Núria Pujol‐Moix

Mutations in ANKRD26 are responsible for a frequent form of inherited thrombocytopenia: analysis of 78 patients from 21 families

Patrizia Noris, Silverio Perrotta, Marco Seri et al. · Blood · 2011 · 292 citations · Full text

Medicine, Genetics, Hematology +12

Mutations in the 5′ UTR of ANKRD26, the Ankirin Repeat Domain 26 Gene, Cause an Autosomal-Dominant Form of Inherited Thrombocytopenia, THC2

Tommaso Pippucci, Anna Savoia, Silverio Perrotta et al. · The American Journal of Human Genetics · 2011 · 220 citations · Full text

Life Sciences, Genetics, Molecular Genetics +8

<i>MYH9</i>-Related Disease: A Novel Prognostic Model to Predict the Clinical Evolution of the Disease Based on Genotype-Phenotype Correlations

Alessandro Pecci, Catherine Klersy, Paolo Gresele et al. · Human Mutation · 2013 · 200 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Position of nonmuscle myosin heavy chain IIA (NMMHC-IIA) mutations predicts the natural history ofMYH9-related disease

Alessandro Pecci, Emanuele Panza, Núria Pujol‐Moix et al. · Human Mutation · 2007 · 185 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16

Platelet diameters in inherited thrombocytopenias: analysis of 376 patients with all known disorders

Patrizia Noris, Ginevra Biino, Alessandro Pecci et al. · Blood · 2014 · 147 citations · Full text

Medicine, Hematology, Pathology +13