Human Genome Epidemiology Literature Finder
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Records 1 - 10 (of 10 Records) |
| Query Trace: Anemia and SPTA1[original query] |
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| Mutational characteristics of ANK1 and SPTB genes in hereditary spherocytosis. Clinical genetics 2016 Feb . Park Joonhong, Jeong Dae-Chul, Yoo Jaeeun, Jang Woori, Chae Hyojin, Kim Jiyeon, Kwon Ahlm, Choi Hayoung, Lee Jae-Wook, Chung Nack-Gyun, Kim Myungshin, Kim Yongg |
| Three Novel Spectrin Variants in Jaundiced Neonates. Clinical pediatrics 2017 1 57 (1): 19-26. Christensen Robert D, Agarwal Archana M, Yaish Hassan M, Reading N Scott, O'Brien Elizabeth A, Prchal Josef |
| Whole-exome sequencing for the genetic diagnosis of congenital red blood cell membrane disorders in Taiwan. Clinica chimica acta; international journal of clinical chemistry 2018 Dec 487 311-317. Lin Pei-Chin, Chiou Shyh-Shin, Lin Chien-Yu, Wang Shu-Chen, Huang Hsi-Yuan, Chang Ya-Sian, Tseng Yu-Hsin, Kan Tzu-Min, Liao Yu-Mei, Tsai Shih-Pien, Peng Ching-Tien, Chang Jan-Gow |
| Genetic and Clinical Characteristics of Patients With Hereditary Spherocytosis in Hubei Province of China. Frontiers in genetics 2020 10 11 953. Wang Xiong, Zhang Ai, Huang Ming, Chen Li, Hu Qun, Lu Yanjun, Cheng Limi |
| Identification of new mutations in patients with hereditary spherocytosis by next-generation sequencing. Journal of human genetics 2020 1 65 (4): 427-434. Qin Li, Nie Yanbo, Zhang Hong, Chen Long, Zhang Donglei, Lin Yani, Ru K |
Multiple-ancestry genome-wide association study identifies 27 loci associated with measures of hemolysis following blood storage.
The Journal of clinical investigation 2021 May . Page Grier P, Kanias Tamir, Guo Yuelong J, Lanteri Marion C, Zhang Xu, Mast Alan E, Cable Ritchard G, Spencer Bryan R, Kiss Joseph E, Fang Fang, Endres-Dighe Stacy M, Brambilla Donald, Nouraie Mehdi, Gordeuk Victor R, Kleinman Steve, Busch Michael P, Gladwin Mark T, |
| Literature review on genotype-phenotype correlation in patients with hereditary spherocytosis. Clinical genetics 2022 Sep . Yang Liqing, Shu Huiying, Zhou Min, Gong Yupi |
| Effects of SPTA1 Gene Variants on the Hematological Phenotype of Mexican Patients with Hereditary Spherocytosis. Genetic testing and molecular biomarkers 2022 5 26 (5): 270-276. Herrera-Tirado Isis Mariela, Espinoza-Mata Laura Lucia, Rizo-delaTorre Lourdes Del Carmen, Becerra-Solano Luis Eduardo, Ibarra-Cortés Bertha, Perea-Díaz Francisco Javi |
| Genotype-degree of hemolysis correlation in hereditary spherocytosis. BMC genomics 2023 6 24 (1): 304. Yimeng Shi, Yuan Li, Xiawan Yang, Xiaoxia Li, Guangxin Peng, Xin Zhao, Xu Liu, Yufei Zhao, Jing Hu, Xiangrong Hu, Baohang Zhang, Kang Zhou, Yang Yang, Youzhen Xiong, Jianping Li, Huihui Fan, Wenrui Yang, Lei Ye, Liping Jing, Li Zhang, Fengkui Zha |
| Identification of novel variants in hereditary spherocytosis patients by whole-exome sequencing. Clinica chimica acta; international journal of clinical chemistry 2024 10 565 119989. Li Qin, Yujiao Jia, Haoxu Wang, Yuan Feng, Junyan Zou, Jianfeng Zhou, Changshun Yu, Bingqing Huang, Ruixue Zhang, Lihui Shi, Jigang Xiao, Yuping Zhao, Qi Sun, Zhijian Xiao, Huijun Wa |
- Page last reviewed:Feb 1, 2024
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