Lista de obras -

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

artículo científico publicado en 2004

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

artículo científico publicado en 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.

artículo científico publicado en 2012

A second generation human haplotype map of over 3.1 million SNPs

artículo científico publicado en 2007

Abnormal P300 in people with high risk of developing psychosis.

artículo científico publicado en 2008

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

artículo científico publicado en 2017

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

artículo científico publicado en 2014

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

artículo científico publicado en 2017

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

artículo científico publicado en 2012

Association between BDNF val66 met genotype and episodic memory

artículo científico publicado en 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

artículo científico publicado en 2002

Cerebral asymmetry in 14 year olds born very preterm

artículo científico publicado en 2006

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

artículo científico publicado en 2015

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

artículo científico publicado en 2013

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

artículo científico publicado en 2008

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

artículo científico publicado en 2017

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

artículo científico publicado en 2005

Distribution of symptom dimensions across Kraepelinian divisions.

artículo científico publicado en 2006

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

artículo científico publicado en 2006

Erratum

scholarly article published in Genetic Epidemiology

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

artículo científico publicado en 2010

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

artículo científico publicado en 2017

Exome sequencing reveals a high genetic heterogeneity on familial Hirschsprung disease

artículo científico publicado en 2015

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

artículo científico publicado en 2016

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

artículo científico publicado en 2015

Familiality of clinical characteristics in schizophrenia

artículo científico publicado en 2002

Fine mapping of the NRG1 Hirschsprung's disease locus

artículo científico publicado en 2011

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

artículo científico publicado en 2008

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

artículo científico publicado en 2015

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

artículo científico publicado en 2011

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

artículo científico publicado en 2013

Genetic overlap between P300, P50, and duration mismatch negativity

artículo científico publicado en 2006

Genetic overlap between bipolar illness and event-related potentials.

artículo científico publicado en 2007

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

artículo científico publicado en 2014

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

artículo científico publicado en 2016

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.

artículo científico publicado en 2010

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

artículo científico publicado en 2012

Genome-wide copy number variation study in anorectal malformations.

artículo científico publicado en 2012

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

artículo científico publicado en 2007

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

artículo científico publicado en 2012

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

artículo científico publicado en 2010

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

artículo científico publicado en 2011

Heritability and reliability of P300, P50 and duration mismatch negativity.

artículo científico publicado en 2006

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

artículo científico publicado en 2003

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

artículo científico publicado en 2014

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

artículo científico publicado en 2014

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

artículo científico publicado en 2006

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

artículo científico publicado en 2005

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

artículo científico publicado en 2004

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

artículo científico publicado en 2008

Longitudinal heritability of childhood aggression

artículo científico publicado en 2016

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

artículo científico publicado en 2013

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

artículo científico publicado en 2012

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

artículo científico publicado en 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.

artículo científico

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.

artículo científico publicado en 2008

No NRG1 V266L in Chinese patients with schizophrenia

article

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

artículo científico publicado en 2004

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

artículo científico publicado en 2017

Population differences in the International Multi-Centre ADHD Gene Project

article

RET and NRG1 interplay in Hirschsprung disease.

artículo científico publicado en 2013

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

artículo científico publicado en 2011

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

artículo científico publicado en 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

artículo científico publicado en 2006

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

artículo científico publicado en 2005

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

artículo científico publicado en 2016

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

artículo científico publicado en 2007

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

artículo científico publicado en 2014

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

artículo científico publicado en 2009

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

artículo científico publicado en 2011

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

artículo científico publicado en 2013

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

artículo científico publicado en 2016

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

artículo científico publicado en 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.

artículo científico publicado en 2018

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

artículo científico publicado en 2017

Lista de obras de

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

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

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

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

A second generation human haplotype map of over 3.1 million SNPs

Abnormal P300 in people with high risk of developing psychosis.

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

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

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

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

Association between BDNF val66 met genotype and episodic memory

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

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

Cerebral asymmetry in 14 year olds born very preterm

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

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

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

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

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

Distribution of symptom dimensions across Kraepelinian divisions.

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

Erratum

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

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

Exome sequencing reveals a high genetic heterogeneity on familial Hirschsprung disease

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

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

Familiality of clinical characteristics in schizophrenia

Fine mapping of the NRG1 Hirschsprung's disease locus

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

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

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

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

Genetic overlap between P300, P50, and duration mismatch negativity

Genetic overlap between bipolar illness and event-related potentials.

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

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

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

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.

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

Genome-wide copy number variation study in anorectal malformations.

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

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

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

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

Heritability and reliability of P300, P50 and duration mismatch negativity.

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

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

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

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

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

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

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

Longitudinal heritability of childhood aggression

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

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

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

Meta-analysis of the P300 and P50 waveforms in schizophrenia

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

Mutations in the NRG1 gene are associated with Hirschsprung disease

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

No NRG1 V266L in Chinese patients with schizophrenia

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

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

Population differences in the International Multi-Centre ADHD Gene Project

RET and NRG1 interplay in Hirschsprung disease.

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

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

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

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

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

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

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

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

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

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

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