Scientific Meetings Published As Abstracts -International

Publication Types:

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

Scientific Meetings Published As Abstracts -International
Jayawardana SMA, Sumathipala D, Hidellage NT, Abeysekara AAGS, Ratnayake PD, Jayasekara RW, Dissanayake VHW.
8th Annual Academic Sessions of the Association of Sri Lankan Neurologists and the 8th Annual Congress of the Asian Society Against Dementia 2014, Colombo, Sri Lanka. November 14- 16, 2014. (Abstracted in the Proceedings of the 8th Annual Academic Sessions of the Association of Sri Lanakan Neurologists and the 8th Annual Congress of the Asian Society Against Dementia. p77).
Publication year: 2018

Implementation of Genomic Medicine in Sri Lanka.

Scientific Meetings Published As Abstracts -International
Dissanayake VHW, Sirisena N, Sumathipala D, Wetthasinghe K, Jayasekara RW
1. 13th International Congress of Human Genetics. 2 to 8 April 2016. Kyoto, Japan. (Abstracted in the proceedings of the conference).
Publication year: 2016

Two siblings presenting with dysmorphism, developmental delay and intellectual disability due to partial trisomy 8p and partial monosomy 18p resulting from a maternal balanced translocation t(8;18)(p21.3;p11.23)

Scientific Meetings Published As Abstracts -International
U.G.I.U. Kariyawasam, N.D. Sirisena, A.V.L.K. Udalamaththa, N.T. Hidellage, S. Sumanasena, R.W. Jayasekara, V.H.W. Dissanayake
Publication year: 2014

Phenotypic spectrum of Sri Lankan females with Isochromosome X

Scientific Meetings Published As Abstracts -International
S.M.A. Jayawardana, D. Sumathipala, P.K.D.S. Nisansala, R.W. Jayasekara, V.H.W. Dissanayake
Publication year: 2014

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

Scientific Meetings Published As Abstracts -International
S. Kidnapillai, U.G.I.U. Kariyawasam, N.D.W. Dissanayake, R.W. Jayasekara, P.M.G. Punchihewa, V.H.W. Dissanayake
Publication year: 2014

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

Scientific Meetings Published As Abstracts -International
Jayawardana SMA, Sumathipala D, Hidellage NT, Abeysekara AAGS, Ratnayake PD, Jayasekera RW, Dissanayake VHW.
Publication year: 2014

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

Scientific Meetings Published As Abstracts -International
K.M.D. Gunathilake, U.G.I.U. Kariyawasam, S.P. Akmeemana, N.W.D. Dissanayake, R.W. Jayasekara, V.H.W. Dissanayake
Publication year: 2014

henotype of partial trisomy of chromosome 8(p21→pter) and partial monosomy of chromosome 11(q25→qter); A case of dysmorphic features and global developmental delay

Scientific Meetings Published As Abstracts -International
A.V.L.K. Udalamaththa, U.G.I.U. Kariyawasam, D.S. Sumathipala, M. De Silva, R.W. Jayasekara, V.H.W. Dissanayake
Publication year: 2014

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

Scientific Meetings Published As Abstracts -International
Senaratne LDS, Oye AM, Selmer KK, Wanigasinghe J, Sumathipala DS, Jayasekara RW, Dissanayake VHW.
Publication year: 2014

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

Scientific Meetings Published As Abstracts -International
Senaratne LDS, Oye AM, Selmer KK, Wanigasinghe J, Sumathipala DS, Netthikumara NF, Jayasekara RW, Dissanayake VHW
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

Scientific Meetings Published As Abstracts -International
N.D. Sirisena, A.A.G.S. Abeysekara, K.S.H. de Silva, R.W. Jayasekara, Vajira H. W. Dissanayake
Publication year: 2014

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

Scientific Meetings Published As Abstracts -International
A.V.L.K. Udalamaththa, U.G.I.U. Kariyawasam, P.K.D.S. Nisansala, R.W. Jayasekara, V.H.W. Dissanayake
Publication year: 2014

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

Scientific Meetings Published As Abstracts -International
K.N.D. Weerapperuma, B. Gautham, H.W.S.S. Karunaratne, D. Samarasinghe, R.W. Jayasekara, V.H. W. Dissanayake
Publication year: 2014

Child with a Homozygous Mutation in the Treacher Collins-Franceschetti Syndrome 1 gene (TCOF1) Presenting with Ambiguous Genitalia, Cranio-facial Dysmorphism and Multiple Congenital Malformations

Scientific Meetings Published As Abstracts -International
Nirmala D. Sirisena, Kenneth McElreavey, Anu Bashamboo, K.S.H. de Silva, Rohan W. Jayasekara, Vajira H.W. Dissanayake
Publication year: 2014

A study of ninety eight single nucleotide polymorphisms in recurrent spontaneous miscarriage.

Scientific Meetings Published As Abstracts -International
PH Andraweera, GA Dekker, SD Thompson, DL Furness, RC Nowak, A Zhou, V Zhang, VHW Dissanayake, RW Jayasekara, CT Roberts
Publication year: 2014

A ring chromosome 21 in a child with dysmorphic features

Scientific Meetings Published As Abstracts -International
L.A.N Kulathunga, H.W.S.S Karunaratne, L.S.D Senaratne, A.V.L.K Udalamaththa, R.W. Jayasekara, V.H.W Dissanayake
Publication year: 2014

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

Scientific Meetings Published As Abstracts -International
B. Gautam, U.G.I.U. Kariyawasam, P.M.G. Punchihewa, N.D.W. Dissanayake, T. Wanigasekara, R.W. Jayasekara, V.H.W. Dissanayake
Publication year: 2014

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

Scientific Meetings Published As Abstracts -International
U.G.I.U. Kariyawasam, A.V.L.K. Udalamaththa, H.W.S.S. Karunaratne, R.W. Jayasekara,V.H.W. Dissanayake
Publication year: 2014

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

Scientific Meetings Published As Abstracts -International
T.D. Wanigasekera, D. Sumathipala, U.G.I.U. Kariyawasam, A.V.L.K. Udalamaththa, L.P.C. Saman Kumara, R.W. Jayasekara, V.H.W. Dissanayake
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

Scientific Meetings Published As Abstracts -International
N.D. Sirisena, K. McElreavey, A. Bashamboo, K.S.H. de Silva, R.W. Jayasekara, V.H. W. Dissanayake
Publication year: 2014

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

Scientific Meetings Published As Abstracts -International
L.D.S. Senaratne, B. Gautham, D.S. Sumathipala, N.D. Sirisena, R.W. Jayasekera, V.H.W. Dissanayake
Publication year: 2014

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

Scientific Meetings Published As Abstracts -International
S.R. Banstola, S.M.A. Jayawardana, A.V.L.K. Udalamaththa, H.W.S.S. Karunaratne, R.W. Jayasekara, V.H.W. Dissanayake.
Publication year: 2014

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

Scientific Meetings Published As Abstracts -International
P.B. Jeerasinghe, A.V.L.K. Udalamaththa, K.N.D. Weerapperuma, N Jayasinghe, R.W. Jayasekara, V.H.W. Dissanayake
Publication year: 2014

The detection of pathogenic bacteria present in placental tissues of women with preeclampsia using novel molecular genetics techniques

Scientific Meetings Published As Abstracts -International
Amarasekara R, Jayasekara RW, Senanayake H, Dissanayake VHW.
Publication year: 2013

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

Scientific Meetings Published As Abstracts -International
Samaranayaka N, Fernando D, Balaji K, Jayasekara RW, Dissanayake VHW.
Publication year: 2013

A novel de novo mutation in the aristaless domain of the arx gene in a sri lankan male child with acquired microcephaly, psychomotor delay and ambiguous genitalia

Scientific Meetings Published As Abstracts -International
U.N.D. Sirisena, K. McElreavey, A. Bashamboo, R.W. Jayasekara, V.H. Dissanayake.
Publication year: 2013

A novel de novo mutation in the aristaless domain of the arx gene in a sri lankan male child with acquired microcephaly, psychomotor delay and ambiguous genitalia

Scientific Meetings Published As Abstracts -International
U.N.D. Sirisena, K. McElreavey, A. Bashamboo, R.W. Jayasekara, V.H. Dissanayake
Publication year: 2013

A Candidate Gene Association Study of Recurrent Pregnancy Loss in a Sinhalese Population from Sri Lanka

Scientific Meetings Published As Abstracts -International
Prabha Andraweera, Gustaaf Dekker, Steven Thompson, Ang Zhou, Denise Furness, Rachael Nowak, Jamie Zhang,Robert C., Vajira Dissanayake, Rohan Jayasekara.
Publication year: 2012

A Candidate Gene Association Study of preelampsia in Sinhala women

Scientific Meetings Published As Abstracts -International
Prabha Andraweera, Gustaaf Dekker, Steven Thompson, Ang Zhou, Denise Furness, Rachael Nowak, Jamie  Zhang,Robert C., Vajira Dissanayake, Rohan Jayasekara.
Publication year: 2012

A descriptive study of children with ambiguous genitalia in Sri Lanka

Scientific Meetings Published As Abstracts -International
U.N.D. Sirisena, R.W. Jayasekara, V.H.W. Dissanayake
Publication year: 2011
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