author:"Peltonen L." in Literature citations

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Common variants in the HLA-DRB1-HLA-DQA1 HLA class II region are associated with susceptibility to visceral leishmaniasis. LeishGEN Consortium Fakiola M., Strange A., Cordell H.J., Miller E.N., Pirinen M., Su Z., Mishra A., Mehrotra S., Monteiro G.R., Band G. et al. Nat. Genet. 45:208-213(2013) · Mapped (462)
Dense fine-mapping study identifies new susceptibility loci for primary biliary cirrhosis. UK Primary Biliary Cirrhosis (PBC) Consortium Liu J.Z., Almarri M.A., Gaffney D.J., Mells G.F., Jostins L., Cordell H.J., Ducker S.J., Day D.B., Heneghan M.A., Neuberger J.M. et al. Nat. Genet. 44:1137-1141(2012) · Mapped (3)
Sex-specific influence of DRD2 on ADHD-type temperament in a large population-based birth cohort. Nyman E.S., Loukola A., Varilo T., Taanila A., Hurtig T., Moilanen I., Loo S., McGough J.J., Jarvelin M.R., Smalley S.L. et al. Psychiatr. Genet. 22:197-201(2012) · Mapped (4)
A common variant near the KCNJ2 gene is associated with T-peak to T-end interval. Marjamaa A., Oikarinen L., Porthan K., Ripatti S., Peloso G., Noseworthy P.A., Viitasalo M., Nieminen M.S., Toivonen L., Kontula K. et al. Heart Rhythm 9:1099-1103(2012) · Mapped (1)
RANTES/CCL5 and risk for coronary events: results from the MONICA/KORA Augsburg case-cohort, Athero-Express and CARDIoGRAM studies. CARDIoGRAM Consortium Herder C., Peeters W., Illig T., Baumert J., de Kleijn D.P., Moll F.L., Poschen U., Klopp N., Muller-Nurasyid M., Roden M. et al. PLoS ONE 6:e25734-e25734(2011) · Mapped (4)
Post-genomic update on a classical candidate gene for coronary artery disease: ESR1. CARDIoGRAM Consortium Lucas G., Lluis-Ganella C., Subirana I., Senti M., Willenborg C., Musameh M.D., Schwartz S.M., O'Donnell C.J., Melander O., Salomaa V. et al. Circ Cardiovasc Genet 4:647-654(2011) · Mapped (56)
The Lin28/let-7 axis regulates glucose metabolism. DIAGRAM Consortium Zhu H., Shyh-Chang N., Segre A.V., Shinoda G., Shah S.P., Einhorn W.S., Takeuchi A., Engreitz J.M., Hagan J.P., Kharas M.G. et al. Cell 147:81-94(2011) · Mapped (11)
Common variants at VRK2 and TCF4 conferring risk of schizophrenia. Irish Schizophrenia Genomics Consortium Steinberg S., de Jong S., Andreassen O.A., Werge T., Borglum A.D., Mors O., Mortensen P.B., Gustafsson O., Costas J., Pietilainen O.P. et al. Hum. Mol. Genet. 20:4076-4081(2011) · Mapped (18)
Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility. Spondyloarthritis Research Consortium of Canada (SPARCC) Evans D.M., Spencer C.C., Pointon J.J., Su Z., Harvey D., Kochan G., Oppermann U., Opperman U., Dilthey A., Pirinen M. et al. Nat. Genet. 43:761-767(2011) · Mapped (2)
Genetic variation near IRS1 associates with reduced adiposity and an impaired metabolic profile. Kilpelainen T.O., Zillikens M.C., Stancakova A., Finucane F.M., Ried J.S., Langenberg C., Zhang W., Beckmann J.S., Luan J., Vandenput L. et al. Nat. Genet. 43:753-760(2011) · Mapped (1)
An evolutionary genomic approach to identify genes involved in human birth timing. Plunkett J., Doniger S., Orabona G., Morgan T., Haataja R., Hallman M., Puttonen H., Menon R., Kuczynski E., Norwitz E. et al. PLoS Genet. 7:e1001365-e1001365(2011) · Mapped (5)
Genome-wide association and genetic functional studies identify autism susceptibility candidate 2 gene (AUTS2) in the regulation of alcohol consumption. Schumann G., Coin L.J., Lourdusamy A., Charoen P., Berger K.H., Stacey D., Desrivieres S., Aliev F.A., Khan A.A., Amin N. et al. Proc. Natl. Acad. Sci. U.S.A. 108:7119-7124(2011) · Mapped (11)
At-risk variant in TCF7L2 for type II diabetes increases risk of schizophrenia. Hansen T., Ingason A., Djurovic S., Melle I., Fenger M., Gustafsson O., Jakobsen K.D., Rasmussen H.B., Tosato S., Rietschel M. et al. Biol. Psychiatry 70:59-63(2011) · Mapped (31)
Population-prevalent desmosomal mutations predisposing to arrhythmogenic right ventricular cardiomyopathy. Lahtinen A.M., Lehtonen E., Marjamaa A., Kaartinen M., Helio T., Porthan K., Oikarinen L., Toivonen L., Swan H., Jula A. et al. Heart Rhythm 8:1214-1221(2011) · Mapped (9)
Identification of ADAMTS7 as a novel locus for coronary atherosclerosis and association of ABO with myocardial infarction in the presence of coronary atherosclerosis: two genome-wide association studies. Myocardial Infarction Genetics Consortium Reilly M.P., Li M., He J., Ferguson J.F., Stylianou I.M., Mehta N.N., Burnett M.S., Devaney J.M., Knouff C.W., Thompson J.R. et al. Lancet 377:383-392(2011) · Mapped (5)
Primate-specific evolution of noncoding element insertion into PLA2G4C and human preterm birth. Plunkett J., Doniger S., Morgan T., Haataja R., Hallman M., Puttonen H., Menon R., Kuczynski E., Norwitz E., Snegovskikh V. et al. BMC Med Genomics 3:62-62(2010) · Mapped (4)
A population-specific HTR2B stop codon predisposes to severe impulsivity. Bevilacqua L., Doly S., Kaprio J., Yuan Q., Tikkanen R., Paunio T., Zhou Z., Wedenoja J., Maroteaux L., Diaz S. et al. Nature 468:1061-1066(2010) · UniProtKB (7) · Mapped (3)
TTC12-ANKK1-DRD2 and CHRNA5-CHRNA3-CHRNB4 influence different pathways leading to smoking behavior from adolescence to mid-adulthood. Ducci F., Kaakinen M., Pouta A., Hartikainen A.L., Veijola J., Isohanni M., Charoen P., Coin L., Hoggart C., Ekelund J. et al. Biol. Psychiatry 69:650-660(2011) · Mapped (21)
Candidate gene association study of magnetic resonance imaging-based hip osteoarthritis (OA): evidence for COL9A2 gene as a common predisposing factor for hip OA and lumbar disc degeneration. Nakki A., Videman T., Kujala U.M., Suhonen M., Mannikko M., Peltonen L., Battie M.C., Kaprio J., Saarela J. J. Rheumatol. 38:747-752(2011) · Mapped (2)
Four novel Loci (19q13, 6q24, 12q24, and 5q14) influence the microcirculation in vivo. Global BPgen Consortium Ikram M.K., Sim X., Xueling S., Jensen R.A., Cotch M.F., Hewitt A.W., Ikram M.A., Wang J.J., Klein R., Klein B.E. et al. PLoS Genet. 6:e1001184-e1001184(2010) · Mapped (23)
Aire-dependent thymic expression of desmoglein 3, the autoantigen in pemphigus vulgaris, and its role in T-cell tolerance. Wada N., Nishifuji K., Yamada T., Kudoh J., Shimizu N., Matsumoto M., Peltonen L., Nagafuchi S., Amagai M. J. Invest. Dermatol. 131:410-417(2011) · Mapped (9)
Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21. UK Parkinson's Disease Consortium Spencer C.C., Plagnol V., Strange A., Gardner M., Paisan-Ruiz C., Band G., Barker R.A., Bellenguez C., Bhatia K., Blackburn H. et al. Hum. Mol. Genet. 20:345-353(2011) · Mapped (26)
A multilocus genetic risk score for coronary heart disease: case-control and prospective cohort analyses. Ripatti S., Tikkanen E., Orho-Melander M., Havulinna A.S., Silander K., Sharma A., Guiducci C., Perola M., Jula A., Sinisalo J. et al. Lancet 376:1393-1400(2010) · Mapped (60)
A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1. Genetic Analysis of Psoriasis Consortium & the Wellcome Trust Case Control Consortium 2 Strange A., Capon F., Spencer C.C., Knight J., Weale M.E., Allen M.H., Barton A., Band G., Bellenguez C., Bergboer J.G. et al. Nat. Genet. 42:985-990(2010) · Mapped (296)
Candidate gene analysis of the human natural killer-1 carbohydrate pathway and perineuronal nets in schizophrenia: B3GAT2 is associated with disease risk and cortical surface area. Kahler A.K., Djurovic S., Rimol L.M., Brown A.A., Athanasiu L., Jonsson E.G., Hansen T., Gustafsson O., Hall H., Giegling I. et al. Biol. Psychiatry 69:90-96(2011) · Mapped (28)

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