Helena Gil‐Peña

Universidad de Oviedo — Spain

Biochemistry, Genetics and Molecular Biology · Life Sciences

22h-index1.3kcitations82works1.12yr avg
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Research Topics

Ion Transport and Channel Regulation(23), Parathyroid Disorders and Treatments(19), Renal function and acid-base balance(16), Magnesium in Health and Disease(13), Bone health and treatments(10)

Publications82 total

A bibliometric approach to worldwide scientific production of familial hypophosphataemic rickets in Scopus (2000–2022)
Orphanet Journal of Rare Diseases·2025Open Access
Characterization of snRNA-related neurodevelopmental disorders through the Spanish Undiagnosed Rare Disease Programs
2025· 1 citedOpen Access
Urine pH and ammonium paediatric reference intervals in first morning spot urine
Advances in Laboratory Medicine / Avances en Medicina de Laboratorio·2025Open Access
High Dietary Phosphorus Impairs Bone Microarchitecture and Induces Alterations in the LGR4–R-Spondins Axis in Rats with Normal Renal Function
Nutrients·2025Open Access
Contribution of Rare and Common APOE Variants to Familial Hypercholesterolemia in Spanish Cohort
Cardiogenetics·2025Open Access
Polymorphisms of the Vitamin D Binding Protein (VDBP) and Free Vitamin D in Patients with Cystic Fibrosis
Nutrients·2024· 1 citedOpen Access
Polymorphisms of the Vitamin D Binding Protein (VDBP) and Free vitamin D in pediatric and young adult patients with cystic fibrosis
Preprints.org·2024· 1 citedOpen Access
RANKL, but Not R-Spondins, Is Involved in Vascular Smooth Muscle Cell Calcification through LGR4 Interaction
International Journal of Molecular Sciences·2024· 7 citedOpen Access
Hemoglobin Oviedo ( <i>c.115A &gt; G; p.T39A</i> ): A Cause of Low Oxygen Saturation
Hemoglobin·2024
A Bibliometric Approach to Scientific Production on Familial Hypophosphatemic Rickets in Scopus (2000-2022)
2023Open Access
Scientific Production on Familial Hypophosphatemic Rickets in Scopus (2000-2022)
Harvard Dataverse·2023Open Access
Genotypic variability in patients with clinical diagnosis of Bartter syndrome type 3
Scientific Reports·2023· 3 citedOpen Access
Nutritional Assessment and Support in Children with Chronic Kidney Disease: The Benefits of Working with a Registered Dietitian
Nutrients·2023· 4 citedOpen Access
¿Desempeñan un papel relevante los micro-ARN en el desarrollo de la poliquistosis renal del adulto?
NefroPlus.·2023Open Access
Evaluation of urinary acidification in children: Clinical utility
Frontiers in Pediatrics·2022· 3 citedOpen Access
Transcriptomic clustering of critically ill COVID-19 patients
European Respiratory Journal·2022· 30 citedOpen Access
IGHG3 hinge length variation was associated with the risk of critical disease and death in a Spanish COVID-19 cohort
Genes and Immunity·2022· 6 citedOpen Access
Long-term complications of primary distal renal tubular acidosis
Pediatric Nephrology·2022· 5 cited
Transcriptomic Clustering of Severe COVID-19 Patients
2022
Transcriptomic clustering of critically ill COVID-19 patients
2022· 4 citedOpen Access
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Frequent Co-authors

Fernando Santos(38), Eliécer Coto(15), Rocío Fuente(13), Julián Rodrı́guez(11), Flor Á. Ordóñez(9), Juan Gómez(8), Ángela Fernández-Iglesias(7), Enrique García-López(7), Vanessa Loredo(7), Gema Ariceta(5), Guillermo M. Albaiceta(5), Elías Cuesta‐Llavona(5), Laura Amado‐Rodríguez(5), Inés López-Alonso(5), Victoria Álvarez(5), Natalia Mejía(5), Laura Alonso‐Durán(5), Enrique Rodríguez-Rubio(5), Débora Claramunt(5), Olaya Hernández-Frías(5)