Author

Adriana Lo‐Castro

Observed names: A. Lo Castro, A. Lo-Castro, Adriana Lo-Castro, Adriana Lo-castro, Lo-Castro A

Observed institutions: University of Rome Tor Vergata, Akron Children's Hospital, Policlinico Tor Vergata

OpenAlex ID: A5113579444

Deletions and de novo mutations of SOX11 are associated with a neurodevelopmental disorder with features of Coffin–Siris syndrome

2015 · Annmarie Hempel, Alistair T Pagnamenta, et al. · Journal of Medical Genetics · 83

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Epilepsy associated with autism and attention deficit hyperactivity disorder: Is there a genetic link?

2013 · Adriana Lo-Castro, Paolo Curatolo · Brain and Development · 82

ADHD and genetic syndromes

2010 · Adriana Lo-Castro, Elisa D’Agati, et al. · Brain and Development · 68

Sox11 Is Required to Maintain Proper Levels of Hedgehog Signaling during Vertebrate Ocular Morphogenesis

2014 · Lakshmi Pillai-Kastoori, Wen Wen, et al. · PLoS Genetics · 60

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Neurobehavioral phenotype observed in KBG syndrome caused by ANKRD11 mutations

2012 · Adriana Lo‐Castro, Francesco Brancati, et al. · American Journal of Medical Genetics Part B Neuropsychiatric Genetics · 49

Mild Wolf–Hirschhorn phenotype in a girl with unbalanced t(4p;12p) translocation without seizures

2009 · Cinzia Galasso, Adriana Lo‐Castro, et al. · American Journal of Medical Genetics Part A · 37

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Association of Syndromic Mental Retardation and Autism with 22q11.2 Duplication

2009 · A. Lo-Castro, C. Galasso, et al. · Neuropediatrics · 35

Deletion 2q37: An Identifiable Clinical Syndrome With Mental Retardation and Autism

2008 · Cinzia Galasso, Adriana Lo-Castro, et al. · Journal of Child Neurology · 29

Detecting anxiety symptoms in children and youths with neurofibromatosis type I

2012 · Augusto Pasini, Adriana Lo‐Castro, et al. · American Journal of Medical Genetics Part B Neuropsychiatric Genetics · 27

Planning Deficit in Children With Neurofibromatosis Type 1

2014 · Cinzia Galasso, Adriana Lo-Castro, et al. · Journal of Child Neurology · 23

De novo mosaic ring chromosome 18 in a child with mental retardation, epilepsy and immunological problems

2011 · Adriana Lo-Castro, Nadia El-Malhany, et al. · European Journal of Medical Genetics · 19

Deletion 2p25.2: A cryptic chromosome abnormality in a patient with autism and mental retardation detected using aCGH

2008 · Adriana Lo-Castro, Grazia Giana, et al. · European Journal of Medical Genetics · 18

"Idiopathic" mental retardation and new chromosomal abnormalities

2010 · Cinzia Galasso, Adriana Lo-Castro, et al. · The Italian Journal of Pediatrics/Italian journal of pediatrics · 17

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Autism spectrum disorders associated with chromosomal abnormalities

2009 · Adriana Lo-Castro, Arianna Benvenuto, et al. · Research in Autism · 16

Role of ADHD symptoms as a contributing factor to obesity in patients with MC4R mutations

2014 · Maria-Cristina Porfirio, Silvia Giovinazzo, et al. · Medical Hypotheses · 14

Late-Onset Epileptic Spasms in Children With Pallister-Killian Syndrome: A Report of Two New Cases and Review of the Electroclinical Aspects

2009 · Caterina Cerminara, Eliana Compagnone, et al. · Journal of Child Neurology · 14

Neurologic Aspects of Microcephalic Osteodysplastic Primordial Dwarfism Type II

2008 · Cinzia Galasso, Adriana Lo-Castro, et al. · Pediatric Neurology · 10

Attention-deficit hyperactivity disorder and binge eating disorder in a patient with 2q21.1–q22.2 deletion

2012 · Maria Cristina Porfirio, Adriana Lo-Castro, et al. · Psychiatric Genetics · 9

Neuroimaging findings of Sturge–Weber Syndrome in a child with Tuberous Sclerosis

2008 · P. Curatolo, A. Lo-Castro, et al. · Brain and Development · 6

Review article Epilepsy associated with autism and attention deficit hyperactivity disorder: Is there a genetic link?

2014 · Adriana Lo‐Castro, Paolo Curatolo · 1

Neurobehavioral phenotype observed in KBG syndrome caused by ANKRD11 mutations.

2012 · Lo-Castro A, Brancati F, et al. · Archivio Istituzionale della Ricerca - Università degli Studi dell Aquila

P08.6 De novo mosaic ring chromosome 18 in a child with mental retardation, epilepsy and immunological problems.

2011 · A. Lo-Castro, C. Galasso, et al. · European Journal of Paediatric Neurology

P144 Absence of seizures in a case of Wolf Hirschhorn syndrome with LETM1 deletion

2009 · C. Galasso, A. Lo-Castro, et al. · European Journal of Paediatric Neurology

P143 Late-onset epileptic spasms in children with Pallister Killian syndrome: two new cases and review of the electroclinical aspects

2009 · C. Cerminara, E. Compagnone, et al. · European Journal of Paediatric Neurology

Levetiracetam: efficacy and tolerability in patients with childhood and adolescent absence seizures

2008 · C. Cerminara, L. D'Argenzio, et al. · European Journal of Paediatric Neurology

Works count: 31

Citation count: 616

H-index: 14

I10-index: 17