MURGIA, ALESSANDRA

MURGIA, ALESSANDRA  

Dipartimento di Salute della Donna e del Bambino - SDB  

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Titolo Data di pubblicazione Autori Rivista Serie Titolo libro
CAGI6 ID panel challenge: assessment of phenotype and variant predictions in 415 children with neurodevelopmental disorders (NDDs) 2025 Aspromonte, Maria CristinaDel Conte, AlessioMurgia, AlessandraPiovesan, DamianoTosatto, Silvio C. E.Leonardi, Emanuela + HUMAN GENETICS - -
Genetic variants and phenotypic data curated for the CAGI6 intellectual disability panel challenge 2025 Aspromonte, Maria CristinaDel Conte, AlessioPolli, RobertaBettella, ElisaNosadini, MargheritaPiovesan, DamianoTosatto, Silvio C EMurgia, AlessandraLeonardi, Emanuela + HUMAN GENETICS - -
Neurobehavioral Outcomes Relate to Activation Ratio in Female Carriers of Fragile X Syndrome Full Mutation: Two Pediatric Case Studies 2025 Di Giorgio E.Benavides Varela S.Porru A.Caviola S.Lunghi M.Rigo P.Mioni G.Calignano G.Valenza E.Beghetti F.Polli R.Sawacha Z.Murgia A. + INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES - -
CAGI, the Critical Assessment of Genome Interpretation, establishes progress and prospects for computational genetic variant interpretation methods 2024 Piero FariselliManuel GiolloSilvio C E TosattoFederica LovisaElisa BettellaFederica CescaRoberta PolliStefano SartoriIrene ToldoMaria C AspromonteEmanuela LeonardiAlessandra MurgiaRui ChenGiovanni MinerviniAlexander M Monzon + GENOME BIOLOGY - -
Expanding the clinical phenotype of SHANK2-related disorders: childhood apraxia of speech in a patient with a novel SHANK2 pathogenic variant 2024 Leonardi, EmanuelaMurgia, Alessandra + EUROPEAN CHILD & ADOLESCENT PSYCHIATRY - -
Unsupervised cluster approach to identify possible associations between phenotypes and gait motor control in children with Fragile X syndrome 2024 Fabiola SpolaorFederica BeghettiAnnamaria GuiottoElisa Di GiorgioRoberta PolliGiulio RigoniAlessandra MurgiaZimi Sawacha + GAIT & POSTURE - -
Activation Ratio Correlates with IQ in Female Carriers of the FMR1 Premutation 2023 Polli, RobertaMurgia, Alessandra + CELLS - -
CAGI6 ID-Challenge: Assessment of phenotype and variant predictions in 415 children with Neurodevelopmental Disorders (NDDs) 2023 Aspromonte, Maria CristinaConte, Alessio DelMurgia, AlessandraPiovesan, DamianoTosatto, Silvio C. E.Leonardi, Emanuela + HUMAN GENETICS - -
CERT1 mutations perturb human development by disrupting sphingolipid homeostasis 2023 Leonardi, EmanuelaMurgia, Alessandra + THE JOURNAL OF CLINICAL INVESTIGATION - -
DNA methylation episignatures are sensitive and specific biomarkers for detection of patients with KAT6A/KAT6B variants 2023 Murgia, AlessandraLeonardi, Emanuela + EPIGENOMICS - -
Expanding the genetics and phenotypic spectrum of Lysine-specific demethylase 5C (KDM5C): a report of 13 novel mutations 2023 Emanuela LeonardiMaria Cristina AspromonteElisa BettellaRoberta PolliGiulia BonatoSerena PellegrinMiryam CarecchioAlessandra Murgia + EUROPEAN JOURNAL OF HUMAN GENETICS - -
A Supervised Classification of Children with Fragile X Syndrome and Controls Based on Kinematic and sEMG Parameters 2022 Fabiola SpolaorMarco RomanatoRoberta PolliAlessandra MurgiaZimi Sawacha + APPLIED SCIENCES - -
Feasibility of Screening for Chromosome 15 Imprinting Disorders in 16 579 Newborns by Using a Novel Genomic Workflow 2022 Murgia, AlessandraLeonardi, EmanuelaPolli, Roberta + JAMA NETWORK OPEN - -
Gain and loss of TASK3 channel function and its regulation by novel variation cause KCNK9 imprinting syndrome 2022 Leonardi, EmanuelaMurgia, AlessandraOgnibene, Davide + GENOME MEDICINE - -
A Missense de Novo Variant in the CASK -interactor KIRREL3 Gene Leading to Neurodevelopmental Disorder with Mild Cerebellar Hypoplasia 2021 Leonardi E.Polli R.Murgia A. + NEUROPEDIATRICS - -
A supervised classification of children with fragile X syndrome and controls driven by gait analysis data 2021 M. RomanatoF. SpolaorA. MurgiaZ. Sawacha + GAIT & POSTURE - -
Feasibility and reliability assessment of video-based motion analysis and surface electromyography in children with fragile x during gait 2021 Sawacha Z.Spolaor F.Piatkowska W. J.Cibin F.Guiotto A.Polli R.Murgia A. + SENSORS - -
Impact of the COVID-19 Italian Lockdown on the Physiological and Psychological Well-Being of Children with Fragile X Syndrome and Their Families 2021 Di Giorgio, ElisaPolli, RobertaLunghi, MarcoMurgia, Alessandra INTERNATIONAL JOURNAL OF ENVIRONMENTAL RESEARCH AND PUBLIC HEALTH - -
Von Hippel-Lindau disease and multispecialist team 2021 Pavesi G.Scarpa B.Zanoletti E.Murgia A. + JOURNAL OF NEUROSURGICAL SCIENCES - -
A Novel WAC Loss of Function Mutation in an Individual Presenting with Encephalopathy Related to Status Epilepticus during Sleep (ESES) 2020 Leonardi E.Aspromonte M. C.Polli R.Bettella E.Cainelli E.Sartori S.Boniver C.Murgia A. + GENES - -