Search Results - "Haites, N"
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Environmental risk factors for Parkinson’s disease and parkinsonism: the Geoparkinson study
Published in Occupational and environmental medicine (London, England) (01-10-2007)“…Objective:To investigate the associations between Parkinson’s disease and other degenerative parkinsonian syndromes and environmental factors in five European…”
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2
Prothrombotic genotypes are not associated with pre-eclampsia and gestational hypertension: results from a large population-based study and systematic review
Published in Thrombosis and haemostasis (01-05-2002)“…DNA samples collected as part of a large population-based case-control study were genotyped to examine the associations of five prothrombotic gene…”
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3
To tell or not to tell: barriers and facilitators in family communication about genetic risk
Published in Clinical genetics (01-10-2003)“…Communication about genetic risk in families is an important issue for genetic counsellors. The objective of this study was to explore the barriers and…”
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4
Effect of B vitamins and genetics on success of in-vitro fertilisation: prospective cohort study
Published in The Lancet (British edition) (06-05-2006)“…There is a need to understand what affects the success of in-vitro fertilisation (IVF) and the rate of resulting twin births so that pregnancy rates can be…”
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5
CYP3A4 and VDR gene polymorphisms and the risk of prostate cancer in men with benign prostate hyperplasia
Published in British journal of cancer (24-03-2003)“…Prostate cancer (PRCa) is one of the most common causes of cancer death in men and determinants of PRCa risk remain largely unidentified. Benign prostatic…”
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6
Gene-environment interactions in parkinsonism and Parkinson’s disease: the Geoparkinson study
Published in Occupational and environmental medicine (London, England) (01-10-2007)“…Objectives:To investigate associations of Parkinson’s disease (PD) and parkinsonian syndromes with polymorphic genes that influence metabolism of either…”
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7
Cytochrome P450 CYP1B1 over-expression in primary and metastatic ovarian cancer
Published in British journal of cancer (20-07-2001)“…Ovarian cancer is the most frequent cause of death from gynaecological malignancies world wide. Little improvement has been made in the long-term outcome of…”
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8
Folate and breast cancer: the role of polymorphisms in methylenetetrahydrofolate reductase (MTHFR)
Published in Cancer letters (08-07-2002)“…Evidence is growing that low folate status may be a factor in the aetiology of several cancers, including breast cancer. The methylenetetrahydrofolate…”
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9
ATM Mutations and Phenotypes in Ataxia-Telangiectasia Families in the British Isles: Expression of Mutant ATM and the Risk of Leukemia, Lymphoma, and Breast Cancer
Published in American journal of human genetics (01-02-1998)“…We report the spectrum of 59 ATM mutations observed in ataxia-telangiectasia (A-T) patients in the British Isles. Of 51 ATM mutations identified in families…”
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10
Comparative genomic hybridization and chromosomal instability in solid tumours
Published in British Journal of Cancer (01-05-1999)Get full text
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11
Genetic nurse counsellors can be an acceptable and cost-effective alternative to clinical geneticists for breast cancer risk genetic counselling. Evidence from two parallel randomised controlled equivalence trials
Published in British journal of cancer (21-08-2006)“…This study compared genetic nurse counsellors with standard services for breast cancer genetic risk counselling services in two regional genetics centres, in…”
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12
Germ line BRCA1 & BRCA2 mutations in Greek breast/ovarian cancer families: 5382insC is the most frequent mutation observed
Published in Cancer letters (08-11-2002)“…BRCA1 and BRCA2 genes were screened for loss-of-function mutations in a series of 85 patients having at least one first- or second-degree relative affected by…”
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13
Improving the referral process for familial breast cancer genetic counselling: findings of three randomised controlled trials of two interventions
Published in Health technology assessment (Winchester, England) (01-02-2005)“…To evaluate the effectiveness and cost-effectiveness of two complementary interventions, using familial breast cancer as a model condition. The primary care…”
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14
Sources of DNA for studying gene-nutrition interactions
Published in European journal of cancer prevention (01-02-2002)Get full text
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15
Paget's Disease of Bone: Evidence for a Susceptibility Locus on Chromosome 18q and for Genetic Heterogeneity
Published in Journal of bone and mineral research (01-06-1998)“…Paget's disease of bone is a common condition characterized by bone pain, deformity, pathological fracture, and an increased incidence of osteosarcoma. Genetic…”
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16
Epidermal growth factor (EGF) Increases the in vitro invasion, motility and adhesion interactions of the primary renal carcinoma cell line, A704
Published in European journal of cancer (1990) (01-10-1996)“…Metastasis is a multistep process that involves alterations in a tumour cell's invasion, motility and adhesive capabilities. This study examined the effect of…”
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17
Steroid responsive polyneuropathy in a family with a novel myelin protein zero mutation
Published in Journal of neurology, neurosurgery and psychiatry (01-12-2000)“…OBJECTIVE To report a novel hereditary motor and sensory neuropathy (HMSN) phenotype, with partial steroid responsiveness, caused by a novel dominant mutation…”
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18
Current policies for surveillance and management in women at risk of breast and ovarian cancer: a survey among 16 European family cancer clinics
Published in European journal of cancer (1990) (01-11-1998)“…The recent isolation of breast cancer predisposing genes ( BRCA1 and BRCA2) allows the identification of carriers within affected families. These carriers have…”
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The ethical management of genetic testing
Published in European journal of cancer (1990) (01-07-2003)Get full text
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20
The genetic causes of the sequential occurrence of multiple primary malignancies in a young woman - 5 years on
Published in European journal of cancer care (01-03-2010)“…HARRY V.N., CUMMING G.P., NARAYANSINGH G.V., PARKIN D.E. & HAITES N.E. (2010) European Journal of Cancer Care19, 276–278 The genetic causes of the sequential…”
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