Author details

Full Name

Xiuqing Guo

Affiliation

ORCID

Career Start Year

1995

Papers

354

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
37178073	Prevalence of Aortic Valve Calcium and the Long-Term Risk of Incident Severe Aortic Stenosis.	JACC Cardiovasc Imaging	2024
37351609	Systemic Markers of Lung Function and Forced Expiratory Volume in 1 Second Decline across Diverse Cohorts.	Ann Am Thorac Soc	2023
35737188	The association between aging-related monocyte transcriptional networks and comorbidity burden: the Multi-Ethnic Study of Atherosclerosis (MESA).	GeroScience	2023
36444934	Whole-exome sequencing study identifies four novel gene loci associated with diabetic kidney disease.	Hum Mol Genet	2023
37848499	Multi-ancestry epigenome-wide analyses identify methylated sites associated with aortic augmentation index in TOPMed MESA.		2023
37756531	Clonal Hematopoiesis of Indeterminate Potential (CHIP) and Incident Type 2 Diabetes Risk.	Diabetes Care	2023
38028628	Gene-educational attainment interactions in a multi-population genome-wide meta-analysis identify novel lipid loci.	Front Genet	2023
37662265	WHOLE GENOME SEQUENCING ANALYSIS OF BODY MASS INDEX IDENTIFIES NOVEL AFRICAN ANCESTRY-SPECIFIC RISK ALLELE.	medRxiv	2023
38014529	Type 2 Diabetes Modifies the Association of CAD Genomic Risk Variants With Subclinical Atherosclerosis.	Circ Genom Precis Med	2023
37923804	Identification of circulating proteins associated with general cognitive function among middle-aged and older adults.	Commun Biol	2023
37582364	Protein-metabolite association studies identify novel proteomic determinants of metabolite levels in human plasma.	Cell Metab	2023
37905118	Determinants of mosaic chromosomal alteration fitness.	medRxiv	2023
37648373	Ancestral diversity in lipoprotein(a) studies helps address evidence gaps.	Open Heart	2023
37904051	Mosaic chromosomal alterations in blood across ancestries using whole-genome sequencing.	Nat Genet	2023
37804200	Association Between Whole Blood-Derived Mitochondrial DNA Copy Number, Low-Density Lipoprotein Cholesterol, and Cardiovascular Disease Risk.	J Am Heart Assoc	2023
37986948	Genome-Wide Interaction Analysis with DASH Diet Score Identified Novel Loci for Systolic Blood Pressure.	medRxiv	2023
37802043	Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed whole-genome sequencing study.	Am J Hum Genet	2023
37709864	Genome-wide association meta-analysis identifies 17 loci associated with nonalcoholic fatty liver disease.	Nat Genet	2023
37968697	Circulating metabolites may illustrate relationship of alcohol consumption with cardiovascular disease.	BMC Med	2023
37961394	Lac-Phe mediates the anti-obesity effect of metformin.	bioRxiv	2023
37868038	The functional impact of rare variation across the regulatory cascade.	Cell Genom	2023
37770635	Multi-ancestry genome-wide study identifies effector genes and druggable pathways for coronary artery calcification.	Nat Genet	2023
37219552	Coronary Artery Calcium Score and Polygenic Risk Score for the Prediction of Coronary Heart Disease Events.	JAMA	2023
37216410	Canonical correlation analysis for multi-omics: Application to cross-cohort analysis.	PLoS Genet	2023
36716967	DNA methylation analysis is used to identify novel genetic loci associated with circulating fibrinogen levels in blood.	J Thromb Haemost	2023
37398015	Circulating Metabolites May Illustrate Relationship of Alcohol Consumption with Cardiovascular Disease.	medRxiv	2023
37398003	Whole genome analysis of plasma fibrinogen reveals population-differentiated genetic regulators with putative liver roles.	medRxiv	2023
37268629	Evaluating the use of blood pressure polygenic risk scores across race/ethnic background groups.	Nat Commun	2023
36882149	Missense Genetic Variation of ICAM1 and Incident Heart Failure.	J Card Fail	2023
36702996	Multi-ancestry transcriptome-wide association analyses yield insights into tobacco use biology and drug repurposing.	Nat Genet	2023
37126548	The genetic determinants of recurrent somatic mutations in 43,693 blood genomes.	Sci Adv	2023
36941441	Causal effects on complex traits are similar for common variants across segments of different continental ancestries within admixed individuals.	Nat Genet	2023
37186683	Association of Severe Hypercholesterolemia and Familial Hypercholesterolemia Genotype With Risk of Coronary Heart Disease.	Circulation	2023
36927883	Association of Mitochondrial DNA Copy Number With Brain MRI Markers and Cognitive Function: A Meta-analysis of Community-Based Cohorts.	Neurology	2023
36735419	OMEGA-3 FATTY ACIDS ARE ASSOCIATED WITH DECREASED PRESENCE AND SEVERITY OF DIABETIC RETINOPATHY: A Combined Analysis of MESA and GOLDR Cohorts.	Retina	2023
37229091	Differences in BMI obesity measures in a workers compensation population: a cross-sectional study.		2023
37046083	Aberrant activation of TCL1A promotes stem cell expansion in clonal haematopoiesis.	Nature	2023
36791419	Investigating Gene-Diet Interactions Impacting the Association Between Macronutrient Intake and Glycemic Traits.	Diabetes	2023
37425772	Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed Whole Genome Sequencing Study.	medRxiv	2023
37292936	Genome-wide association identifies novel ROP risk loci in a multi-ethnic cohort.	Res Sq	2023
36918541	Genetic architecture of spatial electrical biomarkers for cardiac arrhythmia and relationship with cardiovascular disease.	Nat Commun	2023
36723951	Association of Rare Protein-Truncating DNA Variants in APOB or PCSK9 With Low-density Lipoprotein Cholesterol Level and Risk of Coronary Heart Disease.	JAMA Cardiol	2023
37502922	Multi-ancestry epigenome-wide analyses identify methylated sites associated with aortic augmentation index in TOPMed MESA.	Res Sq	2023
37546893	Time-to-Event Genome-Wide Association Study for Incident Cardiovascular Disease in People with Type 2 Diabetes Mellitus.	medRxiv	2023
35085396	Type 2 Diabetes Partitioned Polygenic Scores Associate With Disease Outcomes in 454,193 Individuals Across 13 Cohorts.	Diabetes Care	2022
36048760	Neurocognitive trajectory and proteomic signature of inherited risk for Alzheimer's disease.	PLoS Genet	2022
35592775	The Value of Rare Genetic Variation in the Prediction of Common Obesity in European Ancestry Populations.	Front Endocrinol (Lausanne)	2022
35654975	A multiancestry genome-wide association study of unexplained chronic ALT elevation as a proxy for nonalcoholic fatty liver disease with histological and radiological validation.	Nat Genet	2022
35652341	Insights From a Large-Scale Whole-Genome Sequencing Study of Systolic Blood Pressure, Diastolic Blood Pressure, and Hypertension.	Hypertension	2022
35822943	Targeted Genome Sequencing Identifies Multiple Rare Variants inÂ Caveolin-1 Associated with Obstructive Sleep Apnea.	Am J Respir Crit Care Med	2022