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List of works by Chao Xing

A CRISPR screen identifies IFI6 as an ER-resident interferon effector that blocks flavivirus replication

scientific article published on 17 September 2018

A Comparison of Approaches to Control for Confounding Factors by Regression Models ⬇️

scientific article published on November 11, 2011

A Comparison of the Likelihood Ratio Test and the Variance‐Stabilising Transformation‐Based Tests for Detecting Association of Rare Variants ⬇️

scientific article published on March 14, 2013

A NIK-SIX signalling axis controls inflammation by targeted silencing of non-canonical NF-κB

scientific article published on 20 March 2019

A calcineurin–Hoxb13 axis regulates growth mode of mammalian cardiomyocytes

scientific article published on 22 April 2020

A comprehensively characterized cell line panel highly representative of clinical ovarian high-grade serous carcinomas

scientific article published on 10 June 2016

A logistic mixture model for a family-based association study

scientific article

A methionine-Mettl3-N<sup>6</sup>-methyladenosine axis promotes polycystic kidney disease

scientific article published on 13 April 2021

A novel ZRS variant causes preaxial polydactyly type I by increased sonic hedgehog expression in the developing limb bud

scientific article published on 09 August 2019

A novel autosomal recessive lipodystrophy syndrome due to homozygous LMNA variant

scientific article published on 19 December 2019

A novel de novo KIF21A mutation in a patient with congenital fibrosis of the extraocular muscles and Möbius syndrome

scientific article published on 28 March 2014

A novel germline mutation in BAP1 predisposes to familial clear-cell renal cell carcinoma.

scientific article

A weighted false discovery rate control procedure reveals alleles at FOXA2 that influence fasting glucose levels

scientific article

Adjusting for covariates in logistic regression models ⬇️

scientific article published on November 1, 2010

Admixture mapping of 15,280 African Americans identifies obesity susceptibility loci on chromosomes 5 and X.

scientific article published on 22 May 2009

Adult-onset liver disease and hepatocellular carcinoma in S-adenosylhomocysteine hydrolase deficiency

scientific article published on 26 October 2015

Adult-onset pulmonary fibrosis caused by mutations in telomerase

scholarly article

Aggressive Behavior in Silent Subtype III Pituitary Adenomas May Depend on Suppression of Local Immune Response: A Whole Transcriptome Analysis

scientific article published in October 2017

An East Asian-specific Common Variant in TNNI3 Predisposes to Hypertrophic Cardiomyopathy

scientific article published on 20 October 2020

Analysis of recent shared ancestry in a familial cohort identifies coding and noncoding autism spectrum disorder variants

scientific article published on 21 February 2022

Analyzing pre-symptomatic tissue to gain insights into the molecular and mechanistic origins of late-onset degenerative trinucleotide repeat disease

scientific article published on 28 May 2020

Androgen Receptor Variants Mediate DNA Repair after Prostate Cancer Irradiation.

scientific article published on 28 July 2017

Another Look at Hereditary Partial Androgen Insensitivity Syndrome in an Indigenous Community in the Northern Territory of Australia

scientific article published in December 2017

Association and familial segregation of CTG18.1 trinucleotide repeat expansion of TCF4 gene in Fuchs' endothelial corneal dystrophy

scientific article published on 02 January 2014

BRD4 Promotes DNA Repair and Mediates the Formation of TMPRSS2-ERG Gene Rearrangements in Prostate Cancer.

scientific article published in January 2018

Bi-allelic POLR3A Loss-of-Function Variants Cause Autosomal-Recessive Wiedemann-Rautenstrauch Syndrome

scientific article published on 07 November 2018

Blindly Using Wald's Test Can Miss Rare Disease‐Causal Variants in Case‐Control Association Studies ⬇️

scientific article published on January 18, 2012

CCR2<sup>+</sup> Macrophages Promote Orthodontic Tooth Movement and Alveolar Bone Remodeling

scientific article published on 04 February 2022

CHD4 promotes breast cancer progression as a coactivator of hypoxia-inducible factors

scientific article published on 22 July 2020

Cellular abundance of sodium phosphate cotransporter SLC20A1/PiT1 and phosphate uptake are controlled post-transcriptionally by ESCRT

scientific article published on 18 April 2022

Chemical intervention of influenza virus mRNA nuclear export

scientific article published on 02 April 2020

Chronic IL-1 Exposed AR<sup>+</sup> PCa Cell Lines Show Conserved Loss of IL-1 Sensitivity and Evolve Both Conserved and Unique Differential Gene Expression Profiles

scientific article published on 01 December 2021

Comparison of microsatellites, single-nucleotide polymorphisms (SNPs) and composite markers derived from SNPs in linkage analysis

scientific article published on 30 December 2005

Comparison of missing data approaches in linkage analysis

scientific article

Complement factor H polymorphisms, renal phenotypes and age-related macular degeneration: the Blue Mountains Eye Study

scientific article published on 13 March 2008

Controlled Ovarian Stimulation Protocols Alter Endometrial Histomorphology and Gene Expression Profiles

scientific article published on 06 January 2020

Correlation of Severity of Fuchs Endothelial Corneal Dystrophy With Triplet Repeat Expansion in TCF4.

scientific article published on 24 September 2015

DNA polymerase-α regulates the activation of type I interferons through cytosolic RNA:DNA synthesis

scientific article

De novo heterozygous FBN1 mutations in the extreme C-terminal region cause progeroid fibrillinopathy.

scientific article

Decomposing Pearson's χ test: A linear regression and its departure from linearity

scholarly article by Zhengyang Zhou et al published September 2018 in Annals of Human Genetics

Dermal adipose tissue has high plasticity and undergoes reversible dedifferentiation in mice

scientific article published on 01 December 2019

Differentiating the Cochran-Armitage Trend Test and Pearson's χ2 Test: Location and Dispersion

scientific article published on 27 June 2017

Distribution and magnitude of type I error of model-based multipoint lod scores: implications for multipoint mod scores

scientific article

Distribution of model-based multipoint heterogeneity lod scores

scientific article

EGFR ligand shifts the role of EGFR from oncogene to tumour suppressor in EGFR-amplified glioblastoma by suppressing invasion through BIN3 upregulation

scientific article published in 2022

Eating disorder predisposition is associated with ESRRA and HDAC4 mutations

scientific article

Enhancing the power to detect low-frequency variants in genome-wide screens

scientific article published on 04 February 2014

Epigenetic inheritance of telomere length obscures identification of causative PARN locus

scientific article published on 23 February 2016

EspFu-Mediated Actin Assembly Enhances Enteropathogenic Escherichia coli Adherence and Activates Host Cell Inflammatory Signaling Pathways

scientific article published on 14 April 2020

Exome sequencing links mutations in PARN and RTEL1 with familial pulmonary fibrosis and telomere shortening

scientific article published on 13 April 2015

Exome sequencing reveals novel homozygous FOXE3 mutation in microphthalmos with staphylomatous malformation

scientific article published on 26 September 2016

Fbxw7 is a driver of uterine carcinosarcoma by promoting epithelial-mesenchymal transition

scientific article published on 26 November 2019

Forward genetic analysis using OCT screening identifies Sfxn3 mutations leading to progressive outer retinal degeneration in mice

scientific article published on 26 May 2020

Fuchs' Endothelial Corneal Dystrophy and RNA Foci in Patients With Myotonic Dystrophy

scientific article published on September 2017

Gender and telomere length: systematic review and meta-analysis

scientific article published on 21 December 2013

Genetic and Epigenetic Features of Rapidly Progressing IDH-Mutant Astrocytomas

scientific article published on 01 July 2018

Genetic defects in surfactant protein A2 are associated with pulmonary fibrosis and lung cancer.

scientific article

Genetic linkage of systemic lupus erythematosus to 13q32 in African American families with affected male members.

scientific article published on 28 September 2005

Genetic variant I148M in PNPLA3 is associated with the ultrasonography-determined steatosis degree in a Chinese population

scientific article

Genetic variant in PNPLA3 is associated with nonalcoholic fatty liver disease in China

scientific article published on January 2012

Genetics and bitter taste responses to goitrin, a plant toxin found in vegetables

scientific article

Genome editing in the unicellular holozoan <i>Capsaspora owczarzaki</i> suggests a premetazoan role for the Hippo pathway in multicellular morphogenesis

scientific article published on 06 June 2022

Genome-Wide Analysis of Glioblastoma Patients with Unexpectedly Long Survival

scientific article published on 01 June 2019

Genome-wide association analysis of radiation resistance in Drosophila melanogaster

scientific article

Genome-wide linkage study of retinal vessel diameters in the Beaver Dam Eye Study

scientific article published on 27 February 2006

Genomic, genetic and functional dissection of bitter taste responses to artificial sweeteners

article

HIF2-Induced Long Noncoding RNA RAB11B-AS1 Promotes Hypoxia-Mediated Angiogenesis and Breast Cancer Metastasis

scientific article published on 03 January 2020

Hand2 Selectively Reorganizes Chromatin Accessibility to Induce Pacemaker-like Transcriptional Reprogramming

scientific article published on 01 May 2019

Hepatic GALE Regulates Whole-Body Glucose Homeostasis by Modulating Tff3 Expression.

scientific article

Hereditary lung cancer syndrome targets never smokers with germline EGFR gene T790M mutations

scientific article

Heterogeneous origins and functions of mouse skeletal muscle-resident macrophages

scientific article published on 13 August 2020

Heterozygous Cystic Fibrosis Transmembrane Regulator Gene Missense Variants Are Associated With Worse Cardiac Function in Patients With Duchenne Muscular Dystrophy

scientific article published on 02 October 2020

Homozygosity mapping identifies a bile acid biosynthetic defect in an adult with cirrhosis of unknown etiology

scientific article published on 08 February 2012

Homozygous LIPE mutation in siblings with multiple symmetric lipomatosis, partial lipodystrophy, and myopathy.

scientific article published on 11 November 2016

Homozygous Rare PARN Missense Mutation in Familial Pulmonary Fibrosis

scientific article published on 01 March 2019

Hypoxia fate mapping identifies cycling cardiomyocytes in the adult heart

scientific article

Hypoxia induces heart regeneration in adult mice

scientific article published on 31 October 2016

IL-1-conferred gene expression pattern in ERα+ BCa and AR+ PCa cells is intrinsic to ERα- BCa and AR- PCa cells and promotes cell survival

scientific article published on 20 January 2020

Identification of an IL-1-induced gene expression pattern in AR PCa cells that mimics the molecular phenotype of AR PCa cells

article

Identification of the Underlying Androgen Receptor Defect in the Dallas Reifenstein Family

scientific article published on 19 May 2017

Instability of TCF4 Triplet Repeat Expansion With Parent-Child Transmission in Fuchs' Endothelial Corneal Dystrophy

article

Interleukin-22 regulates B3GNT7 expression to induce fucosylation of glycoproteins in intestinal epithelial cells

scientific article published on 02 December 2021

Intersection of DNA privacy and whole-genome sequencing.

scientific article published on 5 February 2015

Juvenile-onset generalized lipodystrophy due to a novel heterozygous missense LMNA mutation affecting lamin C.

scientific article published on 7 July 2017

LPA Gene, Ethnicity, and Cardiovascular Events

scientific article published on 9 November 2016

Letter To The Glycoforum: The Lec5 Glycosylation Mutant Links Homeobox Genes with Cholesterol and Lipid-Linked Oligosaccharides

article

Linkage analysis of alcohol dependence using both affected and discordant sib pairs

scientific article published on 30 December 2005

Linkage studies of catechol-O-methyltransferase (COMT) and dopamine-beta-hydroxylase (DBH) cDNA expression levels

scientific article

LncIHAT is induced by hypoxia-inducible factor 1 and promotes breast cancer progression

scientific article published on 30 December 2020

Localization and replication of the systemic lupus erythematosus linkage signal at 4p16: interaction with 2p11, 12q24 and 19q13 in European Americans

article

Long noncoding RNA Hoxb3os is dysregulated in autosomal dominant polycystic kidney disease and regulates mTOR signaling.

scientific article

MCM2-7-dependent cohesin loading during S phase promotes sister-chromatid cohesion

scientific article published on 3 April 2018

MicroRNA-21 Aggravates Cyst Growth in a Model of Polycystic Kidney Disease

scientific article published on 17 December 2015

Minimum Information about a Genotyping Experiment (MIGEN).

scientific article

Mitotic Checkpoint Regulators Control Insulin Signaling and Metabolic Homeostasis

scientific article published on 29 June 2016

Molecular Correlates of Long Survival in IDH-Wildtype Glioblastoma Cohorts

scientific article published on 10 July 2020

Multiple independent genetic factors at NOS1AP modulate the QT interval in a multi-ethnic population

scientific article

Multisystem Progeroid Syndrome With Lipodystrophy, Cardiomyopathy, and Nephropathy Due to an LMNA p.R349W Variant

scientific article published on 27 July 2020

Oligonucleotides Targeting TCF4 Triplet Repeat Expansion Inhibit RNA Foci and Mis-splicing in Fuchs' Dystrophy

scientific article

Overcoming the Odds: Toward a Molecular Profile of Long-Term Survival in Glioblastoma

scientific article published on 01 October 2020

PAN-INTACT enables direct isolation of lineage-specific nuclei from fibrous tissues

scientific article published on 02 April 2019

PSMB8 encoding the β5i proteasome subunit is mutated in joint contractures, muscle atrophy, microcytic anemia, and panniculitis-induced lipodystrophy syndrome

scientific article

Power of Genetic Association Studies with Fixed and Random Genotype Frequencies

article

Power of selective genotyping in genome-wide association studies of quantitative traits

scientific article

Prostaglandin dehydrogenase is a target for successful induction of cervical ripening

scientific article

Prune belly syndrome in surviving males can be caused by Hemizygous missense mutations in the X-linked Filamin A gene

scientific article published on 21 February 2020

RELA is sufficient to mediate interleukin-1 repression of androgen receptor expression and activity in an LNCaP disease progression model

scientific article published on 15 November 2019

RIPK1 dephosphorylation and kinase activation by PPP1R3G/PP1γ promote apoptosis and necroptosis

scientific article published on 03 December 2021

Rare Pathogenic Variants Predispose to Hepatocellular Carcinoma in Nonalcoholic Fatty Liver Disease

scientific article published on 06 March 2019

Rare coding variants in MAPK7 predispose to adolescent idiopathic scoliosis

scientific article published on 17 July 2017

Refined mapping of X-linked reticulate pigmentary disorder and sequencing of candidate genes

scientific article

SOX4-mediated repression of specific tRNAs inhibits proliferation of human glioblastoma cells

scientific article published on 02 March 2020

SRC-2-mediated coactivation of anti-tumorigenic target genes suppresses MYC-induced liver cancer

scientific article

Single-nucleotide polymorphisms in LPA explain most of the ancestry-specific variation in Lp(a) levels in African Americans

scientific article

Subclinical lung disease, macrocytosis, and premature graying in kindreds with telomerase (TERT) mutations

scientific article

Summary of Genetic Analysis Workshop 15: Group 9 linkage analysis of the CEPH expression data

scientific article published on January 2007

Suppression of the SWI/SNF Component Arid1a Promotes Mammalian Regeneration

scientific article

TCF4 Triplet Repeat Expansion and Nuclear RNA Foci in Fuchs' Endothelial Corneal Dystrophy

scientific article

TP53 promotes lineage commitment of human embryonic stem cells through ciliogenesis and sonic hedgehog signaling

scientific article published on 01 February 2022

Targeting TGFβR2-mutant tumors exposes vulnerabilities to stromal TGFβ blockade in pancreatic cancer

scientific article published on 14 October 2019

Telomere lengths, pulmonary fibrosis and telomerase (TERT) mutations

scientific article

Telomere shortening in familial and sporadic pulmonary fibrosis

scientific article published on 17 July 2008

The IFN Response in Bats Displays Distinctive IFN-Stimulated Gene Expression Kinetics with Atypical RNASEL Induction.

scientific article published on 27 November 2017

The affected-/discordant-sib-pair design can guarantee validity of multipoint model-free linkage analysis of incomplete pedigrees when there is marker-marker disequilibrium

scientific article

The cytotoxic type 3 secretion system 1 of Vibrio rewires host gene expression to subvert cell death and activate cell survival pathways

scientific article published on 16 May 2017

The landscape of RNA polymerase II associated chromatin interactions in prostate cancer

scientific article published on 28 April 2020

The rs2294918 E434K variant modulates patatin-like phospholipase domain-containing 3 expression and liver damage

scientific article published on 14 January 2016

Thrombin Alters Human Endometrial Stromal Cell Differentiation During Decidualization.

scientific article published in January 2018

Total copy number variation as a prognostic factor in adult astrocytoma subtypes.

scientific article published on 10 June 2019

Total copy number variation, somatic mutation burden, and histologic grade correlate with clinical outcome in oligodendroglioma

scientific article published on 08 March 2020

Transethnic replication of association of CTG18.1 repeat expansion of TCF4 gene with Fuchs' corneal dystrophy in Chinese implies common causal variant

scientific article

Transmembrane 6 superfamily member 2 gene variant disentangles nonalcoholic steatohepatitis from cardiovascular disease

scientific article published in February 2015

Type 1 Hyperlipoproteinemia Due to Compound Heterozygous Rare Variants in GCKR.

scientific article published on 12 July 2016

Type 1 hyperlipoproteinemia in a child with large homozygous deletion encompassing GPIHBP1.

scientific article

Using arterial-venous analysis to characterize cancer metabolic consumption in patients

scientific article published on 23 June 2020

Whole-exome sequencing identifies ADRA2A mutation in atypical familial partial lipodystrophy

scientific article published on June 2016

Y chromosome gene copy number and lack of autism phenotype in a male with an isodicentric Y chromosome and absent NLGN4Y expression

scientific article published on 03 June 2019

ZMYND8 acetylation mediates HIF-dependent breast cancer progression and metastasis

article published in 2018

eIF5B drives integrated stress response-dependent translation of PD-L1 in lung cancer

scientific article published on 20 April 2020

ΔNp63α induces the expression of FAT2 and Slug to promote tumor invasion

scientific article published on 12 April 2016

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