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Autism genetics: opportunities and challenges for clinical translation.
Vorstman, Jacob A S; Parr, Jeremy R; Moreno-De-Luca, Daniel; Anney, Richard J L; Nurnberger, John I; Hallmayer, Joachim F.
Afiliación
  • Vorstman JAS; Department of Psychiatry, Brain Center Rudolf Magnus, University Medical Center Utrecht, Heidelberglaan 100, 3485 Utrecht, The Netherlands.
  • Parr JR; Institute of Neuroscience, University of Newcastle, Newcastle upon Tyne NE1 4LP, UK.
  • Moreno-De-Luca D; Division of Child and Adolescent Psychiatry, Department of Psychiatry and Human Behavior, Brown University, Providence, Rhode Island 02912, USA.
  • Anney RJL; Medical Research Council Centre for Neuropsychiatric Genetics and Genomics, Division of Psychological Medicine and Clinical Neurosciences, Cardiff University, Hadyn Ellis Building, Maindy Road, Cardiff CF24 4HQ, UK.
  • Nurnberger JI; Department of Psychiatry, Stark Neurosciences Research Institute, Indiana University School of Medicine.
  • Hallmayer JF; Department of Medical &Molecular Genetics, Indiana University School of Medicine, 320 West 15th Street, Indianapolis, Indiana 46202, USA.
Nat Rev Genet ; 18(6): 362-376, 2017 06.
Article en En | MEDLINE | ID: mdl-28260791
Genetic studies have revealed the involvement of hundreds of gene variants in autism. Their risk effects are highly variable, and they are frequently related to other conditions besides autism. However, many different variants converge on common biological pathways. These findings indicate that aetiological heterogeneity, variable penetrance and genetic pleiotropy are pervasive characteristics of autism genetics. Although this advancing insight should improve clinical care, at present there is a substantial discrepancy between research knowledge and its clinical application. In this Review, we discuss the current challenges and opportunities for the translation of autism genetics knowledge into clinical practice.
Asunto(s)

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Trastorno Autístico Límite: Humans Idioma: En Revista: Nat Rev Genet Asunto de la revista: GENETICA Año: 2017 Tipo del documento: Article País de afiliación: Países Bajos

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Trastorno Autístico Límite: Humans Idioma: En Revista: Nat Rev Genet Asunto de la revista: GENETICA Año: 2017 Tipo del documento: Article País de afiliación: Países Bajos