A citation-based method for searching scientific literature

Xinyan Xie, Heng Meng, Hao Wu, Fang Hou, Yanlin Chen, Yu Zhou, Qi Xue, Jiajia Zhang, Jianhua Gong, Li Li, Ranran Song. Sci Rep 2020
Times Cited: 3







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



Times Cited
  Times     Co-cited
Similarity


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
66

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
66

MAGMA: generalized gene-set analysis of GWAS data.
Christiaan A de Leeuw, Joris M Mooij, Tom Heskes, Danielle Posthuma. PLoS Comput Biol 2015
66

rSNPBase: a database for curated regulatory SNPs.
Liyuan Guo, Yang Du, Suhua Chang, Kunlin Zhang, Jing Wang. Nucleic Acids Res 2014
87
33

The GeneMANIA prediction server: biological network integration for gene prioritization and predicting gene function.
David Warde-Farley, Sylva L Donaldson, Ovi Comes, Khalid Zuberi, Rashad Badrawi, Pauline Chao, Max Franz, Chris Grouios, Farzana Kazi, Christian Tannus Lopes,[...]. Nucleic Acids Res 2010
33

Connectivity dynamics in typical development and its relationship to autistic traits and autism spectrum disorder.
Barnaly Rashid, Laura M E Blanken, Ryan L Muetzel, Robyn Miller, Eswar Damaraju, Mohammad R Arbabshirani, Erik B Erhardt, Frank C Verhulst, Aad van der Lugt, Vincent W V Jaddoe,[...]. Hum Brain Mapp 2018
58
33

Patterns and rates of exonic de novo mutations in autism spectrum disorders.
Benjamin M Neale, Yan Kou, Li Liu, Avi Ma'ayan, Kaitlin E Samocha, Aniko Sabo, Chiao-Feng Lin, Christine Stevens, Li-San Wang, Vladimir Makarov,[...]. Nature 2012
33

AutDB: a gene reference resource for autism research.
Saumyendra N Basu, Ravi Kollu, Sharmila Banerjee-Basu. Nucleic Acids Res 2009
263
33

Systematic Review of Genetic Risk Factors for Sustaining a Mild Traumatic Brain Injury.
William J Panenka, Andrew J Gardner, Michael N Dretsch, Gogce C Crynen, Fiona C Crawford, Grant L Iverson. J Neurotrauma 2017
27
33

The senescence-associated secretory phenotype is potentiated by feedforward regulatory mechanisms involving Zscan4 and TAK1.
Boyi Zhang, Da Fu, Qixia Xu, Xianling Cong, Chunyan Wu, Xiaoming Zhong, Yushui Ma, Zhongwei Lv, Fei Chen, Liu Han,[...]. Nat Commun 2018
64
33

Association of MAPT haplotype-tagging polymorphisms with cerebrospinal fluid biomarkers of Alzheimer's disease: A preliminary study in a Croatian cohort.
Mirjana Babić Leko, Nanet Willumsen, Matea Nikolac Perković, Nataša Klepac, Fran Borovečki, Patrick R Hof, Zdenko Sonicki, Nela Pivac, Rohan de Silva, Goran Šimić. Brain Behav 2018
19
33

Potential etiologic and functional implications of genome-wide association loci for human diseases and traits.
Lucia A Hindorff, Praveen Sethupathy, Heather A Junkins, Erin M Ramos, Jayashri P Mehta, Francis S Collins, Teri A Manolio. Proc Natl Acad Sci U S A 2009
33

Analysis of shared heritability in common disorders of the brain.
Verneri Anttila, Brendan Bulik-Sullivan, Hilary K Finucane, Raymond K Walters, Jose Bras, Laramie Duncan, Valentina Escott-Price, Guido J Falcone, Padhraig Gormley, Rainer Malik,[...]. Science 2018
911
33

A survey of genetic human cortical gene expression.
Amanda J Myers, J Raphael Gibbs, Jennifer A Webster, Kristen Rohrer, Alice Zhao, Lauren Marlowe, Mona Kaleem, Doris Leung, Leslie Bryden, Priti Nath,[...]. Nat Genet 2007
393
33

Transcriptomic analysis of autistic brain reveals convergent molecular pathology.
Irina Voineagu, Xinchen Wang, Patrick Johnston, Jennifer K Lowe, Yuan Tian, Steve Horvath, Jonathan Mill, Rita M Cantor, Benjamin J Blencowe, Daniel H Geschwind. Nature 2011
33

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
297
33

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
372
33

TRANSFAC and its module TRANSCompel: transcriptional gene regulation in eukaryotes.
V Matys, O V Kel-Margoulis, E Fricke, I Liebich, S Land, A Barre-Dirrie, I Reuter, D Chekmenev, M Krull, K Hornischer,[...]. Nucleic Acids Res 2006
33

Integrative analyses of major histocompatibility complex loci in the genome-wide association studies of major depressive disorder.
Huijuan Li, Hong Chang, Xueqin Song, Weipeng Liu, Lingyi Li, Lu Wang, Yongfeng Yang, Luwen Zhang, Wenqiang Li, Yan Zhang,[...]. Neuropsychopharmacology 2019
19
33

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
159
33

Maintenance of Genome Stability.
Jiadong Wang, Tomas Lindahl. Genomics Proteomics Bioinformatics 2016
16
33

Genome-wide Association Study of Autism Spectrum Disorder in the East Asian Populations.
Xiaoxi Liu, Takafumi Shimada, Takeshi Otowa, Yu-Yu Wu, Yoshiya Kawamura, Mamoru Tochigi, Yasuhide Iwata, Tadashi Umekage, Tomoko Toyota, Motoko Maekawa,[...]. Autism Res 2016
59
33



Correspondence between Resting-State Activity and Brain Gene Expression.
Guang-Zhong Wang, T Grant Belgard, Deng Mao, Leslie Chen, Stefano Berto, Todd M Preuss, Hanzhang Lu, Daniel H Geschwind, Genevieve Konopka. Neuron 2015
73
33

How to interpret a genome-wide association study.
Thomas A Pearson, Teri A Manolio. JAMA 2008
567
33

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
67
33

Roles of tau protein in health and disease.
Tong Guo, Wendy Noble, Diane P Hanger. Acta Neuropathol 2017
440
33

Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function.
Gail Davies, Max Lam, Sarah E Harris, Joey W Trampush, Michelle Luciano, W David Hill, Saskia P Hagenaars, Stuart J Ritchie, Riccardo E Marioni, Chloe Fawns-Ritchie,[...]. Nat Commun 2018
260
33

Analysis of the expression pattern of the schizophrenia-risk and intellectual disability gene TCF4 in the developing and adult brain suggests a role in development and plasticity of cortical and hippocampal neurons.
Matthias Jung, Benjamin M Häberle, Tristan Tschaikowsky, Marie-Theres Wittmann, Elli-Anna Balta, Vivien-Charlott Stadler, Christiane Zweier, Arnd Dörfler, Christian Johannes Gloeckner, D Chichung Lie. Mol Autism 2018
35
33


Genetic ablation of tau improves mitochondrial function and cognitive abilities in the hippocampus.
Claudia Jara, Alejandra Aránguiz, Waldo Cerpa, Cheril Tapia-Rojas, Rodrigo A Quintanilla. Redox Biol 2018
39
33

Convergent functional genomics of psychiatric disorders.
Alexander B Niculescu. Am J Med Genet B Neuropsychiatr Genet 2013
17
33

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
649
33

Individual common variants exert weak effects on the risk for autism spectrum disorders.
Richard Anney, Lambertus Klei, Dalila Pinto, Joana Almeida, Elena Bacchelli, Gillian Baird, Nadia Bolshakova, Sven Bölte, Patrick F Bolton, Thomas Bourgeron,[...]. Hum Mol Genet 2012
242
33

Association of missense and 5'-splice-site mutations in tau with the inherited dementia FTDP-17.
M Hutton, C L Lendon, P Rizzu, M Baker, S Froelich, H Houlden, S Pickering-Brown, S Chakraverty, A Isaacs, A Grover,[...]. Nature 1998
33



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
33

A genome-wide scan for common alleles affecting risk for autism.
Richard Anney, Lambertus Klei, Dalila Pinto, Regina Regan, Judith Conroy, Tiago R Magalhaes, Catarina Correia, Brett S Abrahams, Nuala Sykes, Alistair T Pagnamenta,[...]. Hum Mol Genet 2010
418
33

AutismKB: an evidence-based knowledgebase of autism genetics.
Li-Ming Xu, Jia-Rui Li, Yue Huang, Min Zhao, Xing Tang, Liping Wei. Nucleic Acids Res 2012
127
33

Characteristics and predictive value of blood transcriptome signature in males with autism spectrum disorders.
Sek Won Kong, Christin D Collins, Yuko Shimizu-Motohashi, Ingrid A Holm, Malcolm G Campbell, In-Hee Lee, Stephanie J Brewster, Ellen Hanson, Heather K Harris, Kathryn R Lowe,[...]. PLoS One 2012
101
33

Different brain networks underlying intelligence in autism spectrum disorders.
Emmanuel Peng Kiat Pua, Charles B Malpas, Stephen C Bowden, Marc L Seal. Hum Brain Mapp 2018
17
33

Annotation of functional variation in personal genomes using RegulomeDB.
Alan P Boyle, Eurie L Hong, Manoj Hariharan, Yong Cheng, Marc A Schaub, Maya Kasowski, Konrad J Karczewski, Julie Park, Benjamin C Hitz, Shuai Weng,[...]. Genome Res 2012
33

Association of MAPT haplotypes with Alzheimer's disease risk and MAPT brain gene expression levels.
Mariet Allen, Michaela Kachadoorian, Zachary Quicksall, Fanggeng Zou, High Seng Chai, Curtis Younkin, Julia E Crook, V Shane Pankratz, Minerva M Carrasquillo, Siddharth Krishnan,[...]. Alzheimers Res Ther 2014
79
33


No association between a common single nucleotide polymorphism, rs4141463, in the MACROD2 gene and autism spectrum disorder.
Sarah Curran, Patrick Bolton, Kinga Rozsnyai, Andreas Chiocchetti, Sabine M Klauck, Eftichia Duketis, Fritz Poustka, Sabine Schlitt, Christine M Freitag, Irene Lee,[...]. Am J Med Genet B Neuropsychiatr Genet 2011
26
33

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
146
33

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
428
33

Common genetic variants influence human subcortical brain structures.
Derrek P Hibar, Jason L Stein, Miguel E Renteria, Alejandro Arias-Vasquez, Sylvane Desrivières, Neda Jahanshad, Roberto Toro, Katharina Wittfeld, Lucija Abramovic, Micael Andersson,[...]. Nature 2015
493
33


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.