Zobrazeno 1 - 10 of 590 pro vyhledávání: '"Baccarin M"'
1
Akademický článek
Diagnostic yield and clinical impact of chromosomal microarray analysis in autism spectrum disorder.
Autor: Cucinotta F; Interdepartmental Program 'Autism 0-90', 'G. Martino' University Hospital of Messina, Messina, Italy.; IRCCS Centro Neurolesi 'Bonino Pulejo', Messina, Italy., Lintas C; Service for Neurodevelopmental Disorders & Laboratory of Molecular Psychiatry and Neurogenetics, University 'Campus Bio-Medico', Rome, Italy., Tomaiuolo P; Interdepartmental Program 'Autism 0-90', 'G. Martino' University Hospital of Messina, Messina, Italy., Baccarin M; Mafalda Luce Center for Pervasive Developmental Disorders, Milan, Italy.; Synlab Genetics, Bioggio, Switzerland., Picinelli C; Mafalda Luce Center for Pervasive Developmental Disorders, Milan, Italy., Castronovo P; Mafalda Luce Center for Pervasive Developmental Disorders, Milan, Italy., Sacco R; Service for Neurodevelopmental Disorders & Laboratory of Molecular Psychiatry and Neurogenetics, University 'Campus Bio-Medico', Rome, Italy., Piras IS; Service for Neurodevelopmental Disorders & Laboratory of Molecular Psychiatry and Neurogenetics, University 'Campus Bio-Medico', Rome, Italy.; Neurogenomics Division, The Translational Genomics Research Institute, Phoenix, Arizona, USA., Turriziani L; Interdepartmental Program 'Autism 0-90', 'G. Martino' University Hospital of Messina, Messina, Italy., Ricciardello A; Interdepartmental Program 'Autism 0-90', 'G. Martino' University Hospital of Messina, Messina, Italy., Scattoni ML; Research Coordination and Support Service, Istituto Superiore di Sanità, Rome, Italy., Persico AM; Child and Adolescent Neuropsychiatry Program, Modena University Hospital & Department of Biomedical, Metabolic and Neural Sciences, University of Modena and Reggio Emilia, Modena, Italy.
Publikováno v: Molecular genetics & genomic medicine [Mol Genet Genomic Med] 2023 Aug; Vol. 11 (8), pp. e2182. Date of Electronic Publication: 2023 Apr 25.
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2
Akademický článek
RNA sequencing of blood from sex- and age-matched discordant siblings supports immune and transcriptional dysregulation in autism spectrum disorder.
Autor: Tomaiuolo P; Mafalda Luce Center for Pervasive Developmental Disorders, Milan, Italy., Piras IS; Neurogenomics Division, The Translational Genomics Research Institute, Phoenix, AZ, USA., Sain SB; Center for Translational Genomics and Bioinformatics, IRCCS San Raffaele Scientific Institute, Milan, Italy., Picinelli C; Mafalda Luce Center for Pervasive Developmental Disorders, Milan, Italy., Baccarin M; Mafalda Luce Center for Pervasive Developmental Disorders, Milan, Italy.; Department of Genetics, Synlab Suisse SA, Bioggio, Switzerland., Castronovo P; Mafalda Luce Center for Pervasive Developmental Disorders, Milan, Italy., Morelli MJ; Center for Translational Genomics and Bioinformatics, IRCCS San Raffaele Scientific Institute, Milan, Italy., Lazarevic D; Center for Translational Genomics and Bioinformatics, IRCCS San Raffaele Scientific Institute, Milan, Italy., Scattoni ML; Research Coordination and Support Service, Istituto Superiore di Sanità, Rome, Italy., Tonon G; Center for Translational Genomics and Bioinformatics, IRCCS San Raffaele Scientific Institute, Milan, Italy., Persico AM; Child and Adolescent Neuropsychiatry Program, Department of Biomedical, Metabolic and Neural Sciences, University of Modena and Reggio Emilia, Via Giuseppe Campi 287, 41125, Modena, Italy. antonio.persico@unimore.it.
Publikováno v: Scientific reports [Sci Rep] 2023 Jan 16; Vol. 13 (1), pp. 807. Date of Electronic Publication: 2023 Jan 16.
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3
Akademický článek
Yield of array-CGH analysis in Tunisian children with autism spectrum disorder.
Autor: Chehbani F; Department of Psychiatry, Research Laboratory 'Vulnerability to Psychotic Disorders LR 05 ES 10', Monastir University Hospital, Monastir, Tunisia.; Faculty of Pharmacy, University of Monastir, Monastir, Tunisia., Tomaiuolo P; Mafalda Luce Center for Pervasive Developmental Disorders, Milan, Italy., Picinelli C; Mafalda Luce Center for Pervasive Developmental Disorders, Milan, Italy., Baccarin M; Mafalda Luce Center for Pervasive Developmental Disorders, Milan, Italy.; Department of Genetics, Synlab Suisse SA, Bioggio, Switzerland., Castronovo P; Mafalda Luce Center for Pervasive Developmental Disorders, Milan, Italy., Scattoni ML; Research Coordination and Support Service, Istituto Superiore di Sanità, Rome, Italy., Gaddour N; Unit of Child Psychiatry, Monastir University Hospital, Monastir, Tunisia., Persico AM; Child & Adolescent Neuropsychiatry Program, Modena University Hospital & Department of Biomedical, Metabolic and Neural Sciences, University of Modena and Reggio Emilia, Modena, Italy.
Publikováno v: Molecular genetics & genomic medicine [Mol Genet Genomic Med] 2022 Aug; Vol. 10 (8), pp. e1939. Date of Electronic Publication: 2022 Jun 27.
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6
Akademický článek
Huntingtin gene CAG repeat size affects autism risk: Family-based and case-control association study.
Autor: Piras IS; Neurogenomics Division, The Translational Genomics Research Institute, Phoenix, Arizona, USA., Picinelli C; Mafalda Luce Center for Pervasive Developmental Disorders, Milan, Italy., Iennaco R; Department of Biosciences, Università degli Studi di Milano, Milan, Italy.; Istituto Nazionale di Genetica Molecolare 'Romeo ed Enrica Invernizzi', Milan, Italy., Baccarin M; Mafalda Luce Center for Pervasive Developmental Disorders, Milan, Italy., Castronovo P; Mafalda Luce Center for Pervasive Developmental Disorders, Milan, Italy., Tomaiuolo P; Interdepartmental Program 'Autism 0-90', 'Gaetano Martino' University Hospital, University of Messina, Messina, Italy., Cucinotta F; Interdepartmental Program 'Autism 0-90', 'Gaetano Martino' University Hospital, University of Messina, Messina, Italy., Ricciardello A; Interdepartmental Program 'Autism 0-90', 'Gaetano Martino' University Hospital, University of Messina, Messina, Italy., Turriziani L; Interdepartmental Program 'Autism 0-90', 'Gaetano Martino' University Hospital, University of Messina, Messina, Italy., Nanetti L; Unit of Medical Genetics and Neurogenetics, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy., Mariotti C; Unit of Medical Genetics and Neurogenetics, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy., Gellera C; Unit of Medical Genetics and Neurogenetics, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy., Lintas C; Unit of Child and Adolescent NeuroPsychiatry & Laboratory of Molecular Psychiatry and Neurogenetics, University Campus Bio-Medico, Rome, Italy., Sacco R; Unit of Child and Adolescent NeuroPsychiatry & Laboratory of Molecular Psychiatry and Neurogenetics, University Campus Bio-Medico, Rome, Italy., Zuccato C; Department of Biosciences, Università degli Studi di Milano, Milan, Italy.; Istituto Nazionale di Genetica Molecolare 'Romeo ed Enrica Invernizzi', Milan, Italy., Cattaneo E; Department of Biosciences, Università degli Studi di Milano, Milan, Italy.; Istituto Nazionale di Genetica Molecolare 'Romeo ed Enrica Invernizzi', Milan, Italy., Persico AM; Interdepartmental Program 'Autism 0-90', 'Gaetano Martino' University Hospital, University of Messina, Messina, Italy.
Publikováno v: American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics [Am J Med Genet B Neuropsychiatr Genet] 2020 Sep; Vol. 183 (6), pp. 341-351. Date of Electronic Publication: 2020 Jul 11.
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7
Akademický článek
Pen sensor made with silver nanoparticles decorating graphite-polyurethane electrodes to detect bisphenol-A in tap and river water samples.
Autor: Baccarin M; São Carlos Institute of Chemistry, University of São Paulo, São Carlos, São Paulo CEP 13566-590, Brazil., Ciciliati MA; São Carlos Institute of Chemistry, University of São Paulo, São Carlos, São Paulo CEP 13566-590, Brazil., Oliveira ON Jr; São Carlos Institute of Physics, University of São Paulo, São Carlos, São Paulo CEP 13566-590, Brazil., Cavalheiro ETG; São Carlos Institute of Chemistry, University of São Paulo, São Carlos, São Paulo CEP 13566-590, Brazil., Raymundo-Pereira PA; São Carlos Institute of Physics, University of São Paulo, São Carlos, São Paulo CEP 13566-590, Brazil. Electronic address: pauloaugustoraymundopereira@gmail.com.
Publikováno v: Materials science & engineering. C, Materials for biological applications [Mater Sci Eng C Mater Biol Appl] 2020 Sep; Vol. 114, pp. 110989. Date of Electronic Publication: 2020 Apr 28.
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8
Akademický článek
FARP-1 deletion is associated with lack of response to autism treatment by early start denver model in a multiplex family.
Autor: Cucinotta F; Interdepartmental Program 'Autism 0-90', 'G. Martino' University Hospital of Messina, Messina, Italy., Ricciardello A; Interdepartmental Program 'Autism 0-90', 'G. Martino' University Hospital of Messina, Messina, Italy., Turriziani L; Interdepartmental Program 'Autism 0-90', 'G. Martino' University Hospital of Messina, Messina, Italy., Calabrese G; Interdepartmental Program 'Autism 0-90', 'G. Martino' University Hospital of Messina, Messina, Italy., Briguglio M; Interdepartmental Program 'Autism 0-90', 'G. Martino' University Hospital of Messina, Messina, Italy., Boncoddo M; Interdepartmental Program 'Autism 0-90', 'G. Martino' University Hospital of Messina, Messina, Italy., Bellomo F; Interdepartmental Program 'Autism 0-90', 'G. Martino' University Hospital of Messina, Messina, Italy., Tomaiuolo P; Interdepartmental Program 'Autism 0-90', 'G. Martino' University Hospital of Messina, Messina, Italy., Martines S; Interdepartmental Program 'Autism 0-90', 'G. Martino' University Hospital of Messina, Messina, Italy., Bruschetta M; Interdepartmental Program 'Autism 0-90', 'G. Martino' University Hospital of Messina, Messina, Italy., La Fauci Belponer F; Interdepartmental Program 'Autism 0-90', 'G. Martino' University Hospital of Messina, Messina, Italy., Di Bella T; Interdepartmental Program 'Autism 0-90', 'G. Martino' University Hospital of Messina, Messina, Italy., Colombi C; Department of Psychiatry, University of Michigan, Ann Arbor, MI, USA., Baccarin M; Mafalda Luce Center for Pervasive Developmental Disorders, Milan, Italy., Picinelli C; Mafalda Luce Center for Pervasive Developmental Disorders, Milan, Italy., Castronovo P; Mafalda Luce Center for Pervasive Developmental Disorders, Milan, Italy., Lintas C; Service for Neurodevelopmental Disorders & Laboratory of Molecular Psychiatry and Neurogenetics, University 'Campus Bio-Medico', Rome, Italy., Sacco R; Service for Neurodevelopmental Disorders & Laboratory of Molecular Psychiatry and Neurogenetics, University 'Campus Bio-Medico', Rome, Italy., Biederer T; Department of Neurology, Yale University School of Medicine, New Haven, CT, USA., Kellam B; Genetics & Genome Biology Program, Toronto, Canada.; The Centre for Applied Genomics, The Hospital for Sick Children, Toronto, Canada., Scherer SW; Genetics & Genome Biology Program, Toronto, Canada.; The Centre for Applied Genomics, The Hospital for Sick Children, Toronto, Canada.; Department of Molecular Genetics, University of Toronto, Toronto, Canada.; McLaughlin Centre, University of Toronto, Toronto, Canada., Persico AM; Interdepartmental Program 'Autism 0-90', 'G. Martino' University Hospital of Messina, Messina, Italy.
Publikováno v: Molecular genetics & genomic medicine [Mol Genet Genomic Med] 2020 Sep; Vol. 8 (9), pp. e1373. Date of Electronic Publication: 2020 Jun 25.
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9
Akademický článek
Appropriateness of array-CGH in the ADHD clinics: A comparative study.
Autor: Baccarin M; Mafalda Luce Center for Pervasive Developmental Disorders, Milan, Italy., Picinelli C; Mafalda Luce Center for Pervasive Developmental Disorders, Milan, Italy., Tomaiuolo P; Mafalda Luce Center for Pervasive Developmental Disorders, Milan, Italy., Castronovo P; Mafalda Luce Center for Pervasive Developmental Disorders, Milan, Italy., Costa A; Service for Neurodevelopmental Disorders, Department of Medicine, University Campus Bio-Medico, Rome, Italy., Verdecchia M; Service for Neurodevelopmental Disorders, Department of Medicine, University Campus Bio-Medico, Rome, Italy., Cannizzaro C; Service for Neurodevelopmental Disorders, Department of Medicine, University Campus Bio-Medico, Rome, Italy., Barbieri G; Service for Neurodevelopmental Disorders, Department of Medicine, University Campus Bio-Medico, Rome, Italy., Sacco R; Service for Neurodevelopmental Disorders, Department of Medicine, University Campus Bio-Medico, Rome, Italy., Persico AM; Interdepartmental Program 'Autism 0-90', 'Gaetano Martino' University Hospital, University of Messina, Messina, Italy., Lintas C; Service for Neurodevelopmental Disorders, Department of Medicine, University Campus Bio-Medico, Rome, Italy.
Publikováno v: Genes, brain, and behavior [Genes Brain Behav] 2020 Jul; Vol. 19 (6), pp. e12651. Date of Electronic Publication: 2020 Apr 12.
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10
Akademický článek
Phenotypic spectrum of NRXN1 mono- and bi-allelic deficiency: A systematic review.
Autor: Castronovo P; Laboratory for Pervasive Developmental Disorders, Mafalda Luce Center, Milan, Italy., Baccarin M; Laboratory for Pervasive Developmental Disorders, Mafalda Luce Center, Milan, Italy., Ricciardello A; Interdepartmental Program 'Autism 0-90', 'Gaetano Martino' University Hospital, University of Messina, Messina, Italy., Picinelli C; Laboratory for Pervasive Developmental Disorders, Mafalda Luce Center, Milan, Italy., Tomaiuolo P; Laboratory for Pervasive Developmental Disorders, Mafalda Luce Center, Milan, Italy., Cucinotta F; Interdepartmental Program 'Autism 0-90', 'Gaetano Martino' University Hospital, University of Messina, Messina, Italy., Frittoli M; Laboratory for Pervasive Developmental Disorders, Mafalda Luce Center, Milan, Italy., Lintas C; Service for Neurodevelopmental Disorders & Laboratory of Molecular Psychiatry and Neurogenetics, University 'Campus Bio-Medico', Rome, Italy., Sacco R; Service for Neurodevelopmental Disorders & Laboratory of Molecular Psychiatry and Neurogenetics, University 'Campus Bio-Medico', Rome, Italy., Persico AM; Interdepartmental Program 'Autism 0-90', 'Gaetano Martino' University Hospital, University of Messina, Messina, Italy.
Publikováno v: Clinical genetics [Clin Genet] 2020 Jan; Vol. 97 (1), pp. 125-137. Date of Electronic Publication: 2019 May 07.
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