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Psychological Medicine|August 30, 2003
Randomized controlled trial of brief cognitive behaviour therapy versus treatment as usual in recurrent deliberate self-harm: the POPMACT studyP Tyrer, S Thompson, U Schmidt, et al.European Journal of Human Genetics : EJHG|February 12, 2025
Exome sequencing identifies HELB as a novel susceptibility gene for non-mucinous, non-high-grade-serous epithelial ovarian cancerEd M Dicks, Jonthan P Tyrer, Suzana Ezquina, et al.Cancer Research|November 30, 2018
Functional Analysis and Fine Mapping of the 9p22.2 Ovarian Cancer Susceptibility LocusMelissa A Buckley, Nicholas T Woods, Jonathan P Tyrer, et al.Human Molecular Genetics|August 1, 2013
A genome-wide association scan (GWAS) for mean telomere length within the COGS project: identified loci show little association with hormone-related cancer riskKaren A Pooley, Stig E Bojesen, Maren Weischer, et al.American Journal of Epidemiology|June 22, 2017
Robust Tests for Additive Gene-Environment Interaction in Case-Control Studies Using Gene-Environment IndependenceGang Liu, Bhramar Mukherjee, Seunggeun Lee, et al.Radiotherapy and Oncology : Journal of the European Society for Therapeutic Radiology and Oncology|May 3, 2014
A genome wide association study (GWAS) providing evidence of an association between common genetic variants and late radiotherapy toxicityGillian C Barnett, Deborah Thompson, Laura Fachal, et al.Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|August 12, 2015
Contribution of Germline Mutations in the RAD51B, RAD51C, and RAD51D Genes to Ovarian Cancer in the PopulationHonglin Song, Ed Dicks, Susan J Ramus, et al.Oncotarget|September 9, 2017
Germline whole exome sequencing and large-scale replication identifies FANCM as a likely high grade serous ovarian cancer susceptibility geneEd Dicks, Honglin Song, Susan J Ramus, et al.Journal of the National Cancer Institute|August 29, 2015
Germline Mutations in the BRIP1, BARD1, PALB2, and NBN Genes in Women With Ovarian CancerSusan J Ramus, Honglin Song, Ed Dicks, et al.Human Molecular Genetics|May 23, 2003
Genetic and functional analyses of FH mutations in multiple cutaneous and uterine leiomyomatosis, hereditary leiomyomatosis and renal cancer, and fumarate hydratase deficiencyN A Alam, A J Rowan, N C Wortham, et al.Pageof 28