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Times Co-cited
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Large-scale genotyping identifies 41 new loci associated with breast cancer risk.
Kyriaki Michailidou, Per Hall, Anna Gonzalez-Neira, Maya Ghoussaini, Joe Dennis, Roger L Milne, Marjanka K Schmidt, Jenny Chang-Claude, Stig E Bojesen, Manjeet K Bolla,[...]. Nat Genet 2013
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Prediction of breast cancer risk based on profiling with common genetic variants.
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Association analysis identifies 65 new breast cancer risk loci.
Kyriaki Michailidou, Sara Lindström, Joe Dennis, Jonathan Beesley, Shirley Hui, Siddhartha Kar, Audrey Lemaçon, Penny Soucy, Dylan Glubb, Asha Rostamianfar,[...]. Nature 2017
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Genome-wide association analysis of more than 120,000 individuals identifies 15 new susceptibility loci for breast cancer.
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Kyriaki Michailidou, Jonathan Beesley, Sara Lindstrom, Sander Canisius, Joe Dennis, Michael J Lush, Mel J Maranian, Manjeet K Bolla, Qin Wang, Mitul Shah,[...]. Nat Genet 2015
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Genome-wide association study in BRCA1 mutation carriers identifies novel loci associated with breast and ovarian cancer risk.
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Breast cancer risk prediction using a polygenic risk score in the familial setting: a prospective study from the Breast Cancer Family Registry and kConFab.
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Evaluation of Polygenic Risk Scores for Breast and Ovarian Cancer Risk Prediction in BRCA1 and BRCA2 Mutation Carriers.
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PALB2, which encodes a BRCA2-interacting protein, is a breast cancer susceptibility gene.
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Genome-wide association study identifies five new breast cancer susceptibility loci.
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Genome-wide association study identifies novel breast cancer susceptibility loci.
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Performance of common genetic variants in breast-cancer risk models.
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Projecting individualized probabilities of developing breast cancer for white females who are being examined annually.
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Polygenic Risk Scores for Prediction of Breast Cancer and Breast Cancer Subtypes.
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The impact of a panel of 18 SNPs on breast cancer risk in women attending a UK familial screening clinic: a case-control study.
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BOADICEA: a comprehensive breast cancer risk prediction model incorporating genetic and nongenetic risk factors.
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Genome-wide association analysis identifies three new breast cancer susceptibility loci.
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Identification of a BRCA2-specific modifier locus at 6p24 related to breast cancer risk.
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BRCA1 R1699Q variant displaying ambiguous functional abrogation confers intermediate breast and ovarian cancer risk.
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Making Sense of SNPs: Women's Understanding and Experiences of Receiving a Personalized Profile of Their Breast Cancer Risks.
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Psychosocial and behavioral impact of breast cancer risk assessed by testing for common risk variants: protocol of a prospective study.
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Genome-wide polygenic scores for common diseases identify individuals with risk equivalent to monogenic mutations.
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Addition of a 161-SNP polygenic risk score to family history-based risk prediction: impact on clinical management in non-BRCA1/2 breast cancer families.
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A breast cancer prediction model incorporating familial and personal risk factors.
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Newly discovered breast cancer susceptibility loci on 3p24 and 17q23.2.
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Truncating mutations in the Fanconi anemia J gene BRIP1 are low-penetrance breast cancer susceptibility alleles.
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Translational Genomic Research: Protocol Development and Initial Outcomes following SNP Testing for Colon Cancer Risk.
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Novel breast cancer susceptibility locus at 9q31.2: results of a genome-wide association study.
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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.