Stephan Menzel

Denmark Hill
London, ENG, United Kingdom

Last Updated: 09/26/2026

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Found 38 publications

Fetal-hemoglobin-expressing red blood cells ("F cells") consist of three distinct types as revealed by single-cell transcriptomic analysis of circulating reticulocytes.

Fetal-hemoglobin-expressing red blood cells ("F cells") consist of three distinct types as revealed by single-cell transcriptomic analysis of circulating reticulocytes.

Journal: HemaSphere

Published: March 04, 2025

Genetic Polymorphisms Associated with Fetal Hemoglobin (HbF) Levels and F-Cell Numbers: A Systematic Review of Genome-Wide Association Studies.

Genetic Polymorphisms Associated with Fetal Hemoglobin (HbF) Levels and F-Cell Numbers: A Systematic Review of Genome-Wide Association Studies.

Journal: International journal of molecular sciences

Published: September 06, 2024

The genetic dissection of fetal haemoglobin persistence in sickle cell disease in Nigeria.

The genetic dissection of fetal haemoglobin persistence in sickle cell disease in Nigeria.

Journal: Human molecular genetics

Published: May 20, 2023

Gender effect on production and enrichment of F cell numbers in sickle cell disease patients in Tanzania.

Gender effect on production and enrichment of F cell numbers in sickle cell disease patients in Tanzania.

Journal: American journal of hematology

Published: June 22, 2022

The pleiotropic effects of α-thalassemia on HbSS and HbSC sickle cell disease: Reduced erythrocyte cation co-transport activity, serum erythropoietin, and transfusion burden, do not translate into increased survival.

The pleiotropic effects of α-thalassemia on HbSS and HbSC sickle cell disease: Reduced erythrocyte cation co-transport activity, serum erythropoietin, and transfusion burden, do not translate into increased survival.

Journal: American journal of hematology

Published: June 04, 2022

Genetic variants of PKLR are associated with acute pain in sickle cell disease.

Genetic variants of PKLR are associated with acute pain in sickle cell disease.

Journal: Blood advances

Published: November 22, 2021

Do we need more Genome Wide Association Studies?

Do we need more Genome Wide Association Studies?

Journal: Haematologica

Published: March 23, 2021

Fetal-haemoglobin enhancing genotype at BCL11A reduces HbA2 levels in patients with sickle cell anaemia.

Fetal-haemoglobin enhancing genotype at BCL11A reduces HbA2 levels in patients with sickle cell anaemia.

Journal: EJHaem

Published: January 29, 2021

Genetic Analysis of Patients With Sickle Cell Anemia and Stroke Before 4 Years of Age Suggest an Important Role for Apoliprotein E.

Genetic Analysis of Patients With Sickle Cell Anemia and Stroke Before 4 Years of Age Suggest an Important Role for Apoliprotein E.

Journal: Circulation. Genomic and precision medicine

Published: September 14, 2020

Genome wide association study of silent cerebral infarction in sickle cell disease (HbSS and HbSC).

Genome wide association study of silent cerebral infarction in sickle cell disease (HbSS and HbSC).

Journal: Haematologica

Published: July 03, 2020

Sickle cell disease in Sri Lanka: clinical and molecular basis and the unanswered questions about disease severity.

Sickle cell disease in Sri Lanka: clinical and molecular basis and the unanswered questions about disease severity.

Journal: Orphanet journal of rare diseases

Published: February 13, 2020

F cell numbers are associated with an X-linked genetic polymorphism and correlate with haematological parameters in patients with sickle cell disease.

F cell numbers are associated with an X-linked genetic polymorphism and correlate with haematological parameters in patients with sickle cell disease.

Journal: British journal of haematology

Published: February 11, 2020

Showing 1-12 of 38

Last Updated: 09/26/2026