Publications in Peer-Reviewed Journals

22q11.2 Deletion Syndrome in Diverse Populations.

Kruszka P, Porras AR, Sobering AK, Ikolo FA, La Qua S, Shotelersuk V, Chung BH, Mok GT, Uwineza A, Mutesa L, Moresco A, Obregon MG, Sokunbi OJ, Kalu N, Joseph DA, Ikebudu D, Ugwu CE, Okoromah CA, Addissie YA, Pardo KL, Brough JJ, Lee NC, Girisha KM, Patil SJ, Ng IS, Min BC, Jamuar SS, Tibrewal S, Wallang B, Ganesh S, Sirisena ND, Dissanayake VHW, Paththinige CS, Prabodha LB, Richieri-Costa A, Muthukumarasamy P, Thong MK, Jones KL, Abdul-Rahman OA, Ekure EN, Adeyemo AA, Summar M, Linguraru MG, Muenke M.

Publication year: 2017

Unsung heroes: Genomic successes in the developing world.

Publications in Peer-Reviewed Journals

Dissanayake VH, Barash CI.

Publication year: 2016

The utility of haematopoietic stem cell karyotyping in the diagnosis of de novo myelodysplastic syndromes.

Publications in Peer-Reviewed Journals

Bandara M, Dissanayake VHW, Goonasekara HWW.

Publication year: 2016

Study on Hereditary Thrombophilia and Stroke in a Cohort from Sri Lanka.

Publications in Peer-Reviewed Journals

Kalpage HA, Sumathipala DS, Goonasekara HW, Dissanayake VHW.

Publication year: 2016

Sri Lanka’s national assessment on innovation and intellectual property for access to medical products.

Publications in Peer-Reviewed Journals

Beneragama G, Shridhar M, Ranasinghe R, Dissanayake VHW.

Publication year: 2016

Ring chromosome 4 in a child with multiple congenital abnormalities: a case report and review of literature.

Publications in Peer-Reviewed Journals

Paththinige CS, Sirisena N, Kariyawasam I, Saman Kumara LP, Dissanayake VHW.

Publication year: 2016

Phenotypic and Cytogenetic Characterization of Mesenchymal Stromal Cells in de novo Myelodysplastic Syndromes.

Publications in Peer-Reviewed Journals

Rathnayake AJI, Goonasekara HWW, Dissanayake VHW.

Publication year: 2016

Optimizing amniotic membrane tissue banking protocols for ophthalmic use.

Publications in Peer-Reviewed Journals

Hettiarachchi D, Dissanayake VHW, Goonasekera HWW.

Publication year: 2016

Novel AGXT gene mutation in a Sri Lankan family with Primary Hyperoxaluria type 1

Publications in Peer-Reviewed Journals

Sirisena ND, Hidellage N, Kariyawasam KJC, Jayasekara RW, Dissanayake VHW.

Publication year: 2016

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

Publications in Peer-Reviewed Journals

Sirisena ND, Neththikumara N, Wetthasinghe K, Dissanayake VHW.

Publication year: 2016

HLA-B27 allele frequency in Sri Lankan patients with spondyloarthritides.

Publications in Peer-Reviewed Journals

Kidnapillai S, Sirisena ND, Dissanayake VHW.

Publication year: 2016

Genetic Diversity of Pharmacogenomic Variants in Sri Lanka: implications for clinical implementation.

Publications in Peer-Reviewed Journals

Chan SL, Samaranayake N, Ross CJD, Toh MT, Carleton B, Hayden MR, Teo YY, Dissanayake VHW, Brunham LR.

Publication year: 2016

Development of Cytogenetic Abnormalities in Myelodysplastic Syndromes.

Publications in Peer-Reviewed Journals

Bandara WMMS, Rathnayake AJIS, Goonasekera HWW, Dissanayake VHW.

Publication year: 2016

Correspondence: Establishing a relationship between clinical features and one specific type of chromosome abnormality.

Publications in Peer-Reviewed Journals

Sirisena N, Dissanayake VHW.

Publication year: 2016

Authors reply re: HLA-B27 allele frequency in Sri Lankan patients with spondyloarthritides.

Publications in Peer-Reviewed Journals

Kidnapillai S, Sirisena ND, Dissanayake VH.

Publication year: 2016

Association of HLA class I and II genes with cutaneous leishmaniasis: a case control study from Sri Lanka and a systematic review.

Publications in Peer-Reviewed Journals

Samaranayake N, Fernando SD, Neththikumara NF, Rodrigo C, Karunaweera ND, Dissanayake VHW.

Publication year: 2016

Applying the Resilient Health System Framework for Universal Health Coverage.

Publications in Peer-Reviewed Journals

Ho K, Al-Shorjabji N, Brown E, Zelmer J, Gabor N, Maeder A, Marcelo A, Ritz D, Messina L, Loyola M, Abbott P, Nazira J, McKinnon A, Dissanayake V, Akeel A, Gardner N, Doyle T.

Publication year: 2016

Androgen Insensititivy Syndrome in a Cohort of Sri Lankan Children with 46,XY Disorders of Sex Development.

Publications in Peer-Reviewed Journals

De Silva KSH, Sirisena ND, Wijenayaka WAHK, Cooray MJG, Jayasekara RW, Dissanayake VHW.

Publication year: 2016

Anatomy of teaching anatomy- Do prosected cross sections improve students understanding of spatial and radiological anatomy?

Publications in Peer-Reviewed Journals

Samarakoon L, Sahathevan V, Selvarajah K, Dissanayake M, Anthony D, Dissanayake VHW, Jayasekara R.

Publication year: 2016

A study of HLA-B1502 in a Sri Lankan Population: Implications for pharmacogenomic testing.

Publications in Peer-Reviewed Journals

Gunathilake KDM, Wettasinghe KT, Dissanayake VHW.

Publication year: 2016

A case series of 7 Sri Lankan patients with type 1 spinal muscular atrophy.

Publications in Peer-Reviewed Journals

Banstola SR, Sirisena ND, Sumathipala DS, Dissanayake VHW.

Publication year: 2016

The obesity related FTO gene variant associates with the risk of recurrent miscarriage.

Publications in Peer-Reviewed Journals

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

Publication year: 2015

Polymorphisms in the inflammatory pathway genes and the risk of preeclampsia in Sinhalese women,

Publications in Peer-Reviewed Journals

Andraweera PH, Dekker GA, Jayasekara RW, Dissanayake VHW, Roberts CT,

Publication year: 2015

Novel COL4A3 Gene Mutations in a Consanguineous Family with Autosomal Recessive Alport Syndrome.

Publications in Peer-Reviewed Journals

Sirisena ND, Thalgahagoda S, Abeyagunawardena A, Neumann M, Schmudlach , Jayasekara RW, Dissanayake VHW.

Publication year: 2015

Global implementation of genomic medicine: We are not alone.

Publications in Peer-Reviewed Journals

Manolio TA, Abramowicz M, Al-Mulla F, Anderson W, Balling R, Berger AC, Bleyl S, Chakravarti A, Chantratita W, Chisholm RL, Dissanayake VHW, Dunn M, Dzau VJ, Han BG, Hubbard T, Kolbe A, Korf B, Kubo M, Lasko P, Leego E, Mahasirimongkol S, Majumdar PP, Matthijs G, McLeod HL, Metspalu A, Meulien P, Miyano S, Naparstek Y, O'Rourke PP, Patrinos GP, Rehm HL, Relling MV, Rennert G, Rodriguez LL, Roden DM, Shuldiner AR, Sinha S, Tan P, Ulfendahl M, Ward R, Williams MS, L Wong JE, Green ED, Ginsburg GS.

Publication year: 2015

Genetics of thromboembolic disorders in Sri Lanka.

Publications in Peer-Reviewed Journals

Dissanayake V H W.

Publication year: 2015

Angelman syndrome presented with a rare seizure type in a patient with 15q11.2 deletion: a case report.

Publications in Peer-Reviewed Journals

Ranasinghe JC, Chandradasa D, Fernando S, Kodithuwakku U, Mandawala DEN, Dissanayake VHW.

Publication year: 2015

Allogeneic bone marrow transplant in a child with thalassaemia.

Publications in Peer-Reviewed Journals

Gooneratne LV, Dissanayake R, Jayawardena A, Jayaweera G, Abayadeera A, Samarasinghe M, Chandrasir P, Dissanayake VHW,

Publication year: 2015

A Sri Lankan family with cerebellar hemangioblastoma due to a heterozygous nonsense mutation in the von Hippel-Lindau tumor suppressor, E3 ubiquitin protein ligase (VHL) gene.

Publications in Peer-Reviewed Journals

Somadasa PKDCT, Sirisena ND, De Silva LSC, Dissanayake, VHW.

Publication year: 2015

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

Publications in Peer-Reviewed Journals

Sumathipala DS, Mandawala EM, Sumanasena SP, Dissanayake VHW.

Publication year: 2015

Vidya Jyothi Prof. Vajira H.W. Dissanayake

Publication Types:

22q11.2 Deletion Syndrome in Diverse Populations.

Unsung heroes: Genomic successes in the developing world.

The utility of haematopoietic stem cell karyotyping in the diagnosis of de novo myelodysplastic syndromes.

Study on Hereditary Thrombophilia and Stroke in a Cohort from Sri Lanka.

Sri Lanka’s national assessment on innovation and intellectual property for access to medical products.

Ring chromosome 4 in a child with multiple congenital abnormalities: a case report and review of literature.

Phenotypic and Cytogenetic Characterization of Mesenchymal Stromal Cells in de novo Myelodysplastic Syndromes.

Optimizing amniotic membrane tissue banking protocols for ophthalmic use.

Novel AGXT gene mutation in a Sri Lankan family with Primary Hyperoxaluria type 1

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

HLA-B27 allele frequency in Sri Lankan patients with spondyloarthritides.

Genetic Diversity of Pharmacogenomic Variants in Sri Lanka: implications for clinical implementation.

Development of Cytogenetic Abnormalities in Myelodysplastic Syndromes.

Correspondence: Establishing a relationship between clinical features and one specific type of chromosome abnormality.

Authors reply re: HLA-B27 allele frequency in Sri Lankan patients with spondyloarthritides.

Association of HLA class I and II genes with cutaneous leishmaniasis: a case control study from Sri Lanka and a systematic review.

Applying the Resilient Health System Framework for Universal Health Coverage.

Androgen Insensititivy Syndrome in a Cohort of Sri Lankan Children with 46,XY Disorders of Sex Development.

Anatomy of teaching anatomy- Do prosected cross sections improve students understanding of spatial and radiological anatomy?

A study of HLA-B1502 in a Sri Lankan Population: Implications for pharmacogenomic testing.

A case series of 7 Sri Lankan patients with type 1 spinal muscular atrophy.

The obesity related FTO gene variant associates with the risk of recurrent miscarriage.

Polymorphisms in the inflammatory pathway genes and the risk of preeclampsia in Sinhalese women,

Novel COL4A3 Gene Mutations in a Consanguineous Family with Autosomal Recessive Alport Syndrome.

Global implementation of genomic medicine: We are not alone.

Genetics of thromboembolic disorders in Sri Lanka.

Angelman syndrome presented with a rare seizure type in a patient with 15q11.2 deletion: a case report.

Allogeneic bone marrow transplant in a child with thalassaemia.

A Sri Lankan family with cerebellar hemangioblastoma due to a heterozygous nonsense mutation in the von Hippel-Lindau tumor suppressor, E3 ubiquitin protein ligase (VHL) gene.

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