Robert W. Lindeman

Noninvasive measurement and imaging of liver iron concentrations using proton magnetic resonance

Timothy G. St. Pierre, Paul R. Clark, Wanida Chua‐anusorn et al. · Blood · 2004 · 895 citations

Integrative Genomics Identifies the Molecular Basis of Resistance to Azacitidine Therapy in Myelodysplastic Syndromes

Ashwin Unnikrishnan, Elli Papaemmanuil, Dominik Beck et al. · Cell Reports · 2017 · 123 citations · Full text

Non-responder Hpc Quiescence, Mixed-phenotype Acute Leukemia, Genetics +19

SLC29A3 gene is mutated in pigmented hypertrichosis with insulin-dependent diabetes mellitus syndrome and interacts with the insulin signaling pathway

Simon T. Cliffe, Jamie M. Kramer, Khalid Hussain et al. · Human Molecular Genetics · 2009 · 117 citations

Metabolic Syndrome, Insulin Signaling, Genetic Disorder +15

Single amino acid mutation of FCγ receptor is associated with the development of heparin‐induced thrombocytopenia

Janette K. Burgess, Robert W. Lindeman, Colin N. Chesterman et al. · British Journal of Haematology · 1995 · 113 citations

Mutations in the gene encoding the PML nuclear body protein Sp110 are associated with immunodeficiency and hepatic veno-occlusive disease

Tony Roscioli, Simon T. Cliffe, Donald B. Bloch et al. · Nature Genetics · 2006 · 97 citations · Full text

Primary Immunodeficiency, Hepatology, Hepatic Veno-occlusive Disease +10