Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 46 Records) |
Query Trace: HBG2[original query] |
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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 |
A Multi-locus Approach to Characterization of Major Quantitative Trait Loci Influencing Hb F Regulation in Chinese ß-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 |
Xmn1-158 ?GVariant in B-Thalassemia Intermediate Patients in South-East of Iran. International journal of hematology-oncology and stem cell research 2017 Apr 11 (2): 165-171. Miri-Moghaddam Ebrahim, Bahrami Sara, Naderi Majid, Bazi Ali, Karimipoor Morte |
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 |
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 |
The Sickle ?-Thalassemia Phenotype. Journal of pediatric hematology/oncology 2017 Jan . Adekile Adekunle D, Akbulut Nagihan, Azab Asmaa F, Al-Sharida Sundus, Thomas Dia |
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 |
The relationship between the variations in G? and A? promotors and the Hereditary Persistence of Fetal Hemoglobin (HPFH). Cellular and molecular biology (Noisy-le-Grand, France) 2018 2 64 (1): 32-39. Aydin Muhsin, Rencuzogullari Eyyup, Dalyan Ayse, Bayram Suleyman, Genc Ahm |
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 |
HBG2 -158 (C>T) polymorphism and its contribution to fetal hemoglobin variability in Iraqi Kurds with beta-thalassemia minor. Journal of laboratory physicians 2018 12 10 (4): 370-373. Albarawi Dilan J, Balatay Amer A, Al-Allawi Nas |
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 |
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 |
Impact of Rare and Common Genetic Variants on Diabetes Diagnosis by Hemoglobin A1c in Multi-Ancestry Cohorts: The Trans-Omics for Precision Medicine Program. American journal of human genetics 2019 Oct 105 (4): 706-718. Sarnowski Chloé, Leong Aaron, Raffield Laura M, Wu Peitao, de Vries Paul S, DiCorpo Daniel, Guo Xiuqing, Xu Huichun, Liu Yongmei, Zheng Xiuwen, Hu Yao, Brody Jennifer A, Goodarzi Mark O, Hidalgo Bertha A, Highland Heather M, Jain Deepti, Liu Ching-Ti, Naik Rakhi P, O'Connell Jeffrey R, Perry James A, Porneala Bianca C, Selvin Elizabeth, Wessel Jennifer, Psaty Bruce M, Curran Joanne E, Peralta Juan M, Blangero John, Kooperberg Charles, Mathias Rasika, Johnson Andrew D, Reiner Alexander P, Mitchell Braxton D, Cupples L Adrienne, Vasan Ramachandran S, Correa Adolfo, Morrison Alanna C, Boerwinkle Eric, Rotter Jerome I, Rich Stephen S, Manning Alisa K, Dupuis Josée, Meigs James B, , , , |
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 |
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 |
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 |
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 |
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 |
The value of single-molecule real-time technology in the diagnosis of rare thalassemia variants and analysis of phenotype-genotype correlation. Journal of human genetics 2021 Oct . Luo Shiqiang, Chen Xingyuan, Zeng Dingyuan, Tang Ning, Yuan Dejian, Zhong Qingyan, Mao Aiping, Xu Ruofan, Yan Tizh |
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 |
[Molecular Epidemiological Characteristics and Differential Diagnosis of Common ??-Thalassemia/HPFH]. Zhongguo shi yan xue ye xue za zhi 2022 8 30 (4): 1182-1187. Ju Ai-Ping, Li Na, Lin Keng, Huang Hui-Hui, Liu Shu-Xian, Jiang F |
[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 |
Mutational analysis of hemoglobin genes and functional characterization of detected variants, through in-silico analysis, in Pakistani beta-thalassemia major patients. Scientific reports 2023 8 13 (1): 13236. Samina Ejaz, Iqra Abdullah, Muhammad Usman, Muhammad Arslan Iqbal, Sidra Munawar, Muhammad Irfan Khan, Nagina Imtiaz, Hanniah Tahir, Muhammad Ihsan Bari, Tayyaba Rasool, Aneeza Fatima, Ramsha Anwar, Ayman Durrani, Yasir Hame |
Detection of Transversions and Transitions in HBG2 Cis-Elements Associated with Sickle Cell Allele in Ghanaians. Biochemical genetics 2023 7 . G K Ababio, I Ekem, J Acquaye, S Y Oppong, A G B Amoah, J Brandful, I K Qua |
Identifying signatures of positive selection in human populations from North Africa. Scientific reports 2023 5 13 (1): 8166. Rocio Caro-Consuegra, Marcel Lucas-Sánchez, David Comas, Elena Bos |
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 22, 2024
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