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2010 1
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32 results

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Page 1
Genetic regulation of fetal hemoglobin across global populations.
Cato LD, Li R, Lu HY, Yu F, Wissman M, Mkumbe BS, Ekwattanakit S, Deelen P, Mwita L, Sangeda R, Suksangpleng T, Riolueang S, Bronson PG, Paul DS, Kawabata E, Astle WJ, Aguet F, Ardlie K, de Lapuente Portilla AL, Kang G, Zhang Y, Nouraie SM, Gordeuk VR, Gladwin MT, Garrett ME, Ashley-Koch A, Telen MJ, Custer B, Kelly S, Dinardo CL, Sabino EC, Loureiro P, Carneiro-Proietti AB, Maximo C; NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium; BIOS Consortium; Méndez A, Hammerer-Lercher A, Sheehan VA, Weiss MJ, Franke L, Nilsson B, Butterworth AS, Viprakasit V, Nkya S, Sankaran VG. Cato LD, et al. Among authors: nkya s. medRxiv [Preprint]. 2023 Mar 28:2023.03.24.23287659. doi: 10.1101/2023.03.24.23287659. medRxiv. 2023. PMID: 36993312 Free PMC article. Preprint.
Genomics of fetal haemoglobin: a targeted approach for reticulocyte transcriptome study.
Nkya S, Kaywanga F, Nzunda C, Karim S, Solomon D, Saukiwa E, Christopher H, Ngowi D, Johansen J, Urio F, Mgaya J, Chamba C, Hashim F, Ambroise E, Acquah SO, Makani J. Nkya S, et al. Res Sq [Preprint]. 2023 Jun 30:rs.3.rs-3061395. doi: 10.21203/rs.3.rs-3061395/v1. Res Sq. 2023. PMID: 37461456 Free PMC article. Preprint.
Implementation of a gene therapy education initiative by the ASGCT and Muhimbili University of Health and Allied Sciences.
Cornetta K, Kay S, Urio F, Minja IK, Mbugi E, Mgaya J, Mselle T, Nkya S, Alimohamed MZ, Ndaki K, Bonamino M, Koya RC, Shah LD, Mahlangu J, Drago D, Rangarajan S, Jayandharan GR. Cornetta K, et al. Among authors: nkya s. Mol Ther. 2023 Sep 6;31(9):2561-2565. doi: 10.1016/j.ymthe.2023.07.019. Epub 2023 Aug 17. Mol Ther. 2023. PMID: 37595584
Neuroimaging in patients with sickle cell anemia: capacity building in Africa.
Jacob M, Saunders DE, Kawadler JM, Mussa B, Murdoch R, Lapidaire W, Tluway F, Kazema RR, Nkya S, Ahmed M, Kija E, Fundikira L, Kussaga F, Darekar A, Tutuba H, Shmueli K, Clark CA, Makani J, Kirkham FJ. Jacob M, et al. Among authors: nkya s. Blood Adv. 2018 Nov 30;2(Suppl 1):26-29. doi: 10.1182/bloodadvances.2018GS112714. Blood Adv. 2018. PMID: 30504194 Free PMC article. No abstract available.
The International Hemoglobinopathy Research Network (INHERENT): An international initiative to study the role of genetic modifiers in hemoglobinopathies.
Kountouris P, Stephanou C, Archer N, Bonifazi F, Giannuzzi V, Kuo KHM, Maggio A, Makani J, Mañú-Pereira MDM, Michailidou K, Nkya S, Nnodu OE, Trompeter S, Tshilolo L, Wonkam A, Zilfalil BA, Inusa BPD, Kleanthous M; on behalf of the International Hemoglobinopathy Research Network (INHERENT). Kountouris P, et al. Among authors: nkya s. Am J Hematol. 2021 Nov 1;96(11):E416-E420. doi: 10.1002/ajh.26323. Epub 2021 Aug 30. Am J Hematol. 2021. PMID: 34406671 Free PMC article. No abstract available.
32 results