Author

Marta Arpone

Observed names: Arpone, Marta, M Arpone

Institutions: Hunter Genetics, Murdoch Children's Research Institute

Observed institutions: University of Technology Sydney, Royal Children's Hospital, University of Padua, Vita-Salute San Raffaele University, The University of Melbourne, Florey Institute of Neuroscience and Mental Health, Hunter Genetics, Victorian Clinical Genetics Services, Murdoch Children's Research Institute, Austin Health

ORCID: 0000-0001-8111-7240

Observed ORCID: 0000-0001-8111-7240

OpenAlex ID: A5068451116

Emotion recognition from facial expressions: a normative study of the Ekman 60-Faces Test in the Italian population

2014 · Alessandra Dodich, Chiara Cerami, et al. · Neurological Sciences · 118

Microstructural white matter correlates of emotion recognition impairment in Amyotrophic Lateral Sclerosis

2014 · Chiara Crespi, Chiara Cerami, et al. · Cortex · 89

Intellectual functioning and behavioural features associated with mosaicism in fragile X syndrome

2019 · Emma K. Baker, Marta Arpone, et al. · Journal of Neurodevelopmental Disorders · 48

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Cognitive, behavioral, and social functioning in children and adults with Dravet syndrome

2020 · Amy Brown, Marta Arpone, et al. · Epilepsy & Behavior · 46

External validation of the DIVA and DIVA3 clinical predictive rules to identify difficult intravenous access in paediatric patients

2020 · Cristian Girotto, Marta Arpone, et al. · Emergency Medicine Journal · 36

Incomplete silencing of full mutation alleles in males with fragile X syndrome is associated with autistic features

2019 · Emma K. Baker, Marta Arpone, et al. · Molecular Autism · 36

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Dysarthria and broader motor speech deficits in Dravet syndrome

2017 · Samantha J. Turner, Amy Brown, et al. · Neurology · 36

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The impact of cognitive aids on resuscitation performance in in-hospital cardiac arrest scenarios: a systematic review and meta-analysis

2022 · Francesco Corazza, Elena Fiorese, et al. · Internal and Emergency Medicine · 34

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Development and Usability of a Novel Interactive Tablet App (PediAppRREST) to Support the Management of Pediatric Cardiac Arrest: Pilot High-Fidelity Simulation-Based Study

2020 · Francesco Corazza, Deborah Snijders, et al. · JMIR mhealth and uhealth · 29

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Partially methylated alleles, microdeletion, and tissue mosaicism in a fragile X male with tremor and ataxia at 30 years of age: A case report

2016 · Yun Tae Hwang, Solange Mabel Aliaga, et al. · American Journal of Medical Genetics Part A · 25

Use of sedation in children receiving computed tomography after head injuries

2014 · Tammy Goldwasser, Silvia Bressan, et al. · European Journal of Emergency Medicine · 22

Effectiveness of a Novel Tablet Application in Reducing Guideline Deviations During Pediatric Cardiac Arrest: A Randomized Clinical Trial

2023 · Francesco Corazza, Marta Arpone, et al. · JAMA Network Open · 19

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Intragenic DNA methylation in buccal epithelial cells and intellectual functioning in a paediatric cohort of males with fragile X

2018 · Marta Arpone, Emma K. Baker, et al. · Scientific Reports · 19

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DNA Methylation at Birth Predicts Intellectual Functioning and Autism Features in Children with Fragile X Syndrome

2020 · Claudine M Kraan, Emma K Baker, et al. · International Journal of Molecular Sciences · 16

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Significantly Elevated FMR1 mRNA and Mosaicism for Methylated Premutation and Full Mutation Alleles in Two Brothers with Autism Features Referred for Fragile X Testing

2019 · Michael Field, Tracy Dudding-Byth, et al. · International Journal of Molecular Sciences · 15

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FMR1 mRNA from full mutation alleles is associated with ABC-CFX scores in males with fragile X syndrome

2020 · Emma K. Baker, Marta Arpone, et al. · Scientific Reports · 14

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Missed intracranial injuries are rare in emergency departments using the PECARN head injury decision rules

2020 · Silvia Bressan, Paola Berlese, et al. · Child s Nervous System · 11

Tissue mosaicism, FMR1 expression and intellectual functioning in males with fragile X syndrome

2022 · Emma K. Baker, Marta Arpone, et al. · American Journal of Medical Genetics Part A · 10

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Accuracy of NEXUS II head injury decision rule in children: a prospective PREDICT cohort study

2018 · Franz E Babl, Ed Oakley, et al. · Emergency Medicine Journal · 9

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Concussion Knowledge and Self-Reported Behaviors in Youth Rugby Players and Their Coaches: A Population-Wide Cross-Sectional Survey

2023 · Marco Bazo, Marta Arpone, et al. · Clinical Journal of Sport Medicine · 8

Molecular Inconsistencies in a Fragile X Male with Early Onset Ataxia

2016 · Yun Hwang, Tracy Dudding, et al. · Genes · 8

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PediAppRREST: effectiveness of an interactive cognitive support tablet app in reducing deviations from guidelines in the management of paediatric cardiac arrest: protocol for a simulation-based randomised controlled trial

2021 · Francesco Corazza, Marta Arpone, et al. · BMJ Open · 6

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Race, ethnicity, and ancestry reporting in genetic counseling research: A focused mapping review and synthesis

2024 · Marta Arpone, Erin Turbitt, et al. · Journal of Genetic Counseling · 4

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Clinical and Molecular Differences between 4-Year-Old Monozygous Male Twins Mosaic for Normal, Premutation and Fragile X Full Mutation Alleles

2019 · Alison Pandelache, Emma K Baker, et al. · Genes · 4

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Agreement between parents' and clinical researchers' ratings of behavioral problems in children with fragile X syndrome and chromosome 15 imprinting disorders

2022 · Marta Arpone, Lesley Bretherton, et al. · Research in Developmental Disabilities · 3

Works count: 42

Citation count: 666

H-index: 15

I10-index: 18