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Genetics (sexual selection) PhD Projects, Programs & Scholarships

We have 7 Genetics (sexual selection) PhD Projects, Programs & Scholarships

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We have 7 Genetics (sexual selection) PhD Projects, Programs & Scholarships

Genomics of sexual trait expression in black grouse

  Research Group: Hoffman research group (molecular ecology)
An outstanding opportunity is available for a PhD student to work on the evolutionary genomics of sexual trait expression in an iconic avian model system, the black grouse (Lyrurus tetrix). The position is available in Joe Hoffman’s research group (www.thehoffmanlab.com) at the Department of Animal Behaviour at Bielefeld University and is fully funded for three years. Read more

Male-male competition vs female choice: same-same or something different?

  Research Group: Centre for Evolutionary Biology
We are looking for a talented student to conduct their PhD on sexual selection in Drosophila. Typically, males compete with one another for access to females, and females choose their preferred suitor among competing males. Read more

Experimental approaches to the evolution of anisogamy in a single celled alga

  Research Group: Centre for Evolutionary Biology
We are looking for a talented student to conduct their PhD on the evolutionary biology of anisogamy. Anisogamy is the difference in size between male and female gametes and is the driver of sexual selection and the evolution of the sexes. Read more

Defence evolution under protective symbiosis: how do nuclear and symbiont defences interact?

Animals live in symbiosis with microbes. The presence of symbionts modifies the biology of the host in fundamental ways. In insects and other arthropods, symbionts have become part of the genetic inheritance – passed from a female to her progeny in or on eggs. Read more

An omics approach to understand and treat KMT2C-related neurodevelopmental disorder using induced pluripotent stem cells and CRISPR-Cas9

Background. We recently identified a novel human syndrome caused by mutations in a gene called KMT2C1. Patients with this condition predominantly have developmental delay and intellectual disability indicating the important function of this gene in brain’s normal development and function. Read more
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