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Artificial neural networks reveal sex differences in gene methylation, and connections between maternal risk factors and symptom severity in autism spectrum disorder.
Stoccoro, Andrea; Gallo, Roberta; Calderoni, Sara; Cagiano, Romina; Muratori, Filippo; Migliore, Lucia; Grossi, Enzo; Coppedè, Fabio.
Afiliação
  • Stoccoro A; Department of Translational Research & of New Surgical & Medical Technologies, University of Pisa, Medical School, Via Roma 55, Pisa, 56126, Italy.
  • Gallo R; Department of Translational Research & of New Surgical & Medical Technologies, University of Pisa, Medical School, Via Roma 55, Pisa, 56126, Italy.
  • Calderoni S; IRCCS Stella Maris Foundation, Calambrone, Pisa, 56128, Italy.
  • Cagiano R; Department of Clinical & Experimental Medicine, University of Pisa, Via Roma 55, Pisa, 56126, Italy.
  • Muratori F; IRCCS Stella Maris Foundation, Calambrone, Pisa, 56128, Italy.
  • Migliore L; IRCCS Stella Maris Foundation, Calambrone, Pisa, 56128, Italy.
  • Grossi E; Department of Clinical & Experimental Medicine, University of Pisa, Via Roma 55, Pisa, 56126, Italy.
  • Coppedè F; Department of Translational Research & of New Surgical & Medical Technologies, University of Pisa, Medical School, Via Roma 55, Pisa, 56126, Italy.
Epigenomics ; 14(19): 1181-1195, 2022 10.
Article em En | MEDLINE | ID: mdl-36325841
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Nascimento Prematuro / Transtorno do Espectro Autista Tipo de estudo: Diagnostic_studies / Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Child / Female / Humans / Male / Newborn Idioma: En Revista: Epigenomics Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Itália
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Nascimento Prematuro / Transtorno do Espectro Autista Tipo de estudo: Diagnostic_studies / Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Child / Female / Humans / Male / Newborn Idioma: En Revista: Epigenomics Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Itália