Author

Linda Warwick

Observed names: L. Warwick, Linda J. Warwick, Warwick, Linda

Institutions: Act Health, ACT Government

Observed institutions: Royal Children's Hospital, QIMR Berghofer Medical Research Institute, Canberra Hospital, Victorian Clinical Genetics Services, Act Health, ACT Government

ORCID: 0000-0002-3378-5479

Observed ORCID: 0000-0002-3378-5479

OpenAlex ID: A5008860729

Standardized practices for RNA diagnostics using clinically accessible specimens reclassifies 75% of putative splicing variants

2021 · Adam M. Bournazos, Lisa G. Riley, et al. · Genetics in Medicine · 102

Biallelic mutations in the 3′ exonuclease TOE1 cause pontocerebellar hypoplasia and uncover a role in snRNA processing

2017 · Rea M Lardelli, Ashleigh E Schaffer, et al. · Nature Genetics · 101

Are videoconferenced consultations as effective as face-to-face consultations for hereditary breast and ovarian cancer genetic counseling?

2011 · Elvira M. Zilliacus, Bettina Meiser, et al. · Genetics in Medicine · 87

Women's Experience of Telehealth Cancer Genetic Counseling

2010 · Elvira M. Zilliacus, Bettina Meiser, et al. · Journal of Genetic Counseling · 79

Neuropsychological functioning in children with early-treated phenylketonuria: impact of white matter abnormalities

2004 · Peter J Anderson, Stephen J Wood, et al. · Developmental Medicine & Child Neurology · 70

Two cases of prenatal analysis for the pathogenic T to G substitution at nucleotide 8993 in mitochondrial DNA

1999 · Sarah L. White, Sara Shanske, et al. · Prenatal Diagnosis · 65

Quantifying family dissemination and identifying barriers to communication of risk information in Australian BRCA families

2017 · Emma Healey, Natalie Taylor, et al. · Genetics in Medicine · 52

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Aligning intuition and theory: enhancing the replicability of behaviour change interventions in cancer genetics

2020 · Natalie Taylor, Emma Healey, et al. · Implementation Science Communications · 42

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A Relational Approach to Genetic Counseling for Hereditary Breast and Ovarian Cancer

2016 · Rowan Forbes Shepherd, Tamara Kayali Browne, et al. · Journal of Genetic Counseling · 26

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Multifactorial Likelihood Assessment of BRCA1 and BRCA2 Missense Variants Confirms That BRCA1:c.122A>G(p.His41Arg) Is a Pathogenic Mutation

2014 · Phillip J. Whiley, Michael T. Parsons, et al. · PLoS ONE · 26

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A tumor focused approach to resolving the etiology of DNA mismatch repair deficient tumors classified as suspected Lynch syndrome

2023 · Romy Walker, Khalid Mahmood, et al. · Journal of Translational Medicine · 23

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Consequences of germline variation disrupting the constitutional translational initiation codon start sites of MLH1 and BRCA2 : Use of potential alternative start sites and implications for predicting variant pathogenicity

2013 · Michael T. Parsons, Phillip J. Whiley, et al. · Molecular Carcinogenesis · 18

Succinic semialdehyde dehydrogenase deficiency: low excretion of metabolites in a neonate

1997 · J. J. Pitt, R. Hawkins, et al. · Journal of Inherited Metabolic Disease · 11

Unintended Diagnosis of Von Hippel Lindau Syndrome Using Array Comparative Genomic Hybridization (CGH): Counseling Challenges Arising from Unexpected Information

2012 · Jennifer Hogan, A. Turner, et al. · Journal of Genetic Counseling · 10

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Breast and ovarian cancer referrals to the ACT Genetic Service: are we meeting guidelines?

2016 · Lucy Aitken, Linda Warwick, et al. · Internal Medicine Journal · 6

Myelodysplastic syndrome and multiple solid tumours in an individual with compound heterozygous deleterious FANCM variants: A case report and review of the literature

2023 · Jun Yen Ng, Linda Warwick, et al. · British Journal of Haematology · 5

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Impact of BRCA1/2 status on young women’s sexual function, relationships, and reproduction after predictive genetic testing

2026 · Laura E. Forrest, Rowan Forbes Shepherd, et al. · European Journal of Human Genetics · 2

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Splenectomy in two siblings with G‐CSF‐dependent glycogen storage disease type Ib

2001 · A. Boneh, A. W. Auldist, et al. · Journal of Inherited Metabolic Disease · 2

Works count: 23

Citation count: 727

H-index: 12

I10-index: 14