Publications in Peer-Reviewed Journals

Gunathilake KMD, Sirisena UND, Nisansala PKD, Goonasekera HWW, Jayasekara RW, Dissanayake VHW.

The prevalence of the Prothrombin (F2) 20210G>A mutation in a cohort of Sri Lankan patients with thromboembolic disorders.

Publication year: 2014

The microbiome of the placenta in preeclampsia supports the role of bacteria in the multifactorial aetiology of pre-eclampsia.

Publications in Peer-Reviewed Journals

Amarasekara R, Jayasekara RW, Senanayake H, Dissanayake VHW.

Publication year: 2014

Polymorphisms in the fibrinolytic pathway genes and the risk of recurrent miscarriage.

Publications in Peer-Reviewed Journals

Andraweera PH, Dekker GA, Thompson SD, Nowak RC, Jayasekara RW, Dissanayake VHW, Roberts CT.

Publication year: 2014

Polymorphism in the Epidermal Growth Factor (EGF) gene is associated with pre-eclampsia and low birth weight.

Publications in Peer-Reviewed Journals

Chenthuran T, Harendra GG, Jayasekara RW, Dissanayake VHW.

Publication year: 2014

Hypoxia-inducible factor-1α gene polymorphisms in early and late onset preeclampsia in Sinhalese women.

Publications in Peer-Reviewed Journals

Andraweera PH, Dissanayake VHW, Jayasekara RJ, Dekker GA, Roberts CT.

Publication year: 2014

Cytogenetic analysis of chromosomal abnormalities in Sri Lankan children

Publications in Peer-Reviewed Journals

Thillainathan S, Sirisena ND, Kariyawasam KWJC, Jayasekara RW, Dissanayake VHW

Publication year: 2014

Challenges in global genomics education.

Publications in Peer-Reviewed Journals

de Abrew A, Dissanayake VHW, Korf BR.

Publication year: 2014

Cancer Genetics and the Surgeon – New Frontiers.

Publications in Peer-Reviewed Journals

Sirisena ND, Dissanayake VHW.

Publication year: 2014

A Survey of Scientist and Policy Makers’ Attitudes Towards Research On Stored Human Biological Materials In Sri Lanka.

Publications in Peer-Reviewed Journals

Dissanayake VHW, Sumathipala WLDS, Kariyawasam UGAC, JMDNMM Jayamanne, Nisansala PKDS, Lie R.

Publication year: 2014

A child with a novel de novo mutation in the aristaless domain of the aristaless-related homeobox (ARX) gene presenting with ambiguous genitalia.

Publications in Peer-Reviewed Journals

Sirisena N, McElreavey K, Bashamboo A, de Silva K, Jayasekara R, Dissanayake VHW.

Publication year: 2014

Thalassaemic Osteopathy:-a cross-sectional preliminary study from Sri Lanka.

Publications in Peer-Reviewed Journals

Dissanayake R, De Silva KSH, Lekamwasam S, Abeysekara AAGS, Dissanayake VHW.

Publication year: 2013

Post-zygotic breakage of a dicentric chromosome results in mosaicism for a telocentric 9p marker chromosome in a boy with developmental delay.

Publications in Peer-Reviewed Journals

Pedurupillay CRJ, Misceo D, Gamage TH, Dissanayake VHW, Frengen E.

Publication year: 2013

Genetic variants in the Cytochrome P4502D6 (CYP2D6) gene in the Sri Lankan population.

Publications in Peer-Reviewed Journals

Tharanga TDP, Jinadasa CMV, Risama MF, Galappatthy P, Jayakody RL, Dissanayake VHW.

Publication year: 2013

Development and implementation of a web-based continuing professional development (CPD) programme on medical genetics.

Publications in Peer-Reviewed Journals

Kulatunga GGAK, Marasinghe RB, Karunathilake IM, Dissanayake VHW.

Publication year: 2013

Clinical and genetic features of Huntington disease in Sri Lanka.

Publications in Peer-Reviewed Journals

Sumathipala DS, Jayasekara RW, Dissanayake VHW

Publication year: 2013

Child with Deletion 9p Syndrome Presenting with Cranio-facial Dysmorphism, Developmental Delay and Multiple Congenital Malformations.

Publications in Peer-Reviewed Journals

Sirisena N, Wijetunge UKS, de Silva R, Dissanayake VHW.

Publication year: 2013

Autosomal dominant hereditary ataxia in Sri Lanka

Publications in Peer-Reviewed Journals

Sumathipala DS, Abeysekara AAGS, Jayasekara RW, Tallaksen CME, Dissanayake VHW

Publication year: 2013

A Sri Lankan Child with 48,XXXX syndrome

Publications in Peer-Reviewed Journals

Padeniya PM, Godapitiya I, Pathirana DR, Jayasekara RW, Dissanayake VHW.

Publication year: 2013

Vascular endothelial growth factor family gene polymorphisms in preeclampsia in Sinhalese women in Sri Lanka.

Publications in Peer-Reviewed Journals

Andraweera PH, Dekker GA, Dissanayake VHW, Bianco-Miotto T, Jayasekara RW, Roberts CT.

Publication year: 2012

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

Publications in Peer-Reviewed Journals

Wettasinghe TK, Jayasekara RW, Dissanayake VHW.

Publication year: 2012

Prevalence of chromosomal abnormalities in Sri Lankan women with primary amenorrhea.

Publications in Peer-Reviewed Journals

Samarakoon L, Sirisena ND, Wettasinghe KT, Kariyawasam KWJC, Jayasekara RW, Dissanayake VHW.

Publication year: 2012

Introduction of Web based Continuous Professional Development to Sri Lanka.

Publications in Peer-Reviewed Journals

Kulatunga GGAK, Marasinghe RB, Karunathilake IM, Dissanayake VHW.

Publication year: 2012

Implementation of District Health Information Software 2 (DHIS2) in Sri Lanka.

Publications in Peer-Reviewed Journals

Manoj S, Wijekoon A, Dharmawardhana M, Wijesuriya D, Rodrigo S, Hewapathirana R, Siribaddana P, Gunasekera T, Dissanayake VHW.

Publication year: 2012

Haplotypes of heparin-binding epidermal-growth-factor-like growth factor gene are associated with pre-eclampsia

Publications in Peer-Reviewed Journals

Harendra GG, Jayasekara RW, Dissanayake VHW.

Publication year: 2012

DocCall: a mobile phone based medical advice service to accommodate health care unmet needs in Sri Lanka.

Publications in Peer-Reviewed Journals

Siriwardena N, Hewage M, Dissanayake VHW.

Publication year: 2012

Candidate Gene Study of Genetic Thrombophilic Polymorphisms in Pre-eclampsia and Recurrent Pregnancy Loss in Sinhalese women.

Publications in Peer-Reviewed Journals

Dissanayake VHW, Sirisena ND, Weerasekera LY, Gammulla CG, Seneviratne HR, Jayasekara RW.

Publication year: 2012

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

Publications in Peer-Reviewed Journals

Sumathipala DS, Wijesiriwardena B, Gamage TH, Jayasekara RW, Dissanayake VHW.

Publication year: 2012

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

Publications in Peer-Reviewed Journals

Katulanda P, Rajapakse JRDK, Kariyawasam KDJC, Jayasekara RW, Dissanayake VHW.

Publication year: 2012

A child with mosaicism for deletion (14)(q11.2q13).

Publications in Peer-Reviewed Journals

Gamage TH, Godapitiya IUH, Nanayakkara S, Jayasekara RW, Dissanayake VHW.

Publication year: 2012

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

Publications in Peer-Reviewed Journals

Wetthasinghe TK, Sirisena ND, Andraweera PH, Jayasekara RW, Dissanayake VHW.

Publication year: 2012

Vidya Jyothi Prof. Vajira H.W. Dissanayake

Publication Types:

Gunathilake KMD, Sirisena UND, Nisansala PKD, Goonasekera HWW, Jayasekara RW, Dissanayake VHW.

The microbiome of the placenta in preeclampsia supports the role of bacteria in the multifactorial aetiology of pre-eclampsia.

Polymorphisms in the fibrinolytic pathway genes and the risk of recurrent miscarriage.

Polymorphism in the Epidermal Growth Factor (EGF) gene is associated with pre-eclampsia and low birth weight.

Hypoxia-inducible factor-1α gene polymorphisms in early and late onset preeclampsia in Sinhalese women.

Cytogenetic analysis of chromosomal abnormalities in Sri Lankan children

Challenges in global genomics education.

Cancer Genetics and the Surgeon – New Frontiers.

A Survey of Scientist and Policy Makers’ Attitudes Towards Research On Stored Human Biological Materials In Sri Lanka.

A child with a novel de novo mutation in the aristaless domain of the aristaless-related homeobox (ARX) gene presenting with ambiguous genitalia.

Thalassaemic Osteopathy:-a cross-sectional preliminary study from Sri Lanka.

Post-zygotic breakage of a dicentric chromosome results in mosaicism for a telocentric 9p marker chromosome in a boy with developmental delay.

Genetic variants in the Cytochrome P4502D6 (CYP2D6) gene in the Sri Lankan population.

Development and implementation of a web-based continuing professional development (CPD) programme on medical genetics.

Clinical and genetic features of Huntington disease in Sri Lanka.

Child with Deletion 9p Syndrome Presenting with Cranio-facial Dysmorphism, Developmental Delay and Multiple Congenital Malformations.

Autosomal dominant hereditary ataxia in Sri Lanka

A Sri Lankan Child with 48,XXXX syndrome

Vascular endothelial growth factor family gene polymorphisms in preeclampsia in Sinhalese women in Sri Lanka.

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

Prevalence of chromosomal abnormalities in Sri Lankan women with primary amenorrhea.

Introduction of Web based Continuous Professional Development to Sri Lanka.

Implementation of District Health Information Software 2 (DHIS2) in Sri Lanka.

Haplotypes of heparin-binding epidermal-growth-factor-like growth factor gene are associated with pre-eclampsia

DocCall: a mobile phone based medical advice service to accommodate health care unmet needs in Sri Lanka.

Candidate Gene Study of Genetic Thrombophilic Polymorphisms in Pre-eclampsia and Recurrent Pregnancy Loss in Sinhalese women.

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

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

A child with mosaicism for deletion (14)(q11.2q13).

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