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Colorectal cancer genomics: evidence for multiple genotypes which influence survival

British journal of cancer, 2001-11, Vol.85 (10), p.1492-1498

2001

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Prothrombotic genotypes are not associated with pre-eclampsia and gestational hypertension: results from a large population-based study and systematic review

Thrombosis and haemostasis, 2002-05, Vol.87 (5), p.779-785

2002

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Folate and breast cancer: the role of polymorphisms in methylenetetrahydrofolate reductase (MTHFR)

Cancer letters, 2002-07, Vol.181 (1), p.65-71

2002

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CYP3A4 and VDR gene polymorphisms and the risk of prostate cancer in men with benign prostate hyperplasia

British journal of cancer, 2003-03, Vol.88 (6), p.928-932

2003

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Cytochrome P450 CYP1B1 over-expression in primary and metastatic ovarian cancer

British journal of cancer, 2001-07, Vol.85 (2), p.242-246

2001

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Germ line BRCA1 & BRCA2 mutations in Greek breast/ovarian cancer families: 5382insC is the most frequent mutation observed

Cancer letters, 2002-11, Vol.185 (1), p.61-70

2002

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Epidermal growth factor (EGF) Increases the in vitro invasion, motility and adhesion interactions of the primary renal carcinoma cell line, A704

European journal of cancer (1990), 1996-10, Vol.32 (11), p.1977-1982

1996

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Comparative genomic hybridization and chromosomal instability in solid tumours

British Journal of Cancer, 1999-05, Vol.80 (5-6), p.862-873

1999

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Paget's Disease of Bone: Evidence for a Susceptibility Locus on Chromosome 18q and for Genetic Heterogeneity

Journal of bone and mineral research, 1998-06, Vol.13 (6), p.911-917

1998

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Current policies for surveillance and management in women at risk of breast and ovarian cancer: a survey among 16 European family cancer clinics

European journal of cancer (1990), 1998-11, Vol.34 (12), p.1922-1926

1998

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The genetic causes of the sequential occurrence of multiple primary malignancies in a young woman - 5 years on

European journal of cancer care, 2010-03, Vol.19 (2), p.276-278

2010

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The ethical management of genetic testing

European journal of cancer (1990), 2003-07, Vol.39 (10), p.1339-1340

Haites, N.E.

2003

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Is random screening of value in detecting glucocorticoid-remediable aldosteronism within a hypertensive population?

Journal of human hypertension, 2001-03, Vol.15 (3), p.173-176

2001

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p53 mutation is a common genetic event in ovarian carcinoma

Cancer research (Chicago, Ill.), 1993-05, Vol.53 (9), p.2128-2132

1993

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Mutations in the connexin 32 gene in X-linked dominant Charcot- Marie - Tooth disease (CMTX1)

Human molecular genetics, 1994-01, Vol.3 (1), p.29-34

1994

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Asthma, wheezy bronchitis, and atopy across two generations

American journal of respiratory and critical care medicine, 1999, Vol.159 (1), p.125-129

1999

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Multifocal transitional cell carcinoma in a patient with hereditary nonpolyposis colon cancer

BJU international, 2003-02, Vol.91 (3), p.297-297

2003

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Breast cancer in two sisters with Friedreich's ataxia

European journal of surgical oncology, 2001-08, Vol.27 (5), p.512-514

2001

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Comparative genomic hybridization analysis of chromosomal alterations induced by the development of resistance to thymidylate synthase inhibitors

Cancer research (Chicago, Ill.), 1998-11, Vol.58 (22), p.5042-5045

1998

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A survey of the current clinical facilities for the management of familial cancer in Europe

Journal of medical genetics, 2000-08, Vol.37 (8), p.605-607

2000

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Adhesion molecule interactions in human glomerulonephritis: Importance of the tubulointerstitium

Kidney international, 1996-01, Vol.49 (1), p.127-134

1996

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Early loss of heterozygosity on 17q in ovarian cancer

Oncogene, 1992, Vol.7 (10), p.2069-2072

1992

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Rapid diagnosis and identification of cross-over sites in patients with glucocorticoid remediable aldosteronism

The journal of clinical endocrinology and metabolism, 1998-12, Vol.83 (12), p.4328-4331

1998

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Upregulation and co-localization of connexin43 and cellular adhesion molecules in inflammatory renal disease

The Journal of pathology, 1997-08, Vol.182 (4), p.373-379

1997

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p53 mutation and expression in lymphoma

British journal of cancer, 1995-07, Vol.72 (1), p.150-154

1995

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Colorectal cancer genomics: evidence for multiple genotypes which influence survival

Prothrombotic genotypes are not associated with pre-eclampsia and gestational hypertension: results from a large population-based study and systematic review

Folate and breast cancer: the role of polymorphisms in methylenetetrahydrofolate reductase (MTHFR)

CYP3A4 and VDR gene polymorphisms and the risk of prostate cancer in men with benign prostate hyperplasia

Cytochrome P450 CYP1B1 over-expression in primary and metastatic ovarian cancer

Germ line BRCA1 & BRCA2 mutations in Greek breast/ovarian cancer families: 5382insC is the most frequent mutation observed

Epidermal growth factor (EGF) Increases the in vitro invasion, motility and adhesion interactions of the primary renal carcinoma cell line, A704

Comparative genomic hybridization and chromosomal instability in solid tumours

Paget's Disease of Bone: Evidence for a Susceptibility Locus on Chromosome 18q and for Genetic Heterogeneity

Current policies for surveillance and management in women at risk of breast and ovarian cancer: a survey among 16 European family cancer clinics

The genetic causes of the sequential occurrence of multiple primary malignancies in a young woman - 5 years on

The ethical management of genetic testing

Is random screening of value in detecting glucocorticoid-remediable aldosteronism within a hypertensive population?

p53 mutation is a common genetic event in ovarian carcinoma

Mutations in the connexin 32 gene in X-linked dominant Charcot- Marie - Tooth disease (CMTX1)

Asthma, wheezy bronchitis, and atopy across two generations

Multifocal transitional cell carcinoma in a patient with hereditary nonpolyposis colon cancer

Breast cancer in two sisters with Friedreich's ataxia

Comparative genomic hybridization analysis of chromosomal alterations induced by the development of resistance to thymidylate synthase inhibitors

A survey of the current clinical facilities for the management of familial cancer in Europe

Adhesion molecule interactions in human glomerulonephritis: Importance of the tubulointerstitium

Early loss of heterozygosity on 17q in ovarian cancer

Rapid diagnosis and identification of cross-over sites in patients with glucocorticoid remediable aldosteronism

Upregulation and co-localization of connexin43 and cellular adhesion molecules in inflammatory renal disease

p53 mutation and expression in lymphoma

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