| Functional consequences of transferrin receptor‐2 mutations causing hereditary hemochromatosis type 3 R Joshi, M Shvartsman, E Morán, S Lois, J Aranda, A Barqué, ... Molecular genetics & genomic medicine 3 (3), 221-232, 2015 | 38 | 2015 |
| Genetic and clinical heterogeneity in thirteen new cases with aceruloplasminemia. Atypical anemia as a clue for an early diagnosis M Vila Cuenca, G Marchi, A Barqué, C Esteban-Jurado, A Marchetto, ... International journal of molecular sciences 21 (7), 2374, 2020 | 35 | 2020 |
| Computational and experimental characterization of the novel ECM glycoprotein SNED1 and prediction of its interactome SD Vallet, MN Davis, A Barqué, AH Thahab, S Ricard-Blum, A Naba Biochemical Journal 478 (7), 1413-1434, 2021 | 14 | 2021 |
| Knockout of the gene encoding the extracellular matrix protein SNED1 results in early neonatal lethality and craniofacial malformations A Barqué, K Jan, E De La Fuente, CL Nicholas, RO Hynes, A Naba Developmental Dynamics 250 (2), 274-294, 2021 | 12 | 2021 |
| Knockout of the gene encoding the extracellular matrix protein Sned1 results in craniofacial malformations and early neonatal lethality A Naba, K Jan, A Barqué, CL Nicholas, RO Hynes bioRxiv 440081, 2018 | 3 | 2018 |
| The matrix in focus: new directions in extracellular matrix research from the 2021 ASMB hybrid meeting BA Nerger, TM Jones, KWJ Rose, A Barqué, JS Weinbaum, RJ Petrie, ... Biology Open 11 (1), bio059156, 2022 | 1 | 2022 |
| SNED1: a Novel ECM Protein Regulating Neural Crest Cells Phenotype and Craniofacial Morphogenesis A Barqué, M Davis, A Naba The FASEB Journal 35, 2021 | | 2021 |
| Cuando el hierro es tóxico A Barqué, M Sanchez Genética Médica y Genómica, 2017 | | 2017 |
| ATRANSFERRINEMIA: AN ULTRA-RARE IRON-LOADING ANAEMIA. REPORT OF 6 CASES FROM 4 FAMILIES A Barque, F Fuster, C Diaz de Heredia, ES Edison, K Moser, E Moran, ... AMERICAN JOURNAL OF HEMATOLOGY 91 (3), E30-E30, 2016 | | 2016 |
