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Eresha Anandanie Jasinge

Observed names: E Jasinge, E. A. Jasinge, E. A. Jasinge, E. Jasinge, E.A. Jasinge, Eresha A. Jasinge, Eresha Jasinge, Eresha Jasinge Jasinge, Eresha. A. Jasinge, Eresha A Jasinge, Jasinge E, Jasinge Eresha
ORCID: 0000-0001-6265-0461
Observed ORCID: 0000-0001-6265-0461
OpenAlex ID: A5049623669
Evaluation of biochemical and haematological changes in dengue fever and dengue hemorrhagic fever in Sri Lankan children: a prospective follow up study
2019 · Grace Angeline Malarnangai Kularatnam, Eresha Jasinge, et al. · BMC Pediatrics · 59
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Novel mutations in the glucocerebrosidase gene of Indian patients with Gaucher disease
2014 · Chitra Ankleshwaria, Mehul Mistri, et al. · Journal of Human Genetics · 34
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An integrated multiomic approach as an excellent tool for the diagnosis of metabolic diseases: our first 3720 patients
2022 · Ligia S. Almeida, Catarina Pereira, et al. · European Journal of Human Genetics · 31
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Lipin-1 Deficiency-Associated Recurrent Rhabdomyolysis and Exercise-Induced Myalgia Persisting into Adulthood: A Case Report and Review of Literature
2020 · Neluwa Liyanage Ruwan Indika, Dinesha Maduri Vidanapathirana, et al. · Case Reports in Medicine · 20
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Phenotypic spectrum and genetic heterogeneity of cystic fibrosis in Sri Lanka
2019 · Neluwa Liyanage Ruwan Indika, Dinesha Maduri Vidanapathirana, et al. · BMC Medical Genetics · 20
Many pitfalls in diagnosis of acute intermittent porphyria: a case report
2018 · N. L. R. Indika, T. Kesavan, et al. · BMC Research Notes · 18
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A rare co-occurrence of duchenne muscular dystrophy, congenital adrenal hypoplasia and glycerol kinase deficiency due to Xp21 contiguous gene deletion syndrome: case report
2021 · Asanka Rathnasiri, Udara Senarathne, et al. · BMC Endocrine Disorders · 13
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A heterozygous variant in the SLC22A12 gene in a Sri Lanka family associated with mild renal hypouricemia
2018 · Dinesha Maduri Vidanapathirana, Subashinie Jayasena, et al. · BMC Pediatrics · 13
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Uric acid, an important screening tool to detect inborn errors of metabolism: a case series
2017 · Eresha Jasinge, Grace Angeline Malarnangai Kularatnam, et al. · BMC Research Notes · 12
Dubin–Johnson syndrome and intrahepatic cholestasis of pregnancy in a Sri Lankan family: a case report
2017 · Grace Angeline Malarnangai Kularatnam, Dilanthi Warawitage, et al. · BMC Research Notes · 11
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Lipoprotein Lipase Deficiency in an Infant With Chylomicronemia, Hepatomegaly, and Lipemia Retinalis
2017 · Dinesha Maduri Vidanapathirana, Thushara Rodrigo, et al. · Global Pediatric Health · 10
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First contiguous gene deletion causing biotinidase deficiency: The enzyme deficiency in three Sri Lankan children
2015 · Danika Nadeen Senanayake, Eresha. A. Jasinge, et al. · Molecular Genetics and Metabolism Reports · 10
A novel mutation in ACADVL causing very long-chain acyl-coenzyme-A dehydrogenase deficiency in a South Asian pediatric patient: a case report and review of the literature
2021 · Visvalingam Arunath, Manoj Sanjeewa Liyanarachchi, et al. · Journal of Medical Case Reports · 8
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Erratum: Novel mutations in the glucocerebrosidase gene of Indian patients with Gaucher disease
2015 · Chitra Ankleshwaria, Mehul Mistri, et al. · Journal of Human Genetics · 8
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Association of Serum Uric acid and Gamma-glutamyltransferase with Obesity Related Metabolic Derangements in a Cohort of Children with Obesity in Sri Lanka
2019 · Dinesha M. Vidanapathirana, Eresha A. Jasinge, et al. · Ceylon Medical Journal · 6
GTP-Cyclohydrolase I deficiency presenting as malignant hyperphenylalaninemia, recurrent hyperthermia and progressive neurological dysfunction in a South Asian child – a case report
2019 · Kavinda Chandimal Dayasiri, Nayani Suraweera, et al. · BMC Pediatrics · 6
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Exome sequencing detected an extremely rare case of foetal onset familial haemophagocytic lymphohistiocytosis type 5 presenting with hydrops foetalis
2021 · V. Thadchanamoorthy, M. T. R. Jayatunga, et al. · BMC Medical Genomics · 5
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Association of fatty liver with serum gamma-glutamyltransferase and uric acid in obese children in a tertiary care centre
2025 · Vidanapathirana Dinesha Maduri, Jasinge Eresha, et al. · BMC Pediatrics · 4
Non-specificity of symptoms in infantile-onset Pompe disease may delay the diagnosis and institution of treatment
2022 · Udara Dilrukshi Senarathne, Eresha Jasinge, et al. · BMJ Case Reports · 4
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A Case of Carbamazepine-Induced Aggravation of Self-Limited Epilepsy with Centrotemporal Spikes Epilepsy and Valproate-Induced Hyperammonemic Encephalopathy in a Child with Heterozygous Gene Variant of Carbomoyl Phosphatase Synthetase Deficiency
2021 · Imalke Kankananarachchi, Eresha Jasinge, et al. · Case Reports in Neurological Medicine · 4
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Cornea Verticillata in classical Fabry disease, first from Sri Lanka: a case report
2020 · Hasani Hewavitharana, Eresha Jasinge, et al. · BMC Pediatrics · 4
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Comparison of urine glycosaminoglycan excretion between children with autism spectrum disorder and typically developed children
2024 · Neluwa-Liyanage R. Indika, Eresha Jasinge, et al. · Research in Autism · 3
Association of selected genetic variants in CBS and MTHFR genes in a cohort of children with homocystinuria in Sri Lanka
2022 · Nadeesha Samarasinghe, Dinithi Mahaliyanage, et al. · Journal of Genetic Engineering and Biotechnology · 3
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Clinical Presentation and Genetic Heterogeneity Including Two Novel Variants in Sri Lankan Patients With Infantile Sandhoff Disease
2022 · Siddiqa Ozaal, Subashinie Jayasena, et al. · Child Neurology Open · 3
A Novel Mutation in ACAT1 Causing Beta-Ketothiolase Deficiency in a 4-Year-Old Sri Lankan Boy with Metabolic Ketoacidosis
2019 · Thivanka Vishwani Manawadu, Eresha Jasinge, et al. · Indian Journal of Clinical Biochemistry · 3
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Works count: 84
Citation count: 343
H-index: 10
I10-index: 12
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