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Inflexible neurobiological signatures precede atypical development in infants at high risk for autism

Scientific reports, 2017-09, Vol.7 (1), p.11285-17, Article 11285

2017

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Reduced structural complexity of the right cerebellar cortex in male children with autism spectrum disorder

PloS one, 2018-07, Vol.13 (7), p.e0196964-e0196964

2018

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Smart pathological brain detection by synthetic minority oversampling technique, extreme learning machine, and Jaya algorithm

Multimedia tools and applications, 2018-09, Vol.77 (17), p.22629-22648

2018

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A metabolomic profile of biological aging in 250,341 individuals from the UK Biobank

Nature communications, 2024-09, Vol.15 (1), p.8081-19, Article 8081

2024

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ATP10B variants in Parkinson’s disease: a large cohort study in Chinese mainland population

Acta neuropathologica, 2021-05, Vol.141 (5), p.805-806

2021

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A Delay-Aware and Reliable Data Aggregation for Cyber-Physical Sensing

Sensors (Basel, Switzerland), 2017-02, Vol.17 (2), p.395-395

2017

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Cross-Disorder Analysis of De Novo Mutations in Neuropsychiatric Disorders

Journal of autism and developmental disorders, 2022-03, Vol.52 (3), p.1299-1313

2022

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Revealing a novel contributing landscape of ferroptosis-related genes in Parkinson’s disease

Computational and structural biotechnology journal, 2022, Vol.20, p.5218-5225

2022

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Functional neural circuits that underlie developmental stuttering

PloS one, 2017-07, Vol.12 (7), p.e0179255-e0179255

2017

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Reward-Based Spatial Learning in Teens With Bulimia Nervosa

Journal of the American Academy of Child and Adolescent Psychiatry, 2016-11, Vol.55 (11), p.962-971.e3

2016

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A comprehensive analysis of the health effects associated with smoking in the largest population using UK Biobank genotypic and phenotypic data

Heliyon, 2024-08, Vol.10 (16), p.e35649, Article e35649

2024

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De novo mutation of cancer-related genes associates with particular neurodevelopmental disorders

Journal of molecular medicine (Berlin, Germany), 2020-12, Vol.98 (12), p.1701-1712

2020

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Interactions of genetic risks for autism and the broad autism phenotypes

Frontiers in psychiatry, 2023-03, Vol.14, p.1110080-1110080

2023

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Fractal Dimension Analysis of Subcortical Gray Matter Structures in Schizophrenia

PloS one, 2016-05, Vol.11 (5), p.e0155415-e0155415

2016

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Gene4PD: A Comprehensive Genetic Database of Parkinson's Disease

Frontiers in neuroscience, 2021-04, Vol.15, p.679568-679568

2021

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Performance Comparison of Computational Methods for the Prediction of the Function and Pathogenicity of Non-coding Variants

Genomics, proteomics & bioinformatics, 2023-06, Vol.21 (3), p.649-661

2023

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Characterizing the Expression Patterns of Parkinson's Disease Associated Genes

Frontiers in neuroscience, 2021-04, Vol.15, p.629156-629156

2021

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The Association Between Lysosomal Storage Disorder Genes and Parkinson’s Disease: A Large Cohort Study in Chinese Mainland Population

Frontiers in aging neuroscience, 2021-11, Vol.13

2021

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Profiling the Genome-Wide Landscape of Short Tandem Repeats by Long-Read Sequencing

Frontiers in genetics, 2022-05, Vol.13, p.810595-810595

2022

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Risk factors associated with age at onset of Parkinson’s disease in the UK Biobank

NPJ Parkinson's Disease, 2024-01, Vol.10 (1), p.3-3, Article 3

2024

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Gene4MND: An Integrative Genetic Database and Analytic Platform for Motor Neuron Disease

Frontiers in molecular neuroscience, 2021-04, Vol.14, p.644202-644202

2021

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Gene4HL: An Integrated Genetic Database for Hearing Loss

Frontiers in genetics, 2021-10, Vol.12, p.773009-773009

2021

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Cross-Disorder Analysis of De Novo Variants Increases the Power of Prioritising Candidate Genes

Life (Basel, Switzerland), 2021-03, Vol.11 (3), p.233

2021

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Two Pathogenic Gene Mutations Identified Associating with Congenital Cataract and Iris Coloboma Respectively in a Chinese Family

Journal of ophthalmology, 2020, Vol.2020 (2020), p.1-9

2020

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GRDR: A Novel Data Gathering and Dissemination Scheme for WSNs

Wangji Wanglu Jishu Xuekan = Journal of Internet Technology, 2018-01, Vol.19 (2), p.425-438

2018

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Inflexible neurobiological signatures precede atypical development in infants at high risk for autism

Reduced structural complexity of the right cerebellar cortex in male children with autism spectrum disorder

Smart pathological brain detection by synthetic minority oversampling technique, extreme learning machine, and Jaya algorithm

A metabolomic profile of biological aging in 250,341 individuals from the UK Biobank

ATP10B variants in Parkinson’s disease: a large cohort study in Chinese mainland population

A Delay-Aware and Reliable Data Aggregation for Cyber-Physical Sensing

Cross-Disorder Analysis of De Novo Mutations in Neuropsychiatric Disorders

Revealing a novel contributing landscape of ferroptosis-related genes in Parkinson’s disease

Functional neural circuits that underlie developmental stuttering

Reward-Based Spatial Learning in Teens With Bulimia Nervosa

A comprehensive analysis of the health effects associated with smoking in the largest population using UK Biobank genotypic and phenotypic data

De novo mutation of cancer-related genes associates with particular neurodevelopmental disorders

Interactions of genetic risks for autism and the broad autism phenotypes

Fractal Dimension Analysis of Subcortical Gray Matter Structures in Schizophrenia

Gene4PD: A Comprehensive Genetic Database of Parkinson's Disease

Performance Comparison of Computational Methods for the Prediction of the Function and Pathogenicity of Non-coding Variants

Characterizing the Expression Patterns of Parkinson's Disease Associated Genes

The Association Between Lysosomal Storage Disorder Genes and Parkinson’s Disease: A Large Cohort Study in Chinese Mainland Population

Profiling the Genome-Wide Landscape of Short Tandem Repeats by Long-Read Sequencing

Risk factors associated with age at onset of Parkinson’s disease in the UK Biobank

Gene4MND: An Integrative Genetic Database and Analytic Platform for Motor Neuron Disease

Gene4HL: An Integrated Genetic Database for Hearing Loss

Cross-Disorder Analysis of De Novo Variants Increases the Power of Prioritising Candidate Genes

Two Pathogenic Gene Mutations Identified Associating with Congenital Cataract and Iris Coloboma Respectively in a Chinese Family

GRDR: A Novel Data Gathering and Dissemination Scheme for WSNs

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