Maria Rodriguez‐Zabala

Mutations in C-natriuretic peptide (NPPC): a novel cause of autosomal dominant short stature

Alfonso Hisado-Oliva, Alba Ruzafa-Martin, Lucia Sentchordi et al. · Genetics in Medicine · 2017 · 66 citations · Full text

Human Growth, Novel Cause, Genetics +4

CXCR4 Signaling Has a CXCL12-Independent Essential Role in Murine MLL-AF9-Driven Acute Myeloid Leukemia

Ramprasad Ramakrishnan, Pablo Peña‐Martínez, Puneet Agarwal et al. · Cell Reports · 2020 · 43 citations · Full text

Hematological Malignancy, Cxcl12-independent Essential Role, Cell Surface Genes +11

FGF9 mutation causes craniosynostosis along with multiple synostoses

Maria Rodriguez‐Zabala, Miriam Aza‐Carmona, Carlos I Rivera-Pedroza et al. · Human Mutation · 2017 · 34 citations

Sclerostin, Developmental Biology, Bone Morphogenic Protein +12

Combined GLUT1 and OXPHOS inhibition eliminates acute myeloid leukemia cells by restraining their metabolic plasticity

Maria Rodriguez‐Zabala, Ramprasad Ramakrishnan, Katrin Reinbach et al. · Blood Advances · 2023 · 24 citations · Full text

Engineering, Mixed-phenotype Acute Leukemia, Oxphos Inhibition +19

Biallelic cGMP-dependent type II protein kinase gene (<i>PRKG2</i>) variants cause a novel acromesomelic dysplasia

Francisca Díaz, Saruchi Wadhwa, Maria Rodriguez‐Zabala et al. · Journal of Medical Genetics · 2020 · 21 citations