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Self-learning neural network as a prediction model in non-invasive prenatal testing to detect fetal SNVs

Journal of translational medicine, 2024-07, Vol.22 (1), p.707-4, Article 707

2024

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Analysis of 59 cases of congenital leukemia reported between 2001 and 2016

Journal of International Medical Research, 2019-10, Vol.47 (10), p.4625-4635

2019

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Emergence and circulation of enterovirus B species in infants in southern China: A multicenter retrospective analysis

Virulence, 2024-12, Vol.15 (1), p.2329569-2329569

2024

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Association between cell-free DNA fetal fraction and pregnant character: a retrospective cohort study of 27,793 maternal plasmas

Scientific reports, 2023-07, Vol.13 (1), p.11420-11420, Article 11420

2023

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Cervical HPV infection in Guangzhou, China: an epidemiological study of 198,111 women from 2015 to 2021

Emerging microbes & infections, 2023-12, Vol.12 (1), p.e2176009-e2176009

2023

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High burden of human papillomavirus infection among men in Guangzhou, South China: Implications for HPV vaccination strategies

Human vaccines & immunotherapeutics, 2024-12, Vol.20 (1), p.2337161-2337161

2024

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Factors affecting cell-free DNA fetal fraction: statistical analysis of 13,661 maternal plasmas for non-invasive prenatal screening

Human genomics, 2019-12, Vol.13 (1), p.62-62, Article 62

2019

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Intrauterine phenotype features of fetuses with 7q11.23 microduplication syndrome

Orphanet journal of rare diseases, 2023-09, Vol.18 (1), p.1-305, Article 305

2023

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Prenatal diagnosis of fetal right ventricular diverticulum with massive pericardial effusion in one of monochorionic diamniotic twins: a case report with a favorable outcome following in utero pericardiocentesis

Journal of international medical research, 2021-01, Vol.49 (1), p.300060520986668

2021

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CIR-Net: Automatic Classification of Human Chromosome Based on Inception-ResNet Architecture

IEEE/ACM transactions on computational biology and bioinformatics, 2022-05, Vol.19 (3), p.1285-1293

2022

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Compound heterozygosity for hemoglobin variant Hb-Broomhill and the Southeast Asian α-thalassemia deletion does not worsen outcome: a case report of two unrelated patients

Journal of international medical research, 2020-11, Vol.48 (11), p.300060520967825-300060520967825

2020

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A spectrum of clinical severity of recessive titinopathies in prenatal

Frontiers in genetics, 2023-01, Vol.13, p.1064474-1064474

2023

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The prevalence and molecular spectrum of α- and β-globin gene mutations in 14,332 families of Guangdong Province, China

PloS one, 2014-02, Vol.9 (2), p.e89855-e89855

2014

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Disruption of maternal vascular remodeling by a fetal endoretrovirus-derived gene in preeclampsia

Genome Biology, 2024-05, Vol.25 (1), p.117-46, Article 117

2024

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Exome sequencing in fetuses with short long bones detected by ultrasonography: A retrospective cohort study

Frontiers in genetics, 2023-02, Vol.14, p.1032346-1032346

2023

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Novel Biallelic Variant in the BRAT1 Gene Caused Nonprogressive Cerebellar Ataxia Syndrome

Frontiers in genetics, 2022-03, Vol.13, p.821587-821587

2022

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When NIPT meets WES, prenatal diagnosticians face the dilemma: genetic etiological analysis of 2,328 cases of NT thickening and follow-up of pregnancy outcomes

Frontiers in genetics, 2023-08, Vol.14, p.1227724-1227724

2023

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Establishment and application of a novel method based on single nucleotide polymorphism analysis for detecting β-globin gene cluster deletions

Scientific reports, 2020-10, Vol.10 (1), p.18298, Article 18298

2020

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Clinical features and phylogenetic analysis of severe hand-foot-and-mouth disease caused by Coxsackievirus A6

Infection, genetics and evolution, 2020-01, Vol.77, p.104054-104054, Article 104054

2020

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Performances of NIPT for copy number variations at different sequencing depths using the semiconductor sequencing platform

Human genomics, 2021-07, Vol.15 (1), p.41-41, Article 41

2021

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Noninvasive prenatal detection of fetal sex chromosome abnormalities using the semiconductor sequencing platform (SSP) in Southern China

Journal of assisted reproduction and genetics, 2021-03, Vol.38 (3), p.727-734

2021

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Identification of Key Modules and Genes Associated with Major Depressive Disorder in Adolescents

Genes, 2022-03, Vol.13 (3), p.464

2022

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A novel non-sense variant in the OFD1 gene caused Joubert syndrome

Frontiers in genetics, 2023-01, Vol.13, p.1064762-1064762

2023

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Outcomes of pregnancies with trisomy 16 mosaicism detected by NIPT: a series of case reports

Molecular cytogenetics, 2021-09, Vol.14 (1), p.1-44, Article 44

2021

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Self-learning neural network as a prediction model in non-invasive prenatal testing to detect fetal SNVs

Analysis of 59 cases of congenital leukemia reported between 2001 and 2016

Emergence and circulation of enterovirus B species in infants in southern China: A multicenter retrospective analysis

Association between cell-free DNA fetal fraction and pregnant character: a retrospective cohort study of 27,793 maternal plasmas

Cervical HPV infection in Guangzhou, China: an epidemiological study of 198,111 women from 2015 to 2021

High burden of human papillomavirus infection among men in Guangzhou, South China: Implications for HPV vaccination strategies

Factors affecting cell-free DNA fetal fraction: statistical analysis of 13,661 maternal plasmas for non-invasive prenatal screening

Intrauterine phenotype features of fetuses with 7q11.23 microduplication syndrome

Prenatal diagnosis of fetal right ventricular diverticulum with massive pericardial effusion in one of monochorionic diamniotic twins: a case report with a favorable outcome following in utero pericardiocentesis

CIR-Net: Automatic Classification of Human Chromosome Based on Inception-ResNet Architecture

Compound heterozygosity for hemoglobin variant Hb-Broomhill and the Southeast Asian α-thalassemia deletion does not worsen outcome: a case report of two unrelated patients

A spectrum of clinical severity of recessive titinopathies in prenatal

The prevalence and molecular spectrum of α- and β-globin gene mutations in 14,332 families of Guangdong Province, China

Disruption of maternal vascular remodeling by a fetal endoretrovirus-derived gene in preeclampsia

Exome sequencing in fetuses with short long bones detected by ultrasonography: A retrospective cohort study

Novel Biallelic Variant in the BRAT1 Gene Caused Nonprogressive Cerebellar Ataxia Syndrome

Dietary Modulation of Gut Microbiota Contributes to Alleviation of Both Genetic and Simple Obesity in Children

When NIPT meets WES, prenatal diagnosticians face the dilemma: genetic etiological analysis of 2,328 cases of NT thickening and follow-up of pregnancy outcomes

Establishment and application of a novel method based on single nucleotide polymorphism analysis for detecting β-globin gene cluster deletions

Clinical features and phylogenetic analysis of severe hand-foot-and-mouth disease caused by Coxsackievirus A6

Performances of NIPT for copy number variations at different sequencing depths using the semiconductor sequencing platform

Noninvasive prenatal detection of fetal sex chromosome abnormalities using the semiconductor sequencing platform (SSP) in Southern China

Identification of Key Modules and Genes Associated with Major Depressive Disorder in Adolescents

A novel non-sense variant in the OFD1 gene caused Joubert syndrome

Outcomes of pregnancies with trisomy 16 mosaicism detected by NIPT: a series of case reports

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