The Hong Kong Polytechnic University Featured PhD Programmes
University College London Featured PhD Programmes
Birkbeck, University of London Featured PhD Programmes
University of Warwick Featured PhD Programmes
The Hong Kong Polytechnic University Featured PhD Programmes
"child"×
10 miles

Genetics (child) PhD Projects, Programs & Scholarships

We have 6 Genetics (child) PhD Projects, Programs & Scholarships

  • "child" ×
  • Genetics×
  • clear all
Order by 
Showing 1 to 6 of 6
  Identification of blood biomarkers for antenatal diagnosis of a common congenital heart defect, Tetralogy of Fallot.
  Dr I Dykes
Application Deadline: 1 December 2019

Funding Type

PhD Type

Almost 1 in every 100 babies born in the UK has a congenital heart defect (CHD). CHD is the leading cause of infant mortality and affected children often require surgery at birth.
  Fully-funded PhD positions in Biomedical Sciences at the MDC Berlin

Funding Type

PhD Type

Max Delbrück Center for Molecular Medicine (MDC) invites applicants for PhD positions.  .  . Are you passionate about understanding the molecular basis of health and disease, and translating your findings into clinical applications? Are you interested in one of the following topics?.
  Type 1 diabetes; novel insights from molecular analysis of single B cells.
  Prof K Gillespie
Application Deadline: 25 November 2019

Funding Type

PhD Type

Overview. The University of Bristol is offering a 3.5 year full time PhD to start in 2019. This studentship is funded through GW4 BioMed MRC Doctoral Training Partnership.
  Genetic risk factors underlying impaired cognitive flexibility and neural plasticity in psychiatric disorders.
  Prof J Mellor, Dr MC Ashby
Application Deadline: 25 November 2019

Funding Type

PhD Type

Supervisors. Prof Jack Mellor (Bristol), Jeremy Hall (Cardiff), Dr Michael Ashby (Bristol), Prof Lawrence Wilkinson (Cardiff). Cian O’Donnell (Bristol.
  De Novo Mutations and Human Disease
  Prof A Goriely, Prof A Wilkie
Application Deadline: 10 January 2020

Funding Type

PhD Type

De novo mutations (DNMs) are a significant contributor to human disease, affecting ~1:300 new births. We study the mechanisms by which these spontaneous mutations arise in the first instance, concentrating on the tissue where most of them originate, the human testis.
  De Novo Mutations and Human Disease
  Prof A Goriely, Prof A Wilkie
Application Deadline: 10 January 2020

Funding Type

PhD Type

De novo mutations (DNMs) are a significant contributor to human disease, affecting ~1:300 new births. We study the mechanisms by which these spontaneous mutations arise in the first instance, concentrating on the tissue where most of them originate, the human testis.
Show 10 15 30 per page
  • 1


FindAPhD. Copyright 2005-2019
All rights reserved.