Hongdan Wang

发表

Development of the decision tree model for distinguishing individuals of Chinese four surnames from Zhanjiang Han population based on Y-STR haplotypes.

X. Jin, Yating Fang, Wei Cui, 2021, Legal medicine.

Gene mapping and functional annotation of GWAS of oral ulcers using FUMA software

X. Jin, Hongdan Wang, Yijie Wang, 2020, Scientific Reports.

Prenatal diagnosis and genetic counseling for Waardenburg syndrome type I and II in Chinese families

Hongdan Wang, Dong Wu, S. Liao, 2017, Molecular medicine reports.

Population Differentiations and Phylogenetic Analysis of Tibet and Qinghai Tibetan Groups Based on 30 InDel Loci.

H. Meng, Hongdan Wang, Chun-mei Shen, 2016, DNA and cell biology.

Targeted next-generation sequencing-based molecular diagnosis of congenital hand malformations in Chinese population

Hong-yan Liu, Hongdan Wang, Xichuan Li, 2018, Scientific Reports.

Genetic polymorphisms and association of KIR-HLA system of Chinese Henan Han population and an extensive KIR gene diversity study between populations distributed worldwide

Caiyong Yin, X. Jin, Hongdan Wang, 2018 .

Detection of fetal epigenetic biomarkers through genome-wide DNA methylation study for non-invasive prenatal diagnosis

Jingbin Yan, Hongdan Wang, B. Zhu, 2017, Molecular medicine reports.

Maternal natural killer cell immunoglobulin receptor genes and human leukocyte antigen-C ligands influence recurrent spontaneous abortion in the Han Chinese population

Hongdan Wang, S. Liao, Hai Xiao, 2017, Experimental and therapeutic medicine.

Application of array-comparative genomic hybridization in tetralogy of Fallot

Hongdan Wang, Taibing Fan, B. Peng, 2016, Medicine.

Prenatal diagnosis for a Chinese family with a de novo DMD gene mutation

Xin Ma, X. Lv, Hong-yan Liu, 2017, Medicine.

Genotype/phenotype analysis in a male patient with partial trisomy 4p and monosomy 20q due to maternal reciprocal translocation (4;20): A case report.

Hongdan Wang, Tao Wang, Dong Wu, 2017, Molecular medicine reports.

Preparation and luminescent properties of YBO3:Eu nanofibers by electrospinning

Hongquan Yu, Tao Li, Hongdan Wang, 2012, Journal of nanoscience and nanotechnology.

Novel heterozygous mutations of the INSR gene in a familial case of Donohue syndrome.

Hong-yan Liu, Hongdan Wang, Xichuan Li, 2017, Clinica chimica acta; international journal of clinical chemistry.

Clinical and molecular cytogenetic analyses of four families with 1q21.1 microdeletion or microduplication

Hongdan Wang, Cunying Cui, Dong Wu, 2017, The journal of gene medicine.

DNA methylation study of fetus genome through a genome-wide analysis

M. He, Hongdan Wang, B. Zhu, 2014, BMC Medical Genomics.

A Novel Panel of 43 Insertion/Deletion Loci for Human Identifications of Forensic Degraded DNA Samples: Development and Validation

X. Jin, Yating Fang, Wei Cui, 2021, Frontiers in Genetics.

Genetic Background of Kirgiz Ethnic Group From Northwest China Revealed by Mitochondrial DNA Control Region Sequences on Massively Parallel Sequencing

Yating Fang, Wei Cui, Chong Chen, 2022, Frontiers in Genetics.

Investigating the characteristics of echocardiogram, surgical treatment, chromosome and prognosis for fetal right heart enlargement

Hongdan Wang, Lei Huang, Taibing Fan, 2018, Medicine.

Autosomal DIPs for population genetic structure and differentiation analyses of Chinese Xinjiang Kyrgyz ethnic group

X. Jin, Wei Cui, Chong Chen, 2018, Scientific Reports.

Integrated miRNA and mRNA expression profiling in fetal hippocampus with Down syndrome

Hongdan Wang, Dong Wu, S. Liao, 2016, Journal of Biomedical Science.

Whole exome sequencing identifies novel mutation in eight Chinese children with isolated tetralogy of Fallot

Hongdan Wang, Taibing Fan, B. Peng, 2017, Oncotarget.

Forensic effectiveness and population differentiations study of AGCU 21+1 fluorescence multiplex in Chinese Henan Han population.

H. Meng, Hongdan Wang, Chun-mei Shen, 2017, Forensic science international. Genetics.

Autosomal DIPs for population genetic structure and differentiation analyses of Chinese Xinjiang Kyrgyz ethnic group

X. Jin, Wei Cui, Chong Chen, 2018, Scientific Reports.

Cloning, expression and enzyme activity delineation of two novel CANT1 mutations: the disappearance of dimerization may indicate the change of protein conformation and even function

Da-Wei Zhang, Hongdan Wang, B. Zhu, 2020, Orphanet Journal of Rare Diseases.

Identification of a novel de novo mutation of SETBP1 and new findings of SETBP1 in tumorgenesis

Hongdan Wang, Bofeng Zhu, S. Liao, 2023, Orphanet Journal of Rare Diseases.

Parental Genetic Variants, MTHFR 677C>T and MTRR 66A>G, Associated Differently with Fetal Congenital Heart Defect

Hongdan Wang, Jian-Gang Long, S. Liao, 2017, BioMed research international.

A novel MIP mutation in familial congenital nuclear cataracts.

Hong-yan Liu, Hongdan Wang, Zhe Liu, 2016, European journal of medical genetics.

Targeted next-generation sequencing-based molecular diagnosis of congenital hand malformations in Chinese population

Hong-yan Liu, Hongdan Wang, Xichuan Li, 2018, Scientific Reports.

Selection and Validation of Reference Genes for RT-PCR Expression Analysis of Candidate Genes Involved in Morphine-Induced Conditioned Place Preference Mice

Hongdan Wang, Jiaqi Li, Dong Wu, 2018, Journal of Molecular Neuroscience.

Integrated miRNA and mRNA expression profiling in fetal hippocampus with Down syndrome

Hongdan Wang, Dong Wu, S. Liao, 2016, Journal of Biomedical Science.

A novel mutation within intron 17 of the CUL7 gene results in appearance of premature termination codon.

Shanshan Yin, X. Jin, Hongdan Wang, 2020, Clinica chimica acta; international journal of clinical chemistry.

Genetic polymorphisms of 20 short tandem repeat loci from the Han population in Henan, China

Hongdan Wang, B. Zhu, Dong Wu, 2014 .

Collagen Type I Alpha 1 Mutation Causes Osteogenesis Imperfecta from Mild to Perinatal Death in a Chinese Family

Jia Huang, Yue Wang, Hong-yan Liu, 2016, Chinese Medical Journal.

Identification of novel TMEM231 gene splice variants and pathological findings in a fetus with Meckel Syndrome

Hongdan Wang, S. Liao, Shuya Yang, 2023, Frontiers in Genetics.

Selection and Validation of Reference Genes for RT-PCR Expression Analysis of Candidate Genes Involved in Morphine-Induced Conditioned Place Preference Mice

Hongdan Wang, Jiaqi Li, Dong Wu, 2018, Journal of Molecular Neuroscience.