Author details

Full Name

Zilin Li

Affiliation

ORCID

Career Start Year

2012

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
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
34780860	Leisure sedentary time and suicide risk among young adolescents: Data from 54 low- and middle-income countries.	Journal of Affective Disorders	2022
35845434	Simultaneous Detection of Signal Regions Using Quadratic Scan Statistics With Applications to Whole Genome Association Studies.	J Am Stat Assoc	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
36538421	Cigarette access and purchase patterns among adolescent smokers aged 12-16 years in 140 countries/territories, Global Youth Tobacco Survey 2010-2018.		2022
35216679	A multi-dimensional integrative scoring framework for predicting functional variants in the human genome.	Am J Hum Genet	2022
34571047	Global trends in the prevalence of secondhand smoke exposure among adolescents aged 12-16 years from 1999 to 2018: an analysis of repeated cross-sectional surveys.	Lancet Global Health,The	2021
33545071	Prevalence and trends in tobacco use among adolescents aged 13-15 years in 143 countries, 1999-2018: findings from the Global Youth Tobacco Surveys.		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
32589645	Exploring the young demographic profile of COVID-19 cases in Hong Kong: Evidence from migration and travel history data.	PLoS ONE	2020
31209392	Genome sequencing analysis identifies Epstein-Barr virus subtypes associated with high risk of nasopharyngeal carcinoma.	Nat Genet	2019
30982610	Dynamic Scan Procedure for Detecting Rare-Variant Association Regions in Whole-Genome Sequencing Studies.	Am J Hum Genet	2019
30849328	ACAT: A Fast and Powerful p Value Combination Method for Rare-Variant Analysis in Sequencing Studies.	Am J Hum Genet	2019
26229047	Test for rare variants by environment interactions in sequencing association studies.	Biometrics	2016
27018471	Control for Population Structure and Relatedness for Binary Traits in Genetic Association Studies via Logistic Mixed Models.	Am J Hum Genet	2016
23519603	Variable selection and estimation in generalized linear models with the seamless <i>L</i><sub>0</sub> penalty.	Can J Stat	2012