Annemieke Jmh Verkerk

5PUBLICATIONS
23CO-AUTHORS
Haematological tumoursEpigenetics (incl. genome methylation and epigenomics)Medical infection agents (incl. prions)Gene expression (incl. microarray and other genome-wide approaches)Developmental genetics (incl. sex determination)
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Publications (5)

|Nov 01, 2024
Family-based whole-exome sequencing implicates a variant in lysyl oxidase like 4 in atypical femur fractures.

Wei Zhou, Denise M van de Laarschot, Jeroen G J van Rooij

|Sep 07, 2023
Low-Cost High-Throughput Genotyping for Diagnosing Familial Hypercholesterolemia.

Shirin Ibrahim, Jeroen van Rooij, Annemieke J M H Verkerk

|Apr 20, 2023
Prevalence of Monogenic Bone Disorders in a Dutch Cohort of Atypical Femur Fracture Patients.

Wei Zhou, Jeroen Gj van Rooij, Denise M van de Laarschot

|Jun 18, 2021
A comparison of genotyping arrays.

Joost A M Verlouw, Eva Clemens, Jard H de Vries

|Jan 28, 2018
CXorf56, a dendritic neuronal protein, identified as a new candidate gene for X-linked intellectual disability.

Annemieke J M H Verkerk, Shimriet Zeidler, Guido Breedveld

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Frequent Collaborators

3 joint publications

André G Uitterlinden

2 joint publications

M Carola Zillikens

2 joint publications

Peter R Ebeling

2 joint publications

Denise M van de Laarschot