G. Anandagoda

Germline variants of uncertain significance, their frequency, and clinico-pathological features in a cohort of Sri Lankan patients with hereditary breast cancer

V. Dissanayake, K. Gunawardena, Nilaksha Neththikumara, 2023, BMC Research Notes.

Diversity of pharmacogenomic variants affecting warfarin metabolism in Sri Lankans.

P. Ranasinghe, N. Sirisena, V. Dissanayake, 2022, Pharmacogenomics (London).

Novel frameshift variant in the PCNT gene associated with Microcephalic Osteodysplastic Primordial Dwarfism (MOPD) Type II and small kidneys

P. Lai, D. Hettiarachchi, V. Dissanayake, 2022, BMC medical genomics.

Parathyroid carcinoma during pregnancy: a novel pathogenic CDC73 mutation – a case report

C. Perera, M. Sumanatilleke, Piyumi S A Wijewickrama, 2022, BMC Endocrine Disorders.

Novel frameshift variant in the PCNT gene associated with Microcephalic Osteodysplastic Primordial Dwarfism (MOPD) Type II and small kidneys

P. Lai, D. Hettiarachchi, V. Dissanayake, 2022, BMC Medical Genomics.