Medicine

Investigating placental function and fetal programming in Prader–Willi Syndrome

Cardiff University

Not stated

Location
Cardiff, United Kingdom, United Kingdom
Funding
Competition Funded PhD Project (Students Worldwide)
Application deadline
21 October 2026

About the project

About the Project Summary By bringing together transcriptomics and cutting edge imaging, and data analysis techniques, this PhD project aims to examine how abnormalities in placental function leads to altered programming of the developing fetal brain in a neurodevelopmental disorder. This interdisciplinary project will provide the student with preclinical lab-based skills, and bioinformatic and data-handling skills that will be applicable to a wide range of career pathways. A full description of the project can be found on the GW4 BioMed website . Academic criteria: Applicants for a studentship must have obtained, or be about to obtain, a first or upper second-class UK honours degree, or the equivalent qualification gained outside the UK. English requirements: IELTS with an overall score of 6.5 with 5.5 in all subskills, or acceptable alternative. Please see our English Language Requirements guidance for more details. How to Apply A list of all the projects and how to apply is available on the GW4 BioMed website . You may select up to 2 projects and submit one application per candidate only. Please complete an application to the GW4 BioMed3 for an ‘offer of funding’. If successful, you will also need to make an application for an 'offer to study' to your chosen institution later. Please note that we may close the application process before the stated deadline if an unprecedented number of applications are received– check the GW4 BioMed website for details and updates. If you are shortlisted for interview, you will be notified from Tuesday, 22nd December 2026. Interviews will be held virtually on 26th and 27th January 2027. Studentships will start on 1 st October 2027.

Research areas

MedicineInvestigatingplacentalfunctionandfetalprogramminginPrader–WilliSyndrome