Human Genome Epidemiology Literature Finder
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Records 1 - 30 (of 35 Records) |
| Query Trace: Anemia and BCL11A[original query] |
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| Genetic variants at HbF-modifier loci moderate anemia and leukocytosis in sickle cell disease in Tanzania. American journal of hematology 2015 Jan 90 (1): E1-4. Mtatiro Siana Nkya, Makani Julie, Mmbando Bruno, Thein Swee Lay, Menzel Stephan, Cox Sharon |
| DNA polymorphisms at BCL11A, HBS1L-MYB and Xmn1-HBG2 site loci associated with fetal hemoglobin levels in sickle cell anemia patients from Northern Brazil. Blood cells, molecules & diseases 2014 Dec 53 (4): 176-9. Cardoso Greice Lemos, Diniz Isabela Guerreiro, Silva Aylla Núbia Lima Martins da, Cunha Daniele Almeida, Silva Junior Josivaldo Soares da, Uchôa Camila Tavares Carvalho, Santos Sidney Emanuel Batista dos, Trindade Saide Maria Sarmento, Cardoso Maria do Socorro de Oliveira, Guerreiro João Fari |
The genetics of hemoglobin A2 regulation in sickle cell anemia.
American journal of hematology 2014 Nov 89 (11): 1019-23. Griffin Paula J, Sebastiani Paola, Edward Heather, Baldwin Clinton T, Gladwin Mark T, Gordeuk Victor R, Chui David H K, Steinberg Martin |
| Prediction of fetal hemoglobin in sickle cell anemia using an ensemble of genetic risk prediction models. Circulation. Cardiovascular genetics 2014 Apr 7 (2): 110-5. Milton Jacqueline N, Gordeuk Victor R, Taylor James G, Gladwin Mark T, Steinberg Martin H, Sebastiani Pao |
| Genetic variant in the BCL11A (rs1427407), but not HBS1-MYB (rs6934903) loci associate with fetal hemoglobin levels in Indian sickle cell disease patients. Blood cells, molecules & diseases 2015 Jan 54 (1): 4-8. Bhanushali Aparna A, Patra P K, Nair D, Verma H, Das B |
| rs11886868 and rs4671393 of BCL11A associated with HbF level variation and modulate clinical events among sickle cell anemia patients. Hematology (Amsterdam, Netherlands) 2015 Jun . Chaouch Leila, Moumni Imen, Ouragini Houyem, Darragi Imen, Kalai Miniar, Chaouachi Dorra, Boudrigua Imen, Hafsia Raouf, Abbes Sal |
| BCL11A enhancer haplotypes and fetal hemoglobin in sickle cell anemia. Blood cells, molecules & diseases 2015 Mar 54 (3): 224-30. Sebastiani P, Farrell J J, Alsultan A, Wang S, Edward H L, Shappell H, Bae H, Milton J N, Baldwin C T, Al-Rubaish A M, Naserullah Z, Al-Muhanna F, Alsuliman A, Patra P K, Farrer L A, Ngo D, Vathipadiekal V, Chui D H K, Al-Ali A K, Steinberg M |
| APOL1, a-thalassemia, and BCL11A variants as a genetic risk profile for progression of chronic kidney disease in sickle cell anemia. Haematologica 2016 Sep . Saraf Santosh L, Shah Binal N, Zhang Xu, Han Jin, Tayo Bamidele O, Abbasi Taimur, Ostrower Adam, Guzman Elizabeth, Molokie Robert E, Gowhari Michel, Hassan Johara, Jain Shivi, Cooper Richard S, Machado Roberto F, Lash James P, Gordeuk Victor |
| rs11886868 and rs4671393 of BCL11A associated with HbF level variation and modulate clinical events among sickle cell anemia patients. Hematology (Amsterdam, Netherlands) 2016 Aug 21 (7): 425-9. Chaouch Leila, Moumni Imen, Ouragini Houyem, Darragi Imen, Kalai Miniar, Chaouachi Dorra, Boudrigua Imen, Hafsia Raouf, Abbes Sal |
| The role of BCL11A and HMIP-2 polymorphisms on endogenous and hydroxyurea induced levels of fetal hemoglobin in sickle cell anemia patients from southern Brazil. Blood cells, molecules & diseases 2016 Nov 62 32-37. Friedrisch João Ricardo, Sheehan Vivien, Flanagan Jonathan M, Baldan Alessandro, Summarell Carly C Ginter, Bittar Christina Matzembacher, Friedrisch Bruno Kras, Wilke Ianaê Indiara, Ribeiro Camila Blos, Daudt Liane Esteves, da Rocha Silla Lucia Maria |
| A candidate transacting modulator of fetal hemoglobin gene expression in the Arab-Indian haplotype of sickle cell anemia. American journal of hematology 2016 Aug . Vathipadiekal Vinod, Farrell John J, Wang Shuai, Edward Heather L, Shappell Heather, Al-Rubaish A M, Al-Muhanna Fahad, Naserullah Z, Alsuliman A, Qutub Hatem Othman, Simkin Irene, Farrer Lindsay A, Jiang Zhihua, Luo Hong-Yuan, Huang Shengwen, Mostoslavsky Gustavo, Murphy George, Patra Pradeep K, Chui David H K, Alsultan Abdulrahman, Al-Ali Amein K, Sebastiani Paola, Steinberg Martin |
| Associations of ?-thalassemia and BCL11A with stroke in Nigerian, United States, and United Kingdom sickle cell anemia cohorts. Blood advances 2017 9 1 (11): 693-698. Saraf Santosh L, Akingbola Titilola S, Shah Binal N, Ezekekwu Chinedu A, Sonubi Omowunmi, Zhang Xu, Hsu Lewis L, Gladwin Mark T, Machado Roberto F, Cooper Richard S, Gordeuk Victor R, Tayo Bamidele |
| Protective BCL11A and HBS1L-MYB polymorphisms in a cohort of 102 Congolese patients suffering from sickle cell anemia. Journal of clinical laboratory analysis 2017 Mar . Mikobi Tite Minga, Tshilobo Lukusa Prosper, Aloni Michel Ntetani, Lumaka Aimé Zola, Kaba Didine Kinkodi, Devriendt Koenraad, Matthijs Gert, Mbuyi Muamba Jean Marie, Race Valér |
| Quantitative Trait Loci Influencing Hb F Levels in Southern Thai Hb E (HBB: c.79G>A) Heterozygotes. Hemoglobin 2018 Feb 1-7. Kesornsit Aumpika, Jeenduang Nutjaree, Horpet Dararat, Plyduang Thunyaluk, Nuinoon Man |
| BCL11A rs1427407 Genotypes in Sickle Cell Anemia Patients Undergo to Stroke Problems in Sudan. Korean journal of family medicine 2018 12 40 (1): 53-57. Hassan Fathelrahman Mahdi, Al-Zahrani Faisal Mou |
| Genetic modulators of fetal hemoglobin expression and ischemic stroke occurrence in African descendant children with sickle cell anemia. Annals of hematology 2019 9 98 (12): 2673-2681. Nicolau Marta, Vargas Sofia, Silva Marisa, Coelho Andreia, Ferreira Emanuel, Mendonça Joana, Vieira Luís, Kjöllerström Paula, Maia Raquel, Silva Rita, Dias Alexandra, Ferreira Teresa, Morais Anabela, Soares Isabel Mota, Lavinha João, Faustino Pau |
| Combined and differential effects of alpha-thalassemia and HbF-quantitative trait loci in Senegalese hydroxyurea-free children with sickle cell anemia. Pediatric blood & cancer 2019 Jul e27934. Gueye Tall Fatou, Martin Cyril, Ndour El Hadji Malick, Renoux Céline, Ly Indou Déme, Connes Philippe, Gueye Papa Madieye, Diallo Rokhaya Ndiaye, Diagne Ibrahima, Diop Pape Amadou, Cissé Aynina, Lopez Sall Philomène, Joly Philip |
| High fetal hemoglobin level is associated with increased risk of cerebral vasculopathy in children with sickle cell disease in Mayotte. BMC pediatrics 2020 6 20 (1): 302. Chamouine Abdourahim, Saandi Thoueiba, Muszlak Mathias, Larmaraud Juliette, Lambrecht Laurent, Poisson Jean, Balicchi Julien, Pissard Serge, Elenga Narcis |
| Functional polymorphisms of BCL11A and HBS1L-MYB genes affect both fetal hemoglobin level and clinical outcomes in a cohort of children with sickle cell anemia. Annals of hematology 2020 May . Sales Rahyssa Rodrigues, Belisário André Rolim, Faria Gabriela, Mendes Fabiola, Luizon Marcelo Rizzatti, Viana Marcos Bora |
| Detection of BCL11A and HBS1L-MYB Genotypes in Sickle Cell Anemia. Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion 2020 Oct 36 (4): 705-710. Qadah Talal, Noorwali Abdulwahab, Alzahrani Fatma, Banjar Alaa, Filimban Najlaa, Felimban Ra |
| Genotypic Diversity among Angolan Children with Sickle Cell Anemia. International journal of environmental research and public health 2021 6 18 (10): . Delgadinho Mariana, Ginete Catarina, Santos Brígida, Miranda Armandina, Brito Migu |
| Significance of genetic modifiers of hemoglobinopathies leading towards precision medicine. Scientific reports 2021 Oct 11 (1): 20906. Hariharan Priya, Gorivale Manju, Sawant Pratibha, Mehta Pallavi, Nadkarni Ani |
| Fetal hemoglobin-boosting haplotypes of BCL11A gene and HBS1L-MYB intergenic region in the prediction of clinical and hematological outcomes in a cohort of children with sickle cell anemia. Journal of human genetics 2022 9 67 (12): 701-709. Sales Rahyssa Rodrigues, Nogueira Bárbara Lisboa, Belisário André Rolim, Faria Gabriela, Mendes Fabiola, Viana Marcos Borato, Luizon Marcelo Rizzat |
| Fetal hemoglobin regulating genetic variants identified in homozygous (HbSS) and heterozygous (HbSA) subjects from South Mexico. Journal of tropical pediatrics 2022 9 68 (5): . Rizo-de la Torre L C, Borrayo-López F J, Perea-Díaz F J, Aquino E, Venegas M, Hernández-Carbajal C, Espinoza-Mata L L, Ibarra-Cortés |
| Effects of Senegal haplotype (Xmn1-rs7412844), alpha-thalassemia (3.7kb HBA1/HBA2 deletion), NPRL3-rs11248850 and BCL11A-rs4671393 variants on sickle cell nephropathy. International journal of biochemistry and molecular biology 2022 5 13 (2): 5-16. Ndour El Hadji Malick, Mnika Khuthala, Guèye Tall Fatou, Seck Moussa, Dème Ly Indou, Nembaware Victoria, Sagna-Bassène Hélène Ange Thérèse, Dione Rokhaya, Ndongo Aliou Abdoulaye, Diop Jean Pascal Demba, Barry Nènè Oumou Kesso, Djité Moustapha, Ndiaye Diallo Rokhaya, Guèye Papa Madièye, Diop Saliou, Diagne Ibrahima, Cissé Aynina, Wonkam Ambroise, Lopez Sall Philomè |
| Fetal hemoglobin modulates neurocognitive performance in sickle cell anemia. Current research in translational medicine 2022 3 70 (3): 103335. Heitzer Andrew M, Longoria Jennifer, Rampersaud Evadnie, Rashkin Sara R, Estepp Jeremie H, Okhomina Victoria I, Wang Winfred C, Raches Darcy, Potter Brian, Steinberg Martin H, King Allison A, Kang Guolian, Hankins Jane |
| Do Genetic Polymorphisms Affect Fetal Hemoglobin (HbF) Levels in Patients With Sickle Cell Anemia Treated With Hydroxyurea? A Systematic Review and Pathway Analysis. Frontiers in pharmacology 2021 12 779497. Sales Rahyssa Rodrigues, Nogueira Bárbara Lisboa, Tosatti Jéssica Abdo Gonçalves, Gomes Karina Braga, Luizon Marcelo Rizzat |
| BCL11A Polymorphism in Egyptian Children with ?-Thalassemia: Relation to Phenotypic Heterogeneity. Journal of pediatric genetics 2023 1 12 (1): 16-22. Salah Nouran Y, Ali Heba G A, Bassiouny Noha, Salem Lamya, Taha Sara I, Youssef Mariam K, Annaka Layla, Barakat Noha |
| Detection of Asymptomatic Sickle Cell Hemoglobin Carriers and Fetal Hemoglobin Regulating Genetic Variants in African Descendants from Oaxaca, Mexico. Anemia 2024 5 2024 4940760. María De Los Ángeles Romero-Tlalolini, Sergio Roberto Aguilar-Ruiz, Rafael Baltiérrez-Hoyos, Jaime Vargas-Arzola, Luis Alberto Hernández-Osorio, Verónica Rocío Vásquez-Garzón, Héctor Ulises Bernardino-Hernández, Honorio Torres-Aguil |
| Genetic Modifiers of Sickle Cell Anemia Phenotype in a Cohort of Angolan Children. Genes 2024 4 15 (4): . Catarina Ginete, Mariana Delgadinho, Brígida Santos, Armandina Miranda, Carina Silva, Paulo Guerreiro, Emile R Chimusa, Miguel Bri |
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