Gert‐Jan B. van Ommen - Researcher Profile

Publications

4 shown

Transcriptome and genome sequencing uncovers functional variation in humans

Tuuli Lappalainen , Michael Sammeth , Marc R. Friedländer +54 more

2013 Nature 2095 citations

Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome

Annemieke J.M.H. Verkerk , Maura Pieretti , James S. Sutcliffe +18 more

1991 Cell 3476 citations

Deep sequencing-based expression analysis shows major advances in robustness, resolution and inter-lab portability over five microarray platforms

Peter A.C. ’t Hoen , Yavuz Ariyürek , Helene Thygesen +6 more

The hippocampal expression profiles of wild-type mice and mice transgenic for deltaC-doublecortin-like kinase were compared with Solexa/Illumina deep sequencing technology and f...

2008 Nucleic Acids Research 751 citations

Phenotypically Concordant and Discordant Monozygotic Twins Display Different DNA Copy-Number-Variation Profiles

Carl E.G. Bruder , Arkadiusz Piotrowski , Antoinet A.C.J. Gijsbers +19 more

2008 The American Journal of Human Genetics 591 citations

Frequent Co-Authors

Researcher Info

h-index: 4
Publications: 4
Citations: 6,913
Institution: Leiden University Medical Center

External Links

ORCID Profile Google Scholar

Identifiers

ORCID: 0000-0002-8603-218X

Impact Metrics

h-index 4

h-index: Number of publications with at least h citations each.