Albertien M van Eerde

7PUBLICATIONS
61CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)NeurogeneticsMolecular targetsGene expression (incl. microarray and other genome-wide approaches)Gene mapping
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Publications (7)

|Oct 09, 2025
Author Correction: Exome analysis links kidney malformations to developmental disorders and reveals causal genes.

Hila Milo Rasouly, Sarath Babu Krishna Murthy, Natalie Vena

|Aug 07, 2025
Exome analysis links kidney malformations to developmental disorders and reveals causal genes.

Hila Milo Rasouly, Sarath Babu Krishna Murthy, Natalie Vena

|Oct 07, 2024
Translational strategies to uncover the etiology of congenital anomalies of the kidney and urinary tract.

Lisanne M Vendrig, Mayke A C Ten Hoor, Benthe H König

|Sep 17, 2024
The Role of Genetic Testing in Adult CKD.

Nine V A M Knoers, Albertien M van Eerde

|Jul 31, 2024
Bardet-Biedl syndrome improved diagnosis criteria and management: Inter European Reference Networks consensus statement and recommendations.

Hélène Dollfus, Marc R Lilien, Pietro Maffei

|Feb 22, 2023
KidneyNetwork: using kidney-derived gene expression data to predict and prioritize novel genes involved in kidney disease.

Floranne Boulogne, Laura R Claus, Henry Wiersma

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Frequent Collaborators

3 joint publications

Rik Westland

2 joint publications

Atlas Khan

2 joint publications

Adele Mittrori

2 joint publications

Jun Y Zhang