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Joint application of A-InDels and miniSTRs for forensic personal, full and half sibling identifications, and genetic differentiation analyses in two populations from China

BMC genomics, 2024-04, Vol.25 (1), p.329-329, Article 329

2024

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

Orphanet journal of rare diseases, 2023-05, Vol.18 (1), p.107-107, Article 107

2023

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

Clinica chimica acta, 2017-10, Vol.473, p.26-31

2017

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Evaluation of the genetic parameters and mutation analysis of 22 STR loci in the central Chinese Han population

International Journal of Legal Medicine, 2017, Vol.131 (1), p.103-105

2017

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A novel MIP mutation in familial congenital nuclear cataracts

European journal of medical genetics, 2016-09, Vol.59 (9), p.488-491

2016

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Prenatal diagnosis and genetic analysis of a fetus with 6q27 microdeletion

Zhonghua yi xue yi chuan xue za zhi, 2017-10, Vol.34 (5), p.718

2017

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The covalent organic framework based nylon membrane extraction coupled with UHPLC-MS/MS for highly efficiency determination of hexabromocyclododecanes in environmental water

Journal of hazardous materials, 2023-06, Vol.451, p.131191-131191, Article 131191

2023

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Methylenetetrahydrofolate reductase (MTHFR) and methionine synthase reductase (MTRR) gene polymorphisms and five related serum molecular levels in 2587 patients: Associated differentially with adverse pregnancy

Molecular biology reports, 2024-12, Vol.51 (1), p.1014, Article 1014

2024

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Autosomal deletion/insertion polymorphisms for global stratification analyses and ancestry origin inferences of different continental populations by machine learning methods

Electrophoresis, 2021-08, Vol.42 (14-15), p.1473-1479

2021

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Genetic diagnosis for a family without exonic deletions and duplications of dystrophin gene

Zhonghua yi xue yi chuan xue za zhi, 2015-02, Vol.32 (1), p.81

2015

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Competing Endogenous RNAs Crosstalk in Hippocampus: A Potential Mechanism for Neuronal Developing Defects in Down Syndrome

Journal of molecular neuroscience, 2024-03, Vol.74 (2), p.32, Article 32

2024

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Correlation between maternal serum biomarkers and the risk of fetal chromosome copy number variants: a single-center retrospective study

Archives of gynecology and obstetrics, 2024-08, Vol.310 (2), p.933-942

2024

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Prenatal echocardiographic classification and prognostic evaluation strategy in fetal pulmonary atresia with intact ventricular septum

Medicine (Baltimore), 2019-10, Vol.98 (42), p.e17492-e17492

2019

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Effect of preoperative smoking cessation on postoperative pain outcomes in elderly patients with high nicotine dependence

Medicine (Baltimore), 2019-01, Vol.98 (3), p.e14209

2019

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

Scientific reports, 2018-07, Vol.8 (1), p.11054-8, Article 11054

2018

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

Scientific reports, 2020-07, Vol.10 (1), p.12205-12205, Article 12205

2020

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

Clinica chimica acta, 2020-08, Vol.507, p.23-30

2020

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Genetic analysis of a Chinese pedigree with Cohen syndrome due to compound heterozygous variants of VPS13B gene

Zhonghua yi xue yi chuan xue za zhi, 2023-08, Vol.40 (8), p.966

2023

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Genomic characteristics and prognosis of lung cancer patients with MSI-H: A cohort study

Lung cancer (Amsterdam, Netherlands), 2023-07, Vol.181, p.107255-107255, Article 107255

2023

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

DNA and cell biology, 2016-12, Vol.35 (12), p.787-794

2016

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Analysis of a fetus with unbalanced translocation derived from a balanced t(6;14) maternal translocation

Zhonghua yi xue yi chuan xue za zhi, 2023-02, Vol.40 (2), p.230

2023

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HNRNPC mediated m 6 A methylation of 5-methyltetrahydrofolate-homocysteine methyltransferase and involved in the occurrence of RSA

Journal of reproductive immunology, 2023-12, Vol.160, p.104160

2023

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Identification of pathogenic variant in a Chinese pedigree affected with non-syndromic cleft lip and palate

Zhonghua yi xue yi chuan xue za zhi, 2021-01, Vol.38 (1), p.52

2021

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Genetic analysis of 90 families affected with spinal muscular atrophy

Zhonghua yi xue yi chuan xue za zhi, 2020-02, Vol.37 (2), p.116

2020

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Hereditary spherocytosis due to a novel c.5798+1G>A variant of the SPTB gene

Zhonghua yi xue yi chuan xue za zhi, 2020-01, Vol.37 (1), p.17

2020

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Joint application of A-InDels and miniSTRs for forensic personal, full and half sibling identifications, and genetic differentiation analyses in two populations from China

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

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

Evaluation of the genetic parameters and mutation analysis of 22 STR loci in the central Chinese Han population

A novel MIP mutation in familial congenital nuclear cataracts

Prenatal diagnosis and genetic analysis of a fetus with 6q27 microdeletion

The covalent organic framework based nylon membrane extraction coupled with UHPLC-MS/MS for highly efficiency determination of hexabromocyclododecanes in environmental water

Methylenetetrahydrofolate reductase (MTHFR) and methionine synthase reductase (MTRR) gene polymorphisms and five related serum molecular levels in 2587 patients: Associated differentially with adverse pregnancy

Autosomal deletion/insertion polymorphisms for global stratification analyses and ancestry origin inferences of different continental populations by machine learning methods

Genetic diagnosis for a family without exonic deletions and duplications of dystrophin gene

Competing Endogenous RNAs Crosstalk in Hippocampus: A Potential Mechanism for Neuronal Developing Defects in Down Syndrome

Correlation between maternal serum biomarkers and the risk of fetal chromosome copy number variants: a single-center retrospective study

Prenatal echocardiographic classification and prognostic evaluation strategy in fetal pulmonary atresia with intact ventricular septum

Effect of preoperative smoking cessation on postoperative pain outcomes in elderly patients with high nicotine dependence

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

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

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

Genetic analysis of a Chinese pedigree with Cohen syndrome due to compound heterozygous variants of VPS13B gene

Genomic characteristics and prognosis of lung cancer patients with MSI-H: A cohort study

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

Analysis of a fetus with unbalanced translocation derived from a balanced t(6;14) maternal translocation

HNRNPC mediated m 6 A methylation of 5-methyltetrahydrofolate-homocysteine methyltransferase and involved in the occurrence of RSA

Identification of pathogenic variant in a Chinese pedigree affected with non-syndromic cleft lip and palate

Genetic analysis of 90 families affected with spinal muscular atrophy

Hereditary spherocytosis due to a novel c.5798+1G>A variant of the SPTB gene

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