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Did you mean kemps e[Author] (134 results)?
Allelic variants in HTR3C show association with autism.
Rehnström K, Ylisaukko-oja T, Nummela I, Ellonen P, Kempas E, Vanhala R, von Wendt L, Järvelä I, Peltonen L. Rehnström K, et al. Among authors: kempas e. Am J Med Genet B Neuropsychiatr Genet. 2009 Jul 5;150B(5):741-6. doi: 10.1002/ajmg.b.30882. Am J Med Genet B Neuropsychiatr Genet. 2009. PMID: 19035560 Free PMC article.
Analysis of four neuroligin genes as candidates for autism.
Ylisaukko-oja T, Rehnström K, Auranen M, Vanhala R, Alen R, Kempas E, Ellonen P, Turunen JA, Makkonen I, Riikonen R, Nieminen-von Wendt T, von Wendt L, Peltonen L, Järvelä I. Ylisaukko-oja T, et al. Among authors: kempas e. Eur J Hum Genet. 2005 Dec;13(12):1285-92. doi: 10.1038/sj.ejhg.5201474. Eur J Hum Genet. 2005. PMID: 16077734
Genome-wide scan for loci of Asperger syndrome.
Ylisaukko-oja T, Nieminen-von Wendt T, Kempas E, Sarenius S, Varilo T, von Wendt L, Peltonen L, Järvelä I. Ylisaukko-oja T, et al. Among authors: kempas e. Mol Psychiatry. 2004 Feb;9(2):161-8. doi: 10.1038/sj.mp.4001385. Mol Psychiatry. 2004. PMID: 14966474
MECP2 mutation analysis in patients with mental retardation.
Ylisaukko-Oja T, Rehnström K, Vanhala R, Kempas E, von Koskull H, Tengström C, Mustonen A, Ounap K, Lähdetie J, Järvelä I. Ylisaukko-Oja T, et al. Among authors: kempas e. Am J Med Genet A. 2005 Jan 15;132A(2):121-4. doi: 10.1002/ajmg.a.30416. Am J Med Genet A. 2005. PMID: 15578581
11 results