A citation-based method for searching scientific literature

Xin Cai, Zhi-Hui Yang, Hui-Juan Li, Xiao Xiao, Ming Li, Hong Chang. Schizophr Bull 2021
Times Cited: 9







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



Times Cited
  Times     Co-cited
Similarity


A human-specific AS3MT isoform and BORCS7 are molecular risk factors in the 10q24.32 schizophrenia-associated locus.
Ming Li, Andrew E Jaffe, Richard E Straub, Ran Tao, Joo Heon Shin, Yanhong Wang, Qiang Chen, Chao Li, Yankai Jia, Kazutaka Ohi,[...]. Nat Med 2016
93
77

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
352
66

The genome-wide risk alleles for psychiatric disorders at 3p21.1 show convergent effects on mRNA expression, cognitive function, and mushroom dendritic spine.
Zhihui Yang, Danyang Zhou, Huijuan Li, Xin Cai, Weipeng Liu, Lu Wang, Hong Chang, Ming Li, Xiao Xiao. Mol Psychiatry 2020
23
66


Integration of summary data from GWAS and eQTL studies predicts complex trait gene targets.
Zhihong Zhu, Futao Zhang, Han Hu, Andrew Bakshi, Matthew R Robinson, Joseph E Powell, Grant W Montgomery, Michael E Goddard, Naomi R Wray, Peter M Visscher,[...]. Nat Genet 2016
689
55

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
424
44

The Role of Noncoding Variants in Heritable Disease.
J D French, S L Edwards. Trends Genet 2020
11
44

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
580
44

Gene expression elucidates functional impact of polygenic risk for schizophrenia.
Menachem Fromer, Panos Roussos, Solveig K Sieberts, Jessica S Johnson, David H Kavanagh, Thanneer M Perumal, Douglas M Ruderfer, Edwin C Oh, Aaron Topol, Hardik R Shah,[...]. Nat Neurosci 2016
480
44

Genetic Control of Expression and Splicing in Developing Human Brain Informs Disease Mechanisms.
Rebecca L Walker, Gokul Ramaswami, Christopher Hartl, Nicholas Mancuso, Michael J Gandal, Luis de la Torre-Ubieta, Bogdan Pasaniuc, Jason L Stein, Daniel H Geschwind. Cell 2019
50
44

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
935
33

Schizophrenia risk variants influence multiple classes of transcripts of sorting nexin 19 (SNX19).
Liang Ma, Stephen A Semick, Qiang Chen, Chao Li, Ran Tao, Amanda J Price, Joo Heon Shin, Yankai Jia, Nicholas J Brandon, Alan J Cross,[...]. Mol Psychiatry 2020
18
33

Dendritic structural plasticity and neuropsychiatric disease.
Marc P Forrest, Euan Parnell, Peter Penzes. Nat Rev Neurosci 2018
165
33

Dendritic spine pathology in neuropsychiatric disorders.
Peter Penzes, Michael E Cahill, Kelly A Jones, Jon-Eric VanLeeuwen, Kevin M Woolfrey. Nat Neurosci 2011
903
33

Integrative analysis of omics summary data reveals putative mechanisms underlying complex traits.
Yang Wu, Jian Zeng, Futao Zhang, Zhihong Zhu, Ting Qi, Zhili Zheng, Luke R Lloyd-Jones, Riccardo E Marioni, Nicholas G Martin, Grant W Montgomery,[...]. Nat Commun 2018
95
33

Identification of a functional 339 bp Alu insertion polymorphism in the schizophrenia-associated locus at 10q24.32.
Zhi-Hui Yang, Xin Cai, Na Qu, Li-Juan Zhao, Bao-Liang Zhong, Shu-Fang Zhang, Jing Chen, Bin Xia, Hong-Yan Jiang, Dan-Yang Zhou,[...]. Zool Res 2020
7
42

Genetic effects on gene expression across human tissues.
Alexis Battle, Christopher D Brown, Barbara E Engelhardt, Stephen B Montgomery. Nature 2017
33

Transcriptome-wide association study of schizophrenia and chromatin activity yields mechanistic disease insights.
Alexander Gusev, Nicholas Mancuso, Hyejung Won, Maria Kousi, Hilary K Finucane, Yakir Reshef, Lingyun Song, Alexias Safi, Steven McCarroll, Benjamin M Neale,[...]. Nat Genet 2018
166
33

Developmental and genetic regulation of the human cortex transcriptome illuminate schizophrenia pathogenesis.
Andrew E Jaffe, Richard E Straub, Joo Heon Shin, Ran Tao, Yuan Gao, Leonardo Collado-Torres, Tony Kam-Thong, Hualin S Xi, Jie Quan, Qiang Chen,[...]. Nat Neurosci 2018
137
33

Comparative genetic architectures of schizophrenia in East Asian and European populations.
Max Lam, Chia-Yen Chen, Zhiqiang Li, Alicia R Martin, Julien Bryois, Xixian Ma, Helena Gaspar, Masashi Ikeda, Beben Benyamin, Brielin C Brown,[...]. Nat Genet 2019
131
33

Functional Genomics Identify a Regulatory Risk Variation rs4420550 in the 16p11.2 Schizophrenia-Associated Locus.
Hong Chang, Xin Cai, Hui-Juan Li, Wei-Peng Liu, Li-Juan Zhao, Chu-Yi Zhang, Jun-Yang Wang, Jie-Wei Liu, Xiao-Lei Ma, Lu Wang,[...]. Biol Psychiatry 2021
5
60

CNNM2 mutations cause impaired brain development and seizures in patients with hypomagnesemia.
Francisco J Arjona, Jeroen H F de Baaij, Karl P Schlingmann, Anke L L Lameris, Erwin van Wijk, Gert Flik, Sabrina Regele, G Christoph Korenke, Birgit Neophytou, Stephan Rust,[...]. PLoS Genet 2014
72
33

limma powers differential expression analyses for RNA-sequencing and microarray studies.
Matthew E Ritchie, Belinda Phipson, Di Wu, Yifang Hu, Charity W Law, Wei Shi, Gordon K Smyth. Nucleic Acids Res 2015
22

Identification of a functional human-unique 351-bp Alu insertion polymorphism associated with major depressive disorder in the 1p31.1 GWAS risk loci.
Weipeng Liu, Wenqiang Li, Xin Cai, Zhihui Yang, Huijuan Li, Xi Su, Meng Song, Dong-Sheng Zhou, Xingxing Li, Chen Zhang,[...]. Neuropsychopharmacology 2020
7
28

Moderated estimation of fold change and dispersion for RNA-seq data with DESeq2.
Michael I Love, Wolfgang Huber, Simon Anders. Genome Biol 2014
22

Integrative analysis of 111 reference human epigenomes.
Anshul Kundaje, Wouter Meuleman, Jason Ernst, Misha Bilenky, Angela Yen, Alireza Heravi-Moussavi, Pouya Kheradpour, Zhizhuo Zhang, Jianrong Wang, Michael J Ziller,[...]. Nature 2015
22

Comprehensive functional genomic resource and integrative model for the human brain.
Daifeng Wang, Shuang Liu, Jonathan Warrell, Hyejung Won, Xu Shi, Fabio C P Navarro, Declan Clarke, Mengting Gu, Prashant Emani, Yucheng T Yang,[...]. Science 2018
243
22


Functional genomics reveal gene regulatory mechanisms underlying schizophrenia risk.
Yongxia Huo, Shiwu Li, Jiewei Liu, Xiaoyan Li, Xiong-Jian Luo. Nat Commun 2019
31
22


Identification of the primate-specific gene BTN3A2 as an additional schizophrenia risk gene in the MHC loci.
Yong Wu, Rui Bi, Chunhua Zeng, Changguo Ma, Chunli Sun, Jingzheng Li, Xiao Xiao, Ming Li, Deng-Feng Zhang, Ping Zheng,[...]. EBioMedicine 2019
15
22

A global reference for human genetic variation.
Adam Auton, Lisa D Brooks, Richard M Durbin, Erik P Garrison, Hyun Min Kang, Jan O Korbel, Jonathan L Marchini, Shane McCarthy, Gil A McVean, Gonçalo R Abecasis. Nature 2015
22

Chromosome conformation elucidates regulatory relationships in developing human brain.
Hyejung Won, Luis de la Torre-Ubieta, Jason L Stein, Neelroop N Parikshak, Jerry Huang, Carli K Opland, Michael J Gandal, Gavin J Sutton, Farhad Hormozdiari, Daning Lu,[...]. Nature 2016
258
22

Genetic insights and neurobiological implications from NRXN1 in neuropsychiatric disorders.
Zhonghua Hu, Xiao Xiao, Zhuohua Zhang, Ming Li. Mol Psychiatry 2019
27
22

SZDB2.0: an updated comprehensive resource for schizophrenia research.
Yong Wu, Xiaoyan Li, Jiewei Liu, Xiong-Jian Luo, Yong-Gang Yao. Hum Genet 2020
13
22

Synaptic loss in schizophrenia: a meta-analysis and systematic review of synaptic protein and mRNA measures.
Emanuele Felice Osimo, Katherine Beck, Tiago Reis Marques, Oliver D Howes. Mol Psychiatry 2019
68
22

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
22

Schizophrenia.
Stephen R Marder, Tyrone D Cannon. N Engl J Med 2019
78
22


Genetic insights into the neurodevelopmental origins of schizophrenia.
Rebecca Birnbaum, Daniel R Weinberger. Nat Rev Neurosci 2017
180
22


The Psychiatric Risk Gene NT5C2 Regulates Adenosine Monophosphate-Activated Protein Kinase Signaling and Protein Translation in Human Neural Progenitor Cells.
Rodrigo R R Duarte, Nathaniel D Bachtel, Marie-Caroline Côtel, Sang H Lee, Sashika Selvackadunco, Iain A Watson, Gary A Hovsepian, Claire Troakes, Gerome D Breen, Douglas F Nixon,[...]. Biol Psychiatry 2019
15
22

Mapping DNA methylation across development, genotype and schizophrenia in the human frontal cortex.
Andrew E Jaffe, Yuan Gao, Amy Deep-Soboslay, Ran Tao, Thomas M Hyde, Daniel R Weinberger, Joel E Kleinman. Nat Neurosci 2016
244
22

Sherlock: detecting gene-disease associations by matching patterns of expression QTL and GWAS.
Xin He, Chris K Fuller, Yi Song, Qingying Meng, Bin Zhang, Xia Yang, Hao Li. Am J Hum Genet 2013
140
22

Integrative approaches for large-scale transcriptome-wide association studies.
Alexander Gusev, Arthur Ko, Huwenbo Shi, Gaurav Bhatia, Wonil Chung, Brenda W J H Penninx, Rick Jansen, Eco J C de Geus, Dorret I Boomsma, Fred A Wright,[...]. Nat Genet 2016
598
22

Bayesian test for colocalisation between pairs of genetic association studies using summary statistics.
Claudia Giambartolomei, Damjan Vukcevic, Eric E Schadt, Lude Franke, Aroon D Hingorani, Chris Wallace, Vincent Plagnol. PLoS Genet 2014
615
22

CNNM2 homozygous mutations cause severe refractory hypomagnesemia, epileptic encephalopathy and brain malformations.
Andrea Accogli, Marcello Scala, Annalisa Calcagno, Flavia Napoli, Natascia Di Iorgi, Serena Arrigo, Maria Margherita Mancardi, Giulia Prato, Livia Pisciotta, Mato Nagel,[...]. Eur J Med Genet 2019
14
22

The polygenic architecture of schizophrenia - rethinking pathogenesis and nosology.
Olav B Smeland, Oleksandr Frei, Anders M Dale, Ole A Andreassen. Nat Rev Neurol 2020
29
22




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.