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1 - 10 of 58 search results for `family history and genetic`
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  2. genes | University of Cambridge

    https://www.cam.ac.uk/topics/genes
    2 Jun 2024: 29 Oct 2019. People with a higher genetic likelihood of autism are more likely to report higher childhood maltreatment, self-harm and suicidal thoughts according. ... 24 Apr 2017. The largest genomic analysis of puberty timing in men and women conducted
  3. Home - Centre for Cancer Genetic Epidemiology

    https://ccge.medschl.cam.ac.uk/
    Site Search. Centre for Cancer Genetic Epidemiology. 1 of 10. 2 of 10. ... This study provides the basis for a long term, comprehensive evaluation of genetic and lifestyle modifiers of cancer risk.
  4. Family history and location of genetic fault affect risk for carriers …

    https://www.cam.ac.uk/research/news/family-history-and-location-of-genetic-fault-affect-risk-for-carriers-of-key-breast-and-ovarian
    Thumbnail for Family history and location of genetic fault affect risk for carriers of key breast and ovarian cancer genes | University of Cambridge 20 Jun 2017: Search. Search. Family history and location of genetic fault affect risk for carriers of key breast and ovarian cancer genes. ... Research. Family history and location of genetic fault affect risk for carriers of key breast and ovarian cancer genes..
  5. Genetics and GPs | University of Cambridge

    https://www.cam.ac.uk/news/genetics-and-gps
    4 May 2001: Dr Emery believes that UK primary care is well placed to support an integrated genetic service because of its traditional focus on the family and relatively well computerised longitudinal health records: ... But if they are to fulfil their new roles then
  6. DNA Family Secrets | Jesus College in the University of Cambridge

    https://www.jesus.cam.ac.uk/articles/dna-family-secrets
    Thumbnail for DNA Family Secrets | Jesus College in the University of Cambridge 31 May 2024: The programme is presented by Stacey Dooley and Professor King, and uses the latest DNA technology to solve family mysteries around ancestry, missing relatives and genetic disease. ... Each episode focuses on three people: two of these trying to find out
  7. SPS Annual Report 1998-1999 | Department of Psychology

    https://www.psychol.cam.ac.uk/archivesdp/spsannualreport98_99
    2 Jun 2024: Ms B Lindley. Child protection and family rights; child care issues and legal framework; adoption. ... 105-129. Juliet Mitchell. Gender differences from a psychoanalytic and social history perspective with particular reference to hysteria; changes in the
  8. Annual-Report-1998 - 1999 | Department of Sociology

    https://www.sociology.cam.ac.uk/reports/annual-report-1998%20-%201999
    1 Jun 2024: 105-129. Juliet Mitchell. Gender differences from a psychoanalytic and social history perspective with particular reference to hysteria; changes in the contemporary western family with particular reference to issues concerning women ... Oxford:Hart
  9. Genetic basis of thinness - Institute of Metabolic Science-Metabolic…

    https://www.mrl.ims.cam.ac.uk/blog/genetic-basis-of-thinness/
    24 Feb 2024: The team found new genetic regions involved in severe obesity and some involved in healthy thinness. ... Three out of four people (74%) in the STILTS cohort had a family history of being thin and healthy and the team found some genetic changes that were
  10. Publications - Centre for Cancer Genetic Epidemiology

    https://ccge.medschl.cam.ac.uk/publications/
    Lee A, et al … Easton DF, Antoniou AC. (2019) BOADICEA: a comprehensive breast cancer risk prediction model incorporating genetic and nongenetic risk factors Genet Med. ... Mcinnis RJ, et al … (2011) A risk prediction algorithm based on family
  11. Professor Douglas Easton (Director) - Centre for Cancer Genetic

    https://ccge.medschl.cam.ac.uk/prof-douglas-easton/
    Varghese JS, et al … Easton DF (2012) Mammographic breast density and breast cancer: evidence of a shared genetic basis. ... Macinnis RJ, et al … Easton DF (2011) A risk prediction algorithm based on family history and common genetic variants:

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