The molecular genetics of migraineWESSMAN, Maija; KAUNISTO, Mari A; KALLELA, Mikko et al.Annals of medicine (Helsinki). 2004, Vol 36, Num 6, pp 462-473, issn 0785-3890, 12 p.Article

Patterns of inheritance of Constitutional delay of growth and puberty in families of adolescent girls and boys referred to specialist pediatric careWEHKALAMPI, Karoliina; WIDEN, Elisabeth; LAINE, Tiina et al.The Journal of clinical endocrinology and metabolism. 2008, Vol 93, Num 3, pp 723-728, issn 0021-972X, 6 p.Article

Association of the Timing of Puberty with a Chromosome 2 LocusWEHKALAMPI, Karoliina; WIDEN, Elisabeth; LAINE, Tiina et al.The Journal of clinical endocrinology and metabolism. 2008, Vol 93, Num 12, pp 4833-4839, issn 0021-972X, 7 p.Article

Antenatal gene tests in low-risk pregnancies: molecular screening for aspartylglucosaminuria (AGU) and infantile neuronal ceroid lipofuscinosis (INCL) in FinlandKALLINEN, Juuso; HEINONEN, Seppo; PALOTIE, Aarno et al.Prenatal diagnosis. 2001, Vol 21, Num 5, pp 409-412, issn 0197-3851Article

Genetic similarity of chromosome 6 between patients receiving hematopoietic stem cell transplantation and HLA matched sibling donorsTURPEINEN, Hannu; VOLIN, Liisa; NIKKINEN, Lauri et al.Haematologica (Roma). 2009, Vol 94, Num 4, pp 528-535, issn 0390-6078, 8 p.Article

Wide scope prenatal diagnosis at Kuopio University Hospital 1997-1998: integration of gene tests and fetal karyotypingKALLINEN, Juuso; MARIN, Katja; HEINONEN, Seppo et al.BJOG (Oxford. Print). 2001, Vol 108, Num 5, pp 505-509, issn 1470-0328Conference Paper

Lessons from studying monogenic disease for common diseasePELTONEN, Leena; PEROLA, Markus; NAUKKARINEN, Jussi et al.Human molecular genetics (Print). 2006, Vol 15, issn 0964-6906, R67-R74, NSArticle

Relative levels of SCCA2 and scca1 mRNA in primary tumors predicts recurrent disease in squamous cell cancer of the head and neckSTENMAN, Jakob; HEDSTRÖM, Johan; GRENMAN, Reidar et al.International journal of cancer. 2001, Vol 95, Num 1, pp 39-43, issn 0020-7136Article

Sweet taste preferences are partly genetically determined : identification of a trait locus on chromosome 16KESKITALO, Kaisu; KNAAPILA, Antti; KALLELA, Mikko et al.The American journal of clinical nutrition. 2007, Vol 86, Num 1, pp 55-63, issn 0002-9165, 9 p.Article

Tissue microarray analysis of cytoskeletal actin-associated biomarkers Gelsolin and E-cadherin in urothelial carcinomaJIANYU RAO; SELIGSON, David; VISAPAA, Harri et al.Cancer. 2002, Vol 95, Num 6, pp 1247-1257, issn 0008-543XArticle

CD14 and TNFα promoter polymorphisms in patients with acute arthritis: Special reference to development of chronic spondyloarthropathyREPO, Heikki; ANTTONEN, Krista; KILPINEN, Sami K et al.Scandinavian journal of rheumatology. 2002, Vol 31, Num 6, pp 355-361, issn 0300-9742, 7 p.Article

Genetic component of identification, intensity and pleasantness of odours : a Finnish family studyKNAAPILA, Antti; KESKITALO, Kaisu; KALLELA, Mikko et al.European journal of human genetics. 2007, Vol 15, Num 5, pp 596-602, issn 1018-4813, 7 p.Article

Describing the genetic architecture of epilepsy through heritability analysisSPEED, Doug; O'BRIEN, Terence J; PALOTIE, Aarno et al.Brain. 2014, Vol 137, pp 2680-2689, issn 0006-8950, 10 p., 10Article

Identification of BPESC1, a novel gene disrupted by a balanced chromosomal translocation, t(3;4)(q23;p15.2), in a patient with BPESDE BAERE, Elfride; FUKUSHIMA, Yoshimitsu; SMALL, Kent et al.Genomics (San Diego, Calif.). 2000, Vol 68, Num 3, pp 296-304, issn 0888-7543Article

μ-Opioid Receptor Gene (OPRM1) Polymorphism A118G: Lack of Association in Finnish Populations with Alcohol Dependence or Alcohol ConsumptionROUVINEN-LAGERSTRÖM, Noora; LAHTI, Jari; PALOTIE, Aarno et al.Alcohol and alcoholism (Oxford). 2013, Vol 48, Num 5, pp 519-525, issn 0735-0414, 7 p.Article

Analysis of the phosphatidylinositol 3'-kinase signaling pathway in glioblastoma patients in vivoCHOE, Gheeyoung; HORVATH, Steve; CLOUGHESY, Timothy F et al.Cancer research (Baltimore). 2003, Vol 63, Num 11, pp 2742-2746, issn 0008-5472, 5 p.Article

Quantitative-trait-locus analysis of body-mass index and of stature, by combined analysis of genome scans of five Finnish study groupsPEROLA, Markus; ÖHMAN, Miina; PELTONEN, Leena et al.American journal of human genetics. 2001, Vol 69, Num 1, pp 117-123, issn 0002-9297Article

A Genome-Wide Association Study of Depressive SymptomsHEK, Karin; DEMIRKAN, Ayse; YONGMEI LIU et al.Biological psychiatry (1969). 2013, Vol 73, Num 7, pp 667-678, issn 0006-3223, 12 p.Article

Phenotype mining in CNV carriers from a population cohortPIETILÄINEN, OlliP H; REHNSTRÖM, Karola; RIPATTI, Samuli et al.Human molecular genetics (Print). 2011, Vol 20, Num 13, pp 2686-2695, issn 0964-6906, 10 p.Article

The GENCODE exome: sequencing the complete human exomeCOFFEY, Alison J; KOKOCINSKI, Felix; LEHESJOKI, Anna-Elina et al.European journal of human genetics. 2011, Vol 19, Num 7, pp 827-831, issn 1018-4813, 5 p.Article

Use of a genetic isolate to identify rare disease variants : C7 on 5p associated with MSKALLIO, Suvi P; JAKKULA, Eveliina; VIANDER, Markku et al.Human molecular genetics (Print). 2009, Vol 18, Num 9, pp 1670-1683, issn 0964-6906, 14 p.Article

A susceptibility locus for migraine with aura, on chromosome 4q24WESSMAN, Maija; KALLELA, Mikko; BROAS, Petra et al.American journal of human genetics. 2002, Vol 70, Num 3, pp 652-662, issn 0002-9297Article

A genome-wide association meta-analysis identifies new childhood obesity lociBRADFIELD, Jonathan P; ROB TAAL, H; SALEM, Rany M et al.Nature genetics. 2012, Vol 44, Num 5, pp 526-531, issn 1061-4036, 6 p.Article

Genome-Wide Screen for Metabolic Syndrome Susceptibility Loci Reveals Strong Lipid Gene Contribution But No Evidence for Common Genetic Basis for Clustering of Metabolic Syndrome TraitsKRISTIANSSON, Kati; PEROLA, Markus; ERIKSSON, Johan G et al.Circulation. Cardiovascular genetics (Print). 2012, Vol 5, Num 2, pp 242-249, issn 1942-325X, 8 p.Article

Pubertal Timing and Growth Influences Cardiometabolic Risk Factors in Adult Males and FemalesWIDEN, Elisabeth; SILVENTOINEN, Karri; PELTONEN, Leena et al.Diabetes care. 2012, Vol 35, Num 4, pp 850-856, issn 0149-5992, 7 p.Article