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High N-glycan multiplicity is critical for neuronal adhesion and sensitizes the developing cerebellum to N-glycosylation defect

eLife, 2018-10, Vol.7

2018

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ZC4H2 Mutations Are Associated with Arthrogryposis Multiplex Congenita and Intellectual Disability through Impairment of Central and Peripheral Synaptic Plasticity

American journal of human genetics, 2013-05, Vol.92 (5), p.681-695

2013

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Whole-exome sequence analysis highlights the role of unmasked recessive mutations in copy number variants with incomplete penetrance

European journal of human genetics : EJHG, 2018-06, Vol.26 (6), p.912-918

2018

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Nonsense-mediated mRNA decay: inter-individual variability and human disease

Neuroscience and biobehavioral reviews, 2014-10, Vol.46 Pt 2, p.175-186

2014

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The emerging roles of MicroRNAs in autism spectrum disorders

Neuroscience and biobehavioral reviews, 2016-12, Vol.71, p.729-738

2016

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Mutations in USP9X Are Associated with X-Linked Intellectual Disability and Disrupt Neuronal Cell Migration and Growth

American journal of human genetics, 2014-03, Vol.94 (3), p.470-478

2014

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Loss of the neurodevelopmental disease-associated gene miR-146a impairs neural progenitor differentiation and causes learning and memory deficits

Molecular autism, 2020-03, Vol.11 (1), p.22-22, Article 22

2020

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Role of miR-146a in neural stem cell differentiation and neural lineage determination: relevance for neurodevelopmental disorders

Molecular autism, 2018-06, Vol.9 (1), p.38-38, Article 38

2018

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Rare copy number variation in cerebral palsy

European journal of human genetics : EJHG, 2014-01, Vol.22 (1), p.40-45

2014

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Profiling olfactory stem cells from living patients identifies miRNAs relevant for autism pathophysiology

Molecular autism, 2016-01, Vol.7 (1), p.1-1, Article 1

2016

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Study on the reducibility of iron ore pellets at high temperature

Vietnam Journal of Science, Technology and Engineering, 2022-03, Vol.63 (4), p.3-7

2022

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Distal duplication of chromosome 16q22.1q23.1 in a Vietnamese patient with midface hypoplasia and intellectual disability

American journal of medical genetics. Part A, 2018-09, Vol.176 (9), p.1981-1984

2018

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Broadening the phenotype associated with mutations in UPF3B: Two further cases with renal dysplasia and variable developmental delay

European journal of medical genetics, 2012-08, Vol.55 (8), p.476-479

2012

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Simian virus 40 may be associated with developing malignant pleural mesothelioma

Oncology letters, 2016-03, Vol.11 (3), p.2051-2056

2016

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Rôle de miR-146a dans la différenciation et l’acquisition de l’identité neurale des cellules souches humaines : pertinence pour les troubles du spectre autistique

Morphologie, 2017-12, Vol.101 (335), p.242-242

2017

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A Novel Radio-Aware and Adaptive Numerology Configuration in V2X 5G NR Communications

ICC 2023 - IEEE International Conference on Communications, 2023, p.1652-1657

2023

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Machine learning based classification model for screening of infected patients using vital signs

Informatics in medicine unlocked, 2021, Vol.24, p.100592, Article 100592

2021

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A Flexible Numerology Configuration for Efficient Resource Allocation in 3GPP V2X 5G New Radio

GLOBECOM 2022 - 2022 IEEE Global Communications Conference, 2022, p.4449-4454

2022

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AHB-master controller formal compliance verification

2014 IEEE Fifth International Conference on Communications and Electronics (ICCE), 2014, p.340-345

2014

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Impact of network delays on Hyperledger Fabric

IEEE INFOCOM 2019 - IEEE Conference on Computer Communications Workshops (INFOCOM WKSHPS), 2019, p.222-227

2019

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WCN24-588 LIMITED AWARENESS OF PREDIALYSIS STAGE AND KIDNEY REPLACEMENT THERAPY AMONG CHRONIC KIDNEY DISEASE G45 AND DIALYSIS PATIENTS: A SURVEY AT CHO RAY HOSPITAL, VIETNAM

Kidney international reports, 2024-04, Vol.9 (4), p.S580-S580

2024

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A nonsense variant in HERC1 is associated with intellectual disability, megalencephaly, thick corpus callosum and cerebellar atrophy

European journal of human genetics : EJHG, 2016-03, Vol.24 (3), p.455-458

2016

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Quality Management Models of Project Management in the Construction Sector

Webology, 2021-10, Vol.18 (SI05), p.844-856

2021

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DeTrAP: A Novel AI/ML V2X 5G NR Adaptive Physical Layer Configuration

GLOBECOM 2023 - 2023 IEEE Global Communications Conference, 2023, p.1938-1943

2023

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Ultra-deep massively parallel sequencing with unique molecular identifier tagging achieves comparable performance to droplet digital PCR for detection and quantification of circulating tumor DNA from lung cancer patients

High N-glycan multiplicity is critical for neuronal adhesion and sensitizes the developing cerebellum to N-glycosylation defect

ZC4H2 Mutations Are Associated with Arthrogryposis Multiplex Congenita and Intellectual Disability through Impairment of Central and Peripheral Synaptic Plasticity

Whole-exome sequence analysis highlights the role of unmasked recessive mutations in copy number variants with incomplete penetrance

Nonsense-mediated mRNA decay: inter-individual variability and human disease

The emerging roles of MicroRNAs in autism spectrum disorders

Mutations in USP9X Are Associated with X-Linked Intellectual Disability and Disrupt Neuronal Cell Migration and Growth

Loss of the neurodevelopmental disease-associated gene miR-146a impairs neural progenitor differentiation and causes learning and memory deficits

Role of miR-146a in neural stem cell differentiation and neural lineage determination: relevance for neurodevelopmental disorders

Rare copy number variation in cerebral palsy

Profiling olfactory stem cells from living patients identifies miRNAs relevant for autism pathophysiology

Study on the reducibility of iron ore pellets at high temperature

Distal duplication of chromosome 16q22.1q23.1 in a Vietnamese patient with midface hypoplasia and intellectual disability

Broadening the phenotype associated with mutations in UPF3B: Two further cases with renal dysplasia and variable developmental delay

Simian virus 40 may be associated with developing malignant pleural mesothelioma

Rôle de miR-146a dans la différenciation et l’acquisition de l’identité neurale des cellules souches humaines : pertinence pour les troubles du spectre autistique

A Novel Radio-Aware and Adaptive Numerology Configuration in V2X 5G NR Communications

Machine learning based classification model for screening of infected patients using vital signs

A Flexible Numerology Configuration for Efficient Resource Allocation in 3GPP V2X 5G New Radio

AHB-master controller formal compliance verification

Impact of network delays on Hyperledger Fabric

WCN24-588 LIMITED AWARENESS OF PREDIALYSIS STAGE AND KIDNEY REPLACEMENT THERAPY AMONG CHRONIC KIDNEY DISEASE G45 AND DIALYSIS PATIENTS: A SURVEY AT CHO RAY HOSPITAL, VIETNAM

A nonsense variant in HERC1 is associated with intellectual disability, megalencephaly, thick corpus callosum and cerebellar atrophy

Quality Management Models of Project Management in the Construction Sector

DeTrAP: A Novel AI/ML V2X 5G NR Adaptive Physical Layer Configuration

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