HuGE Literature Finder
Records 1-30
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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 |
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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, Alias H, Khai L C, Aziz N A, Muda Z, Ibrahim H, Jamal R, Latif Z |
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The association of HBG2, BCL11A, and HMIP polymorphisms with fetal hemoglobin and clinical phenotype in Iraqi Kurds with sickle cell disease.
International journal of laboratory hematology 2018 Sep . Al-Allawi Nasir, Qadir Shatha M A, Puehringer Helene, Chui David H K, Farrell John J, Oberkanins Christi |
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Clinical and genetic factors are associated with pain and hospitalisation rates in sickle cell anaemia in Cameroon.
British journal of haematology 2017 Dec . Wonkam Ambroise, Mnika Khuthala, Ngo Bitoungui Valentina J, Chetcha Chemegni Bernard, Chimusa Emile R, Dandara Collet, Kengne Andre |
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An enhancer haplotype may influence BCL11A expression levels and the response to hydroxyurea in ?-thalassemia patients.
Pharmacogenomics 2017 Jun . Maroofi Nahal, Azarkeivan Azita, Banihashemi Soosan, Mohammadparast Saeid, Aghajanirefah Ali, Banan Meh |
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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 |
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The association between four SNPs (rs7482144, rs4671393, rs28384513 and rs4895441) and fetal hemoglobin levels in Chinese Zhuang ß-thalassemia intermedia patients.
Blood cells, molecules & diseases 2017 03 63 52-57. Lai Yunli, Zhou Lin, Yi Sheng, Chen Yun, Tang Yanqing, Yi Shang, Yang Ze, Wei Hongwei, Zheng Chenguang, He She |
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Genetic Variants at BCL11A and HBS1L-MYB loci Influence Hb F Levels in Chinese Zhuang ?-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 |
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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 |
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A Multi-Locus Approach to Characterization of Major Quantitative Trait Loci Influencing Hb F Regulation in Chinese ?-Thalassemia Carriers.
Hemoglobin 2016 Oct 1-12. Chan Nelson C N, Lau Kin-Mang, Cheng Kelvin C K, Chan Natalie P H, Ng Margaret H |
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Molecular Understanding of Non-Transfusion-Dependent Thalassemia Associated with Hemoglobin E-?-Thalassemia in Northeast Thailand.
Acta haematologica 2016 Oct 136 (4): 233-239. Yamsri Supawadee, Pakdee Naruwat, Fucharoen Goonnapa, Sanchaisuriya Kanokwan, Fucharoen Sup |
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APOL1, Alpha 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 |
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A Candidate Trans-acting Modulator of Fetal Hemoglobin Gene Expression in the Arab-Indian Haplotype of Sickle Cell Anemia: -ANTXR1 Variants and HbF.
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 |
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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 |
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Modifying effect of XmnI, BCL11A, and HBS1L-MYB on clinical appearances: A study on ß-thalassemia and hemoglobin E/ß-thalassemia patients in Indonesia.
Hematology/oncology and stem cell therapy 2016 Jun 9 (2): 55-63. Rujito Lantip, Basalamah Muhammad, Siswandari Wahyu, Setyono Joko, Wulandari Gondo, Mulatsih Sri, Sofro Abdul Salam M, Sadewa Ahmad Hamim, Sutaryo Sutar |
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Association of BCL11A genetic variant (rs11886868) with severity in ?-thalassaemia major & sickle cell anaemia.
The Indian journal of medical research 2016 Apr 143 (4): 449-54. Dadheech Sneha, Madhulatha D, Jainc Suman, Joseph James, Jyothy A, Munshi Anja |
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Influence of single nucleotide polymorphisms in the BCL11A and HBS1L-MYB gene on the HbF levels and clinical severity of sickle cell anaemia patients.
Annals of hematology 2016 Apr . Upadhye Dipti, Jain Dipty, Trivedi Yogesh, Nadkarni Anita, Ghosh Kanjaksha, Colah Rosh |
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Reduced rate of sickle-related complications in Brazilian patients carrying HbF-promoting alleles at the BCL11A and HMIP-2 loci.
British journal of haematology 2016 Feb . Leonardo Flávia C, Brugnerotto Ana F, Domingos Igor F, Fertrin Kleber Y, de Albuquerque Dulcinéia M, Bezerra Marcos A C, Araújo Aderson S, Saad Sara T O, Costa Fernando F, Menzel Stephan, Conran Nicola, Thein Swee L |
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The genetic basis of asymptomatic codon 8 frame-shift (HBB:c25_26delAA) ?(0) -thalassaemia homozygotes.
British journal of haematology 2016 Jan . Jiang Zhihua, Luo Hong-Yuan, Huang Shengwen, Farrell John J, Davis Lance, Théberge Roger, Benson Katherine A, Riolueang Suchada, Viprakasit Vip, Al-Allawi Nasir A S, Ünal Sule, Gümrük Fatma, Akar Nejat, Ba?ak A Nazli, Osorio Leonor, Badens Catherine, Pissard Serge, Joly Philippe, Campbell Andrew D, Gallagher Patrick G, Steinberg Martin H, Forget Bernard G, Chui David H |
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Association between Variants at BCL11A Erythroid-Specific Enhancer and Fetal Hemoglobin Levels among Sickle Cell Disease Patients in Cameroon: Implications for Future Therapeutic Interventions.
Omics : a journal of integrative biology 2015 Sep . Pule Gift Dineo, Ngo Bitoungui Valentina Josiane, Chetcha Chemegni Bernard, Kengne Andre Pascal, Antonarakis Stylianos, Wonkam Ambroi |
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Genetics of fetal hemoglobin in tribal Indian patients with sickle cell anemia.
Translational research : the journal of laboratory and clinical medicine 2015 Jun 165 (6): 696-703. Bhanushali Aparna A, Patra Pradip K, Pradhan Smarnika, Khanka Suraj S, Singh Sujata, Das Bibhu |
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Rs 11886868 and rs 4671393 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 |
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A genetic score for the prediction of beta-thalassemia severity.
Haematologica 2015 Apr 100 (4): 452-7. Danjou Fabrice, Francavilla Marcella, Anni Franco, Satta Stefania, Demartis Franca-Rosa, Perseu Lucia, Manca Matteo, Sollaino Maria Carla, Manunza Laura, Mereu Elisabetta, Marceddu Giuseppe, Pissard Serge, Joly Philippe, Thuret Isabelle, Origa Raffaella, Borg Joseph, Forni Gian Luca, Piga Antonio, Lai Maria Eliana, Badens Catherine, Moi Paolo, Galanello Ren |
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Polymorphic variations influencing fetal hemoglobin levels: association study in beta-thalassemia carriers and in normal individuals of Portuguese origin.
Blood cells, molecules & diseases 2015 Apr 54 (4): 315-20. Pereira Clara, Relvas Luís, Bento Celeste, Abade Augusto, Ribeiro M Letícia, Manco Licín |
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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 |
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Genetic Modifiers in ß-Thalassemia Intermedia: A Study on 102 Iraqi Arab Patients.
Genetic testing and molecular biomarkers 2015 Mar . Al-Allawi Nasir A S, Puehringer Helene, Raheem Ruzaiqah A, Oberkanins Christi |
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Polymorphism at BCL11A compared to HBS1L-MYB loci explains less of the variance in HbF in patients with sickle cell disease in Cameroon.
Blood cells, molecules & diseases 2015 Mar 54 (3): 268-9. Bitoungui Valentina Josiane Ngo, Ngogang Jeanne, Wonkam Ambroi |
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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 |
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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 |
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Genetic Modifiers of Sickle Cell Disease: A Genotype-Phenotype Relationship Study in a Cohort of 82 Children on Mayotte Island.
Hemoglobin 2015 39 (3): 156-61. Muszlak Mathias, Pissard Serge, Badens Catherine, Chamouine Abdourahim, Maillard Olivier, Thuret Isabel |
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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 |
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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 |
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Association of variants at BCL11A and HBS1L-MYB with hemoglobin F and hospitalization rates among sickle cell patients in Cameroon.
PloS one 2014 9 (3): e92506. Wonkam Ambroise, Ngo Bitoungui Valentina J, Vorster Anna A, Ramesar Raj, Cooper Richard S, Tayo Bamidele, Lettre Guillaume, Ngogang Jean |
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Genome wide association study of fetal hemoglobin in sickle cell anemia in Tanzania.
PloS one 2014 9 (11): e111464. Mtatiro Siana Nkya, Singh Tarjinder, Rooks Helen, Mgaya Josephine, Mariki Harvest, Soka Deogratius, Mmbando Bruno, Msaki Evarist, Kolder Iris, Thein Swee Lay, Menzel Stephan, Cox Sharon E, Makani Julie, Barrett Jeffrey |
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The influence of the BCL11A polymorphism on the phenotype of patients with beta thalassemia could be affected by the beta globin locus control region and/or the Xmn1-HBG2 genotypic background.
Blood cells, molecules & diseases 2013 Aug 51 (2): 80-4. Neishabury Maryam, Zamani Fahimeh, Keyhani Elahe, Azarkeivan Azita, Abedini Seyedeh Sedigheh, Eslami Masumeh Sadat, Kakroodi Setareh Talebi, Vesiehsari Mahjoobeh Jafari, Najmabadi Hosse |
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Genetic modifiers of sickle cell anemia in the BABY HUG cohort: influence on laboratory and clinical phenotypes.
American journal of hematology 2013 Jul 88 (7): 571-6. Sheehan Vivien A, Luo Zhaoyu, Flanagan Jonathan M, Howard Thad A, Thompson Bruce W, Wang Winfred C, Kutlar Abdullah, Ware Russell E, |
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Candidate sequence variants and fetal hemoglobin in children with sickle cell disease treated with hydroxyurea.
PloS one 2013 8 (2): e55709. Green Nancy S, Ender Katherine L, Pashankar Farzana, Driscoll Catherine, Giardina Patricia J, Mullen Craig A, Clark Lorraine N, Manwani Deepa, Crotty Jennifer, Kisselev Sergey, Neville Kathleen A, Hoppe Carolyn, Barral Sand |
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Utility of the multivariate approach in predicting ?-thalassemia intermedia or ?-thalassemia major types In Iranian patients.
Hemoglobin 2013 37 (5): 413-22. Banan Mehdi, Bayat Hadi, Namdar-Aligoodarzi Pegah, Azarkeivan Azita, Kamali Koorosh, Daneshmand Parvaneh, Zaker-Kandjani Behzad, Najmabadi Hosse |
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Genetic modifiers of ?-thalassemia and clinical severity as assessed by age at first transfusion.
Haematologica 2012 Jul 97 (7): 989-93. Danjou Fabrice, Anni Franco, Perseu Lucia, Satta Stefania, Dessì Carlo, Lai Maria Eliana, Fortina Paolo, Devoto Marcella, Galanello Ren |
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[Correlation between hemoglobin F levels and single nucleotide polymorphism at BCL11A gene rs11886868 locus in ?-thalassemia patients].
Zhongguo shi yan xue ye xue za zhi / Zhongguo bing li sheng li xue hui = Journal of experimental hematology / Chinese Association of Pathophysiology 2012 Jun 20 (3): 650-3. Chen Qun-Rong, Sun Shun-Chang, Peng Yun-Sheng, Wang Qing, Mo Bao-M |
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Influence of BCL11A, HBS1L-MYB, HBBP1 single nucleotide polymorphisms and the HBG2 XmnI polymorphism On Hb F levels.
Hemoglobin 2012 36 (6): 592-9. Roy Papai, Bhattacharya Gargi, Mandal Amrita, Dasgupta Uma B, Banerjee Debasis, Chandra Sarmila, Das Manikanch |
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Influences of genetic variation on fetal hemoglobin.
Pediatric hematology and oncology 2011 Nov 28 (8): 708-17. He Yunyan, Lin Weixiong, Luo Jianmi |
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Pharmacokinetics, pharmacodynamics, and pharmacogenetics of hydroxyurea treatment for children with sickle cell anemia.
Blood 2011 Nov 118 (18): 4985-91. Ware Russell E, Despotovic Jenny M, Mortier Nicole A, Flanagan Jonathan M, He Jin, Smeltzer Matthew P, Kimble Amy C, Aygun Banu, Wu Song, Howard Thad, Sparreboom Al |
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Variants in genetic modifiers of ?-thalassemia can help to predict the major or intermedia type of the disease.
Haematologica 2011 Nov 96 (11): 1712-4. Badens Catherine, Joly Philippe, Agouti Imane, Thuret Isabelle, Gonnet Katia, Fattoum Synda, Francina Alain, Simeoni Marie-Claude, Loundou Anderson, Pissard Ser |
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Genetics of fetal hemoglobin in Tanzanian and British patients with sickle cell anemia.
Blood 2011 Jan 117 (4): 1390-2. Makani Julie, Menzel Stephan, Nkya Siana, Cox Sharon E, Drasar Emma, Soka Deogratius, Komba Albert N, Mgaya Josephine, Rooks Helen, Vasavda Nisha, Fegan Gregory, Newton Charles R, Farrall Martin, Thein Swee L |
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The XmnI (G)gamma polymorphism influences hemoglobin F synthesis contrary to BCL11A and HBS1L-MYB SNPs in a cohort of 57 beta-thalassemia intermedia patients.
Blood cells, molecules & diseases 2010 Aug 45 (2): 124-7. Nguyen Thi Khanh Tien, Joly Philippe, Bardel Claire, Moulsma Mustapha, Bonello-Palot Nathalie, Francina Ala |
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A genome-wide association identified the common genetic variants influence disease severity in beta0-thalassemia/hemoglobin E.
Human genetics 2010 Mar 127 (3): 303-14. Nuinoon Manit, Makarasara Wattanan, Mushiroda Taisei, Setianingsih Iswari, Wahidiyat Pustika Amalia, Sripichai Orapan, Kumasaka Natsuhiko, Takahashi Atsushi, Svasti Saovaros, Munkongdee Thongperm, Mahasirimongkol Surakameth, Peerapittayamongkol Chayanon, Viprakasit Vip, Kamatani Naoyuki, Winichagoon Pranee, Kubo Michiaki, Nakamura Yusuke, Fucharoen Suth |
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Fetal hemoglobin in sickle cell anemia: genome-wide association studies suggest a regulatory region in the 5' olfactory receptor gene cluster.
Blood 2010 Mar 115 (9): 1815-22. Solovieff Nadia, Milton Jacqueline N, Hartley Stephen W, Sherva Richard, Sebastiani Paola, Dworkis Daniel A, Klings Elizabeth S, Farrer Lindsay A, Garrett Melanie E, Ashley-Koch Allison, Telen Marilyn J, Fucharoen Supan, Ha Shau Yin, Li Chi-Kong, Chui David H K, Baldwin Clinton T, Steinberg Martin |
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A genome-wide association identified the common genetic variants influence disease severity in beta(0)-thalassemia/hemoglobin E.
Human genetics 2009 Nov . Nuinoon M, Makarasara W, Mushiroda T, Setianingsih I, Wahidiyat PA, Sripichai O, Kumasaka N, Takahashi A, Svasti S, Munkongdee T, Mahasirimongkol S, Peerapittayamongkol C, Viprakasit V, Kamatani N, Winichagoon P, Kubo M, Nakamura Y, Fucharoen S |
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Amelioration of Sardinian beta0 thalassemia by genetic modifiers.
Blood 2009 Oct 114 (18): 3935-7. Galanello Renzo, Sanna Serena, Perseu Lucia, Sollaino Maria Carla, Satta Stefania, Lai Maria Eliana, Barella Susanna, Uda Manuela, Usala Gianluca, Abecasis Goncalo R, Cao Anton |
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DNA polymorphisms at the BCL11A, HBS1L-MYB, and beta-globin loci associate with fetal hemoglobin levels and pain crises in sickle cell disease.
Proceedings of the National Academy of Sciences of the United States of America 2008 Aug 105 (33): 11869-74. Lettre Guillaume, Sankaran Vijay G, Bezerra Marcos André C, Araújo Aderson S, Uda Manuela, Sanna Serena, Cao Antonio, Schlessinger David, Costa Fernando F, Hirschhorn Joel N, Orkin Stuart |
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Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of beta-thalassemia.
Proceedings of the National Academy of Sciences of the United States of America 2008 Feb 105 (5): 1620-5. Uda Manuela, Galanello Renzo, Sanna Serena, Lettre Guillaume, Sankaran Vijay G, Chen Weimin, Usala Gianluca, Busonero Fabio, Maschio Andrea, Albai Giuseppe, Piras Maria Grazia, Sestu Natascia, Lai Sandra, Dei Mariano, Mulas Antonella, Crisponi Laura, Naitza Silvia, Asunis Isadora, Deiana Manila, Nagaraja Ramaiah, Perseu Lucia, Satta Stefania, Cipollina Maria Dolores, Sollaino Carla, Moi Paolo, Hirschhorn Joel N, Orkin Stuart H, Abecasis Gonçalo R, Schlessinger David, Cao Anton |
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A QTL influencing F cell production maps to a gene encoding a zinc-finger protein on chromosome 2p15.
Nature genetics 2007 Oct 39 (10): 1197-9. Menzel Stephan, Garner Chad, Gut Ivo, Matsuda Fumihiko, Yamaguchi Masao, Heath Simon, Foglio Mario, Zelenika Diana, Boland Anne, Rooks Helen, Best Steve, Spector Tim D, Farrall Martin, Lathrop Mark, Thein Swee L |
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Variability of hemoglobin F expression in hemoglobin EE disease: hematological and molecular analysis.
Blood cells, molecules & diseases 0 53 (1-2): 11-5. Pakdee Naruwat, Yamsri Supawadee, Fucharoen Goonnapa, Sanchaisuriya Kanokwan, Pissard Serge, Fucharoen Sup |
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- Page last updated:Apr 07, 2020
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