Rosa Vargas‐Poussou

Inserm — France

Biochemistry, Genetics and Molecular Biology · Life Sciences

38h-index4.7kcitations155works4.42yr avg
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Research Topics

Ion Transport and Channel Regulation(90), Magnesium in Health and Disease(29), Ion channel regulation and function(27), Electrolyte and hormonal disorders(27), Biomedical Research and Pathophysiology(26)

Publications152 total

SLC4A1 mutations that cause distal renal tubular acidosis alter cytoplasmic pH and cellular autophagy
2025Open Access
SLC4A1 mutations that cause distal renal tubular acidosis alter cytoplasmic pH and cellular autophagy
2025· 1 citedOpen Access
Clinical Characteristics, Symptoms, and Long-Term Outcomes in Gitelman Syndrome
Kidney International Reports·2025Open Access
Trastornos de la magnesemia
EMC - Tratado de Medicina·2025Open Access
Dent disease: clinical practice recommendations
Nephrology Dialysis Transplantation·2025· 6 citedOpen Access
A puzzling renal Fanconi syndrome
Clinical Kidney Journal·2024Open Access
<i>SLC4A1</i> MUTATIONS THAT CAUSE DISTAL RENAL TUBULAR ACIDOSIS ALTER CYTOPLASMIC PH AND CELLULAR AUTOPHAGY
2024Open Access
International expert consensus statement on the diagnosis and management of congenital nephrogenic diabetes insipidus (arginine vasopressin resistance)
Nature Reviews Nephrology·2024· 18 citedOpen Access
Analyse de la réponse transcriptionnelle aiguë à l’aldostérone dans les cellules du néphron distal par snRNA-seq
Annales d Endocrinologie·2024Open Access
CCDC158: A novel regulator in renal proximal tubular endocytosis unveiled through exome sequencing and interactome analysis
Journal of Cellular Physiology·2024· 2 citedOpen Access
Prevalence of kidney failure in adults diagnosed with hereditary tubulopathies
Journal of Nephrology·2024· 6 cited
X-linked transient antenatal Bartter syndrome related to MAGED2 gene: Enriching the phenotypic description and pathophysiologic investigation
Genetics in Medicine·2024· 1 cited
The SLC6A18 Transporter Is Most Likely a Na-Dependent Glycine/Urea Antiporter Responsible for Urea Secretion in the Proximal Straight Tubule: Influence of This Urea Secretion on Glomerular Filtration Rate
˜The œNephron journals/Nephron journals·2024· 3 citedOpen Access
Hypomagnesaemia with varying degrees of extrarenal symptoms as a consequence of heterozygous CNNM2 variants
Scientific Reports·2024· 2 citedOpen Access
Clinical Findings and Genetic Analysis of Nine Mexican Families with Bartter Syndrome
Archives of Medical Research·2023· 1 cited
#2568 LONG-READ SEQUENCING IDENTIFIES NOVEL PATHOGENIC INTRONIC VARIANTS IN GITELMAN SYNDROME
Nephrology Dialysis Transplantation·2023Open Access
Les grandes avancées en néphro-génétique pédiatrique
médecine/sciences·2023Open Access
Relationship between clinical phenotype and in vitro analysis of 13 NPT2c/SCL34A3 mutants
Scientific Reports·2023· 14 citedOpen Access
Tubulopathies and Alterations of the RAAS
Endocrinology·2023· 2 cited
Genetic basis of nephrogenic diabetes insipidus
Molecular and Cellular Endocrinology·2022· 25 cited
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Frequent Co-authors

Anne Blanchard(21), Pascal Houillier(15), Xavier Jeunemaı̂tre(13), Olivier Devuyst(12), Martin Konrad(10), Detlef Böckenhauer(8), Georges Deschênes(8), Karin Dahan(7), Marguerite Hureaux(7), Nine V.A.M. Knoers(6), Robert Novo(6), Rémi Salomon(6), Stephen B. Walsh(6), Stéphanie Baron(6), Cyrielle Tréard(6), Stéphane Lourdel(6), Corinne Antignac(5), Ivan Tack(5), Chantal Loirat(5), Stéphane Decramer(5)