Dr. Klaus L. Rasmussen

• Lead/participant, Center for Rare and Complex Diseases (CAKS) and Clinical Genome Center (CGC)

• Member, European Reference Network for Rare Malformation Syndromes and Disorders (ERN-ITHACA)

• Involvement with multiple national and European advisory boards, expert panels, and societies for genetics

• Author/co-author of over 50 peer-reviewed publications in clinical genetics (2023 alone)

• Supervisor and mentor for PhD students and young doctors

• Editor/reviewer for major genetics and endocrinology journals internationally

• Professor and head of major genetics research initiatives at OUH

• Major national/international research projects and partnerships

Professor Klaus L. Rasmussen is a leader in clinical genetics and rare disease research at Odense University Hospital and the University of Southern Denmark. He leads collaborative diagnostic and research initiatives in rare diseases and hereditary cancer, supervising PhD students and publishing widely. His clinical and academic leadership helps ensure OUH remains a center of excellence for next-generation diagnostics, patient care, and interdisciplinary genetics research in Denmark and Europe.