Related Experiment Video
Updated: Aug 12, 2026

07:34
FISH for Pre-implantation Genetic Diagnosis
Published on: February 23, 2011
Genetics and genetic testing: are GPs likely to attend training courses?
Siobhan McCann1, Domhnall Macauley, Yvonne Barnett
1School of Nursing, University of Ulster, Magee, Northland Road, Londonderry, UK. sm.mccann@ulster.ac.uk
Summary
General practitioners (GPs) are interested in genetics training courses to aid cancer screening and diagnosis. Recent female GPs showed the most interest, suggesting targeted education strategies are needed.
Area of Science:
- Medical Education
- Genetics
- Oncology
Background:
- General Practitioners (GPs) face challenges in cancer screening and genetic testing decisions.
- Educational interventions can enhance GP knowledge and improve cancer referral practices.
Purpose of the Study:
- To assess the interest of GPs in attending genetics training courses.
- To identify factors influencing GP participation in genetics education.
Main Methods:
- A postal survey was distributed to 534 General Practitioners in Northern Ireland.
- The survey assessed willingness to attend three distinct types of genetics training courses.
Main Results:
- Approximately 75% of GPs expressed high likelihood of attending genetics training.
- Recently qualified GPs and female GPs were significantly more likely to attend training.
Conclusions:
- GPs demonstrate a clear interest in continuing education regarding genetics.
- Targeted recruitment strategies should focus on male GPs and those with longer qualification periods.
Related Concept Videos
Genetic Screens
Genetic screens are tools used to identify genes and mutations responsible for phenotypes of interest. Genetic screens help identify individuals or a group of people at risk of developing genetic diseases and help them with early intervention, targeted therapy, and reproductive options.
Forward genetic screens
Forward or “classical” genetic screens involve creating random mutations in an organism’s DNA using radiation, mutagens, or insertion of additional bases, which result in visible changes...
Forward genetic screens
Forward or “classical” genetic screens involve creating random mutations in an organism’s DNA using radiation, mutagens, or insertion of additional bases, which result in visible changes...
Pharmacogenetics and Pharmacogenomics: Overview
Pharmacogenetics and pharmacogenomics examine how genetic factors influence an individual's response to drugs. While pharmacogenetics focuses on the impact of specific genetic variants on drug effects, pharmacogenomics takes a broader approach, studying how genetic variation across populations contributes to differences in drug responses. These fields aim to explain why individuals may experience varying levels of efficacy or adverse reactions to the same medication.Variability in drug...
Pharmacogenomics: Identification of New Drug Targets
Advances in genomics have profoundly influenced drug discovery by increasing both the speed and accuracy of pharmaceutical development. Pharmacogenomics, which examines how genetic variation influences drug response, facilitates the identification of novel therapeutic targets and enables patient stratification for personalized treatment. These strategies contribute to improved drug efficacy, minimized adverse effects, and more efficient clinical trial design.Mapping genetic differences...
Human Genetics
Human genetics provides a profound framework for understanding the interplay between genetic predispositions and human psychology. At the heart of this discipline lies the study of how genes influence physical traits, behaviors, and susceptibility to diseases. Each person carries a unique genetic code that subtly or significantly shapes their psychological and behavioral landscape.
The complex relationship between genetics and psychology is observable through common biological components such...
The complex relationship between genetics and psychology is observable through common biological components such...
Genetic Material
Within the human body, a complex and detailed system of trillions of cells works in unison to sustain life. Each cell houses a nucleus, which contains 46 chromosomes divided into 23 pairs. Chromosomes are highly coiled structures made of the genetic material DNA. These chromosomes are essential carriers of genetic information, with half inherited from the mother through her egg and the other half from the father's sperm, combining to create the unique genetic makeup of an individual.
Behavioral Genetics and Its Designs
Behavior genetics explores how genetic inheritance influences human behavior. It focuses on how genes, passed from parents to offspring, contribute to the development of behavioral traits and tendencies. This branch of genetics seeks to understand the complex interplay between inherited genetic factors and environmental influences in shaping our behaviors.
The primary methodologies used in behavior genetics include family studies, twin studies, and adoption studies, each providing unique...
The primary methodologies used in behavior genetics include family studies, twin studies, and adoption studies, each providing unique...

