Below are links to research studies in genetics. If you are thinking of taking part in one, please talk to your doctor.

• A trial investigating the communication effects caused by Genetic Learning Difficulties in children

• CONVERGE - understanding genetics (impact of copy number variants) in neurodevelopmental disorders

• EMBRACE Study: Epidemiological study of BRCA1 and BRCA2 mutation carriers

• Genetic basis of craniofacial malformations.

• Genetic disorders of human brain development.

• Genetic disorders of human neurological and immune function.

• Genetic Investigations of Rare Disorders of Metabolism and/or Growth (Musketeers Memorandum study)

• Genetics of endocrine tumours

• Genetics of Perrault Syndrome (hearing loss and ovarian insufficiency).

• GENROC: GENetic Rare disease Observational Cohort (Musketeers Study)

• Investigating the cause of abnormal human development - a study to identify aberrations of imprinting.

• Investigating the role of genetics in disease predisposition

• Li Fraumeni Syndrome - Trial investigating the use of Metformin as a cancer prevention in patient with LFS

• Molecular Pathology of Human Genetic Disease.

• REGAIN - Rolandic Epilepsy Genomewide Association International Study

• Scottish Participation in Genomics England 100,000 Genomes Project

• Splicing and Disease.

• Understanding the conditions of the RAS-MAPK pathway.

• Genetics of susceptibility and mortality in critical care (GenOMICC)