Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 58 Records) |
Query Trace: HBA1[original query] |
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Molecular Genetic Analysis of ?-Thalassemia in Hamadan Province, West Iran. Hemoglobin 2020 9 44 (5): 319-324. Moradi Keivan, Aznab Mozaffar, Biglari Mostafa, Shafieenia Samaneh, Azimi Azam, Bijari Nushin, Alibakhshi Re |
Hb Manitoba [?102(G9)Ser?Arg] in Pasifika: Tongan Case Report. Hemoglobin 2020 7 44 (4): 290-293. Pullon Beverley M, Moore Jordyn |
?-Thalassemia Intermedia Results from Interactions of Unstable Hb Prato [?31(B12)Arg?Ser (HBA1 or HBA2 c.96G>T or C)] with the ?-Thalassemia-1 [- - (Southeast Asian)] Deletion in Thailand. Hemoglobin 2020 7 44 (4): 264-271. Panyasai Sitthichai, Phasit Amph |
The Spectrum of ?-Thalassemia Mutations in Kurdistan Province, West Iran. Hemoglobin 2020 6 44 (3): 156-161. Alibakhshi Reza, Moradi Keivan, Aznab Mozaffar, Dastafkan Zahra, Tahmasebi Susan, Ahmadi Mahsa, Omidniakan Lei |
[Effect of high-throughput sequencing for the prevention and control of thalassemia]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2020 5 37 (6): 645-649. Chen Yang, Zhang Shufang, Wang Chan, Chen Shiping, Feng Nyu, Liu Haifang, Tang Xiaoyan, Wang J |
A More Universal Approach to Comprehensive Analysis of Thalassemia Alleles (CATSA). The Journal of molecular diagnostics : JMD 2021 7 23 (9): 1195-1204. Liang Qiaowei, Gu Wanqian, Chen Ping, Li Yuezhen, Liu Yanqiu, Tian Mao, Zhou Qiaomiao, Qi Hongbo, Zhang Yuhong, He Jun, Li Qing, Tang Lingfang, Tang Juan, Teng Yanling, Zhou Yulin, Huang Shengwen, Lu Zongjie, Xu Mengnan, Hou Wei, Huang Ting, Li Youqiong, Li Rong, Hu Lanping, Li Shaoying, Guo Qiwei, Zhuo Zhaozhen, Mou Yan, Cram David S, Wu Lingqi |
Molecular classification of blood and bleeding disorder genes. NPJ genomic medicine 2021 Jul 6 (1): 62. Baz Batoul, Abouelhoda Mohamed, Owaidah Tarek, Dasouki Majed, Monies Dorota, Al Tassan Na |
Influence of various risk factors on the level of ST2 biomarker in patients with heart failure and diabetes mellitus type 2. Polski merkuriusz lekarski : organ Polskiego Towarzystwa Lekarskiego 2021 Apr 49 (290): 95-98. Rudyk Iurii Stepanovich, Medentseva Olena Oleksandrivna, Gasanov Iurii Chigizovich, Babichev Denys Petrovi |
Identification of Two Novel Thalassemia Variants, HBA1: c.263delA and HBA2: c.376dupC, in Chinese Individuals. Hemoglobin 2021 4 45 (1): 49-51. Liu Li, Sun Yan, Chen Shiping, Yu Churen, Cao Peijie, Sun Jun, Peng Zhiyu, Mao Pi |
Alpha thalassemia and alpha-MRE haplotypes in Uruguayan patients with microcytosis and hypochromia without anemia. Genetics and molecular biology 2021 44 (2): e20200399. Soler Ana María, Piellusch Bruna Facanali, Silveira Lorena da, Pedroso Gisele Audrei, López Pablo, Savio Enrique, Sonati María de Fatima, Luz Julio |
Molecular and Hematological Analysis of Alpha- and Beta-Thalassemia in a Cohort of Mexican Patients. Genetic testing and molecular biomarkers 2021 3 25 (3): 247-252. Rizo-de la Torre Lourdes Del Carmen, Rentería-López Víctor Manuel, Sánchez-López Josefina Yoaly, Magaña-Torres María Teresa, Ibarra-Cortés Bertha, Perea-Díaz Francisco Javi |
Eleven Cases of Hb J-Paris-I [HBA2: c.38C>A (or HBA1)]: A Stable ? Chain Variant Elutes in the P3 Window on High-Performance Liquid Chromatography. Hemoglobin 2021 11 45 (5): 322-324. Khalil Mohamed S M, Timbs Adele T, Henderson Shirley J, Schuh Anna, Old John |
Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed program.
American journal of human genetics 2021 4 108 (5): 874-893. Hu Yao, Stilp Adrienne M, McHugh Caitlin P, Rao Shuquan, Jain Deepti, Zheng Xiuwen, Lane John, Méric de Bellefon Sébastian, Raffield Laura M, Chen Ming-Huei, Yanek Lisa R, Wheeler Marsha, Yao Yao, Ren Chunyan, Broome Jai, Moon Jee-Young, de Vries Paul S, Hobbs Brian D, Sun Quan, Surendran Praveen, Brody Jennifer A, Blackwell Thomas W, Choquet Hélène, Ryan Kathleen, Duggirala Ravindranath, Heard-Costa Nancy, Wang Zhe, Chami Nathalie, Preuss Michael H, Min Nancy, Ekunwe Lynette, Lange Leslie A, Cushman Mary, Faraday Nauder, Curran Joanne E, Almasy Laura, Kundu Kousik, Smith Albert V, Gabriel Stacey, Rotter Jerome I, Fornage Myriam, Lloyd-Jones Donald M, Vasan Ramachandran S, Smith Nicholas L, North Kari E, Boerwinkle Eric, Becker Lewis C, Lewis Joshua P, Abecasis Goncalo R, Hou Lifang, O'Connell Jeffrey R, Morrison Alanna C, Beaty Terri H, Kaplan Robert, Correa Adolfo, Blangero John, Jorgenson Eric, Psaty Bruce M, Kooperberg Charles, Walton Russell T, Kleinstiver Benjamin P, Tang Hua, Loos Ruth J F, Soranzo Nicole, Butterworth Adam S, Nickerson Debbie, Rich Stephen S, Mitchell Braxton D, Johnson Andrew D, Auer Paul L, Li Yun, Mathias Rasika A, Lettre Guillaume, Pankratz Nathan, Laurie Cathy C, Laurie Cecelia A, Bauer Daniel E, Conomos Matthew P, Reiner Alexander P, |
Analysis of genotype-phenotype correlation in patients with ?-thalassemia from Fujian province, Southeastern China. Journal of clinical laboratory analysis 2022 9 36 (10): e24696. Pan Yali, Chen Meihuan, Zhang YanHong, Zhang Min, Chen Lingji, Lin Na, Xu Liangpu, Huang Hailo |
Molecular Determination of Vascular Endothelial Growth Factor, miRNA-423 Gene Abnormalities by Utilizing ARMS-PCR and Their Association with Fetal Hemoglobin Expression in the Patients with Sickle Cell Disease. Current issues in molecular biology 2022 6 44 (6): 2569-2582. Hamadi Abdullah, Mir Rashid, Mahzari Ali, Hakami Abdulrahim, Almotairi Reema, Dobie Gasim, Hamdi Fawaz, Nahari Mohammed Hassan, Alhefzi Razan, Alasseiri Mohammed, Hakami Nora Y, Al Sadoun Hadeel, Al-Amer Osama M, Barnawi Jameel, Madkhali Hassan |
Third-Generation Sequencing as a New Comprehensive Technology for Identifying Rare ?- and ?-Globin Gene Variants in Thalassemia Alleles in the Chinese Population. Archives of pathology & laboratory medicine 2022 5 147 (2): 208-214. Zhuang Jianlong, Chen Chunnuan, Fu Wanyu, Wang Yuanbai, Zhuang Qianmei, Lu Yulin, Xie Tiantian, Xu Ruofan, Zeng Shuhong, Jiang Yuying, Xie Yingjun, Wang Gaoxio |
Effects of Senegal haplotype (Xmn1-rs7412844), alpha-thalassemia (3.7kb HBA1/HBA2 deletion), NPRL3-rs11248850 and BCL11A-rs4671393 variants on sickle cell nephropathy. International journal of biochemistry and molecular biology 2022 5 13 (2): 5-16. Ndour El Hadji Malick, Mnika Khuthala, Guèye Tall Fatou, Seck Moussa, Dème Ly Indou, Nembaware Victoria, Sagna-Bassène Hélène Ange Thérèse, Dione Rokhaya, Ndongo Aliou Abdoulaye, Diop Jean Pascal Demba, Barry Nènè Oumou Kesso, Djité Moustapha, Ndiaye Diallo Rokhaya, Guèye Papa Madièye, Diop Saliou, Diagne Ibrahima, Cissé Aynina, Wonkam Ambroise, Lopez Sall Philomè |
Polymorphism in Adiponectin and Adiponectin Receptor Genes in Diabetes Mellitus Pathogenesis. Pathophysiology : the official journal of the International Society for Pathophysiology 2022 4 29 (1): 81-91. Shramko Iuliana, Ageeva Elizaveta, Krutikov Eugene, Maliy Konstantin, Repinskaya Irina, Fomochkina Iryna, Kubishkin Anatolii, Gurtovaya Anna, Tarimov Cyrill, Shekhar Sum |
Integrated multi-omic analysis of low-grade ovarian serous carcinoma collected from short and long-term survivors. Journal of translational medicine 2022 12 20 (1): 606. Wong Kwong-Kwok, Bateman Nicholas W, Ng Chun Wai, Tsang Yvonne T M, Sun Charlotte S, Celestino Joseph, Nguyen Tri V, Malpica Anais, Hillman R Tyler, Zhang Jianhua, Futreal P Andrew, Rojas Christine, Conrads Kelly A, Hood Brian L, Dalgard Clifton L, Wilkerson Matthew D, Phippen Neil T, Conrads Thomas P, Maxwell George L, Sood Anil K, Gershenson David |
Association of Met420del Variant of Metformin Transporter Gene SLC22A1 with Metformin Treatment Response in Ethiopian Patients with Type 2 Diabetes. Diabetes, metabolic syndrome and obesity : targets and therapy 2023 8 16 2523-2535. Abraham Degaga, Sisay Sirgu, Hasniza Zaman Huri, Maw Shin Sim, Tedla Kebede, Birhanemeskel Tegene, Navin Kumar Loganadan, Ephrem Engidawork, Workineh Shibes |
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 |
Clinical significance of mutational variants in beta and alpha genes in patients with hemoglobinopathies from two large Greek centers: a complex interplay between genotype and phenotype. Journal of molecular medicine (Berlin, Germany) 2023 7 . Michael D Diamantidis, Rebecca-Anastasia Karanikola, Chrysoula Polyzoudi, Sophia Delicou, Achilles Manafas, Helen Savera, Aikaterini Xydaki, Angeliki Kotsiafti, Evangelos Tsangalas, Georgia Ikonomou, Eirini Mani, Konstantinos Ntoulas, Evangelos Alexiou, Ioanna Argyrakouli, John Koskinas, Paraskevi Foti |
Combination of HBA1, TTR, and SERPINF2 in plasma defines phenotype correlated with severe burn outcome. iScience 2023 7 26 (8): 107271. Shinya Onishi, Hisatake Matsumoto, Fuminori Sugihara, Takeshi Ebihara, Hiroshi Matsuura, Akinori Osuka, Daisuke Okuzaki, Hiroshi Ogura, Jun O |
Gene Mutation Spectrum among Alpha-Thalassaemia Patients in Northeast Peninsular Malaysia. Diagnostics (Basel, Switzerland) 2023 3 13 (5): . Vijian Divashini, Wan Ab Rahman Wan Suriana, Ponnuraj Kannan Thirumulu, Zulkafli Zefarina, Bahar Rosnah, Yasin Norafiza, Hassan Syahzuwan, Esa Ezal |
Mutation spectrum of thalassemia among pre-pregnant adults in the Jiangsu Province by capillary electrophoresis-based multiplex PCR assay. Molecular genetics & genomic medicine 2023 12 e2344. Binbin Shao, Yuguo Wang, Jingjing Zhang, Yan Wang, Juan Tan, Lulu Wang, Ping Hu, Jianxin Tan, Zhengfeng |
Functional mutation, splice, distribution, and divergence analysis of impactful genes associated with heart failure and other cardiovascular diseases. Scientific reports 2023 10 13 (1): 16769. Ishani Mhatre, Habiba Abdelhalim, William Degroat, Shreya Ashok, Bruce T Liang, Zeeshan Ahm |
Causal links of ?-thalassemia indices and cardiometabolic traits and diabetes: MR study. Life science alliance 2023 10 6 (12): . Lung-An Hsu, Semon Wu, Ming-Sheng Teng, Yu-Lin |
Determination of Carrier Frequency of Actionable Pathogenic Variants in Autosomal Recessive Genetic Diseases in the Turkish Cypriot Population. Genes 2023 10 14 (10): . Aziz Suat Gunsel, Mahmut Cerkez Ergoren, Hatice Kemal, Haniyeh Rahbar Kafshboran, Levent Cerit, Ayla Turgay, Hamza Duy |
[Effects of Hemoglobin Variants on Glycosylated Hemoglobin Testing]. Sichuan da xue xue bao. Yi xue ban = Journal of Sichuan University. Medical science edition 2023 10 54 (5): 1019-1023. Dan Ye, Yan Tang, Mei Zha |
Clinical, laboratory, and molecular characteristics of a cohort of children with hemoglobinopathy S/beta-thalassemia. Hematology, transfusion and cell therapy 2024 1 . Érica Louback Oliveira, André Rolim Belisário, Natiely Pereira Silva, Paulo Val Rezende, Maristela Braga Muniz, Larissa Maira Moura Oliveira, Cibele Velloso-Rodrigues, Marcos Borato Via |
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- Page last updated:Apr 22, 2024
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