Lebenslauf Dr. med. Mathias Herr - DRK Kliniken Berlin
Lebenslauf Dr. med. Mathias Herr - DRK Kliniken Berlin
Lebenslauf Dr. med. Mathias Herr - DRK Kliniken Berlin
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Mitgliedschaften<br />
Publikationen<br />
Deutsche Gesellschaft für Kinder- und Jugend<strong>med</strong>izin (DGKJM)<br />
Deutsche Diabetes Gesellschaft (DDG)<br />
International Society for Pediatric and Adolescent Diabetes (ISPAD)<br />
<strong>Berlin</strong>er Diabetes Gesellschaft<br />
• <strong>Herr</strong> M, Dudbridge F, Zavattari P, Cucca F, Guja C, March R, Campbell DC, Barnett AH, Bain<br />
SC, Todd JA & Koeleman BPC<br />
Evaluation of fine mapping strategies for a multifactorial disease locus: systematic linkage and<br />
association analysis of IDDM1 in the HLA region on chromosome 6p21.<br />
Hum Mol Genet (2000) 9, 1291-1301<br />
• Koeleman BPC, <strong>Herr</strong> M, Zavattari P, Dudbridge F, March R, Campbell D, Barnett AH, Bain SC,<br />
Mulargia AP, Loddo M, Amos W, Cucca F & Todd JA<br />
Conditional ETDT analysis of the Human Leukocyte Antigen region in type 1 diabetes.<br />
Ann Hum Genet (2000) 22, 1291-301<br />
• Toivonen HT, Onkamo P, Vasko K, Ollikainen V, Sevon P, Mannila H, <strong>Herr</strong> M & Kere J<br />
Data mining applied to linkage disequilibrium mapping.<br />
Am J Hum Genet (2000) 67, 133-45<br />
• Ionescu-Tîrgovişte C, Guja C, <strong>Herr</strong> M, Merriman M, Cucca F, Welsh K, Bunce M, Marshall S,<br />
Todd JA<br />
Low frequency of HLA DRB1*03-DQB1*02 and DQB1*0302 haplotypes in Romania is<br />
consistent with the country’s low incidence of type 1 diabetes.<br />
Diabetologia (2001) 44 Suppl 3, B60-6<br />
• Ueda H, Howson JM, Esposito L, Heward J, Snook H, Chamberlain G, Rainbow DB, Hunter KM,<br />
Smith AN, Di Genova G, <strong>Herr</strong> M, […], Todd JA & Gough SC<br />
Association of the T-cell regulatory gene CTLA4 with susceptibility to autoimmune disease.<br />
Nature (2003) 423, 506-11<br />
• Höffe J, Hartmann R, Deiss D, <strong>Herr</strong> M, Kordonouri O<br />
Ergebnisse der Therapieumstellung auf Insulin Glargin bei 84 Kindern und Jugendlichen mit<br />
Typ 1 Diabetes<br />
Diabetologie und Stoffwechsel (2006) 1, 374-78<br />
• Ellard S, Bellanné-Chantelot C, Hattersley AT, European Molecular Genetics Quality Network<br />
(EMQN) MODY group (<strong>Herr</strong> M als Mitglied)<br />
Best practice guidelines for the molecular genetic diagnosis of maturity-onset diabetes of the<br />
young<br />
Diabetologia (2008) 51, 546-53<br />
• Rubio-Cabezas O, Minton JA, Caswell R, Shield JP, Deiss D, Sumnik Z, Cayssials A, <strong>Herr</strong> M,<br />
Loew A, Lewis V, Ellard S, Hattersley AT<br />
Clinical heterogeneity in patients with FOXP3 mutations presenting with permanent neonatal<br />
diabetes<br />
Diabetes Care (2008), 17 [Epub ahead of print]
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