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Loss-of-function mutations in SPEF2 cause multiple morphological abnormalities of the sperm flagella (MMAF)

Journal of medical genetics, 2019-10, Vol.56 (10), p.678-684

2019

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Biallelic mutations of CFAP74 may cause human primary ciliary dyskinesia and MMAF phenotype

Journal of human genetics, 2020-11, Vol.65 (11), p.961-969

2020

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Overall and individual associations between per- and polyfluoroalkyl substances and liver function indices and the metabolic mechanism

Environment international, 2024-01, Vol.183, p.108405-108405, Article 108405

2024

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Effect of exposures to mixtures of lead and various metals on hypertension, pre-hypertension, and blood pressure: A cross-sectional study from the China National Human Biomonitoring

Environmental pollution (1987), 2022-04, Vol.299, p.118864-118864, Article 118864

2022

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A novel TEX11 mutation induces azoospermia: a case report of infertile brothers and literature review

BMC medical genetics, 2018-04, Vol.19 (1), p.63-63, Article 63

2018

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When a vesicular placenta meets a live fetus: case report of twin pregnancy with a partial hydatidiform mole

BMC pregnancy and childbirth, 2021-10, Vol.21 (1), p.694-694, Article 694

2021

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Cohort profile: China National Human Biomonitoring (CNHBM)—A nationally representative, prospective cohort in Chinese population

Environment international, 2021-01, Vol.146, p.106252-106252, Article 106252

2021

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Prenatal exposure to organochlorine pesticides and infant birth weight in China

Chemosphere (Oxford), 2014-09, Vol.110, p.1-7

2014

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Integrative profiling of extrachromosomal circular DNA in placenta and maternal plasma provides insights into the biology of fetal growth restriction and reveals potential biomarkers

Frontiers in genetics, 2023-07, Vol.14, p.1128082-1128082

2023

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Evaluation of a Microhaplotype-Based Noninvasive Prenatal Test in Twin Gestations: Determination of Paternity, Zygosity, and Fetal Fraction

Genes, 2020-12, Vol.12 (1), p.26

2020

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Contribution of genetic variants to congenital heart defects in both singleton and twin fetuses: a Chinese cohort study

Molecular cytogenetics, 2024-01, Vol.17 (1), p.2-2, Article 2

2024

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Case Report: Low-Level Maternal Mosaicism of a Novel CREBBP Variant Causes Recurrent Rubinstein-Taybi Syndrome in Two Siblings of a Chinese Family

Frontiers in genetics, 2021-03, Vol.12, p.640992

2021

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Mosaic duplication of 8q24.1q24.3 detected by chromosomal microarray but not karyotyping in two unrelated fetuses with cardiac defects

Molecular cytogenetics, 2021-05, Vol.14 (1), p.26-26, Article 26

2021

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The association between prenatal exposure to organochlorine pesticides and thyroid hormone levels in newborns in Yancheng, China

Environmental research, 2014-02, Vol.129, p.47-51

2014

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A child with a novel DDX3X variant mimicking cerebral palsy: a case report

Italian journal of pediatrics, 2020-06, Vol.46 (1), p.1-88, Article 88

2020

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Clinical value of genetic analysis in prenatal diagnosis of short femur

Molecular genetics & genomic medicine, 2019-11, Vol.7 (11), p.e978-n/a

2019

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Is an analysis of copy number variants necessary for various types of kidney ultrasound anomalies in fetuses?

Molecular cytogenetics, 2019-07, Vol.12 (Suppl 1), p.31-31, Article 31

2019

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Determination of nine phthalate ester metabolites in human urine using ultra high performance liquid chromatography-tandem triple quadrupole mass spectrometry

Sepu, 2018-09, Vol.36 (9), p.895

2018

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EIF4G1 is a novel candidate gene associated with severe asthenozoospermia

Molecular genetics & genomic medicine, 2019-08, Vol.7 (8), p.e807-n/a

2019

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Determination of eight bisphenol diglycidyl ethers in water by solid phase extraction-high performance liquid chromatography-tandem mass spectrometry

Sepu, 2014, Vol.32 (7), p.730

2014

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Prenatal evaluation of genetic variants in fetuses with small head circumference: A single-center retrospective study

European journal of obstetrics & gynecology and reproductive biology, 2024-02, Vol.293, p.57-66

2024

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Study on Clean Coal Technology with Oil Agglomeration in Fujian Province

Procedia engineering, 2012, Vol.45, p.986-992

2012

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Confirmation of a maternal cryptal balanced translocation through analysis of a fetus using microarray

Zhonghua yi xue yi chuan xue za zhi, 2015-02, Vol.32 (1), p.69

2015

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Sensitive and quick electrochemiluminescence biosensor for the detection of reactive oxygen species in seminal plasma based on the valence regulation of gold nanoclusters

Analytica chimica acta, 2024-11, Vol.1330, p.343284, Article 343284

2024

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Simple and rapid multicolor sensor for seminal plasma ROS detection based on synergistic catalytic etching of gold nanobipyramids dopped agarose composite gel

Talanta (Oxford), 2025-01, Vol.282, p.127042, Article 127042

2025

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Loss-of-function mutations in SPEF2 cause multiple morphological abnormalities of the sperm flagella (MMAF)

Biallelic mutations of CFAP74 may cause human primary ciliary dyskinesia and MMAF phenotype

Overall and individual associations between per- and polyfluoroalkyl substances and liver function indices and the metabolic mechanism

Effect of exposures to mixtures of lead and various metals on hypertension, pre-hypertension, and blood pressure: A cross-sectional study from the China National Human Biomonitoring

A novel TEX11 mutation induces azoospermia: a case report of infertile brothers and literature review

When a vesicular placenta meets a live fetus: case report of twin pregnancy with a partial hydatidiform mole

Cohort profile: China National Human Biomonitoring (CNHBM)—A nationally representative, prospective cohort in Chinese population

Prenatal exposure to organochlorine pesticides and infant birth weight in China

Integrative profiling of extrachromosomal circular DNA in placenta and maternal plasma provides insights into the biology of fetal growth restriction and reveals potential biomarkers

Evaluation of a Microhaplotype-Based Noninvasive Prenatal Test in Twin Gestations: Determination of Paternity, Zygosity, and Fetal Fraction

Contribution of genetic variants to congenital heart defects in both singleton and twin fetuses: a Chinese cohort study

Case Report: Low-Level Maternal Mosaicism of a Novel CREBBP Variant Causes Recurrent Rubinstein-Taybi Syndrome in Two Siblings of a Chinese Family

Mosaic duplication of 8q24.1q24.3 detected by chromosomal microarray but not karyotyping in two unrelated fetuses with cardiac defects

The association between prenatal exposure to organochlorine pesticides and thyroid hormone levels in newborns in Yancheng, China

A child with a novel DDX3X variant mimicking cerebral palsy: a case report

Clinical value of genetic analysis in prenatal diagnosis of short femur

Is an analysis of copy number variants necessary for various types of kidney ultrasound anomalies in fetuses?

Determination of nine phthalate ester metabolites in human urine using ultra high performance liquid chromatography-tandem triple quadrupole mass spectrometry

EIF4G1 is a novel candidate gene associated with severe asthenozoospermia

Determination of eight bisphenol diglycidyl ethers in water by solid phase extraction-high performance liquid chromatography-tandem mass spectrometry

Prenatal evaluation of genetic variants in fetuses with small head circumference: A single-center retrospective study

Study on Clean Coal Technology with Oil Agglomeration in Fujian Province

Confirmation of a maternal cryptal balanced translocation through analysis of a fetus using microarray

Sensitive and quick electrochemiluminescence biosensor for the detection of reactive oxygen species in seminal plasma based on the valence regulation of gold nanoclusters

Simple and rapid multicolor sensor for seminal plasma ROS detection based on synergistic catalytic etching of gold nanobipyramids dopped agarose composite gel

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