Projects per year
Search results
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Active
Understanding the molecular regulation of erythroid cells that express both HBG1 and HBG2
Menzel, S. (Primary Investigator) & Stroumpoulis, J. S. (Co-Investigator)
1/12/2024 → 30/11/2027
Project: Research
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Not started
Genetic characterisation of a disease modifier locus in patients with sickle cell disease.
Menzel, S. (Primary Investigator)
Project: Research
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Finished
Strengthened research alliance on genetics of sickle cell disease
Menzel, S. (Primary Investigator) & Stroumpoulis, J. S. (Co-Investigator)
EPSRC Engineering and Physical Sciences Research Council
1/10/2022 → 31/03/2023
Project: Research
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Identification of novel mechanisms of fetal-haemoglobin induction by common genetic variation in patients with sickle cell disease
Menzel, S. (Primary Investigator) & Stroumpoulis, J. S. (Co-Investigator)
1/12/2019 → 30/11/2022
Project: Research
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Genome-wide association study to identify quantitative trait loci influencing transcranial Doppler velocities in children with sickle cell anaemia
Rees, D. (Primary Investigator) & Menzel, S. (Co-Investigator)
1/04/2017 → 31/03/2020
Project: Research
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GLOBINOMICS - Molecular and cellular therapeutic implications of the globin gene switch mechanism
Menzel, S. (Primary Investigator)
1/10/2016 → 30/09/2021
Project: Research
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Genetic determinants of cerebral vasculopathy in very young children with sickle cell anaemia
Rees, D. (Primary Investigator) & Menzel, S. (Co-Investigator)
7/09/2016 → 6/09/2019
Project: Research
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Genetic modifiers of phenotypic variability in Sickle Cell Disease
Menzel, S. (Primary Investigator)
1/09/2016 → 31/08/2020
Project: Research
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Genetic modifiers of phenotypic variability in Sickle Cell Disease
Menzel, S. (Primary Investigator)
1/09/2016 → 31/08/2020
Project: Research
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Genetic determinants of cerebral vasculopathy in very young children with sickle cell anaemia
Rees, D. (Primary Investigator) & Menzel, S. (Co-Investigator)
1/08/2016 → 30/07/2019
Project: Research
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Diversity of a single genetic condition in a cosmopolitan urban environment: Sickle Cell disease in London.
Menzel, S. (Primary Investigator)
1/05/2016 → 30/04/2019
Project: Research
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The investigation for the genes of severe early onset preeclampsia: a pilot study (GENESIA)
Poon, L. (Primary Investigator) & Menzel, S. (Co-Investigator)
1/01/2016 → 31/12/2020
Project: Research
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Sickle Cell Disease - Environmental and Genetic Factors Influencing Clinical Outcome
Rees, D. (Primary Investigator) & Menzel, S. (Co-Investigator)
1/04/2015 → 31/03/2017
Project: Research
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Genetic modifiers of foetal haemoglobin and response to pharmacological induction in various haematological malignancies and sickle cell disease: A cross-sectional and cohort study.
Menzel, S. (Primary Investigator)
British Society for Haematology
1/03/2015 → 31/08/2016
Project: Research
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Whole genome-sequence analysis: influence of mutations on globin gene regulation and erythropoiesis
Menzel, S. (Primary Investigator)
1/07/2013 → 30/06/2014
Project: Research
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Bilateral BBSRC - FAPESP F cells - a distinct fraction of red blood cells in humans
Menzel, S. (Primary Investigator), Mayr, M. (Co-Investigator) & Thein, S. L. (Co-Investigator)
1/02/2013 → 31/01/2016
Project: Research
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Sickle Cell Anaemia: The role of endogenous biomarkers and genome wide associationstudies(GWAS) in determining the risk factors for renal impairment
Dalton, N. (Primary Investigator), Menzel, S. (Primary Investigator) & Rees, D. (Primary Investigator)
1/01/2013 → 31/12/2018
Project: Research
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ThALAMOSS - THALAssaemia MOdular Stratification System for personalized therapy ofbeta-thalassemia
Thein, S. L. (Primary Investigator) & Menzel, S. (Co-Investigator)
1/11/2012 → 31/12/2016
Project: Research
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Sickle cell disease: a UK patient cohort to support translational research
Thein, S. L. (Primary Investigator), Menzel, S. (Co-Investigator) & Rees, D. (Co-Investigator)
1/09/2012 → 31/08/2017
Project: Research
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Sickle cell disease: a UK patient cohort to support translational research
Thein, S. L. (Primary Investigator), Menzel, S. (Co-Investigator) & Rees, D. (Co-Investigator)
1/05/2012 → 30/04/2017
Project: Research
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Genetic characterisation of a disease modifier locus in patients with sickle cell disease
Menzel, S. (Primary Investigator)
British Society for Haematology
1/08/2010 → 31/07/2011
Project: Research
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Development of a predictive genetic test for sickle cell disease modifying loci
Thein, S. L. (Primary Investigator) & Menzel, S. (Co-Investigator)
2/04/2010 → 1/04/2013
Project: Research