A Swedish Familial Genome-Wide Haplotype Analysis Identified Five Novel Breast Cancer Susceptibility Loci on 9p24.3, 11q22.3, 15q11.2, 16q24.1 and Xq21.31

Most breast cancer heritability is unexplained. We hypothesized that analysis of unrelated familial cases in a GWAS context could enable the identification of novel susceptibility loci. In order to examine the association of a haplotype with breast cancer risk, we performed a genome-wide haplotype a...

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Detalles Bibliográficos
Autores principales: Barnekow, Elin, Hasslow, Johan, Liu, Wen, Bryant, Patrick, Thutkawkorapin, Jessada, Wendt, Camilla, Czene, Kamila, Hall, Per, Margolin, Sara, Lindblom, Annika
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10003706/
https://www.ncbi.nlm.nih.gov/pubmed/36901898
http://dx.doi.org/10.3390/ijms24054468

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10003706/
https://www.ncbi.nlm.nih.gov/pubmed/36901898
http://dx.doi.org/10.3390/ijms24054468

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