Jiao H - Search Results

1

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. 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

2

alpha2-Heremans-Schmid glycoprotein gene polymorphisms are associated with adipocyte insulin action.

Dahlman I, Eriksson P, Kaaman M, Jiao H, Lindgren CM, Kere J, Arner P. Dahlman I, et al. Among authors: jiao h. Diabetologia. 2004 Nov;47(11):1974-9. doi: 10.1007/s00125-004-1556-7. Epub 2004 Dec 1. Diabetologia. 2004. PMID: 15599699

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: jiao h. 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. 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: jiao h. 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: jiao h. 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: jiao h. Mol Vis. 2007 Jul 13;13:1154-60. Mol Vis. 2007. PMID: 17653060

8

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. 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

9

ROCK2 allelic variants are not associated with pre-eclampsia susceptibility in the Finnish population.

Peterson H, Laivuori H, Kerkelä E, Jiao H, Hiltunen L, Heino S, Tiala I, Knuutila S, Rasi V, Kere J, Kivinen K. Peterson H, et al. Among authors: jiao h. Mol Hum Reprod. 2009 Jul;15(7):443-9. doi: 10.1093/molehr/gap032. Epub 2009 May 12. Mol Hum Reprod. 2009. PMID: 19435756

10

Molecular genetic and epigenetic analysis of NCX2/SLC8A2 at 19q13.3 in human gliomas.

Qu M, Jiao H, Zhao J, Ren ZP, Smits A, Kere J, Nistér M. Qu M, et al. Among authors: jiao h. Neuropathol Appl Neurobiol. 2010 Apr;36(3):198-210. doi: 10.1111/j.1365-2990.2010.01070.x. Epub 2010 Feb 26. Neuropathol Appl Neurobiol. 2010. PMID: 20132488

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