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Robust Mixed H2/H∞ Power Control Algorithm for Cognitive Radio Networks

Wireless personal communications, 2022, Vol.123 (1), p.135-163

2022

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Generation of a TSC2 knockout embryonic stem cell line by CRISPR/Cas9 editing

Stem cell research, 2024-06, Vol.77, p.103399, Article 103399

2024

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A novel intron mutation in FBN-1 gene identified in a pregnant woman with Marfan syndrome

Hereditas, 2021-01, Vol.158 (1), p.6-6, Article 6

2021

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Rapid fabrication of hierarchical porous SiC/C hybrid structure: toward high-performance capacitive energy storage with ultrahigh cyclability

Journal of materials science, 2021-10, Vol.56 (28), p.16068-16081

2021

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Expanding the phenotype associated with SMARCC2 variants: a fetus with tetralogy of Fallot

BMC medical genomics, 2022-03, Vol.15 (1), p.40-40, Article 40

2022

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Prognostic significance of IDH mutation in adult low-grade gliomas: a meta-analysis

Journal of neuro-oncology, 2013-06, Vol.113 (2), p.277-284

2013

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Diverse cardiac phenotypes among different carriers of the same MYH7 splicing variant allele (c.732+1G>A) from a family

BMC medical genomics, 2022-02, Vol.15 (1), p.36-36, Article 36

2022

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Evaluating Bicycling Environments with Trajectory Data on Shared Bikes: A Case Study of Beijing

Journal of advanced transportation, 2023-04, Vol.2023, p.1-20

2023

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Genetic abnormalities in fetal congenital heart disease with aberrant right subclavian artery

Scientific reports, 2022-09, Vol.12 (1), p.15899-15899, Article 15899

2022

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Case Report: Characterization of a Novel NONO Intronic Mutation in a Fetus With X-Linked Syndromic Mental Retardation-34

Frontiers in genetics, 2020-11, Vol.11, p.593688

2020

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Case Report: Biventricular Noncompaction Cardiomyopathy With Pulmonary Stenosis and Bradycardia in a Fetus With KCNH2 Mutation

Frontiers in genetics, 2022-02, Vol.13, p.821226

2022

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Placental DNA Methylation Abnormalities in Prenatal Conotruncal Heart Defects

Frontiers in genetics, 2022-05, Vol.13, p.878063-878063

2022

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Generation of a NONO homozygous knockout human induced pluripotent stem cell line by CRISPR/Cas9 editing

Stem cell research, 2020-08, Vol.47, p.101893-101893, Article 101893

2020

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Genetic and Clinical Features of Heterotaxy in a Prenatal Cohort

Frontiers in genetics, 2022-04, Vol.13, p.818241-818241

2022

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Genetic aetiology distribution of 398 foetuses with congenital heart disease in the prenatal setting

ESC Heart Failure, 2023-04, Vol.10 (2), p.917-930

2023

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Genetics and Clinical Features of Noncompaction Cardiomyopathy in the Fetal Population

Frontiers in cardiovascular medicine, 2021-01, Vol.7, p.617561-617561

2021

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Increased frequency of FBN1 frameshift and nonsense mutations in Marfan syndrome patients with aortic dissection

Molecular genetics & genomic medicine, 2020-01, Vol.8 (1), p.e1041-n/a

2020

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Expanding the phenotype of STRA6‐related disorder to include left ventricular non‐compaction

Molecular genetics & genomic medicine, 2020-09, Vol.8 (9), p.e1377-n/a

2020

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Detection of TSC1/TSC2 mosaic variants in patients with cardiac rhabdomyoma and tuberous sclerosis complex by hybrid‐capture next‐generation sequencing

Molecular genetics & genomic medicine, 2021-10, Vol.9 (10), p.e1802-n/a

2021

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Enhancement and Broadening of the Internal Electric Field of Hole-Transport-Layer-Free Perovskite Solar Cells by Quantum Dot Interface Modification

ACS applied materials & interfaces, 2024-02, Vol.16 (5), p.6665-6673

2024

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Analysis of MYRF gene variant in a fetus with Cardiac-urogenital syndrome

Zhonghua yi xue yi chuan xue za zhi, 2023-05, Vol.40 (5), p.563

2023

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Regarding “The Role of Minimally Invasive Surgery in the Care of Women with Ovarian Cancer: A Systematic Review and Meta-analysis”

Journal of minimally invasive gynecology, 2022-10, Vol.29 (10), p.1197-1197

2022

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Efficient hole extraction with Eu3+-doped CsPbBr3 QD interface modification for HTL-free CH3NH3PbI3:Na perovskite solar cells

Solar energy, 2022-10, Vol.245, p.224-230

2022

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Robust Mixed $$\text {H}_{2} / \text {H}_{\infty }$$ Power Control Algorithm for Cognitive Radio Networks

Wireless personal communications, 2022-03, Vol.123 (1), p.135-163

2022

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Association between placental DNA methylation and fetal congenital heart disease

Molecular genetics and genomics : MGG, 2023, Vol.298 (1), p.243-251

2023

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Robust Mixed H2/H∞ Power Control Algorithm for Cognitive Radio Networks

Generation of a TSC2 knockout embryonic stem cell line by CRISPR/Cas9 editing

A novel intron mutation in FBN-1 gene identified in a pregnant woman with Marfan syndrome

Rapid fabrication of hierarchical porous SiC/C hybrid structure: toward high-performance capacitive energy storage with ultrahigh cyclability

Expanding the phenotype associated with SMARCC2 variants: a fetus with tetralogy of Fallot

Prognostic significance of IDH mutation in adult low-grade gliomas: a meta-analysis

Diverse cardiac phenotypes among different carriers of the same MYH7 splicing variant allele (c.732+1G>A) from a family

Evaluating Bicycling Environments with Trajectory Data on Shared Bikes: A Case Study of Beijing

Genetic abnormalities in fetal congenital heart disease with aberrant right subclavian artery

Case Report: Characterization of a Novel NONO Intronic Mutation in a Fetus With X-Linked Syndromic Mental Retardation-34

Case Report: Biventricular Noncompaction Cardiomyopathy With Pulmonary Stenosis and Bradycardia in a Fetus With KCNH2 Mutation

Placental DNA Methylation Abnormalities in Prenatal Conotruncal Heart Defects

Generation of a NONO homozygous knockout human induced pluripotent stem cell line by CRISPR/Cas9 editing

Genetic and Clinical Features of Heterotaxy in a Prenatal Cohort

Genetic aetiology distribution of 398 foetuses with congenital heart disease in the prenatal setting

Genetics and Clinical Features of Noncompaction Cardiomyopathy in the Fetal Population

Increased frequency of FBN1 frameshift and nonsense mutations in Marfan syndrome patients with aortic dissection

Expanding the phenotype of STRA6‐related disorder to include left ventricular non‐compaction

Detection of TSC1/TSC2 mosaic variants in patients with cardiac rhabdomyoma and tuberous sclerosis complex by hybrid‐capture next‐generation sequencing

Enhancement and Broadening of the Internal Electric Field of Hole-Transport-Layer-Free Perovskite Solar Cells by Quantum Dot Interface Modification

Analysis of MYRF gene variant in a fetus with Cardiac-urogenital syndrome

Regarding “The Role of Minimally Invasive Surgery in the Care of Women with Ovarian Cancer: A Systematic Review and Meta-analysis”

Efficient hole extraction with Eu3+-doped CsPbBr3 QD interface modification for HTL-free CH3NH3PbI3:Na perovskite solar cells

Robust Mixed $$\text {H}_{2} / \text {H}_{\infty }$$ Power Control Algorithm for Cognitive Radio Networks

Association between placental DNA methylation and fetal congenital heart disease

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