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Giulia Valente

Observed names: Giulia M Valente, Giulia M. Valente, Valente, Giulia
ORCID: 0000-0002-1449-2515
Observed ORCID: 0000-0002-1449-2515
OpenAlex ID: A5032938783
Clinical impact of genomic testing in patients with suspected monogenic kidney disease
2020 · Kushani Jayasinghe, Zornitza Stark, et al. · Genetics in Medicine · 128
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A cost-effectiveness analysis of genomic sequencing in a prospective versus historical cohort of complex pediatric patients
2020 · Alison Yeung, Natalie B. Tan, et al. · Genetics in Medicine · 37
Mosaicism in tuberous sclerosis complex: Lowering the threshold for clinical reporting
2022 · Zimeng Ye, Sufang Lin, et al. · Human Mutation · 27
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Implementation and Evaluation of a National Multidisciplinary Kidney Genetics Clinic Network Over 10 Years
2024 · Kushani Jayasinghe, Erik Biros, et al. · Kidney International Reports · 25
Genomic Testing in Patients with Kidney Failure of an Unknown Cause
2024 · Amali C. Mallawaarachchi, Lindsay Fowles, et al. · Clinical Journal of the American Society of Nephrology · 24
Genetic Counseling in the Era of Genomics: What's all the Fuss about?
2018 · Gemma R Brett, Ella J Wilkins, et al. · Journal of Genetic Counseling · 21
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Titin-related familial dilated cardiomyopathy: factors associated with disease onset
2025 · Renee Johnson, Robert A Fletcher, et al. · European Heart Journal · 20
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A novel approach to offering additional genomic findings—A protocol to test a two‐step approach in the healthcare system
2019 · Melissa Martyn, Anaita Kanga‐Parabia, et al. · Journal of Genetic Counseling · 15
Clinical impact of whole-genome sequencing in patients with early-onset dementia
2022 · Aamira J Huq, Bryony Thompson, et al. · Journal of Neurology Neurosurgery & Psychiatry · 14
Experience of the first adult-focussed undiagnosed disease program in Australia (AHA-UDP): solving rare and puzzling genetic disorders is ageless
2024 · Mathew Wallis, Simon D. Bodek, et al. · Orphanet Journal of Rare Diseases · 10
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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
Shaping the future of kidney genetics in Australia: proceedings from the KidGen policy implementation workshop 2023
2024 · Amali Mallawaarachchi, Erik Biros, et al. · Human Genomics · 5
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Factors influencing medical practitioner participation in population carrier screening for cystic fibrosis
2020 · Giulia M. Valente, David J. Amor, et al. · Australian and New Zealand Journal of Obstetrics and Gynaecology · 4
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Scaling up Genomics
2026 · Kushani Jayasinghe, Rigan Tytherleigh, et al. · Clinical Journal of the American Society of Nephrology
A cost-effectiveness and utility analysis of genomic sequencing in a prospective versus historical cohort of complex pediatric patients
2020 · Alison Yeung, NB Tan, et al. · European Journal of Human Genetics
A Demonstration of the Diagnostic and Clinical Utility of Genomic Sequencing in Primary Immunodeficiency Diseases in Australia
2019 · C Slade, Fiona Moghaddas, et al. · Journal of Clinical Immunology
Works count: 20
Citation count: 339
H-index: 10
I10-index: 10
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