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Targeted DNA Sequencing from Autism Spectrum Disorder Brains Implicates Multiple Genetic Mechanisms

Neuron (Cambridge, Mass.), 2015-12, Vol.88 (5), p.910-917

2015

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Somatic Mutations in Cerebral Cortical Malformations

The New England journal of medicine, 2014-08, Vol.371 (8), p.733-743

2014

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Capitalizing on the heterogeneous effects of CFTR nonsense and frameshift variants to inform therapeutic strategy for cystic fibrosis

PLoS genetics, 2018-11, Vol.14 (11), p.e1007723-e1007723

2018

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Mutations in QARS, Encoding Glutaminyl-tRNA Synthetase, Cause Progressive Microcephaly, Cerebral-Cerebellar Atrophy, and Intractable Seizures

American journal of human genetics, 2014-04, Vol.94 (4), p.547-558

2014

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CRISPR Del/Rei: a simple, flexible, and efficient pipeline for scarless genome editing

Scientific reports, 2022-07, Vol.12 (1), p.11928-4, Article 11928

2022

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Biallelic mutations in human DCC cause developmental split-brain syndrome

Nature genetics, 2017-04, Vol.49 (4), p.606-612

2017

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Transcriptome analysis of human induced excitatory neurons supports a strong effect of clozapine on cholesterol biosynthesis

Schizophrenia research, 2021-02, Vol.228, p.324-326

2021

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Transcriptomic data of Clozapine-treated Ngn2-induced Human Excitatory Neurons

Data in brief, 2021-04, Vol.35, p.106897-106897, Article 106897

2021

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Prevalence and Determinants of Medication Adherence among Patients with HIV/AIDS in Southern Vietnam

Infectious disease reports, 2021-02, Vol.13 (1), p.126-135

2021

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Knowledge of Antiretroviral Treatment and Associated Factors in HIV-Infected Patients

Healthcare (Basel), 2021-04, Vol.9 (4), p.483

2021

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Increased expression of anion transporter SLC26A9 delays diabetes onset in cystic fibrosis

The Journal of clinical investigation, 2020-01, Vol.130 (1), p.272-286

2020

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Systematic Computational Identification of Variants That Activate Exonic and Intronic Cryptic Splice Sites

American journal of human genetics, 2017-05, Vol.100 (5), p.751-765

2017

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Drug-Related Problems in Prescribing for Pediatric Outpatients in Vietnam

Healthcare (Basel), 2021-03, Vol.9 (3), p.327

2021

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Deletions in GRID2 lead to a recessive syndrome of cerebellar ataxia and tonic upgaze in humans

Neurology, 2013-10, Vol.81 (16), p.1378

2013

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Homozygous deletions implicate non-coding epigenetic marks in Autism spectrum disorder

Scientific reports, 2020-08, Vol.10 (1), p.14045, Article 14045

2020

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SLC26A9 SNP rs7512462 is not associated with lung disease severity or lung function response to ivacaftor in cystic fibrosis patients with G551D-CFTR

Journal of cystic fibrosis, 2021-09, Vol.20 (5), p.851-856

2021

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Mutations in mitochondrial enzyme GPT2 cause metabolic dysfunction and neurological disease with developmental and progressive features

Proceedings of the National Academy of Sciences - PNAS, 2016-09, Vol.113 (38), p.E5598-E5607

2016

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Hand, foot and mouth disease in southern Vietnam during 2015–2018

International journal of infectious diseases, 2020-12, Vol.101, p.258-258

2020

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Coxsackievirus A16 in Viet Nam

International journal of infectious diseases, 2020-12, Vol.101, p.228-228

2020

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Pleiotropic modifiers of age-related diabetes and neonatal intestinal obstruction in cystic fibrosis

American journal of human genetics, 2022-10, Vol.109 (10), p.1894-1908

2022

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SLC26A9 SNP RS7512462 IS NOT ASSOCIATED WITH LUNG DISEASE SEVERITY OR LUNG FUNCTION RESPONSE TO IVACAFTOR IN CYSTIC FIBROSIS PATIENTS WITH G551D-CFTR

Journal of cystic fibrosis, 2021-03, Vol.20 (5), p.851-856

2021

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Non-enzymatic electrochemical sensor based on ZnO nanoparticles/porous graphene for the detection of hypoxanthine in pork meat

AIP advances, 2024-02, Vol.14 (2), p.025034-025034-11

2024

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A Trial of Itraconazole or Amphotericin B for HIV-Associated Talaromycosis

The New England journal of medicine, 2017-06, Vol.376 (24), p.2329-2340

2017

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VinDr-CXR: An open dataset of chest X-rays with radiologist’s annotations

Scientific data, 2022-07, Vol.9 (1), p.429-429, Article 429

2022

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Targeted DNA Sequencing from Autism Spectrum Disorder Brains Implicates Multiple Genetic Mechanisms

Somatic Mutations in Cerebral Cortical Malformations

Capitalizing on the heterogeneous effects of CFTR nonsense and frameshift variants to inform therapeutic strategy for cystic fibrosis

Mutations in QARS, Encoding Glutaminyl-tRNA Synthetase, Cause Progressive Microcephaly, Cerebral-Cerebellar Atrophy, and Intractable Seizures

CRISPR Del/Rei: a simple, flexible, and efficient pipeline for scarless genome editing

Biallelic mutations in human DCC cause developmental split-brain syndrome

Integrated genome and transcriptome sequencing identifies a noncoding mutation in the genome replication factor DONSON as the cause of microcephaly-micromelia syndrome

Transcriptome analysis of human induced excitatory neurons supports a strong effect of clozapine on cholesterol biosynthesis

Transcriptomic data of Clozapine-treated Ngn2-induced Human Excitatory Neurons

Prevalence and Determinants of Medication Adherence among Patients with HIV/AIDS in Southern Vietnam

Knowledge of Antiretroviral Treatment and Associated Factors in HIV-Infected Patients

Increased expression of anion transporter SLC26A9 delays diabetes onset in cystic fibrosis

Systematic Computational Identification of Variants That Activate Exonic and Intronic Cryptic Splice Sites

Drug-Related Problems in Prescribing for Pediatric Outpatients in Vietnam

Deletions in GRID2 lead to a recessive syndrome of cerebellar ataxia and tonic upgaze in humans

Homozygous deletions implicate non-coding epigenetic marks in Autism spectrum disorder

SLC26A9 SNP rs7512462 is not associated with lung disease severity or lung function response to ivacaftor in cystic fibrosis patients with G551D-CFTR

Mutations in mitochondrial enzyme GPT2 cause metabolic dysfunction and neurological disease with developmental and progressive features

Hand, foot and mouth disease in southern Vietnam during 2015–2018

Coxsackievirus A16 in Viet Nam

Pleiotropic modifiers of age-related diabetes and neonatal intestinal obstruction in cystic fibrosis

SLC26A9 SNP RS7512462 IS NOT ASSOCIATED WITH LUNG DISEASE SEVERITY OR LUNG FUNCTION RESPONSE TO IVACAFTOR IN CYSTIC FIBROSIS PATIENTS WITH G551D-CFTR

Non-enzymatic electrochemical sensor based on ZnO nanoparticles/porous graphene for the detection of hypoxanthine in pork meat

A Trial of Itraconazole or Amphotericin B for HIV-Associated Talaromycosis

VinDr-CXR: An open dataset of chest X-rays with radiologist’s annotations

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