Genetics of Human Disease

The MSc in Genetics of Human Disease at University College London offers a comprehensive and cutting-edge exploration of the genetic factors underlying human diseases. This multidisciplinary programme is designed for students interested in understanding the molecular and genetic basis of various health conditions, including cancer, neurodegenerative disorders, cardiovascular diseases, and rare genetic syndromes. Throughout the course, students will gain in-depth knowledge of genetic variation, gene expression, epigenetics, and molecular biology techniques relevant to modern medical research. The programme combines lectures, seminars, laboratory work, and practical sessions to ensure a well-rounded learning experience. Students will explore advances in genomic technologies, such as next-generation sequencing, bioinformatics, and data analysis, to understand how these tools are transforming disease diagnosis and treatment. The curriculum covers fundamental concepts in human genetics, developmental biology, and pathology, along with the latest research on the genetic basis of disease susceptibility, inheritance patterns, and gene-environment interactions. Emphasis is placed on critical analysis of current scientific literature and the application of research methods in experimental and clinical settings. The programme also offers opportunities for students to undertake a research project, working closely with leading experts in the field. This prepares graduates for careers in biomedical research, clinical genetics, pharmaceuticals, biotechnology, and healthcare. The MSc in Genetics of Human Disease at UCL provides students with the analytical skills, scientific knowledge, and practical experience necessary to contribute to advancements in understanding, diagnosing, and treating genetic disorders. It is suitable for graduates with backgrounds in biological sciences, medicine, or related disciplines seeking to deepen their expertise in human genetics and molecular medicine.

The programme provides a thorough grounding in modern approaches to the understanding of the genetics of disease alongside the cutting-edge research methods and techniques used to advance our understanding of development of disease. Core modules provide a broad coverage of the genetics of disease, research skills and social aspects, whilst specialised streams in Inherited Diseases, Pharmacogenetics and Computational Genomics, in which students can qualify, and the research project allow more in-depth analysis in areas of genetics.

Students undertake modules to the value of 180 credits.

The programme consists of four core modules (60 credits) and two specialist modules (30 credits) and a research project culminating in a dissertation (90 credits).

A Postgraduate Diploma consisting of six modules (four core modules in term one and two modules within the selected stream in term two) is offered, full-time nine months.

A Postgraduate Certificate consisting of four core modules in term one (60 credits) is offered, full-time three months.

Core modules

• Advanced Human Genetics: Research Principles
• Understanding Bioinformatics Resources and their Applications
• Core Skills
• Basic Statistics for Medical Sciences

Specialist modules

In term two you will take specialist modules depending on the specialist stream you select: Inherited Disease (A); Pharmacogenetics (B); Computational Genomics (C). 

• Applications in Human Genetics (A)
• Either Genetics of Cardiovascular Disease or Genetics of Neurological Disease (A)
• Clinical Applications of Pharmacogenetic Tests (B)
• Anti-Cancer Personalised Medicine or Pharmacogenomics, adverse drug reactions and biomarkers (B)
• Applications in Human Genetics (C)
• Statistics for Interpreting Genetic Data (C)

Dissertation/report

Students undertake an original research project investigating topical questions in genetics and genetics of human disease which culminates in a dissertation of 12,000 to 14,000 words and an oral presentation.

Teaching and learning

Students develop their knowledge and understanding of genetics of human diseases through a combination of lectures, seminars, tutorials, presentations and journal clubs. Taught modules are assessed by unseen written examination and/or, written reports, oral presentations and coursework. The research project is assessed by the dissertation and oral presentation. 

Normally, a minimum of an upper-second class Bachelor's degree from a UK university in a relevant discipline such as in biomedical sciences, life sciences or a medical degree (MBBS), or an overseas qualification of an equivalent standard. Applicants with an appropriate professional qualification and relevant work experience may also apply.

Want to improve your English level for admission?

Prepare for the program requirements with English Online by the British Council.

• ✔️ Flexible study schedule
• ✔️ Experienced teachers
• ✔️ Certificate upon completion

📘 Recommended for students with an IELTS level of 6.0 or below.

Enroll in the course

Scholarships relevant to this department are displayed below.

Commonwealth Shared Scholarship Scheme (CSSS)

Value:

Full fees, flights, stipend, and other allowances (1 year)

Eligibility:

Overseas students

Criteria:

Based on both academic merit and financial need

The MSc in Genetics of Human Disease at University College London (UCL) offers a comprehensive curriculum designed to explore the genetic basis of human diseases. The program integrates advanced genetic and genomic techniques with clinical insights, preparing students for careers in biomedical research, diagnostics, or further academic study. Students will examine a wide variety of genetic disorders, including their molecular mechanisms, inheritance patterns, and potential treatments. The program emphasizes both theoretical knowledge and practical skills, including laboratory techniques such as DNA sequencing, genotyping, and bioinformatics analysis.

Throughout the course, students have the opportunity to engage with leading experts in genetics, participate in research seminars, and undertake a substantial research project. The curriculum covers fundamental concepts in human genetics, population genetics, molecular biology, and systems biology, alongside specialized topics such as cancer genetics, neurogenetics, and rare inherited disorders. The program also focuses on translating scientific discoveries into clinical practice, highlighting the role of genetic testing and personalized medicine.

The MSc is designed for students with backgrounds in biological sciences, medicine, or related disciplines, seeking to deepen their understanding of genetic contributions to human disease. It aims to develop critical thinking, research skills, and the ability to interpret complex genetic data. Students are encouraged to attend conferences, collaborate with research groups, and participate in placements where possible.

Graduates from this program are well-equipped to pursue PhDs, enter genetic counseling, work in biotech or pharmaceutical industries, or engage in clinical research roles. UCL provides excellent facilities and resources, including access to cutting-edge laboratories, extensive bioinformatics infrastructure, and strong links with hospitals and research institutes. This ensures students receive a high-quality education that is directly relevant to current challenges and innovations in biomedical sciences. Overall, the MSc in Genetics of Human Disease offers an intellectually stimulating environment focused on solving real-world health problems through genetic research.