Laurens Wiel

5PUBLICATIONS
48CO-AUTHORS
Cardiology (incl. cardiovascular diseases)Gene expression (incl. microarray and other genome-wide approaches)Developmental genetics (incl. sex determination)Epigenetics (incl. genome methylation and epigenomics)
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Publications (5)

|Jul 12, 2026
Scaled Multidimensional Assays of Variant Effect Identify Sequence-Function Relationships in Hypertrophic Cardiomyopathy.

|Nov 12, 2025
GREGoR: accelerating genomics for rare diseases.

Moez Dawood, Ben Heavner, Marsha M Wheeler

|Oct 15, 2020
Evidence for 28 genetic disorders discovered by combining healthcare and research data.

Joanna Kaplanis, Kaitlin E Samocha, Laurens Wiel

|May 23, 2019
MetaDome: Pathogenicity analysis of genetic variants through aggregation of homologous human protein domains.

Laurens Wiel, Coos Baakman, Daan Gilissen

|Aug 18, 2017
Aggregation of population-based genetic variation over protein domain homologues and its potential use in genetic diagnostics.

Laurens Wiel, Hanka Venselaar, Joris A Veltman

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Frequent Collaborators

2 joint publications

Christian Gilissen

2 joint publications

Kaitlin E Samocha

2 joint publications

Matthew T Wheeler

1 joint publications

Hanka Venselaar