A citation-based method for searching scientific literature

Jianmin Yuan, Jianlin Hu, Zhiqiang Li, Fuquan Zhang, Dexiang Zhou, Chunhui Jin. Hereditas 2017
Times Cited: 4







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



Times Cited
  Times     Co-cited
Similarity


Microduplications of 16p11.2 are associated with schizophrenia.
Shane E McCarthy, Vladimir Makarov, George Kirov, Anjene M Addington, Jon McClellan, Seungtai Yoon, Diana O Perkins, Diane E Dickel, Mary Kusenda, Olga Krastoshevsky,[...]. Nat Genet 2009
478
75

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
298
75

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
50

Genome-wide association study identifies genetic variation in neurocan as a susceptibility factor for bipolar disorder.
Sven Cichon, Thomas W Mühleisen, Franziska A Degenhardt, Manuel Mattheisen, Xavier Miró, Jana Strohmaier, Michael Steffens, Christian Meesters, Stefan Herms, Moritz Weingarten,[...]. Am J Hum Genet 2011
191
50

Association at SYNE1 in both bipolar disorder and recurrent major depression.
E K Green, D Grozeva, L Forty, K Gordon-Smith, E Russell, A Farmer, M Hamshere, I R Jones, L Jones, P McGuffin,[...]. Mol Psychiatry 2013
62
50

Genome-wide association study reveals two new risk loci for bipolar disorder.
Thomas W Mühleisen, Markus Leber, Thomas G Schulze, Jana Strohmaier, Franziska Degenhardt, Jens Treutlein, Manuel Mattheisen, Andreas J Forstner, Johannes Schumacher, René Breuer,[...]. Nat Commun 2014
199
50

Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder.
Manuel A R Ferreira, Michael C O'Donovan, Yan A Meng, Ian R Jones, Douglas M Ruderfer, Lisa Jones, Jinbo Fan, George Kirov, Roy H Perlis, Elaine K Green,[...]. Nat Genet 2008
845
50


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
50

Meta-analysis of genome-wide association data identifies a risk locus for major mood disorders on 3p21.1.
Francis J McMahon, Nirmala Akula, Thomas G Schulze, Pierandrea Muglia, Federica Tozzi, Sevilla D Detera-Wadleigh, C J M Steele, René Breuer, Jana Strohmaier, Jens R Wendland,[...]. Nat Genet 2010
130
50

A genome-wide association study identifies two novel susceptibility loci and trans population polygenicity associated with bipolar disorder.
M Ikeda, A Takahashi, Y Kamatani, Y Okahisa, H Kunugi, N Mori, T Sasaki, T Ohmori, Y Okamoto, H Kawasaki,[...]. Mol Psychiatry 2018
70
50

Genome-wide association study meta-analysis of European and Asian-ancestry samples identifies three novel loci associated with bipolar disorder.
D T Chen, X Jiang, N Akula, Y Y Shugart, J R Wendland, C J M Steele, L Kassem, J-H Park, N Chatterjee, S Jamain,[...]. Mol Psychiatry 2013
134
50

Genome-wide association study of 40,000 individuals identifies two novel loci associated with bipolar disorder.
Liping Hou, Sarah E Bergen, Nirmala Akula, Jie Song, Christina M Hultman, Mikael Landén, Mazda Adli, Martin Alda, Raffaella Ardau, Bárbara Arias,[...]. Hum Mol Genet 2016
88
50

Polygenic dissection of diagnosis and clinical dimensions of bipolar disorder and schizophrenia.
Douglas M Ruderfer, Ayman H Fanous, Stephan Ripke, Andrew McQuillin, Richard L Amdur, Pablo V Gejman, Michael C O'Donovan, Ole A Andreassen, Srdjan Djurovic, Christina M Hultman,[...]. Mol Psychiatry 2014
209
50

Genome-wide association study of bipolar disorder in Canadian and UK populations corroborates disease loci including SYNE1 and CSMD1.
Wei Xu, Sarah Cohen-Woods, Qian Chen, Abdul Noor, Jo Knight, Georgina Hosang, Sagar V Parikh, Vincenzo De Luca, Federica Tozzi, Pierandrea Muglia,[...]. BMC Med Genet 2014
77
50

Genome-wide association study identifies 30 loci associated with bipolar disorder.
Eli A Stahl, Gerome Breen, Andreas J Forstner, Andrew McQuillin, Stephan Ripke, Vassily Trubetskoy, Manuel Mattheisen, Yunpeng Wang, Jonathan R I Coleman, Héléna A Gaspar,[...]. Nat Genet 2019
408
50

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
50

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
50

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
180
50

Rare and common variants at 16p11.2 are associated with schizophrenia.
Hong Chang, Lingyi Li, Ming Li, Xiao Xiao. Schizophr Res 2017
19
25

The association between rare large duplication of 16p11.2 and schizophrenia in the Singaporean Chinese population.
Xuebin Zheng, Jin-Xin Bei, Haiyan Xu, Jimmy Lee, Siow-Ann Chong, Kang Sim, Herty Liany, Tai E Shyong, Tian Liu, Jia Nee Foo,[...]. Schizophr Res 2013
9
25

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
128
25

Rapid detection of subtelomeric deletion/duplication by novel real-time quantitative PCR using SYBR-green dye.
Detlef Boehm, Sabine Herold, Alma Kuechler, Thomas Liehr, Franco Laccone. Hum Mutat 2004
63
25

Beyond GWASs: illuminating the dark road from association to function.
Stacey L Edwards, Jonathan Beesley, Juliet D French, Alison M Dunning. Am J Hum Genet 2013
412
25

Genetic risk between the CACNA1I gene and schizophrenia in Chinese Uygur population.
Wei Xu, Yahui Liu, Jianhua Chen, Qingli Guo, Ke Liu, Zujia Wen, Zhaowei Zhou, Zhijian Song, Juan Zhou, Lin He,[...]. Hereditas 2017
6
25

Further Evidence of an Association between NCAN rs1064395 and Bipolar Disorder.
Lu Wang, Weiqing Liu, Xingxing Li, Xiao Xiao, Lingyi Li, Fang Liu, Yuanfang He, Yan Bai, Hong Chang, Dong-Sheng Zhou,[...]. Mol Neuropsychiatry 2018
7
25

Genetics of bipolar disorder.
Nick Craddock, Pamela Sklar. Lancet 2013
286
25

Bipolar disorders.
Eduard Vieta, Michael Berk, Thomas G Schulze, André F Carvalho, Trisha Suppes, Joseph R Calabrese, Keming Gao, Kamilla W Miskowiak, Iria Grande. Nat Rev Dis Primers 2018
196
25

Bipolar disorder.
Iria Grande, Michael Berk, Boris Birmaher, Eduard Vieta. Lancet 2016
526
25

Haploview: analysis and visualization of LD and haplotype maps.
J C Barrett, B Fry, J Maller, M J Daly. Bioinformatics 2005
25

Genetic variants in the bipolar disorder risk locus SYNE1 that affect CPG2 expression and protein function.
Mette Rathje, Hannah Waxman, Marc Benoit, Prasad Tammineni, Costin Leu, Sven Loebrich, Elly Nedivi. Mol Psychiatry 2021
8
25

Association of genetic variation in CACNA1C with bipolar disorder in Han Chinese.
Xu Zhang, Chen Zhang, Zhiguo Wu, Zuowei Wang, Daihui Peng, Jun Chen, Wu Hong, Chengmei Yuan, Zezhi Li, Shunying Yu,[...]. J Affect Disord 2013
23
25

An integrated map of genetic variation from 1,092 human genomes.
Goncalo R Abecasis, Adam Auton, Lisa D Brooks, Mark A DePristo, Richard M Durbin, Robert E Handsaker, Hyun Min Kang, Gabor T Marth, Gil A McVean. Nature 2012
25


Common SNPs and haplotypes in DGKH are associated with bipolar disorder and schizophrenia in the Chinese Han population.
Z Zeng, T Wang, T Li, Y Li, P Chen, Q Zhao, J Liu, J Li, G Feng, L He,[...]. Mol Psychiatry 2011
39
25

A Genome-Wide Search for Bipolar Disorder Risk Loci Modified by Mitochondrial Genome Variation.
Euijung Ryu, Malik Nassan, Gregory D Jenkins, Sebastian M Armasu, Ana Andreazza, Susan L McElroy, Marquis P Vawter, Mark A Frye, Joanna M Biernacka. Mol Neuropsychiatry 2018
12
25


Genome-wide association study of bipolar I disorder in the Han Chinese population.
M T M Lee, C H Chen, C S Lee, C C Chen, M Y Chong, W C Ouyang, N Y Chiu, L J Chuo, C Y Chen, H K L Tan,[...]. Mol Psychiatry 2011
115
25

Replicated associations of FADS1, MAD1L1, and a rare variant at 10q26.13 with bipolar disorder in Chinese population.
Lijuan Zhao, Hong Chang, Dong-Sheng Zhou, Jun Cai, Weixing Fan, Wei Tang, Wenxin Tang, Xingxing Li, Weiqing Liu, Fang Liu,[...]. Transl Psychiatry 2018
12
25


A primate-specific, brain isoform of KCNH2 affects cortical physiology, cognition, neuronal repolarization and risk of schizophrenia.
Stephen J Huffaker, Jingshan Chen, Kristin K Nicodemus, Fabio Sambataro, Feng Yang, Venkata Mattay, Barbara K Lipska, Thomas M Hyde, Jian Song, Dan Rujescu,[...]. Nat Med 2009
180
25


Signals of recent positive selection in a worldwide sample of human populations.
Joseph K Pickrell, Graham Coop, John Novembre, Sridhar Kudaravalli, Jun Z Li, Devin Absher, Balaji S Srinivasan, Gregory S Barsh, Richard M Myers, Marcus W Feldman,[...]. Genome Res 2009
495
25

Patterns of cis regulatory variation in diverse human populations.
Barbara E Stranger, Stephen B Montgomery, Antigone S Dimas, Leopold Parts, Oliver Stegle, Catherine E Ingle, Magda Sekowska, George Davey Smith, David Evans, Maria Gutierrez-Arcelus,[...]. PLoS Genet 2012
330
25

Further evidence for the genetic association between CACNA1I and schizophrenia.
Yijun Xie, Di Huang, Li Wei, Xiong-Jian Luo. Hereditas 2018
7
25

Molecular and Genetic Characterization of Depression: Overlap with other Psychiatric Disorders and Aging.
Ying Ding, Lun-Ching Chang, Xingbin Wang, Jean-Philippe Guilloux, Jenna Parrish, Hyunjung Oh, Beverly J French, David A Lewis, George C Tseng, Etienne Sibille. Mol Neuropsychiatry 2015
36
25

Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection.
Antonio F Pardiñas, Peter Holmans, Andrew J Pocklington, Valentina Escott-Price, Stephan Ripke, Noa Carrera, Sophie E Legge, Sophie Bishop, Darren Cameron, Marian L Hamshere,[...]. Nat Genet 2018
506
25

VRK2, a Candidate Gene for Psychiatric and Neurological Disorders.
Ming Li, Weihua Yue. Mol Neuropsychiatry 2018
15
25

Genetic variants on 3q21 and in the Sp8 transcription factor gene (SP8) as susceptibility loci for psychotic disorders: a genetic association study.
Kenji Kondo, Masashi Ikeda, Yusuke Kajio, Takeo Saito, Yoshimi Iwayama, Branko Aleksic, Kazuo Yamada, Tomoko Toyota, Eiji Hattori, Hiroshi Ujike,[...]. PLoS One 2013
17
25

Allelic differences between Europeans and Chinese for CREB1 SNPs and their implications in gene expression regulation, hippocampal structure and function, and bipolar disorder susceptibility.
M Li, X-J Luo, M Rietschel, C M Lewis, M Mattheisen, B Müller-Myhsok, S Jamain, M Leboyer, M Landén, P M Thompson,[...]. Mol Psychiatry 2014
46
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.