A citation-based method for searching scientific literature

Derek W Morris, Richard D Pearson, Paul Cormican, Elaine M Kenny, Colm T O'Dushlaine, Louis-Philippe Lemieux Perreault, Eleni Giannoulatou, Daniela Tropea, Brion S Maher, Brandon Wormley, Eric Kelleher, Ciara Fahey, Ines Molinos, Stefania Bellini, Matti Pirinen, Amy Strange, Colin Freeman, Dawn L Thiselton, Rachel L Elves, Regina Regan, Sean Ennis, Timothy G Dinan, Colm McDonald, Kieran C Murphy, Eadbhard O'Callaghan, John L Waddington, Dermot Walsh, Michael O'Donovan, Detelina Grozeva, Nick Craddock, Jennifer Stone, Ed Scolnick, Shaun Purcell, Pamela Sklar, Bradley Coe, Evan E Eichler, Roel Ophoff, Jacobine Buizer, Jin Szatkiewicz, Christina Hultman, Patrick Sullivan, Hugh Gurling, Andrew Mcquillin, David St Clair, Elliott Rees, George Kirov, James Walters, Douglas Blackwood, Mandy Johnstone, Gary Donohoe, Francis A O'Neill, Kenneth S Kendler, Michael Gill, Brien P Riley, Chris C A Spencer, Aiden Corvin. Hum Mol Genet 2014
Times Cited: 25







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



Times Cited
  Times     Co-cited
Similarity


Large recurrent microdeletions associated with schizophrenia.
Hreinn Stefansson, Dan Rujescu, Sven Cichon, Olli P H Pietiläinen, Andres Ingason, Stacy Steinberg, Ragnheidur Fossdal, Engilbert Sigurdsson, Thordur Sigmundsson, Jacobine E Buizer-Voskamp,[...]. Nature 2008
36



Copy number variants in schizophrenia: confirmation of five previous findings and new evidence for 3q29 microdeletions and VIPR2 duplications.
Douglas F Levinson, Jubao Duan, Sang Oh, Kai Wang, Alan R Sanders, Jianxin Shi, Nancy Zhang, Bryan J Mowry, Ann Olincy, Farooq Amin,[...]. Am J Psychiatry 2011
316
24

A polygenic burden of rare disruptive mutations in schizophrenia.
Shaun M Purcell, Jennifer L Moran, Menachem Fromer, Douglas Ruderfer, Nadia Solovieff, Panos Roussos, Colm O'Dushlaine, Kimberly Chambert, Sarah E Bergen, Anna Kähler,[...]. Nature 2014
875
24

De novo mutations in schizophrenia implicate synaptic networks.
Menachem Fromer, Andrew J Pocklington, David H Kavanagh, Hywel J Williams, Sarah Dwyer, Padhraig Gormley, Lyudmila Georgieva, Elliott Rees, Priit Palta, Douglas M Ruderfer,[...]. Nature 2014
955
24

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
24


CNV analysis in a large schizophrenia sample implicates deletions at 16p12.1 and SLC1A1 and duplications at 1p36.33 and CGNL1.
Elliott Rees, James T R Walters, Kimberly D Chambert, Colm O'Dushlaine, Jin Szatkiewicz, Alexander L Richards, Lyudmila Georgieva, Gerwyn Mahoney-Davies, Sophie E Legge, Jennifer L Moran,[...]. Hum Mol Genet 2014
54
20

New copy number variations in schizophrenia.
Chiara Magri, Emilio Sacchetti, Michele Traversa, Paolo Valsecchi, Rita Gardella, Cristian Bonvicini, Alessandra Minelli, Massimo Gennarelli, Sergio Barlati. PLoS One 2010
69
20

Genetic architectures of psychiatric disorders: the emerging picture and its implications.
Patrick F Sullivan, Mark J Daly, Michael O'Donovan. Nat Rev Genet 2012
709
20

A genome-wide CNV analysis of schizophrenia reveals a potential role for a multiple-hit model.
Danielle S Rudd, Michael Axelsen, Eric A Epping, Nancy C Andreasen, Thomas H Wassink. Am J Med Genet B Neuropsychiatr Genet 2014
19
26

Implication of a rare deletion at distal 16p11.2 in schizophrenia.
Saurav Guha, Elliott Rees, Ariel Darvasi, Dobril Ivanov, Masashi Ikeda, Sarah E Bergen, Patrik K Magnusson, Paul Cormican, Derek Morris, Michael Gill,[...]. JAMA Psychiatry 2013
49
20

Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia.
Tom Walsh, Jon M McClellan, Shane E McCarthy, Anjené M Addington, Sarah B Pierce, Greg M Cooper, Alex S Nord, Mary Kusenda, Dheeraj Malhotra, Abhishek Bhandari,[...]. Science 2008
20

Copy number variation in schizophrenia in Sweden.
J P Szatkiewicz, C O'Dushlaine, G Chen, K Chambert, J L Moran, B M Neale, M Fromer, D Ruderfer, S Akterin, S E Bergen,[...]. Mol Psychiatry 2014
159
20

De novo CNV analysis implicates specific abnormalities of postsynaptic signalling complexes in the pathogenesis of schizophrenia.
G Kirov, A J Pocklington, P Holmans, D Ivanov, M Ikeda, D Ruderfer, J Moran, K Chambert, D Toncheva, L Georgieva,[...]. Mol Psychiatry 2012
515
16


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
16

Microdeletions of 3q29 confer high risk for schizophrenia.
Jennifer Gladys Mulle, Anne F Dodd, John A McGrath, Paula S Wolyniec, Adele A Mitchell, Amol C Shetty, Nara L Sobreira, David Valle, M Katharine Rudd, Glen Satten,[...]. Am J Hum Genet 2010
158
16

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
16

Schizophrenia as a complex trait: evidence from a meta-analysis of twin studies.
Patrick F Sullivan, Kenneth S Kendler, Michael C Neale. Arch Gen Psychiatry 2003
16


Copy number variants in German patients with schizophrenia.
Lutz Priebe, Franziska Degenhardt, Jana Strohmaier, René Breuer, Stefan Herms, Stephanie H Witt, Per Hoffmann, Rebecca Kulbida, Manuel Mattheisen, Susanne Moebus,[...]. PLoS One 2013
19
21

Genome-wide Analysis of the Role of Copy Number Variation in Schizophrenia Risk in Chinese.
Zhiqiang Li, Jianhua Chen, Yifeng Xu, Qizhong Yi, Weidong Ji, Peng Wang, Jiawei Shen, Zhijian Song, Meng Wang, Ping Yang,[...]. Biol Psychiatry 2016
36
16

Copy number variation in schizophrenia in the Japanese population.
Masashi Ikeda, Branko Aleksic, George Kirov, Yoko Kinoshita, Yoshio Yamanouchi, Tsuyoshi Kitajima, Kunihiro Kawashima, Tomo Okochi, Taro Kishi, Irina Zaharieva,[...]. Biol Psychiatry 2010
89
16

Genome-wide analysis shows increased frequency of copy number variation deletions in Dutch schizophrenia patients.
Jacobine E Buizer-Voskamp, Jan-Willem Muntjewerff, Eric Strengman, Chiara Sabatti, Hreinn Stefansson, Jacob A S Vorstman, Roel A Ophoff. Biol Psychiatry 2011
52
16

Pathogenic rare copy number variants in community-based schizophrenia suggest a potential role for clinical microarrays.
Gregory Costain, Anath C Lionel, Daniele Merico, Pamela Forsythe, Kathryn Russell, Chelsea Lowther, Tracy Yuen, Janice Husted, Dimitri J Stavropoulos, Marsha Speevak,[...]. Hum Mol Genet 2013
83
16

Disruption of the neurexin 1 gene is associated with schizophrenia.
Dan Rujescu, Andres Ingason, Sven Cichon, Olli P H Pietiläinen, Michael R Barnes, Timothea Toulopoulou, Marco Picchioni, Evangelos Vassos, Ulrich Ettinger, Elvira Bramon,[...]. Hum Mol Genet 2009
334
16

Genome-wide association analysis identifies 13 new risk loci for schizophrenia.
Stephan Ripke, Colm O'Dushlaine, Kimberly Chambert, Jennifer L Moran, Anna K Kähler, Susanne Akterin, Sarah E Bergen, Ann L Collins, James J Crowley, Menachem Fromer,[...]. Nat Genet 2013
979
12

Duplications of the neuropeptide receptor gene VIPR2 confer significant risk for schizophrenia.
Vladimir Vacic, Shane McCarthy, Dheeraj Malhotra, Fiona Murray, Hsun-Hua Chou, Aine Peoples, Vladimir Makarov, Seungtai Yoon, Abhishek Bhandari, Roser Corominas,[...]. Nature 2011
232
12

Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs.
S Hong Lee, Stephan Ripke, Benjamin M Neale, Stephen V Faraone, Shaun M Purcell, Roy H Perlis, Bryan J Mowry, Anita Thapar, Michael E Goddard, John S Witte,[...]. Nat Genet 2013
12

De novo mutations in epileptic encephalopathies.
Andrew S Allen, Samuel F Berkovic, Patrick Cossette, Norman Delanty, Dennis Dlugos, Evan E Eichler, Michael P Epstein, Tracy Glauser, David B Goldstein, Yujun Han,[...]. Nature 2013
915
12

Functional impact of global rare copy number variation in autism spectrum disorders.
Dalila Pinto, Alistair T Pagnamenta, Lambertus Klei, Richard Anney, Daniele Merico, Regina Regan, Judith Conroy, Tiago R Magalhaes, Catarina Correia, Brett S Abrahams,[...]. Nature 2010
12


Recurrent rearrangements in synaptic and neurodevelopmental genes and shared biologic pathways in schizophrenia, autism, and mental retardation.
Audrey Guilmatre, Christèle Dubourg, Anne-Laure Mosca, Solenn Legallic, Alice Goldenberg, Valérie Drouin-Garraud, Valérie Layet, Antoine Rosier, Sylvain Briault, Frédérique Bonnet-Brilhault,[...]. Arch Gen Psychiatry 2009
302
12

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
12

Common variant at 16p11.2 conferring risk of psychosis.
S Steinberg, S de Jong, M Mattheisen, J Costas, D Demontis, S Jamain, O P H Pietiläinen, K Lin, S Papiol, J Huttenlocher,[...]. Mol Psychiatry 2014
66
12

Reduced dendritic spine density on cerebral cortical pyramidal neurons in schizophrenia.
L J Garey, W Y Ong, T S Patel, M Kanani, A Davis, A M Mortimer, T R Barnes, S R Hirsch. J Neurol Neurosurg Psychiatry 1998
463
12


Linkage of a neurophysiological deficit in schizophrenia to a chromosome 15 locus.
R Freedman, H Coon, M Myles-Worsley, A Orr-Urtreger, A Olincy, A Davis, M Polymeropoulos, J Holik, J Hopkins, M Hoff,[...]. Proc Natl Acad Sci U S A 1997
895
12


Analysis of copy number variations in brain DNA from patients with schizophrenia and other psychiatric disorders.
Tianzhang Ye, Barbara K Lipska, Ran Tao, Thomas M Hyde, Liqin Wang, Chao Li, Kwang H Choi, Richard E Straub, Joel E Kleinman, Daniel R Weinberger. Biol Psychiatry 2012
28
12

A recurrent 15q13.3 microdeletion syndrome associated with mental retardation and seizures.
Andrew J Sharp, Heather C Mefford, Kelly Li, Carl Baker, Cindy Skinner, Roger E Stevenson, Richard J Schroer, Francesca Novara, Manuela De Gregori, Roberto Ciccone,[...]. Nat Genet 2008
403
12

Rare copy number variants in neuropsychiatric disorders: Specific phenotype or not?
Maarten J Van Den Bossche, Mandy Johnstone, Mojca Strazisar, Benjamin S Pickard, Dirk Goossens, An-Sofie Lenaerts, Sonia De Zutter, Annelie Nordin, Karl-Fredrik Norrback, Julien Mendlewicz,[...]. Am J Med Genet B Neuropsychiatr Genet 2012
26
12

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
12

A role for p21-activated kinase 7 in the development of gastric cancer.
Jun Gu, Keqiang Li, Maolan Li, Xiangsong Wu, Lin Zhang, Qichen Ding, Wenguang Wu, Jiahua Yang, Jiasheng Mu, Hao Wen,[...]. FEBS J 2013
42
12

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
12

Cognitive Performance Among Carriers of Pathogenic Copy Number Variants: Analysis of 152,000 UK Biobank Subjects.
Kimberley M Kendall, Elliott Rees, Valentina Escott-Price, Mark Einon, Rhys Thomas, Jonathan Hewitt, Michael C O'Donovan, Michael J Owen, James T R Walters, George Kirov. Biol Psychiatry 2017
74
12

Synaptic, transcriptional and chromatin genes disrupted in autism.
Silvia De Rubeis, Xin He, Arthur P Goldberg, Christopher S Poultney, Kaitlin Samocha, A Erucment Cicek, Yan Kou, Li Liu, Menachem Fromer, Susan Walker,[...]. Nature 2014
12

CNVs in neuropsychiatric disorders.
George Kirov. Hum Mol Genet 2015
77
12


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.