A citation-based method for searching scientific literature

M Y M Ng, D F Levinson, S V Faraone, B K Suarez, L E DeLisi, T Arinami, B Riley, T Paunio, A E Pulver, Irmansyah, P A Holmans, M Escamilla, D B Wildenauer, N M Williams, C Laurent, B J Mowry, L M Brzustowicz, M Maziade, P Sklar, D L Garver, G R Abecasis, B Lerer, M D Fallin, H M D Gurling, P V Gejman, E Lindholm, H W Moises, W Byerley, E M Wijsman, P Forabosco, M T Tsuang, H-G Hwu, Y Okazaki, K S Kendler, B Wormley, A Fanous, D Walsh, F A O'Neill, L Peltonen, G Nestadt, V K Lasseter, K Y Liang, G M Papadimitriou, D G Dikeos, S G Schwab, M J Owen, M C O'Donovan, N Norton, E Hare, H Raventos, H Nicolini, M Albus, W Maier, V L Nimgaonkar, L Terenius, J Mallet, M Jay, S Godard, D Nertney, M Alexander, R R Crowe, J M Silverman, A S Bassett, M-A Roy, C Mérette, C N Pato, M T Pato, J Louw Roos, Y Kohn, D Amann-Zalcenstein, G Kalsi, A McQuillin, D Curtis, J Brynjolfson, T Sigmundsson, H Petursson, A R Sanders, J Duan, E Jazin, M Myles-Worsley, M Karayiorgou, C M Lewis. Mol Psychiatry 2009
Times Cited: 173







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



Times Cited
  Times     Co-cited
Similarity


Common polygenic variation contributes to risk of schizophrenia and bipolar disorder.
Shaun M Purcell, Naomi R Wray, Jennifer L Stone, Peter M Visscher, Michael C O'Donovan, Patrick F Sullivan, Pamela Sklar. Nature 2009
50

Common variants conferring risk of schizophrenia.
Hreinn Stefansson, Roel A Ophoff, Stacy Steinberg, Ole A Andreassen, Sven Cichon, Dan Rujescu, Thomas Werge, Olli P H Pietiläinen, Ole Mors, Preben B Mortensen,[...]. Nature 2009
41


Genome scan meta-analysis of schizophrenia and bipolar disorder, part II: Schizophrenia.
Cathryn M Lewis, Douglas F Levinson, Lesley H Wise, Lynn E DeLisi, Richard E Straub, Iiris Hovatta, Nigel M Williams, Sibylle G Schwab, Ann E Pulver, Stephen V Faraone,[...]. Am J Hum Genet 2003
878
33

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
33


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
27

Common variants on chromosome 6p22.1 are associated with schizophrenia.
Jianxin Shi, Douglas F Levinson, Jubao Duan, Alan R Sanders, Yonglan Zheng, Itsik Pe'er, Frank Dudbridge, Peter A Holmans, Alice S Whittemore, Bryan J Mowry,[...]. Nature 2009
822
25

Systematic meta-analyses and field synopsis of genetic association studies in schizophrenia: the SzGene database.
Nicole C Allen, Sachin Bagade, Matthew B McQueen, John P A Ioannidis, Fotini K Kavvoura, Muin J Khoury, Rudolph E Tanzi, Lars Bertram. Nat Genet 2008
785
24

Identification of loci associated with schizophrenia by genome-wide association and follow-up.
Michael C O'Donovan, Nicholas Craddock, Nadine Norton, Hywel Williams, Timothy Peirce, Valentina Moskvina, Ivan Nikolov, Marian Hamshere, Liam Carroll, Lyudmila Georgieva,[...]. Nat Genet 2008
810
22

Common genetic determinants of schizophrenia and bipolar disorder in Swedish families: a population-based study.
Paul Lichtenstein, Benjamin H Yip, Camilla Björk, Yudi Pawitan, Tyrone D Cannon, Patrick F Sullivan, Christina M Hultman. Lancet 2009
19


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
17

Common variants on 8p12 and 1q24.2 confer risk of schizophrenia.
Yongyong Shi, Zhiqiang Li, Qi Xu, Ti Wang, Tao Li, Jiawei Shen, Fengyu Zhang, Jianhua Chen, Guoquan Zhou, Weidong Ji,[...]. Nat Genet 2011
185
17

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
17

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
919
17

Haploview: analysis and visualization of LD and haplotype maps.
J C Barrett, B Fry, J Maller, M J Daly. Bioinformatics 2005
16

PLINK: a tool set for whole-genome association and population-based linkage analyses.
Shaun Purcell, Benjamin Neale, Kathe Todd-Brown, Lori Thomas, Manuel A R Ferreira, David Bender, Julian Maller, Pamela Sklar, Paul I W de Bakker, Mark J Daly,[...]. Am J Hum Genet 2007
16

Convergent functional genomics of schizophrenia: from comprehensive understanding to genetic risk prediction.
M Ayalew, H Le-Niculescu, D F Levey, N Jain, B Changala, S D Patel, E Winiger, A Breier, A Shekhar, R Amdur,[...]. Mol Psychiatry 2012
291
16


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
14

Genome-wide association study identifies a susceptibility locus for schizophrenia in Han Chinese at 11p11.2.
Wei-Hua Yue, Hai-Feng Wang, Liang-Dan Sun, Fu-Lei Tang, Zhong-Hua Liu, Hong-Xing Zhang, Wen-Qiang Li, Yan-Ling Zhang, Yang Zhang, Cui-Cui Ma,[...]. Nat Genet 2011
212
14

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
538
13

Strong association of de novo copy number mutations with sporadic schizophrenia.
Bin Xu, J Louw Roos, Shawn Levy, E J van Rensburg, Joseph A Gogos, Maria Karayiorgou. Nat Genet 2008
593
12

A systematic review of the prevalence of schizophrenia.
Sukanta Saha, David Chant, Joy Welham, John McGrath. PLoS Med 2005
12

Estimating the proportion of variation in susceptibility to schizophrenia captured by common SNPs.
S Hong Lee, Teresa R DeCandia, Stephan Ripke, Jian Yang, Patrick F Sullivan, Michael E Goddard, Matthew C Keller, Peter M Visscher, Naomi R Wray. Nat Genet 2012
394
12

Genetic architectures of psychiatric disorders: the emerging picture and its implications.
Patrick F Sullivan, Mark J Daly, Michael O'Donovan. Nat Rev Genet 2012
751
12

Disruption of two novel genes by a translocation co-segregating with schizophrenia.
J K Millar, J C Wilson-Annan, S Anderson, S Christie, M S Taylor, C A Semple, R S Devon, D M St Clair, W J Muir, D H Blackwood,[...]. Hum Mol Genet 2000
966
11

Schizophrenia: a common disease caused by multiple rare alleles.
Jon M McClellan, Ezra Susser, Mary-Claire King. Br J Psychiatry 2007
202
11


SZGR: a comprehensive schizophrenia gene resource.
P Jia, J Sun, A Y Guo, Z Zhao. Mol Psychiatry 2010
67
14

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
10

Neuregulin 1 and susceptibility to schizophrenia.
Hreinn Stefansson, Engilbert Sigurdsson, Valgerdur Steinthorsdottir, Soley Bjornsdottir, Thordur Sigmundsson, Shyamali Ghosh, Jon Brynjolfsson, Steinunn Gunnarsdottir, Omar Ivarsson, Thomas T Chou,[...]. Am J Hum Genet 2002
9

Association between genetic variation in a region on chromosome 11 and schizophrenia in large samples from Europe.
M Rietschel, M Mattheisen, F Degenhardt, T W Mühleisen, P Kirsch, C Esslinger, S Herms, D Demontis, M Steffens, J Strohmaier,[...]. Mol Psychiatry 2012
94
9

Common variants at VRK2 and TCF4 conferring risk of schizophrenia.
Stacy Steinberg, Simone de Jong, Ole A Andreassen, Thomas Werge, Anders D Børglum, Ole Mors, Preben B Mortensen, Omar Gustafsson, Javier Costas, Olli P H Pietiläinen,[...]. Hum Mol Genet 2011
154
9

Rethinking schizophrenia.
Thomas R Insel. Nature 2010
9

Genomewide association for schizophrenia in the CATIE study: results of stage 1.
P F Sullivan, D Lin, J-Y Tzeng, E van den Oord, D Perkins, T S Stroup, M Wagner, S Lee, F A Wright, F Zou,[...]. Mol Psychiatry 2008
277
9

Spatial and temporal mapping of de novo mutations in schizophrenia to a fetal prefrontal cortical network.
Suleyman Gulsuner, Tom Walsh, Amanda C Watts, Ming K Lee, Anne M Thornton, Silvia Casadei, Caitlin Rippey, Hashem Shahin, Vishwajit L Nimgaonkar, Rodney C P Go,[...]. Cell 2013
358
9

The structure of haplotype blocks in the human genome.
Stacey B Gabriel, Stephen F Schaffner, Huy Nguyen, Jamie M Moore, Jessica Roy, Brendan Blumenstiel, John Higgins, Matthew DeFelice, Amy Lochner, Maura Faggart,[...]. Science 2002
8

De novo gene mutations highlight patterns of genetic and neural complexity in schizophrenia.
Bin Xu, Iuliana Ionita-Laza, J Louw Roos, Braden Boone, Scarlet Woodrick, Yan Sun, Shawn Levy, Joseph A Gogos, Maria Karayiorgou. Nat Genet 2012
294
8

Genome-wide association identifies a common variant in the reelin gene that increases the risk of schizophrenia only in women.
Sagiv Shifman, Martina Johannesson, Michal Bronstein, Sam X Chen, David A Collier, Nicholas J Craddock, Kenneth S Kendler, Tao Li, Michael O'Donovan, F Anthony O'Neill,[...]. PLoS Genet 2008
248
8

Genome-wide significant associations in schizophrenia to ITIH3/4, CACNA1C and SDCCAG8, and extensive replication of associations reported by the Schizophrenia PGC.
M L Hamshere, J T R Walters, R Smith, A L Richards, E Green, D Grozeva, I Jones, L Forty, L Jones, K Gordon-Smith,[...]. Mol Psychiatry 2013
180
8

Genomewide linkage scan of schizophrenia in a large multicenter pedigree sample using single nucleotide polymorphisms.
P A Holmans, B Riley, A E Pulver, M J Owen, D B Wildenauer, P V Gejman, B J Mowry, C Laurent, K S Kendler, G Nestadt,[...]. Mol Psychiatry 2009
51
13

Neurexin 1 (NRXN1) deletions in schizophrenia.
George Kirov, Dan Rujescu, Andres Ingason, David A Collier, Michael C O'Donovan, Michael J Owen. Schizophr Bull 2009
165
7

The endophenotype concept in psychiatry: etymology and strategic intentions.
Irving I Gottesman, Todd D Gould. Am J Psychiatry 2003
7

Severe mental disorders in offspring with 2 psychiatrically ill parents.
Irving I Gottesman, Thomas Munk Laursen, Aksel Bertelsen, Preben Bo Mortensen. Arch Gen Psychiatry 2010
139
7

Converging evidence for a pseudoautosomal cytokine receptor gene locus in schizophrenia.
T Lencz, T V Morgan, M Athanasiou, B Dain, C R Reed, J M Kane, R Kucherlapati, A K Malhotra. Mol Psychiatry 2007
202
7


Spatio-temporal transcriptome of the human brain.
Hyo Jung Kang, Yuka Imamura Kawasawa, Feng Cheng, Ying Zhu, Xuming Xu, Mingfeng Li, André M M Sousa, Mihovil Pletikos, Kyle A Meyer, Goran Sedmak,[...]. Nature 2011
7

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
321
7


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.