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Association of the T-cell regulatory gene CTLA4 with susceptibility to autoimmune disease.
Nature. 2003 May 29;423(6939):506-11. doi: 10.1038/nature01621. Epub 2003 Apr 30.
Nature. 2003.
PMID: 12724780
Evaluation of fine mapping strategies for a multifactorial disease locus: systematic linkage and association analysis of IDDM1 in the HLA region on chromosome 6p21.
Herr M, Dudbridge F, Zavattari P, Cucca F, Guja C, March R, Campbell RD, Barnett AH, Bain SC, Todd JA, Koeleman BP.
Herr M, et al.
Hum Mol Genet. 2000 May 22;9(9):1291-301. doi: 10.1093/hmg/9.9.1291.
Hum Mol Genet. 2000.
PMID: 10814711
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Conditional ETDT analysis of the human leukocyte antigen region in type 1 diabetes.
Koeleman BP, Herr MH, Zavattari P, Dudbridge F, March R, Campbell D, Barnett AH, Bain SC, Mulargia AP, Loddo M, Amos W, Cucca F, Todd JA.
Koeleman BP, et al. Among authors: herr mh.
Ann Hum Genet. 2000 May;64(Pt 3):215-21. doi: 10.1017/S0003480000008101.
Ann Hum Genet. 2000.
PMID: 11246473
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Low frequency of HLA DRB1*03 - DQB1*02 and DQB1*0302 haplotypes in Romania is consistent with the country's low incidence of Type I diabetes.
Ionescu-Tîrgoviste C, Guja C, Herr M, Cucca E, Welsh K, Bunce M, Marshall S, Todd JA.
Ionescu-Tîrgoviste C, et al.
Diabetologia. 2001 Oct;44 Suppl 3:B60-6. doi: 10.1007/pl00002956.
Diabetologia. 2001.
PMID: 11724419
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Clinical heterogeneity in patients with FOXP3 mutations presenting with permanent neonatal diabetes.
Rubio-Cabezas O, Minton JA, Caswell R, Shield JP, Deiss D, Sumnik Z, Cayssials A, Herr M, Loew A, Lewis V, Ellard S, Hattersley AT.
Rubio-Cabezas O, et al.
Diabetes Care. 2009 Jan;32(1):111-6. doi: 10.2337/dc08-1188. Epub 2008 Oct 17.
Diabetes Care. 2009.
PMID: 18931102
Free PMC article.
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Data mining applied to linkage disequilibrium mapping.
Toivonen HT, Onkamo P, Vasko K, Ollikainen V, Sevon P, Mannila H, Herr M, Kere J.
Toivonen HT, et al.
Am J Hum Genet. 2000 Jul;67(1):133-45. doi: 10.1086/302954. Epub 2000 Jun 9.
Am J Hum Genet. 2000.
PMID: 10848493
Free PMC article.
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Best practice guidelines for the molecular genetic diagnosis of maturity-onset diabetes of the young.
Ellard S, Bellanné-Chantelot C, Hattersley AT; European Molecular Genetics Quality Network (EMQN) MODY group.
Ellard S, et al.
Diabetologia. 2008 Apr;51(4):546-53. doi: 10.1007/s00125-008-0942-y. Epub 2008 Feb 23.
Diabetologia. 2008.
PMID: 18297260
Free PMC article.
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Diabetes and neurodegeneration in Wolfram syndrome: a multicenter study of phenotype and genotype.
Rohayem J, Ehlers C, Wiedemann B, Holl R, Oexle K, Kordonouri O, Salzano G, Meissner T, Burger W, Schober E, Huebner A, Lee-Kirsch MA; Wolfram Syndrome Diabetes Writing Group.
Rohayem J, et al.
Diabetes Care. 2011 Jul;34(7):1503-10. doi: 10.2337/dc10-1937. Epub 2011 May 20.
Diabetes Care. 2011.
PMID: 21602428
Free PMC article.
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