Menzel, Stephan

A QTL influencing F cell production maps to a gene encoding a zinc-finger protein on chromosome 2p15

Menzel, S., Garner, C., Gut, I., Matsuda, F., Yamaguchi, M., Heath, S., Foglio, M., Zelenika, D., Boland, A., Rooks, H., et al. (2007) · Nature Genetics

Hemoglobinopathies and Related DisordersGenetic Associations and Epidemiology

Cited by 529

Control of fetal hemoglobin: new insights emerging from genomics and clinical implications

Thein, S. L., Menzel, S., Lathrop, M., & Garner, C. (2009) · Human Molecular Genetics

Hemoglobinopathies and Related DisordersHemoglobin structure and function

Cited by 250

Genetic modifiers of fetal haemoglobin in sickle cell disease

Menzel, S., & Thein, S. L. (2019) · Molecular Diagnosis & Therapy

Hemoglobinopathies and Related DisordersHemoglobin structure and function

Cited by 50

g(HbF): a genetic model of fetal hemoglobin in sickle cell disease

Gardner, K., Fulford, T., Silver, N., Rooks, H., Angelis, N., Allman, M., Nkya, S., Makani, J., Howard, J., Kesse-Adu, R., et al. (2018) · Blood Advances

Hemoglobinopathies and Related DisordersHemoglobin structure and function

Cited by 43

Prognostic factors of disease severity in infants with sickle cell anemia: A comprehensive longitudinal cohort study

Brousse, V., El Hoss, S., Bouazza, N., Arnaud, C., Bernaudin, F., Pellegrino, B., Guitton, C., Odièvre‐Montanié, M., Mames, D., Brouzes, C., et al. (2018) · American Journal of Hematology

Hemoglobinopathies and Related DisordersBlood groups and transfusion

Cited by 25

Fetal hemoglobin is associated with peripheral oxygen saturation in sickle cell disease in Tanzania

Nkya, S., Mgaya, J., Urio, F., Makubi, A., Thein, S. L., Menzel, S., Cox, S. E., Newton, C. R., Kirkham, F. J., Mmbando, B. P., et al. (2017) · EBioMedicine

Hemoglobinopathies and Related DisordersHemoglobin structure and function

Cited by 13