Principal Investigator

Satoshi Koyama, MD, PhD

Dr. Koyama studies how human genetic variation contributes to disease risk, molecular mechanisms, and precision prevention across a broad range of human diseases, with a particular focus on cardiometabolic traits. His training in cardiovascular medicine, human genetics, and computational biology grounds the lab's work in rigorous statistical genetics and patient-centered translation.

Satoshi Koyama, MD, PhD

Academic Appointments & Affiliations

Assistant Director of Bioinformatics

Personalized Medicine, Mass General Brigham

Investigator

Heart and Vascular Institute, Mass General Brigham

Associate Member

Cardiovascular Disease Initiative, Broad Institute of MIT and Harvard

Member of the Faculty of Medicine

Harvard Medical School

Education

PhD

Kyoto University

MD

Kobe University

Training

Postdoctoral Fellow

Broad Institute of MIT and Harvard

Postdoctoral Fellow

RIKEN

Cardiology Fellow

Hyogo Prefectural Amagasaki Hospital

Resident Physician

Kobe City General Hospital

Grant Support

Whole genome sequence interpretation for lipids to discover new genes and mechanisms for coronary artery disease

NIH/NHLBI Pathway to Independence Award (R00), R00HL169733 / PI

Extends the genetic understanding of familial hypercholesterolemia and coronary artery disease through whole-genome sequence interpretation.

Past Grant Support

Whole genome sequence interpretation for lipids to discover new genes and mechanisms for coronary artery disease

NIH/NHLBI Pathway to Independence Award (K99), K99HL169733 / PI

Characterized rare coding and non-coding variants in familial hypercholesterolemia and developed integrated risk prediction approaches.

Defining the pathophysiology of coronary artery disease through rare variants and lipid traits

The Uehara Memorial Foundation / PI

Defined how rare variants shape coronary artery disease risk, with a focus on blood lipid traits.

The pathophysiology of coronary artery disease utilizing whole-genome sequencing

JSPS Overseas Research Fellowship, 202160643 / PI

Identified rare effector variants for coronary artery disease using whole-genome sequencing datasets.

Elucidation of the pathophysiology of microRNA in acute heart failure

JSPS Research Fellowship for Young Scientists (DC1), 15J00784 / PI

Described blood microRNA dynamics during acute decompensation in heart failure.

Awards and Honors

Gill Award for Early Contributions to Cardiovascular Research

University of Kentucky Gill Heart & Vascular Institute

Recognized contributions to genetic analysis in atherosclerotic cardiovascular disease.

Academic Leadership

Analytic Lead & PRS Working Group Chair

CARDIoGRAMplusC4D Consortium

Member, GPM Early Career Committee

American Heart Association Council on Genomic and Precision Medicine