King's College London

Research portal

Mr Thomas Hansen

  1. The Genetics of the Mood Disorder Spectrum: Genome-wide Association Analyses of More Than 185,000 Cases and 439,000 Controls

    Bipolar Disorder Working Group of the Psychiatric Genomics Consortium & Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium, 1 Jan 2020, In : Biological psychiatry.

    Research output: Contribution to journalArticle

  2. Publisher Correction: Gene expression imputation across multiple brain regions provides insights into schizophrenia risk (Nature Genetics, (2019), 51, 4, (659-674), 10.1038/s41588-019-0364-4)

    iPSYCH-GEMS Schizophrenia Working Group, CommonMind Consortium & The Schizophrenia Working Group of the Psychiatric Genomics Consortium, 1 Jun 2019, In : Nature Genetics. 51, 6, 1 p.

    Research output: Contribution to journalComment/debate

  3. Identification of common genetic risk variants for autism spectrum disorder

    Autism Spectrum Disorder Working Group of the Psychiatric Genomics Consortium, BUPGEN, Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium & 23andMe Research Team, 25 Feb 2019, In : Nature Genetics. 51, 3, p. 431-444 14 p.

    Research output: Contribution to journalArticle

  4. Genetic influences on schizophrenia and subcortical brain volumes: Large-scale proof of concept

    Psychosis Endophenotypes International Consortium, 23 Feb 2016, In : Nature Neuroscience. 19, 3, p. 420-431 12 p.

    Research output: Contribution to journalArticle

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

    Breast Cancer Family Registry, 31 Dec 2014, In : Breast Cancer Research. 16, 6, p. 3416

    Research output: Contribution to journalArticle

  6. Genome-wide association study in BRCA1 mutation carriers identifies novel loci associated with breast and ovarian cancer risk

    KConFab Investigators, 2013, In : PLoS Genetics. 9, 3, p. e1003212

    Research output: Contribution to journalArticle

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

    SWE-BRCA, Apr 2012, In : Human Mutation. 33, 4, p. 690-702 13 p.

    Research output: Contribution to journalArticle

  8. Common variants of the BRCA1 wild-type allele modify the risk of breast cancer in BRCA1 mutation carriers

    Ontario Cancer Genetics Network, 1 Dec 2011, In : Human Molecular Genetics. 20, 23, p. 4732-47 16 p.

    Research output: Contribution to journalArticle

  9. Haplotype structure in Ashkenazi Jewish BRCA1 and BRCA2 mutation carriers

    HEBON, Nov 2011, In : Human Genetics. 130, 5, p. 685-99 15 p.

    Research output: Contribution to journalArticle

  10. Common alleles at 6q25.1 and 1p11.2 are associated with breast cancer risk for BRCA1 and BRCA2 mutation carriers

    SWE-BRCA, 15 Aug 2011, In : Human Molecular Genetics. 20, 16, p. 3304-21 18 p.

    Research output: Contribution to journalArticle

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

    OCGN, 19 Jan 2011, In : Journal of the National Cancer Institute. 103, 2, p. 105-16 12 p.

    Research output: Contribution to journalArticle

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

    Ontario Cancer Genetics Network, 1 Dec 2010, In : Cancer Research. 70, 23, p. 9742-54 13 p.

    Research output: Contribution to journalArticle

  13. Common variants in LSP1, 2q35 and 8q24 and breast cancer risk for BRCA1 and BRCA2 mutation carriers

    Kathleen Cuningham Foundation Consortium for Research into Familial Breast Cancer, 15 Nov 2009, In : Human Molecular Genetics. 18, 22, p. 4442-56 15 p.

    Research output: Contribution to journalArticle

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