Kere J - Search Results

1

CELSR2 is a candidate susceptibility gene in idiopathic scoliosis.

Einarsdottir E, Grauers A, Wang J, Jiao H, Escher SA, Danielsson A, Simony A, Andersen M, Christensen SB, Åkesson K, Kou I, Khanshour AM, Ohlin A, Wise C, Ikegawa S, Kere J, Gerdhem P. Einarsdottir E, et al. Among authors: kere j. PLoS One. 2017 Dec 14;12(12):e0189591. doi: 10.1371/journal.pone.0189591. eCollection 2017. PLoS One. 2017. PMID: 29240829 Free PMC article.

2

Transgenic mouse models support HCR as an effector gene in the PSORS1 locus.

Elomaa O, Majuri I, Suomela S, Asumalahti K, Jiao H, Mirzaei Z, Rozell B, Dahlman-Wright K, Pispa J, Kere J, Saarialho-Kere U. Elomaa O, et al. Among authors: kere j. Hum Mol Genet. 2004 Aug 1;13(15):1551-61. doi: 10.1093/hmg/ddh178. Epub 2004 Jun 9. Hum Mol Genet. 2004. PMID: 15190014

3

The CIDEA gene V115F polymorphism is associated with obesity in Swedish subjects.

Dahlman I, Kaaman M, Jiao H, Kere J, Laakso M, Arner P. Dahlman I, et al. Among authors: kere j. Diabetes. 2005 Oct;54(10):3032-4. doi: 10.2337/diabetes.54.10.3032. Diabetes. 2005. PMID: 16186410

4

A common beta2-adrenoceptor gene haplotype protects against obesity in Swedish women.

Jiao H, Dahlman I, Eriksson P, Kere J, Arner P. Jiao H, et al. Among authors: kere j. Obes Res. 2005 Oct;13(10):1645-50. doi: 10.1038/oby.2005.202. Obes Res. 2005. PMID: 16286511 Free article.

5

Liver X receptor gene polymorphisms and adipose tissue expression levels in obesity.

Dahlman I, Nilsson M, Jiao H, Hoffstedt J, Lindgren CM, Humphreys K, Kere J, Gustafsson JA, Arner P, Dahlman-Wright K. Dahlman I, et al. Among authors: kere j. Pharmacogenet Genomics. 2006 Dec;16(12):881-9. doi: 10.1097/01.fpc.0000236334.49422.48. Pharmacogenet Genomics. 2006. PMID: 17108812

6

A common haplotype in the G-protein-coupled receptor gene GPR74 is associated with leanness and increased lipolysis.

Dahlman I, Dicker A, Jiao H, Kere J, Blomqvist L, van Harmelen V, Hoffstedt J, Borch-Johnsen K, Jorgensen T, Hansen T, Pedersen O, Laakso M, Arner P. Dahlman I, et al. Among authors: kere j. Am J Hum Genet. 2007 Jun;80(6):1115-24. doi: 10.1086/518445. Epub 2007 May 2. Am J Hum Genet. 2007. PMID: 17503329 Free PMC article.

7

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. Lu S, et al. Among authors: kere j. Mol Vis. 2007 Jul 13;13:1154-60. Mol Vis. 2007. PMID: 17653060

8

Myosin IXB gene region and gluten intolerance: linkage to coeliac disease and a putative dermatitis herpetiformis association.

Koskinen LL, Korponay-Szabo IR, Viiri K, Juuti-Uusitalo K, Kaukinen K, Lindfors K, Mustalahti K, Kurppa K, Adány R, Pocsai Z, Széles G, Einarsdottir E, Wijmenga C, Mäki M, Partanen J, Kere J, Saavalainen P. Koskinen LL, et al. Among authors: kere j. J Med Genet. 2008 Apr;45(4):222-7. doi: 10.1136/jmg.2007.053991. Epub 2007 Dec 12. J Med Genet. 2008. PMID: 18077767

9

Association analysis of positional obesity candidate genes based on integrated data from transcriptomics and linkage analysis.

Jiao H, Kaaman M, Dungner E, Kere J, Arner P, Dahlman I. Jiao H, et al. Among authors: kere j. Int J Obes (Lond). 2008 May;32(5):816-25. doi: 10.1038/sj.ijo.0803789. Epub 2008 Jan 8. Int J Obes (Lond). 2008. PMID: 18180783

10

Novel and recurrent STAT3 mutations in hyper-IgE syndrome patients from different ethnic groups.

Jiao H, Tóth B, Erdos M, Fransson I, Rákóczi E, Balogh I, Magyarics Z, Dérfalvi B, Csorba G, Szaflarska A, Megarbane A, Akatcherian C, Dbaibo G, Rajnavölgyi E, Hammarström L, Kere J, Lefranc G, Maródi L. Jiao H, et al. Among authors: kere j. Mol Immunol. 2008 Nov;46(1):202-6. doi: 10.1016/j.molimm.2008.07.001. Epub 2008 Aug 15. Mol Immunol. 2008. PMID: 18706697

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