🏆 Finalist — NIH Data Sharing Index (“S-Index”) Challenge

Yoshinori Murakami

Tokyo Medical University

ORCID: 0000-0002-2826-4396

Also affiliated with Institute of Medicinal Molecular Design, The University of Tokyo, Nippon Medical School

MedicineBiochemistry, Genetics and Molecular Biology

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 3%percentile
1.1Author DataRank

Indexed papers

1in pilot corpus
datarank_citation_only_1hop_v6· scope data_onlyMethodology
Why this DataRank?

An author's DataRank is the sum of the DataRanks of all 1 indexed paper attributed to them. A prolific author with many moderate-impact papers can outrank one with a single high-impact paper.

Author scores recompute whenever paper DataRanks are refreshed, so this number lags the underlying paper scores by at most one batch run.

Read the full methodology →

Top data-sharing exemplar

The highest-impact dataset this researcher has shared, ranked by DataRank — the single contribution doing the most to lift their data-sharing standing.

Pan-cancer and cross-population genome-wide association studies dissect shared genetic backgrounds underlying carcinogenesis

Nature Communications(2023)10.1038/s41467-023-39136-7
Top 18%
1.1DataRank
Top 18%49 citations

Yuya Shirai, Shinichi Namba, Ryuya Edahiro, Kyuto Sonehara, Tsuyoshi Hata +30 more

Papers

Driven by 13 papers — median percentile 82. Top paper: “Leveraging fine-mapping and multipopulation training data to improve cross-population polygenic risk scores”.

Leveraging fine-mapping and multipopulation training data to improve cross-population polygenic risk scores

Nature Genetics(2022)10.1038/s41588-022-01036-9
N/A
6.6DataRank · unranked
284 citations

Masahiro Kanai, Huwenbo Shi, Steven Gazal, Wouter J. Peyrot, Amit V. Khera +30 more

Genetic analysis of right heart structure and function in 40,000 people

Nature Genetics(2022)10.1038/s41588-022-01090-3
N/A
2.2DataRank · unranked
99 citations

Paolo Di Achille, Victor Nauffal, Mahan Nekoui, Sam Friedman, Marcus D. R. Klarqvist +46 more

Mobile element variation contributes to population-specific genome diversification, gene regulation and disease risk

Nature Genetics(2023)10.1038/s41588-023-01390-2
N/A
1.3DataRank · unranked
49 citations

Satoshi Koyama, Mirei Ka, Yuka Saito, Erica H. Parrish, Mikiko Endo +42 more

Pan-cancer and cross-population genome-wide association studies dissect shared genetic backgrounds underlying carcinogenesis

Nature Communications(2023)10.1038/s41467-023-39136-7
Top 18%
1.1DataRank
Top 18%49 citations

Yuya Shirai, Shinichi Namba, Ryuya Edahiro, Kyuto Sonehara, Tsuyoshi Hata +30 more

Improving the trans-ancestry portability of polygenic risk scores by prioritizing variants in predicted cell-type-specific regulatory elements

Nature Genetics(2020)10.1038/s41588-020-00740-8
N/A
0.805DataRank · unranked
213 citations

Kazuyoshi Ishigaki, Hiroki Sugishita, Tazro Ohta, Masaru Koido, Kushal K. Dey +7 more

Global biobank analyses provide lessons for developing polygenic risk scores across diverse cohorts

medRxiv(2021)10.1101/2021.11.18.21266545
N/A
0DataRank · unranked
25 citations

Shinichi Namba, Esteban A. Lopera-Maya, Sini Kerminen, Kristin Tsuo, Kristi Läll +25 more

Leveraging supervised learning for functionally informed fine-mapping of cis-eQTLs identifies an additional 20,913 putative causal eQTLs

Nature Communications(2021)10.1038/s41467-021-23134-8
N/A
0DataRank · unranked
101 citations

David R. Kelley, Jacob C. Ulirsch, Masahiro Kanai, Shuvom Sadhuka, Ran Cui +33 more

Global Biobank analyses provide lessons for developing polygenic risk scores across diverse cohorts

Cell Genomics(2023)10.1016/j.xgen.2022.100241
N/A
0DataRank · unranked
113 citations

Shinichi Namba, Esteban A. Lopera-Maya, Sini Kerminen, Kristin Tsuo, Kristi Läll +83 more

Genome-wide association study of lung adenocarcinoma in East Asia and comparison with a European population

Nature Communications(2023)10.1038/s41467-023-38196-z
N/A
0DataRank · unranked
71 citations

Kouya Shiraishi, Jiyeon Choi, Keitaro Matsuo, Tzu-Yu Chen, Juncheng Dai +95 more

In silico integration of thousands of epigenetic datasets into 707 cell type regulatory annotations improves the trans-ethnic portability of polygenic risk scores

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.02.21.959510
N/A
0DataRank · unranked
3 citations

Kazuyoshi Ishigaki, Hiroki Sugishita, Tazro Ohta, Koichi Matsuda, Yoshinori Murakami +5 more

Genome-wide association meta-analysis identifies GP2 gene risk variants for pancreatic cancer

Nature Communications(2020)10.1038/s41467-020-16711-w
N/A
0DataRank · unranked
62 citations

Masahiro Nakatochi, Yasuyuki Hosono, Hidemi Ito, Yoichiro Kamatani, Akihito Inoko +81 more

ENIGMA CHEK2 gether Project: A Comprehensive Study Identifies Functionally Impaired CHEK2 Germline Missense Variants Associated with Increased Breast Cancer Risk

Clinical Cancer Research(2023)10.1158/1078-0432.ccr-23-0212
N/A
0DataRank · unranked
31 citations

Petra Kleiblova, Petra Zemánková, Barbora Šťastná, Marketa Janatova, Jana Soukupová +95 more

The power of genetic diversity in genome-wide association studies of lipids

UNC Libraries(2024)10.17615/539b-tz69
N/A
0DataRank · unranked
5 citations

Joel N. Hirschhorn, Zoltán Kutalik, Sanni Ruotsalainen, Daniela Ruggiero, Prashantha Hebbar +95 more