Raija Vanhala

Genetic and Functional Analyses of SHANK2 Mutations Suggest a Multiple Hit Model of Autism Spectrum Disorders

Claire S. Leblond, Jutta Heinrich, Richard Delorme et al. · PLoS Genetics · 2012 · 443 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Speech–sound-selective auditory impairment in children with autism: They can perceive but do not attend

Rita Čėponiené, T. Lepistö, Raija Vanhala et al. · Proceedings of the National Academy of Sciences · 2003 · 396 citations

Health Professions, Neuroscience, Speech-language Pathology +17

The discrimination of and orienting to speech and non-speech sounds in children with autism

T. Lepistö, Teija Kujala, Raija Vanhala et al. · Brain Research · 2005 · 325 citations

Education, Psychology, Speech-language Pathology +11

A Genomewide Screen for Autism-Spectrum Disorders: Evidence for a Major Susceptibility Locus on Chromosome 3q25-27

Mari Auranen, Raija Vanhala, Teppo Varilo et al. · The American Journal of Human Genetics · 2002 · 234 citations · Full text

Life Sciences, Genetics, Molecular Genetics +13

Association of DISC1 with autism and Asperger syndrome

Helena Kilpinen, Tero Ylisaukko‐oja, William Hennah et al. · Molecular Psychiatry · 2007 · 192 citations

Medicine, Neuroscience, Psychiatry +6