Publications

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Child with maternally inherited pericentric inversion of chromosome 9 presenting with dysmorphism, developmental delay and multiple congenital malformations

Communications at Scientific Meetings - International
Weerapperuma KND, Gautam B, Karunaratne HWSS, Samarasinghe D, Jayasekara RW, Dissanayake VHW.
p35
Publication year: 2014

Child with a novel homozygous mutation in the Treacher Collins-Franceschetti syndrome 1 (TCOF1) gene presenting with ambiguous genitalia, cranio-facial dysmorphism and multiple congenital malformations

Communications at Scientific Meetings - National
Sirisena UND, McElreavey K, Bashamboo A, de Silva KSH, Jayasekara RW, Dissanayake VHW.
p197
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

BRCA1 mutation is three Sri Lanka families with hereditary breast and ovarian cancer syndrome

Communications at Scientific Meetings - International
Gautam B, Sirisena UND, Dissanayake NDW, Dissanayake VHW
p58
Publication year: 2014

Anthropometric patterns among patients with chronic mechanical low back pain

Communications at Scientific Meetings - National
Perera GLRS, Wijayarathna LS, Senarath U, Dissanayake PH, Karunanayake AL, Dissanayake VHW.
Ceylon Medical Journal 2014, 59 (Suppl 1):66).
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 study of skeletal dysplasia in a selected cohort of Sri Lankan Patients

Communications at Scientific Meetings - National
Wanigasekara T, Liyanage U, Dissanayake VHW, Jayasekera RW.
p154
Publication year: 2014

A ring chromosome 21 in a child with dysmorphic features

Communications at Scientific Meetings - International
Kulathunga LAN, Karunaratne HWSS, Senaratne LSD, Udalamaththa AVLK, Jayasekara RW, Dissanayake VHW
p39
Publication year: 2014

A ring chromosome 18 in a Sri Lankan female child with congenital malformations and global developmental delay

Communications at Scientific Meetings - International
Somadasa PKDCT, Udalamaththa AVLK, Liyanage JC, Jayawardana SMA, Arambepola WMM, Dissanayake VHW.
p28
Publication year: 2014

A patient with Turner Syndrome with a karyotype of 45,X[38]/46,X,r(X)[16].

Communications at Scientific Meetings - National
Gunathilake KMD, Kariyawasam UGIU, Udalamaththa AVLK, Sumathipala DS, Sirisena UND, Dissanayake VHW.
p202
Publication year: 2014

A paternally inherited unbalanced Chromosomal (8;11) Translocation in a Child Presenting with Dysmorphic Features and Seizures

Communications at Scientific Meetings - International
Gautam B, Kariyawasam UGIU, Punchihewa PMG, Dissanayake NDW, Wanigasekara T, Jayasekara RW, Dissanayake VHW
p30
Publication year: 2014

A maternally inherited partial trisomy 1q (q44->qter) and partial trisomy 15 (pter->q22) in a child with Silver Russell & Partial trisomy 15q Syndrome

Communications at Scientific Meetings - National
Jeerasinghe PB, Sirisena ND, Kariyawasam I, Udalamaththa V, Dissanayake VHW.
p196
Publication year: 2014

A maternally inherited partial trisomy 1(q44qter) and partial trisomy 15(pterq22) in a child with Silver Russell phenotype

Communications at Scientific Meetings - International
Kariyawasam UGIU, Udalamaththa AVLK, Karunaratne HWSS, Jayasekara RW, Dissanayake VHW
p32
Publication year: 2014

A Male Infant with Partial Monosomy of 7p21 Syndrome Associated with Craniosynostois, Craniofacial Dysmorphism and Non Communicating Hydrocephalus

Communications at Scientific Meetings - International
Wanigasekara TD, Sumathipala D, Kariyawasam UGIU, Udalamaththa AVLK, Saman Kumara LPC, Jayasekara RW, Dissanayake VHW.
p37
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

A Child with a novel de novo mutation in the Aristaless Domain of the Aristaless-Related Homeobox (ARX) gene presenting with ambiguous genitalia

Communications at Scientific Meetings - International
Sirisena ND, McElreavey K, Bashamboo A, de Silva KSH, Jayasekara RW, Dissanayake VHW
p34
Publication year: 2014

A case series of four Sri Lankan patients with 5p deletion

Communications at Scientific Meetings - International
Senaratne LDS, Gautam B, Sumathipala DS, Sirisena ND, Jayasekara RW, Dissanayake VHW
p36
Publication year: 2014

A case report of a Sri Lankan child with mosaic cell lines for ring chromosome 6 and monosomy 6

Communications at Scientific Meetings - International
Banstola SR, Jayawardana SMA, Udalamaththa AVLK, Karunaratne HWSS, Jayasekara RW, Dissanayake VHW
p27
Publication year: 2014

A case report of a patient with mosaicism for ring chromosome 6 and monosomy 6 cell lines: FOXC1 gene deletion with no associated eye anomalies

Communications at Scientific Meetings - National
Banstola SR, Udalamaththa AVLK, Kariyawasam UGIU, Sirisena UND, Dissanayake VHW.
p205
Publication year: 2014

A case report of a child with trisomy 21 and reciprocal translocation between chromosome 1 and 18

Communications at Scientific Meetings - International
Jeerasinghe PB, Udalamaththa AVLK, Weerapperuma KND, Jayasinghe N, Jayasekara RW, Dissanayake VHW.
p27
Publication year: 2014

A baby with a de novo derivative Chromosome 5

Communications at Scientific Meetings - International
IUH Godapitiya, FM Jainlabdeen, NDW Dissanayake, UGIU Kariyawasam, R Senevirathne, Dissanayake VHW
p32
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

HLA-DQ alleles as susceptibility to Cutaeneous Leishmaniasis in Sri Lanka

Communications at Scientific Meetings - International
Samaranayaka N, Fernando D, Balaji K, Jayasekara RW, Dissanayake VHW.
p226
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

Detection of microbes in the placental tissues of women with pre-eclampsia

Communications at Scientific Meetings - International
Amarasekara R, Jayasekara RW, Senanayake H, 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
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