Oliver Klaas
Muenster, NW, Germany
Last Updated: 09/26/2026
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Found 9 publications
Bi-allelic MED16 variants cause a MEDopathy with intellectual disability, motor delay, and craniofacial, cardiac, and limb malformations.
Journal: American journal of human genetics
Published: September 13, 2024
Variant-specific pathophysiological mechanisms of AFF3 differently influence transcriptome profiles.
Variant-specific pathophysiological mechanisms of AFF3 differently influence transcriptome profiles.
Journal: medRxiv : the preprint server for health sciences
Published: January 31, 2024
Variant-specific pathophysiological mechanisms of AFF3 differently influence transcriptome profiles.
Variant-specific pathophysiological mechanisms of AFF3 differently influence transcriptome profiles.
Journal: Genome medicine
Published: December 12, 2023
De novo missense variants in RRAGC lead to a fatal mTORopathy of early childhood.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: November 17, 2022
Author Correction: Loss-of-function uORF mutations in human malignancies.
Journal: Scientific reports
Published: January 29, 2021
Loss-of-function uORF mutations in human malignancies.
Journal: Scientific reports
Published: March 07, 2017
ITIH5 mediates epigenetic reprogramming of breast cancer cells.
Journal: Molecular cancer
Published: October 21, 2016
Showing 1-9 of 9
Last Updated: 09/26/2026