Stephan Menzel
7PUBLICATIONS
9CO-AUTHORS
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Publications (7)
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|Jul 18, 2022
Fetal-haemoglobin enhancing genotype at BCL11A reduces HbA2 levels in patients with sickle cell anaemia.Titilope A Adeyemo, Oyesola O Ojewunmi, Idayat Ajoke Oyetunji
|Mar 10, 2022
Genetic variants of PKLR are associated with acute pain in sickle cell disease.Xunde Wang, Kate Gardner, Mickias B Tegegn
|Oct 19, 2020
F cell numbers are associated with an X-linked genetic polymorphism and correlate with haematological parameters in patients with sickle cell disease.Florence Urio, Siana Nkya, Helen Rooks
|May 30, 2019
The effects of hydroxycarbamide on the plasma proteome of children with sickle cell anaemia.John Brewin, Sanjay Tewari, Stephan Menzel
|Jun 08, 2018
A survey of genetic fetal-haemoglobin modifiers in Nigerian patients with sickle cell anaemia.Titilope A Adeyemo, Oyesola O Ojewunmi, Idat A Oyetunji
|Feb 14, 2018
g(HbF): a genetic model of fetal hemoglobin in sickle cell disease.Kate Gardner, Tony Fulford, Nicholas Silver
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Frequent Collaborators
1 joint publications
Alani S Akanmu
1 joint publications
David C Rees
1 joint publications
Florence Urio
1 joint publications
Lucio Luzzatto
1 joint publications
Kate Gardner
1 joint publications
Hamel Patel
1 joint publications
Fayaz T Seifuddin
1 joint publications
Swee Lay Thein
1 joint publications
Titilope A Adeyemo
