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New myotonic dystrophy type 1 mouse model

Cell research, 2020-02, Vol.30 (2), p.99-100

2020

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Actuation enhances patterning in human neural tube organoids

Nature communications, 2021-05, Vol.12 (1), p.3192-3192, Article 3192

2021

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Somatic mutations in planar cell polarity genes in neural tissue from human fetuses with neural tube defects

Human genetics, 2020-10, Vol.139 (10), p.1299-1314

2020

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Digenic variants of planar cell polarity genes in human neural tube defect patients

Molecular genetics and metabolism, 2018-05, Vol.124 (1), p.94-100

2018

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Gene Environment Interactions in the Etiology of Neural Tube Defects

Frontiers in genetics, 2021-05, Vol.12, p.659612

2021

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Editorial: Health effects and pathophysiological mechanisms of one-carbon metabolism nutrients intake throughout the life cycle

Frontiers in nutrition (Lausanne), 2023-08, Vol.10, p.1269038-1269038

2023

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Biomass Calculations of Individual Trees Based on Unmanned Aerial Vehicle Multispectral Imagery and Laser Scanning Combined with Terrestrial Laser Scanning in Complex Stands

Remote sensing (Basel, Switzerland), 2022-10, Vol.14 (19), p.4715

2022

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Hypermethylation of PI3K-AKT signalling pathway genes is associated with human neural tube defects

Epigenetics, 2022-02, Vol.17 (2), p.133-146

2022

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Identification of novel CELSR1 mutations in spina bifida

PloS one, 2014-03, Vol.9 (3), p.e92207-e92207

2014

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Genetic analysis of Wnt/PCP genes in neural tube defects

BMC medical genomics, 2018-04, Vol.11 (1), p.38-38, Article 38

2018

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Planar cell polarity genes Celsr1 and Vangl2 are necessary for kidney growth, differentiation, and rostrocaudal patterning

Kidney international, 2016-12, Vol.90 (6), p.1274-1284

2016

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Functional characterization of age-dependent p16 epimutation reveals biological drivers and therapeutic targets for colorectal cancer

Journal of experimental & clinical cancer research, 2023-05, Vol.42 (1), p.113-113, Article 113

2023

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Mutations in planar cell polarity gene SCRIB are associated with spina bifida

PloS one, 2013-07, Vol.8 (7), p.e69262-e69262

2013

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Gene-environment interactions underlying the etiology of neural tube defects

Current topics in developmental biology, 2023, Vol.152, p.193

2023

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The TFAP2A-IRF6-GRHL3 genetic pathway is conserved in neurulation

Human molecular genetics, 2019-05, Vol.28 (10), p.1726-1737

2019

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Whole-Exome Sequencing Identifies Damaging de novo Variants in Anencephalic Cases

Frontiers in neuroscience, 2019-11, Vol.13, p.1285

2019

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Whole-exome sequencing study of hypospadias

iScience, 2023-05, Vol.26 (5), p.106663-106663, Article 106663

2023

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KDM6B Variants May Contribute to the Pathophysiology of Human Cerebral Folate Deficiency

Biology (Basel, Switzerland), 2022-12, Vol.12 (1), p.74

2022

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Genome-wide association study in Chinese cohort identifies one novel hypospadias risk associated locus at 12q13.13

BMC medical genomics, 2019-12, Vol.12 (1), p.196-196, Article 196

2019

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Excess folic acid intake increases DNA de novo point mutations

Cell discovery, 2023-02, Vol.9 (1), p.22-5, Article 22

2023

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Angiotensinogen Gene M235T and T174M Polymorphisms and Susceptibility of Pre-Eclampsia: A Meta-Analysis

Annals of human genetics, 2012-09, Vol.76 (5), p.377-386

2012

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Homozygous Mutation in the MTHFS Gene May Contribute to the Development of Cerebral Folate Deficiency Syndrome

Reproductive and developmental medicine, 2020-04, Vol.4 (2), p.72-80

2020

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Correction to: Genetic analysis of Wnt/PCP genes in neural tube defects

BMC medical genomics, 2021-01, Vol.14 (1), p.29-29, Article 29

2021

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Somatic and de novo Germline Variants of MEDs in Human Neural Tube Defects

Frontiers in cell and developmental biology, 2021-03, Vol.9, p.641831

2021

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Progress and clinical prospect of genomic structural variants investigation

Science bulletin, 2024-03, Vol.69 (6), p.705-708

2024

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New myotonic dystrophy type 1 mouse model

Actuation enhances patterning in human neural tube organoids

Somatic mutations in planar cell polarity genes in neural tissue from human fetuses with neural tube defects

Digenic variants of planar cell polarity genes in human neural tube defect patients

Gene Environment Interactions in the Etiology of Neural Tube Defects

Editorial: Health effects and pathophysiological mechanisms of one-carbon metabolism nutrients intake throughout the life cycle

Biomass Calculations of Individual Trees Based on Unmanned Aerial Vehicle Multispectral Imagery and Laser Scanning Combined with Terrestrial Laser Scanning in Complex Stands

Hypermethylation of PI3K-AKT signalling pathway genes is associated with human neural tube defects

Identification of novel CELSR1 mutations in spina bifida

Genetic analysis of Wnt/PCP genes in neural tube defects

Planar cell polarity genes Celsr1 and Vangl2 are necessary for kidney growth, differentiation, and rostrocaudal patterning

Functional characterization of age-dependent p16 epimutation reveals biological drivers and therapeutic targets for colorectal cancer

Mutations in planar cell polarity gene SCRIB are associated with spina bifida

Gene-environment interactions underlying the etiology of neural tube defects

The TFAP2A-IRF6-GRHL3 genetic pathway is conserved in neurulation

Whole-Exome Sequencing Identifies Damaging de novo Variants in Anencephalic Cases

Whole-exome sequencing study of hypospadias

KDM6B Variants May Contribute to the Pathophysiology of Human Cerebral Folate Deficiency

Genome-wide association study in Chinese cohort identifies one novel hypospadias risk associated locus at 12q13.13

Excess folic acid intake increases DNA de novo point mutations

Angiotensinogen Gene M235T and T174M Polymorphisms and Susceptibility of Pre-Eclampsia: A Meta-Analysis

Homozygous Mutation in the MTHFS Gene May Contribute to the Development of Cerebral Folate Deficiency Syndrome

Correction to: Genetic analysis of Wnt/PCP genes in neural tube defects

Somatic and de novo Germline Variants of MEDs in Human Neural Tube Defects

Progress and clinical prospect of genomic structural variants investigation

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