Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 231 Records) |
Query Trace: HBB[original query] |
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Genome-wide association study identifies novel candidate malaria resistance genes in Cameroon.
Human molecular genetics 2023 2 32 (12): 1946-1958. Esoh Kevin K, Apinjoh Tobias O, Amambua-Ngwa Alfred, Nyanjom Steven G, Chimusa Emile R, Amenga-Etego Lucas, Wonkam Ambroise, Achidi Eric |
Exploring the host factors affecting asymptomatic Plasmodium falciparum infection: insights from a rural Burkina Faso study. Malaria journal 2023 9 22 (1): 252. Peter J Neyer, Bérenger Kaboré, Christos T Nakas, Britta Hartmann, Annelies Post, Salou Diallo, Halidou Tinto, Angelika Hammerer-Lercher, Carlo R Largiadèr, Andre J van der Ven, Andreas R Hub |
Molecular Detection of Hemoglobin O-Arab in the Sudanese Population. International journal of general medicine 2023 8 16 3323-3330. Izzeldin Elbashir, Tagwa Yousif Elsayed Yous |
Detecting rare thalassemia in children with anemia using third-generation sequencing. Hematology (Amsterdam, Netherlands) 2023 8 28 (1): 2241226. Zhen-Min Ren, Wu-Jiao Li, Zhi-Hao Xing, Xiao-Ying Fu, Ju-Yan Zhang, Yun-Sheng Chen, De-Fa |
The Spectrum of HBB Mutations among 2315 Beta Thalassemia Patients of a Reference Clinic in Tehran-Iran. Hemoglobin 2023 8 1-5. Niloofar Bazazzadegan, Seyedeh Sedigheh Abedini, Azita Azarkeivan, Susan Banihashemi, Nooshin Nikzat, Hossein Najmabadi, Maryam Neishabu |
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 |
A Rare Case of Abnormal Hemoglobin Variant Hb Mizuho: [HBB: c.206T?>?C ? 68(E12) Leu-Pro]: A First Report in the Chinese Population. Hemoglobin 2023 7 1-5. Ya-Ping Chen, Peng Wu, Heng Wang, Jiang-Fen Wu, Dan Xie, Lei Wang, Bangquan An, Shengwen Hua |
Whole Exome Sequencing Reveals Novel Variants in Unexplained Erythrocytosis. Omics : a journal of integrative biology 2023 7 . Harshit Khurana, Babylakshmi Muthusamy, Uday Yanamandra, Kishore Garapati, Harikrishnan Premdeep, Shankar Subramanian, Akhilesh Pand |
Mutation Spectrum of ?-Thalassemia in Some Ethnic Groups of North Maharashtra, India. Hemoglobin 2023 6 1-6. Ranjeet Kumar, Syed Abrar Ahmad, Mustafa Ozdemir, Sakthivel Sadayappan, Varsha Wankha |
Association of sickle cell trait with adverse pregnancy outcomes in a population-based cohort. Acta obstetricia et gynecologica Scandinavica 2023 6 . Joseph Hulsizer, Andrew S Rifkin, Zhuqing Shi, Jun Wei, S Lilly Zheng, Brian T Helfand, Jessica Morgan, David W Ouyang, Michael S Caplan, Jianfeng |
A review of the main genetic factors influencing the course of COVID-19 in Sardinia: the role of human leukocyte antigen-G. Frontiers in immunology 2023 6 14 1138559. Stefano Mocci, Roberto Littera, Luchino Chessa, Marcello Campagna, Maurizio Melis, Carla Maria Ottelio, Ignazio S Piras, Sara Lai, Davide Firinu, Stefania Tranquilli, Alessia Mascia, Monica Vacca, Daniele Schirru, Luigi Isaia Lecca, Stefania Rassu, Federica Cannas, Celeste Sanna, Mauro Giovanni Carta, Francesca Sedda, Erika Giuressi, Selene Cipri, Michela Miglianti, Andrea Perra, Sabrina Gigl |
Molecular Basis and Hematologic Phenotype of Hemoglobin H Disease Combined with Two Rare ?-Globin Mutations. Hemoglobin 2023 6 1-4. Yuling Qiu, Shilu Wei, Wei Hou, Ketong Lai, Hengying Zhu, Wenwei Li, Qi Li, Zheng Yang, Qisheng Shu, Ping Chen, Wuning |
The frequency of HK?? allele in silent deletional ?-thalassemia carriers in the Yulin region of southern China using the third-generation sequencing. Gene 2023 5 875 147505. Sisi Ning, Yunrong Qin, Yunning Liang, Yi Liang, Yuling Xie, Yinghong Lu, Guanghong Wei, Ruofan Xu, Yinyin Liu, Jihui |
Clinical and biological profile of Sickle Cell Anemia children in a rural area in Central Africa. Hematology (Amsterdam, Netherlands) 2023 4 28 (1): 2193770. Mbayabo Gloire, Ngole Mamy, Lumbala Paul Kabuyi, Lumaka Aimé, Race Valerie, Matthijs Gert, Mikobi Tite Minga, Devriendt Koenraad, Van Geet Chris, Lukusa Prosper Tshilo |
HBB Gene Mutations and Their Pathological Impacts on HbE/?-Thalassaemia in Kuala Terengganu, Malaysia. Diagnostics (Basel, Switzerland) 2023 4 13 (7): . Saad Hanan Kamel M, Taib Wan Rohani Wan, Ab Ghani Azly Sumanty, Ismail Imilia, Al-Rawashde Futoon Abedrabbu, Almajali Belal, Alhawamdeh Maysa, Abd Rahman Alawiyah Awang, Al-Wajeeh Abdullah Saleh, Al-Jamal Hamid Ali Na |
?- and ?-Globin Gene Mutations in Individuals with Hemoglobinopathies in the Chattogram and Sylhet Regions of Bangladesh. Hemoglobin 2023 3 1-8. Kabir Tamanna, Anwar Saeed, Mourosi Jarin Taslem, Akter Shanjida, Hosen Mohammad Jak |
Alpha globin gene copy number and incident ischemic stroke risk among Black Americans. medRxiv : the preprint server for health sciences 2023 3 . Ruhl A Parker, Jeffries Neal, Yang Yu, Brooks Steven, Naik Rakhi P, Pecker Lydia H, Mott Bryan T, Winkler Cheryl A, Armstrong Nicole D, Zakai Neil A, Gutierrez Orlando M, Judd Suzanne, Howard Virginia, Howard George, Irvin Marguerite R, Cushman Mary, Ackerman Hans |
Pilot study of correlation of selected genetic factors with cribra orbitalia in individuals from a medieval population from Slovakia. International journal of paleopathology 2023 2 41 1-7. B?andová Gabriela, Patlevi?ová Andrea, Palkovi?ová Jana, Pavlíková Štefánia, Be?uš Radoslav, Repiská Vanda, Baldovi? Mari |
Two novel deletion mutations in ?-globin gene cause ?-thalassemia trait in two Chinese families. Human genomics 2023 12 17 (1): 111. Xiuqin Bao, Danqing Qin, Jicheng Wang, Jing Chen, Cuize Yao, Jie Liang, Kailing Liang, Yixia Wang, Yousheng Wang, Li Du, Aihua Y |
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 |
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 |
Reliability of hemoglobin A value as measured by the Premier Resolution system for screening of ?-thalassemia carriers. Clinical chemistry and laboratory medicine 2023 10 . Surada Satthakarn, Kesorn Panyasai, Amphai Phasit, Sitthichai Panyas |
First report of a patient with homozygous hemoglobin Ernz: Evidence to support a non-pathogenic variant. Blood cells, molecules & diseases 2023 10 104 102797. Zohreh Shojaei, Maryam Abiri, Fatemeh Zafarghandi Motlagh, Masoume Amini, Samira Dabbagh Bagheri, Sadaf Asnavandi, Sedighe Asadi, Hamideh Bagherian, Sirous Zeina |
Evaluating the Clinical Utility of a Long-Read Sequencing-Based Approach in Prenatal Diagnosis of Thalassemia. Clinical chemistry 2023 1 69 (3): 239-250. Liang Qiaowei, He Jun, Li Qing, Zhou Yulin, Liu Yanqiu, Li Youqiong, Tang Lingfang, Huang Shengwen, Li Rong, Zeng Fanqian, Mao Aiping, Liu Yinyin, Liang Desheng, Wu Lingqi |
First Report of Filipino ?-Thalassemia/?-Thalassemia in a Chinese Family. Hemoglobin 2024 1 1-5. Meihuan Chen, Aixiang Lv, Siwen Zhang, Junhao Zheng, Min Zhang, Lingji Chen, Qianqian He, Jianlong Zhuang, Na Lin, Liangpu Xu, Hailong Hua |
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 |
Genetic Association and Transferability for Urinary Albumin-Creatinine Ratio as a Marker of Kidney Function in four Sub-Saharan African Populations and non-continental Individuals of African Ancestry. medRxiv : the preprint server for health sciences 2024 1 . Jean-Tristan Brandenburg, Wenlong Carl Chen, Palwende Romuald Boua, Melanie Ann Govender, Godfred Agongo, Lisa K Micklesfield, Hermann Sorgho, Stephen Tollman, Gershim Asiki, Felistas Mashinya, Scott Hazelhurst, Andrew P Morris, June Fabian, Michèle Ramsay, |
Genetic epidemiology of thalassemia in couples of childbearing age: over 6 years of a thalassemia intervention project. Molecular biology reports 2024 1 51 (1): 138. Xiujie Zheng, Yantao Bao, Qunyan Wu, Fang Yao, Jindi Su, Yuankai Yang, Zhiqiang Liu, Shan Du |
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- Page last updated:Mar 25, 2024
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