Leena Peltonen

Exclusion of eight genes as mutated loci in congenital nephrotic syndrome of the Finnish type.

L. Peltonen, E. Savolainen, K. Tryggvason, 1994, Kidney international.

A genomewide screen for schizophrenia genes in an isolated Finnish subpopulation, suggesting multiple susceptibility loci.

J. Suvisaari, L. Peltonen, J. Terwilliger, 1999, American journal of human genetics.

Genome-wide scan in a nationwide study sample of schizophrenia families in Finland reveals susceptibility loci on chromosomes 2q and 5q.

J D Terwilliger, T Varilo, J Ekelund, 2001, Human molecular genetics.

Evidence of a predisposing locus to bipolar disorder on Xq24-q27.1 in an extended Finnish pedigree.

L. Peltonen, J. Terwilliger, J. Lönnqvist, 1995, Genome research.

Assignment of the locus for hydrolethalus syndrome to a highly restricted region on 11q23-25.

L. Peltonen, R. Salonen, T. Varilo, 1999, American journal of human genetics.