R. Snoek

Pregnancy in Advanced Kidney Disease: Clinical Practice Considerations on a Challenging Combination

N. Knoers, R. van der Graaf, K. Bloemenkamp, 2020, Nephron.

Preimplantation Genetic Testing for Monogenic Kidney Disease.

A. Paulussen, N. Knoers, J. Dreesen, 2020, Clinical journal of the American Society of Nephrology : CJASN.

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

N. Knoers, A. V. van Eerde, R. Snoek, 2022, American journal of medical genetics. Part C, Seminars in medical genetics.

Review of genetic testing in kidney disease patients: SNV and CNV diagnostic yield evaluated across and within kidney phenotype groups

N. Knoers, A. V. Eerde, R. Snoek, 2022 .

Fleas as Vectors of Emerging Zoonoses

R. Snoek, 2011 .

Accuracy of diagnosis and counseling of fetal brain anomalies prior to 24 weeks of gestational age

L. D. de Vries, K. Lichtenbelt, P. Nikkels, 2018, The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians.

Genetics-first approach improves diagnostics of ESKD patients younger than 50 years.

B. van der Zwaag, A. V. van Zuilen, R. Goldschmeding, 2020, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Defects in t6A tRNA modification due to GON7 and YRDC mutations lead to Galloway-Mowat syndrome

N. Boddaert, D. Magen, P. Revy, 2019, Nature Communications.

NPHP1 (Nephrocystin-1) Gene Deletions Cause Adult-Onset ESRD.

A. Israni, H. Snieder, B. van der Zwaag, 2018, Journal of the American Society of Nephrology : JASN.

Importance of Genetic Diagnostics in Adult-Onset Focal Segmental Glomerulosclerosis

B. van der Zwaag, A. V. van Zuilen, R. Goldschmeding, 2019, Nephron.

Assessing Nephron Hyperplasia in Fetal Congenital Solitary Functioning Kidneys by Measuring Renal Papilla Number.

L. Pistorius, M. Lilien, M. Bekker, 2018, American journal of kidney diseases : the official journal of the National Kidney Foundation.

Importance of reliable variant calling and clear phenotyping when reporting on gene panel testing in renal disease.

N. Knoers, A. V. van Eerde, R. Snoek, 2017, Kidney international.

Perspectives of patients and clinicians on reproductive healthcare and autosomal dominant polycystic kidney disease

A. V. van Eerde, N. Crombag, R. Snoek, 2024, Kidney International Reports.