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Human Genetics|November 5, 2003
Identification of two AGTR2 mutations in male patients with non-syndromic mental retardationTero Ylisaukko-oja, Karola Rehnström, Raija Vanhala, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|August 28, 2007
No association between common variants in glyoxalase 1 and autism spectrum disordersKarola Rehnström, Tero Ylisaukko-Oja, Raija Vanhala, et al.
Autism Research : Official Journal of the International Society for Autism Research|April 11, 2009
Mitochondrial aspartate/glutamate carrier SLC25A12 gene is associated with autismJoni A Turunen, Karola Rehnström, Helena Kilpinen, et al.
Genomics|June 1, 2005
Characterization of a novel cation transporter ATPase gene (ATP13A4) interrupted by 3q25-q29 inversion in an individual with language delayDorota A Kwasnicka-Crawford, Andrew R Carson, Wendy Roberts, et al.
European Journal of Human Genetics : EJHG|October 8, 2004
Family-based association study of DYX1C1 variants in autismTero Ylisaukko-Oja, Myriam Peyrard-Janvid, Cecilia M Lindgren, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|November 28, 2008
Allelic variants in HTR3C show association with autismKarola Rehnström, Tero Ylisaukko-oja, Ilona Nummela, et al.
Autism Research : Official Journal of the International Society for Autism Research|March 9, 2011
Fine mapping of Xq11.1-q21.33 and mutation screening of RPS6KA6, ZNF711, ACSL4, DLG3, and IL1RAPL2 for autism spectrum disorders (ASD)Katri Kantojärvi, Ilona Kotala, Karola Rehnström, et al.
Human Molecular Genetics|May 21, 2009
Linkage and linkage disequilibrium scan for autism loci in an extended pedigree from FinlandHelena Kilpinen, Tero Ylisaukko-oja, Karola Rehnström, et al.
American Journal of Medical Genetics. Part A|December 4, 2004
MECP2 mutation analysis in patients with mental retardationTero Ylisaukko-Oja, Karola Rehnström, Raija Vanhala, et al.
American Journal of Medical Genetics. Part A|September 14, 2007
PAK3 related mental disability: further characterization of the phenotypeMaarit Peippo, Anne M Koivisto, Teppo Särkämö, et al.
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