A citation-based method for searching scientific literature

Han Wu, Liu-Tao Zhai, Xue-Xue Guo, Stephane Rety, Xu-Guang Xi. Biochem J 2020
Times Cited: 1







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



Times Cited
  Times     Co-cited
Similarity


A Fast and Accurate Algorithm to Test for Binary Phenotypes and Its Application to PheWAS.
Rounak Dey, Ellen M Schmidt, Goncalo R Abecasis, Seunggeun Lee. Am J Hum Genet 2017
40
100


Reproducible association with type 1 diabetes in the extended class I region of the major histocompatibility complex.
M K Viken, A Blomhoff, M Olsson, H E Akselsen, F Pociot, J Nerup, I Kockum, A Cambon-Thomsen, E Thorsby, D E Undlien,[...]. Genes Immun 2009
37
100

Gene expression imputation across multiple brain regions provides insights into schizophrenia risk.
Laura M Huckins, Amanda Dobbyn, Douglas M Ruderfer, Gabriel Hoffman, Weiqing Wang, Antonio F Pardiñas, Veera M Rajagopal, Thomas D Als, Hoang T Nguyen, Kiran Girdhar,[...]. Nat Genet 2019
64
100


General framework for meta-analysis of rare variants in sequencing association studies.
Seunggeun Lee, Tanya M Teslovich, Michael Boehnke, Xihong Lin. Am J Hum Genet 2013
126
100

Genome-wide association study identifies novel risk variants from RPS6KA1, CADPS, VARS, and DHX58 for fasting plasma glucose in Arab population.
Prashantha Hebbar, Mohamed Abu-Farha, Fadi Alkayal, Rasheeba Nizam, Naser Elkum, Motasem Melhem, Sumi Elsa John, Arshad Channanath, Jehad Abubaker, Abdullah Bennakhi,[...]. Sci Rep 2020
7
100

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
144
100

Evolution of human-specific neural SRGAP2 genes by incomplete segmental duplication.
Megan Y Dennis, Xander Nuttle, Peter H Sudmant, Francesca Antonacci, Tina A Graves, Mikhail Nefedov, Jill A Rosenfeld, Saba Sajjadian, Maika Malig, Holland Kotkiewicz,[...]. Cell 2012
192
100

Cis-eQTLs regulate reduced LST1 gene and NCR3 gene expression and contribute to increased autoimmune disease risk.
Guiyou Liu, Yang Hu, Shuilin Jin, Fang Zhang, Qinghua Jiang, Junwei Hao. Proc Natl Acad Sci U S A 2016
19
100



Compensated deleterious mutations in insect genomes.
Rob J Kulathinal, Brian R Bettencourt, Daniel L Hartl. Science 2004
74
100

Genetic association of the major histocompatibility complex with rheumatoid arthritis implicates two non-DRB1 loci.
Charlotte Vignal, Aruna T Bansal, David J Balding, Michael H Binks, Marion C Dickson, Doug S Montgomery, Anthony G Wilson. Arthritis Rheum 2009
58
100

Rare-variant association testing for sequencing data with the sequence kernel association test.
Michael C Wu, Seunggeun Lee, Tianxi Cai, Yun Li, Michael Boehnke, Xihong Lin. Am J Hum Genet 2011
100

Notch signaling in diabetic nephropathy.
Ramon Bonegio, Katalin Susztak. Exp Cell Res 2012
42
100


Leveraging molecular quantitative trait loci to understand the genetic architecture of diseases and complex traits.
Farhad Hormozdiari, Steven Gazal, Bryce van de Geijn, Hilary K Finucane, Chelsea J-T Ju, Po-Ru Loh, Armin Schoech, Yakir Reshef, Xuanyao Liu, Luke O'Connor,[...]. Nat Genet 2018
51
100

A unified association analysis approach for family and unrelated samples correcting for stratification.
Xiaofeng Zhu, Shengchao Li, Richard S Cooper, Robert C Elston. Am J Hum Genet 2008
93
100


Compensatory mutations restore fitness during the evolution of dihydrofolate reductase.
Kyle M Brown, Marna S Costanzo, Wenxin Xu, Scott Roy, Elena R Lozovsky, Daniel L Hartl. Mol Biol Evol 2010
60
100

A restriction fragment of the C2 gene is a unique marker for C2 deficiency and the uncommon C2 allele C2*B (a marker for type 1 diabetes).
S Simon, Z Awdeh, R D Campbell, P Ronco, S J Brink, G S Eisenbarth, E J Yunis, C A Alper. J Clin Invest 1991
10
100

The cerebellum, sensitive periods, and autism.
Samuel S-H Wang, Alexander D Kloth, Aleksandra Badura. Neuron 2014
304
100

A gene-based association method for mapping traits using reference transcriptome data.
Eric R Gamazon, Heather E Wheeler, Kaanan P Shah, Sahar V Mozaffari, Keston Aquino-Michaels, Robert J Carroll, Anne E Eyler, Joshua C Denny, Dan L Nicolae, Nancy J Cox,[...]. Nat Genet 2015
581
100

Comprehensive Multiple eQTL Detection and Its Application to GWAS Interpretation.
Biao Zeng, Luke R Lloyd-Jones, Grant W Montgomery, Andres Metspalu, Tonu Esko, Lude Franke, Urmo Vosa, Annique Claringbould, Kenneth L Brigham, Arshed A Quyyumi,[...]. Genetics 2019
11
100

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
100


Detecting disease-associated genotype patterns.
Quan Long, Qingrun Zhang, Jurg Ott. BMC Bioinformatics 2009
19
100


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
544
100

A transcriptome-wide association study identifies PALMD as a susceptibility gene for calcific aortic valve stenosis.
Sébastien Thériault, Nathalie Gaudreault, Maxime Lamontagne, Mickael Rosa, Marie-Chloé Boulanger, David Messika-Zeitoun, Marie-Annick Clavel, Romain Capoulade, François Dagenais, Philippe Pibarot,[...]. Nat Commun 2018
36
100

A Fast and Accurate Method for Genome-Wide Time-to-Event Data Analysis and Its Application to UK Biobank.
Wenjian Bi, Lars G Fritsche, Bhramar Mukherjee, Sehee Kim, Seunggeun Lee. Am J Hum Genet 2020
4
100

Exploring the diabetogenicity of the HLA-B18-DR3 CEH: independent association with T1D genetic risk close to HLA-DOA.
I Santin, A Castellanos-Rubio, A M Aransay, G Gutierrez, S Gaztambide, I Rica, J L Vicario, J A Noble, L Castaño, J R Bilbao. Genes Immun 2009
13
100


The type 1 diabetes - HLA susceptibility interactome--identification of HLA genotype-specific disease genes for type 1 diabetes.
Caroline Brorsson, Niclas Tue Hansen, Regine Bergholdt, Søren Brunak, Flemming Pociot. PLoS One 2010
19
100

Retinal transcriptome and eQTL analyses identify genes associated with age-related macular degeneration.
Rinki Ratnapriya, Olukayode A Sosina, Margaret R Starostik, Madeline Kwicklis, Rebecca J Kapphahn, Lars G Fritsche, Ashley Walton, Marios Arvanitis, Linn Gieser, Alexandra Pietraszkiewicz,[...]. Nat Genet 2019
71
100

Integrative transcriptome imputation reveals tissue-specific and shared biological mechanisms mediating susceptibility to complex traits.
Wen Zhang, Georgios Voloudakis, Veera M Rajagopal, Ben Readhead, Joel T Dudley, Eric E Schadt, Johan L M Björkegren, Yungil Kim, John F Fullard, Gabriel E Hoffman,[...]. Nat Commun 2019
17
100

Massive genomic variation and strong selection in Arabidopsis thaliana lines from Sweden.
Quan Long, Fernando A Rabanal, Dazhe Meng, Christian D Huber, Ashley Farlow, Alexander Platzer, Qingrun Zhang, Bjarni J Vilhjálmsson, Arthur Korte, Viktoria Nizhynska,[...]. Nat Genet 2013
214
100

Exome sequencing identifies novel rheumatoid arthritis-susceptible variants in the BTNL2.
Shigeki Mitsunaga, Kazuyoshi Hosomichi, Yuko Okudaira, Hirofumi Nakaoka, Nanae Kunii, Yasuo Suzuki, Masataka Kuwana, Shinji Sato, Yuko Kaneko, Yasuhiko Homma,[...]. J Hum Genet 2013
32
100

ALDH2 Inhibition Potentiates High Glucose Stress-Induced Injury in Cultured Cardiomyocytes.
Guodong Pan, Mandar Deshpande, Rajarajan A Thandavarayan, Suresh Selvaraj Palaniyandi. J Diabetes Res 2016
12
100


A deep auto-encoder model for gene expression prediction.
Rui Xie, Jia Wen, Andrew Quitadamo, Jianlin Cheng, Xinghua Shi. BMC Genomics 2017
20
100

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
100

Proteome-wide association studies identify biochemical modules associated with a wing-size phenotype in Drosophila melanogaster.
Hirokazu Okada, H Alexander Ebhardt, Sibylle Chantal Vonesch, Ruedi Aebersold, Ernst Hafen. Nat Commun 2016
24
100

Using extended pedigrees to identify novel autism spectrum disorder (ASD) candidate genes.
Marc Woodbury-Smith, Andrew D Paterson, Bhooma Thiruvahindrapduram, Anath C Lionel, Christian R Marshall, Daniele Merico, Bridget A Fernandez, Eric Duku, James S Sutcliffe, Irene O'Conner,[...]. Hum Genet 2015
13
100

Polygenic modeling with bayesian sparse linear mixed models.
Xiang Zhou, Peter Carbonetto, Matthew Stephens. PLoS Genet 2013
328
100

Large-scale transcriptome-wide association study identifies new prostate cancer risk regions.
Nicholas Mancuso, Simon Gayther, Alexander Gusev, Wei Zheng, Kathryn L Penney, Zsofia Kote-Jarai, Rosalind Eeles, Matthew Freedman, Christopher Haiman, Bogdan Pasaniuc. Nat Commun 2018
40
100

Efficiently controlling for case-control imbalance and sample relatedness in large-scale genetic association studies.
Wei Zhou, Jonas B Nielsen, Lars G Fritsche, Rounak Dey, Maiken E Gabrielsen, Brooke N Wolford, Jonathon LeFaive, Peter VandeHaar, Sarah A Gagliano, Aliya Gifford,[...]. Nat Genet 2018
183
100

Transcriptome-Wide Association Study Identifies New Candidate Susceptibility Genes for Glioma.
Isabelle Atkins, Ben Kinnersley, Quinn T Ostrom, Karim Labreche, Dora Il'yasova, Georgina N Armstrong, Jeanette E Eckel-Passow, Minouk J Schoemaker, Markus M Nöthen, Jill S Barnholtz-Sloan,[...]. Cancer Res 2019
10
100



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.