Peter A. Smethurst

Compound inheritance of a low-frequency regulatory SNP and a rare null mutation in exon-junction complex subunit RBM8A causes TAR syndrome

Cornelis A. Albers, Dirk S. Paul, Harald Schulze et al. · Nature Genetics · 2012 · 419 citations

Compound Inheritance, Mendelian Disorder, Genetic Disorder +8

Genome-wide Analysis of Simultaneous GATA1/2, RUNX1, FLI1, and SCL Binding in Megakaryocytes Identifies Hematopoietic Regulators

Marloes R. Tijssen, Ana Cvejic, Anagha Joshi et al. · Developmental Cell · 2011 · 278 citations · Full text

Identification in Collagen Type I of an Integrin α2β1-binding Site Containing an Essential GER Sequence

Christopher G. Knight, Laurence F. Morton, David J. Onley et al. · Journal of Biological Chemistry · 1998 · 276 citations · Full text

Exome sequencing identifies NBEAL2 as the causative gene for gray platelet syndrome

Cornelis A. Albers, Ana Cvejic, Rémi Favier et al. · Nature Genetics · 2011 · 274 citations · Full text

Thrombopoiesis, Thrombosis, Blood Platelet +11

Platelet receptor interplay regulates collagen-induced thrombus formation in flowing human blood

Pia Siljander, Imke C.A. Munnix, Peter A. Smethurst et al. · Blood · 2003 · 202 citations