Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 77 Records) |
Query Trace: HBS1L[original query] |
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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 |
Germline variations at JAK2, TERT, HBS1L-MYB and MECOM and the risk of myeloproliferative neoplasms in Taiwanese population. Oncotarget 2017 Sep 8 (44): 76204-76213. Chiang Yi-Hao, Chang Yu-Cheng, Lin Huan-Chau, Huang Ling, Cheng Chun-Chia, Wang Wei-Ting, Cheng Hung-I, Su Nai-Wen, Chen Caleb Gon-Shen, Lin Johnson, Chang Yi-Fang, Chang Ming-Chih, Hsieh Ruey-Kuen, Chou Wen-Chien, Lim Ken-Hong, Kuo Yuan-Y |
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 |
A genome-wide association study of red-blood cell fatty acids and ratios incorporating dietary covariates: Framingham Heart Study Offspring Cohort. PloS one 2018 13 (4): e0194882. Kalsbeek Anya, Veenstra Jenna, Westra Jason, Disselkoen Craig, Koch Kristin, McKenzie Katelyn A, O'Bott Jacob, Vander Woude Jason, Fischer Karen, Shearer Greg C, Harris William S, Tintle Nathan |
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 |
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 |
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 |
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 |
Association of HMIP1 C-893A polymorphism and disease severity in patients with sickle cell anemia. Hematology, transfusion and cell therapy 2020 Jun . Pereira-Martins Diego A, Domingos Igor F, Belini-Junior Edis, Coelho-Silva Juan L, Weinhäuser Isabel, Araújo Aderson S, Lobo Clarisse L, Bonini-Domingos Claudia R, Bezerra Marcos A, Lucena-Araujo Antonio |
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 |
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 |
Ancestry-specific associations identified in genome-wide combined-phenotype study of red blood cell traits emphasize benefits of diversity in genomics.
BMC genomics 2020 Mar 21 (1): 228. Hodonsky Chani J, Baldassari Antoine R, Bien Stephanie A, Raffield Laura M, Highland Heather M, Sitlani Colleen M, Wojcik Genevieve L, Tao Ran, Graff Marielisa, Tang Weihong, Thyagarajan Bharat, Buyske Steve, Fornage Myriam, Hindorff Lucia A, Li Yun, Lin Danyu, Reiner Alex P, North Kari E, Loos Ruth J F, Kooperberg Charles, Avery Christy |
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 |
Mitochondrial genome copy number measured by DNA sequencing in human blood is strongly associated with metabolic traits via cell-type composition differences. Human genomics 2021 6 15 (1): 34. Ganel Liron, Chen Lei, Christ Ryan, Vangipurapu Jagadish, Young Erica, Das Indraniel, Kanchi Krishna, Larson David, Regier Allison, Abel Haley, Kang Chul Joo, Scott Alexandra, Havulinna Aki, Chiang Charleston W K, Service Susan, Freimer Nelson, Palotie Aarno, Ripatti Samuli, Kuusisto Johanna, Boehnke Michael, Laakso Markku, Locke Adam, Stitziel Nathan O, Hall Ira |
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 |
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 |
A genome-wide meta-analysis yields 46 new loci associating with biomarkers of iron homeostasis.
Communications biology 2021 Feb 4 (1): 156. Bell Steven, Rigas Andreas S, Magnusson Magnus K, Ferkingstad Egil, Allara Elias, Bjornsdottir Gyda, Ramond Anna, Sørensen Erik, Halldorsson Gisli H, Paul Dirk S, Burgdorf Kristoffer S, Eggertsson Hannes P, Howson Joanna M M, Thørner Lise W, Kristmundsdottir Snaedis, Astle William J, Erikstrup Christian, Sigurdsson Jon K, Vuckovic Dragana, Dinh Khoa M, Tragante Vinicius, Surendran Praveen, Pedersen Ole B, Vidarsson Brynjar, Jiang Tao, Paarup Helene M, Onundarson Pall T, Akbari Parsa, Nielsen Kaspar R, Lund Sigrun H, Juliusson Kristinn, Magnusson Magnus I, Frigge Michael L, Oddsson Asmundur, Olafsson Isleifur, Kaptoge Stephen, Hjalgrim Henrik, Runarsson Gudmundur, Wood Angela M, Jonsdottir Ingileif, Hansen Thomas F, Sigurdardottir Olof, Stefansson Hreinn, Rye David, , Peters James E, Westergaard David, Holm Hilma, Soranzo Nicole, Banasik Karina, Thorleifsson Gudmar, Ouwehand Willem H, Thorsteinsdottir Unnur, Roberts David J, Sulem Patrick, Butterworth Adam S, Gudbjartsson Daniel F, Danesh John, Brunak Søren, Di Angelantonio Emanuele, Ullum Henrik, Stefansson Ka |
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 |
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 |
[Predictors of Hematologic Responses in Patients with Non-Transfusion-Dependent ?-Thalassemia Receiving Thalidomide Therapy]. Zhongguo shi yan xue ye xue za zhi 2022 Oct 30 (5): 1519-1526. Yang Kun, Yin Xiao-Lin, Liu Xiao-Dong, Hua Fang, Peng Wei, Li Lan, Chen Kun, Zhang Jin, Luo Shan, Xiao Ji |
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 |
Nuclear and mitochondrial genetic variants associated with mitochondrial DNA copy number. Scientific reports 2024 1 14 (1): 2083. Adriana Koller, Michele Filosi, Hansi Weissensteiner, Federica Fazzini, Mathias Gorski, Cristian Pattaro, Sebastian Schönherr, Lukas Forer, Janina M Herold, Klaus J Stark, Patricia Döttelmayer, Andrew A Hicks, Peter P Pramstaller, Reinhard Würzner, Kai-Uwe Eckardt, Iris M Heid, Christian Fuchsberger, Claudia Lamina, Florian Kronenbe |
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- Page last updated:Apr 16, 2024
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