Michael A. Simpson

Assessment of Minimal Residual Disease in Standard-Risk AML

Adam Ivey, Robert K. Hills, Michael A. Simpson et al. · New England Journal of Medicine · 2016 · 812 citations · Full text

Mutations in IL36RN/IL1F5 Are Associated with the Severe Episodic Inflammatory Skin Disease Known as Generalized Pustular Psoriasis

Alexandros Onoufriadis, Michael A. Simpson, Andrew Pink et al. · The American Journal of Human Genetics · 2011 · 521 citations · Full text

Inflammation, Rheumatology, Autoimmune Disease +8

Mutations in GATA2 cause primary lymphedema associated with a predisposition to acute myeloid leukemia (Emberger syndrome)

Pia Østergaard, Michael A. Simpson, Fiona Connell et al. · Nature Genetics · 2011 · 494 citations

Hematological Malignancy, Genetic Disorder, Mixed-phenotype Acute Leukemia +8

Structural Insights into Histone Demethylation by JMJD2 Family Members

Zhongzhou Chen, Jianye Zang, Johnathan R. Whetstine et al. · Cell · 2006 · 399 citations · Full text

Histone Modifications, Chromatin, Chromatin Structure +9

Infantile-onset symptomatic epilepsy syndrome caused by a homozygous loss-of-function mutation of GM3 synthase

Michael A. Simpson, Christos Proukakis, David A. Priestman et al. · Nature Genetics · 2004 · 381 citations · Full text

Mendelian Disorder, Genetic Disorder, Genetics +7