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Blood Advances|October 19, 2018
The platelet NLRP3 inflammasome is upregulated in sickle cell disease via HMGB1/TLR4 and Bruton tyrosine kinaseSebastian Vogel, Taruna Arora, Xunde Wang, et al.
British Journal of Haematology|January 28, 2021
A phenotypic risk score for predicting mortality in sickle cell diseaseVandana Sachdev, Xin Tian, Yuan Gu, et al.
Haematologica|December 23, 2020
Genome wide association study of silent cerebral infarction in sickle cell disease (HbSS and HbSC)John N Brewin, Helen Rooks, Kate Gardner, et al.
British Journal of Haematology|September 28, 2007
Circulating DNA: a potential marker of sickle cell crisisNisha Vasavda, Pinar Ulug, Sheila Kondaveeti, et al.
Blood Advances|March 10, 2022
Genetic variants of PKLR are associated with acute pain in sickle cell diseaseXunde Wang, Kate Gardner, Mickias B Tegegn, et al.
Ebiomedicine|August 29, 2017
Fetal Hemoglobin is Associated with Peripheral Oxygen Saturation in Sickle Cell Disease in TanzaniaSiana Nkya, Josephine Mgaya, Florence Urio, et al.
British Journal of Haematology|October 23, 2024
A machine learning-based workflow for predicting transplant outcomes in patients with sickle cell diseaseHaiou Li, Vandana Sachdev, Xin Tian, et al.
The Journal of Clinical Investigation|March 12, 2014
HBS1L-MYB intergenic variants modulate fetal hemoglobin via long-range MYB enhancersRalph Stadhouders, Suleyman Aktuna, Supat Thongjuea, et al.
BMC Medical Genetics|May 1, 2015
Genetic association of fetal-hemoglobin levels in individuals with sickle cell disease in Tanzania maps to conserved regulatory elements within the MYB core enhancerSiana N Mtatiro, Josephine Mgaya, Tarjinder Singh, et al.
Biorxiv : the Preprint Server for Biology|December 11, 2023
Random forest classifiers trained on simulated data enable accurate short read-based genotyping of structural variants in the alpha globin region at Chr16p13.3Nancy F Hansen, Xunde Wang, Mickias B Tegegn, et al.
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