.
Elise B Robinson, Paul Lichtenstein, Henrik Anckarsäter, Francesca Happé, Angelica Ronald. Proc Natl Acad Sci U S A 2013
193
14

Risk factors in autism: Thinking outside the brain.
Lauren Matelski, Judy Van de Water. J Autoimmun 2016
60
14


Impaired Gas Exchange at Birth and Risk of Intellectual Disability and Autism: A Meta-analysis.
Amirhossein Modabbernia, Josephine Mollon, Paolo Boffetta, Abraham Reichenberg. J Autism Dev Disord 2016
26
14

Modulation of mu attenuation to social stimuli in children and adults with 16p11.2 deletions and duplications.
Caitlin M Hudac, Anna Kresse, Benjamin Aaronson, Trent D DesChamps, Sara Jane Webb, Raphael A Bernier. J Neurodev Disord 2015
6
16

The cognitive and behavioral phenotype of the 16p11.2 deletion in a clinically ascertained population.
Ellen Hanson, Raphael Bernier, Ken Porche, Frank I Jackson, Robin P Goin-Kochel, LeeAnne Green Snyder, Anne V Snow, Arianne Stevens Wallace, Katherine L Campe, Yuan Zhang,[...]. Biol Psychiatry 2015
128
14

A general framework for estimating the relative pathogenicity of human genetic variants.
Martin Kircher, Daniela M Witten, Preti Jain, Brian J O'Roak, Gregory M Cooper, Jay Shendure. Nat Genet 2014
14

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
14

Perinatal and neonatal risk factors for autism: a comprehensive meta-analysis.
Hannah Gardener, Donna Spiegelman, Stephen L Buka. Pediatrics 2011
291
14

Narrowly versus broadly defined autism spectrum disorders: differences in pre- and perinatal risk factors.
Janne C Visser, Nanda Rommelse, Lianne Vink, Margo Schrieken, Iris J Oosterling, Rutger J van der Gaag, Jan K Buitelaar. J Autism Dev Disord 2013
32
14

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
14

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
14

Estimates of penetrance for recurrent pathogenic copy-number variations.
Jill A Rosenfeld, Bradley P Coe, Evan E Eichler, Howard Cuckle, Lisa G Shaffer. Genet Med 2013
184
14

Maternal infection during pregnancy and risk of autism spectrum disorders: A systematic review and meta-analysis.
Hai-Yin Jiang, Lian-Lian Xu, Li Shao, Rong-Man Xia, Zheng-He Yu, Zong-Xin Ling, Fan Yang, Min Deng, Bing Ruan. Brain Behav Immun 2016
130
14

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
250
14

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
601
14

The variant call format and VCFtools.
Petr Danecek, Adam Auton, Goncalo Abecasis, Cornelis A Albers, Eric Banks, Mark A DePristo, Robert E Handsaker, Gerton Lunter, Gabor T Marth, Stephen T Sherry,[...]. Bioinformatics 2011
14

Prenatal, perinatal, and neonatal risk factors of autism spectrum disorder.
Elizabeth Hisle-Gorman, Apryl Susi, Theophil Stokes, Gregory Gorman, Christine Erdie-Lalena, Cade M Nylund. Pediatr Res 2018
34
14

A 600 kb deletion syndrome at 16p11.2 leads to energy imbalance and neuropsychiatric disorders.
Flore Zufferey, Elliott H Sherr, Noam D Beckmann, Ellen Hanson, Anne M Maillard, Loyse Hippolyte, Aurélien Macé, Carina Ferrari, Zoltán Kutalik, Joris Andrieux,[...]. J Med Genet 2012
154
14

A Short Review on the Current Understanding of Autism Spectrum Disorders.
Hye Ran Park, Jae Meen Lee, Hyo Eun Moon, Dong Soo Lee, Bung-Nyun Kim, Jinhyun Kim, Dong Gyu Kim, Sun Ha Paek. Exp Neurobiol 2016
63
14

Prenatal risk factors for autism: comprehensive meta-analysis.
Hannah Gardener, Donna Spiegelman, Stephen L Buka. Br J Psychiatry 2009
331
14

Microduplications of 16p11.2 are associated with schizophrenia.
Shane E McCarthy, Vladimir Makarov, George Kirov, Anjene M Addington, Jon McClellan, Seungtai Yoon, Diana O Perkins, Diane E Dickel, Mary Kusenda, Olga Krastoshevsky,[...]. Nat Genet 2009
478
14

The penetrance of copy number variations for schizophrenia and developmental delay.
George Kirov, Elliott Rees, James T R Walters, Valentina Escott-Price, Lyudmila Georgieva, Alexander L Richards, Kimberly D Chambert, Gerwyn Davies, Sophie E Legge, Jennifer L Moran,[...]. Biol Psychiatry 2014
194
14


Recurrent 16p11.2 microdeletions in autism.
Ravinesh A Kumar, Samer KaraMohamed, Jyotsna Sudi, Donald F Conrad, Camille Brune, Judith A Badner, T Conrad Gilliam, Norma J Nowak, Edwin H Cook, William B Dobyns,[...]. Hum Mol Genet 2008
461
14

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
14

Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations.
Brian J O'Roak, Pelagia Deriziotis, Choli Lee, Laura Vives, Jerrod J Schwartz, Santhosh Girirajan, Emre Karakoc, Alexandra P Mackenzie, Sarah B Ng, Carl Baker,[...]. Nat Genet 2011
760
14

An assessment of sex bias in neurodevelopmental disorders.
Andrew Polyak, Jill A Rosenfeld, Santhosh Girirajan. Genome Med 2015
40
14

Maternal autoimmune diseases and the risk of autism spectrum disorders in offspring: A systematic review and meta-analysis.
Shao-Wei Chen, Xue-Shan Zhong, Li-Na Jiang, Xue-Yan Zheng, Yi-Quan Xiong, Shu-Juan Ma, Min Qiu, Shu-Ting Huo, Jing Ge, Qing Chen. Behav Brain Res 2016
72
14

Prenatal and perinatal risk factors and the clinical implications on autism spectrum disorder.
Yi-Ling Chien, Miao-Chun Chou, Wen-Jiun Chou, Yu-Yu Wu, Wen-Che Tsai, Yen-Nan Chiu, Susan Shur-Fen Gau. Autism 2019
11
14

ASD in females: are we overstating the gender difference in diagnosis?
Nicole L Kreiser, Susan W White. Clin Child Fam Psychol Rev 2014
83
14

Quantifying the Effects of 16p11.2 Copy Number Variants on Brain Structure: A Multisite Genetic-First Study.
Sandra Martin-Brevet, Borja Rodríguez-Herreros, Jared A Nielsen, Clara Moreau, Claudia Modenato, Anne M Maillard, Aurélie Pain, Sonia Richetin, Aia E Jønch, Abid Y Qureshi,[...]. Biol Psychiatry 2018
27
14

De novo mutations in moderate or severe intellectual disability.
Fadi F Hamdan, Myriam Srour, Jose-Mario Capo-Chichi, Hussein Daoud, Christina Nassif, Lysanne Patry, Christine Massicotte, Amirthagowri Ambalavanan, Dan Spiegelman, Ousmane Diallo,[...]. PLoS Genet 2014
224
14


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.