A former Lord Mayor of Manchester has become the 3,000th person in GM to take part in research aimed at understanding and tackling the higher rates of serious disease in South Asian people.
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A ground-breaking research study treating rare genetic conditions in newborn babies has reached a major milestone with the recruitment of its 1,000th baby at MFT.
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To celebrate International Day of the Midwife, Research Midwife, Deborah Pillar shares her midwifery research journey and why she is proud to contribute to research that aims to make pregnancy safer.
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An aspiring researcher is encouraging other health and care professionals to be part of a NIHR development programme which has inspired her to become a Principal Investigator.
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Latest research led from Manchester could revolutionise the diagnosis of Perrault syndrome, a rare genetic condition that results in hearing loss.
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An international team of scientists are to set to use thousands of MRI brain scans from research teams around the world in a bid to study NF1, a lifelong neurological condition.
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In the largest study of its kind, UK clinicians and researchers at RMCH and GOSH have jointly developed a highly innovative, life-changing surgery for children with a rare genetic condition.
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The Pharmacogenetics Roll Out – Gauging Response to Service [PROGRESS] programme is an NHS England funded transformation project led by researchers at Manchester University NHS Foundation Trust.
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