1 - 25 of
105
results
for author:"Kere J."
in Literature Citations
| Variation in STAT4 is associated with systemic lupus erythematosus (SLE) in a Finnish family cohort. Hellquist A., Sandling J.K., Zucchelli M., Koskenmies S., Julkunen H., D'Amato M., Garnier S., Syvanen A.C., Kere J. Ann. Rheum. Dis. 0:0-0(2009) · Mapped (8) |
| Evidence for genetic association and interaction between the TYK2 and IRF5 genes in systemic lupus erythematosus. Hellquist A., Jarvinen T.M., Koskenmies S., Zucchelli M., Orsmark-Pietras C., Berglind L., Panelius J., Hasan T., Julkunen H., D'Amato M. et al. J. Rheumatol. 36:1631-1638(2009) · Mapped (17) |
| ROCK2 allelic variants are not associated with pre-eclampsia susceptibility in the Finnish population. Peterson H., Laivuori H., Kerkela E., Jiao H., Hiltunen L., Heino S., Tiala I., Knuutila S., Rasi V., Kere J. et al. Mol. Hum. Reprod. 15:443-449(2009) · Mapped (3) |
| Functional interaction of DYX1C1 with estrogen receptors suggests involvement of hormonal pathways in dyslexia. Massinen S., Tammimies K., Tapia-Paez I., Matsson H., Hokkanen M.E., Soderberg O., Landegren U., Castren E., Gustafsson J.A., Treuter E. et al. Hum. Mol. Genet. 18:2802-2812(2009) · Mapped (66) |
| Lack of association between neuropeptide S receptor 1 gene (NPSR1) and eczema in five European populations. Ekelund E., Bradley M., Weidinger S., Jovanovic D.L., Johansson C., Lindgren C.M., Todorova A., Jakob T., Illig T., von Mutius E. et al. Acta Derm. Venereol. 89:115-121(2009) · Mapped (4) |
| Further evidence for DYX1C1 as a susceptibility factor for dyslexia. Dahdouh F., Anthoni H., Tapia-Paez I., Peyrard-Janvid M., Schulte-Korne G., Warnke A., Remschmidt H., Ziegler A., Kere J., Muller-Myhsok B. et al. Psychiatr. Genet. 19:59-63(2009) · Mapped (4) |
| IL23R in the Swedish, Finnish, Hungarian and Italian populations: association with IBD and psoriasis, and linkage to celiac disease. Einarsdottir E., Koskinen L.L., Dukes E., Kainu K., Suomela S., Lappalainen M., Ziberna F., Korponay-Szabo I.R., Kurppa K., Kaukinen K. et al. BMC Med. Genet. 10:8-8(2009) · Mapped (23) |
| Blood group AB and factor V Leiden as risk factors for pre-eclampsia: a population-based nested case-control study. Hiltunen L.M., Laivuori H., Rautanen A., Kaaja R., Kere J., Krusius T., Paunio M., Rasi V. Thromb. Res. 124:167-173(2009) · Mapped (130) |
| Association study of the IL18RAP locus in three European populations with coeliac disease. Koskinen L.L., Einarsdottir E., Dukes E., Heap G.A., Dubois P., Korponay-Szabo I.R., Kaukinen K., Kurppa K., Ziberna F., Vatta S. et al. Hum. Mol. Genet. 18:1148-1155(2009) · Mapped (4) |
| Investigation of the DCDC2 intron 2 deletion/compound short tandem repeat polymorphism in a large German dyslexia sample. Ludwig K.U., Schumacher J., Schulte-Korne G., Konig I.R., Warnke A., Plume E., Anthoni H., Peyrard-Janvid M., Meng H., Ziegler A. et al. Psychiatr. Genet. 18:310-312(2008) · Mapped (2) |
| No association between the eczema genes COL29A1 and IL31 and inflammatory bowel disease. Zucchelli M., Torkvist L., Bresso F., Halfvarson J., Soderhall C., Lee Y.A., Lofberg R., Kere J., D'Amato M. Inflamm. Bowel Dis. 15:961-962(2009) · Mapped (2) |
| Interactions between glutathione S-transferase P1, tumor necrosis factor, and traffic-related air pollution for development of childhood allergic disease. Melen E., Nyberg F., Lindgren C.M., Berglind N., Zucchelli M., Nordling E., Hallberg J., Svartengren M., Morgenstern R., Kere J. et al. Environ. Health Perspect. 116:1077-1084(2008) · Mapped (11) |
| Novel and recurrent STAT3 mutations in hyper-IgE syndrome patients from different ethnic groups. Jiao H., Toth B., Erdos M., Fransson I., Rakoczi E., Balogh I., Magyarics Z., Derfalvi B., Csorba G., Szaflarska A. et al. Mol. Immunol. 46:202-206(2008) · Mapped (7) |
| The complex of TFII-I, PARP1, and SFPQ proteins regulates the DYX1C1 gene implicated in neuronal migration and dyslexia. Tapia-Paez I., Tammimies K., Massinen S., Roy A.L., Kere J. FASEB J. 22:3001-3009(2008) · Mapped (23) |
| Biological and genetic interaction between tenascin C and neuropeptide S receptor 1 in allergic diseases. Orsmark-Pietras C., Melen E., Vendelin J., Bruce S., Laitinen A., Laitinen L.A., Lauener R., Riedler J., von Mutius E., Doekes G. et al. Hum. Mol. Genet. 17:1673-1682(2008) · Mapped (10) |
| The protective effect of farm animal exposure on childhood allergy is modified by NPSR1 polymorphisms. Bruce S., Nyberg F., Melen E., James A., Pulkkinen V., Orsmark-Pietras C., Bergstrom A., Dahlen B., Wickman M., von Mutius E. et al. J. Med. Genet. 46:159-167(2009) · Mapped (4) |
| Familial non-syndromic cleft lip and palate--analysis of the IRF6 gene and clinical phenotypes. Pegelow M., Peyrard-Janvid M., Zucchelli M., Fransson I., Larson O., Kere J., Larsson C., Karsten A. Eur J Orthod 30:169-175(2008) · Mapped (4) |
| The PSORS1 locus gene CCHCR1 affects keratinocyte proliferation in transgenic mice. Tiala I., Wakkinen J., Suomela S., Puolakkainen P., Tammi R., Forsberg S., Rollman O., Kainu K., Rozell B., Kere J. et al. Hum. Mol. Genet. 17:1043-1051(2008) · Mapped (25) |
| Myosin IXB gene region and gluten intolerance: linkage to coeliac disease and a putative dermatitis herpetiformis association. Koskinen L.L., Korponay-Szabo I.R., Viiri K., Juuti-Uusitalo K., Kaukinen K., Lindfors K., Mustalahti K., Kurppa K., Adany R., Pocsai Z. et al. J. Med. Genet. 45:222-227(2008) · Mapped (5) |
| Neuropeptide s receptor 1 gene polymorphism is associated with susceptibility to inflammatory bowel disease. D'Amato M., Bruce S., Bresso F., Zucchelli M., Ezer S., Pulkkinen V., Lindgren C., Astegiano M., Rizzetto M., Gionchetti P. et al. Gastroenterology 133:808-817(2007) · Mapped (4) |
| Physical exercise-induced hypoglycemia caused by failed silencing of monocarboxylate transporter 1 in pancreatic beta cells. Otonkoski T., Jiao H., Kaminen-Ahola N., Tapia-Paez I., Ullah M.S., Parton L.E., Schuit F., Quintens R., Sipilae I., Mayatepek E. et al. Am. J. Hum. Genet. 81:467-474(2007) · UniProtKB (1) · Mapped (16) |
| Mutations in the gene encoding the 3'-5' DNA exonuclease TREX1 are associated with systemic lupus erythematosus. Lee-Kirsch M.A., Gong M., Chowdhury D., Senenko L., Engel K., Lee Y.A., de Silva U., Bailey S.L., Witte T., Vyse T.J. et al. |
| Two Chinese families with pulverulent congenital cataracts and deltaG91 CRYBA1 mutations. Lu S., Zhao C., Jiao H., Kere J., Tang X., Zhao F., Zhang X., Zhao K., Larsson C. Mol. Vis. 13:1154-1160(2007) · Mapped (1) |
| Expression of allograft inflammatory factor-1 in inflammatory skin disorders. Orsmark C., Skoog T., Jeskanen L., Kere J., Saarialho-Kere U. Acta Derm. Venereol. 87:223-227(2007) · Mapped (5) |
| Expression of ion transport-associated proteins in human efferent and epididymal ducts. Kujala M., Hihnala S., Tienari J., Kaunisto K., Hastbacka J., Holmberg C., Kere J., Hoglund P. Reproduction 133:775-784(2007) · UniProtKB (1) |
