Kawmadi Gunawardena

4PUBLICATIONS
6CO-AUTHORS
Gene and molecular therapyMedical biochemistry and metabolomics not elsewhere classifiedGene expression (incl. microarray and other genome-wide approaches)Vision science
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Publications (4)

|Apr 13, 2026
Spectrum of Congenital Anomalies in Myhre Syndrome-Insights Into Effects Brought by Altered TGF-β Signaling via Gain-of-Function Variants in SMAD4.

Kawmadi Gunawardena, Alessandro De Falco, Deborah Osio

|Sep 09, 2024
Mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes with coexisting nemaline myopathy: a case report.

Kawmadi Gunawardena, Somasundaram Praveenan, Vajira H W Dissanayake

|Jun 05, 2023
Germline variants of uncertain significance, their frequency, and clinico-pathological features in a cohort of Sri Lankan patients with hereditary breast cancer.

Kawmadi Gunawardena, Nirmala D Sirisena, Gayani Anandagoda

|Feb 04, 2023
The first genetically authenticated case of Leber hereditary optic neuropathy in Sri Lanka: a case report and review of the literature.

Kawmadi Gunawardena, Vajira H W Dissanayake, Thashi Chang

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Frequent Collaborators

1 joint publications

Nirmala D Sirisena

1 joint publications

Vajira H W Dissanayake

1 joint publications

Alessandro De Falco

1 joint publications

Erina Sasaki