W. V. Vermeulen - Genetic Mutations

Author Information

Wim Vermeulen is a prominent researcher affiliated with the Department of Molecular Genetics at the Oncode Institute, Erasmus MC, University Medical Center Rotterdam, located at Dr. Molewaterplein 40, 3015 GD, Rotterdam, the Netherlands. His work primarily focuses on the mechanisms of DNA repair and genome stability.

Research Contributions

Wim Vermeulen has made significant contributions to the field of genetics, particularly in understanding DNA repair mechanisms. His research has elucidated various aspects of nucleotide excision repair (NER) and transcription-coupled repair, providing insights into how cells maintain genome integrity. His recent work includes studies on the roles of proteins like XPG, HLTF, and ELOF1 in genome maintenance, as well as the impact of mutations in genes like AARS1 and MARS1 on protein stability and disease.

Aliases

Wim Vermeulen is also known by the following aliases:

W Vermeulen W. V. Vermeulen W. Vermeulen

Publication and Citation Metrics

Metric	Value
Citation Count	19,938
h-index	74
Paper Count	231

Publications:

XPG: a multitasking genome caretaker

DOI: 10.1007/s00018-022-04194-5

Year: 2022

Active DNA damage eviction by HLTF stimulates nucleotide excision repair.

DOI: 10.1016/j.molcel.2022.02.020

Year: 2022

Global and transcription-coupled repair of 8-oxoG is initiated by nucleotide excision repair proteins

DOI: 10.1038/s41467-022-28642-9

Year: 2022

Publisher Correction: Elongation factor ELOF1 drives transcription-coupled repair and prevents genome instability

DOI: 10.1038/s41556-021-00720-y

Year: 2021

Elongation factor ELOF1 drives transcription-coupled repair and prevents genome instability

DOI: 10.1101/2021.05.11.443558

Year: 2021

USP44 Stabilizes DDB2 to Facilitate Nucleotide Excision Repair and Prevent Tumors

DOI: 10.3389/fcell.2021.663411

Year: 2021

Elongation factor ELOF1 drives transcription-coupled repair and prevents genome instability

DOI: 10.1038/s41556-021-00692-z

Year: 2021

Protein instability associated with AARS1 and MARS1 mutations causes trichothiodystrophy

DOI: 10.1093/hmg/ddab123

Year: 2021

Retraction Notice to: Cockayne Syndrome A and B Proteins Differentially Regulate Recruitment of Chromatin Remodeling and Repair Factors to Stalled RNA Polymerase II In Vivo.

DOI: 10.1016/j.molcel.2021.11.021

Year: 2021

C. elegans TFIIH subunit GTF-2H5/TTDA is a non-essential transcription factor indispensable for DNA repair

DOI: 10.1101/2021.06.04.447037

Year: 2021

What is an Insertion Mutation?

What are Genetic Duplications?

What Are the Successes of Gene Therapy?

How do Genetic Mutations Influence Medication Response?

What are the Options for Individuals with BRCA1 or BRCA2 Mutations?

What are Examples of Diseases Caused by Missense Mutations?

What is a Substitution Mutation?

What is CRISPR-Cas9?

What are the ethical considerations of using ZFNs?

Why are Improved Diagnostic Tools Important?

Partnered Content Networks

Relevant Topics