Publicacións en colaboración con investigadores/as de Lund University (14)

2021

  1. Combined Associations of a Polygenic Risk Score and Classical Risk Factors With Breast Cancer Risk

    Journal of the National Cancer Institute, Vol. 113, Núm. 3, pp. 329-337

2020

  1. Author Correction: Retrospective evaluation of whole exome and genome mutation calls in 746 cancer samples (Nature Communications, (2020), 11, 1, (4748), 10.1038/s41467-020-18151-y)

    Nature Communications

  2. Pan-cancer analysis of whole genomes

    Nature, Vol. 578, Núm. 7793, pp. 82-93

  3. Retrospective evaluation of whole exome and genome mutation calls in 746 cancer samples

    Nature Communications, Vol. 11, Núm. 1

  4. Sex differences in oncogenic mutational processes

    Nature Communications, Vol. 11, Núm. 1

2019

  1. Genome-wide association study of germline variants and breast cancer-specific mortality

    British Journal of Cancer, Vol. 120, Núm. 6, pp. 647-657

2017

  1. Association analysis identifies 65 new breast cancer risk loci

    Nature, Vol. 551, Núm. 7678, pp. 92-94

  2. Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer

    Nature Genetics, Vol. 49, Núm. 12, pp. 1767-1778

2015

  1. Frequent somatic transfer of mitochondrial DNA into the nuclear genome of human cancer cells

    Genome Research, Vol. 25, Núm. 6, pp. 814-824

2014

  1. Alcohol consumption and survival after a breast cancer diagnosis: A literature-based meta-analysis and collaborative analysis of data for 29,239 cases

    Cancer Epidemiology Biomarkers and Prevention, Vol. 23, Núm. 6, pp. 934-945

  2. Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization

    Nature Genetics, Vol. 46, Núm. 8, pp. 826-836

  3. Processed pseudogenes acquired somatically during cancer development

    Nature Communications, Vol. 5

2010

  1. Common variants at 2q37.3, 8q24.21, 15q21.3 and 16q24.1 influence chronic lymphocytic leukemia risk

    Nature Genetics, Vol. 42, Núm. 2, pp. 132-136

  2. Verification that common variation at 2q37.1, 6p25.3, 11q24.1, 15q23, and 19q13.32 influences chronic lymphocytic leukaemia risk

    British Journal of Haematology, Vol. 150, Núm. 4, pp. 473-479