Published in Genet Med on February 01, 2008
Interpretation of genetic association studies: markers with replicated highly significant odds ratios may be poor classifiers. PLoS Genet (2009) 4.22
Confidence of primary care physicians in their ability to carry out basic medical genetic tasks-a European survey in five countries-Part 1. J Community Genet (2010) 1.47
Genetic educational needs and the role of genetics in primary care: a focus group study with multiple perspectives. BMC Fam Pract (2011) 1.37
A systematic review of interventions to provide genetics education for primary care. BMC Fam Pract (2016) 0.84
General practitioner management of genetic aspects of a cardiac disease: a scenario-based study to anticipate providers' practices. J Community Genet (2010) 0.82
Family physicians' management of genetic aspects of a cardiac disease: a scenario-based study from slovenia. Balkan J Med Genet (2014) 0.81
The use of family history in primary health care: a qualitative study. Adv Prev Med (2013) 0.81
Cancer risk communication, predictive testing and management in France, Germany, the Netherlands and the UK: general practitioners' and breast surgeons' current practice and preferred practice responsibilities. J Community Genet (2013) 0.81
A primary care specialist genetics service: a cluster-randomised factorial trial. Br J Gen Pract (2012) 0.78
Immune Reactions following Cord Blood Transplantations in Adults. Stem Cells Int (2011) 0.76
Family physicians' self-perceived importance of providing genetic test information to patients: a cross-sectional study from Slovenia. Med Sci Monit (2014) 0.76
General Practitioners and Breast Surgeons in France, Germany, Netherlands and the UK show variable breast cancer risk communication profiles. BMC Cancer (2015) 0.76
Association between BRCA1 and BRCA2 mutations and survival in women with invasive epithelial ovarian cancer. JAMA (2012) 3.85
EuroGentest: DNA-based testing for heritable disorders in Europe. Community Genet (2008) 1.63
Regulations and practices of genetic counselling in 38 European countries: the perspective of national representatives. Eur J Hum Genet (2008) 1.63
Genetic testing and common disorders in a public health framework: how to assess relevance and possibilities. Background Document to the ESHG recommendations on genetic testing and common disorders. Eur J Hum Genet (2011) 1.57
Perioperative outcome in adults undergoing elective deep hypothermic circulatory arrest with retrograde cerebral perfusion in proximal aortic arch repair: evaluation of protocol-based care. J Cardiothorac Vasc Anesth (2006) 1.57
WRN mutations in Werner syndrome patients: genomic rearrangements, unusual intronic mutations and ethnic-specific alterations. Hum Genet (2010) 1.50
Confidence of primary care physicians in their ability to carry out basic medical genetic tasks-a European survey in five countries-Part 1. J Community Genet (2010) 1.47
Provision of genetic services in Europe: current practices and issues. Eur J Hum Genet (2003) 1.43
Maximising recruitment and retention of general practices in clinical trials: a case study. Br J Gen Pract (2008) 1.42
Community genetics. Its definition 2010. J Community Genet (2010) 1.42
Genetic variation at 9p22.2 and ovarian cancer risk for BRCA1 and BRCA2 mutation carriers. J Natl Cancer Inst (2010) 1.41
Fatal thrombosis after mitral valve replacement for endocarditis: aprotinin and disseminated intravascular coagulation. Anesthesiology (2006) 1.31
Virtual Screening with AutoDock: Theory and Practice. Expert Opin Drug Discov (2010) 1.30
Genetic testing for familial/hereditary breast cancer-comparison of guidelines and recommendations from the UK, France, the Netherlands and Germany. J Community Genet (2011) 1.23
The contribution of the hereditary nonpolyposis colorectal cancer syndrome to the development of ovarian cancer. Gynecol Oncol (2005) 1.23
The wide variation of definitions of genetic testing in international recommendations, guidelines and reports. J Community Genet (2012) 1.19
Assessing educational priorities in genetics for general practitioners and specialists in five countries: factor structure of the Genetic-Educational Priorities (Gen-EP) scale. Genet Med (2008) 1.14
Scope of definitions of genetic testing: evidence from a EuroGentest survey. J Community Genet (2010) 1.11
Definitions of genetic testing in European legal documents. J Community Genet (2012) 1.10
An excess of chromosome 1 breakpoints in male infertility. Eur J Hum Genet (2004) 1.06
Report of an international survey of molecular genetic testing laboratories. Community Genet (2007) 1.04
Reflecting on earlier experiences with unsolicited findings: points to consider for next-generation sequencing and informed consent in diagnostics. Hum Mutat (2013) 1.04
Association of the variants CASP8 D302H and CASP10 V410I with breast and ovarian cancer risk in BRCA1 and BRCA2 mutation carriers. Cancer Epidemiol Biomarkers Prev (2010) 1.01
Higher occurrence of childhood cancer in families with germline mutations in BRCA2, MMR and CDKN2A genes. Fam Cancer (2008) 1.00
What is ideal genetic counselling? A survey of current international guidelines. Eur J Hum Genet (2008) 0.99
Ovarian cancer susceptibility alleles and risk of ovarian cancer in BRCA1 and BRCA2 mutation carriers. Hum Mutat (2012) 0.98
Allosteric regulation of substrate channeling in tryptophan synthase: modulation of the L-serine reaction in stage I of the beta-reaction by alpha-site ligands. Biochemistry (2007) 0.98
Educational priorities and current involvement in genetic practice: a survey of midwives in the Netherlands, UK and Sweden. Midwifery (2008) 0.98
Synthesis and characterization of allosteric probes of substrate channeling in the tryptophan synthase bienzyme complex. Biochemistry (2007) 0.96
Genetically modified donor leukocyte transfusion and graft-versus-leukemia effect after allogeneic stem cell transplantation. Hum Gene Ther (2011) 0.93
Cytogenetic Guidelines and Quality Assurance: a common European framework for quality assessment for constitutional and acquired cytogenetic investigations. Eur J Hum Genet (2007) 0.92
Outcomes of pregnancies diagnosed with Klinefelter syndrome: the possible influence of health professionals. Prenat Diagn (2002) 0.90
A nonsynonymous polymorphism in IRS1 modifies risk of developing breast and ovarian cancers in BRCA1 and ovarian cancer in BRCA2 mutation carriers. Cancer Epidemiol Biomarkers Prev (2012) 0.89
Genetic education for non-geneticist health professionals. Community Genet (2006) 0.89
Genetic education and nongenetic health professionals: educational providers and curricula in Europe. Genet Med (2005) 0.88
Prevalence of stroke and vascular risk factors among first-degree relatives of stroke patients and control subjects. A prospective consecutive study. Cerebrovasc Dis (2005) 0.87
Intranasal vaccination with ISCOMATRIX adjuvanted influenza vaccine. Vaccine (2003) 0.86
Ischaemic stroke in hypertensive patients is associated with variations in the PDE4D genome region. Eur J Hum Genet (2008) 0.86
Major incident planning in primary care trusts in north-west England: a cross-sectional survey. Health Serv Manage Res (2010) 0.86
Association of HTRA1 and ARMS2 gene variation with drusen formation in rhesus macaques. Exp Eye Res (2008) 0.86
A large-sample assessment of possible association between ischaemic stroke and rs12188950 in the PDE4D gene. Eur J Hum Genet (2012) 0.85
Testing the children: do non-genetic health-care providers differ in their decision to advise genetic presymptomatic testing on minors? A cross-sectional study in five countries in the European Union. Genet Test Mol Biomarkers (2009) 0.85
Preparedness of emergency departments in northwest England for managing chemical incidents: a structured interview survey. BMC Emerg Med (2007) 0.84
Long-term prognosis of early-onset breast cancer in a population-based cohort with a known BRCA1/2 mutation status. Breast Cancer Res Treat (2014) 0.84
The need for oncogenetic counselling. Ten years' experience of a regional oncogenetic clinic. Acta Oncol (2004) 0.83
Evidence for SMAD3 as a modifier of breast cancer risk in BRCA2 mutation carriers. Breast Cancer Res (2010) 0.82
General practitioner management of genetic aspects of a cardiac disease: a scenario-based study to anticipate providers' practices. J Community Genet (2010) 0.82
Developing a framework for implementation of genetic services: learning from examples of testing for monogenic forms of common diseases. J Community Genet (2014) 0.82
Cancer risk communication, predictive testing and management in France, Germany, the Netherlands and the UK: general practitioners' and breast surgeons' current practice and preferred practice responsibilities. J Community Genet (2013) 0.81
Increased incidence of childhood, prostate and breast cancers in relatives of childhood cancer patients. Fam Cancer (2012) 0.81
Testing the parents to confirm genotypes of CF patients is highly recommended: report of two cases. Eur J Hum Genet (2008) 0.81
Color-flow Doppler recognition of intraoperative brachiocephalic malperfusion during operative repair of acute type a aortic dissection: utility of transcutaneous carotid artery ultrasound scanning. J Cardiothorac Vasc Anesth (2006) 0.80
Emergency management in health: key issues and challenges in the UK. BMC Public Health (2012) 0.80
Education in medical genetics for non-genetic health care providers in Sweden. Community Genet (2006) 0.80
Direct innominate artery cannulation in acute type a dissection and severe thoracic aortic atheroma. J Cardiothorac Vasc Anesth (2006) 0.78
Establishment of an Australian motor neurone disease registry. Med J Aust (2006) 0.78
Risk stratification of patients with acute chest pain without a rise in troponin: current practice in England. Emerg Med J (2010) 0.78
Broad phenotypic spectrum in familial adenomatous polyposis; from early onset and severe phenotypes to late onset of attenuated polyposis with the first manifestation at age 72. BMC Med Genet (2008) 0.78
Primary care and genetic services. Health care in evolution. Eur J Public Health (2002) 0.77
High risk of in-breast tumor recurrence after BRCA1/2-associated breast cancer. Breast Cancer Res Treat (2014) 0.77
Clinician adherence to a standardized assessment battery across settings and disciplines in a poststroke rehabilitation population. Arch Phys Med Rehabil (2013) 0.76
Biparental inheritance of chromosomal abnormalities in male twins with non-syndromic mental retardation. Eur J Med Genet (2011) 0.76
Conservation of 5'-upstream region of the FBN1 gene in primates. Eur J Hum Genet (2008) 0.76
TGFBR3 variation is not a common cause of Marfan-like syndrome and Loeys-Dietz-like syndrome. J Negat Results Biomed (2012) 0.76
Editorial: genetics and democracy. J Community Genet (2012) 0.75
Physiological-social scoring is important in pandemic flu. BMJ (2006) 0.75
Severity of illness assessment in community-acquired pneumonia. Intensive Care Med (2008) 0.75
More on pneumonia: clinical judgment is also needed with CURB score. BMJ (2006) 0.75
Genetics and democracy-what is the issue? J Community Genet (2012) 0.75
Prevalence of germline TP53 mutations and history of Li-Fraumeni syndrome in families with childhood adrenocortical tumors, choroid plexus tumors, and rhabdomyosarcoma: a population-based survey. Pediatr Blood Cancer (2012) 0.75
Mortality predictors are not triage scores. Thorax (2007) 0.75