Web Images Videos Maps News Shopping Gmail more »
Sign in
Scholar Home  
  Advanced Scholar Search
Scholar Preferences
Scholar Results 1 - 10 of about 111 citing Barratt: Remapping the insulin gene/IDDM2 locus in type 1 diabetes. (0.08 sec) 

Replication of an association between the lymphoid tyrosine phosphatase locus ( …


D Smyth, JD Cooper, JE Collins, JM Heward, JA … - Diabetes, 2004 - Am Diabetes Assoc
In the genetic analysis of common, multifactorial diseases, such as type 1 diabetes, true positive
irrefutable linkage and association results have been rare to date. Recently, it has been reported
that a single nucleotide polymorphism (SNP), 1858C>T, in the gene PTPN22, encoding ...
Cited by 244 - Related articles - BL Direct - All 5 versions

A genome-wide association study of nonsynonymous SNPs identifies a type 1 …


DJ Smyth, JD Cooper, R Bailey, S Field, O Burren, LJ … - Nature genetics, 2006 - nature.com
2 Clinic of Diabetes, Institute of Diabetes, Nutrition and Metabolic Diseases 'N.Paulescu', Bucharest
79811, Romania. ... 3 Department of Paediatrics, University of Cambridge, Addenbrooke's
Hospital, Cambridge CB2 2XY, UK. ... 4 Department of Medical Genetics, Queen's ...
Cited by 190 - Related articles - BL Direct - All 6 versions

Localization of a type 1 diabetes locus in the IL2RA/CD25 region by use of tag …

- nih.gov
A Vella, JD Cooper, CE Lowe, N Walker, S Nutland, … - The American Journal of …, 2005 - Elsevier
Despite hundreds of association studies, few have been consistently replicated (Dahlman et
al. 2002; Hirschhorn et al. 2003; Ioannidis et al. 2003; Lohmueller et al. 2003). In type 1 diabetes
(T1D [MIM 222100]), only four loci have been identified and successfully replicated: the ...
Cited by 137 - Related articles - All 6 versions

Regulatory polymorphisms underlying complex disease traits


JC Knight - Journal of molecular medicine, 2005 - Springer
Abstract There is growing evidence that genetic variation plays an important role in the determination
of individual susceptibility to complex disease traits. In contrast to coding sequence
polymorphisms, where the consequences of non-synonymous variation may be resolved ...
Cited by 101 - Related articles - All 4 versions

Genetic epidemiology of diabetes

- nih.gov
MA Permutt, J Wasson, N Cox - Journal of Clinical Investigation, 2005 - Am Soc Clin Investig
Conventional genetic analysis focuses on the genes that account for specific phenotypes, while
traditional epidemiology is more concerned with the environmental causes and risk factors related
to traits. Genetic epidemiology is an alliance of the 2 fields that focuses on both genetics, ...
Cited by 91 - Related articles - All 9 versions

Genetic association between a lymphoid tyrosine phosphatase (PTPN22) and type …


W Zheng, JX She - Diabetes, 2005 - Am Diabetes Assoc
The lymphoid-specific phosphatase (LYP) encoded by PTPN22 is involved in preventing spontaneous
T-cell activation by dephosphorylating and inactivating T-cell receptor-associated Csk
kinase. We have genotyped 396 type 1 diabetic patients and 1,178 control subjects of ...
Cited by 63 - Related articles - All 5 versions

Genetic progress towards the molecular basis of autoimmunity

- cell.com
SHS Pearce, TR Merriman - Trends in molecular medicine, 2006 - Elsevier
The past few years have seen the identification of PTPN22 and the confirmation of CTLA-4 as
common autoimmune disease genes. Together with MHC and INS, these developments have
increased the collection of confirmed susceptibility loci for autoimmunity. In this article, the ...
Cited by 46 - Related articles - All 5 versions

Genetic insights into disease mechanisms of autoimmunity

- oxfordjournals.org
MJ Simmonds, SCL Gough - British medical bulletin, 2005 - British Council
Educating the immune system to distinguish between self and non-self is critical to ensure that
an immune response is mounted against foreign antigens and not against self. A breakdown
in these mechanisms can lead to the onset of autoimmune disease. Clinical and ...
Cited by 43 - Related articles - All 5 versions

Type 1 diabetes genes and pathways shared by humans and NOD mice

- harvard.edu [PDF] 
LS Wicker, J Clark, HI Fraser, VES Garner, A … - Journal of Autoimmunity, 2005 - Elsevier
The identification of causative genes for the autoimmune disease type 1 diabetes (T1D) in humans
and candidate genes in the NOD mouse has made significant progress in recent years. In addition
to sharing structural aspects of the MHC class II molecules that confer susceptibility or ...
Cited by 42 - Related articles - All 6 versions

Genetic approaches to studying common diseases and complex traits


JN HIRSCHHORN - Pediatric research, 2005 - journals.lww.com
Most common diseases and most quantitative traits that can be measured in human populations
are complex genetic traits. That is, many genetic and nongenetic factors interact to determine
the final phenotype, whether that phenotype is susceptibility to disease, or a quantifiable ...
Cited by 40 - Related articles - All 4 versions


Result Page: 

1

2

3

4

5

6

7

8

9

10

Next


 


Go to Google Home - About Google - About Google Scholar

©2009 Google