Human Genome Epidemiology Literature Finder
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Records 1 - 30 (of 57 Records) |
| Query Trace: Thalassemia and BCL11A[original query] |
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| 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 |
| In Vitro Hb Production in B-thalassemia Patients Is Not a Predictor of Clinical Responsiveness to Hydroxyurea. Iranian journal of public health 2017 8 46 (7): 948-956. Mahdavi Mohammad Reza, Pourfarzad Farzin, Kosaryan Mehrnoush, Akbari Mohammad Tag |
| An enhancer haplotype may influence BCL11A expression levels and the response to hydroxyurea in ß-thalassemia patients. Pharmacogenomics 2017 Jun . Maroofi Nahal, Azarkeivan Azita, Banihashemi Soosan, Mohammadparast Saeid, Aghajanirefah Ali, Banan Meh |
| Genetic Variants at BCL11A and HBS1L-MYB loci Influence Hb F Levels in Chinese Zhuang ß-Thalassemia Intermedia Patients. Hemoglobin 2016 Nov 40 (6): 405-410. Lai Yunli, Chen Yun, Chen Biyan, Zheng Haiyang, Yi Sheng, Li Guojian, Wei Hongwei, He Sheng, Zheng Chengua |
| 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 |
| g(HbF): a genetic model of fetal hemoglobin in sickle cell disease. Blood advances 2018 2 2 (3): 235-239. Gardner Kate, Fulford Tony, Silver Nicholas, Rooks Helen, Angelis Nikolaos, Allman Marlene, Nkya Siana, Makani Julie, Howard Jo, Kesse-Adu Rachel, Rees David C, Stuart-Smith Sara, Yeghen Tullie, Awogbade Moji, Sangeda Raphael Z, Mgaya Josephine, Patel Hamel, Newhouse Stephen, Menzel Stephan, Thein Swee L |
| Common fetal hemoglobin variants in Lebanese patients bearing the codon 29 beta gene mutation associated with different thalassemia phenotypes. Annals of hematology 2018 12 98 (4): 833-840. Brancaleoni Valentina, Moukhadder Hassan M, Consonni Dario, Koussa Suzanne, Di Pierro Elena, Cappellini Maria Domenica, Taher A |
| Genetic Modifiers of Fetal Haemoglobin (HbF) and Phenotypic Severity in ?-Thalassemia Patients. Current molecular medicine 2018 Oct . Razak S A A, Murad N A A, Masra F, Chong D L S, Abdullah N, Jalil N, Alauddin H, Sabudin R Z A R, Ithnin A, Khai L C, Aziz N A, Muda Z, Ibrahim H, Latiff Z |
| 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 |
| Molecular Analysis of Non-Transfusion Dependent Thalassemia Associated with Hemoglobin E-?-Thalassemia Disease without ?-Thalassemia. Mediterranean journal of hematology and infectious diseases 2019 11 (1): e2019038. Phanrahan Paramee, Yamsri Supawadee, Teawtrakul Nattiya, Fucharoen Goonnapa, Sanchaisuriya Kanokwan, Fucharoen Sup |
| A novel SNP rs11759328 on Rho GTPase-activating protein 18 gene is associated with the expression of Hb F in hemoglobin E-related disorders. Annals of hematology 2019 11 99 (1): 23-29. Jomoui Wittaya, Tepakhan Wanicha, Yamsri Supawadee, Srivorakun Hataichanok, Fucharoen Goonnapa, Fucharoen Sup |
| Association Between Genetic Polymorphisms and Hb F Levels in Heterozygous ?-Thalassemia 3.5?kb Deletions. Hemoglobin 2020 Sep 1-6. Tepakhan Wanicha, Kanjanaopas Sataron, Srewaradachpisal Kornt |
| 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 |
| The association of HBG2, BCL11A, and HBS1L-MYB polymorphisms to thalidomide response in Chinese ?-thalassemia patients. Blood cells, molecules & diseases 2020 Apr 84 102442. Yang Kun, Wu Yi, Ma Yanni, Xiao Jian, Zhou Yali, Yin Xiaol |
| Multi-Locus Models to Address Hb F Variability in Portuguese ß-Thalassemia Carriers. Hemoglobin 2020 Apr 1-5. Manco Licínio, Bento Celeste, Relvas Luís, Cunha Elisabete, Pereira Janet, Moreira Valeria, Alvarez Manuela, Maia Tabita, Ribeiro M Letíc |
| Haemoglobin switching modulator SNPs rs5006884 is associated with increased HbA in ?-thalassaemia carriers. Archives of medical science : AMS 2021 8 17 (4): 1064-1074. Cyrus Cyril, Vatte Chittibabu, Chathoth Shahanas, Sayed Abdul Azeez, Borgio J Francis, Alrubaish Mohammed Abdullah, Alfalah Rawan, Alsaikhan Jana, Al Ali Amein |
| A polygenic score for acute vaso-occlusive pain in pediatric sickle cell disease. Blood advances 2021 07 5 (14): 2839-2851. Rampersaud Evadnie, Kang Guolian, Palmer Lance E, Rashkin Sara R, Wang Shuoguo, Bi Wenjian, Alberts Nicole M, Anghelescu Doralina, Barton Martha, Birch Kirby, Boulos Nidal, Brandow Amanda M, Brooke Russell John, Chang Ti-Cheng, Chen Wenan, Cheng Yong, Ding Juan, Easton John, Hodges Jason R, Kanne Celeste K, Levy Shawn, Mulder Heather, Patel Ashwin P, Puri Latika, Rosencrance Celeste, Rusch Michael, Sapkota Yadav, Sioson Edgar, Sharma Akshay, Tang Xing, Thrasher Andrew, Wang Winfred, Yao Yu, Yasui Yutaka, Yergeau Donald, Hankins Jane S, Sheehan Vivien A, Downing James R, Estepp Jeremie H, Zhang Jinghui, DeBaun Michael, Wu Gang, Weiss Mitchell |
| Modulatory effect of single nucleotide polymorphism in Xmn1, BCL11A and HBS1L-MYB loci on foetal haemoglobin levels in ?-thalassemia major and Intermedia patients. JPMA. The Journal of the Pakistan Medical Association 2021 May 71 (5): 1394-1398. Bashir Shabnam, Mahmood Saqib, Mohsin Shahida, Tabassum Iqra, Ghafoor Mahmood, Sajjad Oshe |
| Predictive SNPs for ?-thalassemia/HbE disease severity. Scientific reports 2021 5 11 (1): 10352. Munkongdee Thongperm, Tongsima Sissades, Ngamphiw Chumpol, Wangkumhang Pongsakorn, Peerapittayamongkol Chayanon, Hashim Hafizah Binti, Fucharoen Suthat, Svasti Saovar |
| A Pragmatic Scoring Tool to Predict Hydroxyurea Response Among ?-Thalassemia Major Patients in Pakistan. Journal of pediatric hematology/oncology 2021 3 44 (1): e77-e83. Ansari Saqib H, Hussain Zeeshan, Zohaib Muhammad, Parveen Sadia, Kaleem Bushra, Qamar Hina, Adil Omair, Khan Muhammad T, Shamsi Tahir |
| 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 |
| 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 |
| Frequency of secondary modifiers in Beta Thalassemia intermedia in patients from Northern Punjab. Pakistan journal of medical sciences 2023 9 39 (5): 1517-1520. Fariha Nasreen, Attika Khalid, Lubna Zafar, Suhaib Ahmad, Asma Shai |
| Correlations between Multiple SNPs and HbF Levels in ?-Thalassemia Carriers. Clinical laboratory 2023 9 69 (9): . Qin Xu, Ling Huang, Tingting Jin, Yuanyuan Han, Juan Liu, Wenqiu Zhang, Yao Biao, Bangquan An, Shengwen Hua |
| Molecular basis of a high Hb A/Hb F?-thalassemia trait: a retrospective analysis, genotype-phenotype interaction, diagnostic implication, and identification of a novel interaction with ?-globin gene triplication. PeerJ 2023 5 11 e15308. Chayada Soontornpanawet, Kritsada Singha, Hataichanok Srivorakun, Wanicha Tepakhan, Goonnapa Fucharoen, Supan Fucharo |
| Responses of ?-thalassemia and compound heterozygote of Sickle/?thalassemia of BCL11A Gene Polymorphism in Pakistani Patients. Pakistan journal of medical sciences 2023 11 39 (6): 1788-1792. Nayab Soomro, Mohsin Wahid, Mehreen Mehmood, Syed Hasan Dani |
| 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 |
| Systematic Review of Genetic Modifiers Associated with the Development and/or Progression of Nephropathy in Patients with Sickle Cell Disease. International journal of molecular sciences 2024 5 25 (10): . Veerle Labarque, Emmanuel Chide Okocha, |
| Associations between BCL11A and HBS1L-MYB polymorphisms and thalassemia risk. Journal of Taibah University Medical Sciences 2024 11 19 (5): 1039-1048. Kashif Bashir, Uzma K Niazi, Raheela Shahzadi, Kaynat Azam, Asma Idrees, Qurrat U Ain, Amin A Alam |
- Page last reviewed:Feb 1, 2024
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