| Live imaging of axolotl digit regeneration reveals spatiotemporal choreography of diverse connective tissue progenitor pools JD Currie, A Kawaguchi, RM Traspas, M Schuez, O Chara, EM Tanaka Developmental cell 39 (4), 411-423, 2016 | 145 | 2016 |
| DPP9 deficiency: an inflammasomopathy that can be rescued by lowering NLRP1/IL-1 signaling CR Harapas, KS Robinson, K Lay, J Wong, R Moreno Traspas, ... Science immunology 7 (75), eabi4611, 2022 | 24 | 2022 |
| Loss of C2orf69 defines a fatal autoinflammatory syndrome in humans and zebrafish that evokes a glycogen-storage-associated mitochondriopathy HH Wong, SH Seet, M Maier, A Gurel, RM Traspas, C Lee, S Zhang, ... The American Journal of Human Genetics 108 (7), 1301-1317, 2021 | 12 | 2021 |
| C10orf99/GPR15L regulates proinflammatory response of keratinocytes and barrier formation of the skin T Dainichi, Y Nakano, H Doi, S Nakamizo, S Nakajima, R Matsumoto, ... Frontiers in Immunology 13, 825032, 2022 | 9 | 2022 |
| Loss of FOCAD, operating via the SKI messenger RNA surveillance pathway, causes a pediatric syndrome with liver cirrhosis R Moreno Traspas, TS Teoh, PM Wong, M Maier, CY Chia, K Lay, NA Ali, ... Nature genetics 54 (8), 1214-1226, 2022 | 8 | 2022 |
| Notch3-dependent effects on adult neurogenesis and hippocampus-dependent learning in a modified transgenic model of CADASIL F Ehret, R Moreno Traspas, MT Neumuth, B Hamann, D Lasse, ... Frontiers in aging neuroscience 13, 617733, 2021 | 5 | 2021 |
| A progeroid syndrome caused by a deep intronic variant in TAPT1 is revealed by RNA/SI‐NET sequencing N Nabavizadeh, A Bressin, M Shboul, R Moreno Traspas, PH Chia, ... EMBO Molecular Medicine 15 (2), e16478, 2023 | 4 | 2023 |
| New insights in melanoma biomarkers: long-noncoding RNAs R Moreno-Traspas, I Vujic, M Sanlorenzo, S Ortiz-Urda Melanoma Management 3 (3), 195-205, 2016 | 1 | 2016 |
| A progeroid syndrome with severe osteogenesis imperfecta segregates with an intronic TAPT1 homozygous variant that creates a knockout allele N Nabavizadeh, A Bressin, PH Chia, RM Traspas, N Escande-Beillard, ... EUROPEAN JOURNAL OF HUMAN GENETICS 31, 402-403, 2023 | | 2023 |
| Commentary: Loss of FOCAD, Operating via the SKI Messenger RNA Surveillance Pathway, Causes a Pediatric Syndrome with Liver Cirrhosis RM Traspas Appl Cell Biol 11 (2), 2023 | | 2023 |
| 176 C10orf99/2610528A11Rik induces keratinocyte proinflammatory response and regulates lipid metabolism and barrier formation of the skin T Dainichi, Y Nakano, H Doi, S Nakamizo, S Nakajima, T Farkas, P Wong, ... Journal of Investigative Dermatology 142 (12), S210, 2022 | | 2022 |
| Deciphering the consequence of deep intronic variants: a progeroid syndrome caused by a TAPT1 mutation is revealed by combined RNA/SI-NET sequencing N Nabavizadeh, A Bressin, PH Chia, RM Traspas, N Escande-Beillard, ... medRxiv, 2022.07. 15.22276800, 2022 | | 2022 |
| Loss of Focad, Operating in the SKI mRNA Surveillance Pathway, is Responsible for a Syndromic form of Pediatric Liver Cirrhosis RM Traspas PQDT-Global, 2022 | | 2022 |
| Live imaging of axolotl appendage regeneration reveals the cellular source and coordination of regenerated connective tissue and skeletal tissue via PDGF-dependent cell migration. JD Currie, A Kawaguchi, RM Traspas, M Schuez, O Chara, EM Tanaka MOLECULAR BIOLOGY OF THE CELL 29 (26), 2018 | | 2018 |
| LncRNAs as Biomarkers for Melanoma YJ Zheng, RM Traspas, S Ortiz-Urda Human Skin Cancers: Pathways, Mechanisms, Targets and Treatments, 25, 2018 | | 2018 |
