Skip to Main Content
CKG
Home
Home
Home
TKG
Author details
Breadcrumb
Author Details
Full Name
Hailiang Huang
Affiliation
Massachusetts General Hospital
ORCID
Career Start Year
2007
Papers
83
H Index
37
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36273448
MCPIP-1-Mediated Immunosuppression of Neutrophils Exacerbates Acute Bacterial Peritonitis and Liver Injury.
J Innate Immun
2023
37868036
Polygenic prediction across populations is influenced by ancestry, genetic architecture, and methodology.
Cell Genom
2023
37055591
A lncRNA from an inflammatory bowel disease risk locus maintains intestinal host-commensal homeostasis.
Cell Res
2023
37207277
Using brain cell-type-specific protein interactomes to interpret neurodevelopmental genetic signals in schizophrenia.
iScience
2023
36651666
GWAS quality score for evaluating associated regions in GWAS analyses.
Bioinformatics
2023
36869767
Haplotype-specific MAPK3 expression in 16p11.2 deletion contributes to variable neurodevelopment.
Brain
2023
35040433
Wnt activation promotes memory T cell polyfunctionality via epigenetic regulator PRMT1.
J Clin Invest
2022
37724326
Potential diagnostic biomarkers for schizophrenia.
Med Rev (Berl)
2022
35578829
Non-rapid eye movement sleep and wake neurophysiology in schizophrenia.
Elife
2022
35765100
Development and validation of a trans-ancestry polygenic risk score for type 2 diabetes in diverse populations.
Genome Med
2022
35396580
Mapping genomic loci implicates genes and synaptic biology in schizophrenia.
Nature
2022
35396579
Rare coding variants in ten genes confer substantial risk for schizophrenia.
Nature
2022
35460606
Powerful and robust inference of complex phenotypes' causal genes with dependent expression quantitative loci by a median-based Mendelian randomization.
Am J Hum Genet
2022
35662508
miR143-3p-Mediated NRG-1-Dependent Mitochondrial Dysfunction Contributes to Olanzapine Resistance in Refractory Schizophrenia.
Biol Psychiatry
2022
35449187
Genome-wide association study of actinic keratosis identifies new susceptibility loci implicated in pigmentation and immune regulation pathways.
Commun Biol
2022
35513724
Improving polygenic prediction in ancestrally diverse populations.
Nat Genet
2022
36369282
Collective genomic segments with differential pleiotropic patterns between cognitive dimensions and psychopathology.
Nat Commun
2022
36038634
Large-scale sequencing identifies multiple genes and rare variants associated with Crohn's disease susceptibility.
Nat Genet
2022
36065016
Multi-omics analysis identifies rare variation in leptin/PPAR gene sets and hypermethylation of ABCG1 contribute to antipsychotics-induced metabolic syndromes.
Mol Psychiatry
2022
35041074
Methods for statistical fine-mapping and their applications to auto-immune diseases.
Semin Immunopathol
2022
33263741
Genetic Architecture of Bipolar Disorder in Individuals of Han Chinese and European Ancestries.
JAMA Psychiatry
2021
33828297
Genome-wide enhancer maps link risk variants to disease genes.
Nature
2021
33597505
Population-specific causal disease effect sizes in functionally important regions impacted by selection.
Nat Commun
2021
33634990
Cyclosporine modulates neutrophil functions via the SIRT6-HIF-1α-glycolysis axis to alleviate severe ulcerative colitis.
Clin Transl Med
2021
34732149
Comparison of resting-state spontaneous brain activity between treatment-naive schizophrenia and obsessive-compulsive disorder.
BMC Psychiatry
2021
34628353
Genome-wide analysis of DNA methylation in 106 schizophrenia family trios in Han Chinese.
EBioMedicine
2021
34118560
Large-scale evaluation of the Positive and Negative Syndrome Scale (PANSS) symptom architecture in schizophrenia.
Asian J Psychiatr
2021
34052317
A next generation sequencing combined genome-wide association study identifies novel tuberculosis susceptibility loci in Chinese population.
Genomics
2021
31388929
GABAergic Abnormalities Associated with Sensorimotor Cortico-striatal Community Structural Deficits in ErbB4 Knockout Mice and First-Episode Treatment-Naïve Patients with Schizophrenia.
Neurosci Bull
2020
31813014
Identifying common genome-wide risk genes for major psychiatric traits.
Hum Genet
2020
31926482
Polygenic prediction and GWAS of depression, PTSD, and suicidal ideation/self-harm in a Peruvian cohort.
Neuropsychopharmacology
2020
32066673
Novel genetic susceptibility loci identified by family based whole exome sequencing in Han Chinese schizophrenia patients.
Transl Psychiatry
2020
33264322
Genetic liability in individuals at ultra-high risk of psychosis: A comparison study of 9 psychiatric traits.
PLoS One
2020
32665544
Correction: Multi-trait analysis for genome-wide association study of five psychiatric disorders.
Transl Psychiatry
2020
32606422
Multi-trait analysis for genome-wide association study of five psychiatric disorders.
Transl Psychiatry
2020
32961455
Genome-wide association analysis of opioid use disorder: A novel approach using clinical data.
Drug Alcohol Depend
2020
32678187
Novel susceptibility loci for A(H7N9) infection identified by next generation sequencing and functional analysis.
Sci Rep
2020
32332799
Genome-wide association analysis of insomnia using data from Partners Biobank.
Sci Rep
2020
30478444
Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder.
Nat Genet
2019
31740837
Comparative genetic architectures of schizophrenia in East Asian and European populations.
Nat Genet
2019
31607513
Genome-wide Association Studies in Ancestrally Diverse Populations: Opportunities, Methods, Pitfalls, and Recommendations.
Cell
2019
31145742
Correction: Insights into the genetic epidemiology of Crohn's and rare diseases in the Ashkenazi Jewish population.
PLoS Genet
2019
30827414
Host Genetic Variant in CXCL16 May Be Associated With Hepatitis B Virus-Related Acute Liver Failure.
Cell Mol Gastroenterol Hepatol
2019
29795570
Insights into the genetic epidemiology of Crohn's and rare diseases in the Ashkenazi Jewish population.
PLoS Genet
2018
30054501
Using whole genome scores to compare three clinical phenotyping methods in complex diseases.
Sci Rep
2018
29860388
Late-Onset Crohn's Disease Is A Subgroup Distinct in Genetic and Behavioral Risk Factors With UC-Like Characteristics.
Inflamm Bowel Dis
2018
29930110
Analysis of shared heritability in common disorders of the brain.
Science
2018
29899441
Author Correction: Discovery of stimulation-responsive immune enhancers with CRISPR activation.
Nature
2018
29579042
Genetic variants in cellular transport do not affect mesalamine response in ulcerative colitis.
PLoS One
2018
29549319
Publisher Correction: Whole genome sequencing in psychiatric disorders: the WGSPD consortium.
Nat Neurosci
2018
1 - 50 of 83
Column Actions
Search
Recommended Authors
Xia Shen
Usher Institute, University of Edinburgh
Career Start Year
2011
Number of shared co-authors
39
Benjamin Lehne
School of Public Health, Imperial College London
Career Start Year
2009
Number of shared co-authors
65
Liping Hou
Harrison International Peace Hospital
Career Start Year
2009
Number of shared co-authors
55
Karol Estrada
Brandeis University
Career Start Year
2009
Number of shared co-authors
99
Eric R Gamazon
Vanderbilt University Medical Center
Career Start Year
2009
Number of shared co-authors
57
Xiangjun Xiao
Institute for Clinical and Translational Research, Baylor College of Medicine
Career Start Year
2008
Number of shared co-authors
55
Elizabeth T Cirulli
Duke University
Career Start Year
2007
Number of shared co-authors
29
Hongsheng Gui
Behavioral Health Services
Career Start Year
2007
Number of shared co-authors
22
Yun Li
University of British Columbia
Career Start Year
2007
Number of shared co-authors
105
Andrew J Schork
The Lundbeck Foundation Initiative for Integrative Psychiatric Research (iPSYCH)
Career Start Year
2007
Number of shared co-authors
74
Alexander Gusev
The Center for Functional Cancer Epigenetics, Dana Farber Cancer Institute
Career Start Year
2006
Number of shared co-authors
56
William S Bush
Cleveland Institute for Computational Biology, Case Western Reserve University
Career Start Year
2006
Number of shared co-authors
49
Gabriel E Hoffman
Center for Disease Neurogenomics, Icahn School of Medicine at Mount Sinai
Career Start Year
2006
Number of shared co-authors
22
Ian B Stanaway
Kidney Research Institute and Division of Nephrology, University of Washington
Career Start Year
2006
Number of shared co-authors
23
Ali Torkamani
Scripps Science Institute
Career Start Year
2005
Number of shared co-authors
26
Benjamin F Voight
Perelman School of Medicine, University of Pennsylvania
Career Start Year
2005
Number of shared co-authors
89
Degui Zhi
University of Texas Health Science Center at Houston
Career Start Year
2004
Number of shared co-authors
41
Sarah S Murray
University of California San Diego Health System
Career Start Year
2004
Number of shared co-authors
100
Steven J Schrodi
University of Wisconsin Madison
Career Start Year
2004
Number of shared co-authors
12
Tushar Bhangale
Genentech Inc.
Career Start Year
2004
Number of shared co-authors
59
Zolt??n Kutalik
University of Lausanne
Career Start Year
2004
Number of shared co-authors
122
Sarah A Pendergrass
Biomedical and Translational Informatics Institute
Career Start Year
2003
Number of shared co-authors
58
Yufeng Shen
Columbia University
Career Start Year
2002
Number of shared co-authors
28
Kai Wang
University of Pennsylvania
Career Start Year
2001
Number of shared co-authors
68
Eric E Schadt
Icahn School of Medicine at Mount Sinai
Career Start Year
1998
Number of shared co-authors
113
Nicole Soranzo
Wellcome Sanger Institute
Career Start Year
1998
Number of shared co-authors
125
Michael R Barnes
William Harvey Research Institute, Queen Mary University of London
Career Start Year
1997
Number of shared co-authors
132
Mathieu Lemire
The Hospital for Sick Children
Career Start Year
1997
Number of shared co-authors
31
Hongyu Zhao
Yale University
Career Start Year
1995
Number of shared co-authors
81
Panos Deloukas
William Harvey Research Institute, Queen Mary University of London
Career Start Year
1992
Number of shared co-authors
163
row(s) 1 - 30 of 30
Collaborators
Mark J Daly
Massachusetts General Hospital
Co-authored papers
30
Benjamin M Neale
Massachusetts General Hospital
Co-authored papers
13
Aarno Palotie
Co-authored papers
11
Stephan Ripke
Massachusetts General Hospital and Harvard Medical School
Co-authored papers
10
Ramnik J Xavier
Broad Institute of MIT and Harvard
Co-authored papers
10
Joel S Bader
Johns Hopkins University
Co-authored papers
9
Lin He
Heilongjiang Bayi Agricultural University
Co-authored papers
8
Dermot P B McGovern
F. Widjaja Inflammatory Bowel Disease Institute
Co-authored papers
8
Thomas Werge
Co-authored papers
8
Patrick F Sullivan
University of North Carolina at Chapel Hill
Co-authored papers
8
Andre Franke
Institute of Clinical Molecular Biology, Kiel University
Co-authored papers
7
John D Rioux
Co-authored papers
7
Judy H Cho
Co-authored papers
7
Jeffrey C Barrett
Co-authored papers
7
Veikko Salomaa
Co-authored papers
6
Alicia R Martin
Co-authored papers
6
Richard H Duerr
Co-authored papers
6
Steven A McCarroll
Co-authored papers
6
Stephen V Faraone
SUNY Upstate Medical University
Co-authored papers
6
Talin Haritunians
Co-authored papers
6
Carlos N Pato
Co-authored papers
6
Nelson B Freimer
Co-authored papers
6
Jordan W Smoller
Center for Genomic Medicine, Massachusetts General Hospital
Co-authored papers
6
Stefan Schreiber
Co-authored papers
6
Lude Franke
Co-authored papers
5
Tõnu Esko
Co-authored papers
5
Phil H Lee
Center for Genomic Medicine, Massachusetts General Hospital
Co-authored papers
5
Eli A Stahl
Co-authored papers
5
Eija Hämäläinen
Co-authored papers
5
Markus M N??then
Institute of Human Genetics, University Hospital Bonn
Co-authored papers
5
1 - 30