N. Ordóñez

ADAMTS19‐associated heart valve defects: Novel genetic variants consolidating a recognizable cardiac phenotype

P. Bauer, A. Bertoli-Avella, C. Beetz, 2020, Clinical genetics.

Inflammatory cytokine expression is correlated with the level of human immunodeficiency virus (HIV) transcripts in HIV-infected placental trophoblastic cells

J. Reuben, N. Eriksen, C. Langston, 1997, Journal of virology.

Physiology and pathophysiology of dendritic cells.

Z. Estrov, M. Talpaz, N. Ordóñez, 1997, Human pathology.

Loss of C2orf69 defines a fatal autoinflammatory syndrome in humans and zebrafish that evokes a glycogen storage-associated mitochondriopathy.

Fernanda L. Sirota, J. Lupski, J. Casanova, 2021, American journal of human genetics.

De novo MCM6 variants in neurodevelopmental disorders: a recognizable phenotype related to zinc binding residues

H. Van Esch, G. Mancini, T. Roscioli, 2023, Human Genetics.

ANTI-TUMOR EFFECTS OF SIMVASTATIN ON UMR-106 OSTEOSARCOMA CELL LINE

L. Fernández-Pérez, Adriana Umaña-Pérez, N. Ordóñez, 2011 .

A pleiotropic recurrent dominant ITPR3 variant causes a complex multisystemic disease

Nurit Assia Batzir, S. Ehl, R. Hite, 2024, Science advances.

FBXO22 deficiency defines a pleiotropic syndrome of growth restriction and multi-system anomalies associated with a unique epigenetic signature

F. Alkuraya, A. Bertoli-Avella, A. A. Tayoun, 2024, medRxiv.