Maria Pontillo

ORCID: 0000-0002-0083-0093
Publications
Citations
Views
---
Saved
---
About
Contact & Profiles
Research Areas
  • Congenital heart defects research
  • Schizophrenia research and treatment
  • Autism Spectrum Disorder Research
  • Obsessive-Compulsive Spectrum Disorders
  • Child and Adolescent Psychosocial and Emotional Development
  • Coronary Artery Anomalies
  • Genetics and Neurodevelopmental Disorders
  • Attention Deficit Hyperactivity Disorder
  • Bipolar Disorder and Treatment
  • Congenital Heart Disease Studies
  • Anxiety, Depression, Psychometrics, Treatment, Cognitive Processes
  • Mental Health Research Topics
  • COVID-19 and Mental Health
  • Personality Disorders and Psychopathology
  • Reading and Literacy Development
  • Body Image and Dysmorphia Studies
  • Mental Health and Psychiatry
  • Psychosomatic Disorders and Their Treatments
  • Eating Disorders and Behaviors
  • Tryptophan and brain disorders
  • Family and Disability Support Research
  • Cognitive and developmental aspects of mathematical skills
  • Child Nutrition and Feeding Issues
  • Child Development and Digital Technology
  • Hearing Impairment and Communication

Bambino Gesù Children's Hospital
2016-2025

Istituti di Ricovero e Cura a Carattere Scientifico
2015-2024

Sapienza University of Rome
2012-2020

University of Padua
2020

University of Rome Tor Vergata
2019

Università Cattolica del Sacro Cuore
2016

Office Médico Pédagogique
2016

University of Geneva
2016

Creative Research Enterprises (United States)
2016

Fondazione Santa Lucia
2012-2014

Isabelle Cleynen Worrawat Engchuan Matthew S. Hestand Tracy Heung Aaron M. Holleman and 95 more H. Richard Johnston Thomas Monfeuga Donna M. McDonald‐McGinn Raquel E. Gur Bernice E. Morrow Ann Swillen Jacob Vorstman Carrie E. Bearden Eva W. C. Chow Marianne B. M. van den Bree B S Emanuel Joris Vermeesch Stephen T. Warren Michael J. Owen Pankaj Chopra David J. Cutler Richard Duncan Alex Kotlar Jennifer G. Mulle Anna J. Voss Michael E. Zwick Alexander Diacou Aaron Golden Tingwei Guo Jhih-Rong Lin Tao Wang Zhengdong Zhang Yingjie Zhao Christian R. Marshall Daniele Merico Andrea Jin Brenna Lilley Harold I. Salmons Oanh Tran Peter Holmans Antonio F. Pardiñas James Walters Wolfram Demaerel Erik Boot Nancy J. Butcher Gregory Costain Chelsea Lowther Rens Evers Thérèse van Amelsvoort Esther van Duin Claudia Vingerhoets Jeroen Breckpot Koenraad Devriendt Elfi Vergaelen Annick Vogels T. Blaine Crowley Daniel E. McGinn Edward Moss Robert Sharkus Marta Unolt Elaine H. Zackai Monica E. Calkins Robert S. Gallagher Ruben C. Gur Sunny X. Tang Rosemarie Fritsch Claudia Ornstein Gabriela M. Repetto Elemi Breetvelt Sasja N. Duijff Ania Fiksinski Hayley Moss Maria Niarchou Kieran C. Murphy Sarah E. Prasad Eileen Daly Maria Gudbrandsen Clodagh M. Murphy Declan Murphy Antonio Buzzanca Fabio Di Fabio Maria Cristina Digilio Maria Pontillo Bruno Marino Stefano Vicari Karlene Coleman Joseph F. Cubells Opal Ousley Miri Carmel Doron Gothelf Ehud Mekori‐Domachevsky Elena Michaelovsky Ronnie Weinberger Abraham Weizman Leila Kushan Maria Jalbrzikowski Marco Armando Stéphan Eliez Corrado Sandini Maude Schneider

10.1038/s41380-020-0654-3 article EN Molecular Psychiatry 2020-02-03
Yingjie Zhao Alexander Diacou H. Richard Johnston Fadi I. Musfee Donna M. McDonald‐McGinn and 85 more Daniel E. McGinn T. Blaine Crowley Gabriela M. Repetto Ann Swillen Jeroen Breckpot Joris Vermeesch Wendy R. Kates M. Cristina Digilio Marta Unolt Bruno Marino Maria Pontillo Marco Armando Fabio Di Fabio Stefano Vicari Marianne B. M. van den Bree Hayley Moss Michael J. Owen Kieran C. Murphy Clodagh M. Murphy Declan Murphy Kelly Schoch Vandana Shashi Flora Tassone Tony J. Simon Robert J. Shprintzen Linda Campbell Nicole Philip Damián Heine‐Suñer Sixto García‐Miñaúr Luis C. Fernández Carrie E. Bearden Claudia Vingerhoets Thérèse van Amelsvoort Stéphan Eliez Maude Schneider Jacob Vorstman Doron Gothelf Elaine H. Zackai A. J. Agopian Raquel E. Gur Anne S. Bassett Beverly S. Emanuel Elizabeth Goldmuntz Laura E. Mitchell Tao Wang Bernice E. Morrow Stylianos E. Antonarakis Massimo Biondi Erik Boot Elemi Breetvelt Tiffany Busa Nancy J. Butcher Antonino Buzzanca Miri Carmel Isabelle Cleynen David J. Cutler Bruno Dallapiccola María Angeles de la Fuente Sanches Michael P. Epstein Rens Evers Luis C. Fernández Rosemarie Fritsch Fernando García Algas Tingwei Guo Raquel E. Gur Matthew S. Hestand Tracy Heung Stephen R. Hooper Andrea Jin Leila Kushan Alejandra Laorden-Nieto Guido Maria Lattanzi Christian Marshall Kathryn McCabe Elena Michaelovsky Claudia Ornstein Candice K. Silversides Oanh Tran Esther D.A. van Duin Elfi Vergaelen Steve T. Warren Ronnie Weinberger Abraham Weizman Zhengdong Zhang Michael E. Zwick

10.1016/j.ajhg.2019.11.010 article EN publisher-specific-oa The American Journal of Human Genetics 2019-12-20

Down's syndrome (DS) is the most frequent genetic cause of intellectual disability and patients with DS show significant psychopathology (18-23%). Moreover, individuals often a cognitive decline associated ageing characterized by deterioration in memory, language functioning. According to these relevant findings, an overview presented state-of-the-art knowledge neurocognitive, neurobiological psychopathological profile, assessment treatment DS. The linguistic characteristics develop...

10.1097/ypg.0b013e32835fe426 article EN Psychiatric Genetics 2013-03-22

In this study, we examined the effect of multiple versus single stimulus presentation in typically developing readers and children with developmental dyslexia. The tasks involved either reading words or arrays naming colors digits (rapid automatized RAN). To be able to compare these sets conditions, recorded total response times (i.e., time between onset end participant's vocal response) all cases. study included 43 25 Results indicate that have a clear advantage over items on both RAN...

10.1080/09297049.2012.718325 article EN Child Neuropsychology 2012-08-28

The 22q11.2 deletion syndrome (22q11DS) is characterized by high rates of psychotic symptoms and schizophrenia, making this condition a promising human model for studying risk factors psychosis. We explored the predictive value ultra (UHR) criteria in sample patients with 22q11DS. also examined additional contribution socio-demographic, clinical cognitive variables to predict transition psychosis within mean interval 32.5 ± 17.6 months after initial assessment. Eighty-nine participants...

10.1002/wps.20347 article EN World Psychiatry 2016-09-22

Nearly one-third of individuals with 22q11.2 deletion syndrome (22q11.2DS) develop a psychotic disorder during life, most them by early adulthood. Importantly, full-blown episode is usually preceded subthreshold symptoms. In the current study, 760 participants (aged 6–55 years) confirmed hemizygous microdeletion have been recruited through 10 medical sites worldwide, as part an international research consortium. Of them, 692 were nonpsychotic and complete measurement data. Subthreshold...

10.1093/schbul/sbx005 article EN Schizophrenia Bulletin 2017-01-30

The 22q11.2 deletion syndrome is caused by non‐allelic homologous recombination events during meiosis between low copy repeats (LCR22) termed A, B, C, and D. Most patients have a typical LCR22A‐D (AD) of 3 million base pairs (Mb). In this report, we evaluated IQ scores in 1,478 subjects with 22q11.2DS. mean full scale IQ, verbal performance our cohort were 72.41 (standard deviation‐ SD 13.72), 75.91( 14.46), 73.01( 13.71), respectively. To investigate whether are associated size, examined...

10.1002/ajmg.a.40359 article EN American Journal of Medical Genetics Part A 2018-10-01

Abstract Antipsychotics are the most widely used medications for treatment of schizophrenia spectrum disorders. While such drugs generally ameliorate positive symptoms, clinical responses highly variable in terms negative symptoms and cognitive impairments. However, predictors individual have been elusive. Here, we report a pharmacogenetic interaction related to core dysfunction patients with schizophrenia. We show that genetic variations reducing dysbindin-1 expression can identify...

10.1038/s41467-018-04711-w article EN cc-by Nature Communications 2018-06-05

The aim of the study was to explore clinical significance school refusal behavior, its negative impact on psychological well-being children and adolescents relationship with most common psychopathological conditions during childhood adolescence (e.g. neurodevelopmental disorders, psychiatric disorders). School behavior refers a distressing condition experienced by that compromise regular attendance determine consequences mental health adaptive functioning. A narrative review literature...

10.1186/s13052-024-01667-0 article EN cc-by ˜The œItalian Journal of Pediatrics/Italian journal of pediatrics 2024-05-30

In reading aloud, the eye typically leads over voice position. present study, movements and utterances were simultaneously recorded tracked during of a meaningful text to evaluate eye-voice lead in 16 dyslexic same-age control readers. Dyslexic children slower than peers texts. Their slowness was characterized by great number silent pauses sounding-out behaviors small lengthening word articulation times. Regarding movements, readers made many more fixations (and generally smaller rightward...

10.3389/fnhum.2013.00696 article EN cc-by Frontiers in Human Neuroscience 2013-01-01

Autism Spectrum Disorder (ASD) affects millions of individuals worldwide, presenting challenges in social communication, repetitive behaviors, and sensory processing. Despite its prevalence, diagnosis can be lengthy, access to appropriate treatment varies greatly. This project utilizes the power Artificial Intelligence (AI), particularly Machine Learning (ML) Deep (DL), improve treatment. A central data hub, Master Data Plan (MDP), will aggregate analyze information from diverse sources,...

10.3389/fpsyt.2024.1512818 article EN cc-by Frontiers in Psychiatry 2025-01-22

Anxiety disorders (ADs) are common among children and adolescents frequently co-occur with specific learning disorder (SLD). Approximately 20% of SLD meet criteria for ADs, while those anxiety six times more likely to have a premorbid SLD. The strong relationship between ADs underscores the importance examining developmental trajectories manifestations neuropsychiatric conditions like particularly when is present. In this context, study investigates clinical profiles first diagnosis an AD...

10.1186/s12991-025-00555-z article EN cc-by-nc-nd Annals of General Psychiatry 2025-03-19

Despite evidence suggesting increased rates of psychosis in individuals with autism spectrum disorder (ASD), the detection prodromal psychotic symptoms, including attenuated syndrome (APS), remains underexplored this population. The primary aim present study was to characterize clinical phenotype young ASD who also APS (ASD/APS; n = 48) comparison only (n 93) and those 30) (age range 9-23 years). Assessments included standardized measures autistic symptoms (Autism Diagnostic Observation...

10.3389/fpsyt.2025.1536361 article EN cc-by Frontiers in Psychiatry 2025-03-31

Abstract The catechol- o -methyltransferase ( COMT ) genetic variations produce pleiotropic behavioral/neuroanatomical effects. Some of these effects may vary among sexes. However, the developmental trajectories -by-sex interactions are unclear. Here we found that extreme reduction, in both humans (22q11.2 deletion syndrome Met) and mice −/−), was associated to cortical thinning only after puberty females. Molecular biomarkers, such as tyrosine hydroxylase, Akt neuronal/cellular counting,...

10.1038/tp.2017.109 article EN cc-by Translational Psychiatry 2017-05-30

Aims: Recent meta-analytic data show that approximately 40% of individuals at clinical high risk for psychosis (CHR) receive least one personality disorder (PD) diagnosis. Personality pathology could significantly influence CHR patients' prognosis and response to treatment. We aimed exploring the PD traits adolescents, in order outline a prototypic description their most frequently observed characteristics. Methods: One hundred twenty-three psychiatrists psychologists used Q-sort procedure...

10.3389/fpsyt.2020.562835 article EN cc-by Frontiers in Psychiatry 2020-12-08

Abstract To be relevant to healthcare systems, the clinical high risk for psychosis (CHR-P) concept should denote a specific (i.e., unique) population and provide useful information guide choice of intervention. The current study applied network analyses examine specificities CHR-P youths compared general help-seekers non–CHR-P youth. 146 (mean age = 14.32 years) 103 12.58 help-seeking youth were recruited from neuropsychiatric unit assessed using Structured Interview Psychosis-Risk...

10.1007/s00787-024-02491-x article EN cc-by European Child & Adolescent Psychiatry 2024-06-19
Coming Soon ...