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List of works by Pak Chung Sham

A developmental model for similarities and dissimilarities between schizophrenia and bipolar disorder

scientific article

A genetic variant in the gene encoding fibrinogen beta chain predicted development of hypertension in Chinese men.

scientific article published on 2 February 2010

A genome-wide association study identifies colorectal cancer susceptibility loci on chromosomes 10p14 and 8q23.3

article

A genome-wide linkage and association scan reveals novel loci for hypertension and blood pressure traits.

scientific article

A second generation human haplotype map of over 3.1 million SNPs

scientific article

Abnormal P300 in people with high risk of developing psychosis

scientific article published on 4 January 2008

Actionable secondary findings from whole-genome sequencing of 954 East Asians

scientific article published on 11 November 2017

Alleles that increase risk for type 2 diabetes mellitus are not associated with increased risk for Alzheimer's disease

scientific article published on 24 July 2014

An Exome-Chip Association Analysis in Chinese Subjects Reveals a Functional Missense Variant of GCKR That Regulates FGF21 Levels.

scientific article published on 6 April 2017

Assessment of gene-by-sex interaction effect on bone mineral density

scientific article (publication date: October 2012)

Association between BDNF val66 met genotype and episodic memory

scientific article published in April 2005

Association of Genetic Risks for Schizophrenia and Bipolar DisorderWith Specific and Generic Brain Structural Endophenotypes

scientific article published on 01 October 2004

Brain volumes in familial and non-familial schizophrenic probands and their unaffected relatives

scientific article published in August 2002

Cerebral asymmetry in 14 year olds born very preterm

scientific article published on 11 May 2006

Chinese family with diffuse oesophageal leiomyomatosis: a new COL4A5/COL4A6 deletion and a case of gonosomal mosaicism

scientific article published on 16 July 2015

Common genetic variants regulating ADD3 gene expression alter biliary atresia risk.

scientific article published on 19 July 2013

DSM-IV combined type ADHD shows familial association with sibling trait scores: a sampling strategy for QTL linkage

scientific article published in December 2008

De novo mutations in Caudal Type Homeo Box transcription Factor 2 (CDX2) in patients with persistent cloaca

scientific article published on 21 November 2017

Dermatoglyphics and Schizophrenia: a meta-analysis and investigation of the impact of obstetric complications upon a-b ridge count.

scientific article

Distribution of symptom dimensions across Kraepelinian divisions.

scientific article published in October 2006

Episodic memory performance predicted by the 2bp deletion in exon 6 of the "alpha 7-like" nicotinic receptor subunit gene

scientific article

Erratum

scholarly article published in Genetic Epidemiology

Excellent school performance at age 16 and risk of adult bipolar disorder: national cohort study

scientific article

Exome chip meta-analysis identifies novel loci and East Asian-specific coding variants that contribute to lipid levels and coronary artery disease.

scientific article published on 30 October 2017

Exome sequencing reveals a high genetic heterogeneity on familial Hirschsprung disease

scientific article

Exome-chip association analysis reveals an Asian-specific missense variant in PAX4 associated with type 2 diabetes in Chinese individuals.

scientific article published on 15 October 2016

Exome-wide association analysis reveals novel coding sequence variants associated with lipid traits in Chinese

scientific article

Familiality of clinical characteristics in schizophrenia

scientific article published on 01 September 2002

Fine mapping of the NRG1 Hirschsprung's disease locus

scientific article

Further evidence for shared genetic effects between psychotic bipolar disorder and P50 suppression: a combined twin and family study

scientific article published in July 2008

GWASdb v2: an update database for human genetic variants identified by genome-wide association studies

scientific article

GWASdb: a database for human genetic variants identified by genome-wide association studies

scientific article published on December 2011

Genetic Analyses of a Three Generation Family Segregating Hirschsprung Disease and Iris Heterochromia.

scientific article

Genetic overlap between P300, P50, and duration mismatch negativity

scientific article published in June 2006

Genetic overlap between bipolar illness and event-related potentials

scientific article published on 16 January 2007

Genetic predisposition to increased blood cholesterol and triglyceride lipid levels and risk of Alzheimer disease: a Mendelian randomization analysis

scientific article

Genetic study of congenital bile-duct dilatation identifies de novo and inherited variants in functionally related genes

scientific article

Genome-wide association study identifies NRG1 as a susceptibility locus for Hirschsprung's disease

scientific journal article

Genome-wide association study identifies a susceptibility locus for biliary atresia on 10q24.2

Genome-wide association study identifies a susceptibility locus for biliary atresia on 10q24.2.

scientific article

Genome-wide copy number analysis uncovers a new HSCR gene: NRG3

scientific article

Genome-wide copy number variation study in anorectal malformations.

scientific article published on 29 October 2012

Genome-wide detection and characterization of positive selection in human populations

scientific article

Genome-wide meta-analysis identifies 56 bone mineral density loci and reveals 14 loci associated with risk of fracture

scientific article

Haplotype analysis reveals a possible founder effect of RET mutation R114H for Hirschsprung's disease in the Chinese population.

scientific article

Hedgehog/Notch-induced premature gliogenesis represents a new disease mechanism for Hirschsprung disease in mice and humans

scientific article

Heritability and reliability of P300, P50 and duration mismatch negativity

scientific article published on 7 July 2006

Hippocampal volume in familial and nonfamilial schizophrenic probands and their unaffected relatives

scientific article

Identifying gene-environment interactions in schizophrenia: contemporary challenges for integrated, large-scale investigations

scientific article

Influence of Alzheimer's disease genes on cognitive decline: the Guangzhou Biobank Cohort Study

scientific article

Intellectual asymmetry and genetic liability in first-degree relatives of probands with schizophrenia.

scientific article

Is the P300 wave an endophenotype for schizophrenia? A meta-analysis and a family study.

scientific article

Joint analysis of the DRD5 marker concludes association with attention-deficit/hyperactivity disorder confined to the predominantly inattentive and combined subtypes

scientific article

Jumping To Conclusions, General Intelligence, And Psychosis Liability: Findings From The Multicentric EU-GEI Case-Control Study

Linkage to chromosome 1p36 for attention-deficit/hyperactivity disorder traits in school and home settings

scientific article published on 24 April 2008

Longitudinal heritability of childhood aggression

scientific article published on 19 January 2016

Lumbar disc degeneration is linked to a carbohydrate sulfotransferase 3 variant.

scientific article

Meta-analyses of genome-wide linkage scans of anxiety-related phenotypes

scientific article

Meta-analysis of GWAS on two Chinese populations followed by replication identifies novel genetic variants on the X chromosome associated with systemic lupus erythematosus.

scientific article published on 22 August 2014

Meta-analysis of the P300 and P50 waveforms in schizophrenia

article

Molecular genetic gene-environment studies using candidate genes in schizophrenia: a systematic review.

scientific article published on 02 October 2013

Mutations in the NRG1 gene are associated with Hirschsprung disease

article

Neuregulin-1 and the P300 waveform--a preliminary association study using a psychosis endophenotype

scientific article published on 20 June 2008

No NRG1 V266L in Chinese patients with schizophrenia

article

Normal cerebral asymmetry in familial and non-familial schizophrenic probands and their unaffected relatives

scientific article published in March 2004

Patient complexity and genotype-phenotype correlations in biliary atresia: a cross-sectional analysis.

scientific article

Population differences in the International Multi-Centre ADHD Gene Project

article

RET and NRG1 interplay in Hirschsprung disease.

scientific article published on 12 February 2013

RET mutational spectrum in Hirschsprung disease: evaluation of 601 Chinese patients.

scientific article

Reaction time performance in ADHD: improvement under fast-incentive condition and familial effects

scientific article published on 31 May 2007

Refinement of the basis and impact of common 11q23.1 variation to the risk of developing colorectal cancer

article

Regional brain morphometry in patients with schizophrenia or bipolar disorder and their unaffected relatives

scientific article

Regional volume deviations of brain structure in schizophrenia and psychotic bipolar disorder: computational morphometry study

scientific article published in May 2005

Sacral agenesis: a pilot whole exome sequencing and copy number study

scientific article

Substantial shared genetic influences on schizophrenia and event-related potentials.

scientific article published on May 2007

Targeted Next-Generation Sequencing on Hirschsprung Disease: A Pilot Study Exploits DNA Pooling

scientific article published on 20 June 2014

The early auditory gamma-band response is heritable and a putative endophenotype of schizophrenia.

scientific article

The genetic and environmental influences of event-related gamma oscillations on bipolar disorder

scientific article

Three SNPs in chromosome 11q23.3 are independently associated with systemic lupus erythematosus in Asians.

scientific article published on 2 September 2013

Trans-ethnic meta-analysis of genome-wide association studies for Hirschsprung disease.

scientific article published on 3 October 2016

Two subtypes of intervertebral disc degeneration distinguished by large-scale population-based study.

scientific article published on 5 May 2016

Two-stage genome-wide association study identifies variants in CAMSAP1L1 as susceptibility loci for epilepsy in Chinese

article

Uncovering the genetic lesions underlying the most severe form of Hirschsprung disease by whole-genome sequencing

scientific article published on 26 February 2018

Whole exome sequencing coupled with unbiased functional analysis reveals new Hirschsprung disease genes

scientific article

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