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Author Details

Marta Romani
Sapienza University of Rome
2004
41
18
Trey Ideker (CM4AI)
PMIDPaper TitleJournal TitlePublished Year
36285951Diagnostic and Therapeutic Challenges of Comorbid ASD, ADHD and Psychosis: A Case Report.Behav Sci (Basel)2022
36138971Feasibility of Screening Programs for Domestic Violence in Pediatric and Child and Adolescent Mental Health Services: A Literature Review.Brain Sci2022
36360447Clinical, Cognitive and Neurodevelopmental Profile in Tetrasomies and Pentasomies: A Systematic Review.Children (Basel)2022
36291492A Narrative Review about Prosocial and Antisocial Behavior in Childhood: The Relationship with Shame and Moral Development.Children (Basel)2022
33237526Riders on the Storm: Did COVID-19 Change Children's Emotional and Behavioral Profile? A Brief Exploratory Survey.Indian J Pediatr2021
34220569Link Between Topographic Memory and the Combined Presentation of ADHD (ADHD-C): A Pilot Study.Front Psychiatry2021
34178884Risks and Protective Factors Associated With Mental Health Symptoms During COVID-19 Home Confinement in Italian Children and Adolescents: The #Understandingkids Study.Front Pediatr2021
30403813Impaired urinary concentration ability is a sensitive predictor of renal disease progression in Joubert syndrome.Nephrol Dial Transplant2020
32916583ADHD and ADHD-related neural networks in benign epilepsy with centrotemporal spikes: A systematic review.Epilepsy Behav2020
32672063Two Cases of Selective Mutism: To Speak Does Not Mean to Recover.Clin Pediatr (Phila)2020
32349379Hyperacusis in Children with Attention Deficit Hyperactivity Disorder: A Preliminary Study.Int J Environ Res Public Health2020
31516627Atypical Childhood-onset Neuroaxonal Dystrophy in an Indian Girl.J Pediatr Neurosci2019
30070380Negative Regulation of Mitochondrial Antiviral Signaling Protein-Mediated Antiviral Signaling by the Mitochondrial Protein LRPPRC During Hepatitis C Virus Infection.Hepatology2019
31242533Intellectual functioning and executive functions in children and adolescents with attention deficit hyperactivity disorder (ADHD) and specific learning disorder (SLD).Scand J Psychol2019
29081005Children's and parent's psychological profiles in selective mutism and generalized anxiety disorder: a clinical study.Eur Child Adolesc Psychiatry2018
29604300Face memory and face recognition in children and adolescents with attention deficit hyperactivity disorder: A systematic review.Neurosci Biobehav Rev2018
28965847Hypomorphic Recessive Variants in SUFU Impair the Sonic Hedgehog Pathway and Cause Joubert Syndrome with Cranio-facial and Skeletal Defects.Am J Hum Genet2017
28357411<i>GNAO1</i> encephalopathy: Broadening the phenotype and evaluating treatment and outcome.Neurol Genet2017
27000981Elevated aspartate aminotransferase and lactate dehydrogenase levels are a constant finding in PLA2G6-associated neurodegeneration.Eur J Neurol2016
27208211Mutations in CEP120 cause Joubert syndrome as well as complex ciliopathy phenotypes.J Med Genet2016
27123480"Fork and bracket" syndrome expands the spectrum of SBF1-related sensory motor polyneuropathies.Neurol Genet2016
27530364Cognitive, adaptive, and behavioral features in Joubert syndrome.Am J Med Genet A2016
27251579Very mild features of dysequilibrium syndrome associated with a novel VLDLR missense mutation.Neurogenetics2016
26982032MKS5 and CEP290 Dependent Assembly Pathway of the Ciliary Transition Zone.PLoS Biol2016
26932191Clinical, neuroradiological and molecular characterization of cerebellar dysplasia with cysts (Poretti-Boltshauser syndrome).Eur J Hum Genet2016
25164370Infantile and childhood onset PLA2G6-associated neurodegeneration in a large North African cohort.Eur J Neurol2015
26489806Cognitive rehabilitation in a child with Joubert Syndrome: Developmental trends and adaptive changes in a single case report.Res Dev Disabil2015
26073777Loss-of-Function Mutations in APPL1 in Familial Diabetes Mellitus.Am J Hum Genet2015
26026149Functional genome-wide siRNA screen identifies KIAA0586 as mutated in Joubert syndrome.Elife2015
25407461Oral-facial-digital syndrome type VI: is C5orf42 really the major gene?Hum Genet2015
24166846A homozygous PDE6D mutation in Joubert syndrome impairs targeting of farnesylated INPP5E protein to the primary cilium.Hum Mutat2014
24886560Mutations in B9D1 and MKS1 cause mild Joubert syndrome: expanding the genetic overlap with the lethal ciliopathy Meckel syndrome.Orphanet J Rare Dis2014
21784762Ex vivo acidic preconditioning enhances bone marrow ckit+ cell therapeutic potential via increased CXCR4 expression.Eur Heart J2013
23870701Joubert syndrome: congenital cerebellar ataxia with the molar tooth.Lancet Neurol2013
22877770A solid quality-control analysis of AB SOLiD short-read sequencing data.Brief Bioinform2013
21656024High mobility group box 1 is a novel substrate of dipeptidyl peptidase-IV.Diabetologia2012
22508326Lack of sequence variations in THAP1 gene and THAP1-binding sites in TOR1A promoter of DYT1 patients.Mov Disord2012
22437320C/EBPγ regulates wound repair and EGF receptor signaling.J Invest Dermatol2012
20007689Role of HIF-1alpha in proton-mediated CXCR4 down-regulation in endothelial cells.Cardiovasc Res2010
17619141Psychiatric comorbidity in learning disorder: analysis of family variables.Child Psychiatry Hum Dev2008
15542633Conventional protein kinase C inhibition prevents alpha interferon-mediated hepatitis C virus replicon clearance by impairing STAT activation.J Virol2004
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University of Pavia
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Co-authored papers 6
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University of Pavia
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Franco Stanzial
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Jennifer L Silhavy
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Nardo Nardocci
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Rose-Mary Boustany
American University of Beirut Medical Center
Co-authored papers 1
Petter Str??mme
University of Oslo
Co-authored papers 1
Colin A Johnson
University of Leeds Leeds Institute of Medical Research at St James's
Co-authored papers 1
Stacey Gabriel
Broad Institute of MIT and Harvard
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Ji Eun Lee
Soonchunhyang University College of Medicine, Bucheon Hospital
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Peter K Jackson
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