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Nannochloropsis genomes reveal evolution of microalgal oleaginous traits

PLoS genetics, 2014-01, Vol.10 (1), p.e1004094-e1004094

2014

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Saliva microbiomes distinguish caries-active from healthy human populations

The ISME Journal, 2012-01, Vol.6 (1), p.1-10

2012

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Modeling and analysis of distribution network with photovoltaic cells based on Markov global sensitivity

Frontiers in energy research, 2024-03, Vol.12

2024

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A novel binary genetic differential evolution optimization algorithm for wind layout problems

AIMS energy, 2024-01, Vol.12 (1), p.321-349

2024

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Design of high-precision displacement safety monitoring and three-dimensional spatial alarm system for Beidou based on intelligent algorithms

Measurement. Sensors, 2024-06, Vol.33, p.101099, Article 101099

2024

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Design of a 3D space early warning system for high precision positioning technology of Beidou and analysis of differential positioning accuracy

Measurement. Sensors, 2024-06, Vol.33, p.101103, Article 101103

2024

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Design and implementation of a monitoring platform based on beidou high precision positioning technology

Measurement. Sensors, 2024-06, Vol.33, p.101105, Article 101105

2024

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Clinical and genetic analysis of a case with centronuclear myopathy caused by SPEG gene mutation: a case report and literature review

BMC pediatrics, 2021-04, Vol.21 (1), p.209-209, Article 209

2021

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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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Genetic variations and clinical spectrum of dystroglycanopathy in a large cohort of Chinese patients

Clinical genetics, 2021-03, Vol.99 (3), p.384-395

2021

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Clinical and genetic features of infancy-onset congenital myopathies from a Chinese paediatric centre

BMC pediatrics, 2022-01, Vol.22 (1), p.65-65, Article 65

2022

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Treatment of childhood intraneural perineurioma: A case report and literature review

Heliyon, 2024-03, Vol.10 (5), p.e26089, Article e26089

2024

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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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Pediatric Autoimmune Encephalitis: Case Series From Two Chinese Tertiary Pediatric Neurology Centers

Frontiers in neurology, 2019-08, Vol.10, p.906-906

2019

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Natural history and genetic study of LAMA2-related muscular dystrophy in a large Chinese cohort

Orphanet journal of rare diseases, 2021-07, Vol.16 (1), p.1-319, Article 319

2021

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Correlation of Phenotype-Genotype and Protein Structure in RYR1 -Related Myopathy

Frontiers in neurology, 2022-05, Vol.13, p.870285-870285

2022

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A splice site mutation c.1251G>A of ISPD gene is a common cause of congenital muscular dystrophy in Chinese patients

Clinical genetics, 2020-05, Vol.97 (5), p.789-790

2020

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Efficacy of vigabatrin in the treatment of infantile epileptic spasms syndrome: A systematic review and meta‐analysis

Epilepsia open, 2023-06, Vol.8 (2), p.268-277

2023

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Unique genotype-phenotype correlations within LAMA2 -related limb girdle muscular dystrophy in Chinese patients

Frontiers in neurology, 2023-05, Vol.14, p.1158094-1158094

2023

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Novel SEPN1 Mutations in Exon 1 Are Common in Rigid Spine With Muscular Dystrophy Type 1 in Chinese Patients

Frontiers in genetics, 2022-03, Vol.13, p.825793-825793

2022

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Congenital muscular dystrophies in China

Clinical genetics, 2019-09, Vol.96 (3), p.207-215

2019

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Centronuclear myopathy due to a de novo nonsense variant and a maternally inherited splice‐site variant in TTN: A case report

Clinical case reports, 2021-07, Vol.9 (7), p.e04478-n/a

2021

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Link prediction in multilayer social networks using reliable local random walk and boosting ensemble classifier

Chaos, solitons and fractals, 2024-11, Vol.188, p.115530, Article 115530

2024

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Clinical and electrophysiological characteristics of startle epilepsy in childhood

Clinical neurophysiology, 2010-05, Vol.121 (5), p.658-664

2010

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Saliva microbiota carry caries-specific functional gene signatures

PloS one, 2014-02, Vol.9 (2), p.e76458

2014

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Nannochloropsis genomes reveal evolution of microalgal oleaginous traits

Saliva microbiomes distinguish caries-active from healthy human populations

Modeling and analysis of distribution network with photovoltaic cells based on Markov global sensitivity

A novel binary genetic differential evolution optimization algorithm for wind layout problems

Design of high-precision displacement safety monitoring and three-dimensional spatial alarm system for Beidou based on intelligent algorithms

Design of a 3D space early warning system for high precision positioning technology of Beidou and analysis of differential positioning accuracy

Design and implementation of a monitoring platform based on beidou high precision positioning technology

Clinical and genetic analysis of a case with centronuclear myopathy caused by SPEG gene mutation: a case report and literature review

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

Genetic variations and clinical spectrum of dystroglycanopathy in a large cohort of Chinese patients

Clinical and genetic features of infancy-onset congenital myopathies from a Chinese paediatric centre

Treatment of childhood intraneural perineurioma: A case report and literature review

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

Pediatric Autoimmune Encephalitis: Case Series From Two Chinese Tertiary Pediatric Neurology Centers

Natural history and genetic study of LAMA2-related muscular dystrophy in a large Chinese cohort

Correlation of Phenotype-Genotype and Protein Structure in RYR1 -Related Myopathy

A splice site mutation c.1251G>A of ISPD gene is a common cause of congenital muscular dystrophy in Chinese patients

Efficacy of vigabatrin in the treatment of infantile epileptic spasms syndrome: A systematic review and meta‐analysis

Unique genotype-phenotype correlations within LAMA2 -related limb girdle muscular dystrophy in Chinese patients

Novel SEPN1 Mutations in Exon 1 Are Common in Rigid Spine With Muscular Dystrophy Type 1 in Chinese Patients

Congenital muscular dystrophies in China

Centronuclear myopathy due to a de novo nonsense variant and a maternally inherited splice‐site variant in TTN: A case report

Link prediction in multilayer social networks using reliable local random walk and boosting ensemble classifier

Clinical and electrophysiological characteristics of startle epilepsy in childhood

Saliva microbiota carry caries-specific functional gene signatures

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