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Author Details

Hailiang Huang
Massachusetts General Hospital
2007
83
37
PMIDPaper TitleJournal TitlePublished Year
36273448MCPIP-1-Mediated Immunosuppression of Neutrophils Exacerbates Acute Bacterial Peritonitis and Liver Injury.J Innate Immun2023
37868036Polygenic prediction across populations is influenced by ancestry, genetic architecture, and methodology.Cell Genom2023
37055591A lncRNA from an inflammatory bowel disease risk locus maintains intestinal host-commensal homeostasis.Cell Res2023
37207277Using brain cell-type-specific protein interactomes to interpret neurodevelopmental genetic signals in schizophrenia.iScience2023
36651666GWAS quality score for evaluating associated regions in GWAS analyses.Bioinformatics2023
36869767Haplotype-specific MAPK3 expression in 16p11.2 deletion contributes to variable neurodevelopment.Brain2023
35040433Wnt activation promotes memory T cell polyfunctionality via epigenetic regulator PRMT1.J Clin Invest2022
37724326Potential diagnostic biomarkers for schizophrenia.Med Rev (Berl)2022
35578829Non-rapid eye movement sleep and wake neurophysiology in schizophrenia.Elife2022
35765100Development and validation of a trans-ancestry polygenic risk score for type 2 diabetes in diverse populations.Genome Med2022
35396580Mapping genomic loci implicates genes and synaptic biology in schizophrenia.Nature2022
35396579Rare coding variants in ten genes confer substantial risk for schizophrenia.Nature2022
35460606Powerful and robust inference of complex phenotypes' causal genes with dependent expression quantitative loci by a median-based Mendelian randomization.Am J Hum Genet2022
35662508miR143-3p-Mediated NRG-1-Dependent Mitochondrial Dysfunction Contributes to Olanzapine Resistance in Refractory Schizophrenia.Biol Psychiatry2022
35449187Genome-wide association study of actinic keratosis identifies new susceptibility loci implicated in pigmentation and immune regulation pathways.Commun Biol2022
35513724Improving polygenic prediction in ancestrally diverse populations.Nat Genet2022
36369282Collective genomic segments with differential pleiotropic patterns between cognitive dimensions and psychopathology.Nat Commun2022
36038634Large-scale sequencing identifies multiple genes and rare variants associated with Crohn's disease susceptibility.Nat Genet2022
36065016Multi-omics analysis identifies rare variation in leptin/PPAR gene sets and hypermethylation of ABCG1 contribute to antipsychotics-induced metabolic syndromes.Mol Psychiatry2022
35041074Methods for statistical fine-mapping and their applications to auto-immune diseases.Semin Immunopathol2022
33263741Genetic Architecture of Bipolar Disorder in Individuals of Han Chinese and European Ancestries.JAMA Psychiatry2021
33828297Genome-wide enhancer maps link risk variants to disease genes.Nature2021
33597505Population-specific causal disease effect sizes in functionally important regions impacted by selection.Nat Commun2021
33634990Cyclosporine modulates neutrophil functions via the SIRT6-HIF-1α-glycolysis axis to alleviate severe ulcerative colitis.Clin Transl Med2021
34732149Comparison of resting-state spontaneous brain activity between treatment-naive schizophrenia and obsessive-compulsive disorder.BMC Psychiatry2021
34628353Genome-wide analysis of DNA methylation in 106 schizophrenia family trios in Han Chinese.EBioMedicine2021
34118560Large-scale evaluation of the Positive and Negative Syndrome Scale (PANSS) symptom architecture in schizophrenia.Asian J Psychiatr2021
34052317A next generation sequencing combined genome-wide association study identifies novel tuberculosis susceptibility loci in Chinese population.Genomics2021
31388929GABAergic Abnormalities Associated with Sensorimotor Cortico-striatal Community Structural Deficits in ErbB4 Knockout Mice and First-Episode Treatment-Naïve Patients with Schizophrenia.Neurosci Bull2020
31813014Identifying common genome-wide risk genes for major psychiatric traits.Hum Genet2020
31926482Polygenic prediction and GWAS of depression, PTSD, and suicidal ideation/self-harm in a Peruvian cohort.Neuropsychopharmacology2020
32066673Novel genetic susceptibility loci identified by family based whole exome sequencing in Han Chinese schizophrenia patients.Transl Psychiatry2020
33264322Genetic liability in individuals at ultra-high risk of psychosis: A comparison study of 9 psychiatric traits.PLoS One2020
32665544Correction: Multi-trait analysis for genome-wide association study of five psychiatric disorders.Transl Psychiatry2020
32606422Multi-trait analysis for genome-wide association study of five psychiatric disorders.Transl Psychiatry2020
32961455Genome-wide association analysis of opioid use disorder: A novel approach using clinical data.Drug Alcohol Depend2020
32678187Novel susceptibility loci for A(H7N9) infection identified by next generation sequencing and functional analysis.Sci Rep2020
32332799Genome-wide association analysis of insomnia using data from Partners Biobank.Sci Rep2020
30478444Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder.Nat Genet2019
31740837Comparative genetic architectures of schizophrenia in East Asian and European populations.Nat Genet2019
31607513Genome-wide Association Studies in Ancestrally Diverse Populations: Opportunities, Methods, Pitfalls, and Recommendations.Cell2019
31145742Correction: Insights into the genetic epidemiology of Crohn's and rare diseases in the Ashkenazi Jewish population.PLoS Genet2019
30827414Host Genetic Variant in CXCL16 May Be Associated With Hepatitis B Virus-Related Acute Liver Failure.Cell Mol Gastroenterol Hepatol2019
29795570Insights into the genetic epidemiology of Crohn's and rare diseases in the Ashkenazi Jewish population.PLoS Genet2018
30054501Using whole genome scores to compare three clinical phenotyping methods in complex diseases.Sci Rep2018
29860388Late-Onset Crohn's Disease Is A Subgroup Distinct in Genetic and Behavioral Risk Factors With UC-Like Characteristics.Inflamm Bowel Dis2018
29930110Analysis of shared heritability in common disorders of the brain.Science2018
29899441Author Correction: Discovery of stimulation-responsive immune enhancers with CRISPR activation.Nature2018
29579042Genetic variants in cellular transport do not affect mesalamine response in ulcerative colitis.PLoS One2018
29549319Publisher Correction: Whole genome sequencing in psychiatric disorders: the WGSPD consortium.Nat Neurosci2018
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Collaborators

Massachusetts General Hospital
Co-authored papers 30
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Co-authored papers 13
Co-authored papers 11
Massachusetts General Hospital and Harvard Medical School
Co-authored papers 10
Broad Institute of MIT and Harvard
Co-authored papers 10
Johns Hopkins University
Co-authored papers 9
Heilongjiang Bayi Agricultural University
Co-authored papers 8
F. Widjaja Inflammatory Bowel Disease Institute
Co-authored papers 8
Co-authored papers 8
University of North Carolina at Chapel Hill
Co-authored papers 8
Institute of Clinical Molecular Biology, Kiel University
Co-authored papers 7
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Co-authored papers 7
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Co-authored papers 6
Co-authored papers 6
Co-authored papers 6
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SUNY Upstate Medical University
Co-authored papers 6
Co-authored papers 6
Co-authored papers 6
Co-authored papers 6
Center for Genomic Medicine, Massachusetts General Hospital
Co-authored papers 6
Co-authored papers 6
Co-authored papers 5
Co-authored papers 5
Center for Genomic Medicine, Massachusetts General Hospital
Co-authored papers 5
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Institute of Human Genetics, University Hospital Bonn
Co-authored papers 5