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Genetics (cognitive neuroscience) PhD Projects, Programs & Scholarships

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

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  The genetics of cognitive ageing: neuromodulators and prefrontal cortex
  Dr M Chechlacz, Prof G Gkoutos, Dr P C Hansen
Application Deadline: 6 January 2020

Funding Type

PhD Type

Neuromodulators including dopamine, noradrenaline, serotonin, and acetylcholine have been implicated in numerous cognitive functions and behaviours.
  Personalized quantification and prediction of epilepsy surgery on seizure control and memory function
  Dr D Atan
Application Deadline: 25 November 2019

Funding Type

PhD Type

The University of Bristol is offering a 3.5 year full time PhD in research around Translational Health to start in 2020. This studentship is funded through GW4 BioMed MRC Doctoral Training Partnership.
  Epigenetic mechanisms of behavioural, placental and cognitive impairment in a neurodevelopmental model for schizophrenia
  Dr R Hager, Prof J Neill, Dr J Glazier
Applications accepted all year round

Funding Type

PhD Type

A fundamental question in disease research is how stressors experienced during critical developmental periods influence the genesis or ‘programming’ of adult disease (Estes & McAllister 2016).
  Investigating the remodelling of inhibitory brain circuits in early Alzheimer’s disease. PhD in Medical Studies (MRC GW4 BioMed DTP)
  Prof A Randall
Application Deadline: 25 November 2019

Funding Type

PhD Type

Supervisory team. Professor Andrew Randall, Medical School, College of Medicine and Health, University of Exeter. Dr Jonathan Witton, College of Medicine and Health, University of Exeter.
  Simons Initiative for the Developing Brain (SIDB) PhD Studentships 2020

Funding Type

PhD Type

Applications are invited for 3.5 year full-time fully funded PhD studentships spanning basic and translational brain sciences in the biological mechanisms underlying autism.
  Oral vitamin D spray as a novel treatment for 22q11 deletion syndrome
  Dr A McNeill, Dr C Mazzà
Applications accepted all year round

Funding Type

PhD Type

22q11 deletion syndrome is the most common genetic disorder, affecting about 1/2500 people (as common as cystic fibrosis). It is due to a small missing piece of chromosome 22 on the long arm (q) at position 11.
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