Genomic landscape of positive natural selection in Northern European populationsLAPPALAINEN, Tuuli; SALMELA, Elina; ANDERSEN, Peter M et al.European journal of human genetics. 2010, Vol 18, Num 4, pp 471-478, issn 1018-4813, 8 p.Article

Psoriasis susceptibility locus on 18p revealed by genome scan in finnish families not associated with PSORS1ASUMALAHTI, Kati; LAITINEN, Tarja; UURASMAA, Tutta et al.Journal of investigative dermatology. 2003, Vol 121, Num 4, pp 735-740, issn 0022-202X, 6 p.Article

A novel low-penetrance locus for familial glioma at 15q23-q26.3PAUNU, Niina; LAHERMO, Päivi; ONKAMO, Päivi et al.Cancer research (Baltimore). 2002, Vol 62, Num 13, pp 3798-3802, issn 0008-5472Article

Mutations in AXIN2 cause familial tooth agenesis and predispose to colorectal cancerLAMMI, Laura; ARTE, Sirpa; SOMER, Mirja et al.American journal of human genetics. 2004, Vol 74, Num 5, pp 1043-1050, issn 0002-9297, 8 p.Article

European lactase persistence genotype shows evidence of association with increase in body mass indexKETTUNEN, Johannes; SILANDER, Kaisa; POUTA, Anneli et al.Human molecular genetics (Print). 2010, Vol 19, Num 6, pp 1129-1136, issn 0964-6906, 8 p.Article

Association Between Genes of Disrupted in Schizophrenia 1 (DISC1) Interactors and Schizophrenia Supports the Role of the DISC1 Pathway in the Etiology of Major Mental IllnessesTOMPPO, Liisa; HENNAH, William; LAHERMO, Päivi et al.Biological psychiatry (1969). 2009, Vol 65, Num 12, pp 1055-1062, issn 0006-3223, 8 p.Article

ELMOD2 is a candidate gene for familial idiopathic pulmonary fibrosisHODGSON, Ulla; PULKKINEN, Ville; TUKIAINEN, Pentti et al.American journal of human genetics. 2006, Vol 79, Num 1, pp 149-154, issn 0002-9297, 6 p.Article

Fine mapping of the 2p11 dyslexia locus and exclusion of TACR1 as a candidate genePEYRARD-JANVID, Myriam; ANTHONI, Heidi; KERE, Juha et al.Human genetics. 2004, Vol 114, Num 5, pp 510-516, issn 0340-6717, 7 p.Article

High prevalence of four long QT syndrome founder mutations in the Finnish populationMARJAMAA, Annukka; SALOMAA, Veikko; SWAN, Heikki et al.Annals of medicine (Helsinki). 2009, Vol 41, Num 3, pp 234-240, issn 0785-3890, 7 p.Article

Association of Variants in DISC1 With Psychosis-Related Traits in a Large Population CohortTOMPPO, Liisa; HENNAH, William; MIETTUNEN, Jouko et al.Archives of general psychiatry. 2009, Vol 66, Num 2, pp 134-141, issn 0003-990X, 8 p.Article

Genome-wide search in Finnish families with inflammatory bowel disease provides evidence for novel susceptibility lociPAAVOLA-SAKKI, Paulina; OLLIKAINEN, Vesa; HELIÖ, Tiina et al.European journal of human genetics. 2003, Vol 11, Num 2, pp 112-120, issn 1018-4813, 9 p.Article

Susceptibility loci for preeclampsia on chromosomes 2p25 and 9p13 in finnish familiesLAIVUORI, Hannele; LAHERMO, Päivi; OLLIKAINEN, Vesa et al.American journal of human genetics. 2003, Vol 72, Num 1, pp 168-177, issn 0002-9297, 10 p.Article

Low-level microsatellite instability in most colorectal carcinomasLAIHO, Päivi; LAUNONEN, Virpi; SHIBATA, Darryl et al.Cancer research (Baltimore). 2002, Vol 62, Num 4, pp 1166-1170, issn 0008-5472Article

Methylation of H19 and its imprinted control region (H19 ICR1) in Müllerian aplasiaSANDBACKA, Maria; BRUCE, Sara; HALTTUNEN, Mervi et al.Fertility and sterility. 2011, Vol 95, Num 8, pp 2703-2706, issn 0015-0282, 4 p.Article