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Abstract P3-08-01: The prospective risk of ovarian cancer in 1433 women in a breast cancer family history clinic: no increased risk in families testing negative for BRCA1 and BRCA2

Cancer research (Chicago, Ill.), 2012-12, Vol.72 (24_Supplement), p.P3-P3-08-01

2012

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Abstract PD1-05: Transgenerational epigenetic silencing of BRCA1 due to a germline variant unmasks a new mechanism for familial breast and ovarian cancer

Cancer research (Chicago, Ill.), 2018-02, Vol.78 (4_Supplement), p.PD1-05-PD1-05

2018

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The accuracy of diagnoses as reported in families with cancer: a retrospective study

Journal of medical genetics, 1999-04, Vol.36 (4), p.309-312

1999

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Age related shift in the mutation spectra of germline and somatic NF2 mutations: hypothetical role of DNA repair mechanisms

Journal of medical genetics, 2005-08, Vol.42 (8), p.630-632

2005

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Allele losses in the region 17q12-21 in familial breast and ovarian cancer involve the wild-type chromosome

Nature genetics, 1992-10, Vol.2 (2), p.128-131

1992

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Ankyloblepharon filiforme adnatum in trisomy 18 Edwards syndrome

Journal of medical genetics, 1990-11, Vol.27 (11), p.720-721

1990

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Apo E genotypes in multiple sclerosis, Parkinson's disease, schwannomas and late-onset Alzheimer's disease

Molecular and cellular probes, 1994-12, Vol.8 (6), p.519-525

1994

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Appearances can be deceptive: An APC 1893del4 mutation with unusual properties

Human mutation, 1998-01, Vol.12 (3), p.212-212

1998

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Are There Low-Penetrance TP53 Alleles? Evidence from Childhood Adrenocortical Tumors

American journal of human genetics, 1999-10, Vol.65 (4), p.995-1006

1999

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Assessment of relative risk of second primary tumors after ovarian cancer and of the usefulness of double primary cases as a source of material for genetic studies with a cancer registry

Cancer, 1993-08, Vol.72 (3), p.819-827

1993

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The association between weight at birth and breast cancer risk revisited using Mendelian randomisation

European journal of epidemiology, 2019-06, Vol.34 (6), p.591-600

2019

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Association of superficial plexiform and paraspinal neurofibromas in neurofibromatosis 1 (NF1)

Neurology, 1999-04, Vol.52 (7), p.1519

1999

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Brain tumours and the occurrence of severe invasive basal cell carcinoma in first degree relatives with Gorlin syndrome

British journal of neurosurgery, 1991, Vol.5 (6), p.643-646

1991

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BRCA1/2 mutation analysis in male breast cancer families from North West England

Familial cancer, 2008-06, Vol.7 (2), p.113-117

2008

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BRCA1, BRCA2 and TP53 mutations in very early-onset breast cancer with associated risks to relatives

European journal of cancer (1990), 2006-05, Vol.42 (8), p.1143-1150

2006

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Can hair be used to screen for breast cancer?

Journal of medical genetics, 2000-04, Vol.37 (4), p.297-298

2000

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Can the diagnosis of NF1 be excluded clinically? A lack of pigmentary findings in families with spinal neurofibromatosis demonstrates a limitation of clinical diagnosis

Journal of medical genetics, 2013-09, Vol.50 (9), p.606-613

2013

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Cancer genetics clinics

European journal of cancer (1990), 1996-03, Vol.32 (3), p.391-392

1996

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Cancer Genetics Service Provision: A Comparison of Seven European Centres

Community genetics, 2003, Vol.6 (4), p.192-205

2003

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A case of multiple cutaneous schwannomas; schwannomatosis or neurofibromatosis type 2?

Journal of neurology, neurosurgery and psychiatry, 2006-02, Vol.77 (2), p.269-271

2006

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Clinical and molecular correlates of somatic mosaicism in neurofibromatosis 2

Journal of medical genetics, 2000-07, Vol.37 (7), p.542-543

2000

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A clinical study of type 1 neurofibromatosis in north west England

Journal of medical genetics, 1999-03, Vol.36 (3), p.197-203

1999

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A clinical study of type 2 neurofibromatosis

Quarterly journal of medicine, 1992-08, Vol.84 (304), p.603-618

1992

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A common MSH2 mutation in English and North American HNPCC families: origin, phenotypic expression, and sex specific differences in colorectal cancer

Journal of medical genetics, 1999-02, Vol.36 (2), p.97-102

1999

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Comparison of proactive and usual approaches to offering predictive testing for BRCA1/2 mutations in unaffected relatives

Clinical genetics, 2009-02, Vol.75 (2), p.124-132

2009

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Abstract P3-08-01: The prospective risk of ovarian cancer in 1433 women in a breast cancer family history clinic: no increased risk in families testing negative for BRCA1 and BRCA2

Abstract PD1-05: Transgenerational epigenetic silencing of BRCA1 due to a germline variant unmasks a new mechanism for familial breast and ovarian cancer

The accuracy of diagnoses as reported in families with cancer: a retrospective study

Age related shift in the mutation spectra of germline and somatic NF2 mutations: hypothetical role of DNA repair mechanisms

Allele losses in the region 17q12-21 in familial breast and ovarian cancer involve the wild-type chromosome

Ankyloblepharon filiforme adnatum in trisomy 18 Edwards syndrome

Apo E genotypes in multiple sclerosis, Parkinson's disease, schwannomas and late-onset Alzheimer's disease

Appearances can be deceptive: An APC 1893del4 mutation with unusual properties

Are There Low-Penetrance TP53 Alleles? Evidence from Childhood Adrenocortical Tumors

Assessment of relative risk of second primary tumors after ovarian cancer and of the usefulness of double primary cases as a source of material for genetic studies with a cancer registry

The association between weight at birth and breast cancer risk revisited using Mendelian randomisation

Association of superficial plexiform and paraspinal neurofibromas in neurofibromatosis 1 (NF1)

Brain tumours and the occurrence of severe invasive basal cell carcinoma in first degree relatives with Gorlin syndrome

BRCA1/2 mutation analysis in male breast cancer families from North West England

BRCA1, BRCA2 and TP53 mutations in very early-onset breast cancer with associated risks to relatives

Can hair be used to screen for breast cancer?

Can the diagnosis of NF1 be excluded clinically? A lack of pigmentary findings in families with spinal neurofibromatosis demonstrates a limitation of clinical diagnosis

Cancer genetics clinics

Cancer Genetics Service Provision: A Comparison of Seven European Centres

A case of multiple cutaneous schwannomas; schwannomatosis or neurofibromatosis type 2?

Clinical and molecular correlates of somatic mosaicism in neurofibromatosis 2

A clinical study of type 1 neurofibromatosis in north west England

A clinical study of type 2 neurofibromatosis

A common MSH2 mutation in English and North American HNPCC families: origin, phenotypic expression, and sex specific differences in colorectal cancer

Comparison of proactive and usual approaches to offering predictive testing for BRCA1/2 mutations in unaffected relatives

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