Jürgen Herwig

CTLA4 Alanine-17 Confers Genetic Susceptibility to Graves’ Disease and to Type 1 Diabetes Mellitus¹

H. Donner, Harald Rau, Paul G. Walfish et al. · The Journal of Clinical Endocrinology & Metabolism · 1997 · 396 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

CYP2R1 (vitamin D 25‐hydroxylase) gene is associated with susceptibility to type 1 diabetes and vitamin D levels in Germans

Elizabeth Ramos‐Lopez, Patrick T. Bruck, Thomas Jansen et al. · Diabetes/Metabolism Research and Reviews · 2007 · 163 citations

Medicine, Genetics, Molecular Genetics +15

The cblD Defect Causes Either Isolated or Combined Deficiency of Methylcobalamin and Adenosylcobalamin Synthesis

Terttu Suormala, Matthias R. Baumgartner, David Coelho et al. · Journal of Biological Chemistry · 2004 · 119 citations · Full text

Life Sciences, Molecular Biology, Molecular Genetics +8

3-methylcrotonyl-CoA carboxylase deficiency: Clinical, biochemical, enzymatic and molecular studies in 88 individuals

Sarah C. Grünert, Martin Stucki, Raphael J. Morscher et al. · Orphanet Journal of Rare Diseases · 2012 · 93 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Detection of mutations in the apolipoprotein CII gene by denaturing gradient gel electrophoresis. Identification of the splice site variant apolipoprotein CII-Hamburg in a patient with severe hypertriglyceridemia

Markus Nauck, Henrik Nissen, Michael M. Hoffmann et al. · Clinical Chemistry · 1998 · 22 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17