A citation-based method for searching scientific literature

Ziqi Wang, Jishui Zhang, Tianlan Lu, Tian Zhang, Meixiang Jia, Yanyan Ruan, Dai Zhang, Jun Li, Lifang Wang. Prog Neuropsychopharmacol Biol Psychiatry 2019
Times Cited: 6







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



Times Cited
  Times     Co-cited
Similarity



Prevalence of Autism Spectrum Disorder Among Children Aged 8 Years - Autism and Developmental Disabilities Monitoring Network, 11 Sites, United States, 2014.
Jon Baio, Lisa Wiggins, Deborah L Christensen, Matthew J Maenner, Julie Daniels, Zachary Warren, Margaret Kurzius-Spencer, Walter Zahorodny, Cordelia Robinson Rosenberg, Tiffany White,[...]. MMWR Surveill Summ 2018
50

Common genetic variants on 5p14.1 associate with autism spectrum disorders.
Kai Wang, Haitao Zhang, Deqiong Ma, Maja Bucan, Joseph T Glessner, Brett S Abrahams, Daria Salyakina, Marcin Imielinski, Jonathan P Bradfield, Patrick M A Sleiman,[...]. Nature 2009
677
50


Comprehensive integrative analyses identify GLT8D1 and CSNK2B as schizophrenia risk genes.
Cui-Ping Yang, Xiaoyan Li, Yong Wu, Qiushuo Shen, Yong Zeng, Qiuxia Xiong, Mengping Wei, Chunhui Chen, Jiewei Liu, Yongxia Huo,[...]. Nat Commun 2018
62
33

Quality control parameters on a large dataset of regionally dissected human control brains for whole genome expression studies.
Daniah Trabzuni, Mina Ryten, Robert Walker, Colin Smith, Sabaena Imran, Adaikalavan Ramasamy, Michael E Weale, John Hardy. J Neurochem 2011
169
33


Identification of common genetic risk variants for autism spectrum disorder.
Jakob Grove, Stephan Ripke, Thomas D Als, Manuel Mattheisen, Raymond K Walters, Hyejung Won, Jonatan Pallesen, Esben Agerbo, Ole A Andreassen, Richard Anney,[...]. Nat Genet 2019
666
33

3DIV: A 3D-genome Interaction Viewer and database.
Dongchan Yang, Insu Jang, Jinhyuk Choi, Min-Seo Kim, Andrew J Lee, Hyunwoong Kim, Junghyun Eom, Dongsup Kim, Inkyung Jung, Byungwook Lee. Nucleic Acids Res 2018
60
33

A genome-wide association study of autism reveals a common novel risk locus at 5p14.1.
Deqiong Ma, Daria Salyakina, James M Jaworski, Ioanna Konidari, Patrice L Whitehead, Ashley N Andersen, Joshua D Hoffman, Susan H Slifer, Dale J Hedges, Holly N Cukier,[...]. Ann Hum Genet 2009
160
33


Impact of the Autism-Associated Long Noncoding RNA MSNP1AS on Neuronal Architecture and Gene Expression in Human Neural Progenitor Cells.
Jessica J DeWitt, Nicole Grepo, Brent Wilkinson, Oleg V Evgrafov, James A Knowles, Daniel B Campbell. Genes (Basel) 2016
17
33

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
300
16

Analysis of two language-related genes in autism: a case-control association study of FOXP2 and CNTNAP2.
Claudio Toma, Amaia Hervás, Bàrbara Torrico, Noemí Balmaña, Marta Salgado, Marta Maristany, Elisabet Vilella, Rafael Martínez-Leal, Ma Inmaculada Planelles, Ivon Cuscó,[...]. Psychiatr Genet 2013
39
16

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
16

Association of CACNA1C and SYNE1 in offspring of patients with psychiatric disorders.
Patricia Gassó, Vanessa Sánchez-Gistau, Sergi Mas, Gisela Sugranyes, Natalia Rodríguez, Daniel Boloc, Elena de la Serna, Soledad Romero, Dolores Moreno, Carmen Moreno,[...]. Psychiatry Res 2016
7
16

A method for meta-analysis of molecular association studies.
Ammarin Thakkinstian, Patrick McElduff, Catherine D'Este, David Duffy, John Attia. Stat Med 2005
522
16

Neurexin gene family variants as risk factors for autism spectrum disorder.
Jia Wang, Jianhua Gong, Li Li, Yanlin Chen, Lingfei Liu, HuaiTing Gu, Xiu Luo, Fang Hou, Jiajia Zhang, Ranran Song. Autism Res 2018
28
16

Reduced Hippocampal Functional Connectivity During Episodic Memory Retrieval in Autism.
Rose A Cooper, Franziska R Richter, Paul M Bays, Kate C Plaisted-Grant, Simon Baron-Cohen, Jon S Simons. Cereb Cortex 2017
57
16

Speech perception in autism spectrum disorder: An activation likelihood estimation meta-analysis.
Ana Tryfon, Nicholas E V Foster, Megha Sharda, Krista L Hyde. Behav Brain Res 2018
14
16

How to interpret a genome-wide association study.
Thomas A Pearson, Teri A Manolio. JAMA 2008
560
16

Inter-α-inhibitor deficiency in the mouse is associated with alterations in anxiety-like behavior, exploration and social approach.
David R Goulding, Viktoriya D Nikolova, Lopa Mishra, Lisheng Zhuo, Koji Kimata, Sandra J McBride, Sheryl S Moy, G J Harry, Stavros Garantziotis. Genes Brain Behav 2019
9
16



Most genetic risk for autism resides with common variation.
Trent Gaugler, Lambertus Klei, Stephan J Sanders, Corneliu A Bodea, Arthur P Goldberg, Ann B Lee, Milind Mahajan, Dina Manaa, Yudi Pawitan, Jennifer Reichert,[...]. Nat Genet 2014
616
16


ITIH3 polymorphism may confer susceptibility to psychiatric disorders by altering the expression levels of GLT8D1.
Daimei Sasayama, Hiroaki Hori, Noriko Yamamoto, Seiji Nakamura, Toshiya Teraishi, Masahiko Tatsumi, Kotaro Hattori, Miho Ota, Teruhiko Higuchi, Hiroshi Kunugi. J Psychiatr Res 2014
22
16

Association of a Schizophrenia-Risk Nonsynonymous Variant With Putamen Volume in Adolescents: A Voxelwise and Genome-Wide Association Study.
Qiang Luo, Qiang Chen, Wenjia Wang, Sylvane Desrivières, Erin Burke Quinlan, Tianye Jia, Christine Macare, Gabriel H Robert, Jing Cui, Mickaël Guedj,[...]. JAMA Psychiatry 2019
26
16

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
16

Identification of a Bipolar Disorder Vulnerable Gene CHDH at 3p21.1.
Hong Chang, Lingyi Li, Tao Peng, Maria Grigoroiu-Serbanescu, Sarah E Bergen, Mikael Landén, Christina M Hultman, Andreas J Forstner, Jana Strohmaier, Julian Hecker,[...]. Mol Neurobiol 2017
5
20

Association study between autistic-like traits and polymorphisms in the autism candidate regions RELN, CNTNAP2, SHANK3, and CDH9/10.
Lina Jonsson, Anna Zettergren, Erik Pettersson, Daniel Hovey, Henrik Anckarsäter, Lars Westberg, Paul Lichtenstein, Sebastian Lundström, Jonas Melke. Mol Autism 2014
24
16



Genome-Wide Association Study Detected Novel Susceptibility Genes for Schizophrenia and Shared Trans-Populations/Diseases Genetic Effect.
Masashi Ikeda, Atsushi Takahashi, Yoichiro Kamatani, Yukihide Momozawa, Takeo Saito, Kenji Kondo, Ayu Shimasaki, Kohei Kawase, Takaya Sakusabe, Yoshimi Iwayama,[...]. Schizophr Bull 2019
55
16

Learning induces long-term potentiation in the hippocampus.
Jonathan R Whitlock, Arnold J Heynen, Marshall G Shuler, Mark F Bear. Science 2006
16

Rare deletions at the neurexin 3 locus in autism spectrum disorder.
Andrea K Vaags, Anath C Lionel, Daisuke Sato, McKinsey Goodenberger, Quinn P Stein, Sarah Curran, Caroline Ogilvie, Joo Wook Ahn, Irene Drmic, Lili Senman,[...]. Am J Hum Genet 2012
144
16

A genome-wide linkage and association scan reveals novel loci for autism.
Lauren A Weiss, Dan E Arking, Mark J Daly, Aravinda Chakravarti. Nature 2009
423
16


Neurexin and neuroligin mediate retrograde synaptic inhibition in C. elegans.
Zhitao Hu, Sabrina Hom, Tambudzai Kudze, Xia-Jing Tong, Seungwon Choi, Gayane Aramuni, Weiqi Zhang, Joshua M Kaplan. Science 2012
74
16

Genome-Wide Association Study for Autism Spectrum Disorder in Taiwanese Han Population.
Po-Hsiu Kuo, Li-Chung Chuang, Mei-Hsin Su, Chia-Hsiang Chen, Chien-Hsiun Chen, Jer-Yuarn Wu, Chung-Jen Yen, Yu-Yu Wu, Shih-Kai Liu, Miao-Chun Chou,[...]. PLoS One 2015
21
16

Status of essential elements in autism spectrum disorder: systematic review and meta-analysis.
Amene Saghazadeh, Narges Ahangari, Kasra Hendi, Fatemeh Saleh, Nima Rezaei. Rev Neurosci 2017
38
16

Decoupling through synchrony in neuronal circuits with propagation delays.
Evgueniy V Lubenov, Athanassios G Siapas. Neuron 2008
109
16

Common genetic variants on 1p13.2 associate with risk of autism.
K Xia, H Guo, Z Hu, G Xun, L Zuo, Y Peng, K Wang, Y He, Z Xiong, L Sun,[...]. Mol Psychiatry 2014
58
16

Autism prevalence in China is comparable to Western prevalence.
Xiang Sun, Carrie Allison, Liping Wei, Fiona E Matthews, Bonnie Auyeung, Yu Yu Wu, Sian Griffiths, Jie Zhang, Simon Baron-Cohen, Carol Brayne. Mol Autism 2019
84
16


Polymorphisms of Ionotropic Glutamate Receptor-Related Genes and the Risk of Autism Spectrum Disorder in a Chinese Population.
Xinyan Xie, Fang Hou, Li Li, Yanlin Chen, Lingfei Liu, Xiu Luo, Huaiting Gu, Xin Li, Jiajia Zhang, Jianhua Gong,[...]. Psychiatry Investig 2019
1
100

Meta-analyses of molecular association studies: methodologic lessons for genetic epidemiology.
John Attia, Ammarin Thakkinstian, Catherine D'Este. J Clin Epidemiol 2003
270
16

The role of the ITIH3 rs2535629 variant in antipsychotic response.
E J Brandl, T A Lett, N I Chowdhury, A K Tiwari, G Bakanidze, H Y Meltzer, S G Potkin, J A Lieberman, J L Kennedy, D J Müller. Schizophr Res 2016
13
16

Sensory perception in autism.
Caroline E Robertson, Simon Baron-Cohen. Nat Rev Neurosci 2017
286
16

Stress response genes associated with attention deficit hyperactivity disorder: A case-control study in Chinese children.
Xinzhen Chen, Min Wang, Qi Zhang, Yuwei Hou, Xin Huang, Shanyawen Li, Jing Wu. Behav Brain Res 2019
2
50


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.