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TKG
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Author Details
Full Name
Pak C Sham
Affiliation
the University of Hong Kong
ORCID
Career Start Year
1989
Papers
770
H Index
105
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
38086974
Correction: Cross-phenotype relationship between opioid use disorder and suicide attempts: new evidence from polygenic association and Mendelian randomization analyses.
Mol Psychiatry
2024
35164887
Ameliorative patterns of grey matter in patients with first-episode and treatment-naïve schizophrenia.
Psychol Med
2023
37633278
Dissecting the high-resolution genetic architecture of complex phenotypes by accurately estimating gene-based conditional heritability.
Am J Hum Genet
2023
38078747
Cannabis use as a potential mediator between childhood adversity and first-episode psychosis: results from the EU-GEI case-control study.
Psychol Med
2023
37602215
Inferring CTCF-binding patterns and anchored loops across human tissues and cell types.
Patterns (N Y)
2023
37292649
Association of neurotransmitter pathway polygenic risk with specific symptom profiles in psychosis.
medRxiv
2023
37061531
Transcriptomics of Hirschsprung disease patient-derived enteric neural crest cells reveals a role for oxidative phosphorylation.
Nat Commun
2023
37285136
Preliminary Evidence for Genetic Nurture in Depression and Neuroticism Through Polygenic Scores.
JAMA Psychiatry
2023
37211699
YBX1-Mediated DNA Methylation-Dependent SHANK3 Expression in PBMCs and Developing Cortical Interneurons in Schizophrenia.
Adv Sci (Weinh)
2023
37443193
Neural variability in three major psychiatric disorders.
Mol Psychiatry
2023
37310339
Synergistic effects of childhood adversity and polygenic risk in first-episode psychosis: the EU-GEI study.
Psychol Med
2023
37441552
The genetic basis of onset age in schizophrenia: evidence and models.
Front Genet
2023
37340172
Cross-phenotype relationship between opioid use disorder and suicide attempts: new evidence from polygenic association and Mendelian randomization analyses.
Mol Psychiatry
2023
37438366
Unveiling common psychological characteristics of proneness to aggression and general psychopathology in a large community youth cohort.
Transl Psychiatry
2023
37129249
The association between reasons for first using cannabis, later pattern of use, and risk of first-episode psychosis: the EU-GEI case-control study.
Psychol Med
2023
37092861
Brain transcriptome-wide association study implicates novel risk genes underlying schizophrenia risk.
Psychol Med
2023
37062770
Exploring the mediation of DNA methylation across the epigenome between childhood adversity and First Episode of Psychosis-findings from the EU-GEI study.
Mol Psychiatry
2023
36889182
Functional dysconnectivity of anterior cingulate subregions in schizophrenia and psychotic and nonpsychotic bipolar disorder.
Schizophr Res
2023
36854672
Reciprocal causation mixture model for robust Mendelian randomization analysis using genome-scale summary data.
Nat Commun
2023
36746926
Common and rare variant associations with latent traits underlying depression, bipolar disorder, and schizophrenia.
Transl Psychiatry
2023
36711134
Third-generation genome sequencing implicates medium-sized structural variants in chronic schizophrenia.
Front Neurosci
2023
36869052
An autoimmune pleiotropic SNP modulates IRF5 alternative promoter usage through ZBTB3-mediated chromatin looping.
Nat Commun
2023
36709613
White matter changes and its relationship with clinical symptom in medication-naive first-episode early onset schizophrenia.
Asian J Psychiatr
2023
35947471
First-Episode Psychosis Patients Who Deteriorated in the Premorbid Period Do Not Have Higher Polygenic Risk Scores Than Others: A Cluster Analysis of EU-GEI Data.
Schizophr Bull
2023
35076361
Use of multiple polygenic risk scores for distinguishing schizophrenia-spectrum disorder and affective psychosis categories in a first-episode sample; the EU-GEI study.
Psychol Med
2023
35144700
Effectiveness and optimal duration of early intervention treatment in adult-onset psychosis: a randomized clinical trial.
Psychol Med
2023
33032663
Evaluation of bi-directional causal association between depression and cardiovascular diseases: a Mendelian randomization study.
Psychol Med
2022
35652173
Clarifying the causes of consistent and inconsistent findings in genetics.
Genet Epidemiol
2022
35668084
Associations between childhood maltreatment and psychiatric disorders: analysis from electronic health records in Hong Kong.
Transl Psychiatry
2022
35396580
Mapping genomic loci implicates genes and synaptic biology in schizophrenia.
Nature
2022
35527273
Comprehensive and integrative analyses identify TYW5 as a schizophrenia risk gene.
BMC Med
2022
35750329
Improved nonparametric penalized maximum likelihood estimation for arbitrarily censored survival data.
Stat Med
2022
35779326
Extended gene set analysis of human neuro-psychiatric traits shows enrichment in brain-expressed human accelerated regions across development.
Schizophr Res
2022
36443333
Whole genome sequencing reveals epistasis effects within RET for Hirschsprung disease.
Sci Rep
2022
35873260
Abnormal Brain Structure Morphology in Early-Onset Schizophrenia.
Front Psychiatry
2022
36299579
Polygenic power calculator: Statistical power and polygenic prediction accuracy of genome-wide association studies of complex traits.
Front Genet
2022
36380119
Discovering the structure and organization of a free Cantonese emotion-label word association graph to understand mental lexicons of emotions.
Sci Rep
2022
36195640
A causal association of ANKRD37 with human hippocampal volume.
Mol Psychiatry
2022
35093020
Mendelian randomization analysis of vitamin D in the secondary prevention of hypertensive-diabetic subjects: role of facilitating blood pressure control.
Genes Nutr
2022
35211769
Striatal dopamine synthesis capacity and its association with negative symptoms upon resolution of positive symptoms in first-episode schizophrenia and delusional disorder.
Psychopharmacology (Berl)
2022
34872833
Structural network alterations and their association with neurological soft signs in schizophrenia: Evidence from clinical patients and unaffected siblings.
Schizophr Res
2022
35325253
Facial Emotion Recognition in Psychosis and Associations With Polygenic Risk for Schizophrenia: Findings From the Multi-Center EU-GEI Case-Control Study.
Schizophr Bull
2022
34931221
Deviation from baseline mutation burden provides powerful and robust rare-variants association test for complex diseases.
Nucleic Acids Res
2022
35170024
Potential role of regulatory DNA variants in modifying the risk of severe cutaneous reactions induced by aromatic anti-seizure medications.
Epilepsia
2022
35195259
A polygenic risk score improves risk stratification of coronary artery disease: a large-scale prospective Chinese cohort study.
Eur Heart J
2022
34570217
VannoPortal: multiscale functional annotation of human genetic variants for interrogating molecular mechanism of traits and diseases.
Nucleic Acids Res
2022
34564762
Integrative analysis of metabolomic, genomic, and imaging-based phenotypes identify very-low-density lipoprotein as a potential risk factor for lumbar Modic changes.
Eur Spine J
2022
34099189
Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders.
Biol Psychiatry
2022
34193973
Integrative omics of schizophrenia: from genetic determinants to clinical classification and risk prediction.
Mol Psychiatry
2022
32173736
MTMR4 SNVs modulate ion channel degradation and clinical severity in congenital long QT syndrome: insights in the mechanism of action of protective modifier genes.
Cardiovasc Res
2021
1 - 50 of 770
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George Kirov
Co-authored papers
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Kenneth S Kendler
Virginia Commonwealth University
Co-authored papers
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Benjamin M Neale
Massachusetts General Hospital
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Robert Plomin
Co-authored papers
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Panwen Wang
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Nattiya Hirankarn
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Anne Farmer
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