project title: Frequency of HLA-B27 Allele in a Cohort of Sri Lankan Patients Referred for Suspected Spondyloarthritides, Implementation of a Multiplex Tetra-Primer Amplification Refractory Mutation System (T-ARMS) PCR Assay to Genotype APOE alleles, Partial Monosomy of the Long Arm of Chromosome 13 Involving 13q32 Band: A Case Report (MSc awarded - 1 October 2014).
Project title: Frequency of the MTHFR 677 C>T (rs1801133) Gene Polymorphism in Patients Referred for Thrombophilia Screening, Design and Implementation of Allele Specific Tetra-Primer Amplification Refractory Mutation System Polymerase Chain Reaction (T-ARMS-PCR) Genotyping Assays for 1639 G>A and 1173 C>T Polymorphisms in the VKORC1 Gene, A Ring Chromosome 21 in a Child with Dysmorphic Features (MSc awarded - 1 October 2014).
Project title: The Frequency of the Factor V Leiden (F5)1691G>A allele among Sri Lankan Patients with Thromboembolism, Design and Implementation of a Novel Genotyping Assay for CYP2C9, CYP4F2 And GGCX Polymorphisms to Predict Warfarin Maintenance Dose, Design and Implementation of a Tetra Primer Amplification Refractory Mutation System (T-ARMS) Polymerase Chain Reaciton Genotyping Assay for CYP2C19*2 and CYP2C19*17 Polymorphisms, Molecular Cytogenetic Characterization of the First Reported Sri Lankan Child with a De Novo 9p Inverted Duplication (P13.3;P23) (MSc awarded - 1 October 2014).
Project title: The Prevalence of the Prothrombin (F2) 20210G>A Mutation in a Cohort of Sri Lankan Patients with Thromboembolic Disorders, Implementation of an HLA-B*1502 Sequence Specific Polymerase Chain Reaction Assay and Determination of the Frequency of HLA-B*1502 Allele Carriers in a Cohort of Sri Lankans, Implementation of an Allele Specific- Polymerase Chain Reaction Assay for rs2395029 in HCP5 Gene to Detect HLA-B*5701 in a Cohort of Sri Lankans, A Patient With Turner Syndrome with a Karyotype of 45,X`{`38`}`/46,X,r(X)`{`16`}` (MSc awarded - 1 October 2014).
Project title: 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, Design and Implementation of a New Assay for Genotyping Pharmocogenomicaly Important Cytochrome P450 2D6 Gene Variants, Molecular- Cytogenetic Analysis of a Ring Chromosome 18 in a Sri Lankan Female Child with Congenital Malformation, Heart Defects and Global Development Delay (MSc awarded - 1 October 2014).
Project title: BRCA1 Gene Mutations in Sri Lankan Families with Hereditary Breast and Ovarian Cancer Syndrome, Design and Implementation of Novel Allele Specific Multiplex Polymerase Chain Reaction Assay to Genotype Exon 19 Deletion and L858R Mutation in the EGFR Gene in Patients with Non-Small Cell Lung Carcinoma, Paternally Inherited Chromosomal Translocation (8; 11) in a Child with Dysmorphic Features and Seizures (MSc awarded - 1 October 2014).
Project title: Descriptive Study of the Clinical and Genetic Features of Spinal Muscular Atrophy in Sri Lanka, Design and Implementation of a Polymerase Chain Reaction (PCR) test to Genotype the CCR5 Delta 32 Base Pairs Deletion Design and Implementation of Allele Specific Polymerase Chain Reaction (AS-PCR) Assay to Genotype the V600E Mutation in the BRAF Gene, A Case Report of a Patient with Mosaicism for Ring Chromosome 6 and Monosomy 6 Cell Lines: FOXC1 Gene Deletion Without a Correlation for Eye Anomaly Phenotype (MSc awarded - 1 October 2014).
Project title: Frequency of Haemoglobin Beta Gene (HBB) Mutations in a Cohort of Sri Lankan Patients Referred for Β Thalassaemia Screening, Design and Implementation of a New Assay to Genotype 460G>A and 719A>G Polymorphisms in the Thiopurine S-Methyltransferase (TPMT) Gene, A Maternally Inherited Partial Trisomy 1 (q44qter) and Partial Trisomy 15 (pterq22) in a Child with Silver Russell & Partial Trisomy 15q Syndrome” (MSc awarded - 1 October 2014).