R. Singaraja

TREM2: a new risk factor for Alzheimer's disease

R. Singaraja, 2013, Clinical genetics.

Loss‐of‐function mutations in CCDC114 cause primary ciliary dyskinesia

R. Singaraja, D. H. Wu, Dh Wu, 2013, Clinical genetics.

Schwartz-Jampel Syndrome (SJS1), Type 1 a Novel Variant in the HSPG2 Gene

B. Venkatesh, C. Bonnard, B. Reversade, 2018 .

Spectrum of low-density lipoprotein receptor (LDLR) mutations in a cohort of Sri Lankan patients with familial hypercholesterolemia – a preliminary report

V. Dissanayake, G. Constantine, G. Constantine, 2018, Lipids in Health and Disease.

Novel mutations in scavenger receptor BI associated with high HDL cholesterol in humans

M. Hayden, J. Kastelein, I. Tietjen, 2011, Clinical genetics.