Yoichiro Kamatani

The University of Texas at San Antonio Health Science Center

Also affiliated with The University of Tokyo

Biochemistry, 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 1%percentile

4.7Author DataRank

Indexed papers

5in 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 5 indexed papers 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 →

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

Trans-ethnic Mendelian-randomization study reveals causal relationships between cardiometabolic factors and chronic kidney disease

International Journal of Epidemiology(2021)10.1093/ije/dyab203

Top 7%

3.0DataRank

Top 7%122 citations

Yuemiao Zhang, Humaira Rasheed, Venexia Walker, Yuka Sugawara, Jiachen Li +38 more

Papers

Driven by 60 papers — median percentile 68. Top paper: “Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations”.

Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations

Cell(2020)10.1016/j.cell.2020.06.045

N/A

8.3DataRank · unranked

739 citations

Laura M. Raffield, Abdou Mousas, Saori Sakaue, Jennifer E. Huffman, Arden Moscati +95 more

Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants

Nature Genetics(2022)10.1038/s41588-022-01233-6

N/A

7.7DataRank · unranked

721 citations

Tao Jiang, Anuj Goel, Stavroula Kanoni, Brooke N. Wolford, Deepak Atri +92 more

Large-scale genome-wide association study of coronary artery disease in genetically diverse populations

Nature Medicine(2022)10.1038/s41591-022-01891-3

N/A

6.8DataRank · unranked

363 citations

Xiang Zhu, Austin T. Hilliard, Shoa L. Clarke, Valerio Napolioni, Shining Ma +78 more

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 diversity fuels gene discovery for tobacco and alcohol use

Nature(2022)10.1038/s41586-022-05477-4

N/A

5.9DataRank · unranked

513 citations

Xingyan Wang, Fang Chen, Seon-Kyeong Jang, Mengzhen Liu, Chen Wang +95 more

Cerebral small vessel disease genomics and its implications across the lifespan

Nature Communications(2020)10.1038/s41467-020-19111-2

N/A

4.3DataRank · unranked

209 citations

Hideaki Suzuki, Xueqiu Jian, Chloé Sarnowski, Tavia E. Evans, Joshua C. Bis +94 more

Trans-ethnic Mendelian-randomization study reveals causal relationships between cardiometabolic factors and chronic kidney disease

International Journal of Epidemiology(2021)10.1093/ije/dyab203

Top 7%

3.0DataRank

Top 7%122 citations

Yuemiao Zhang, Humaira Rasheed, Venexia Walker, Yuka Sugawara, Jiachen Li +38 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

Model-based assessment of replicability for genome-wide association meta-analysis

Nature Communications(2021)10.1038/s41467-021-21226-z

N/A

1.5DataRank · unranked

40 citations

Yu Jiang, Mengzhen Liu, J. Dylan Weissenkampen, Scott A. Eckert, Lina Yang +125 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

Clinical use of current polygenic risk scores may exacerbate health disparities

Nature Genetics(2019)10.1038/s41588-019-0379-x

N/A

1.2DataRank · unranked

2850 citations

Masahiro Kanai, Yoichiro Kamatani, Karen L. Mohlke, Michael C O'Donovan, Coleen Damcott +1 more

Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use

Nature Genetics(2019)10.1038/s41588-018-0307-5

N/A

1.1DataRank · unranked

2128 citations

Mengzhen Liu, HUNT All-In Psychiatry, Yu Jiang, Robbee Wedow, Yue Li +120 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

Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases

Nature Genetics(2018)10.1038/s41588-018-0047-6

N/A

1.0DataRank · unranked

901 citations

Masato Akiyama, Atsushi Takahashi, Nana Matoba, Yukihide Momozawa, Masashi Ikeda +8 more

Seven new loci associated with age-related macular degeneration

Nature Genetics(2013)10.1038/ng.2578

N/A

1.0DataRank · unranked

798 citations

Lars G. Fritsche, Wei Chen, Brian L. Yaspan, Yi Yu, Guðmar Þorleifsson +141 more

The Polygenic and Monogenic Basis of Blood Traits and Diseases

Cell(2020)10.1016/j.cell.2020.08.008

N/A

0.988DataRank · unranked

722 citations

Erik L. Bao, Parsa Akbari, Caleb A. Lareau, Abdou Mousas, Tao Jiang +95 more

Genetic susceptibility to hepatocellular carcinoma in chromosome 22q13.31, findings of a genome‐wide association study

JGH Open(2021)10.1002/jgh3.12682

N/A

0.915DataRank · unranked

23 citations

Anuradha Budhu, Yi Shen, Linda L. Wong, Brenda Y. Hernandez, Maarit Tiirikainen +34 more

Multi-ancestry genome-wide association analyses identify novel genetic mechanisms in rheumatoid arthritis

Nature Genetics(2022)10.1038/s41588-022-01213-w

N/A

0.882DataRank · unranked

356 citations

Saori Sakaue, Chikashi Terao, Yang Luo, Kyuto Sonehara, Kensuke Yamaguchi +86 more

The genetic basis of endometriosis and comorbidity with other pain and inflammatory conditions

Nature Genetics(2023)10.1038/s41588-023-01323-z

N/A

0.853DataRank · unranked

293 citations

Sally Mortlock, Marzieh Ghiasi, Peter Möller, Lilja Stefánsdóttir, Geneviève Galarneau +95 more

Discerning asthma endotypes through comorbidity mapping

Nature Communications(2022)10.1038/s41467-022-33628-8

N/A

0.775DataRank · unranked

28 citations

Xue Zhong, Hae Kyung Im, Nathan Schoettler, Milton Pividori, D. Kyle Hogarth +14 more

Genomics yields biological and phenotypic insights into bipolar disorder

Nature(2025)10.1038/s41586-024-08468-9

N/A

0.775DataRank · unranked

174 citations

Maria Koromina, Tracey van der Veen, Toni Boltz, Friederike S. David, Jessica Yang +95 more

Characterizing prostate cancer risk through multi-ancestry genome-wide discovery of 187 novel risk variants

Nature Genetics(2023)10.1038/s41588-023-01534-4

N/A

0.753DataRank · unranked

150 citations

Jiayi Shen, Alex A Rodriguez, Edward J. Saunders, Fei Chen, Rohini Janivara +95 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

0.694DataRank · unranked

101 citations

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

0.646DataRank · unranked

73 citations

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

Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants

medRxiv(2021)10.1101/2021.05.24.21257377

N/A

0.637DataRank · unranked

69 citations

Tao Jiang, Anuj Goel, Stavroula Kanoni, Brooke N. Wolford, Elle M. Weeks +87 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

0.621DataRank · unranked

62 citations

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

Current clinical use of polygenic scores will risk exacerbating health disparities

bioRxiv (Cold Spring Harbor Laboratory)(2018)10.1101/441261

N/A

0.568DataRank · unranked

43 citations

Masahiro Kanai, Yoichiro Kamatani, Karen L. Mohlke, Michael C O'Donovan, Coleen Damcott +1 more

A large-scale multi-ethnic genome-wide association study of coronary artery disease

Research Square(2021)10.21203/rs.3.rs-275591/v1

N/A

0.561DataRank · unranked

11 citations

Catherine Tcheandjieu, Xiang Zhu, Austin T. Hilliard, Shoa L. Clarke, Valerio Napolioni +77 more

Contribution of Common Genetic Variants to Risk of Early-Onset Ischemic Stroke

Neurology(2022)10.1212/wnl.0000000000201006

N/A

0.546DataRank · unranked

37 citations

Huichun Xu, Brady Gaynor, John W. Cole, Kristiina Rannikmäe, Tara M. Stanne +95 more

Genetic Risk Score for Intracranial Aneurysms: Prediction of Subarachnoid Hemorrhage and Role in Clinical Heterogeneity

Stroke(2023)10.1161/strokeaha.122.040715

N/A

0.520DataRank · unranked

31 citations

Jos P. Kanning, Gad Abraham, Amy E. Martinsen, Bendik Slagsvold Winsvold, John‐Anker Zwart +95 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

0.520DataRank · unranked

31 citations

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

Whole genome sequence analyses of eGFR in 23,732 people representing multiple ancestries in the NHLBI trans-omics for precision medicine (TOPMed) consortium

EBioMedicine(2021)10.1016/j.ebiom.2020.103157

N/A

0.505DataRank · unranked

28 citations

Kelsey Grinde, Jennifer A. Brody, Charles E. Breeze, Laura M. Raffield, Josyf C. Mychaleckyj +68 more

Hematopoietic mosaic chromosomal alterations and risk for infection among 767,891 individuals without blood cancer

Research Square(2020)10.21203/rs.3.rs-100817/v1

N/A

0.436DataRank · unranked

6 citations

Seyedeh M. Zekavat, Shu‐Hong Lin, Alexander G. Bick, Aoxing Liu, Kaavya Paruchuri +26 more

The high-dimensional space of human diseases built from diagnosis records and mapped to genetic loci

Nature Computational Science(2023)10.1038/s43588-023-00453-y

Top 46%

0.393DataRank

Top 46%9 citations

Yu Li, Xue Zhong, Kanix Wang, Milton Pividori, Rabab Alomairy +15 more

Genetic variants for head size share genes and pathways with cancer

Cell Reports Medicine(2024)10.1016/j.xcrm.2024.101529

N/A

0.380DataRank · unranked

10 citations

Raymond A. Poot, Tavia E. Evans, Claudia L. Satizábal, Aniket Mishra, Muralidharan Sargurupremraj +95 more

Proteogenomics in cerebrospinal fluid and plasma reveals new biological fingerprint of cerebral small vessel disease

Research Square(2024)10.21203/rs.3.rs-4535534/v1

N/A

0.331DataRank · unranked

5 citations

Ilana Caro, Daniel Western, Shinichi Namba, Na Sun, Shuji Kawaguchi +52 more

Genetic variants for head size share genes and pathways with cancer

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.07.15.191114

N/A

0.312DataRank · unranked

7 citations

Raymond A. Poot, Tavia E. Evans, Claudia L. Satizábal, Aniket Mishra, Sandra Van der Auwera +95 more

Polygenic Risk Score and Lung Adenocarcinoma Risk Among Never-Smokers by EGFR Mutation Status: A Brief Report

Journal of Thoracic Oncology(2024)10.1016/j.jtho.2024.11.019

N/A

0.312DataRank · unranked

6 citations

Chao A. Hsiung, Xiaoyu Wang, Haoyu Zhang, Wei Jie Seow, Jianxin Shi +95 more

Genetically proxied HTRA1 protease activity and circulating levels independently predict risk of ischemic stroke and coronary artery disease

Research Square(2023)10.21203/rs.3.rs-3523612/v1

N/A

0.269DataRank · unranked

5 citations

Rainer Malik, Nathalie Beaufort, Koki Tanaka, Marios K. Georgakis, Yunye He +5 more

Multi-ancestry polygenic risk scores for the prediction of type 2 diabetes and complications in diverse ancestries

The Lancet Diabetes & Endocrinology(2026)10.1016/s2213-8587(25)00405-x

N/A

0.208DataRank · unranked

3 citations

Joohyun Kim, Ravi Mandla, Yingchang Lu, Ken Suzuki, Lauren E Petty +255 more

Trans-ethnic Mendelian randomization study reveals causal relationships between cardio-metabolic factors and chronic kidney disease

medRxiv(2020)10.1101/2020.09.04.20188284

N/A

0.165DataRank · unranked

2 citations

YueMiao Zhang, Humaira Rasheed, Venexia Walker, Yuka Sugawara, Jiachen Li +38 more

Proteogenomics in cerebrospinal fluid and plasma reveals new biological fingerprint of cerebral small vessel disease

Nature Aging(2025)10.1038/s43587-025-01006-w

N/A

0.165DataRank · unranked

2 citations

Daniel Western, Shinichi Namba, Na Sun, Shuji Kawaguchi, Yunye He +56 more

The Ethnic/Racial Variations of Intracerebral Hemorrhage Genetics (ERICH-GENE) Study Protocol

medRxiv(2025)10.1101/2025.06.11.25329301

Top 78%

0.104DataRank

Top 78%1 citations

Stacey Q Wolfe, Marialuisa Zedde, Rosario Pascarella, Jordi Jiménez‐Conde, Marta Vallverdú Prats +61 more

Hematopoietic mosaic chromosomal alterations increase the risk for diverse types of infection

Nature Medicine(2021)10.1038/s41591-021-01371-0

N/A

0DataRank · unranked

193 citations

Shu‐Hong Lin, Alexander G. Bick, Aoxing Liu, Kaavya Paruchuri, Chen Wang +95 more

Genome-Wide Meta-analysis Identifies Genetic Variants Associated With Glycemic Response to Sulfonylureas

Diabetes Care(2021)10.2337/dc21-1152

N/A

0DataRank · unranked

44 citations

Sook Wah Yee, Kaixin Zhou, Nienke van Leeuwen, Yanfei Zhang, Moneeza K. Siddiqui +50 more

Trans-ancestry genome-wide association study identifies novel genetic mechanisms in rheumatoid arthritis

medRxiv(2021)10.1101/2021.12.01.21267132

N/A

0DataRank · unranked

14 citations

Saori Sakaue, Chikashi Terao, Yang Luo, Kyuto Sonehara, Kensuke Yamaguchi +86 more

Evidence of causality of low body mass index on risk of adolescent idiopathic scoliosis: a Mendelian randomization study

Frontiers in Endocrinology(2023)10.3389/fendo.2023.1089414

N/A

0DataRank · unranked

9 citations

Anas M. Khanshour, Masaru Koido, Kazuki Takeda, Yukihide Momozawa, Michiaki Kubo +43 more

A large-scale microRNA transcriptome-wide association study identifies two susceptibility microRNAs, miR-1307-5p and miR-192-3p, for colorectal cancer risk

Human Molecular Genetics(2023)10.1093/hmg/ddad185

N/A

0DataRank · unranked

4 citations

Weiqiang Lin, Qiuyin Cai, Sun‐Seog Kweon, Xiao‐Ou Shu, Chizu Tanikawa +27 more

Variants encoding a restricted carboxy-terminal domain of SLC12A2 cause hereditary hearing loss in humans

PLoS Genetics(2020)10.1371/journal.pgen.1008643

N/A

0DataRank · unranked

58 citations

Koichiro Wasano, Yukihide Momozawa, Yoichiro Kamatani, Fuyuki Miya, Sawako Masuda +8 more

Genetic risk score for intracranial aneurysms to predict aneurysmal subarachnoid hemorrhage and identify associations with patient characteristics

medRxiv(2022)10.1101/2022.04.29.22274404

N/A

0DataRank · unranked

0 citations

Jos P. Kanning, Gad Abraham, Amy E. Martinsen, Bendik S Winsvold, John‐Anker Zwart +19 more

Mobile elements in human population-specific genome and phenotype divergence

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.03.25.485726

N/A

0DataRank · unranked

9 citations

Satoshi Koyama, Mirei Ka, Yuka Saito, Erica H. Parrish, Mikiko Endo +19 more

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

medRxiv(2024)10.1101/2024.06.26.24309127

N/A

0DataRank · unranked

0 citations

Xiaoyu Wang, Juncheng Dai, Christiana Karsonaki, Jianxin Shi, Kouya Shiraishi +95 more

Genetic variants for head size share genes and pathways with cancer

UNC Libraries(2024)10.17615/0jt9-4n49

N/A

0DataRank · unranked

0 citations

Vince D. Calhoun, Manabu Nagata, Raymond A. Poot, Aad van der Lugt, Svenja Caspers +95 more

Polygenic score integrating neurodegenerative and vascular risk informs dementia risk stratification

Alzheimer s & Dementia(2025)10.1002/alz.70014

N/A

0DataRank · unranked

9 citations

Santiago Clocchiatti‐Tuozzo, Cyprien Rivier, Aniket Mishra, Tsuyoshi Hachiya, Benjamin Grenier‐Boley +21 more

Genome-wide analysis of heart failure yields insights into disease heterogeneity and enables prognostic prediction in the Japanese population

Nature Communications(2025)10.1038/s41467-025-64659-6

N/A

0DataRank · unranked

7 citations

Kazuo Miyazawa, Satoshi Koyama, Ryo Kurosawa, Hirotaka Ieki, Hiroki Yoshida +26 more

Stratifying lung adenocarcinoma risk with multi-ancestry polygenic risk scores in East Asian never-smokers

JNCI Journal of the National Cancer Institute(2025)10.1093/jnci/djaf272

N/A

0DataRank · unranked

0 citations

Xiaoyu Wang, Juncheng Dai, Christiana Karsonaki, Jianxin Shi, Kouya Shiraishi +95 more

Claudin-2 deficiency associates with hypercalciuria in mice and human kidney stone disease

Journal of Clinical Investigation(2020)10.1172/jci127750

N/A

0DataRank · unranked

111 citations

Matthew Saurette, Masomeh Askari, Lei Pei, Michael B. Filla, Megan R. Beggs +11 more

Mendelian randomization of genetically independent aging phenotypes identifies LPA and VCAM1 as biological targets for human aging

Nature Aging(2022)10.1038/s43587-021-00159-8

N/A

0DataRank · unranked

60 citations

Evgeny Tiys, Saori Sakaue, Masato Akiyama, Tuomo Kiiskinen, Wei Zhou +13 more

Genome-wide analysis identifies novel susceptibility loci for myocardial infarction

European Heart Journal(2020)10.1093/eurheartj/ehaa1040

N/A

0DataRank · unranked

279 citations

Yi Han, Qiong Jia, James R. Hilser, Pin Huang, Janet Gukasyan +55 more

Genetically independent phenotype analysis identifies LPA and VCAM1 as drug targets for human ageing

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.01.22.427837

N/A

0DataRank · unranked

2 citations

Evgeny Tiys, Saori Sakaue, Masato Akiyama, Tuomo Kiiskinen, Wei Zhou +13 more

Yoichiro Kamatani

Indexed papers

Top data-sharing exemplar

Papers