Diabetes

Citations 11-20 of 88 total displayed.

Letters to JMG
Severe neonatal manifestations of Costello syndrome

I F M Lo, C Brewer, N Shannon, J Shorto, B Tang, G Black, M T Soo, D K K Ng, S T S Lam, B Kerr
J. Med. Genet. 2008 45: 167 -171; published online before print as 10.1136/jmg.2007.054411 [Abstract] [Full text] [PDF] [Request Permissions]  

Letters to JMG
Psoriasis is associated with pleiotropic susceptibility loci identified in type II diabetes and Crohn disease

N Wolf, M Quaranta, N J Prescott, M Allen, R Smith, A D Burden, J Worthington, C E M Griffiths, C G Mathew, J N Barker, F Capon, R C Trembath
J. Med. Genet. 2008 45: 114 -116; published online before print as 10.1136/jmg.2007.053595 [Abstract] [Full text] [PDF] [Request Permissions]  

Letters to JMG
The IRF5 polymorphism in type 1 diabetes

Hui-Qi Qu, Luc Marchand, Rosemary Grabs, Constantin Polychronakos
J. Med. Genet. 2007 44: 670 -672; published online before print as 10.1136/jmg.2007.050971 [Abstract] [Full text] [PDF] [Request Permissions]  

Letters to JMG
Genetic association analysis of inositol polyphosphate phosphatase-like 1 (INPPL1, SHIP2) variants with essential hypertension

Ana Carolina Braga Marçano, Beverley Burke, Johannie Gungadoo, Chris Wallace, Pamela J Kaisaki, Peng Y Woon, Martin Farrall, David Clayton, Morris Brown, Anna Dominiczak, John M Connell, John Webster, Mark Lathrop, Mark Caulfield, Nilesh Samani, Dominique Gauguier, Patricia B Munroe
J. Med. Genet. 2007 44: 603 -605; published online before print as 10.1136/jmg.2007.049718 [Abstract] [Full text] [PDF] [Request Permissions]  

Online mutation reports
Mitochondrial DNA haplogroups and type 2 diabetes: a study of 897 cases and 1010 controls

P F Chinnery, C Mowbray, S K Patel, J L Elson, M Sampson, G A Hitman, M I McCarthy, A T Hattersley, M Walker
J. Med. Genet. 2007; 44: e80. [Abstract] [Full text] [PDF] [Request Permissions]  

Original articles
The human GIMAP5 gene has a common polyadenylation polymorphism increasing risk to systemic lupus erythematosus

Anna Hellquist, Marco Zucchelli, Katja Kivinen, Ulpu Saarialho-Kere, Sari Koskenmies, Elisabeth Widen, Heikki Julkunen, Andrew Wong, Marja-Liisa Karjalainen-Lindsberg, Tiina Skoog, Johanna Vendelin, Deborah S Cunninghame-Graham, Timothy J Vyse, Juha Kere, Cecilia M Lindgren
J. Med. Genet. 2007 44: 314 -321; published online before print as 10.1136/jmg.2006.046185 [Abstract] [Full text] [PDF] [Request Permissions] [ web only appendix ]  

Original articles
Genetic and epigenetic defects at the 6q24 imprinted locus in a cohort of 13 patients with transient neonatal diabetes: new hypothesis raised by the finding of a unique case with hemizygotic deletion in the critical region

C Diatloff-Zito, A Nicole, G Marcelin, H Labit, E Marquis, C Bellanné-Chantelot, J J Robert
J. Med. Genet. 2007 44: 31 -37; published online before print as 10.1136/jmg.2006.044404 [Abstract] [Full text] [PDF] [Request Permissions]  

Original articles
Polymorphisms of the low-density lipoprotein receptor-related protein 5 (LRP5) gene are associated with obesity phenotypes in a large family-based association study

Yan-fang Guo, Dong-hai Xiong, Hui Shen, Lan-juan Zhao, Peng Xiao, Yan Guo, Wei Wang, Tie-lin Yang, Robert R Recker, Hong-wen Deng
J. Med. Genet. 2006 43: 798 -803; published online before print as 10.1136/jmg.2006.041715 [Abstract] [Full text] [PDF] [Request Permissions]  

Short reports
Autosomal dominant optic atrophy associated with hearing impairment and impaired glucose regulation caused by a missense mutation in the WFS1 gene

H Eiberg, L Hansen, B Kjer, T Hansen, O Pedersen, M Bille, T Rosenberg, L Tranebjærg
J. Med. Genet. 2006; 43: 435-440. [Abstract] [Full text] [PDF] [Request Permissions]  

Letters to JMG
Congenital hyperinsulinism and mosaic abnormalities of the ploidy

I Giurgea, D Sanlaville, J-C Fournet, C Sempoux, C Bellanné-Chantelot, G Touati, L Hubert, M-S Groos, F Brunelle, J Rahier, J-C Henquin, M J Dunne, F Jaubert, J-J Robert, C Nihoul-Fékété, M Vekemans, C Junien, P de Lonlay
J. Med. Genet. 2006 43: 248 -254; published online before print as 10.1136/jmg.2005.034116 [Abstract] [Full text] [PDF] [Request Permissions]