Michael Henri Duyzend

8PUBLICATIONS
196CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)Infant and child healthMedical molecular engineering of nucleic acids and proteinsGenomics and transcriptomicsMedical biotechnology diagnostics (incl. biosensors)
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Publications (8)

|Mar 17, 2025
GA4GH Phenopacket-Driven Characterization of Genotype-Phenotype Correlations in Mendelian Disorders.

Lauren Rekerle, Daniel Danis, Filip Rehburg

|Dec 05, 2024
Going Back in Time: Prenatal Presentations of Postnatal Genetic Diagnoses Made in a Neonatal Intensive Care Unit.

Michael Duyzend, Malika Sud, Alissa M D'Gama

|Jan 23, 2024
Lethal phenotypes in Mendelian disorders.

Pilar Cacheiro, Samantha Lawson, Ignatia B Van den Veyver

|Jan 19, 2024
Improving prenatal diagnosis through standards and aggregation.

Michael H Duyzend, Pilar Cacheiro, Julius O B Jacobsen

|Nov 12, 2023
The Human Phenotype Ontology in 2024: phenotypes around the world.

Michael A Gargano, Nicolas Matentzoglu, Ben Coleman

|Jul 25, 2022
Prenatal phenotyping: A community effort to enhance the Human Phenotype Ontology.

Ferdinand Dhombres, Patricia Morgan, Bimal P Chaudhari

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Frequent Collaborators

5 joint publications

Peter N Robinson

4 joint publications

Damian Smedley

3 joint publications

Markus S Ladewig

3 joint publications

Pilar Cacheiro