A citation-based method for searching scientific literature

Samuel J R A Chawner, Joanne L Doherty, Richard J L Anney, Kevin M Antshel, Carrie E Bearden, Raphael Bernier, Wendy K Chung, Caitlin C Clements, Sarah R Curran, Goran Cuturilo, Ania M Fiksinski, Louise Gallagher, Robin P Goin-Kochel, Raquel E Gur, Ellen Hanson, Sebastien Jacquemont, Wendy R Kates, Leila Kushan, Anne M Maillard, Donna M McDonald-McGinn, Marina Mihaljevic, Judith S Miller, Hayley Moss, Milica Pejovic-Milovancevic, Robert T Schultz, LeeAnne Green-Snyder, Jacob A Vorstman, Tara L Wenger, Jeremy Hall, Michael J Owen, Marianne B M van den Bree. Am J Psychiatry 2021
Times Cited: 4







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



Times Cited
  Times     Co-cited
Similarity


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

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

Genotype-phenotype associations in children with copy number variants associated with high neuropsychiatric risk in the UK (IMAGINE-ID): a case-control cohort study.
Samuel J R A Chawner, Michael J Owen, Peter Holmans, F Lucy Raymond, David Skuse, Jeremy Hall, Marianne B M van den Bree. Lancet Psychiatry 2019
32
50

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
50

Reciprocal White Matter Changes Associated With Copy Number Variation at 15q11.2 BP1-BP2: A Diffusion Tensor Imaging Study.
Ana I Silva, Magnus O Ulfarsson, Hreinn Stefansson, Omar Gustafsson, G Bragi Walters, David E J Linden, Lawrence S Wilkinson, Mark Drakesmith, Michael J Owen, Jeremy Hall,[...]. Biol Psychiatry 2019
18
50

Association of Copy Number Variation of the 15q11.2 BP1-BP2 Region With Cortical and Subcortical Morphology and Cognition.
Dennis van der Meer, Ida E Sønderby, Tobias Kaufmann, G Bragi Walters, Abdel Abdellaoui, David Ames, Katrin Amunts, Micael Andersson, Nicola J Armstrong, Manon Bernard,[...]. JAMA Psychiatry 2020
20
50

Medical consequences of pathogenic CNVs in adults: analysis of the UK Biobank.
Karen Crawford, Matthew Bracher-Smith, David Owen, Kimberley M Kendall, Elliott Rees, Antonio F Pardiñas, Mark Einon, Valentina Escott-Price, James T R Walters, Michael C O'Donovan,[...]. J Med Genet 2019
38
50

CNVs conferring risk of autism or schizophrenia affect cognition in controls.
Hreinn Stefansson, Andreas Meyer-Lindenberg, Stacy Steinberg, Brynja Magnusdottir, Katrin Morgen, Sunna Arnarsdottir, Gyda Bjornsdottir, G Bragi Walters, Gudrun A Jonsdottir, Orla M Doyle,[...]. Nature 2014
371
50

Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects.
Christian R Marshall, Daniel P Howrigan, Daniele Merico, Bhooma Thiruvahindrapuram, Wenting Wu, Douglas S Greer, Danny Antaki, Aniket Shetty, Peter A Holmans, Dalila Pinto,[...]. Nat Genet 2017
398
50

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
50

Autism-like behaviours and germline transmission in transgenic monkeys overexpressing MeCP2.
Zhen Liu, Xiao Li, Jun-Tao Zhang, Yi-Jun Cai, Tian-Lin Cheng, Cheng Cheng, Yan Wang, Chen-Chen Zhang, Yan-Hong Nie, Zhi-Fang Chen,[...]. Nature 2016
141
25

Antibodies From Children With PANDAS Bind Specifically to Striatal Cholinergic Interneurons and Alter Their Activity.
Jian Xu, Rong-Jian Liu, Shaylyn Fahey, Luciana Frick, James Leckman, Flora Vaccarino, Ronald S Duman, Kyle Williams, Susan Swedo, Christopher Pittenger. Am J Psychiatry 2021
8
25

Harmonizing the Neurobiology and Treatment of Obsessive-Compulsive Disorder.
Wayne K Goodman, Eric A Storch, Sameer A Sheth. Am J Psychiatry 2021
4
25

Diagnostic Classification for Human Autism and Obsessive-Compulsive Disorder Based on Machine Learning From a Primate Genetic Model.
Yafeng Zhan, Jianze Wei, Jian Liang, Xiu Xu, Ran He, Trevor W Robbins, Zheng Wang. Am J Psychiatry 2021
5
25


Obsessive-compulsive disorder: an integrative genetic and neurobiological perspective.
David L Pauls, Amitai Abramovitch, Scott L Rauch, Daniel A Geller. Nat Rev Neurosci 2014
315
25

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
458
25

Genotype-Phenotype Predictions in Autism: Are We There Yet?
Elisabeth B Binder. Am J Psychiatry 2021
2
50

Can Transgenic Monkeys Help Us Innovate Transdiagnostic Therapies?
Odile A van den Heuvel. Am J Psychiatry 2021
1
100

PANDAS: Too Narrow a View of the Neuroimmune Landscape.
Steven E Hyman. Am J Psychiatry 2021
1
100

Obsessive-compulsive disorder.
Dan J Stein, Daniel L C Costa, Christine Lochner, Euripedes C Miguel, Y C Janardhan Reddy, Roseli G Shavitt, Odile A van den Heuvel, H Blair Simpson. Nat Rev Dis Primers 2019
60
25

Treatment-Specific Associations Between Brain Activation and Symptom Reduction in OCD Following CBT: A Randomized fMRI Trial.
Luke J Norman, Kristin A Mannella, Huan Yang, Mike Angstadt, James L Abelson, Joseph A Himle, Kate D Fitzgerald, Stephan F Taylor. Am J Psychiatry 2021
6
25

Autism Spectrum Disorder Genetics and the Search for Pathological Mechanisms.
Devanand S Manoli, Matthew W State. Am J Psychiatry 2021
4
25

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
25

Quantifying the polygenic contribution to variable expressivity in eleven rare genetic disorders.
M T Oetjens, M A Kelly, A C Sturm, C L Martin, D H Ledbetter. Nat Commun 2019
28
25

Insufficient Evidence for "Autism-Specific" Genes.
Scott M Myers, Thomas D Challman, Raphael Bernier, Thomas Bourgeron, Wendy K Chung, John N Constantino, Evan E Eichler, Sebastien Jacquemont, David T Miller, Kevin J Mitchell,[...]. Am J Hum Genet 2020
24
25

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
25

Getting to the Cores of Autism.
Lilia M Iakoucheva, Alysson R Muotri, Jonathan Sebat. Cell 2019
56
25

Autistic symptomatology and language ability in autism spectrum disorder and specific language impairment.
Tom Loucas, Tony Charman, Andrew Pickles, Emily Simonoff, Susie Chandler, David Meldrum, Gillian Baird. J Child Psychol Psychiatry 2008
85
25

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
25

Identification of common genetic risk variants for autism spectrum disorder.
Jakob Grove, Stephan Ripke, Thomas D Als, Manuel Mattheisen, Raymond K Walters, Hyejung Won, Jonatan Pallesen, Esben Agerbo, Ole A Andreassen, Richard Anney,[...]. Nat Genet 2019
437
25

Autism in children with 22q11.2 deletion syndrome.
Stephan Eliez. J Am Acad Child Adolesc Psychiatry 2007
26
25


European guidelines for constitutional cytogenomic analysis.
Marisa Silva, Nicole de Leeuw, Kathy Mann, Heleen Schuring-Blom, Sian Morgan, Daniela Giardino, Katrina Rack, Ros Hastings. Eur J Hum Genet 2019
31
25

22q11.2 deletion syndrome.
Donna M McDonald-McGinn, Kathleen E Sullivan, Bruno Marino, Nicole Philip, Ann Swillen, Jacob A S Vorstman, Elaine H Zackai, Beverly S Emanuel, Joris R Vermeesch, Bernice E Morrow,[...]. Nat Rev Dis Primers 2015
381
25

A common cognitive, psychiatric, and dysmorphic phenotype in carriers of NRXN1 deletion.
Marina Viñas-Jornet, Susanna Esteba-Castillo, Elisabeth Gabau, Núria Ribas-Vidal, Neus Baena, Joan San, Anna Ruiz, Maria Dolors Coll, Ramon Novell, Miriam Guitart. Mol Genet Genomic Med 2014
23
25

Psychiatric disorders in children with autism spectrum disorders: prevalence, comorbidity, and associated factors in a population-derived sample.
Emily Simonoff, Andrew Pickles, Tony Charman, Susie Chandler, Tom Loucas, Gillian Baird. J Am Acad Child Adolesc Psychiatry 2008
25

Prenatal and postnatal diagnosis of 22q11.2 deletion syndrome.
Florence Bretelle, Laura Beyer, Marie Christine Pellissier, Chantal Missirian, Sabine Sigaudy, Marc Gamerre, Claude D'Ercole, Nicole Philip. Eur J Med Genet 2010
31
25

Identifying schizophrenia patients who carry pathogenic genetic copy number variants using standard clinical assessment: retrospective cohort study.
Claire Foley, Elizabeth A Heron, Denise Harold, James Walters, Michael Owen, Michael O'Donovan, Jonathan Sebat, Eric Kelleher, Christina Mooney, Amy Durand,[...]. Br J Psychiatry 2020
3
33


22q11.2 duplication syndrome: elevated rate of autism spectrum disorder and need for medical screening.
Tara L Wenger, Judith S Miller, Lauren M DePolo, Ashley B de Marchena, Caitlin C Clements, Beverly S Emanuel, Elaine H Zackai, Donna M McDonald-McGinn, Robert T Schultz. Mol Autism 2016
40
25


Rare Copy Number Variations and Predictors in Children With Intellectual Disability and Epilepsy.
Miriam Kessi, Juan Xiong, Liwen Wu, Lifen Yang, Fang He, Chen Chen, Nan Pang, Haolin Duan, Wen Zhang, Ahmed Arafat,[...]. Front Neurol 2018
10
25

Education and employment trajectories from childhood to adulthood in individuals with 22q11.2 deletion syndrome.
Mariela Mosheva, Virginie Pouillard, Yael Fishman, Lydia Dubourg, Dafna Sofrin-Frumer, Yaffa Serur, Abraham Weizman, Stephan Eliez, Doron Gothelf, Maude Schneider. Eur Child Adolesc Psychiatry 2019
8
25

Identification of Neuropsychiatric Copy Number Variants in a Health Care System Population.
Christa Lese Martin, Karen E Wain, Matthew T Oetjens, Kasia Tolwinski, Emily Palen, Abby Hare-Harris, Lukas Habegger, Evan K Maxwell, Jeffrey G Reid, Lauren Kasparson Walsh,[...]. JAMA Psychiatry 2020
11
25

The psychiatric phenotypes of 1q21 distal deletion and duplication.
Stefanie C Linden, Cameron J Watson, Jacqueline Smith, Samuel J R A Chawner, Thomas M Lancaster, Ffion Evans, Nigel Williams, David Skuse, F Lucy Raymond, Jeremy Hall,[...]. Transl Psychiatry 2021
1
100

The 15q11.2 BP1-BP2 microdeletion syndrome: a review.
Devin M Cox, Merlin G Butler. Int J Mol Sci 2015
94
25



Predicting Cognition and Psychosis in Young Adults With 22q11.2 Deletion Syndrome.
Kevin M Antshel, Wanda Fremont, Seetha Ramanathan, Wendy R Kates. Schizophr Bull 2017
21
25


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.