Publications by authors named "Keqin Lin"

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Establishment of a humanized SCA2 mouse model carrying a CAA disruption preventing CAG repeat expansion in pathogenic genes.
Yao Zhang, Yufei Li, Lin Zhang, Zhaoqing Li, Keqin Lin

Animal Model Exp Med· September 2025

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A novel mutation alters GNE bifunctional enzyme activity and leads to familial inherited GNE diseases.
Yufei Li, Wenwu Li, Baitong Fan, Yao Zhang, Zhaoqing Li, Keqin Lin

Gene· November 2024

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Difference in microbial community structure along a gradient of crater altitude: insights from the Nushan volcano.
Jin Chen, Ye Cui, Qingchen Xiao, Keqin Lin, Boyan Wang

Appl Environ Microbiol· August 2024

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FLT4 gene polymorphisms influence isolated ventricular septal defect predisposition in a Southwest China population.
Yunhan Zhang, Xiaoli Dong, Jun Zhang, Miao Zhao, Jiang Wang, Keqin Lin, Zhiling Luo

BMC Med Genomics· August 2024

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Exploring Genetic Diversity of SOD2 and POU5F1 for Congenital Heart Disease in the Southwest Chinese Population.
Ye Jin, Jun Zhang, Qiuzhe Guo, Xiaoli Dong, Jian Li, Keqin Lin, Zhiling Luo

Int Heart J· July 2024

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Association study of FLT4 and HYDIN single nucleotide polymorphisms with atrial septal defect susceptibility in the Han Chinese population of Southwest China.
Ye Jin, Miao Zhao, Qiuzhe Guo, Wanyu Zhao, Min Lei, Keqin Lin, Zhiling Luo

Ital J Pediatr· April 2024

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Determination of the 3'UTR region of HLA-B*53:01:03 sequence by next generation sequencing.
Zi-An Cheng, Cheng Bian, Ke-Qin Lin, Hao Sun, Zhao-Qing Yang

HLA· January 2024

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Comprehensive research on the distribution of HLA-DRB1 in Chinese populations.
Baitong Fan, Xiaoqin Huang, Xiaochao Zhang, Lifan Huang, Zhaoqing Yang, Lin Zhang, Keqin Lin

HLA· March 2023

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A novel splice site variant in the POPDC3 causes autosomal recessive limb-girdle muscular dystrophy type 26.
Lin Zhang, Wenwu Li, Yuting Weng, Keqin Lin, Kai Huang

Clin Genet· October 2022

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Three Novel Genetic Variants in the FAM110D, CACNA1A, and NLRP12 Genes Are Associated With Susceptibility to Hypertension Among Dai People.
Lin Zhang, Yun Sun, Xiaochao Zhang, Xiyun Shan, Jianmei Li, Keqin Lin

Am J Hypertens· August 2021

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Characterization of a novel echovirus 21 strain isolated from a healthy child in China in 2013.
Hongbo Liu, Shanri Cong, Danhan Xu, Keqin Lin, Xiaoqin Huang

Arch Virol· March 2020

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Association between gene polymorphisms of voltage-dependent Ca channels and hypertension in the Dai people of China: a case-control study.
Lifan Huang, Yan Chu, Xiaoqin Huang, Shaohui Ma, Keqin Lin

BMC Med Genet· February 2020

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Interactions of unstable hemoglobin Rush with thalassemia and hemoglobin E result in thalassemia intermedia.
Kai Huang, Shijun Ge, Wei Yi, Hui Bi, Keqin Lin

Hematology· December 2019

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A novel mutation causes Hermansky-Pudlak syndrome type 4 with pulmonary fibrosis in 2 siblings from China.
Wenjuan Wu, Keqin Lin, Yanni Yang, ZhaoXing Dong, Tao Zhang

Medicine (Baltimore)· August 2019

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Characterization of the novel KIR3DL1*0150213 and KIR3DL1*112 alleles using sequence-based typing.
Jie Jia, Ke-Qin Lin, Kai Huang, Jie-Jie Dai, Zhao-Qing Yang

HLA· July 2019

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Identification of two novel KIR3DL1 subtypes, KIR3DL1*0010104 and KIR3DL1*0010105.
Jie Jia, Keqin Lin, Hao Sun, Jie-Jie Dai, Zhao-Qing Yang

HLA· February 2019

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Molecular characterization of Coxsackievirus A16 strains isolated from children with severe hand, foot, and mouth disease in Yunnan, Southwest China, during 2009-2015.
Ming Zhang, Yilin Zhao, Haihao Zhang, Keqin Lin, Hongbo Liu

J Med Virol· January 2019

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Molecular characterization of echovirus 12 strains isolated from healthy children in China.
Hongbo Liu, Jie Zhang, Yilin Zhao, Haihao Zhang, Keqin Lin

Sci Rep· August 2018

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Strong association of and gene variants with idiopathic male infertility in Han Chinese.
Shu-Yuan Liu, Chang-Jun Zhang, Hai-Ying Peng, Hao Sun, Ke-Qin Lin

Asian J Androl· March 2018

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Molecular evolution of two asymptomatic echovirus 6 strains that constitute a novel branch of recently epidemic echovirus 6 in China.
Hao Sun, Xiaoqin Huang, Keqin Lin, Kai Huang, Jiayou Chu

Virol J· July 2017

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Complete Genome Sequence of an Enterovirus 71 Strain Isolated from the Cerebrospinal Fluid of a Child with Severe Hand-Foot-and-Mouth Disease in Yunnan, China, 2013.
Keqin Lin, Haihao Zhang, Wei Bai, Yiling Zhao, Hongbo Liu

Genome Announc· May 2017

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β-globin gene cluster haplotypes in ethnic minority populations of southwest China.
Hao Sun, Hongxian Liu, Kai Huang, Keqin Lin, Xiaoqin Huang

Sci Rep· February 2017

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Mitochondrial haplogroup M9a1a1c1b is associated with hypoxic adaptation in the Tibetans.
Qian Li, Keqin Lin, Hao Sun, Shuyuan Liu, Kai Huang

J Hum Genet· December 2016

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Gene frequency and haplotype distribution of hemoglobin E among seven minority groups of Yunnan, China.
Hongxian Liu, Kai Huang, Shuyuan Liu, Hao Sun, Keqin Lin

Am J Hum Biol· November 2016

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[Impact of natural selection on the polymorphism of HLA-G 3'UTR among five ethnic Chinese populations].
Hao Sun, Qianqian Sun, Kai Huang, Keqin Lin, Shuyuan Liu

Zhonghua Yi Xue Yi Chuan Xue Za Zhi· August 2016

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