Helger Yntema

12PUBLICATIONS
82CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Epigenetics (incl. genome methylation and epigenomics)Translation and interpretation studiesNeurogeneticsOther biomedical and clinical sciences not elsewhere classified
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Publications (12)

|Jun 26, 2026
Near-perfect genome sequencing in medical genetics.

|May 21, 2026
Towards responsible genome-wide screening: normative and stakeholder considerations.

|Mar 23, 2026
Distinct mechanisms of CNV formation at the human 15q13.3 locus.

Wolfram Höps, David Porubsky, DongAhn Yoo

|Apr 23, 2025
Cochlear Implantation Outcomes in Genotyped Subjects with Sensorineural Hearing Loss.

M L A Fehrmann, L Haer-Wigman, H Kremer

|Sep 27, 2024
Uncovering recessive alleles in rare Mendelian disorders by genome sequencing of 174 individuals with monoallelic pathogenic variants.

Gaby Schobers, Maartje Pennings, Juliette de Vries

|Oct 27, 2023
Systematic analysis of paralogous regions in 41,755 exomes uncovers clinically relevant variation.

Wouter Steyaert, Lonneke Haer-Wigman, Rolph Pfundt

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Frequent Collaborators

6 joint publications

Christian Gilissen

4 joint publications

Hannie Kremer

4 joint publications

Lisenka E L M Vissers

3 joint publications

Susanne Roosing