Alexander P.A. Stegmann

<i>MAX</i> Mutations Cause Hereditary and Sporadic Pheochromocytoma and Paraganglioma

Nelly Burnichon, Alberto Cascón, Francesca Schiavi et al. · Clinical Cancer Research · 2012 · 321 citations · Full text

Inhibition of T Cell and Promotion of Natural Killer Cell Development by the Dominant Negative Helix Loop Helix Factor Id3

Mirjam H.M. Heemskerk, Bianca Blom, Garry P. Nolan et al. · The Journal of Experimental Medicine · 1997 · 270 citations

Human Thymus, Lymphocyte Development, T-regulatory Cell +16

Further clinical and molecular delineation of the 9q subtelomeric deletion syndrome supports a major contribution of <i>EHMT1</i> haploinsufficiency to the core phenotype

Tjitske Kleefstra, W. A. van Zelst‐Stams, Willy M. Nillesen et al. · Journal of Medical Genetics · 2009 · 257 citations

Fourteen new cases contribute to the characterization of the 7q11.23 microduplication syndrome

Nathalie Van der Aa, Liesbeth Rooms, Geert Vandeweyer et al. · European Journal of Medical Genetics · 2009 · 215 citations

Developmental Biology, Genetic Disorder, Genetics +7

Distinct Roles of the Phosphatidylinositol 3-Kinase and STAT5 Pathways in IL-7-Mediated Development of Human Thymocyte Precursors

C. Pallard, Alexander P.A. Stegmann, Titia van Kleffens et al. · Immunity · 1999 · 202 citations · Full text

Inflammation, Cytokine, Signal Transduction +14