Publications

Molecular cytogenetic characterization of the first reported Sri Lankan child with a de novo 9p inverted duplication (p13.3; p23)

Communications at Scientific Meetings - National

Godapitiya IUH, Kariyawasam I, Udalamaththa V, Sirisena UND, Dissanayake VHW.

p208

Publication year: 2014

Moebius syndrome: A rare neuro-developmental disorder restricting ocular movements, causing marked facial dysmorphism and amelia: Case report

Communications at Scientific Meetings - International

Weerapperuma KND, Abeysekera H, Irugalbandara D, Dissanayake MM, Dissanayake VHW.

Publication year: 2014

Maternally inherited unbalanced chromosomal (1;17) translocation presenting with craniofacial dysmorphism, developmental delay, and multiple congenital malformations

Communications at Scientific Meetings - International

Weerapperuma KND, Mandawala EDN, Sumathipala DS, De Silva R, Dissanayake VHW.

p34

Publication year: 2014

Karyotype-phenotype correlation in partial monosomy of the long arm of chromosome 13: A case report

Communications at Scientific Meetings - International

Kidnapillai S, Kariyawasam UGIU, Dissanayake NDW, Jayasekara RW, Punchihewa PMG, Dissanayake VHW.

p36

Publication year: 2014

Initial report of MECP2 gene mutations in three girls with Rett syndrome in Sri Lanka

Communications at Scientific Meetings - International

Jayawardana SMA, Sumathipala D, Hidellage NT, Abeysekara AAGS, Ratnayake PD, Jayasekara RW, Dissanayake VHW.

p77

Publication year: 2014

Implementation of an Allele Specific Amplification Refractory Mutation System Polymerase Chain Reaction (AS-ARMS-PCR)

Communications at Scientific Meetings - National

Kulathunga LAN, Wettasinghe KT, Sirisena UND, Dissanayake VHW.

p144-5

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

Hypergonadotrophic hypogonadism associated with 46,X,inv(X)(p11.2p21)

Communications at Scientific Meetings - International

Gunathilake KMD, Kariyawasam UGIU, Akmeemana SP, Dissanayake NDW, Jayasekara RW, Dissanayake VHW

p28

Publication year: 2014

Heredity and Globe Preservation Rates of Retinoblastoma in Sri Lanka

Communications at Scientific Meetings - International

Weerapperuma KND, Abeysekera H, Irugalbandara D, Dissanayake MM, Dissanayake VHW

Publication year: 2014

Hereditary Breast Cancer

Books/Book Chapter

Sirisena N, Dissanayake N, Dissanayake VHW

28-32. [ISBN 978-955-0505-21-0]

Publication year: 2014

Haplotypes of Heparin Binding Epidermal Growth Factor (HBEGF) gene and its association with birth weight of Sinhalese mothers

Communications at Scientific Meetings - National

Galena GH, Dissanayake VHW, Jayasekara RW.

p140-1

Publication year: 2014

Haemachromotosis gene (HFE) in transfusion dependant thalassaemia: phenotype genotype relationship in a Sri Lankan population

Communications at Scientific Meetings - National

Padeniya AGPM, Abeysekara AAGS, Goonasekara HWW, Jayasekara RW, Dissanayake VHW.

Ceylon Medical Journal 2014, 59 (suppl 1):77).

Publication year: 2014

Genetic services provided at De Soysa Hospital for Women from September 2012 to March 2014: a retrospective analysis

Communications at Scientific Meetings - National

Padeniya AGPM, Senewiratne NAJP, Dissanayake VHW.

Ceylon Medical Journal 2014, 59 (Suppl 1):76-7).

Publication year: 2014

Genetic Evaluation and Counseling of a Sri Lankan Family with Autosomal Dominant Blepharophimosis, Ptosis, and Epicanthus Inversus Syndrome Type I

Communications at Scientific Meetings - International

Weerapperuma KND, Dissanayake MM, Sithambarapillai A, Dissanayake VHW

Publication year: 2014

Evaluation of infantile spasms in a cohort of Sri Lankan children with Tuberous Sclerosis Complex

Communications at Scientific Meetings - International

Senaratne LDS, Oye AM, Selmer KK, Wanigasinghe J, Sumathipala DS, Jayasekara RW, Dissanayake VHW.

p32

Publication year: 2014

Digital health: The path to good health on the information superhighway

Books/Book Chapter

Solaiman Juman. Rohan Maharaj, Vajira H. W. Dissanayake, Clive C. James, Roshan Hewapathirana, Pandula Siribaddana, Sundaram Arulrhaj

48-51. [ISBN: 978-1-908609-11-3]

Publication year: 2014

Determination of frequency of HLA-B1502 allele carriers in a cohort of Sri Lankans by HLA-B1502 sequence specific polymerase chain reaction

Communications at Scientific Meetings - National

Gunathilake KMD, Wettasinghe KT, Sirisena UND, Dissanayake VHW.

Publication year: 2014

Design and implementation of novel allele specific multiplex polymerase chain reaction assay to genotype the exon 19 deletion and L858R mutation in the EGFR gene in patients with non-small cell lung carcinoma

Communications at Scientific Meetings - National

Gautam B, Wetthasinghe TK, Sirisena UND, Dissanayake VHW.

p190

Publication year: 2014

Design and implementation of allele specific polymerase chain reaction (AS-PCR) assay to Genotype the V600E mutation in the BRAF gene

Communications at Scientific Meetings - National

Banstola SR, Wettasinghe TK, Sirisena UND, Dissanayake VHW.

p189

Publication year: 2014

Design and implementation of a polymerase chain reaction (PCR) test to genotype the CCR5 delta 32 base pairs deletion

Communications at Scientific Meetings - National

Wetthasinghe TK, Banstola SR, Sirisena UND, Dissanayake VHW.

p192

Publication year: 2014

Design and implementation of a new assay to genotype 460G>A and 719A>G polymorphisms in the Thiopurine S-methyltransferase (TPMT) gene

Communications at Scientific Meetings - National

Jeerasinghe PB, Wettasinghe KT, Sirisena ND, Dissanayake VHW.

p194

Publication year: 2014

Design and implementation of a new assay for genotyping pharmocogenomicaly important Cytochrome P450 2D6 (CYP 2D6) gene variants

Communications at Scientific Meetings - National

Somadasa PKDCT, Wettasinghe KT, Sirisena UND, Dissanayake VHW.

p176

Publication year: 2014

Descriptive study of genetic services provided at De Soysa Hospital for Women from September 2012 to December 2013

Communications at Scientific Meetings - International

Padeniya AGPM, Senewiratne N, Dissanayake VHW.

p38

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

Clinical evaluation and genetic study of Tuberous Sclerosis Complex in a cohort of Sri Lankan children

Communications at Scientific Meetings - International

Senaratne LDS, Oye AM, Selmer KK, Wanigasinghe J, Sumathipala DS, Netthikumara NF, Jayasekara RW, Dissanayake VHW.

p33

Publication year: 2014

Clinical evaluation and genetic study of Tuberous Sclerosis Complex in a cohort of Sri Lankan Children

Communications at Scientific Meetings - National

Senaratne LDS, Oye AM, Selmer KK, Wanigasinghe J, Sumathipala DS, Jayasekara RW, Dissanayake VHW.

p142

Publication year: 2014

Clinical characterization of a cohort of Sri Lankan families with inherited cancer syndromes

Communications at Scientific Meetings - National

Dissanayake NDW, Sirisena ND, Sumathipala D, Dissanayake VHW.

p172

Publication year: 2014

Clinical and genetic features of Spinal Muscular Atrophy in Sri Lanka.

Communications at Scientific Meetings - National

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

Ceylon Medical Journal 2014, 59 (suppl 1):79).

Publication year: 2014

Clinical and genetic characterization of Androgen Receptor (AR) gene mutations in a cohort of Sri Lankan patients with 46,XY Disorders of Sex Development

Communications at Scientific Meetings - International

Sirisena ND, Abeysekara AAGS, de Silva KSH, Jayasekara RW, Dissanayake VHW.

p33

Publication year: 2014

Chromosomal aetiology of 669 cases of syndromic and non-syndromic birth defects: A summary report

Communications at Scientific Meetings - International

Udalamaththa AVLK, Kariyawasam UGIU, Nisansala PKDS, Jayasekara RW, Dissanayake VHW.

p37

Publication year: 2014

Vidya Jyothi Prof. Vajira H.W. Dissanayake

Filter by type:

Molecular cytogenetic characterization of the first reported Sri Lankan child with a de novo 9p inverted duplication (p13.3; p23)

Moebius syndrome: A rare neuro-developmental disorder restricting ocular movements, causing marked facial dysmorphism and amelia: Case report

Maternally inherited unbalanced chromosomal (1;17) translocation presenting with craniofacial dysmorphism, developmental delay, and multiple congenital malformations

Karyotype-phenotype correlation in partial monosomy of the long arm of chromosome 13: A case report

Initial report of MECP2 gene mutations in three girls with Rett syndrome in Sri Lanka

Implementation of an Allele Specific Amplification Refractory Mutation System Polymerase Chain Reaction (AS-ARMS-PCR)

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

Hypergonadotrophic hypogonadism associated with 46,X,inv(X)(p11.2p21)

Heredity and Globe Preservation Rates of Retinoblastoma in Sri Lanka

Hereditary Breast Cancer

Haplotypes of Heparin Binding Epidermal Growth Factor (HBEGF) gene and its association with birth weight of Sinhalese mothers

Haemachromotosis gene (HFE) in transfusion dependant thalassaemia: phenotype genotype relationship in a Sri Lankan population

Genetic services provided at De Soysa Hospital for Women from September 2012 to March 2014: a retrospective analysis

Genetic Evaluation and Counseling of a Sri Lankan Family with Autosomal Dominant Blepharophimosis, Ptosis, and Epicanthus Inversus Syndrome Type I

Evaluation of infantile spasms in a cohort of Sri Lankan children with Tuberous Sclerosis Complex

Digital health: The path to good health on the information superhighway

Determination of frequency of HLA-B1502 allele carriers in a cohort of Sri Lankans by HLA-B1502 sequence specific polymerase chain reaction

Design and implementation of novel allele specific multiplex polymerase chain reaction assay to genotype the exon 19 deletion and L858R mutation in the EGFR gene in patients with non-small cell lung carcinoma

Design and implementation of allele specific polymerase chain reaction (AS-PCR) assay to Genotype the V600E mutation in the BRAF gene

Design and implementation of a polymerase chain reaction (PCR) test to genotype the CCR5 delta 32 base pairs deletion

Design and implementation of a new assay to genotype 460G>A and 719A>G polymorphisms in the Thiopurine S-methyltransferase (TPMT) gene

Design and implementation of a new assay for genotyping pharmocogenomicaly important Cytochrome P450 2D6 (CYP 2D6) gene variants

Descriptive study of genetic services provided at De Soysa Hospital for Women from September 2012 to December 2013

Cytogenetic analysis of chromosomal abnormalities in Sri Lankan children

Clinical evaluation and genetic study of Tuberous Sclerosis Complex in a cohort of Sri Lankan children

Clinical evaluation and genetic study of Tuberous Sclerosis Complex in a cohort of Sri Lankan Children

Clinical characterization of a cohort of Sri Lankan families with inherited cancer syndromes

Clinical and genetic features of Spinal Muscular Atrophy in Sri Lanka.

Clinical and genetic characterization of Androgen Receptor (AR) gene mutations in a cohort of Sri Lankan patients with 46,XY Disorders of Sex Development

Chromosomal aetiology of 669 cases of syndromic and non-syndromic birth defects: A summary report