Publicacións en colaboración con investigadores/as de Dana–Farber Cancer Institute (22)

2022

  1. Author Correction: Expanded encyclopaedias of DNA elements in the human and mouse genomes (Nature, (2020), 583, 7818, (699-710), 10.1038/s41586-020-2493-4)

    Nature

  2. Author Correction: Perspectives on ENCODE (Nature, (2020), 583, 7818, (693-698), 10.1038/s41586-020-2449-8)

    Nature

  3. Mortality in Persons with Autism Spectrum Disorder or Attention-Deficit/Hyperactivity Disorder: A Systematic Review and Meta-analysis

    JAMA Pediatrics, Vol. 176, Núm. 4, pp. E216401

  4. Standardized annotation of translated open reading frames

    Nature Biotechnology

2020

  1. Chronic lymphocytic leukemia patients with IGH translocations are characterized by a distinct genetic landscape with prognostic implications

    International Journal of Cancer, Vol. 147, Núm. 10, pp. 2780-2792

  2. Expanded encyclopaedias of DNA elements in the human and mouse genomes

    Nature, Vol. 583, Núm. 7818, pp. 699-710

  3. Fine-mapping of 150 breast cancer risk regions identifies 191 likely target genes

    Nature Genetics, Vol. 52, Núm. 1, pp. 56-73

  4. Perspectives on ENCODE

    Nature, Vol. 583, Núm. 7818, pp. 693-698

2019

  1. Association of Anorexia Nervosa With Risk of Cancer: A Systematic Review and Meta-analysis

    JAMA network open, Vol. 2, Núm. 6, pp. e195313

2017

  1. Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer

    Nature Genetics, Vol. 49, Núm. 5, pp. 680-691

2014

  1. Associations of common breast cancer susceptibility alleles with risk of breast cancer subtypes in BRCA1 and BRCA2 mutation carriers

    Breast Cancer Research, Vol. 16

  2. DNA Glycosylases Involved in Base Excision Repair May Be Associated with Cancer Risk in BRCA1 and BRCA2 Mutation Carriers

    PLoS Genetics, Vol. 10, Núm. 4

2013

  1. Genome-Wide Association Study in BRCA1 Mutation Carriers Identifies Novel Loci Associated with Breast and Ovarian Cancer Risk

    PLoS Genetics, Vol. 9, Núm. 3

2012

  1. Common variants at the 19p13.1 and ZNF365 loci are associated with ER subtypes of breast cancer and ovarian cancer risk in BRCA1 and BRCA2 mutation carriers

    Cancer Epidemiology Biomarkers and Prevention, Vol. 21, Núm. 4, pp. 645-657

  2. Ovarian cancer susceptibility alleles and risk of ovarian cancer in BRCA1 and BRCA2 mutation carriers

    Human Mutation, Vol. 33, Núm. 4, pp. 690-702

2011

  1. Common breast cancer susceptibility alleles are associated with tumour subtypes in BRCA1 and BRCA2 mutation carriers: results from the Consortium of Investigators of Modifiers of BRCA1/2

    Breast Cancer Research, Vol. 13, Núm. 6

  2. Genetic variation at 9p22.2 and ovarian cancer risk for BRCA1 and BRCA2 mutation carriers

    Journal of the National Cancer Institute, Vol. 103, Núm. 2, pp. 105-116

2010

  1. Common breast cancer susceptibility alleles and the risk of breast cancer for BRCA1 and BRCA2 mutation carriers: Implications for risk prediction

    Cancer Research, Vol. 70, Núm. 23, pp. 9742-9754

  2. Fast kinase domain-containing protein 3 is a mitochondrial protein essential for cellular respiration

    Biochemical and Biophysical Research Communications, Vol. 401, Núm. 3, pp. 440-446

2007

  1. Fas-activated serine/threonine phosphoprotein (FAST) is a regulator of alternative splicing

    Proceedings of the National Academy of Sciences of the United States of America, Vol. 104, Núm. 27, pp. 11370-11375