Author

Sadaaki Takata

RIKEN Center for Integrative Medical SciencesORCID 0000-0002-5354-5341Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetics· 2

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Research Focus:variant calling· 2 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1 Research Focus:GWAS / association mapping· 1 Research Focus:variant effect prediction· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Chikashi C. TeraoiD· 2 shared Yoichiro KamataniiD· 2 shared Yukihide MomozawaiD· 2 shared Anselmo Jiro KamadaiD· 1 shared Asami F. Gelinas· 1 shared Atsushi Takeda· 1 shared Chihiro Inai· 1 shared Erica H. Parrish· 1 shared

Activity by Year

2020-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 35 mutual co-author links

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2 shared papersGenetics

Chikashi C. TeraoORCID

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2 papers

Recent·Most cited

GeneticsbioRxivPreprintMar 25, 2022

Mobile elements in human population-specific genome and phenotype divergence

Shohei Kojima, Satoshi Koyama, Mirei Ka…·Nicholas F. Parrish

The paper develops a tool to genotype mobile element variants (MEVs) using short-read data and identifies population-specific MEs linked to disease and gene regulation.

9 citations

humanwhole-genome sequencing

𝕏 PostBluesky

GeneticsbioRxivPreprintMar 15, 2020

Population-wide Screening for Germline Variants of Hereditary Cancer Genes in 12K Unselected Japanese Colorectal Cancers and 27K Controls

Masashi Fujita, Xiaoxi Liu, Yusuke Iwasaki…·Yukihide Momozawa

The paper screens 12,503 Japanese CRC patients and 23,705 controls for germline variants in 27 cancer genes, finding 3.3% of patients have pathogenic variants linked to CRC risk.

2 citations

humanwhole-exome sequencing

𝕏 PostBluesky