Author details

Full Name

Xiaohui Li

Affiliation

ORCID

Career Start Year

2003

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
37292936	Genome-wide association identifies novel ROP risk loci in a multi-ethnic cohort.	Res Sq	2023
36931367	Results of corneal collagen cross-linking in patients with corneal ectasia after laser refractive surgery-A prospective study.		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
35069183	The Pharmacogenetics of Statin Therapy on Clinical Events: No Evidence that Genetic Variation Affects Statin Response on Myocardial Infarction.	Front Pharmacol	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
36220816	Whole genome sequence analysis of blood lipid levels in >66,000 individuals.	Nat Commun	2022
36268164	Erratum: Ancestral diversity improves discovery and fine-mapping of genetic loci for anthropometric traits-The Hispanic/Latino Anthropometry Consortium.	HGG Adv	2022
35659450	Erratum to Gene Set Enrichment Analyses Identify Pathways Involved in Genetic Risk for Diabetic Retinopathy. Am J Ophthalmol 2022;233:111-123.	Am J Ophthalmol	2022
35399580	Ancestral diversity improves discovery and fine-mapping of genetic loci for anthropometric traits-The Hispanic/Latino Anthropometry Consortium.	HGG Adv	2022
34166655	Gene Set Enrichment Analsyes Identify Pathways Involved in Genetic Risk for Diabetic Retinopathy.	Am J Ophthalmol	2022
34849546	Clinical and biomarker modifiers of vitamin D treatment response: the Multi-Ethnic Study of Atherosclerosis.	Am J Clin Nutr	2022
34721828	Meta-Analysis Study on Treatment of Children's Attention Deficit Disorder with Hyperactivity.	Journal of Healthcare Engineering	2021
33588078	The Multi-Ethnic Study of Atherosclerosis individual response to vitamin D trial: Building a randomized clinical trial into an observational cohort study.	Contemp Clin Trials	2021
33769766	Results of corneal crosslinking in adolescents with progressive keratoconus: prospective study.	Journal of Cataract and Refractive Surgery	2021
33654115	Identification of candidate genes and pathways in retinopathy of prematurity by whole exome sequencing of preterm infants enriched in phenotypic extremes.	Sci Rep	2021
33649486	A multi-ethnic genome-wide association study implicates collagen matrix integrity and cell differentiation pathways in keratoconus.	Commun Biol	2021
31855235	Association of Genetic Variation With Keratoconus.	JAMA Ophthalmol	2020
30779634	Common Genetic Variation in Relation to Brachial Vascular Dimensions and Flow-Mediated Vasodilation.	Circ Genom Precis Med	2019
31852976	PPIP5K2 and PCSK1 are Candidate Genetic Contributors to Familial Keratoconus.	Sci Rep	2019
30487263	Multiethnic Genome-Wide Association Study of Diabetic Retinopathy Using Liability Threshold Modeling of Duration of Diabetes and Glycemic Control.	Diabetes	2019
27958378	Large-scale pharmacogenomic study of sulfonylureas and the QT, JT and QRS intervals: CHARGE Pharmacogenomics Working Group.	Pharmacogenomics J	2018
30250936	The genetics of retinopathy of prematurity: a model for neovascular retinal disease.	Ophthalmol Retina	2018
30388399	Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders.	Am J Hum Genet	2018
30178632	A genome-wide association study suggests new evidence for an association of the NADPH Oxidase 4 (NOX4) gene with severe diabetic retinopathy in type 2 diabetes.	Acta Ophthalmol	2018
29703846	LPA Variants Are Associated With Residual Cardiovascular Risk in Patients Receiving Statins.	Circulation	2018
27911294	Deleterious Effect of Butyrylcholinesterase K-Variant in Donepezil Treatment of Mild Cognitive Impairment.	J Alzheimers Dis	2017
28768753	<i>PCSK9</i> Loss-of-Function Variants, Low-Density Lipoprotein Cholesterol, and Risk of Coronary Heart Disease and Stroke: Data From 9 Studies of Blacks and Whites.	Circ Cardiovasc Genet	2017
28951389	Genetically Determined Plasma Lipid Levels and Risk of Diabetic Retinopathy: A Mendelian Randomization Study.	Diabetes	2017
28039329	A genome-wide interaction analysis of tricyclic/tetracyclic antidepressants and RR and QT intervals: a pharmacogenomics study from the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) consortium.	J Med Genet	2017
24555746	Linkage Analysis of High-density SNPs Confirms Keratoconus Locus at 5q Chromosomal Region.	Ophthalmic Genetics	2016
27020472	Meta-analysis of gene-environment-wide association scans accounting for education level identifies additional loci for refractive error.	Nat Commun	2016
27321945	Trans-ethnic Meta-analysis and Functional Annotation Illuminates theÂ Genetic Architecture of Fasting Glucose and Insulin.	Am J Hum Genet	2016
26896123	Incidence of Age-Related Macular Degeneration in a Multi-Ethnic United States Population: The Multi-Ethnic Study of Atherosclerosis.	Ophthalmology	2016
26567291	Novel Genetic Loci Associated With Retinal Microvascular Diameter.	Circ Cardiovasc Genet	2016
27648687	Rooted in risk: genetic predisposition for low-density lipoprotein cholesterol level associates with diminished low-density lipoprotein cholesterol response to statin treatment.	Pharmacogenomics	2016
27722758	Comparison of the Effect of Epithelial Removal by Transepithelial Phototherapeutic Keratectomy or Manual Debridement on Cross-linking Procedures for Progressive Keratoconus.	Journal of Refractive Surgery	2016
27587472	Meta-analysis of genome-wide association studies of HDL cholesterol response to statins.	J Med Genet	2016
27618452	The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals.	Nat Genet	2016
26516778	Drug-Gene Interactions of Antihypertensive Medications and Risk of Incident Cardiovascular Disease: A Pharmacogenomics Study from the CHARGE Consortium.	PLoS One	2015
25373792	Independent origin of c.57 Câ¿¿>â¿¿T mutation in MIR184 associated with inherited corneal and lens abnormalities.	Ophthalmic Genet	2015
25968104	HIV infection is associated with an increased prevalence of coronary noncalcified plaque among participants with a coronary artery calcium score of zero: Multicenter AIDS Cohort Study (MACS).	HIV Med	2015
26098467	African Ancestry Analysis and Admixture Genetic Mapping for Proliferative Diabetic Retinopathy in African Americans.	Invest Ophthalmol Vis Sci	2015
24763472	Optical coherence tomography combined with videokeratography to differentiate mild keratoconus subtypes.	Journal of Refractive Surgery	2014
25350695	Pharmacogenetic meta-analysis of genome-wide association studies of LDL cholesterol response to statins.	Nat Commun	2014
23459443	Drug-gene interactions and the search for missing heritability: a cross-sectional pharmacogenomics study of the QT interval.	Pharmacogenomics J	2014
25233373	Genome-wide meta-analysis of myopia and hyperopia provides evidence for replication of 11 loci.	PLoS One	2014
23449483	An association between the calpastatin (CAST) gene and keratoconus.	Cornea	2013
23776548	Genetic loci for retinal arteriolar microcirculation.	PLoS One	2013
24075760	No association of 9p21 with arterial elasticity and retinal microvascular findings.	Atherosclerosis	2013
23938121	Associations of candidate genes to age-related macular degeneration among racial/ethnic groups in the multi-ethnic study of atherosclerosis.	Am J Ophthalmol	2013