Selaus tekijän mukaan kokoelmassa Vertaisarvioidut artikkelit (Peer-reviewed articles)

Viitteet 1-3 / 3

    • Attitudes towards genetic testing and information: does parenthood shape the views? 

      Saastamoinen, Antti; Hyttinen, Virva; Kortelainen, Mika; Aaltio, Juho; Auranen, Mari; Ylikallio, Emil; Lönnqvist, Tuula; Sainio, Markus; Suomalainen, Anu; Tyynismaa, Henna; Isohanni, Pirjo
      Journal of Community Genetics : 4 (Open Access) (Springer, 2020)
      This study examines how parents of pediatric patients might differ in their views and attitudes towards genetic technology and information when compared to adult patients. There is surprisingly little evidence on how parents ...

    • Cost-effectiveness of whole-exome sequencing in progressive neurological disorders of children 

      Aaltio, Juho; Hyttinen, Virva; Kortelainen, Mika; Frederix, Gerardus W.J.; Lönnqvist, Tuula; Suomalainen, Anu; Isohanni, Pirjo
      European Journal of Paediatric Neurology : Open Access (Elsevier, 2022)
      Objectives: To clarify the diagnostic utility and the cost-effectiveness of whole-exome sequencing (WES) as a routine early-diagnostic tool in children with progressive neurological disorders. Methods: Patients with ...

    • Effectiveness of clinical exome sequencing in adult patients with difficult-to-diagnose neurological disorders 

      Sainio, Markus T.; Aaltio, Juho; Hyttinen, Virva; Kortelainen, Mika; Ojanen, Simo; Paetau, Anders; Tienari, Pentti; Ylikallio, Eemil; Auranen, Mari; Tyynismaa, Henna
      Acta Neurologica Scandinavica : 1, Open Access (Wiley, 2021)
      Objectives: Clinical diagnostics in adults with hereditary neurological diseases is complicated by clinical and genetic heterogeneity, as well as lifestyle effects. Here, we evaluate the effectiveness of exome sequencing ...