Publications by authors named "Decio Brunoni"

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Delayed diagnosis in children with autism spectrum disorder or intellectual disability.
Janaína Aparecida de Oliveira Augusto, Carolina Kulcsar Caravieri, Rodrigo Genaro Arduini, Décio Brunoni, Sylvia Maria Ciasca

Dement Neuropsychol· September 2025

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Dataset of pharmacotherapy in autism spectrum disorder.
Sebastião Gonçalves de Barros Neto, Catherine Oliveira de Araújo, Renandro de Carvaho Reis, Kelson James da Silva Almeida, Decio Brunoni

Data Brief· August 2025

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A Normative Model Representing Autistic Individuals Amidst Autism Spectrum Phenotypic Heterogeneity.
Joana Portolese, Catarina Santos Gomes, Vinicius Daguano Gastaldi, Cristiane Silvestre Paula, Sheila C Caetano, Décio Brunoni

Brain Sci· December 2024

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Exploring the Acquisition of Social Communication Skills in Children with Autism: Preliminary Findings from Applied Behavior Analysis (ABA), Parent Training, and Video Modeling.
Daniela Bordini, Ana Cláudia Moya, Graccielle Rodrigues da Cunha Asevedo, Cristiane Silvestre Paula, Décio Brunoni

Brain Sci· February 2024

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H NMR Metabolomics and Lipidomics To Monitor Positive Responses in Children with Autism Spectrum Disorder Following a Guided Parental Intervention: A Pilot Study.
Banny Silva Barbosa Correia, João Guilherme de Moraes Pontes, João Victor Silva Nani, Fabian Villalta, Natalia Cristina Mor, Décio Brunoni

ACS Chem Neurosci· March 2023

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Phenotypic and mutational spectrum of ROR2-related Robinow syndrome.
Ariadne R Lima, Barbara M Ferreira, Chaofan Zhang, Angad Jolly, Haowei Du, Décio Brunoni

Hum Mutat· July 2022

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SARS-CoV-2 pandemic in the Brazilian community of rare diseases: A patient reported survey.
Ida Vanessa Doederlein Schwartz, Dévora Natalia Randon, Natan Monsores, Carolina Fischinger Moura de Souza, Dafne Dain Gandelman Horovitz, Decio Brunoni

Am J Med Genet C Semin Med Genet· September 2021

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Environmental Influences Measured by Epigenetic Clock and Vulnerability Components at Birth Impact Clinical ASD Heterogeneity.
Viviane Neri de Souza Reis, Ana Carolina Tahira, Vinícius Daguano Gastaldi, Paula Mari, Joana Portolese, Décio Brunoni

Genes (Basel)· September 2021

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TRANSLATION, CULTURAL ADAPTATION, AND EVIDENCE OF INSTRUMENT VALIDITY FOR A MORPHOLOGICAL EXAMINATION PERFORMED IN CHILDREN WITH AUTISM SPECTRUM DISORDER.
Thais Arbocese Zanolla, Eduardo Perrone, Rodrigo Ambrosio Fock, Daniela Bordini, Helena Paula Brentani, Decio Brunoni

Rev Paul Pediatr· November 2020

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Identifying Autism with a Brief and Low-Cost Screening Instrument-OERA: Construct Validity, Invariance Testing, and Agreement Between Judges.
Cristiane S Paula, Graccielle Rodrigues Cunha, Daniela Bordini, Decio Brunoni, Ana Claudia Moya

J Autism Dev Disord· May 2018

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Determining the frequency of morphological characteristics in a sample of Brazilian children.
Eduardo Perrone, Thais Arbocese Zanolla, Rodrigo Ambrosio Fock, Ana Beatriz Alvarez Perez, Decio Brunoni

J Pediatr (Rio J)· November 2017

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Procedures and compliance of a video modeling applied behavior analysis intervention for Brazilian parents of children with autism spectrum disorders.
Leila F Bagaiolo, Jair de J Mari, Daniela Bordini, Tatiane C Ribeiro, Maria Carolina C Martone, Decio Brunoni

Autism· July 2017

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Mismatch between diagnostic reports and special educational needs classification in a public educational system.
Maria Cristina Triguero Veloz Teixeira, Décio Brunoni, Luiz Renato Rodrigues Carreiro, Ana Claudia Braga, Naiara Adorna da Silva

Arq Neuropsiquiatr· April 2017

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Microcephaly and other Zika virus related events: the impact on children, families and health teams.
Decio Brunoni, Silvana Maria Blascovi-Assis, Ana Alexandra Caldas Osório, Alessandra Gotuzo Seabra, Cibelle Albuquerque de la Higuera Amato

Cien Saude Colet· October 2016

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Divorce in families of children with Down Syndrome or Rett Syndrome.
Vivian Renne Gerber Lederman, Bianca dos Santos Alves, Juliana Negrão, José Salomão Schwartzman, Maria Eloisa Famá D'Antino, Decio Brunoni

Cien Saude Colet· May 2015

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Novel Deletion of SERPINF1 Causes Autosomal Recessive Osteogenesis Imperfecta Type VI in Two Brazilian Families.
Renata Moldenhauer Minillo, Nara Sobreira, Maria de Fatima de Faria Soares, Julie Jurgens, Hua Ling, Decio Brunoni

Mol Syndromol· December 2014

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Clinical, cytogenetic, and molecular characterization of six patients with ring chromosomes 22, including one with concomitant 22q11.2 deletion.
Roberta Santos Guilherme, Karina Cunha Soares, Milena Simioni, Tarsis Paiva Vieira, Vera Lúcia Gil-da-Silva-Lopes, Décio Brunoni

Am J Med Genet A· July 2014

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Sclerocornea in a patient with van den Ende-Gupta syndrome homozygous for a SCARF2 microdeletion.
Michele P Migliavacca, Nara L M Sobreira, Graziela P M Antonialli, Mariana M Oliveira, Maria Isabel S A Melaragno, Decio Brunoni

Am J Med Genet A· May 2014

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Twenty-year cytogenetic and molecular follow-up of a patient with ring chromosome 15: a case report.
Roberta S Guilherme, Vera de Fa Meloni, Sylvia S Takeno, Renata Pellegrino, Decio Brunoni

J Med Case Rep· September 2012

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Cytogenomic characterization of an unexpected 17.6 Mb 9p deletion associated to a 14.8 Mb 20p duplication in a dysmorphic patient with multiple congenital anomalies presenting a normal G-banding karyotype.
Vera de Freitas Ayres Meloni, Flavia Balbo Piazzon, Maria de Fátima de Faria Soares, Sylvia Satomi Takeno, Denise Maria Christofolini, Decio Brunoni

Gene· March 2012

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Cytogenetic and molecular evaluation and 20-year follow-up of a patient with ring chromosome 14.
Roberta Santos Guilherme, Vera de Freitas Ayres Meloni, Claudete Palmer Sodré, Denise Maria Christofolini, Renata Pellegrino, Decio Brunoni

Am J Med Genet A· November 2010

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[Use of the Internet to report congenital malformations on birth certificates at four public maternity hospitals in the city of São Paulo, Brazil].
Pablo Domingos Rodrigues De Nicola, Mirlene Cecília Soares Pinho Cernach, Ana Beatriz Alvarez Perez, Decio Brunoni

Cad Saude Publica· July 2010

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Novel mutations in the TBX5 gene in patients with Holt-Oram Syndrome.
Marianna P R Porto, Naja Vergani, Antonio Carlos C Carvalho, Mirlene C S P Cernach, Decio Brunoni

Genet Mol Biol· April 2010

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Genotype-phenotype correlation in Brazillian Rett syndrome patients.
Fernanda T de Lima, Decio Brunoni, José Salomão Schwartzman, Maria Cristina Pozzi, Fernando Kok

Arq Neuropsiquiatr· September 2009

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Evaluation of clinical checklists for fragile X syndrome screening in Brazilian intellectually disabled males: proposal for a new screening tool.
Denise M Christofolini, Eduardo M Abbud, Monica V N Lipay, Silvia S Costa, Angela M Vianna-Morgante, Décio Brunoni

J Intellect Disabil· September 2009

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