Unsung heroes: Genomic successes in the developing world

por Dissanayake, Vajira H.W., Barash, Carol Isaacson
Publicado 2016

Genetics and genomic medicine in Sri Lanka

por Sirisena, Nirmala D., Dissanayake, Vajira H. W.
Publicado 2019

Strategies for Genomic Medicine Education in Low- and Middle-Income Countries

por Sirisena, Nirmala D., Dissanayake, Vajira H. W.
Publicado 2019

Copy Number Variants Captured by the Array Comparative Genomic Hybridization in a Cohort of Patients Affected with Hereditary Colorectal Cancer in Sri Lanka: The First CNV Analysis...

por Wijesiriwardhana, Prabhavi, Wetthasinghe, Kalum, Dissanayake, Vajira H W
Publicado 2021

Genetic determinants of syndactyly: perspectives on pathogenesis and diagnosis

por Cassim, Afraah, Hettiarachchi, Dineshani, Dissanayake, Vajira H. W.
Publicado 2022

The first genetically authenticated case of Leber hereditary optic neuropathy in Sri Lanka: a case report and review of the literature

por Gunawardena, Kawmadi, Dissanayake, Vajira H. W., Chang, Thashi
Publicado 2023

Relative normalized luciferase activity for the recombinant vector constructs carrying the ancestral and variant alleles for XRCC2:rs3218550 and PHB:rs6917

por Sirisena, Nirmala Dushyanthi, Samaranayake, Nilakshi, Dissanayake, Vajira H. W.
Publicado 2018

Genotype data for single nucleotide polymorphism markers in sporadic breast cancer related genes in a Sri Lankan case–control cohort of postmenopausal women

por Sirisena, Nirmala Dushyanthi, Samaranayake, Nilakshi, Dissanayake, Vajira H. W.
Publicado 2019

Electrophoretic mobility shift assays implicate XRCC2:rs3218550C>T as a potential low-penetrant susceptibility allele for sporadic breast cancer

por Sirisena, Nirmala D., Samaranayake, Nilakshi, Dissanayake, Vajira H. W.
Publicado 2019

Spontaneous coronary artery dissection with leucoencephalopathy associated with thrombospondin Type 1 domain containing 1 gene mutation: a case report

por Ranasinghe, Gotabhaya, Sovis, Rasika, Shellvacumar, Sajeev, Dissanayake, Vajira H W
Publicado 2023

The low frequency of Y chromosome microdeletions in subfertile males in a Sinhalese population of Sri Lanka

por Wettasinghe, Tithila Kalum, Jayasekara, Rohan W., Dissanayake, Vajira H. W.
Publicado 2012

Implementation of genomic medicine in Sri Lanka: Initial experience and challenges

por Sirisena, Nirmala D., Neththikumara, Nilaksha, Wetthasinghe, Kalum, Dissanayake, Vajira H.W.
Publicado 2016

17p11.2 and Xq28 duplication detected in a girl diagnosed with Potocki–Lupski syndrome

por Sumathipala, Dulika S., Mandawala, Eranda N., Sumanasena, Samanmalee P., Dissanayake, Vajira H. W.
Publicado 2015

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

por Gunawardena, Kawmadi, Sirisena, Nirmala D., Anandagoda, Gayani, Neththikumara, Nilaksha, Dissanayake, Vajira H.W.
Publicado 2023

A Sri Lankan child with 49,XXXXY syndrome

por Dissanayake, Vajira H. W., Bandarage, Palinda, Pedurupillay, Christeen R. J., Jayasekara, Rohan W.
Publicado 2010

An Infant Born to a Mother with Gestational Diabetes Presenting with 49,XXXXY Syndrome and Renal Agenesis-A Case Report

por Sumathipala, Dulika, Gamage, Thilini, Wijesiriwardena, Bandula, Jayasekara, Rohan W., Dissanayake, Vajira H.W.
Publicado 2012

Child with Deletion 9p Syndrome Presenting with Craniofacial Dysmorphism, Developmental Delay, and Multiple Congenital Malformations

por Sirisena, Nirmala D., Wijetunge, U. Kalpani S., de Silva, Ramya, Dissanayake, Vajira H. W.
Publicado 2013

The Frequency and Spectrum of Chromosomal Translocations in a Cohort of Sri Lankans

por Paththinige, Chamara S., Sirisena, Nirmala D., Kariyawasam, U. G. I. U., Dissanayake, Vajira H. W.
Publicado 2019

An adolescent with 48,XXYY syndrome with hypergonadotrophic hypogonadism, attention deficit hyperactive disorder and renal malformations

por Katulanda, Prasad, Rajapakse, J. Rasika D. K., Kariyawasam, Jayani, Jayasekara, Rohan, Dissanayake, Vajira H. W.
Publicado 2012

A Case Series of Five Sri Lankan Patients with Ovotesticular Disorder of Sex Development

por Wettasinghe, Kalum T., Sirisena, Nirmala D., Andraweera, Prabha H., Jayasekara, Rohan W., Dissanayake, Vajira H. W.
Publicado 2012