Diabetes

Citations 1-10 of 88 total displayed.

Letters to JMG
A common UCP2 polymorphism predisposes to stress hyperglycaemia in severe sepsis

A Pyle, I M Ibbett, C Gordon, S M Keers, M Walker, P F Chinnery, S V Baudouin
J. Med. Genet. 2009 46: 773 -775; published online before print as 10.1136/jmg.2009.067173 [Abstract] [Full text] [PDF] [Request Permissions]  

Letters to JMG
Association of RASGRP1 with type 1 diabetes is revealed by combined follow-up of two genome-wide studies

H Q Qu, S F A Grant, J P Bradfield, C Kim, E Frackelton, H Hakonarson, C Polychronakos
J. Med. Genet. 2009 46: 553 -554; published online before print as 10.1136/jmg.2009.067140 [Abstract] [Full text] [PDF] [Request Permissions] [ Web only appendix ]  

Letters to JMG
The effect of the MHC locus on autoantibodies in type 1 diabetes

H-Q Qu, C Polychronakos
J. Med. Genet. 2009 46: 469 -471; published online before print as 10.1136/jmg.2009.066647 [Abstract] [Full text] [PDF] [Request Permissions] [ Web only appendix ]  

Letters to JMG
Genome-wide linkage scan for plasma high density lipoprotein cholesterol, apolipoprotein A-1 and triglyceride variation among American Indian populations: the Strong Heart Family Study

X Li, K L Monda, H H H Göring, K Haack, S A Cole, V P Diego, L Almasy, S Laston, B V Howard, N M Shara, E T Lee, L G Best, R R Fabsitz, J W MacCluer, Kari E North
J. Med. Genet. 2009 46: 472 -479; published online before print as 10.1136/jmg.2008.063891 [Abstract] [Full text] [PDF] [Request Permissions] [ Web only appendicies ]  

Review
The genetic basis of congenital hyperinsulinism

C James, R R Kapoor, D Ismail, K Hussain
J. Med. Genet. 2009 46: 289 -299; published online before print as 10.1136/jmg.2008.064337 [Abstract] [Full text] [PDF] [Request Permissions]  

Original articles
Genetic analysis of 56 polymorphisms in 17 genes involved in methionine metabolism in patients with abdominal aortic aneurysm

B Giusti, C Saracini, P Bolli, A Magi, I Sestini, E Sticchi, G Pratesi, R Pulli, C Pratesi, R Abbate
J. Med. Genet. 2008 45: 721 -730; published online before print as 10.1136/jmg.2008.057851 [Abstract] [Full text] [PDF] [Request Permissions] [ web only appendices ]  

Original articles
Prevalence and heritability of the metabolic syndrome and its individual components in a Dutch isolate: the Erasmus Rucphen Family study

P Henneman, Y S Aulchenko, R R Frants, K W van Dijk, B A Oostra, C M van Duijn
J. Med. Genet. 2008 45: 572 -577; published online before print as 10.1136/jmg.2008.058388 [Abstract] [Full text] [PDF] [Request Permissions]  

Review
Double outlet right ventricle: aetiologies and associations

D Obler, A L Juraszek, L B Smoot, M R Natowicz
J. Med. Genet. 2008 45: 481 -497; published online before print as 10.1136/jmg.2008.057984 [Abstract] [Full text] [PDF] [Request Permissions]  

Original articles
Termination of damaged protein repair defines the occurrence of symptoms in carriers of the m.3243A>G tRNA^Leu mutation

R G E van Eijsden, L M T Eijssen, P J Lindsey, C M M van den Burg, L E A de Wit, M E Rubio-Gozalbo, C E M de Die, T Ayoubi, W Sluiter, I F M de Coo, H J M Smeets
J. Med. Genet. 2008 45: 525 -534; published online before print as 10.1136/jmg.2008.057497 [Abstract] [Full text] [PDF] [Request Permissions] [ web only appendix ]  

Original articles
Genetic risk for myocardial infarction determined by polymorphisms of candidate genes in a Japanese population

Y Yamada, K Kato, M Oguri, T Fujimaki, K Yokoi, H Matsuo, S Watanabe, N Metoki, H Yoshida, K Satoh, S Ichihara, Y Aoyagi, A Yasunaga, H Park, M Tanaka, Y Nozawa
J. Med. Genet. 2008 45: 216 -221; published online before print as 10.1136/jmg.2007.054387 [Abstract] [Full text] [PDF] [Request Permissions] [ web only table ]