N. Klopp

ASXL1 exon 12 mutations are frequent in AML with intermediate risk karyotype and are independently associated with an adverse outcome

Susanne Schnittger, Christiane Eder, Sabine Jeromin et al. · Leukemia · 2012 · 211 citations

Life Sciences, Genetics, Molecular Genetics +11

Putative association of a <i>TLR9</i> promoter polymorphism with atopic eczema

Natalija Novak, Chunfeng Yu, Laura Maintz et al. · Allergy · 2007 · 174 citations

Life Sciences, Genetics, Immunology +17

Genome-wide association study identifies a new locus for coronary artery disease on chromosome 10p11.23

Jeanette Erdmann, Christina Willenborg, Janja Nahrstaedt et al. · European Heart Journal · 2010 · 144 citations · Full text

Medicine, Cardiology, Genetics +17

Effect of macrophage migration inhibitory factor (MIF) gene variants and MIF serum concentrations on the risk of type 2 diabetes: results from the MONICA/KORA Augsburg Case–Cohort Study, 1984–2002

Christian Herder, N. Klopp, Jens Baumert et al. · Diabetologia · 2007 · 92 citations · Full text

Medicine, Endocrinology, Immunology +9

Prion protein codon 129 polymorphism and risk of Alzheimer disease

Markus J. Riemenschneider, N. Klopp, Wei Xiang et al. · Neurology · 2004 · 91 citations

Life Sciences, Genetics, Molecular Genetics +14