Human Genome Epidemiology Literature Finder
|
Records 1 - 30 (of 39 Records) |
| Query Trace: Disease and HBS1L[original query] |
|---|
| 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 |
| 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 |
| 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 |
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 |
| Genetic association of fetal-hemoglobin levels in individuals with sickle cell disease in Tanzania maps to conserved regulatory elements within the MYB core enhancer. BMC medical genetics 2015 16 4. Mtatiro Siana N, Mgaya Josephine, Singh Tarjinder, Mariki Harvest, Rooks Helen, Soka Deogratius, Mmbando Bruno, Thein Swee Lay, Barrett Jeffrey C, Makani Julie, Cox Sharon E, Menzel Steph |
| Genetic variation at MECOM, TERT, JAK2 and HBS1L-MYB predisposes to myeloproliferative neoplasms.
Nature communications 2015 6 6691. Tapper William, Jones Amy V, Kralovics Robert, Harutyunyan Ashot S, Zoi Katerina, Leung William, Godfrey Anna L, Guglielmelli Paola, Callaway Alison, Ward Daniel, Aranaz Paula, White Helen E, Waghorn Katherine, Lin Feng, Chase Andrew, Baxter E Joanna, Maclean Cathy, Nangalia Jyoti, Chen Edwin, Evans Paul, Short Michael, Jack Andrew, Wallis Louise, Oscier David, Duncombe Andrew S, Schuh Anna, Mead Adam J, Griffiths Michael, Ewing Joanne, Gale Rosemary E, Schnittger Susanne, Haferlach Torsten, Stegelmann Frank, Döhner Konstanze, Grallert Harald, Strauch Konstantin, Tanaka Toshiko, Bandinelli Stefania, Giannopoulos Andreas, Pieri Lisa, Mannarelli Carmela, Gisslinger Heinz, Barosi Giovanni, Cazzola Mario, Reiter Andreas, Harrison Claire, Campbell Peter, Green Anthony R, Vannucchi Alessandro, Cross Nicholas C |
| 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 |
| 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 |
| The Impact of XmnI-HBG2, BCL11A and HBS1L-MYB Single Nucleotide Polymorphisms on Hb F Variation of Hematologically Normal Iranian Individuals. Hemoglobin 2016 Jun 40 (3): 198-201. Keyhani Elaheh, Jafari Vesiehsari Mahjoobeh, Talebi Kakroodi Setareh, Darabi Elham, Zamani Fahimeh, Karimlou Masoud, Kamali Koorosh, Neishabury Mary |
| 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 |
| Molecular Understanding of Non-Transfusion-Dependent Thalassemia Associated with Hemoglobin E-ß-Thalassemia in Northeast Thailand. Acta haematologica 2016 Oct 136 (4): 233-239. Yamsri Supawadee, Pakdee Naruwat, Fucharoen Goonnapa, Sanchaisuriya Kanokwan, Fucharoen Sup |
| 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 |
| 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 |
| 2SNP heritability and effects of genetic variants for neutrophil-to-lymphocyte and platelet-to-lymphocyte ratio.
Journal of human genetics 2017 Nov 62 (11): 979-988. Lin Bochao Danae, Carnero-Montoro Elena, Bell Jordana T, Boomsma Dorret I, de Geus Eco J, Jansen Rick, Kluft Cornelis, Mangino Massimo, Penninx Brenda, Spector Tim D, Willemsen Gonneke, Hottenga Jouke-J |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| Dietary contributions in the genetic variation of liver fibrosis: a genome-wide association study of fibrosis-4 index in the liver fibrosis development. Cell & bioscience 2024 11 14 (1): 141. Poppy Diah Palupi, Chun-Yu Wei, Wan-Hsuan Chou, Min-Rou Lin, Yu-Jui Yvonne Wan, Wei-Chiao Cha |
- Page last reviewed:Feb 1, 2024
- Content source: