Lista de obras - Ming Li - Dominio Público Uruguay

A human-specific AS3MT isoform and BORCS7 are molecular risk factors in the 10q24.32 schizophrenia-associated locus.

artículo científico publicado en 2016

Allelic variation at 5-HTTLPR is associated with brain morphology in a Chinese population

artículo científico publicado en 2015

Analysis of common genetic variants identifiesRELNas a risk gene for schizophrenia in Chinese population ⬇️

artículo científico publicado el 11 de julio de 2011

Association of RELN promoter SNPs with schizophrenia in the Chinese population ⬇️

artículo científico publicado el 1 de octubre de 2011

Author Correction: Comprehensive integrative analyses identify GLT8D1 and CSNK2B as schizophrenia risk genes

artículo científico publicado en 2018

Common variants at 2q11.2, 8q21.3, and 11q13.2 are associated with major mood disorders.

artículo científico publicado en 2017

Common variants on 2p16.1, 6p22.1 and 10q24.32 are associated with schizophrenia in Han Chinese population.

artículo científico publicado en 2016

Common variants on 6q16.2, 12q24.31 and 16p13.3 are associated with major depressive disorder

artículo científico publicado en 2018

Complement C7 is a novel risk gene for Alzheimer's disease in Han Chinese

scientific article published on 05 November 2018

Comprehensive integrative analyses identify GLT8D1 and CSNK2B as schizophrenia risk genes

artículo científico publicado en 2018

Convergent Lines of Evidence Support LRP8 as a Susceptibility Gene for Psychosis

artículo científico publicado en 2015

Convergent lines of evidence support NOTCH4 as a schizophrenia risk gene

artículo científico publicado en 2020

DEGS2 polymorphism associated with cognition in schizophrenia is associated with gene expression in brain

artículo científico publicado en 2015

Failure of replicating the association between hippocampal volume and 3 single-nucleotide polymorphisms identified from the European genome-wide association study in Asian populations

artículo científico publicado en 2014

Further confirmation of netrin 1 receptor (DCC) as a depression risk gene via integrations of multi-omics data

artículo científico publicado en 2020

Further evidence for the association between LRP8 and schizophrenia

artículo científico publicado en 2017

Genetic association and identification of a functional SNP at GSK3β for schizophrenia susceptibility

artículo científico publicado el 12 de octubre de 2011

Genetic association and meta-analysis of a schizophrenia GWAS variant rs10489202 in East Asian populations

article

Genetic insights and neurobiological implications from NRXN1 in neuropsychiatric disorders

artículo científico publicado en 2019

Genome wide association study identifies four loci for early onset schizophrenia

artículo científico publicado en 2021

Identification of a Bipolar Disorder Vulnerable Gene CHDH at 3p21.1.

artículo científico publicado en 2016

Identification of a Tibetan-specific mutation in the hypoxic gene EGLN1 and its contribution to high-altitude adaptation

artículo científico publicado en 2013

Identification of a functional human-unique 351-bp Alu insertion polymorphism associated with major depressive disorder in the 1p31.1 GWAS risk loci

artículo científico publicado en 2020

Impact of the genome-wide schizophrenia risk single nucleotide polymorphism (rs1625579) in miR-137 on brain structures in healthy individuals

artículo científico publicado en 2013

Independent replications and integrative analyses confirm TRANK1 as a susceptibility gene for bipolar disorder

artículo científico publicado en 2020

Integrative analyses of major histocompatibility complex loci in the genome-wide association studies of major depressive disorder

artículo científico publicado en 2019

MAOA Variants and Genetic Susceptibility to Major Psychiatric Disorders

artículo científico publicado en 2015

Meta-analysis supports association of a non-synonymous SNP in ZNF804A with schizophrenia

artículo científico publicado en 2013

Molecular mechanisms underlying noncoding risk variations in psychiatric genetic studies

artículo científico publicado en 2017

No association between schizophrenia susceptibility variants and macroscopic structural brain volume variation in healthy subjects

artículo científico publicado en 2015

Protein-protein interaction analysis reveals common molecular processes/pathways that contribute to risk of schizophrenia

artículo científico publicado en 2012

Regulatory mechanisms of major depressive disorder risk variants

scientific article published on 25 March 2020

Replicated associations of FADS1, MAD1L1, and a rare variant at 10q26.13 with bipolar disorder in Chinese population

article

Replication of Han Chinese GWAS loci for schizophrenia via meta-analysis of four independent samples

artículo científico publicado en 2016

SLC6A15 rs1545843 and depression: implications from brain imaging data

artículo científico publicado en 2013

Shared genetic architecture and causal relationship between sleep behaviors and lifespan

artículo científico publicado en 2024

Systems-level analysis of risk genes reveals the modular nature of schizophrenia

artículo científico publicado en 2018

The Gene Encoding Protocadherin 9 (PCDH9), a Novel Risk Factor for Major Depressive Disorder

artículo científico publicado en 2017

The depression GWAS risk allele predicts smaller cerebellar gray matter volume and reduced SIRT1 mRNA expression in Chinese population

scientific article published on 09 December 2019

The genome-wide risk alleles for psychiatric disorders at 3p21.1 show convergent effects on mRNA expression, cognitive function, and mushroom dendritic spine

scientific article published on 13 November 2019

The schizophrenia risk isoform ZNF804AE3E4 affects dendritic spine

artículo científico publicado en 2020

The schizophrenia susceptibility gene ZNF804A confers risk of major mood disorders

artículo científico publicado en 2016

Translational genomics and beyond in bipolar disorder

artículo científico publicado en 2020

Up-regulation of NOTCH4 gene expression in bipolar disorder: future studies

artículo científico publicado en 2013

VRK2, a Candidate Gene for Psychiatric and Neurological Disorders

scientific article published on 07 November 2018

Lista de obras de Ming Li

A human-specific AS3MT isoform and BORCS7 are molecular risk factors in the 10q24.32 schizophrenia-associated locus.

Allelic variation at 5-HTTLPR is associated with brain morphology in a Chinese population

Analysis of common genetic variants identifiesRELNas a risk gene for schizophrenia in Chinese population ⬇️

Association of RELN promoter SNPs with schizophrenia in the Chinese population ⬇️

Author Correction: Comprehensive integrative analyses identify GLT8D1 and CSNK2B as schizophrenia risk genes

Common variants at 2q11.2, 8q21.3, and 11q13.2 are associated with major mood disorders.

Common variants on 2p16.1, 6p22.1 and 10q24.32 are associated with schizophrenia in Han Chinese population.

Common variants on 6q16.2, 12q24.31 and 16p13.3 are associated with major depressive disorder

Complement C7 is a novel risk gene for Alzheimer's disease in Han Chinese

Comprehensive integrative analyses identify GLT8D1 and CSNK2B as schizophrenia risk genes

Convergent Lines of Evidence Support LRP8 as a Susceptibility Gene for Psychosis

Convergent lines of evidence support NOTCH4 as a schizophrenia risk gene

DEGS2 polymorphism associated with cognition in schizophrenia is associated with gene expression in brain

Failure of replicating the association between hippocampal volume and 3 single-nucleotide polymorphisms identified from the European genome-wide association study in Asian populations

Further confirmation of netrin 1 receptor (DCC) as a depression risk gene via integrations of multi-omics data

Further evidence for the association between LRP8 and schizophrenia

Genetic association and identification of a functional SNP at GSK3β for schizophrenia susceptibility

Genetic association and meta-analysis of a schizophrenia GWAS variant rs10489202 in East Asian populations

Genetic insights and neurobiological implications from NRXN1 in neuropsychiatric disorders

Genome wide association study identifies four loci for early onset schizophrenia

Identification of a Bipolar Disorder Vulnerable Gene CHDH at 3p21.1.

Identification of a Tibetan-specific mutation in the hypoxic gene EGLN1 and its contribution to high-altitude adaptation

Identification of a functional human-unique 351-bp Alu insertion polymorphism associated with major depressive disorder in the 1p31.1 GWAS risk loci

Impact of the genome-wide schizophrenia risk single nucleotide polymorphism (rs1625579) in miR-137 on brain structures in healthy individuals

Independent replications and integrative analyses confirm TRANK1 as a susceptibility gene for bipolar disorder

Integrative analyses of major histocompatibility complex loci in the genome-wide association studies of major depressive disorder

MAOA Variants and Genetic Susceptibility to Major Psychiatric Disorders

Meta-analysis supports association of a non-synonymous SNP in ZNF804A with schizophrenia

Molecular mechanisms underlying noncoding risk variations in psychiatric genetic studies

No association between schizophrenia susceptibility variants and macroscopic structural brain volume variation in healthy subjects

Protein-protein interaction analysis reveals common molecular processes/pathways that contribute to risk of schizophrenia

Regulatory mechanisms of major depressive disorder risk variants

Replicated associations of FADS1, MAD1L1, and a rare variant at 10q26.13 with bipolar disorder in Chinese population

Replication of Han Chinese GWAS loci for schizophrenia via meta-analysis of four independent samples

SLC6A15 rs1545843 and depression: implications from brain imaging data

Shared genetic architecture and causal relationship between sleep behaviors and lifespan

Systems-level analysis of risk genes reveals the modular nature of schizophrenia

The Gene Encoding Protocadherin 9 (PCDH9), a Novel Risk Factor for Major Depressive Disorder

The depression GWAS risk allele predicts smaller cerebellar gray matter volume and reduced SIRT1 mRNA expression in Chinese population

The genome-wide risk alleles for psychiatric disorders at 3p21.1 show convergent effects on mRNA expression, cognitive function, and mushroom dendritic spine

The schizophrenia risk isoform ZNF804AE3E4 affects dendritic spine

The schizophrenia susceptibility gene ZNF804A confers risk of major mood disorders

Translational genomics and beyond in bipolar disorder

Up-regulation of NOTCH4 gene expression in bipolar disorder: future studies

VRK2, a Candidate Gene for Psychiatric and Neurological Disorders