A citation-based method for searching scientific literature

Christian G Bouwkamp, Anneke J A Kievit, Sander Markx, Joseph I Friedman, Laura van Zutven, Rick van Minkelen, Terry Vrijenhoek, Bin Xu, Ineke Sterrenburg-van de Nieuwegiessen, Joris A Veltman, Vincenzo Bonifati, Steven A Kushner. Am J Psychiatry 2017
Times Cited: 9







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



Times Cited
  Times     Co-cited
Similarity


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
55


Psychiatric disorders from childhood to adulthood in 22q11.2 deletion syndrome: results from the International Consortium on Brain and Behavior in 22q11.2 Deletion Syndrome.
Maude Schneider, Martin Debbané, Anne S Bassett, Eva W C Chow, Wai Lun Alan Fung, Marianne van den Bree, Michael Owen, Kieran C Murphy, Maria Niarchou, Wendy R Kates,[...]. Am J Psychiatry 2014
386
33

Analysis of Intellectual Disability Copy Number Variants for Association With Schizophrenia.
Elliott Rees, Kimberley Kendall, Antonio F Pardiñas, Sophie E Legge, Andrew Pocklington, Valentina Escott-Price, James H MacCabe, David A Collier, Peter Holmans, Michael C O'Donovan,[...]. JAMA Psychiatry 2016
53
33

Neurodevelopmental risk copy number variants in adults with intellectual disabilities and comorbid psychiatric disorders.
Johan H Thygesen, Kate Wolfe, Andrew McQuillin, Marina Viñas-Jornet, Neus Baena, Nathalie Brison, Greet D'Haenens, Susanna Esteba-Castillo, Elisabeth Gabau, Núria Ribas-Vidal,[...]. Br J Psychiatry 2018
11
33

Rare Genome-Wide Copy Number Variation and Expression of Schizophrenia in 22q11.2 Deletion Syndrome.
Anne S Bassett, Chelsea Lowther, Daniele Merico, Gregory Costain, Eva W C Chow, Therese van Amelsvoort, Donna McDonald-McGinn, Raquel E Gur, Ann Swillen, Marianne Van den Bree,[...]. Am J Psychiatry 2017
40
22

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
22

Practical guidelines for managing adults with 22q11.2 deletion syndrome.
Wai Lun Alan Fung, Nancy J Butcher, Gregory Costain, Danielle M Andrade, Erik Boot, Eva W C Chow, Brian Chung, Cheryl Cytrynbaum, Hanna Faghfoury, Leona Fishman,[...]. Genet Med 2015
110
22

Schizophrenia and the neurodevelopmental continuum:evidence from genomics.
Michael J Owen, Michael C O'Donovan. World Psychiatry 2017
103
22

Missense variants in ATP1A3 and FXYD gene family are associated with childhood-onset schizophrenia.
Boris Chaumette, Vladimir Ferrafiat, Amirthagowri Ambalavanan, Alice Goldenberg, Alexandre Dionne-Laporte, Dan Spiegelman, Patrick A Dion, Priscille Gerardin, Claudine Laurent, David Cohen,[...]. Mol Psychiatry 2020
17
22

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
22

Analysis of copy number variations at 15 schizophrenia-associated loci.
Elliott Rees, James T R Walters, Lyudmila Georgieva, Anthony R Isles, Kimberly D Chambert, Alexander L Richards, Gerwyn Mahoney-Davies, Sophie E Legge, Jennifer L Moran, Steven A McCarroll,[...]. Br J Psychiatry 2014
218
22

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
22

High rate of disease-related copy number variations in childhood onset schizophrenia.
K Ahn, N Gotay, T M Andersen, A A Anvari, P Gochman, Y Lee, S Sanders, S Guha, A Darvasi, J T Glessner,[...]. Mol Psychiatry 2014
78
22

Developmental Delay, Treatment-Resistant Psychosis, and Early-Onset Dementia in a Man With 22q11 Deletion Syndrome and Huntington's Disease.
Martilias Farrell, Maya Lichtenstein, James J Crowley, Dawn M Filmyer, Gabriel Lázaro-Muñoz, Rita A Shaughnessy, Ian R Mackenzie, Veronica Hirsch-Reinshagen, Robert Stowe, James P Evans,[...]. Am J Psychiatry 2018
6
33

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
22


Targeted Treatment of Individuals With Psychosis Carrying a Copy Number Variant Containing a Genomic Triplication of the Glycine Decarboxylase Gene.
J Alexander Bodkin, Michael J Coleman, Laura J Godfrey, Claudia M B Carvalho, Charity J Morgan, Raymond F Suckow, Thea Anderson, Dost Öngür, Marc J Kaufman, Kathryn E Lewandowski,[...]. Biol Psychiatry 2019
15
22

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
22

High-resolution copy number variation analysis of schizophrenia in Japan.
I Kushima, B Aleksic, M Nakatochi, T Shimamura, T Shiino, A Yoshimi, H Kimura, Y Takasaki, C Wang, J Xing,[...]. Mol Psychiatry 2017
54
22

Genomic Disorders in Psychiatry-What Does the Clinician Need to Know?
Chelsea Lowther, Gregory Costain, Danielle A Baribeau, Anne S Bassett. Curr Psychiatry Rep 2017
18
22

21st-Century Genetics in Psychiatric Residency Training: How Do We Get There?
Aaron D Besterman, Daniel Moreno-De-Luca, John I Nurnberger. JAMA Psychiatry 2019
5
40

A copy number variation morbidity map of developmental delay.
Gregory M Cooper, Bradley P Coe, Santhosh Girirajan, Jill A Rosenfeld, Tiffany H Vu, Carl Baker, Charles Williams, Heather Stalker, Rizwan Hamid, Vickie Hannig,[...]. Nat Genet 2011
803
22

High Incidence of Copy Number Variants in Adults with Intellectual Disability and Co-morbid Psychiatric Disorders.
Marina Viñas-Jornet, Susanna Esteba-Castillo, Neus Baena, Núria Ribas-Vidal, Anna Ruiz, David Torrents-Rodas, Elisabeth Gabau, Elisabet Vilella, Lourdes Martorell, Lluís Armengol,[...]. Behav Genet 2018
7
28

Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies.
David T Miller, Margaret P Adam, Swaroop Aradhya, Leslie G Biesecker, Arthur R Brothman, Nigel P Carter, Deanna M Church, John A Crolla, Evan E Eichler, Charles J Epstein,[...]. Am J Hum Genet 2010
22

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
22

American College of Medical Genetics standards and guidelines for interpretation and reporting of postnatal constitutional copy number variants.
Hutton M Kearney, Erik C Thorland, Kerry K Brown, Fabiola Quintero-Rivera, Sarah T South. Genet Med 2011
513
22

Comparative mapping of the 22q11.2 deletion region and the potential of simple model organisms.
Alina Guna, Nancy J Butcher, Anne S Bassett. J Neurodev Disord 2015
50
11

Psychotic illness in patients diagnosed with velo-cardio-facial syndrome and their relatives.
A E Pulver, G Nestadt, R Goldberg, R J Shprintzen, M Lamacz, P S Wolyniec, B Morrow, M Karayiorgou, S E Antonarakis, D Housman. J Nerv Ment Dis 1994
337
11

22q11.2 microdeletions: linking DNA structural variation to brain dysfunction and schizophrenia.
Maria Karayiorgou, Tony J Simon, Joseph A Gogos. Nat Rev Neurosci 2010
297
11

The birth of a psychiatric orphan disorder: postpartum psychosis.
Arianna Di Florio, Trine Munk-Olsen, Veerle Bergink. Lancet Psychiatry 2016
5
20

Low-frequency and rare variants may contribute to elucidate the genetics of major depressive disorder.
Chenglong Yu, Mauricio Arcos-Burgos, Bernhard T Baune, Volker Arolt, Udo Dannlowski, Ma-Li Wong, Julio Licinio. Transl Psychiatry 2018
15
11

Adult Utilization of Psychiatric Drugs and Differences by Sex, Age, and Race.
Thomas J Moore, Donald R Mattison. JAMA Intern Med 2017
88
11


The global burden of mental disorders: an update from the WHO World Mental Health (WMH) surveys.
Ronald C Kessler, Sergio Aguilar-Gaxiola, Jordi Alonso, Somnath Chatterji, Sing Lee, Johan Ormel, T Bedirhan Ustün, Philip S Wang. Epidemiol Psichiatr Soc 2009
735
11

Identification of 15 genetic loci associated with risk of major depression in individuals of European descent.
Craig L Hyde, Michael W Nagle, Chao Tian, Xing Chen, Sara A Paciga, Jens R Wendland, Joyce Y Tung, David A Hinds, Roy H Perlis, Ashley R Winslow. Nat Genet 2016
313
11

Evidence for overlapping genetic influences on autistic and ADHD behaviours in a community twin sample.
Angelica Ronald, Emily Simonoff, Jonna Kuntsi, Philip Asherson, Robert Plomin. J Child Psychol Psychiatry 2008
255
11


The genetic architecture of type 2 diabetes.
Christian Fuchsberger, Jason Flannick, Tanya M Teslovich, Anubha Mahajan, Vineeta Agarwala, Kyle J Gaulton, Clement Ma, Pierre Fontanillas, Loukas Moutsianas, Davis J McCarthy,[...]. Nature 2016
543
11

Autistic traits in the general population: a twin study.
John N Constantino, Richard D Todd. Arch Gen Psychiatry 2003
696
11

Familial recurrence of autism spectrum disorder: evaluating genetic and environmental contributions.
Neil Risch, Thomas J Hoffmann, Meredith Anderson, Lisa A Croen, Judith K Grether, Gayle C Windham. Am J Psychiatry 2014
69
11

Psychiatric Genomics: An Update and an Agenda.
Patrick F Sullivan, Arpana Agrawal, Cynthia M Bulik, Ole A Andreassen, Anders D Børglum, Gerome Breen, Sven Cichon, Howard J Edenberg, Stephen V Faraone, Joel Gelernter,[...]. Am J Psychiatry 2018
209
11

The genetics of autism spectrum disorders and related neuropsychiatric disorders in childhood.
Paul Lichtenstein, Eva Carlström, Maria Råstam, Christopher Gillberg, Henrik Anckarsäter. Am J Psychiatry 2010
388
11


Genetic risk for attention-deficit/hyperactivity disorder contributes to neurodevelopmental traits in the general population.
Joanna Martin, Marian L Hamshere, Evangelia Stergiakouli, Michael C O'Donovan, Anita Thapar. Biol Psychiatry 2014
91
11



Adolescent outcomes of childhood attention-deficit/hyperactivity disorder in a diverse community sample.
Regina Bussing, Dana M Mason, Lindsay Bell, Phillip Porter, Cynthia Garvan. J Am Acad Child Adolesc Psychiatry 2010
111
11

Neurodevelopmental disorders.
Anita Thapar, Miriam Cooper, Michael Rutter. Lancet Psychiatry 2017
143
11

High loading of polygenic risk for ADHD in children with comorbid aggression.
Marian L Hamshere, Kate Langley, Joanna Martin, Sharifah Shameem Agha, Evangelia Stergiakouli, Richard J L Anney, Jan Buitelaar, Stephen V Faraone, Klaus-Peter Lesch, Benjamin M Neale,[...]. Am J Psychiatry 2013
85
11


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.