(Q57266761)

10

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Gareth Evans

object named as

D Gareth Evans

11

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David Craufurd

9

object named as

David Craufurd

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author name string

Lucy Brooks

1

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Fiona Lennard

2

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Andrew Shenton

3

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Fiona Lalloo

4

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Ingrid Ambus

5

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Audrey Ardern-Jones

6

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Bronwyn Kerr

European Journal of Human Genetics

8

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publication date

12 May 2004

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published in

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volume

12

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issue

8

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page(s)

654-662

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exact match

https://scigraph.springernature.com/pub.10.1038/sj.ejhg.5201206

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cites work

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Identification of the breast cancer susceptibility gene BRCA2

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Potential impact of a predictive test on the gene frequency of Huntington disease

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Uptake of presymptomatic predictive testing for Huntington's disease

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Understanding the low uptake of presymptomatic DNA testing for Huntington's disease

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Ten years of presymptomatic testing for Huntington's disease: the experience of the UK Huntington's Disease Prediction Consortium

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Uptake of genetic testing for cancer predisposition.

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Attitudes towards cancer predictive testing and transmission of information to the family

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Interest in genetic testing among first-degree relatives of breast cancer patients

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Proband family uptake of familial-genetic counselling.

21 January 2018

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Psychosocial factors predicting BRCA1/BRCA2 testing decisions in members of hereditary breast and ovarian cancer families.

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Uptake of genetic testing and pre-test levels of mental distress in Norwegian families with known BRCA1 mutations

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Early adoption of BRCA1/2 testing: who and why.

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Psychological responses to BRCA1 mutation testing: preliminary findings.

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Predictive genetic testing for hereditary non-polyposis colorectal cancer: uptake and long-term satisfaction

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Genetic testing in families with hereditary nonpolyposis colon cancer

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Attitudes about genetic testing for breast-ovarian cancer susceptibility

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Uptake of hereditary breast/ovarian cancer genetic testing in a French national sample of BRCA1 families. The French Cancer Genetic Network

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Genetic testing for a BRCA1 mutation: prophylactic surgery and screening behavior in women 2 years post testing

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Presymptomatic DNA testing and prophylactic surgery in families with a BRCA1 or BRCA2 mutation

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