Lista de obras - Zhongsheng Sun - Dominio Público Uruguay

A 17 gene panel for non-small-cell lung cancer prognosis identified through integrative epigenomic-transcriptomic analyses of hypoxia-induced epithelial-mesenchymal transition

scientific article published on 29 May 2019

A Bayesian framework to identify methylcytosines from high-throughput bisulfite sequencing data

artículo científico publicado en 2014

A Statistical Framework for Mapping Risk Genes from De Novo Mutations in Whole-Genome-Sequencing Studies

artículo científico publicado en 2018

A comparative study of the genetic components of three subcategories of autism spectrum disorder

artículo científico publicado en 2018

A differential response of two putative mammalian circadian regulators, mper1 and mper2, to light.

artículo científico publicado en 1997

A novel 10-base pair insertion mutation in exon 5 of the SOD1 gene in a Chinese family with amyotrophic lateral sclerosis.

artículo científico publicado en 2016

Acetylation of hMOF Modulates H4K16ac to Regulate DNA Repair Genes in Response to Oxidative Stress.

artículo científico publicado en 2017

Altered expressions of memory genes in food-entrained circadian rhythm

scientific article published on 01 October 2018

Androgen deprivation drives variation of androgen receptor trinucleotide repeats

scientific article published on 01 September 2019

Anxiety-Related Behaviours Associated with microRNA-206-3p and BDNF Expression in Pregnant Female Mice Following Psychological Social Stress.

artículo científico publicado en 2017

CRISPR Editing in Biological and Biomedical Investigation

artículo científico publicado en 2017

CirGRDB: a database for the genome-wide deciphering circadian genes and regulators

artículo científico publicado en 2017

Circadian clock genes oscillate in human peripheral blood mononuclear cells

artículo científico publicado en 2003

Co-expression Network of mRNAs and lncRNAs Regulated by Stress-Linked Behavioral Assays

scientific article published on 23 November 2019

Comparative RNA-seq analysis reveals potential mechanisms mediating the conversion to androgen independence in an LNCaP progression cell model

artículo científico publicado en 2013

Comprehensive characterization of posttranscriptional impairment-related 3'-UTR mutations in 2413 whole genomes of cancer patients

scientific article published on 02 June 2022

Converging signal on ERK1/2 activity regulates group I mGluR-mediated Arc transcription.

artículo científico publicado en 2009

Deficiency of Antinociception and Excessive Grooming Induced by Acute Immobilization Stress in Per1 Mutant Mice ⬇️

artículo científico publicado el 14 de enero de 2011

Demethylation of c-MYB binding site mediates upregulation of Bdnf IV in cocaine-conditioned place preference

artículo científico publicado en 2016

Dysplastic spondylolysis is caused by mutations in the diastrophic dysplasia sulfate transporter gene

artículo científico publicado en 2015

EpiDenovo: a platform for linking regulatory de novo mutations to developmental epigenetics and diseases.

artículo científico publicado en 2017

Epigenetic Activation of ASCT2 in the Hippocampus Contributes to Depression-Like Behavior by Regulating D-Serine in Mice.

artículo científico publicado en 2017

EpilepsyGene: a genetic resource for genes and mutations related to epilepsy.

artículo científico publicado en 2014

Evolutionary mode and functional divergence of vertebrate NMDA receptor subunit 2 genes

artículo científico publicado en 2010

Expression profiling reveals a positive regulation by mPer2 on circadian rhythm of cytotoxicity receptors: Ly49C and Nkg2d.

artículo científico publicado en 2009

Genes with de novo mutations are shared by four neuropsychiatric disorders discovered from NPdenovo database

artículo científico publicado en 2015

Genes with de novo mutations are shared by four neuropsychiatric disorders discovered from NPdenovo database

artículo científico publicado en 2015

Genetic landscape of papillary thyroid carcinoma in the Chinese population.

artículo científico publicado en 2017

Genome-wide identification and divergent transcriptional expression of StAR-related lipid transfer (START) genes in teleosts.

artículo científico publicado en 2013

Genome-wide identification of differential methylation between primary and recurrent hepatocellular carcinomas.

artículo científico publicado en 2015

Genomic landscapes of Chinese sporadic autism spectrum disorders revealed by whole-genome sequencing

article

Identification and characterization of novel fusion genes in prostate cancer by targeted RNA capture and next-generation sequencing

article

Identification of Novel Compound Mutations in PLA2G6-Associated Neurodegeneration Patient with Characteristic MRI Imaging.

artículo científico publicado en 2016

Identification of a novel missense (C7W) mutation of SOD1 in a large familial amyotrophic lateral sclerosis pedigree.

artículo científico publicado en 2013

Isolation of novel genes from the CMT1A duplication/HNPP deletion critical region in 17p11.2-p12.

artículo científico publicado en 1997

Lamarck rises from his grave: parental environment-induced epigenetic inheritance in model organisms and humans

artículo científico publicado en 2017

MBRidge: an accurate and cost-effective method for profiling DNA methylome at single-base resolution

artículo científico publicado en 2015

MPer1 and mper2 are essential for normal resetting of the circadian clock

artículo científico publicado en 2001

MagicViewer: integrated solution for next-generation sequencing data visualization and genetic variation detection and annotation

artículo científico publicado en 2010

Maternal depression is associated with DNA methylation changes in cord blood T lymphocytes and adult hippocampi

artículo científico publicado en 2015

Mutations in WNT10B Are Identified in Individuals with Oligodontia

artículo científico publicado en 2016

Mutations of ANK3 identified by exome sequencing are associated with autism susceptibility.

artículo científico publicado en 2012

OncoBase: a platform for decoding regulatory somatic mutations in human cancers

scientific article published on 01 January 2019

PAK2 Haploinsufficiency Results in Synaptic Cytoskeleton Impairment and Autism-Related Behavior

scientific article published on 01 August 2018

Performance evaluation of pathogenicity-computation methods for missense variants

artículo científico publicado en 2018

Population genomics reveals speciation and introgression between Brown Norway rats and their sibling species.

artículo científico publicado en 2017

Presence of the pregnant partner regulates microRNA-30a and BDNF levels and protects male mice from social defeat-induced abnormal behaviors

scientific article published on 01 April 2019

Q-RRBS: a quantitative reduced representation bisulfite sequencing method for single-cell methylome analyses.

artículo científico publicado en 2015

RBP-Var: a database of functional variants involved in regulation mediated by RNA-binding proteins

artículo científico publicado en 2015

RIGUI, a Putative Mammalian Ortholog of the Drosophila period Gene ⬇️

artículo científico publicado el 19 de septiembre de 1997

RRBS-analyser: a comprehensive web server for reduced representation bisulfite sequencing data analysis.

artículo científico publicado en 2013

RSPO2-LGR5 signaling has tumour-suppressive activity in colorectal cancer.

artículo científico publicado en 2014

Ras-induced epigenetic inactivation of the RRAD (Ras-related associated with diabetes) gene promotes glucose uptake in a human ovarian cancer model.

artículo científico publicado en 2014

Recent Progress in CRISPR/Cas9 Technology

artículo científico publicado en 2016

Reversal of cocaine-conditioned place preference through methyl supplementation in mice: altering global DNA methylation in the prefrontal cortex

artículo científico publicado en 2012

S-adenosyl-methionine (SAM) alters the transcriptome and methylome and specifically blocks growth and invasiveness of liver cancer cells.

artículo científico publicado en 2017

Screening for possible oligogenic pathogenesis in Chinese sporadic ALS patients.

artículo científico publicado en 2018

Single-cell sequencing technologies: current and future.

artículo científico publicado en 2014

Systematic evaluation of genome-wide methylated DNA enrichment using a CpG island array.

artículo científico publicado en 2011

TET1 modulates H4K16 acetylation by controlling auto-acetylation of hMOF to affect gene regulation and DNA repair function.

artículo científico publicado en 2016

Targeted sequencing and functional analysis reveal brain-size-related genes and their networks in autism spectrum disorders

artículo científico publicado en 2017

Targeted sequencing and integrative analysis to prioritize candidate genes in neurodevelopmental disorders

artículo científico publicado en 2021

The APP-interacting protein FE65 is required for hippocampus-dependent learning and long-term potentiation.

artículo científico

The Circadian Clock Gene Regulates Gamma Interferon Production of NK Cells in Host Response to Lipopolysaccharide-Induced Endotoxic Shock

scientific article published in 2007

The biological basis of sexual orientation: How hormonal, genetic, and environmental factors influence to whom we are sexually attracted

artículo científico publicado en 2019

The circadian clock Period 2 gene regulates gamma interferon production of NK cells in host response to lipopolysaccharide-induced endotoxic shock.

artículo científico publicado en 2006

Transcriptomic signature associated with carcinogenesis and aggressiveness of papillary thyroid carcinoma

scientific article published on 30 July 2018

VarCards: an integrated genetic and clinical database for coding variants in the human genome.

artículo científico publicado en 2017

Vitamin D-related genes are subjected to significant de novo mutation burdens in autism spectrum disorder

artículo científico publicado en 2017

Whole-Genome Sequencing Reveals Genetic Variation in the Asian House Rat.

artículo científico publicado en 2016

mirTools: microRNA profiling and discovery based on high-throughput sequencing

artículo científico publicado en 2010

mirTrios: an integrated pipeline for detection of de novo and rare inherited mutations from trios-based next-generation sequencing

artículo científico publicado en 2015

mirVAFC: A Web Server for Prioritizations of Pathogenic Sequence Variants from Exome Sequencing Data via Classifications.

artículo científico publicado en 2016

Lista de obras de Zhongsheng Sun

A 17 gene panel for non-small-cell lung cancer prognosis identified through integrative epigenomic-transcriptomic analyses of hypoxia-induced epithelial-mesenchymal transition

A Bayesian framework to identify methylcytosines from high-throughput bisulfite sequencing data

A Statistical Framework for Mapping Risk Genes from De Novo Mutations in Whole-Genome-Sequencing Studies

A comparative study of the genetic components of three subcategories of autism spectrum disorder

A differential response of two putative mammalian circadian regulators, mper1 and mper2, to light.

A novel 10-base pair insertion mutation in exon 5 of the SOD1 gene in a Chinese family with amyotrophic lateral sclerosis.

Acetylation of hMOF Modulates H4K16ac to Regulate DNA Repair Genes in Response to Oxidative Stress.

Altered expressions of memory genes in food-entrained circadian rhythm

Androgen deprivation drives variation of androgen receptor trinucleotide repeats

Anxiety-Related Behaviours Associated with microRNA-206-3p and BDNF Expression in Pregnant Female Mice Following Psychological Social Stress.

CRISPR Editing in Biological and Biomedical Investigation

CirGRDB: a database for the genome-wide deciphering circadian genes and regulators

Circadian clock genes oscillate in human peripheral blood mononuclear cells

Co-expression Network of mRNAs and lncRNAs Regulated by Stress-Linked Behavioral Assays

Comparative RNA-seq analysis reveals potential mechanisms mediating the conversion to androgen independence in an LNCaP progression cell model

Comprehensive characterization of posttranscriptional impairment-related 3'-UTR mutations in 2413 whole genomes of cancer patients

Converging signal on ERK1/2 activity regulates group I mGluR-mediated Arc transcription.

Deficiency of Antinociception and Excessive Grooming Induced by Acute Immobilization Stress in Per1 Mutant Mice ⬇️

Demethylation of c-MYB binding site mediates upregulation of Bdnf IV in cocaine-conditioned place preference

Dysplastic spondylolysis is caused by mutations in the diastrophic dysplasia sulfate transporter gene

EpiDenovo: a platform for linking regulatory de novo mutations to developmental epigenetics and diseases.

Epigenetic Activation of ASCT2 in the Hippocampus Contributes to Depression-Like Behavior by Regulating D-Serine in Mice.

EpilepsyGene: a genetic resource for genes and mutations related to epilepsy.

Evolutionary mode and functional divergence of vertebrate NMDA receptor subunit 2 genes

Expression profiling reveals a positive regulation by mPer2 on circadian rhythm of cytotoxicity receptors: Ly49C and Nkg2d.

Genes with de novo mutations are shared by four neuropsychiatric disorders discovered from NPdenovo database

Genes with de novo mutations are shared by four neuropsychiatric disorders discovered from NPdenovo database

Genetic landscape of papillary thyroid carcinoma in the Chinese population.

Genome-wide identification and divergent transcriptional expression of StAR-related lipid transfer (START) genes in teleosts.

Genome-wide identification of differential methylation between primary and recurrent hepatocellular carcinomas.

Genomic landscapes of Chinese sporadic autism spectrum disorders revealed by whole-genome sequencing

Identification and characterization of novel fusion genes in prostate cancer by targeted RNA capture and next-generation sequencing

Identification of Novel Compound Mutations in PLA2G6-Associated Neurodegeneration Patient with Characteristic MRI Imaging.

Identification of a novel missense (C7W) mutation of SOD1 in a large familial amyotrophic lateral sclerosis pedigree.

Isolation of novel genes from the CMT1A duplication/HNPP deletion critical region in 17p11.2-p12.

Lamarck rises from his grave: parental environment-induced epigenetic inheritance in model organisms and humans

MBRidge: an accurate and cost-effective method for profiling DNA methylome at single-base resolution

MPer1 and mper2 are essential for normal resetting of the circadian clock

MagicViewer: integrated solution for next-generation sequencing data visualization and genetic variation detection and annotation

Maternal depression is associated with DNA methylation changes in cord blood T lymphocytes and adult hippocampi

Mutations in WNT10B Are Identified in Individuals with Oligodontia

Mutations of ANK3 identified by exome sequencing are associated with autism susceptibility.

OncoBase: a platform for decoding regulatory somatic mutations in human cancers

PAK2 Haploinsufficiency Results in Synaptic Cytoskeleton Impairment and Autism-Related Behavior

Performance evaluation of pathogenicity-computation methods for missense variants

Population genomics reveals speciation and introgression between Brown Norway rats and their sibling species.

Presence of the pregnant partner regulates microRNA-30a and BDNF levels and protects male mice from social defeat-induced abnormal behaviors

Q-RRBS: a quantitative reduced representation bisulfite sequencing method for single-cell methylome analyses.

RBP-Var: a database of functional variants involved in regulation mediated by RNA-binding proteins

RIGUI, a Putative Mammalian Ortholog of the Drosophila period Gene ⬇️

RRBS-analyser: a comprehensive web server for reduced representation bisulfite sequencing data analysis.

RSPO2-LGR5 signaling has tumour-suppressive activity in colorectal cancer.

Ras-induced epigenetic inactivation of the RRAD (Ras-related associated with diabetes) gene promotes glucose uptake in a human ovarian cancer model.

Recent Progress in CRISPR/Cas9 Technology

Reversal of cocaine-conditioned place preference through methyl supplementation in mice: altering global DNA methylation in the prefrontal cortex

S-adenosyl-methionine (SAM) alters the transcriptome and methylome and specifically blocks growth and invasiveness of liver cancer cells.

Screening for possible oligogenic pathogenesis in Chinese sporadic ALS patients.

Single-cell sequencing technologies: current and future.

Systematic evaluation of genome-wide methylated DNA enrichment using a CpG island array.

TET1 modulates H4K16 acetylation by controlling auto-acetylation of hMOF to affect gene regulation and DNA repair function.

Targeted sequencing and functional analysis reveal brain-size-related genes and their networks in autism spectrum disorders

Targeted sequencing and integrative analysis to prioritize candidate genes in neurodevelopmental disorders

The APP-interacting protein FE65 is required for hippocampus-dependent learning and long-term potentiation.

The Circadian Clock Gene Regulates Gamma Interferon Production of NK Cells in Host Response to Lipopolysaccharide-Induced Endotoxic Shock

The biological basis of sexual orientation: How hormonal, genetic, and environmental factors influence to whom we are sexually attracted

The circadian clock Period 2 gene regulates gamma interferon production of NK cells in host response to lipopolysaccharide-induced endotoxic shock.

Transcriptomic signature associated with carcinogenesis and aggressiveness of papillary thyroid carcinoma

VarCards: an integrated genetic and clinical database for coding variants in the human genome.

Vitamin D-related genes are subjected to significant de novo mutation burdens in autism spectrum disorder

Whole-Genome Sequencing Reveals Genetic Variation in the Asian House Rat.

mirTools: microRNA profiling and discovery based on high-throughput sequencing

mirTrios: an integrated pipeline for detection of de novo and rare inherited mutations from trios-based next-generation sequencing

mirVAFC: A Web Server for Prioritizations of Pathogenic Sequence Variants from Exome Sequencing Data via Classifications.