Kerra Pearce

Identification of mutations in CUL7 in 3-M syndrome

Céline Huber, Dora Dias‐Santagata, Anna Glaser et al. · Nature Genetics · 2005 · 172 citations

Genetic Disorder, Pathology, 3-M Syndrome +2

Targeting acute myeloid leukemia by drug-induced c-MYB degradation

Vanessa Walf-Vorderwülbecke, Kerra Pearce, Tony Brooks et al. · Leukemia · 2017 · 114 citations

Hematological Malignancy, Medicine, Acute Myeloid Leukemia +5

Molecular study of 33 families with Fraser syndrome new data and mutation review

Mieke M. van Haelst, Merel Maiburg, Geneviève Baujat et al. · American Journal of Medical Genetics Part A · 2008 · 85 citations

Fraser Syndrome, Developmental Anomaly, Umbilical Cord +15

Hes1 expression is reduced in Tbx1 null cells and is required for the development of structures affected in 22q11 deletion syndrome

Kelly Lammerts van Bueren, Irinna Papangeli, Francesca Rochais et al. · Developmental Biology · 2010 · 62 citations · Full text

Genetics, Molecular Genetics, Deletion Syndrome +19

Mutations in linker for activation of T cells (LAT) lead to a novel form of severe combined immunodeficiency

Chiara Bacchelli, Federico A. Moretti, Marlene Carmo et al. · Journal of Allergy and Clinical Immunology · 2016 · 55 citations

Primary Immunodeficiency, Autoimmune Disease, Human Retrovirus +9