Author Search Results

1

Unsung heroes: Genomic successes in the developing world by Dissanayake, Vajira H.W., Barash, Carol Isaacson

Published 2016

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Focusing attention on ancestral diversity within genomics research: a potential means for promoting equity in the provision of genomics based healthcare services in developing coun... by Sirisena, Nirmala D., Dissanayake, Vajira H. W.

Published 2017

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Genetics and genomic medicine in Sri Lanka by Sirisena, Nirmala D., Dissanayake, Vajira H. W.

Published 2019

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Strategies for Genomic Medicine Education in Low- and Middle-Income Countries by Sirisena, Nirmala D., Dissanayake, Vajira H. W.

Published 2019

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Copy Number Variants Captured by the Array Comparative Genomic Hybridization in a Cohort of Patients Affected with Hereditary Colorectal Cancer in Sri Lanka: The First CNV Analysis... by Wijesiriwardhana, Prabhavi, Wetthasinghe, Kalum, Dissanayake, Vajira H W

Published 2021

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Genetic determinants of syndactyly: perspectives on pathogenesis and diagnosis by Cassim, Afraah, Hettiarachchi, Dineshani, Dissanayake, Vajira H. W.

Published 2022

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Relative normalized luciferase activity for the recombinant vector constructs carrying the ancestral and variant alleles for XRCC2:rs3218550 and PHB:rs6917 by Sirisena, Nirmala Dushyanthi, Samaranayake, Nilakshi, Dissanayake, Vajira H. W.

Published 2018

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Genotype data for single nucleotide polymorphism markers in sporadic breast cancer related genes in a Sri Lankan case–control cohort of postmenopausal women by Sirisena, Nirmala Dushyanthi, Samaranayake, Nilakshi, Dissanayake, Vajira H. W.

Published 2019

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Electrophoretic mobility shift assays implicate XRCC2:rs3218550C>T as a potential low-penetrant susceptibility allele for sporadic breast cancer by Sirisena, Nirmala D., Samaranayake, Nilakshi, Dissanayake, Vajira H. W.

Published 2019

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The low frequency of Y chromosome microdeletions in subfertile males in a Sinhalese population of Sri Lanka by Wettasinghe, Tithila Kalum, Jayasekara, Rohan W., Dissanayake, Vajira H. W.

Published 2012

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Implementation of genomic medicine in Sri Lanka: Initial experience and challenges by Sirisena, Nirmala D., Neththikumara, Nilaksha, Wetthasinghe, Kalum, Dissanayake, Vajira H.W.

Published 2016

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17p11.2 and Xq28 duplication detected in a girl diagnosed with Potocki–Lupski syndrome by Sumathipala, Dulika S., Mandawala, Eranda N., Sumanasena, Samanmalee P., Dissanayake, Vajira H. W.

Published 2015

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13

A Sri Lankan child with 49,XXXXY syndrome by Dissanayake, Vajira H. W., Bandarage, Palinda, Pedurupillay, Christeen R. J., Jayasekara, Rohan W.

Published 2010

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14

An Infant Born to a Mother with Gestational Diabetes Presenting with 49,XXXXY Syndrome and Renal Agenesis-A Case Report by Sumathipala, Dulika, Gamage, Thilini, Wijesiriwardena, Bandula, Jayasekara, Rohan W., Dissanayake, Vajira H.W.

Published 2012

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Child with Deletion 9p Syndrome Presenting with Craniofacial Dysmorphism, Developmental Delay, and Multiple Congenital Malformations by Sirisena, Nirmala D., Wijetunge, U. Kalpani S., de Silva, Ramya, Dissanayake, Vajira H. W.

Published 2013

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16

The Frequency and Spectrum of Chromosomal Translocations in a Cohort of Sri Lankans by Paththinige, Chamara S., Sirisena, Nirmala D., Kariyawasam, U. G. I. U., Dissanayake, Vajira H. W.

Published 2019

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An adolescent with 48,XXYY syndrome with hypergonadotrophic hypogonadism, attention deficit hyperactive disorder and renal malformations by Katulanda, Prasad, Rajapakse, J. Rasika D. K., Kariyawasam, Jayani, Jayasekara, Rohan, Dissanayake, Vajira H. W.

Published 2012

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A Case Series of Five Sri Lankan Patients with Ovotesticular Disorder of Sex Development by Wettasinghe, Kalum T., Sirisena, Nirmala D., Andraweera, Prabha H., Jayasekara, Rohan W., Dissanayake, Vajira H. W.

Published 2012

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19

Genome-wide linkage search for cancer susceptibility loci in a cohort of non BRCA1/2 families in Sri Lanka by Wijesiriwardhana, Prabhavi, Musolf, Anthony M., Bailey-Wilson, Joan E., Wetthasinghe, T. Kalum, Dissanayake, Vajira H. W.

Published 2022

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A child with mosaicism for deletion (14)(q11.2q13) by Gamage, Thilini H., Godapitiya, Imaya U.H., Nanayakkara, Shakila, Jayasekara, Rohan W., Dissanayake, Vajira H.W.

Published 2012

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Search Results - Dissanayake, Vajira H.W.

Unsung heroes: Genomic successes in the developing world by Dissanayake, Vajira H.W., Barash, Carol Isaacson

Focusing attention on ancestral diversity within genomics research: a potential means for promoting equity in the provision of genomics based healthcare services in developing coun... by Sirisena, Nirmala D., Dissanayake, Vajira H. W.

Genetics and genomic medicine in Sri Lanka by Sirisena, Nirmala D., Dissanayake, Vajira H. W.

Strategies for Genomic Medicine Education in Low- and Middle-Income Countries by Sirisena, Nirmala D., Dissanayake, Vajira H. W.

Copy Number Variants Captured by the Array Comparative Genomic Hybridization in a Cohort of Patients Affected with Hereditary Colorectal Cancer in Sri Lanka: The First CNV Analysis... by Wijesiriwardhana, Prabhavi, Wetthasinghe, Kalum, Dissanayake, Vajira H W

Genetic determinants of syndactyly: perspectives on pathogenesis and diagnosis by Cassim, Afraah, Hettiarachchi, Dineshani, Dissanayake, Vajira H. W.

Relative normalized luciferase activity for the recombinant vector constructs carrying the ancestral and variant alleles for XRCC2:rs3218550 and PHB:rs6917 by Sirisena, Nirmala Dushyanthi, Samaranayake, Nilakshi, Dissanayake, Vajira H. W.

Genotype data for single nucleotide polymorphism markers in sporadic breast cancer related genes in a Sri Lankan case–control cohort of postmenopausal women by Sirisena, Nirmala Dushyanthi, Samaranayake, Nilakshi, Dissanayake, Vajira H. W.

Electrophoretic mobility shift assays implicate XRCC2:rs3218550C>T as a potential low-penetrant susceptibility allele for sporadic breast cancer by Sirisena, Nirmala D., Samaranayake, Nilakshi, Dissanayake, Vajira H. W.

The low frequency of Y chromosome microdeletions in subfertile males in a Sinhalese population of Sri Lanka by Wettasinghe, Tithila Kalum, Jayasekara, Rohan W., Dissanayake, Vajira H. W.

Implementation of genomic medicine in Sri Lanka: Initial experience and challenges by Sirisena, Nirmala D., Neththikumara, Nilaksha, Wetthasinghe, Kalum, Dissanayake, Vajira H.W.

17p11.2 and Xq28 duplication detected in a girl diagnosed with Potocki–Lupski syndrome by Sumathipala, Dulika S., Mandawala, Eranda N., Sumanasena, Samanmalee P., Dissanayake, Vajira H. W.

A Sri Lankan child with 49,XXXXY syndrome by Dissanayake, Vajira H. W., Bandarage, Palinda, Pedurupillay, Christeen R. J., Jayasekara, Rohan W.

An Infant Born to a Mother with Gestational Diabetes Presenting with 49,XXXXY Syndrome and Renal Agenesis-A Case Report by Sumathipala, Dulika, Gamage, Thilini, Wijesiriwardena, Bandula, Jayasekara, Rohan W., Dissanayake, Vajira H.W.

Child with Deletion 9p Syndrome Presenting with Craniofacial Dysmorphism, Developmental Delay, and Multiple Congenital Malformations by Sirisena, Nirmala D., Wijetunge, U. Kalpani S., de Silva, Ramya, Dissanayake, Vajira H. W.

The Frequency and Spectrum of Chromosomal Translocations in a Cohort of Sri Lankans by Paththinige, Chamara S., Sirisena, Nirmala D., Kariyawasam, U. G. I. U., Dissanayake, Vajira H. W.

An adolescent with 48,XXYY syndrome with hypergonadotrophic hypogonadism, attention deficit hyperactive disorder and renal malformations by Katulanda, Prasad, Rajapakse, J. Rasika D. K., Kariyawasam, Jayani, Jayasekara, Rohan, Dissanayake, Vajira H. W.

A Case Series of Five Sri Lankan Patients with Ovotesticular Disorder of Sex Development by Wettasinghe, Kalum T., Sirisena, Nirmala D., Andraweera, Prabha H., Jayasekara, Rohan W., Dissanayake, Vajira H. W.

Genome-wide linkage search for cancer susceptibility loci in a cohort of non BRCA1/2 families in Sri Lanka by Wijesiriwardhana, Prabhavi, Musolf, Anthony M., Bailey-Wilson, Joan E., Wetthasinghe, T. Kalum, Dissanayake, Vajira H. W.

A child with mosaicism for deletion (14)(q11.2q13) by Gamage, Thilini H., Godapitiya, Imaya U.H., Nanayakkara, Shakila, Jayasekara, Rohan W., Dissanayake, Vajira H.W.

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