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Fuzzy sampled‐data exponential synchronization of T‐S fuzzy complex networks with discontinuous activations and mixed time‐varying delays

IET control theory & applications, 2022-05, Vol.16 (8), p.789-798

2022

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Distributed Formation Control of Multi-Robot Systems with Path Navigation via Complex Laplacian

Entropy (Basel, Switzerland), 2023-11, Vol.25 (11), p.1536

2023

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Finite-time Nonfragile Synchronization Control of Time-Varying Delays T-S Fuzzy Discrete Chaotic Network Systems with Deception Attacks

IEEE access, 2024-01, Vol.12, p.1-1

2024

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Gene Mutation Analysis in 253 Chinese Children with Unexplained Epilepsy and Intellectual/Developmental Disabilities

PloS one, 2015-11, Vol.10 (11), p.e0141782-e0141782

2015

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Finite-Time Pinning Synchronization Control for T-S Fuzzy Discrete Complex Networks with Time-Varying Delays via Adaptive Event-Triggered Approach

Entropy (Basel, Switzerland), 2022-05, Vol.24 (5), p.733

2022

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Mosaicism and incomplete penetrance of PCDH19 mutations

Journal of medical genetics, 2019-02, Vol.56 (2), p.81-88

2019

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CHD2‐related epilepsy: novel mutations and new phenotypes

Developmental medicine and child neurology, 2020-05, Vol.62 (5), p.647-653

2020

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Observer-Based Leader-Following Formation Control for Multi-Robot With Obstacle Avoidance

IEEE access, 2019, Vol.7, p.14791-14798

2019

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A VINS Combined With Dynamic Object Detection for Autonomous Driving Vehicles

IEEE access, 2022, Vol.10, p.91127-91136

2022

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Genomic mosaicism in paternal sperm and multiple parental tissues in a Dravet syndrome cohort

Scientific reports, 2017-11, Vol.7 (1), p.15677-13, Article 15677

2017

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The clinical outcome and neuroimaging of acute encephalopathy after status epilepticus in Dravet syndrome

Developmental medicine and child neurology, 2018-06, Vol.60 (6), p.566-573

2018

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ATP1A3 mutations and genotype-phenotype correlation of alternating hemiplegia of childhood in Chinese patients

PloS one, 2014-05, Vol.9 (5), p.e97274-e97274

2014

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Adaptive and Exponential Synchronization of Uncertain Fractional-Order T-S Fuzzy Complex Networks With Coupling Time-Varying Delays via Pinning Control Strategy

IEEE access, 2021, Vol.9, p.2007-2017

2021

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Novel MEF2C point mutations in Chinese patients with Rett (-like) syndrome or non-syndromic intellectual disability: insights into genotype-phenotype correlation

BMC medical genetics, 2018-10, Vol.19 (1), p.191-191, Article 191

2018

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Quantization-Based Event-Triggered H∞ Consensus for Discrete-Time Markov Jump Fractional-Order Multiagent Systems with DoS Attacks

Fractal and fractional, 2024-03, Vol.8 (3), p.147

2024

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Genomic mosaicism in the pathogenesis and inheritance of a Rett syndrome cohort

Genetics in medicine, 2019-06, Vol.21 (6), p.1330-1338

2019

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GRIN2A mutations in epilepsy-aphasia spectrum disorders

Brain & development (Tokyo. 1979), 2018-03, Vol.40 (3), p.205-210

2018

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Adaptive fractional-order non-singular terminal sliding mode control based on fuzzy wavelet neural networks for omnidirectional mobile robot manipulator

ISA transactions, 2022-02, Vol.121, p.258-267

2022

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Phenotype-Genotype Analysis of Chinese Patients with Early-Onset LMNA-Related Muscular Dystrophy

PloS one, 2015-06, Vol.10 (6), p.e0129699-e0129699

2015

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SCN8A mutations in Chinese patients with early onset epileptic encephalopathy and benign infantile seizures

BMC medical genetics, 2017-09, Vol.18 (1), p.104-104, Article 104

2017

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Hypomyelinating disorders in China: The clinical and genetic heterogeneity in 119 patients

PloS one, 2018-02, Vol.13 (2), p.e0188869-e0188869

2018

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The Efficacy of Ketogenic Diet in 60 Chinese Patients With Dravet Syndrome

Frontiers in neurology, 2019-06, Vol.10, p.625-625

2019

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Genetic analysis of benign familial epilepsies in the first year of life in a Chinese cohort

Journal of human genetics, 2018-01, Vol.63 (1), p.9-18

2018

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Functional study of NIPA2 mutations identified from the patients with childhood absence epilepsy

PloS one, 2014-10, Vol.9 (10), p.e109749-e109749

2014

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Rett and Rett‐like syndrome: Expanding the genetic spectrum to KIF1A and GRIN1 gene

Molecular genetics & genomic medicine, 2019-11, Vol.7 (11), p.e968-n/a

2019

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Fuzzy sampled‐data exponential synchronization of T‐S fuzzy complex networks with discontinuous activations and mixed time‐varying delays

Distributed Formation Control of Multi-Robot Systems with Path Navigation via Complex Laplacian

Finite-time Nonfragile Synchronization Control of Time-Varying Delays T-S Fuzzy Discrete Chaotic Network Systems with Deception Attacks

Gene Mutation Analysis in 253 Chinese Children with Unexplained Epilepsy and Intellectual/Developmental Disabilities

Finite-Time Pinning Synchronization Control for T-S Fuzzy Discrete Complex Networks with Time-Varying Delays via Adaptive Event-Triggered Approach

Mosaicism and incomplete penetrance of PCDH19 mutations

CHD2‐related epilepsy: novel mutations and new phenotypes

Observer-Based Leader-Following Formation Control for Multi-Robot With Obstacle Avoidance

A VINS Combined With Dynamic Object Detection for Autonomous Driving Vehicles

Genomic mosaicism in paternal sperm and multiple parental tissues in a Dravet syndrome cohort

The clinical outcome and neuroimaging of acute encephalopathy after status epilepticus in Dravet syndrome

ATP1A3 mutations and genotype-phenotype correlation of alternating hemiplegia of childhood in Chinese patients

Adaptive and Exponential Synchronization of Uncertain Fractional-Order T-S Fuzzy Complex Networks With Coupling Time-Varying Delays via Pinning Control Strategy

Novel MEF2C point mutations in Chinese patients with Rett (-like) syndrome or non-syndromic intellectual disability: insights into genotype-phenotype correlation

Quantization-Based Event-Triggered H∞ Consensus for Discrete-Time Markov Jump Fractional-Order Multiagent Systems with DoS Attacks

Genomic mosaicism in the pathogenesis and inheritance of a Rett syndrome cohort

GRIN2A mutations in epilepsy-aphasia spectrum disorders

Adaptive fractional-order non-singular terminal sliding mode control based on fuzzy wavelet neural networks for omnidirectional mobile robot manipulator

Phenotype-Genotype Analysis of Chinese Patients with Early-Onset LMNA-Related Muscular Dystrophy

SCN8A mutations in Chinese patients with early onset epileptic encephalopathy and benign infantile seizures

Hypomyelinating disorders in China: The clinical and genetic heterogeneity in 119 patients

The Efficacy of Ketogenic Diet in 60 Chinese Patients With Dravet Syndrome

Genetic analysis of benign familial epilepsies in the first year of life in a Chinese cohort

Functional study of NIPA2 mutations identified from the patients with childhood absence epilepsy

Rett and Rett‐like syndrome: Expanding the genetic spectrum to KIF1A and GRIN1 gene

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