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Author Details
Full Name
Yafang Li
Affiliation
University of Michigan ann arbor
ORCID
Career Start Year
2010
Papers
41
H Index
18
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
37150255
Mosaic Chromosomal Alterations Are Associated With Increased Lung Cancer Risk: Insight From the INTEGRAL-ILCCO Cohort Analysis.
J Thorac Oncol
2023
35138370
Genome-wide interaction analysis identified low-frequency variants with sex disparity in lung cancer risk.
Hum Mol Genet
2022
35500836
A Large-Scale Genome-Wide Gene-Gene Interaction Study of Lung Cancer Susceptibility in Europeans With a Trans-Ethnic Validation in Asians.
J Thorac Oncol
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
35272635
Genetic variants associated mRNA stability in lung.
BMC Genomics
2022
34932879
Epigenome-wide three-way interaction study identifies a complex pattern between TRIM27, KIAA0226, and smoking associated with overall survival of early-stage NSCLC.
Mol Oncol
2022
33594163
Rare deleterious germline variants and risk of lung cancer.
NPJ Precis Oncol
2021
33853833
Genetic Variation and Recurrent Haplotypes on Chromosome 6q23-25 Risk Locus in Familial Lung Cancer.
Cancer Res
2021
32855268
Genetics of Smoking Behaviors in American Indians.
Cancer Epidemiol Biomarkers Prev
2020
31826912
Whole Exome Sequencing of Highly Aggregated Lung Cancer Families Reveals Linked Loci for Increased Cancer Risk on Chromosomes 12q, 7p, and 4q.
Cancer Epidemiol Biomarkers Prev
2020
30956756
Genetic interaction analysis among oncogenesis-related genes revealed novel genes and networks in lung cancer development.
Oncotarget
2019
29293537
Gene-level association analysis of systemic sclerosis: A comparison of African-Americans and White populations.
PLoS One
2018
30104567
Identification of susceptibility pathways for the role of chromosome 15q25.1 in modifying lung cancer risk.
Nat Commun
2018
30254314
Fine mapping of MHC region in lung cancer highlights independent susceptibility loci by ethnicity.
Nat Commun
2018
29924316
Genome-wide association study of familial lung cancer.
Carcinogenesis
2018
29059373
Genome-wide interaction study of smoking behavior and non-small cell lung cancer risk in Caucasian population.
Carcinogenesis
2018
27697780
The OncoArray Consortium: A Network for Understanding the Genetic Architecture of Common Cancers.
Cancer Epidemiol Biomarkers Prev
2017
28106732
Familial Lung Cancer: A Brief History from the Earliest Work to the Most Recent Studies.
Genes (Basel)
2017
28426704
Population effect model identifies gene expression predictors of survival outcomes in lung adenocarcinoma for both Caucasian and Asian patients.
PLoS One
2017
29088810
Genetic variants of PDGF signaling pathway genes predict cutaneous melanoma survival.
Oncotarget
2017
28510328
Genetic variants in the genes encoding rho GTPases and related regulators predict cutaneous melanoma-specific survival.
Int J Cancer
2017
28927378
Genome-wide imaging association study implicates functional activity and glial homeostasis of the caudate in smoking addiction.
BMC Genomics
2017
28604730
Large-scale association analysis identifies new lung cancer susceptibility loci and heterogeneity in genetic susceptibility across histological subtypes.
Nat Genet
2017
26961892
FastPop: a rapid principal component derived method to infer intercontinental ancestry using genetic data.
BMC Bioinformatics
2016
28817824
Parametric Linkage Analysis Identifies Five Novel Genome-Wide Significant Loci for Familial Lung Cancer.
Hum Hered
2016
26382192
Component-wise gradient boosting and false discovery control in survival analysis with high-dimensional covariates.
Bioinformatics
2016
26590902
Fine mapping of chromosome 5p15.33 based on a targeted deep sequencing and high density genotyping identifies novel lung cancer susceptibility loci.
Carcinogenesis
2016
27578485
Genetic variants in the PIWI-piRNA pathway gene DCP1A predict melanoma disease-specific survival.
Int J Cancer
2016
25804397
Deciphering associations for lung cancer risk through imputation and analysis of 12,316 cases and 16,831 controls.
Eur J Hum Genet
2015
26327458
RNA-Seq Analysis of Differential Splice Junction Usage and Intron Retentions by DEXSeq.
PLoS One
2015
26394269
International genome-wide meta-analysis identifies new primary biliary cirrhosis risk loci and targetable pathogenic pathways.
Nat Commun
2015
26363033
Identification of lung cancer histology-specific variants applying Bayesian framework variant prioritization approaches within the TRICL and ILCCO consortia.
Carcinogenesis
2015
26282330
The role of haplotype in 15q25.1 locus in lung cancer risk: results of scanning chromosome 15.
Carcinogenesis
2015
26081616
RNA-seq analysis of lung adenocarcinomas reveals different gene expression profiles between smoking and nonsmoking patients.
Tumour Biol
2015
25644374
Informed genome-wide association analysis with family history as a secondary phenotype identifies novel loci of lung cancer.
Genet Epidemiol
2015
25640678
A recurrent mutation in PARK2 is associated with familial lung cancer.
Am J Hum Genet
2015
25329654
Role of a genetic variant on the 15q25.1 lung cancer susceptibility locus in smoking-associated nasopharyngeal carcinoma.
PLoS One
2014
23094028
Genetic association analysis of complex diseases incorporating intermediate phenotype information.
PLoS One
2012
22936693
Immunochip analyses identify a novel risk locus for primary biliary cirrhosis at 13q14, multiple independent associations at four established risk loci and epistasis between 1p31 and 7q32 risk variants.
Hum Mol Genet
2012
20215501
A susceptibility locus on chromosome 6q greatly increases lung cancer risk among light and never smokers.
Cancer Res
2010
21030603
Ordered subset analysis identifies loci influencing lung cancer risk on chromosomes 6q and 12q.
Cancer Epidemiol Biomarkers Prev
2010
1 - 41 of 41
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