Dimuthu Alankarage

Victor Chang Cardiac Research Institute — Australia

Biochemistry, Genetics and Molecular Biology · Life Sciences

6h-index243citations15works4.22yr avg
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Research Topics

Congenital heart defects research(10), Congenital Heart Disease Studies(4), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities(4), Sexual Differentiation and Disorders(4), Sperm and Testicular Function(3)

Publications15 total

Neural crest cell-derived DKK1 and NEDD4 modulate Wnt signalling in the second heart field to orchestrate outflow tract development
Nature Communications·2026Open Access
Haploinsufficient variants in SMAD5 are associated with isolated congenital heart disease
Human Genetics and Genomics Advances·2025Open Access
NKX2-5 congenital heart disease mutations show diverse loss and gain of epigenomic, biochemical and chromatin search functions underpinning pathogenicity
2025Open Access
Neural crest cell derived DKK1 modulates Wnt signalling in the second heart field to orchestrate cardiac outflow tract development
2025
A metabolic signature for NADSYN1-dependent congenital NAD deficiency disorder
Journal of Clinical Investigation·2024· 21 citedOpen Access
Quantitative trait and transcriptome analysis of genetic complexity underpinning cardiac interatrial septation in mice using an advanced intercross line
eLife·2023· 5 citedOpen Access
Author response: Quantitative trait and transcriptome analysis of genetic complexity underpinning cardiac interatrial septation in mice using an advanced intercross line
2023Open Access
Myhre syndrome is caused by dominant-negative dysregulation of SMAD4 and other co-factors
Differentiation·2022· 15 citedOpen Access
Dataset of differentially expressed genes in mouse P12 testes in response to the loss of ATRX in Sertoli cells
Data in Brief·2022· 2 citedOpen Access
Functional genomics and gene-environment interaction highlight the complexity of congenital heart disease caused by Notch pathway variants
Human Molecular Genetics·2019· 49 citedOpen Access
Functional characterization of a novel PBX1 de novo missense variant identified in a patient with syndromic congenital heart disease
Human Molecular Genetics·2019· 32 citedOpen Access
Identification of clinically actionable variants from genome sequencing of families with congenital heart disease
Genetics in Medicine·2018· 84 citedOpen Access
Disorders of Sex Development Loci ☆
Elsevier eBooks·2016
Dataset of differentially expressed genes from SOX9 over-expressing NT2/D1 cells
Data in Brief·2016· 5 citedOpen Access
SOX9 regulates expression of the male fertility gene Ets variant factor 5 (ETV5) during mammalian sex development
The International Journal of Biochemistry & Cell Biology·2016· 30 cited

Frequent Co-authors

Sally L. Dunwoodie(10), Gavin Chapman(7), David T. Humphreys(5), Richard P. Harvey(5), David S. Winlaw(5), Eleni Giannoulatou(5), Justin O. Szot(4), Gillian M. Blue(4), Annabelle Enriquez(4), Edwin P. Kirk(4), Vincent R. Harley(4), Stefan Bagheri‐Fam(3), Hartmut Cuny(2), Michael Troup(2), Kavitha R. Iyer(2), Victoria C. O׳Reilly(2), Ella MMA Martin(2), Duncan B. Sparrow(2), Louisa Ludbrook(2), Stephanie Portelli(2)