Klaas Koop

6PUBLICATIONS
56CO-AUTHORS
Medical biochemistry - amino acids and metabolitesNeonatologyNanometrologyGene expression (incl. microarray and other genome-wide approaches)Genome structure and regulation
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Publications (6)

|Aug 26, 2026
Refining MMA Screening in the Dutch Newborn Screening Program: Lessons from Vitamin B12 Deficiency and Genetic Cases.

|Jan 21, 2026
Too Early to Tell? Balancing Diagnostic Accuracy of Newborn Screening for Propionic Acidemia Versus a Timely Referral.

Nils W F Meijer, Hidde H Huidekoper, Klaas Koop

|Oct 16, 2025
NMNAT3 deficiency: a novel red blood cell enzymopathy causing hemolysis by altering NAD levels and glycolysis.

Titine J J Ruiter, Brigitte A van Oirschot, Esmé Waanders

|Jun 25, 2025
Lymphatic Obstruction and Edema in Neonate due to Left Subclavian Central Venous Catheter.

Klaas Koop, Dominique Valérie Clarence de Jel, Joppe Nijman

|Jan 02, 2024
Molecular and Phenotypic Characterization of the RORB-Related Disorder.

Zeynep Gokce-Samar, Annalisa Vetro, Julitta De Bellescize

|Aug 08, 2023
Macrocephaly and developmental delay caused by missense variants in RAB5C.

Klaas Koop, Weimin Yuan, Federico Tessadori

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Frequent Collaborators

2 joint publications

Monique G M de Sain-van der Velden

2 joint publications

Annet M Bosch

2 joint publications

M Rebecca Heiner-Fokkema

1 joint publications

Federico Tessadori