T. Ylisaukko-oja

Identification of two AGTR2 mutations in male patients with non-syndromic mental retardation

I. Järvelä, J. Lähdetie, K. Rehnström, 2003, Human Genetics.

A heterogeneity-based genome search meta-analysis for autism-spectrum disorders

L. Peltonen, J. Ioannidis, T. Trikalinos, 2006, Molecular Psychiatry.

Mitochondrial aspartate/glutamate carrier SLC25A12 gene is associated with autism

H. Kilpinen, K. Rehnström, M. Kuokkanen, 2008, Autism research : official journal of the International Society for Autism Research.

Independent replication and initial fine mapping of 3p21–24 in Asperger syndrome

L. Peltonen, I. Järvelä, L. von Wendt, 2005, Journal of Medical Genetics.

Analysis of four neuroligin genes as candidates for autism

L. Peltonen, T. N. Wendt, I. Järvelä, 2005, European Journal of Human Genetics.

Evidence for allelic association on chromosome 3q25–27 in families with autism spectrum disorders originating from a subisolate of Finland

L. Peltonen, I. Järvelä, T. Varilo, 2003, Molecular Psychiatry.

Physicians discuss the risks of smoking with their patients, but seldom offer practical cessation support

J. Jokelainen, M. Timonen, T. Ylisaukko-oja, 2015, Substance Abuse Treatment, Prevention, and Policy.

Reelin Associated With Restricted and Stereotyped Behavior Based on Principal Component Analysis on Autism Diagnostic Interview-Revised

L. Peltonen, S. Ripatti, I. Surakka, 2013 .