Author

Dejian Yuan

Central South UniversityORCID 0000-0001-9884-2158Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Cancer Biology· 1 Evolutionary Biology· 1 Genomics· 1

Signature Assays, Organisms & Methods

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Organism:human· 3 Approach:statistical model· 3 Research Focus:gene regulatory network inference· 2 Research Focus:cell type annotation· 1 Research Focus:chromatin & epigenetic regulation· 1 Research Focus:differential expression· 1 Assay:DNA methylation· 1 Assay:GWAS summary statistics· 1

Frequent Co-Authors

Shi HuangiD· 3 shared Zuobin ZhuiD· 2 shared Xiaoyun Lei· 1 shared Xitong Lu· 1 shared

Activity by Year

2016-2018 · peak 1/yr

Co-Author Collaboration Network

4 top collaborators · 5 mutual co-author links

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3 shared papersEvolutionary Biology

Shi HuangORCID

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3 papers

Recent·Most cited

Evolutionary BiologybioRxivPreprintAug 23, 2018

On The Peopling Of The Americas: Molecular Evidence For The Paleoamerican And The Solutrean Models

Dejian Yuan, Shi Huang

The paper reanalyzes public DNA data to assess the Paleoamerican and Solutrean models for the peopling of the Americas, finding genetic links between ancient and modern populations.

DOI 10.1101/130989

humanDNA methylation

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Cancer BiologybioRxivPreprintFeb 8, 2017

Collective effects of common SNPs and improved risk prediction in lung cancer

Xiaoyun Lei, Dejian Yuan, Zuobin Zhu, Shi Huang

The paper identifies a set of SNPs with higher minor allele content in lung cancer cases, leading to a predictive risk score that identifies 2.6% of cases with 100% specificity.

DOI 10.1101/106864

humanGWAS summary statistics

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GenomicsGenomicsPeer-reviewedDec 9, 2016

Close genetic relationships between a spousal pair with autism-affected children and high minor allele content in cases in autism-associated SNPs

Zuobin Zhu, Xitong Lu, Dejian Yuan, Shi Huang

The paper examines genetic relationships in ASD trios, finding smaller genetic distance in spousal pairs with ASD-affected children and higher minor allele content in cases for ASD-associated SNPs.

7 citations

humanwhole-exome sequencing

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