Helen Rooks

Denmark Hill
London, ENG, United Kingdom

Last Updated: 09/26/2026

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Found 18 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

Reduced GATA1 levels are associated with ineffective erythropoiesis in sickle cell anemia.

Reduced GATA1 levels are associated with ineffective erythropoiesis in sickle cell anemia.

Journal: Haematologica
Published: June 04, 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

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

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

A gain of function variant in PIEZO1 (E756del) and sickle cell disease.

A gain of function variant in PIEZO1 (E756del) and sickle cell disease.

Journal: Haematologica
Published: September 22, 2018

A survey of genetic fetal-haemoglobin modifiers in Nigerian patients with sickle cell anaemia.

A survey of genetic fetal-haemoglobin modifiers in Nigerian patients with sickle cell anaemia.

Journal: PloS one
Published: March 22, 2018

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

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

Journal: Blood advances
Published: June 26, 2017

Beta thalassaemia intermedia due to co-inheritance of three unique alpha globin cluster duplications characterised by next generation sequencing analysis.

Beta thalassaemia intermedia due to co-inheritance of three unique alpha globin cluster duplications characterised by next generation sequencing analysis.

Journal: British journal of haematology
Published: July 30, 2016

Genetic association of fetal-hemoglobin levels in individuals with sickle cell disease in Tanzania maps to conserved regulatory elements within the MYB core enhancer.

Genetic association of fetal-hemoglobin levels in individuals with sickle cell disease in Tanzania maps to conserved regulatory elements within the MYB core enhancer.

Journal: BMC medical genetics
Published: January 21, 2015

Genome wide association study of fetal hemoglobin in sickle cell anemia in Tanzania.

Genome wide association study of fetal hemoglobin in sickle cell anemia in Tanzania.

Journal: PloS one
Published: June 25, 2014
Showing 1-12 of 18

Last Updated: 09/26/2026