S. Minami

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

A. Philippakis, Y. Kamatani, E. Benjamin, 2022, Nature Genetics.

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

David R. Kelley, Jacob C. Ulirsch, D. MacArthur, 2020, Nature Communications.

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

Alicia R. Martin, M. Kanai, Y. Kamatani, 2022, Nature Genetics.

Genome-wide association study of colorectal polyps identified highly overlapping polygenic architecture with colorectal cancer

Y. Kamatani, Y. Furukawa, K. Matsuda, 2021, Journal of Human Genetics.

Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases

M. Kanai, Y. Kamatani, Y. Okada, 2020, Nature Genetics.

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

Matthew S. Lebo, Beryl B. Cummings, John D. Eicher, 2021, Nature Medicine.

Functional analysis of three novel cell lines derived from human papillary thyroid carcinomas with three different clinical courses

G. Yoshino, T. Tachibana, S. Minami, 2014, Human Cell.

Identification of serum metabolome signatures associated with retinal and renal complications of type 2 diabetes

Y. Kamatani, Y. Okada, Y. Furukawa, 2023, Communications Medicine.

ENIGMA CHEK2gether Project: A Comprehensive Study Identifies Functionally Impaired CHEK2 Germline Missense Variants Associated with Increased Breast Cancer Risk

James M. Hodge, E. Burnside, Y. Kamatani, 2023, Clinical cancer research : an official journal of the American Association for Cancer Research.

Genome-wide association study identifies risk loci within the major histocompatibility complex region for Hunner-type interstitial cystitis.

S. Ishikawa, H. Kume, Y. Homma, 2023, Cell reports. Medicine.