Genomics and pediatric researchBORIGHT, Andrew P; KERE, Juha; SCHERER, Stephen W et al.Pediatric research. 2003, Vol 53, Num 1, pp 4-9, issn 0031-3998, 6 p.Article

Familial systemic lupus erythematosus in FinlandKOSKENMIES, Sari; WIDEN, Elisabeth; KERE, Juha et al.Journal of rheumatology. 2001, Vol 28, Num 4, pp 758-760, issn 0315-162XConference Paper

Long-range control of expression in yeastMANNILA, Heikki; PATRIKAINEN, Anne; SEPPÄNEN, Jouni K et al.Bioinformatics (Oxford. Print). 2002, Vol 18, Num 3, pp 482-483, issn 1367-4803Article

Expression of allograft inflammatory factor-1 in inflammatory skin disordersORSMARK, Christina; SKOOG, Tiina; JESKANEN, Leila et al.Acta dermato-venereologica. 2007, Vol 87, Num 3, pp 223-227, issn 0001-5555, 5 p.Article

Haplotype associations define target regions for susceptibility loci in systemic lupus erythematosusKOSKENMIES, Sari; WIDEN, Elisabeth; ONKAMO, Päivi et al.European journal of human genetics. 2004, Vol 12, Num 6, pp 489-494, issn 1018-4813, 6 p.Article

Clinically Distinct Epigenetic Subgroups in Silver-Russell Syndrome : The Degree of H19 Hypomethylation Associates with Phenotype Severity and Genital and Skeletal AnomaliesBRUCE, Sara; HANNULA-JOUPPI, Katariina; PELTONEN, Jari et al.The Journal of clinical endocrinology and metabolism. 2009, Vol 94, Num 2, pp 579-587, issn 0021-972X, 9 p.Article

Restriction Site-Specific Methylation Studies of Imprinted Genes with Quantitative Real-Time PCRBRUCE, Sara; HANNULA-JOUPPI, Katariina; LINDGREN, Cecilia M et al.Clinical chemistry (Baltimore, Md.). 2008, Vol 54, Num 3, pp 491-499, issn 0009-9147, 9 p.Article

Exclusion of coding-region mutations in luteinizing hormone and follicle-stimulating hormone receptor genes as the cause of ovarian hyperstimulation syndromeKERKELA, Erja; SKOTTMAN, Heli; FRIDEN, Barbro et al.Fertility and sterility. 2007, Vol 87, Num 3, pp 603-606, issn 0015-0282, 4 p.Article

The CIDEA gene V115F polymorphism is associated with obesity in swedish subjectsDAHLMAN, Ingrid; KAAMAN, Maria; HONG JIAO et al.Diabetes (New York, NY). 2005, Vol 54, Num 10, pp 3032-3034, issn 0012-1797, 3 p.Article

A narrow segment of maternal uniparental disomy of chromosome 7q31-qter in Silver-Russell syndrome delimits a candidate gene regionHANNULA, Katariina; LIPSANEN-NYMAN, Marita; KONTIOKARI, Tero et al.American journal of human genetics. 2001, Vol 68, Num 1, pp 247-253, issn 0002-9297Conference Paper

Two translocations of chromosome 15q associated with dyslexiaNOPOLA-HEMMI, Jaana; TAIPALE, Mikko; HALTIA, Tuomas et al.Journal of medical genetics. 2000, Vol 37, Num 10, pp 771-775, issn 0022-2593Article

Three Dyslexia Susceptibility Genes, DYX1C1, DCDC2, and KIAA0319, Affect Temporo-Parietal White Matter StructureDARKI, Fahimeh; PEYRARD-JANVID, Myriam; MATSSON, Hans et al.Biological psychiatry (1969). 2012, Vol 72, Num 8, pp 671-676, issn 0006-3223, 6 p.Article

Differential regulation of basolateral Cl^-/HCO₃- exchangers SLC26A7 and AE1 in kidney outer medullary collecting ductBARONE, Sharon; AMLAL, Hassane; JIE XU et al.Journal of the American Society of Nephrology. 2004, Vol 15, Num 8, pp 2002-2011, issn 1046-6673, 10 p.Article

Maternal and paternal chromosomes 7 show differential methylation of many genes in lymphoblast DNAHANNULA, Katariina; LIPSANEN-NYMAN, Marita; SCHERER, Stephen W et al.Genomics (San Diego, Calif.). 2001, Vol 73, Num 1, pp 1-9, issn 0888-7543Article

Ectodysplasin is released by proteolytic shedding and binds to the EDAR proteinELOMAA, Outi; PULKKINEN, Kati; HANNELIUS, Ulf et al.Human molecular genetics (Print). 2001, Vol 10, Num 9, pp 953-962, issn 0964-6906Article

Do patients with maternal uniparental disomy for chromosome 7 have a distinct mild Silver-Russell phenotype?HANNULA, Katariina; KERE, Juha; PIRINEN, Sinikka et al.Journal of medical genetics. 2001, Vol 38, Num 4, pp 273-278, issn 0022-2593Article

Mapping of five new putative anion transporter genes in human and characterization of SLC26A6, a candidate gene for pancreatic anion exchangerLOHI, Hannes; KUJALA, Minna; KERKELÄ, Erja et al.Genomics (San Diego, Calif.). 2000, Vol 70, Num 1, pp 102-112, issn 0888-7543Article

Isoforms of SLC26A6 mediate anion transport and have functional PDZ interaction domainsLOHI, Hannes; LAMPRECHT, Georg; MARKOVICH, Daniel et al.American journal of physiology. Cell physiology. 2003, Vol 53, Num 3, pp C769-C779, issn 0363-6143Article

A new locus for coeliac disease mapped to chromosome 15 in a population isolateWOOLLEY, Niina; HOLOPAINEN, Päivi; OLLIKAINEN, Vesa et al.Human genetics. 2002, Vol 111, Num 1, pp 40-45, issn 0340-6717Article

Microsatellite Polymorphism in the Heme Oxygenase-1 Promoter Is Associated With Nonsevere and Late-Onset PreeclampsiaKAARTOKALLIO, Tea; KLEMETTI, Miira M; LAIVUORI, Hannele et al.Hypertension (Dallas, Tex. 1979). 2014, Vol 64, Num 1, pp 172-177, issn 0194-911X, 6 p.Article

An unfavorable combination of factor V Leiden with age, weight, and blood group causes high risk of pregnancy-associated venous thrombosis : a population-based nested case-control studyHILTUNEN, Leena; RAUTANEN, Anna; RASI, Vesa et al.Thrombosis research. 2007, Vol 119, Num 4, pp 423-432, issn 0049-3848, 10 p.Article

Mutations in the gene encoding the 3'-5' DNA exonuclease TREX1 are associated with systemic lupus erythematosusAE LEE-KIRSCH, Min; GONG, Maolian; KERE, Juha et al.Nature genetics. 2007, Vol 39, Num 9, pp 1065-1067, issn 1061-4036, 3 p.Article

Downstream target genes of the neuropeptide S-NPSR1 pathwayVENDELIN, Johanna; BRUCE, Sara; SAARIALHO-KERE, Ulpu et al.Human molecular genetics (Print). 2006, Vol 15, Num 19, pp 2923-2935, issn 0964-6906, 13 p.Article

Physical exercise-induced hyperinsulinemic hypoglycemia is an autosomal-dominant trait characterized by abnormal pyruvate-induced insulin releaseOTONKOSKI, Timo; KAMINEN, Nina; USTINOV, Jarkko et al.Diabetes (New York, NY). 2003, Vol 52, Num 1, pp 199-204, issn 0012-1797, 6 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