A citation-based method for searching scientific literature

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, Steven A McCarroll, Michael C O'Donovan, Michael J Owen. Biol Psychiatry 2014
Times Cited: 190







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



Times Cited
  Times     Co-cited
Similarity


Microdeletion 15q13.3: a locus with incomplete penetrance for autism, mental retardation, and psychiatric disorders.
S Ben-Shachar, B Lanpher, J R German, M Qasaymeh, L Potocki, S C Sreenath Nagamani, L M Franco, A Malphrus, G W Bottenfield, J E Spence,[...]. J Med Genet 2009
158
6

15q11.2 CNV affects cognitive, structural and functional correlates of dyslexia and dyscalculia.
M O Ulfarsson, G B Walters, O Gustafsson, S Steinberg, A Silva, O M Doyle, M Brammer, D F Gudbjartsson, S Arnarsdottir, G A Jonsdottir,[...]. Transl Psychiatry 2017
36
16

Rare variants in the genetic background modulate cognitive and developmental phenotypes in individuals carrying disease-associated variants.
Lucilla Pizzo, Matthew Jensen, Andrew Polyak, Jill A Rosenfeld, Katrin Mannik, Arjun Krishnan, Elizabeth McCready, Olivier Pichon, Cedric Le Caignec, Anke Van Dijck,[...]. Genet Med 2019
50
12

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
124
6

Refining the role of de novo protein-truncating variants in neurodevelopmental disorders by using population reference samples.
Jack A Kosmicki, Kaitlin E Samocha, Daniel P Howrigan, Stephan J Sanders, Kamil Slowikowski, Monkol Lek, Konrad J Karczewski, David J Cutler, Bernie Devlin, Kathryn Roeder,[...]. Nat Genet 2017
146
6

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
23
26

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
9
66

Can Animal Models of Copy Number Variants That Predispose to Schizophrenia Elucidate Underlying Biology?
Annika Forsingdal, Trine Nygaard Jørgensen, Line Olsen, Thomas Werge, Michael Didriksen, Jacob Nielsen. Biol Psychiatry 2019
13
46

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
7

Prevalence of rearrangements in the 22q11.2 region and population-based risk of neuropsychiatric and developmental disorders in a Danish population: a case-cohort study.
Line Olsen, Thomas Sparsø, Shantel M Weinsheimer, Marcelo Bertalan Quintanilha Dos Santos, Wiktor Mazin, Anders Rosengren, Xabier Calle Sanchez, Louise K Hoeffding, Henriette Schmock, Marie Baekvad-Hansen,[...]. Lancet Psychiatry 2018
35
17

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
94
6

Schizophrenia-associated genomic copy number variants and subcortical brain volumes in the UK Biobank.
Anthony Warland, Kimberley M Kendall, Elliott Rees, George Kirov, Xavier Caseras. Mol Psychiatry 2020
23
26

Association of Rare Copy Number Variants With Risk of Depression.
Kimberley Marie Kendall, Elliott Rees, Matthew Bracher-Smith, Sophie Legge, Lucy Riglin, Stanley Zammit, Michael Conlon O'Donovan, Michael John Owen, Ian Jones, George Kirov,[...]. JAMA Psychiatry 2019
23
26

De novo mutations in schizophrenia implicate chromatin remodeling and support a genetic overlap with autism and intellectual disability.
S E McCarthy, J Gillis, M Kramer, J Lihm, S Yoon, Y Berstein, M Mistry, P Pavlidis, R Solomon, E Ghiban,[...]. Mol Psychiatry 2014
226
5

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
199
5

Neurocognitive development in 22q11.2 deletion syndrome: comparison with youth having developmental delay and medical comorbidities.
R E Gur, J J Yi, D M McDonald-McGinn, S X Tang, M E Calkins, D Whinna, M C Souders, A Savitt, E H Zackai, P J Moberg,[...]. Mol Psychiatry 2014
57
8

Reciprocal Effects on Neurocognitive and Metabolic Phenotypes in Mouse Models of 16p11.2 Deletion and Duplication Syndromes.
Thomas Arbogast, Abdel-Mouttalib Ouagazzal, Claire Chevalier, Maksym Kopanitsa, Nurudeen Afinowi, Eugenia Migliavacca, Belinda S Cowling, Marie-Christine Birling, Marie-France Champy, Alexandre Reymond,[...]. PLoS Genet 2016
54
9


The familial risk of autism.
Sven Sandin, Paul Lichtenstein, Ralf Kuja-Halkola, Henrik Larsson, Christina M Hultman, Abraham Reichenberg. JAMA 2014
470
5


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
917
5

Investigation of NRXN1 deletions: clinical and molecular characterization.
Mindy Preston Dabell, Jill A Rosenfeld, Patricia Bader, Luis F Escobar, Dima El-Khechen, Stephanie E Vallee, Mary Beth Palko Dinulos, Cynthia Curry, Jamie Fisher, Raymond Tervo,[...]. Am J Med Genet A 2013
69
7

Support for the involvement of large copy number variants in the pathogenesis of schizophrenia.
George Kirov, Detelina Grozeva, Nadine Norton, Dobril Ivanov, Kiran K Mantripragada, Peter Holmans, Nick Craddock, Michael J Owen, Michael C O'Donovan. Hum Mol Genet 2009
303
5

Schizophrenia.
Michael J Owen, Akira Sawa, Preben B Mortensen. Lancet 2016
561
5

Association Between Schizophrenia-Related Polygenic Liability and the Occurrence and Level of Mood-Incongruent Psychotic Symptoms in Bipolar Disorder.
Judith Allardyce, Ganna Leonenko, Marian Hamshere, Antonio F Pardiñas, Liz Forty, Sarah Knott, Katherine Gordon-Smith, David J Porteous, Caroline Haywood, Arianna Di Florio,[...]. JAMA Psychiatry 2018
43
11

Mapping 22q11.2 Gene Dosage Effects on Brain Morphometry.
Amy Lin, Christopher R K Ching, Ariana Vajdi, Daqiang Sun, Rachel K Jonas, Maria Jalbrzikowski, Leila Kushan-Wells, Laura Pacheco Hansen, Emma Krikorian, Boris Gutman,[...]. J Neurosci 2017
29
17

Psychopathology and cognition in children with 22q11.2 deletion syndrome.
Maria Niarchou, Stanley Zammit, Stephanie H M van Goozen, Anita Thapar, Hayley M Tierling, Michael J Owen, Marianne B M van den Bree. Br J Psychiatry 2014
47
10

Rare Copy Number Variants in NRXN1 and CNTN6 Increase Risk for Tourette Syndrome.
Alden Y Huang, Dongmei Yu, Lea K Davis, Jae Hoon Sul, Fotis Tsetsos, Vasily Ramensky, Ivette Zelaya, Eliana Marisa Ramos, Lisa Osiecki, Jason A Chen,[...]. Neuron 2017
68
7

Dosage-dependent phenotypes in models of 16p11.2 lesions found in autism.
Guy Horev, Jacob Ellegood, Jason P Lerch, Young-Eun E Son, Lakshmi Muthuswamy, Hannes Vogel, Abba M Krieger, Andreas Buja, R Mark Henkelman, Michael Wigler,[...]. Proc Natl Acad Sci U S A 2011
168
5

Genetic architecture of reciprocal CNVs.
Christelle Golzio, Nicholas Katsanis. Curr Opin Genet Dev 2013
32
15


Recurrent reciprocal 16p11.2 rearrangements associated with global developmental delay, behavioural problems, dysmorphism, epilepsy, and abnormal head size.
Marwan Shinawi, Pengfei Liu, Sung-Hae L Kang, Joseph Shen, John W Belmont, Daryl A Scott, Frank J Probst, William J Craigen, Brett H Graham, Amber Pursley,[...]. J Med Genet 2010
315
5

Heritability of Schizophrenia and Schizophrenia Spectrum Based on the Nationwide Danish Twin Register.
Rikke Hilker, Dorte Helenius, Birgitte Fagerlund, Axel Skytthe, Kaare Christensen, Thomas M Werge, Merete Nordentoft, Birte Glenthøj. Biol Psychiatry 2018
123
5

Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression.
Naomi R Wray, Stephan Ripke, Manuel Mattheisen, Maciej Trzaskowski, Enda M Byrne, Abdel Abdellaoui, Mark J Adams, Esben Agerbo, Tracy M Air, Till M F Andlauer,[...]. Nat Genet 2018
802
5

Autism Spectrum Disorder, Developmental and Psychiatric Features in 16p11.2 Duplication.
LeeAnne Green Snyder, Debra D'Angelo, Qixuan Chen, Raphael Bernier, Robin P Goin-Kochel, Arianne Stevens Wallace, Jennifer Gerdts, Stephen Kanne, Leandra Berry, Lisa Blaskey,[...]. J Autism Dev Disord 2016
27
18

The Database of Genomic Variants: a curated collection of structural variation in the human genome.
Jeffrey R MacDonald, Robert Ziman, Ryan K C Yuen, Lars Feuk, Stephen W Scherer. Nucleic Acids Res 2014
617
5

Copy number variations of chromosome 16p13.1 region associated with schizophrenia.
A Ingason, D Rujescu, S Cichon, E Sigurdsson, T Sigmundsson, O P H Pietiläinen, J E Buizer-Voskamp, E Strengman, C Francks, P Muglia,[...]. Mol Psychiatry 2011
178
5


A genotype-first approach to defining the subtypes of a complex disease.
Holly A Stessman, Raphael Bernier, Evan E Eichler. Cell 2014
132
5

Transcriptome-wide isoform-level dysregulation in ASD, schizophrenia, and bipolar disorder.
Michael J Gandal, Pan Zhang, Evi Hadjimichael, Rebecca L Walker, Chao Chen, Shuang Liu, Hyejung Won, Harm van Bakel, Merina Varghese, Yongjun Wang,[...]. Science 2018
265
5

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
5

Genetic identification of brain cell types underlying schizophrenia.
Nathan G Skene, Julien Bryois, Trygve E Bakken, Gerome Breen, James J Crowley, Héléna A Gaspar, Paola Giusti-Rodriguez, Rebecca D Hodge, Jeremy A Miller, Ana B Muñoz-Manchado,[...]. Nat Genet 2018
171
5

Duplication of the 15q11-q13 region: clinical and genetic study of 30 new cases.
Essam Al Ageeli, Séverine Drunat, Catherine Delanoë, Laurence Perrin, Clarisse Baumann, Yline Capri, Jennifer Fabre-Teste, Azzedine Aboura, Céline Dupont, Stéphane Auvin,[...]. Eur J Med Genet 2014
40
12

1q21.1 Microduplication expression in adults.
Alessia Dolcetti, Candice K Silversides, Christian R Marshall, Anath C Lionel, Dimitri J Stavropoulos, Stephen W Scherer, Anne S Bassett. Genet Med 2013
58
8


Attention-deficit hyperactivity disorder shares copy number variant risk with schizophrenia and autism spectrum disorder.
Olafur O Gudmundsson, G Bragi Walters, Andres Ingason, Stefan Johansson, Tetyana Zayats, Lavinia Athanasiu, Ida Elken Sonderby, Omar Gustafsson, Muhammad S Nawaz, Gudbjorn F Jonsson,[...]. Transl Psychiatry 2019
17
29

Phenotypic variability and genetic susceptibility to genomic disorders.
Santhosh Girirajan, Evan E Eichler. Hum Mol Genet 2010
182
4

Premorbid IQ in schizophrenia: a meta-analytic review.
Kristen A Woodberry, Anthony J Giuliano, Larry J Seidman. Am J Psychiatry 2008
344
4

Tbx1: identification of a 22q11.2 gene as a risk factor for autism spectrum disorder in a mouse model.
Takeshi Hiramoto, Gina Kang, Go Suzuki, Yasushi Satoh, Raju Kucherlapati, Yasuhiro Watanabe, Noboru Hiroi. Hum Mol Genet 2011
53
7

Static and dynamic cognitive deficits in childhood preceding adult schizophrenia: a 30-year study.
Abraham Reichenberg, Avshalom Caspi, Honalee Harrington, Renate Houts, Richard S E Keefe, Robin M Murray, Richie Poulton, Terrie E Moffitt. Am J Psychiatry 2010
311
4


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.