Author details

Full Name

Xihao Li

Affiliation

ORCID

Career Start Year

2018

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
37425772	Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed Whole Genome Sequencing Study.	medRxiv	2023
36350676	FAVOR: functional annotation of variants online resource and annotator for variation across the human genome.	Nucleic Acids Res	2023
37857625	Author Correction: Whole-Genome Sequencing Analysis of Human Metabolome in Multi-Ethnic Populations.	Nat Commun	2023
37745480	Whole Genome Sequencing Based Analysis of Inflammation Biomarkers in the Trans-Omics for Precision Medicine (TOPMed) Consortium.	bioRxiv	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
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
37961350	A statistical framework for powerful multi-trait rare variant analysis in large-scale whole-genome sequencing studies.	bioRxiv	2023
37253714	Whole-Genome Sequencing Analysis of Human Metabolome in Multi-Ethnic Populations.	Nat Commun	2023
35216679	A multi-dimensional integrative scoring framework for predicting functional variants in the human genome.	Am J Hum Genet	2022
35441669	STAAR workflow: a cloud-based workflow for scalable and reproducible rare variant analysis.	Bioinformatics	2022
36220816	Whole genome sequence analysis of blood lipid levels in >66,000 individuals.	Nat Commun	2022
35915169	Cross-ancestry genome-wide meta-analysis of 61,047 cases and 947,237 controls identifies new susceptibility loci contributing to lung cancer.	Nat Genet	2022
34986354	Spatiotemporal patterns of neuronal subtype genesis suggest hierarchical development of retinal diversity.	Cell Rep	2022
34496678	Surgical Survival Benefits With Different Metastatic Patterns for Stage IV Extrathoracic Metastatic Non-Small Cell Lung Cancer: A SEER-Based Study.	Technology in Cancer Research and Treatment	2021
33507253	Utility of Restricted Mean Survival Time for Analyzing Time to Nursing Home Placement Among Patients With Dementia.	JAMA network open	2021
33653773	Association between Smoking History and Tumor Mutation Burden in Advanced Non-Small Cell Lung Cancer.	Cancer Res	2021
32924180	Integration of multiomic annotation data to prioritize and characterize inflammation and immune-related risk variants in squamous cell lung cancer.	Genet Epidemiol	2021
33170346	Correction to: Shared genetic architecture between metabolic traits and Alzheimer's disease: a large-scale genome-wide cross-trait analysis.	Human Genetics	2021
30805717	Shared genetic architecture between metabolic traits and Alzheimer's disease: a large-scale genome-wide cross-trait analysis.	Human Genetics	2019
30982610	Dynamic Scan Procedure for Detecting Rare-Variant Association Regions in Whole-Genome Sequencing Studies.	Am J Hum Genet	2019
29288389	Principles and methods of in-silico prioritization of non-coding regulatory variants.	Hum Genet	2018