Skip to Main Content

Author Details

Hongsheng Gui
Behavioral Health Services
2007
58
16
PMIDPaper TitleJournal TitlePublished Year
36907458Self-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 Disord2023
37594966Examining sociodemographic correlates of opioid use, misuse, and use disorders in the All of Us Research Program.PLoS One2023
37557965The interactions between host genome and gut microbiome increase the risk of psychiatric disorders: Mendelian randomization and biological annotation.Brain Behav Immun2023
37516210Shifting as an executive function separate from updating and inhibition in old age: Behavioral and genetic evidence.Behav Brain Res2023
37649700<i>MAP3K19</i> regulatory variation in populations with African ancestry may increase COVID-19 severity.iScience2023
37191882Evaluation 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 Res2023
37340172Cross-phenotype relationship between opioid use disorder and suicide attempts: new evidence from polygenic association and Mendelian randomization analyses.Mol Psychiatry2023
37069653GBC: a parallel toolkit based on highly addressable byte-encoding blocks for extremely large-scale genotypes of species.Genome Biol2023
37126548The genetic determinants of recurrent somatic mutations in 43,693 blood genomes.Sci Adv2023
34193973Integrative omics of schizophrenia: from genetic determinants to clinical classification and risk prediction.Mol Psychiatry2022
35831289Detecting and distinguishing indicators of risk for suicide using clinical records.Transl Psychiatry2022
35912095Patterns of Convergence and Divergence Between Bipolar Disorder Type I and Type II: Evidence From Integrative Genomic Analyses.Front Cell Dev Biol2022
36353114Genome-wide screening of sex-biased genetic variants potentially associated with COVID-19 hospitalization.Front Genet2022
35224615DLRAPom: a hybrid pipeline of Optimized XGBoost-guided integrative multiomics analysis for identifying targetable disease-related lncRNA-miRNA-mRNA regulatory axes.Brief Bioinform2022
34425222Survival Association of Angiotensin Inhibitors in Heart Failure With Reduced Ejection Fraction: Comparisons Using Self-Identified Race and Genomic Ancestry.J Card Fail2022
32966749Mapping the 17q12-21.1 Locus for Variants Associated with Early-Onset Asthma in African Americans.Am J Respir Crit Care Med2021
34480422The genomics of heart failure: design and rationale of the HERMES consortium.ESC Heart Fail2021
34475833Editorial: Genetic Mechanisms of Biomarkers in Schizophrenia, Bipolar Disorder and Depression.Front Psychiatry2021
33999650Plasma Proteomic Profile Predicts Survival in Heart Failure With Reduced Ejection Fraction.Circ Genom Precis Med2021
32327564Lung 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.Genetics2020
32926842Suppression tumorigenicity 2 (ST2) turbidimetric immunoassay compared to enzyme-linked immunosorbent assay in predicting survival in heart failure patients with reduced ejection fraction.Clin Chim Acta2020
30367910Integrative approach identifies corticosteroid response variant in diverse populations with asthma.J Allergy Clin Immunol2019
31728800Association of Regulatory Genetic Variants for Protein Kinase Cα with Mortality and Drug Efficacy in Patients with Heart Failure.Cardiovasc Drugs Ther2019
31266369Performance of the Meta-Analysis Global Group in Chronic Heart Failure Score in Black Patients Compared With Whites.Circ Cardiovasc Qual Outcomes2019
31113495Genetics of heart rate in heart failure patients (GenHRate).Hum Genomics2019
29150900Genetic overlap between epilepsy and schizophrenia: Evidence from cross phenotype analysis in Hong Kong Chinese population.Am J Med Genet B Neuropsychiatr Genet2018
29967385Prenatal immune activation alters the adult neural epigenome but can be partly stabilised by a n-3 polyunsaturated fatty acid diet.Transl Psychiatry2018
29904720Rare variants and de novo variants in mesial temporal lobe epilepsy with hippocampal sclerosis.Neurol Genet2018
30013184Genome-wide association and HLA fine-mapping studies identify risk loci and genetic pathways underlying allergic rhinitis.Nat Genet2018
30116036Author Correction: Genome-wide association and HLA fine-mapping studies identify risk loci and genetic pathways underlying allergic rhinitis.Nat Genet2018
30061609Multiethnic meta-analysis identifies ancestry-specific and cross-ancestry loci for pulmonary function.Nat Commun2018
30896106Analysis of Genetic Polymorphism and Genetic Distance of 19 Autosomal STR Loci in Jiangsu Han Population.Fa Yi Xue Za Zhi2018
28398356SNP-based HLA allele tagging, imputation and association with antiepileptic drug-induced cutaneous reactions in Hong Kong Han Chinese.Pharmacogenomics J2018
29739794Race 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 Assoc2018
29288229Genetic variation in CFH predicts phenytoin-induced maculopapular exanthema in European-descent patients.Neurology2018
28342760Correction of Hirschsprung-Associated Mutations in Human Induced Pluripotent Stem Cells Via Clustered Regularly Interspaced Short Palindromic Repeats/Cas9, Restores Neural Crest Cell Function.Gastroenterology2017
28274275Whole exome sequencing coupled with unbiased functional analysis reveals new Hirschsprung disease genes.Genome Biol2017
28495956Sharing of Genes and Pathways Across Complex Phenotypes: A Multilevel Genome-Wide Analysis.Genetics2017
25876511Association of BDNF Polymorphisms with the Risk of Epilepsy: a Multicenter Study.Mol Neurobiol2016
27702942Trans-ethnic meta-analysis of genome-wide association studies for Hirschsprung disease.Hum Mol Genet2016
25717236Depletion of the IKBKAP ortholog in zebrafish leads to hirschsprung disease-like phenotype.World J Gastroenterol2015
26559152Exome sequencing reveals a high genetic heterogeneity on familial Hirschsprung disease.Sci Rep2015
26261006Identification of GLI Mutations in Patients With Hirschsprung Disease That Disrupt Enteric Nervous System Development in Mice.Gastroenterology2015
24413707A three-stage genome-wide association study combining multilocus test and gene expression analysis for young-onset hypertension in Taiwan Han Chinese.Am J Hypertens2014
24828511The contribution of genetic diversity to subdivide populations living in the silk road of China.PLoS One2014
24863667Influence of Alzheimer's disease genes on cognitive decline: the Guangzhou Biobank Cohort Study.Neurobiol Aging2014
24947032Targeted next-generation sequencing on Hirschsprung disease: a pilot study exploits DNA pooling.Ann Hum Genet2014
22384028A genome-wide linkage and association scan reveals novel loci for hypertension and blood pressure traits.PLoS One2012
23084198Screening of the RET gene of Vietnamese Hirschsprung patients identifies 2 novel missense mutations.J Pediatr Surg2012
22241780A comprehensive framework for prioritizing variants in exome sequencing studies of Mendelian diseases.Nucleic Acids Res2012
  • 1 - 50 of 58

Recommended Authors

Harrison International Peace Hospital
Career Start Year 2009
Number of shared co-authors 2
Osaka University School of Medicine Graduate School of Medicine
Career Start Year 2008
Number of shared co-authors 46
Massachusetts General Hospital
Career Start Year 2007
Number of shared co-authors 22
Duke University
Career Start Year 2007
Number of shared co-authors 5
Cleveland Institute for Computational Biology, Case Western Reserve University
Career Start Year 2006
Number of shared co-authors 13
the Children's Hospital Affiliated to Xi'an Jiaotong University
Career Start Year 2006
Number of shared co-authors 8
Institute of Human Genetics, University of Bonn and University Hospital Bonn
Career Start Year 2005
Number of shared co-authors 40
Scripps Science Institute
Career Start Year 2005
Number of shared co-authors 1
University of California San Diego Health System
Career Start Year 2004
Number of shared co-authors 31
Institute for Medical Information Processing
Career Start Year 2003
Number of shared co-authors 49
Boston Children's Hospital, Seoul National University, Seoul National University Hospital
Career Start Year 2003
Number of shared co-authors 2
Institute of Human Genetics, University of Bonn
Career Start Year 2001
Number of shared co-authors 17
University of Pennsylvania
Career Start Year 2001
Number of shared co-authors 26
Boston University School of Public Health
Career Start Year 2001
Number of shared co-authors 45
University of Groningen, University Medical Center Groningen
Career Start Year 2000
Number of shared co-authors 43
University of Washington Medical Center
Career Start Year 2000
Number of shared co-authors 42
Data Science Institute and Lancaster University Medical School
Career Start Year 2000
Number of shared co-authors 24
Vertex Pharmaceuticals
Career Start Year 1999
Number of shared co-authors 53
Foshan First People's Hospital
Career Start Year 1999
Number of shared co-authors 30
Duke University School of Medicine
Career Start Year 1998
Number of shared co-authors 5
Wellcome Sanger Institute
Career Start Year 1998
Number of shared co-authors 54
The Affiliated Huaian No. 1 People's Hospital of Nanjing Medical University
Career Start Year 1997
Number of shared co-authors 8
Heilongjiang Bayi Agricultural University
Career Start Year 1995
Number of shared co-authors 2
Institute for Genomic Medicine, Columbia University Irving Medical Center
Career Start Year 1992
Number of shared co-authors 23
Broad Institute of Harvard and Massachusetts Institute of Technology (MIT)
Career Start Year 1992
Number of shared co-authors 46
William Harvey Research Institute, Queen Mary University of London
Career Start Year 1992
Number of shared co-authors 59
Max Planck Institute of Psychiatry
Career Start Year 1989
Number of shared co-authors 32
Fudan University
Career Start Year 1988
Number of shared co-authors 10
Massachusetts General Hospital
Career Start Year 1987
Number of shared co-authors 48
Victor Philip Dahdaleh Institute of Genomic Medicine at McGill University
Career Start Year 1975
Number of shared co-authors 40

Collaborators

the University of Hong Kong
Co-authored papers 18
Queen Mary Hospital, The University of Hong Kong
Co-authored papers 8
University of California San Francisco (UCSF)
Co-authored papers 6
Keck School of Medicine, University of Southern California
Co-authored papers 5
Co-authored papers 4
Co-authored papers 4
Co-authored papers 3
Co-authored papers 3
Behavioral Health Services.
Co-authored papers 3
Brigham and Women's Hospital, Harvard Medical School
Co-authored papers 3
Co-authored papers 3
University of Iceland
Co-authored papers 3
Co-authored papers 3
Regeneron Pharmaceuticals Inc.
Co-authored papers 3
Co-authored papers 3
Co-authored papers 3
University of Michigan School of Public Health ann arbor
Co-authored papers 2
University of Washington
Co-authored papers 2
Co-authored papers 2
Institute and Clinic for Occupational, University Hospital
Co-authored papers 2
University of Chicago
Co-authored papers 2
Co-authored papers 2
Co-authored papers 2
Co-authored papers 2
Co-authored papers 2
University of California san francisco
Co-authored papers 2
Co-authored papers 2
Co-authored papers 2
23andMe Inc.
Co-authored papers 2
Co-authored papers 2