Author

Ivan Gorlov

ORCID 0000-0001-8415-5656Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1 Genomics· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Approach:machine learning (classical)· 1 Research Focus:polygenic risk· 1 Research Focus:variant calling· 1 Assay:whole-exome sequencing· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Adeline SeowiD· 1 shared Akiteru GotoiD· 1 shared Allison ReineriD· 1 shared Ann G. SchwartziD· 1 shared Arshi AroraiD· 1 shared Atsushi TakahashiiD· 1 shared Baosen ZhouiD· 1 shared Batel BlechteriD· 1 shared

Activity by Year

2024-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 29 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Adeline SeowORCID

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2 papers

Recent·Most cited

Genetic & Genomic MedicineJNCI Journal of the National Cancer InstitutePeer-reviewedSep 18, 2025

Stratifying Lung Adenocarcinoma Risk with Multi-ancestry Polygenic Risk Scores in East Asian Never-Smokers

Batel Blechter, Xiaoyu Wang, Juncheng Dai…·Ping Yang

The paper develops and validates multi-ancestry polygenic risk scores for LUAD in East Asian never-smokers, showing improved risk prediction compared to East Asian-only models.

4 citations

humanwhole-genome sequencing

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GenomicsbioRxivPreprintOct 28, 2024

Improving Accuracy of Somatic Mutation Profiling in Large Epidemiologic Studies: Addressing Cases without Matched Normal Samples

Arshi Arora, Li Luo, Caroline E. Kostrzewa…·InterMEL

The paper improves somatic mutation detection in tumor samples without matched normal samples by estimating tumor purity and variant allele frequency, reducing false positive and negative rates.

DOI 10.1101/2024.10.28.617052

humanwhole-exome sequencing

𝕏 PostBluesky