Hao Sun

发表

The Adaptive Change of HLA-DRB1 Allele Frequencies Caused by Natural Selection in a Mongolian Population That Migrated to the South of China

Hao Sun, Zhao-Qing Yang, Ke-qin Lin, 2015, PloS one.

Autosomal STRs Provide Genetic Evidence for the Hypothesis That Tai People Originate from Southern China

Hao Sun, Ke-qin Lin, Shuyuan Liu, 2013, PloS one.

Molecular characteristics of hand, foot, and mouth disease for hospitalized pediatric patients in Yunnan, China

Hao Sun, Zhao-Qing Yang, Xiao-qin Huang, 2018, Medicine.

Assessing the outcomes of everolimus on renal angiomyolipoma associated with tuberous sclerosis complex in China: a two years trial

Hao Sun, Han-Zhong Li, Wenda Wang, 2018, Orphanet Journal of Rare Diseases.

[Association between six single nucleotide polymorphisms of EGLN1 gene and adaptation to high-altitude hypoxia].

Hao Sun, Zhao-Qing Yang, Ke-qin Lin, 2013, Yi chuan = Hereditas.

CAG-repeat variant in the polymerase γ gene and male infertility in the Chinese population: a meta-analysis.

Hao Sun, Ke-qin Lin, Shuyuan Liu, 2011, Asian journal of andrology.

Strong association of SLC1A1 and DPF3 gene variants with idiopathic male infertility in Han Chinese

Hao Sun, Zhao-Qing Yang, Ke-qin Lin, 2016, Asian journal of andrology.

Association between gene polymorphisms of voltage-dependent Ca2+ channels and hypertension in the Dai people of China: a case-control study

Hao Sun, Ke-qin Lin, K. Huang, 2019, BMC Medical Genetics.

Genetic evidence of tri-genealogy hypothesis on the origin of ethnic minorities in Yunnan

J. Chu, Yang Gao, Yan Lu, 2022, BMC Biology.

A novel splice site variant in the POPDC3 causes autosomal recessive limb‐girdle muscular dystrophy type 26

Hao Sun, Ke-qin Lin, K. Huang, 2022, Clinical genetics.

Distribution of CCR5-Delta32, CCR2-64I, SDF1-3'A, CX3CR1-249I, and CX3CR1-280M in Chinese populations.

Hao Sun, Ke-qin Lin, J. Chu, 2008, AIDS research and human retroviruses.

RANTES In1.1C allele polymorphisms in 13 Chinese ethnic populations.

Hao Sun, J. Chu, Y. Qian, 2009, Chinese medical journal.

Identification of a new recombinant strain of echovirus 33 from children with hand, foot, and mouth disease complicated by meningitis in Yunnan, China

J. Zhang, Hao Sun, Zhao-Qing Yang, 2019, Virology Journal.

Analysis of whole genome‐wide methylation and gene expression profiles in visceral omental adipose tissue of pregnancies with gestational diabetes mellitus

Yong Duan, Wenjin Qi, Hao Sun, 2018, Journal of the Chinese Medical Association : JCMA.

[Analysis of the 14 bp insertion/deletion polymorphism in human leukocyte antigen-G gene in Chinese Dai and Han ethnic groups in Yunnan Province].

Hao Sun, Ke-qin Lin, J. Chu, 2010, Yi chuan = Hereditas.

[Association study of telomere length with idiopathic male infertility].

Hao Sun, Zhao-Qing Yang, Ke-qin Lin, 2015, Yi chuan = Hereditas.

Waardenburg syndrome type II in a Chinese patient caused by a novel nonsense mutation in the SOX10 gene.

Jing Ma, Hao Sun, Hongchao Jiang, 2016, International journal of pediatric otorhinolaryngology.

A Combination of Species Identification and STR Profiling Identifies Cross-contaminated Cells from 482 Human Tumor Cell Lines

Yuqin Liu, Hao Sun, Hao Sun, 2017, Scientific Reports.

Downregulation of the insulin signaling pathway by SHC may correlate with congenital heart disease in Chinese populations.

Yan Shen, Longjiang Xu, Hao Sun, 2020, Clinical science.

Human and mouse studies establish TBX6 in Mendelian CAKUT and as a potential driver of kidney defects associated with the 16p11.2 microdeletion syndrome.

A. Breman, J. Lupski, Zhihong Wu, 2020, Kidney international.

Gene frequency and haplotype distribution of hemoglobin E among seven minority groups of Yunnan, China

Hao Sun, Ke-qin Lin, Shuyuan Liu, 2016, American journal of human biology : the official journal of the Human Biology Council.

A novel dominant mutation in the SOX10 gene in a Chinese family with Waardenburg syndrome type II.

Jing Ma, Hao Sun, Guomin Wu, 2019, Molecular medicine reports.

TBX6 compound inheritance leads to congenital vertebral malformations in humans and mice

J. Lupski, Zhihong Wu, Shuyang Zhang, 2018, Human molecular genetics.

A rare variant in TOR1A exon 5 associated with isolated dystonia in southwestern Chinese

Hao Sun, J. Chu, Xiao-qin Huang, 2017, Movement disorders : official journal of the Movement Disorder Society.

Epidemiological and etiological characteristics of viral meningitis for hospitalized pediatric patients in Yunnan, China

Hao Sun, Zhaoqing Yang, Shaohui Ma, 2022, Medicine.

Molecular characterization of two novel echovirus 18 recombinants associated with hand-foot-mouth disease

Hao Sun, Zhao-Qing Yang, Xiao-qin Huang, 2017, Scientific Reports.

A 5‐year molecular epidemiology survey of human enterovirus 71 before vaccine application in Yunnan Province, China

Hao Sun, Zhao-Qing Yang, Xiao-qin Huang, 2019, Journal of medical virology.

Molecular characterization of echovirus 9 strains isolated from hand-foot-and-mouth disease in Kunming, Yunnan Province, China

Hao Sun, Zhao-Qing Yang, Shaohui Ma, 2022, Scientific Reports.

Isolation and characterization of a novel clade of coxsackievirus B2 associated with hand, foot, and mouth disease in Southwest China

Hao Sun, Zhao-Qing Yang, Shaohui Ma, 2022, Journal of medical virology.

Complete Genome Sequence of a Human Enterovirus C99 Strain Isolated from a Healthy Child in Yunnan, China, in 2013

Hao Sun, Zhao-Qing Yang, Xiao-qin Huang, 2019, Microbiology Resource Announcements.

Characterization of coxsackievirus A10 strains isolated from children with hand, foot, and mouth disease

J. Zhang, Hao Sun, Zhao-Qing Yang, 2021, Journal of medical virology.

Identification of two novel KIR3DL1 subtypes, KIR3DL1*0010104 and KIR3DL1*0010105

Jiejie Dai, Hao Sun, Zhao-Qing Yang, 2019, HLA.

Diversity of killer cell immunoglobulin-like receptor genes in four ethnic groups in China

Yufeng Yao, Hao Sun, Zhao-Qing Yang, 2011, Immunogenetics.

HLA polymorphism of the Zhuang population reflects the common HLA characteristics among Zhuang-Dong language-speaking populations

K. Tokunaga, Hao Sun, Ke-qin Lin, 2011, Journal of Zhejiang University SCIENCE B.

[Polymorphic Alu insertions and their associations with HLA I alleles in Yugu and Zhuang ethnic populations].

Hao Sun, Zhao-Qing Yang, Ke-qin Lin, 2011, Yi chuan = Hereditas.

Correlation between the linguistic affinity and genetic diversity of Chinese ethnic groups

Hao Sun, Zhao-Qing Yang, Ke-qin Lin, 2013, Journal of Human Genetics.

Interactions of unstable hemoglobin Rush with thalassemia and hemoglobin E result in thalassemia intermedia

Hao Sun, Ke-qin Lin, K. Huang, 2019, Hematology.

Comprehensive research on the distribution of HLA‐DRB1 in Chinese populations

Hao Sun, Ke-qin Lin, K. Huang, 2022, HLA.

Deletion variant rs35153737 in TOR1A is associated with isolated dystonia in a Southwestern Chinese Population

Hao Sun, J. Chu, Xiao-qin Huang, 2017, Neuroscience Letters.

Microarray analysis of differentially expressed genes and their functions in omental visceral adipose tissues of pregnant women with vs. without gestational diabetes mellitus

Xueling Xiao, Hao Sun, Y. Qian, 2017, Biomedical reports.

Genetic and clinical analysis in a Chinese parkinsonism-predominant spinocerebellar ataxia type 2 family

Y. Qian, T. Toda, Shouzhi Fu, 2011, Journal of Human Genetics.

Cellular analysis of a novel mutation p. Ser287Tyr in TOR1A in late-onset isolated dystonia

Longjiang Xu, Hao Sun, Xiuyun Wang, 2020, Neurobiology of Disease.

A pangenome reference of 36 Chinese populations

K. Ye, J. Chu, Baoxun Wang, 2023, Nature.

[Association between polymorphisms of PSMB8, PSMB9 and TAP2 genes with rheumatoid arthritis in ethnic Han Chinese from Yunnan].

Hao Sun, Zhao-Qing Yang, J. Chu, 2013, Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics.

β-globin gene cluster haplotypes in ethnic minority populations of southwest China

Hao Sun, Ke-qin Lin, J. Chu, 2017, Scientific Reports.

[Association between single nucleotide polymorphisms of 5'-untranslated region of GPx4 gene and male infertility].

Hao Sun, Shuyuan Liu, J. Chu, 2011, Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics.

Molecular evolution of two asymptomatic echovirus 6 strains that constitute a novel branch of recently epidemic echovirus 6 in China

Hao Sun, Ke-qin Lin, K. Huang, 2017, Virology Journal.

Molecular characterization of echovirus 12 strains isolated from healthy children in China

Hao Sun, Zhao-Qing Yang, Ke-qin Lin, 2018, Scientific Reports.

Mitochondrial haplogroup M9a1a1c1b is associated with hypoxic adaptation in the Tibetans

Hao Sun, Ke-qin Lin, Shuyuan Liu, 2016, Journal of Human Genetics.

Positive selection of CAG repeats of the ATXN2 gene in Chinese ethnic groups.

Hao Sun, Zhao-Qing Yang, Ke-qin Lin, 2013, Journal of genetics and genomics = Yi chuan xue bao.

Association Analysis of Nonsyndromic Congenital Heart Disease and Tag Single Nucleotide Polymorphisms of TBX20 and Genes in the Ras-MAPK Pathway.

Yan Shen, Hao Sun, Zhao-Qing Yang, 2017, Genetic testing and molecular biomarkers.

[Variation of CAG repeats in coding region of ATXN2 gene in different ethnic groups].

Hao Sun, Zhao-Qing Yang, Ke-qin Lin, 2011, Yi chuan = Hereditas.

[Association of EMILIN1 gene polymorphism with essential hypertension in Mongolian].

Hao Sun, Zhao-Qing Yang, J. Chu, 2011, Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics.

Molecular characterization of two novel echovirus 18 recombinants associated with hand-foot-mouth disease

Hao Sun, Zhao-Qing Yang, Xiao-qin Huang, 2017, Scientific Reports.