Carmen Benito

Hospital General Universitario Gregorio Marañón — Spain

Medicine · Health Sciences

13h-index519citations50works0.02yr avg
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Research Topics

Pancreatic function and diabetes(11), interferon and immune responses(8), NF-κB Signaling Pathways(7), Metabolism and Genetic Disorders(6), Diabetes and associated disorders(6)

Publications50 total

Association between use of enhanced recovery after surgery protocols and postoperative complications after gastric surgery for cancer (POWER 4): a nationwide, prospective multicentre study
Cirugía Española·2023· 6 citedOpen Access
Association between use of enhanced recovery after surgery protocols and postoperative complications after gastric surgery for cancer (POWER 4): a nationwide, prospective multicentre study
Cirugía Española (English Edition)·2023· 4 cited
Data from Increased Susceptibility to Skin Carcinogenesis in TREX2 Knockout Mice
2023Open Access
Supplementary Figure 1 from Increased Susceptibility to Skin Carcinogenesis in TREX2 Knockout Mice
2023Open Access
Supplementary Figure 1 from Increased Susceptibility to Skin Carcinogenesis in TREX2 Knockout Mice
2023Open Access
Supplementary Figure Legend, Tables 1-2 from Increased Susceptibility to Skin Carcinogenesis in TREX2 Knockout Mice
2023Open Access
Supplementary Figure Legend, Tables 1-2 from Increased Susceptibility to Skin Carcinogenesis in TREX2 Knockout Mice
2023Open Access
Data from Increased Susceptibility to Skin Carcinogenesis in TREX2 Knockout Mice
2023Open Access
M274 Cobalamin deficiency detected through expanded newborn screening in Spain
Clinica Chimica Acta·2022
Metabolic Serendipities of Expanded Newborn Screening
Genes·2020· 19 citedOpen Access
Rare Variants in 48 Genes Account for 42% of Cases of Epilepsy With or Without Neurodevelopmental Delay in 246 Pediatric Patients
Frontiers in Neuroscience·2019· 60 citedOpen Access
Further delineation of neuropsychiatric findings in Tatton-Brown-Rahman syndrome due to disease-causing variants in DNMT3A: seven new patients
European Journal of Human Genetics·2019· 30 citedOpen Access
Initial Evaluation of Prospective and Parallel Assessments of Cystic Fibrosis Newborn Screening Protocols in Eastern Andalusia: IRT/IRT versus IRT/PAP/IRT
International Journal of Neonatal Screening·2019· 6 citedOpen Access
El programa MUS-E en Badajoz: análisis comparativo y emergente de resultados de su implantación
SHILAP Revista de lepidopterología·2019Open Access
A new metabolic disorder in human cationic amino acid transporter‐2 that mimics arginase 1 deficiency in newborn screening
Journal of Inherited Metabolic Disease·2019· 8 cited
Infantile sialidosis: natural history in a preterm infant with two new pathogenic mutations and new ocular findings
Journal of American Association for Pediatric Ophthalmology and Strabismus·2018· 3 cited
Ethical Challenges of Early Identification of Advanced Chronic Patients in Need of Palliative Care
Journal of Palliative Care·2018· 13 citedOpen Access
Table of Contents
Journal of Investigative Dermatology·2016Open Access
The Exonuclease Trex2 Shapes Psoriatic Phenotype
Journal of Investigative Dermatology·2016· 21 citedOpen Access
Leber hereditary optic neuropathy: Usefulness of next generation sequencing to study mitochondrial mutations on apparent homoplasmy
Medicina Clínica (English Edition)·2016· 8 cited
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Frequent Co-authors

Joan Manils(10), Concepció Soler(9), Teresa Gallart(9), Arnau Viña‐Vilaseca(8), Bárbara Castellana(7), Eva Morán‐Salvador(7), Nuria Vázquez‐Villoldo(7), Gemma Tarancón(7), Miquel Borràs(7), Sagrario Ortega(7), Marta E Fabregat(7), Ramón Gomis(6), Willy Malaisse(6), Jeremy N. Rich(6), David Parra Monserrat(6), Sara Sancho(6), Raquel Yahyaoui(5), Ramón Gomis(4), Mònica Gudayol(4), Josefa Fernández-Álvarez(4)