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Inferring the molecular and phenotypic impact of amino acid variants with MutPred2

Nature communications, 2020-11, Vol.11 (1), p.5918-13, Article 5918

2020

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Spatiotemporal 16p11.2 Protein Network Implicates Cortical Late Mid-Fetal Brain Development and KCTD13-Cul3-RhoA Pathway in Psychiatric Diseases

Neuron (Cambridge, Mass.), 2015-02, Vol.85 (4), p.742-754

2015

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Haplotype function score improves biological interpretation and cross-ancestry polygenic prediction of human complex traits

eLife, 2024-04, Vol.12

2024

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Spatiotemporal 7q11.23 protein network analysis implicates the role of DNA repair pathway during human brain development

Scientific reports, 2021-04, Vol.11 (1), p.8246-8246, Article 8246

2021

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Reduced motor cortex GABABR function following chronic alcohol exposure

Molecular psychiatry, 2021-02, Vol.26 (2), p.383-395

2021

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Peripheral transcriptome of clinical high‐risk psychosis reflects symptom alteration and helps prognosis prediction

Psychiatry and clinical neurosciences, 2022-06, Vol.76 (6), p.268-270

2022

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Comparisons among two fertile and three male-sterile mitochondrial genomes of maize

Genetics (Austin), 2007-10, Vol.177 (2), p.1173-1192

2007

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Spatiotemporal 22q11.21 Protein Network Implicates DGCR8-Dependent MicroRNA Biogenesis as a Risk for Late Fetal Cortical Development in Psychiatric Diseases

Life (Basel, Switzerland), 2021-05, Vol.11 (6), p.514

2021

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A comparison framework and guideline of clustering methods for mass cytometry data

Genome Biology, 2019-12, Vol.20 (1), p.297-297, Article 297

2019

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De novo Mutations From Whole Exome Sequencing in Neurodevelopmental and Psychiatric Disorders: From Discovery to Application

Frontiers in genetics, 2019-04, Vol.10, p.258

2019

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Emden: A novel method integrating graph and transformer representations for predicting the effect of mutations on clinical drug response

Computers in biology and medicine, 2023-12, Vol.167, p.107678-107678, Article 107678

2023

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Single‐cell RNA sequencing reveals the epithelial cell heterogeneity and invasive subpopulation in human bladder cancer

International journal of cancer, 2021-12, Vol.149 (12), p.2099-2115

2021

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Mendelian randomization studies of brain MRI yield insights into the pathogenesis of neuropsychiatric disorders

BMC genomics, 2021-06, Vol.22 (Suppl 3), p.1-342, Article 342

2021

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Psychological factors as the risk factor of mouth ulcers: A two-sample Mendelian randomization study

Journal of health psychology, 2022-06, Vol.27 (7), p.1556-1568

2022

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An Integrative Analysis of Identified Schizophrenia-Associated Brain Cell Types and Gene Expression Changes

International journal of molecular sciences, 2022-10, Vol.23 (19), p.11581

2022

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When loss-of-function is loss of function: assessing mutational signatures and impact of loss-of-function genetic variants

Bioinformatics (Oxford, England), 2017-07, Vol.33 (14), p.i389-i398

2017

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Interaction between PGRN gene and the early trauma on clinical characteristics in patients with obsessive-compulsive disorder

Journal of affective disorders, 2020-02, Vol.263, p.134-140

2020

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Label propagation-based semi-supervised feature selection on decoding clinical phenotypes with RNA-seq data

BMC medical genomics, 2021-08, Vol.14 (Suppl 1), p.141-141, Article 141

2021

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Mendelian Randomization and GWAS Meta Analysis Revealed the Risk-Increasing Effect of Schizophrenia on Cancers

Biology (Basel, Switzerland), 2022-09, Vol.11 (9), p.1345

2022

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A Generative Adversarial Network Model for Disease Gene Prediction With RNA-seq Data

IEEE access, 2020, Vol.8, p.37352-37360

2020

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Protein interaction network of alternatively spliced isoforms from brain links genetic risk factors for autism

Nature communications, 2014-04, Vol.5 (1), p.3650-3650, Article 3650

2014

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Single-cell spatial transcriptomic analysis reveals common and divergent features of developing postnatal granule cerebellar cells and medulloblastoma

BMC biology, 2021-07, Vol.19 (1), p.135-135, Article 135

2021

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Testosterone in Female Depression: A Meta-Analysis and Mendelian Randomization Study

Biomolecules (Basel, Switzerland), 2021-03, Vol.11 (3), p.409

2021

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Dissection of the Genetic Association between Anorexia Nervosa and Obsessive-Compulsive Disorder at the Network and Cellular Levels

Genes, 2021-03, Vol.12 (4), p.491

2021

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Inferring the molecular and phenotypic impact of amino acid variants with MutPred2

Spatiotemporal 16p11.2 Protein Network Implicates Cortical Late Mid-Fetal Brain Development and KCTD13-Cul3-RhoA Pathway in Psychiatric Diseases

Whole-Genome Sequencing in Autism Identifies Hot Spots for De Novo Germline Mutation

Haplotype function score improves biological interpretation and cross-ancestry polygenic prediction of human complex traits

Spatiotemporal 7q11.23 protein network analysis implicates the role of DNA repair pathway during human brain development

Reduced motor cortex GABABR function following chronic alcohol exposure

Peripheral transcriptome of clinical high‐risk psychosis reflects symptom alteration and helps prognosis prediction

Comparisons among two fertile and three male-sterile mitochondrial genomes of maize

Spatiotemporal 22q11.21 Protein Network Implicates DGCR8-Dependent MicroRNA Biogenesis as a Risk for Late Fetal Cortical Development in Psychiatric Diseases

A comparison framework and guideline of clustering methods for mass cytometry data

De novo Mutations From Whole Exome Sequencing in Neurodevelopmental and Psychiatric Disorders: From Discovery to Application

Emden: A novel method integrating graph and transformer representations for predicting the effect of mutations on clinical drug response

Single‐cell RNA sequencing reveals the epithelial cell heterogeneity and invasive subpopulation in human bladder cancer

Mendelian randomization studies of brain MRI yield insights into the pathogenesis of neuropsychiatric disorders

Psychological factors as the risk factor of mouth ulcers: A two-sample Mendelian randomization study

An Integrative Analysis of Identified Schizophrenia-Associated Brain Cell Types and Gene Expression Changes

When loss-of-function is loss of function: assessing mutational signatures and impact of loss-of-function genetic variants

Interaction between PGRN gene and the early trauma on clinical characteristics in patients with obsessive-compulsive disorder

Label propagation-based semi-supervised feature selection on decoding clinical phenotypes with RNA-seq data

Mendelian Randomization and GWAS Meta Analysis Revealed the Risk-Increasing Effect of Schizophrenia on Cancers

A Generative Adversarial Network Model for Disease Gene Prediction With RNA-seq Data

Protein interaction network of alternatively spliced isoforms from brain links genetic risk factors for autism

Single-cell spatial transcriptomic analysis reveals common and divergent features of developing postnatal granule cerebellar cells and medulloblastoma

Testosterone in Female Depression: A Meta-Analysis and Mendelian Randomization Study

Dissection of the Genetic Association between Anorexia Nervosa and Obsessive-Compulsive Disorder at the Network and Cellular Levels

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