Aurélia Gruber

Clinical and Genetic Spectrum of a Large Cohort With Total and Sub-total Complement Deficiencies

Carine El Sissy, Jérémie Rosain, Paula Vieira‐Martins et al. · Frontiers in Immunology · 2019 · 60 citations · Full text

Life Sciences, Genetics, Immunology +15

SPRED1, a RAS MAPK pathway inhibitor that causes Legius syndrome, is a tumour suppressor downregulated in paediatric acute myeloblastic leukaemia

Éric Pasmant, Brigitte Gilbert‐Dussardier, Arnaud Petit et al. · Oncogene · 2014 · 55 citations

Medicine, Molecular Genetics, Oncology +12

Non-invasive prenatal diagnosis of paternally inherited disorders from maternal plasma: detection of <i>NF1</i> and <i>CFTR</i> mutations using droplet digital PCR

Aurélia Gruber, Mathilde Pacault, Laïla El Khattabi et al. · Clinical Chemistry and Laboratory Medicine (CCLM) · 2018 · 40 citations

Medicine, Genetics, Molecular Genetics +14

<i>NF1</i> mutations identify molecular and clinical subtypes of lung adenocarcinomas

Camille Tlemsani, Nicolas Pécuchet, Aurélia Gruber et al. · Cancer Medicine · 2019 · 18 citations · Full text

Medicine, Molecular Genetics, Oncology +17

Diagnostic performance of high‐throughput sequencing of the T‐cell receptor beta gene for the diagnosis of cutaneous T‐cell lymphoma

Clement Zimmermann, Marie Boisson, C. Ram‐Wolff et al. · British Journal of Dermatology · 2021 · 12 citations

Medicine, Immunology, Oncology +16