Debjani Das
Building 131, Garran Road
Canberra, ACT 2601, Australia
Canberra, ACT 2601, Australia
Last Updated: 09/26/2026
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Found 21 publications
Haploinsufficient variants in SMAD5 are associated with isolated congenital heart disease.
Journal: HGG advances
Published: April 28, 2025
Benchmarking of variant pathogenicity prediction methods using a population genetics approach.
Journal: Bioinformatics advances
Published: April 04, 2025
A three generation family with VACTERL association is found to have a rare form of diamond-blackfan anaemia.
Journal: European journal of human genetics : EJHG
Published: January 20, 2025
A multitiered analysis platform for genome sequencing: Design and initial findings of the Australian Genomics Cardiovascular Disorders Flagship.
Journal: Genetics in medicine open
Published: November 03, 2023
CHDgene: A Curated Database for Congenital Heart Disease Genes.
Journal: Circulation. Genomic and precision medicine
Published: May 06, 2022
Whole genome sequencing in transposition of the great arteries and associations with clinically relevant heart, brain and laterality genes.
Journal: American heart journal
Published: May 20, 2021
Late Onset Alzheimer's Disease Risk Variants in Cognitive Decline: The PATH Through Life Study.
Journal: Journal of Alzheimer's disease : JAD
Published: March 09, 2017
Retrospective assessment of childhood ADHD symptoms for diagnosis in adults: validity of a short 8-item version of the Wender-Utah Rating Scale.
Journal: Attention deficit and hyperactivity disorders
Published: January 31, 2016
Associations between corpus callosum size and ADHD symptoms in older adults: The PATH through life study.
Journal: Psychiatry research. Neuroimaging
Published: January 12, 2016
Association of genetic risk factors with cognitive decline: the PATH through life project.
Journal: Neurobiology of aging
Published: August 08, 2015
Last Updated: 09/26/2026