Author

Angela Overkov

Observed names: A. Overkov, Overkov A

Observed institutions: Princess Margaret Hospital for Children, King Edward Memorial Hospital, Australian Genomics Health Alliance

OpenAlex ID: A5031600934

A germline MTOR mutation in Aboriginal Australian siblings with intellectual disability, dysmorphism, macrocephaly, and small thoraces

2015 · Gareth Baynam, Angela Overkov, et al. · American Journal of Medical Genetics Part A · 49

Titin-related familial dilated cardiomyopathy: factors associated with disease onset

2025 · Renee Johnson, Robert A Fletcher, et al. · European Heart Journal · 20

A recurrence of a hydrop lethal skeletal dysplasia showing similarity to Desbuquois dysplasia and a proposed new sign: The Upsilon sign

2010 · Gareth Baynam, Cathy Kiraly‐Borri, et al. · American Journal of Medical Genetics Part A · 13

A multitiered analysis platform for genome sequencing: Design and initial findings of the Australian Genomics Cardiovascular Disorders Flagship

2024 · Rachel Austin, Jaye S. Brown, et al. · Genetics in Medicine Open · 9

Investigation of current models of care for genetic heart disease in Australia: A national clinical audit

2021 · Rachel Austin, Michael C.J. Quinn, et al. · International Journal of Cardiology · 4

Extending the Benign and Malignant Phenotypes Associated with Germline DICER1 Mutations.

2011 · Marc Tischkowitz, Amin Bahubeshi, et al. · 1

Psychosocial Implications of Genome Sequencing for Inherited Cardiac Disease: Outcomes From the Australian Genomics Cardiovascular Disorders Flagship

2026 · L. Catto, A. Butters, et al. · Heart Lung and Circulation

Works count: 8

Citation count: 96

H-index: 4

I10-index: 3