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Times Cited: 325
Times Cited: 325
Times Cited
Times Co-cited
Similarity
A gene-based association method for mapping traits using reference transcriptome data.
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Integrative approaches for large-scale transcriptome-wide association studies.
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LD Score regression distinguishes confounding from polygenicity in genome-wide association studies.
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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
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Integration of summary data from GWAS and eQTL studies predicts complex trait gene targets.
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MAGMA: generalized gene-set analysis of GWAS data.
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PLINK: a tool set for whole-genome association and population-based linkage analyses.
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Integrating predicted transcriptome from multiple tissues improves association detection.
Alvaro N Barbeira, Milton Pividori, Jiamao Zheng, Heather E Wheeler, Dan L Nicolae, Hae Kyung Im. PLoS Genet 2019
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A statistical framework for cross-tissue transcriptome-wide association analysis.
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An atlas of genetic correlations across human diseases and traits.
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Using an atlas of gene regulation across 44 human tissues to inform complex disease- and trait-associated variation.
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Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms across Eight Psychiatric Disorders.
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Farhad Hormozdiari, Martijn van de Bunt, Ayellet V Segrè, Xiao Li, Jong Wha J Joo, Michael Bilow, Jae Hoon Sul, Sriram Sankararaman, Bogdan Pasaniuc, Eleazar Eskin. Am J Hum Genet 2016
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Trait-associated SNPs are more likely to be eQTLs: annotation to enhance discovery from GWAS.
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The UK Biobank resource with deep phenotyping and genomic data.
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12
Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression.
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11
Heritability enrichment of specifically expressed genes identifies disease-relevant tissues and cell types.
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11
Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection.
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11
Genome-wide association study identifies 30 loci associated with bipolar disorder.
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11
Comprehensive functional genomic resource and integrative model for the human brain.
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10
Transcriptome and genome sequencing uncovers functional variation in humans.
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10
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Discovery and refinement of loci associated with lipid levels.
Cristen J Willer, Ellen M Schmidt, Sebanti Sengupta, Gina M Peloso, Stefan Gustafsson, Stavroula Kanoni, Andrea Ganna, Jin Chen, Martin L Buchkovich, Samia Mora,[...]. Nat Genet 2013
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10
Integrative analysis of 111 reference human epigenomes.
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9
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
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10
Transcriptome-wide association study of schizophrenia and chromatin activity yields mechanistic disease insights.
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9
Next-generation genotype imputation service and methods.
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Sayantan Das, Lukas Forer, Sebastian Schönherr, Carlo Sidore, Adam E Locke, Alan Kwong, Scott I Vrieze, Emily Y Chew, Shawn Levy, Matt McGue,[...]. Nat Genet 2016
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Mendelian randomization with invalid instruments: effect estimation and bias detection through Egger regression.
Jack Bowden, George Davey Smith, Stephen Burgess. Int J Epidemiol 2015
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Genetic architecture of gene expression traits across diverse populations.
Lauren S Mogil, Angela Andaleon, Alexa Badalamenti, Scott P Dickinson, Xiuqing Guo, Jerome I Rotter, W Craig Johnson, Hae Kyung Im, Yongmei Liu, Heather E Wheeler. PLoS Genet 2018
Lauren S Mogil, Angela Andaleon, Alexa Badalamenti, Scott P Dickinson, Xiuqing Guo, Jerome I Rotter, W Craig Johnson, Hae Kyung Im, Yongmei Liu, Heather E Wheeler. PLoS Genet 2018
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Exploiting the GTEx resources to decipher the mechanisms at GWAS loci.
Alvaro N Barbeira, Rodrigo Bonazzola, Eric R Gamazon, Yanyu Liang, YoSon Park, Sarah Kim-Hellmuth, Gao Wang, Zhuoxun Jiang, Dan Zhou, Farhad Hormozdiari,[...]. Genome Biol 2021
Alvaro N Barbeira, Rodrigo Bonazzola, Eric R Gamazon, Yanyu Liang, YoSon Park, Sarah Kim-Hellmuth, Gao Wang, Zhuoxun Jiang, Dan Zhou, Farhad Hormozdiari,[...]. Genome Biol 2021
24
Partitioning heritability by functional annotation using genome-wide association summary statistics.
Hilary K Finucane, Brendan Bulik-Sullivan, Alexander Gusev, Gosia Trynka, Yakir Reshef, Po-Ru Loh, Verneri Anttila, Han Xu, Chongzhi Zang, Kyle Farh,[...]. Nat Genet 2015
Hilary K Finucane, Brendan Bulik-Sullivan, Alexander Gusev, Gosia Trynka, Yakir Reshef, Po-Ru Loh, Verneri Anttila, Han Xu, Chongzhi Zang, Kyle Farh,[...]. Nat Genet 2015
8
Genome-wide meta-analysis of depression identifies 102 independent variants and highlights the importance of the prefrontal brain regions.
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8
Quantifying genetic effects on disease mediated by assayed gene expression levels.
Douglas W Yao, Luke J O'Connor, Alkes L Price, Alexander Gusev. Nat Genet 2020
Douglas W Yao, Luke J O'Connor, Alkes L Price, Alexander Gusev. Nat Genet 2020
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Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder.
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Ditte Demontis, Raymond K Walters, Joanna Martin, Manuel Mattheisen, Thomas D Als, Esben Agerbo, Gísli Baldursson, Rich Belliveau, Jonas Bybjerg-Grauholm, Marie Bækvad-Hansen,[...]. Nat Genet 2019
8
Conditional and joint multiple-SNP analysis of GWAS summary statistics identifies additional variants influencing complex traits.
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PhenomeXcan: Mapping the genome to the phenome through the transcriptome.
Milton Pividori, Padma S Rajagopal, Alvaro Barbeira, Yanyu Liang, Owen Melia, Lisa Bastarache, YoSon Park, GTEx Consortium, Xiaoquan Wen, Hae K Im. Sci Adv 2020
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A reference panel of 64,976 haplotypes for genotype imputation.
Shane McCarthy, Sayantan Das, Warren Kretzschmar, Olivier Delaneau, Andrew R Wood, Alexander Teumer, Hyun Min Kang, Christian Fuchsberger, Petr Danecek, Kevin Sharp,[...]. Nat Genet 2016
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8
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.