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Author Details
Full Name
Hongsheng Gui
Affiliation
Behavioral Health Services
ORCID
Career Start Year
2007
Papers
58
H Index
16
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36907458
Self-rated health as a predictor of hospitalizations in patients with bipolar disorder or major depressive disorder: A prospective cohort study of the UK Biobank.
J Affect Disord
2023
37594966
Examining sociodemographic correlates of opioid use, misuse, and use disorders in the All of Us Research Program.
PLoS One
2023
37557965
The interactions between host genome and gut microbiome increase the risk of psychiatric disorders: Mendelian randomization and biological annotation.
Brain Behav Immun
2023
37516210
Shifting as an executive function separate from updating and inhibition in old age: Behavioral and genetic evidence.
Behav Brain Res
2023
37649700
<i>MAP3K19</i> regulatory variation in populations with African ancestry may increase COVID-19 severity.
iScience
2023
37191882
Evaluation of a New Aptamer-Based Array for Soluble Suppressor of Tumorgenicity (ST2) and N-terminal Pro-B-Type Natriuretic Peptide (NTproBNP) in Heart Failure Patients.
J Cardiovasc Transl Res
2023
37340172
Cross-phenotype relationship between opioid use disorder and suicide attempts: new evidence from polygenic association and Mendelian randomization analyses.
Mol Psychiatry
2023
37069653
GBC: a parallel toolkit based on highly addressable byte-encoding blocks for extremely large-scale genotypes of species.
Genome Biol
2023
37126548
The genetic determinants of recurrent somatic mutations in 43,693 blood genomes.
Sci Adv
2023
34193973
Integrative omics of schizophrenia: from genetic determinants to clinical classification and risk prediction.
Mol Psychiatry
2022
35831289
Detecting and distinguishing indicators of risk for suicide using clinical records.
Transl Psychiatry
2022
35912095
Patterns of Convergence and Divergence Between Bipolar Disorder Type I and Type II: Evidence From Integrative Genomic Analyses.
Front Cell Dev Biol
2022
36353114
Genome-wide screening of sex-biased genetic variants potentially associated with COVID-19 hospitalization.
Front Genet
2022
35224615
DLRAPom: a hybrid pipeline of Optimized XGBoost-guided integrative multiomics analysis for identifying targetable disease-related lncRNA-miRNA-mRNA regulatory axes.
Brief Bioinform
2022
34425222
Survival Association of Angiotensin Inhibitors in Heart Failure With Reduced Ejection Fraction: Comparisons Using Self-Identified Race and Genomic Ancestry.
J Card Fail
2022
32966749
Mapping the 17q12-21.1 Locus for Variants Associated with Early-Onset Asthma in African Americans.
Am J Respir Crit Care Med
2021
34480422
The genomics of heart failure: design and rationale of the HERMES consortium.
ESC Heart Fail
2021
34475833
Editorial: Genetic Mechanisms of Biomarkers in Schizophrenia, Bipolar Disorder and Depression.
Front Psychiatry
2021
33999650
Plasma Proteomic Profile Predicts Survival in Heart Failure With Reduced Ejection Fraction.
Circ Genom Precis Med
2021
32327564
Lung Function in African American Children with Asthma Is Associated with Novel Regulatory Variants of the KIT Ligand <i>KITLG/SCF</i> and Gene-By-Air-Pollution Interaction.
Genetics
2020
32926842
Suppression tumorigenicity 2 (ST2) turbidimetric immunoassay compared to enzyme-linked immunosorbent assay in predicting survival in heart failure patients with reduced ejection fraction.
Clin Chim Acta
2020
30367910
Integrative approach identifies corticosteroid response variant in diverse populations with asthma.
J Allergy Clin Immunol
2019
31728800
Association of Regulatory Genetic Variants for Protein Kinase Cα with Mortality and Drug Efficacy in Patients with Heart Failure.
Cardiovasc Drugs Ther
2019
31266369
Performance of the Meta-Analysis Global Group in Chronic Heart Failure Score in Black Patients Compared With Whites.
Circ Cardiovasc Qual Outcomes
2019
31113495
Genetics of heart rate in heart failure patients (GenHRate).
Hum Genomics
2019
29150900
Genetic overlap between epilepsy and schizophrenia: Evidence from cross phenotype analysis in Hong Kong Chinese population.
Am J Med Genet B Neuropsychiatr Genet
2018
29967385
Prenatal immune activation alters the adult neural epigenome but can be partly stabilised by a n-3 polyunsaturated fatty acid diet.
Transl Psychiatry
2018
29904720
Rare variants and de novo variants in mesial temporal lobe epilepsy with hippocampal sclerosis.
Neurol Genet
2018
30013184
Genome-wide association and HLA fine-mapping studies identify risk loci and genetic pathways underlying allergic rhinitis.
Nat Genet
2018
30116036
Author Correction: Genome-wide association and HLA fine-mapping studies identify risk loci and genetic pathways underlying allergic rhinitis.
Nat Genet
2018
30061609
Multiethnic meta-analysis identifies ancestry-specific and cross-ancestry loci for pulmonary function.
Nat Commun
2018
30896106
Analysis of Genetic Polymorphism and Genetic Distance of 19 Autosomal STR Loci in Jiangsu Han Population.
Fa Yi Xue Za Zhi
2018
28398356
SNP-based HLA allele tagging, imputation and association with antiepileptic drug-induced cutaneous reactions in Hong Kong Han Chinese.
Pharmacogenomics J
2018
29739794
Race and Beta-Blocker Survival Benefit in Patients With Heart Failure: An Investigation of Self-Reported Race and Proportion of African Genetic Ancestry.
J Am Heart Assoc
2018
29288229
Genetic variation in CFH predicts phenytoin-induced maculopapular exanthema in European-descent patients.
Neurology
2018
28342760
Correction of Hirschsprung-Associated Mutations in Human Induced Pluripotent Stem Cells Via Clustered Regularly Interspaced Short Palindromic Repeats/Cas9, Restores Neural Crest Cell Function.
Gastroenterology
2017
28274275
Whole exome sequencing coupled with unbiased functional analysis reveals new Hirschsprung disease genes.
Genome Biol
2017
28495956
Sharing of Genes and Pathways Across Complex Phenotypes: A Multilevel Genome-Wide Analysis.
Genetics
2017
25876511
Association of BDNF Polymorphisms with the Risk of Epilepsy: a Multicenter Study.
Mol Neurobiol
2016
27702942
Trans-ethnic meta-analysis of genome-wide association studies for Hirschsprung disease.
Hum Mol Genet
2016
25717236
Depletion of the IKBKAP ortholog in zebrafish leads to hirschsprung disease-like phenotype.
World J Gastroenterol
2015
26559152
Exome sequencing reveals a high genetic heterogeneity on familial Hirschsprung disease.
Sci Rep
2015
26261006
Identification of GLI Mutations in Patients With Hirschsprung Disease That Disrupt Enteric Nervous System Development in Mice.
Gastroenterology
2015
24413707
A three-stage genome-wide association study combining multilocus test and gene expression analysis for young-onset hypertension in Taiwan Han Chinese.
Am J Hypertens
2014
24828511
The contribution of genetic diversity to subdivide populations living in the silk road of China.
PLoS One
2014
24863667
Influence of Alzheimer's disease genes on cognitive decline: the Guangzhou Biobank Cohort Study.
Neurobiol Aging
2014
24947032
Targeted next-generation sequencing on Hirschsprung disease: a pilot study exploits DNA pooling.
Ann Hum Genet
2014
22384028
A genome-wide linkage and association scan reveals novel loci for hypertension and blood pressure traits.
PLoS One
2012
23084198
Screening of the RET gene of Vietnamese Hirschsprung patients identifies 2 novel missense mutations.
J Pediatr Surg
2012
22241780
A comprehensive framework for prioritizing variants in exome sequencing studies of Mendelian diseases.
Nucleic Acids Res
2012
1 - 50 of 58
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