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Nat Genet 2020
Times Cited: 49
Times Cited: 49
Times Cited
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Similarity
Association analysis identifies 65 new breast cancer risk loci.
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Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer.
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Large-scale genotyping identifies 41 new loci associated with breast cancer risk.
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Polygenic Risk Scores for Prediction of Breast Cancer and Breast Cancer Subtypes.
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Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer.
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Functional variants at the 11q13 risk locus for breast cancer regulate cyclin D1 expression through long-range enhancers.
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A locus on 19p13 modifies risk of breast cancer in BRCA1 mutation carriers and is associated with hormone receptor-negative breast cancer in the general population.
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Chromatin interactome mapping at 139 independent breast cancer risk signals.
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Integrative eQTL-based analyses reveal the biology of breast cancer risk loci.
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Evidence that breast cancer risk at the 2q35 locus is mediated through IGFBP5 regulation.
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Fine-scale mapping of the FGFR2 breast cancer risk locus: putative functional variants differentially bind FOXA1 and E2F1.
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Prediction of breast cancer risk based on profiling with common genetic variants.
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Polymorphisms in a Putative Enhancer at the 10q21.2 Breast Cancer Risk Locus Regulate NRBF2 Expression.
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The OncoArray Consortium: A Network for Understanding the Genetic Architecture of Common Cancers.
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Identification of independent association signals and putative functional variants for breast cancer risk through fine-scale mapping of the 12p11 locus.
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Fine-scale mapping of 8q24 locus identifies multiple independent risk variants for breast cancer.
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An intergenic risk locus containing an enhancer deletion in 2q35 modulates breast cancer risk by deregulating IGFBP5 expression.
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Associations Between Cancer Predisposition Testing Panel Genes and Breast Cancer.
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Genome-wide association analysis identifies three new breast cancer susceptibility loci.
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GWAS meta-analysis and replication identifies three new susceptibility loci for ovarian cancer.
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An integrated map of structural variation in 2,504 human genomes.
Peter H Sudmant, Tobias Rausch, Eugene J Gardner, Robert E Handsaker, Alexej Abyzov, John Huddleston, Yan Zhang, Kai Ye, Goo Jun, Markus Hsi-Yang Fritz,[...]. Nature 2015
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8
Evaluating the power to discriminate between highly correlated SNPs in genetic association studies.
Miriam S Udler, Jonathan Tyrer, Douglas F Easton. Genet Epidemiol 2010
Miriam S Udler, Jonathan Tyrer, Douglas F Easton. Genet Epidemiol 2010
10
Non-coding RNAs underlie genetic predisposition to breast cancer.
Mahdi Moradi Marjaneh, Jonathan Beesley, Tracy A O'Mara, Pamela Mukhopadhyay, Lambros T Koufariotis, Stephen Kazakoff, Nehal Hussein, Laura Fachal, Nenad Bartonicek, Kristine M Hillman,[...]. Genome Biol 2020
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Conditional and joint multiple-SNP analysis of GWAS summary statistics identifies additional variants influencing complex traits.
Jian Yang, Teresa Ferreira, Andrew P Morris, Sarah E Medland, Pamela A F Madden, Andrew C Heath, Nicholas G Martin, Grant W Montgomery, Michael N Weedon, Ruth J Loos,[...]. Nat Genet 2012
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8
Integrating functional data to prioritize causal variants in statistical fine-mapping studies.
Gleb Kichaev, Wen-Yun Yang, Sara Lindstrom, Farhad Hormozdiari, Eleazar Eskin, Alkes L Price, Peter Kraft, Bogdan Pasaniuc. PLoS Genet 2014
Gleb Kichaev, Wen-Yun Yang, Sara Lindstrom, Farhad Hormozdiari, Eleazar Eskin, Alkes L Price, Peter Kraft, Bogdan Pasaniuc. PLoS Genet 2014
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LDlink: a web-based application for exploring population-specific haplotype structure and linking correlated alleles of possible functional variants.
Mitchell J Machiela, Stephen J Chanock. Bioinformatics 2015
Mitchell J Machiela, Stephen J Chanock. Bioinformatics 2015
8
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