Human Genome Epidemiology Literature Finder
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Records 1 - 30 (of 58 Records) |
| Query Trace: Disease 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 |
| Existence of HbF Enhancer Haplotypes at HBS1L-MYB Intergenic Region in Transfusion-Dependent Saudi ß-Thalassemia Patients. BioMed research international 2017 2017 1972429. Cyrus Cyril, Vatte Chittibabu, Borgio J Francis, Al-Rubaish Abdullah, Chathoth Shahanas, Nasserullah Zaki A, Jarrash Sana Al, Sulaiman Ahmed, Qutub Hatem, Alsaleem Hassan, Alzahrani Alhusain J, Steinberg Martin H, Ali Amein K |
| 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 |
| Fetal haemoglobin induction in sickle cell disease. British journal of haematology 2017 11 180 (2): 189-200. Paikari Alireza, Sheehan Vivien |
| 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 |
| A survey of genetic fetal-haemoglobin modifiers in Nigerian patients with sickle cell anaemia. PloS one 2018 6 13 (6): e0197927. Adeyemo Titilope A, Ojewunmi Oyesola O, Oyetunji Idat A, Rooks Helen, Rees David C, Akinsulie Adebola O, Akanmu Alani S, Thein Swee Lay, Menzel Steph |
| 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 |
| 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 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 |
| Fetal Hemoglobin Modulators May Be Associated With Symptomology of Football Players with Sickle Cell Trait. Southern medical journal 2019 May 112 (5): 289-294. Flansburg Carroll, Balentine Christina M, Grieger Ryan W, Lund Justin, Ciambella Michelle, White Deandre, Coris Eric, Gonzalez Eduardo, Stone Anne C, Madrigal Lore |
| 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 BCL11A, HSB1L-MYB, and XmnI ?G-158 (C/T) gene polymorphism and hemoglobin F level in Egyptian sickle cell disease patients. Annals of hematology 2020 Aug . El-Ghamrawy Mona, Yassa Marianne E, Tousson Angie M S, El-Hady Marwa Abd, Mikhaeil Erini, Mohamed Nada B, Khorshied Mervat Mamdo |
| Identifying genetic variants and pathways associated with extreme levels of fetal hemoglobin in sickle cell disease in Tanzania. BMC medical genetics 2020 Jun 21 (1): 125. Nkya Siana, Mwita Liberata, Mgaya Josephine, Kumburu Happiness, van Zwetselaar Marco, Menzel Stephan, Mazandu Gaston Kuzamunu, Sangeda Raphael, Chimusa Emile, Makani Jul |
| 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 |
| Identification of new candidate genes and signalling pathways associated with the development of neuroendocrine pancreatic tumours based on next generation sequencing data. Molecular biology reports 2020 5 47 (6): 4233-4243. Kit Oleg I, Trifanov Vladimir S, Petrusenko Nataliya A, Gvaldin Dmitry Y, Kutilin Denis S, Timoshkina Nataliya |
| 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 |
| F cell numbers are associated with an X-linked genetic polymorphism and correlate with haematological parameters in patients with sickle cell disease. British journal of haematology 2020 Oct . Urio Florence, Nkya Siana, Rooks Helen, Mgaya Josephine A, Masamu Upendo, Zozimus Sangeda Raphael, Mmbando Bruno P, Brumat Marco, Mselle Ted, Menzel Stephan, Luzzatto Lucio, Makani Jul |
| 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 |
| 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 |
| 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 |
| Genetic modifiers of fetal hemoglobin affect the course of sickle cell disease in patients treated with hydroxyurea. Haematologica 2021 10 107 (7): 1577-1588. Allard Pierre, Alhaj Nareen, Lobitz Stephan, Cario Holger, Jarisch Andreas, Grosse Regine, Oevermann Lena, Hakimeh Dani, Tagliaferri Laura, Kohne Elisabeth, Kopp-Schneider Annette, Kulozik Andreas E, Kunz Joachim |
| 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 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 |
| Identification of genetic variants associated with clinical features of sickle cell disease. Scientific reports 2024 8 14 (1): 20070. Katharine Tsukahara, Xiao Chang, Frank Mentch, Kim Smith-Whitley, Anita Bhandari, Cindy Norris, Joseph T Glessner, Hakon Hakonars |
| Genotyping the BCL11A Single Nucleotide Polymorphism and Associated Levels of Fetal Hemoglobin in Mauritanian Sickle Cell Patients. Frontiers in bioscience (Scholar edition) 2024 6 16 (2): 11. Aminetou Taleb Brahim, Mariem Taleb, Harouna Soumaré, Sidi Mohamed Ghaber, Aminetou Mohamed, Ali Ould Mohamed Salem Boukha |
| 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 |
| 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, |
| BCL11A intellectual developmental disorder: defining the clinical spectrum and genotype-phenotype correlations. European journal of human genetics : EJHG 2024 10 . Angela Peron, Felice D'Arco, Kimberly A Aldinger, Constance Smith-Hicks, Christiane Zweier, Gyri A Gradek, Kimberley Bradbury, Andrea Accogli, Erica F Andersen, Ping Yee Billie Au, Roberta Battini, Daniah Beleford, Lynne M Bird, Arjan Bouman, Ange-Line Bruel, Øyvind Løvold Busk, Philippe M Campeau, Valeria Capra, Colleen Carlston, Jenny Carmichael, Anna Chassevent, Jill Clayton-Smith, Michael J Bamshad, Dawn L Earl, Laurence Faivre, Christophe Philippe, Patrick Ferreira, Luitgard Graul-Neumann, Mary J Green, Darrah Haffner, Parthiv Haldipur, Suhair Hanna, Gunnar Houge, Wendy D Jones, Cornelia Kraus, Birgit Elisabeth Kristiansen, James Lespinasse, Karen J Low, Sally Ann Lynch, Sofia Maia, Rong Mao, Ruta Kalinauskiene, Catherine Melver, Kimberly McDonald, Tara Montgomery, Manuela Morleo, Constance Motter, Amanda S Openshaw, Janice Cox Palumbos, Aditi Shah Parikh, Yezmin Perilla-Young, Cynthia M Powell, Richard Person, Megha Desai, Juliette Piard, Rolph Pfundt, Marcello Scala, Margaux Serey-Gaut, Deborah Shears, Anne Slavotinek, Mohnish Suri, Claire Turner, Tatiana Tvrdik, Karin Weiss, Ingrid M Wentzensen, Marcella Zollino, Tzung-Chien Hsieh, , , , Bert B A de Vries, Francois Guillemot, William B Dobyns, David Viskochil, Cristina Di |
- Page last reviewed:Feb 1, 2024
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