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We have 26 quantitative genetics PhD Projects, Programmes & Scholarships

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quantitative genetics PhD Projects, Programmes & Scholarships

We have 26 quantitative genetics PhD Projects, Programmes & Scholarships

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PhD Studentship in quantitative genetics of neurodevelopment

The student will have the opportunity to work on a project analysing data from large-scale longitudinal and developmental cohorts with a focus on infant and child phenotypes. Read more

Understanding the ecological and evolutionary effects of heatwaves in tropical species and ecological communities

Heatwaves are considered one of the most threatening processes for our plants and animal species as the Earth’s climate warms. There is much to understand about how our species and the ecological communities they form will change and adapt through heatwaves. Read more

PHD POSITION IN STATISTICAL GENOMICS/GENETIC EPIDEMIOLOGY

The Max Planck Institute (MPI) for Psycholinguistics, Nijmegen, the Netherlands, is offering a PhD position in Statistical Genomics/Genetic Epidemiology within the population genetics of human communication group, led by Dr Beate St Pourcain and embedded within the Language & Genetics Department at the MPI. Read more

The evolutionary basis of feeding preferences: A Geometric Framework approach

Despite the essential role food plays in our lives, we have little understanding of how different nutrients work together to impact functioning, or the reasons individuals choose certain combinations of food. Read more

Harnessing the genetics of DNA methylation to understand context-specific gene regulation in disease

Genome wide association studies (GWAS) have discovered many genetic associations for traits and diseases. However, most GWAS signals reside in non-coding regions (outside genes), and it is likely that GWAS variants confer their effects through modulating regulatory mechanism. Read more

Harnessing the genetics of DNA methylation to understand context-specific gene regulation in disease

Project Background. Genome wide association studies (GWAS) have discovered many genetic associations with health outcomes. However, most GWAS signals reside in non-coding regions and it is likely that GWAS variants confer their effects through a regulatory mechanism. Read more

Eliminating Harmful Cells to Maintain Homeostatis and Prevent Tumorigenesis

Hamaratoglu Lab studies cell-cell signalling in development, homeostasis and tumourigenesis. We take advantage of outstanding genetic tools in Drosophila, and use larval imaginal discs as model epithelial organs. Read more

Integrative genomics prioritisation of drug targets

The MRC Integrative Epidemiology Unit at the University of Bristol is the leading group for the development and application of causal analysis and evidence triangulation in health research to improve lives. Read more

Self-funded PhD- Exploring changes in well-being across key life transitions

About the Project. We conduct research on the causes and consequences of positive well-being across the life course. Positive well-being includes feelings of happiness, satisfaction with one’s life, and having meaning and purpose. Read more

Self-funded MSc R- Exploring changes in well-being across key life transitions

We conduct research on the causes and consequences of positive well-being across the life course. Positive well-being includes feelings of happiness, satisfaction with one’s life, and having meaning and purpose. Read more

Early life factors in the development of Juvenile idiopathic arthritis

Juvenile idiopathic arthritis (JIA) is an autoimmune inflammatory arthritis with disease onset before the age of 16. Children and young people with this condition develop painful swollen joints and untreated it can lead to long term disability. It may also be associated with comorbid conditions such as uveitis. Read more

Investigating monogenic disorders of the protein synthesis machinery

Translation of mRNA into proteins is a critical cellular biological process. We recently described a novel human disorder, now called Faundes-Banka Syndrome (FABAS), caused by heterozygous variants in EIF5A1 that encodes a translation factor. Read more

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