Albertien M Van Eerde (Albertien M van Eerde)

Publication Activity (10 Years)

Years Active: 2022-2024
Publications (10 Years): 4

Top Topics

Gene Expression

Palliative Care

Top Venues

European journal of human genetics : EJHG

Journal of the American Society of Nephrology : JASN

American journal of medical genetics. Part C, Seminars in medical genetics

This page only lists publications with an associated author ORCID identifier.

Publications

Hélène Dollfus, Marc R Lilien, Pietro Maffei, Alain Verloes, Jean Muller, Giacomo Maria Bacci, Metin Cetiner, Erica L T van den Akker, Monika Grudzinska Pechhacker, Francesco Testa, Didier Lacombe, Marijn F Stokman, Francesca Simonelli, Aurélie Gouronc, Amélie Gavard, Mieke M van Haelst, Jens König, Sylvie Rossignol, Carsten Bergmann, Miriam Zacchia, Bart Peter Leroy, Héléna Mosbah, Albertien M Van Eerde, Djalila Mekahli, Aude Servais, Christine Poitou, Diana Valverde
Bardet-Biedl syndrome improved diagnosis criteria and management: Inter European Reference Networks consensus statement and recommendations. European journal of human genetics : EJHG (2024)
Nine V A M Knoers, Albertien M Van Eerde
The Role of Genetic Testing in Adult CKD. Journal of the American Society of Nephrology : JASN 35 (8) (2024)
Floranne Boulogne, Laura R Claus, Henry Wiersma, Roy Oelen, Floor Schukking, Niek de Klein, Shuang Li, Harm-Jan Westra, Bert van der Zwaag, Franka van Reekum, null null, Dana Sierks, Ria Schönauer, Zhigui Li, Emilia K Bijlsma, Willem Jan W Bos, Jan Halbritter, Nine V A M Knoers, Whitney Besse, Patrick Deelen, Lude Franke, Albertien M Van Eerde
KidneyNetwork: using kidney-derived gene expression data to predict and prioritize novel genes involved in kidney disease. European journal of human genetics : EJHG (2023)
Laura R Claus, Rozemarijn Snoek, Nine V A M Knoers, Albertien M Van Eerde
Review of genetic testing in kidney disease patients: Diagnostic yield of single nucleotide variants and copy number variations evaluated across and within kidney phenotype groups. American journal of medical genetics. Part C, Seminars in medical genetics 190 (3) (2022)