Mariëtte J V Hoffer

8PUBLICATIONS
79CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Epigenetics (incl. genome methylation and epigenomics)Genetic immunologyCancer diagnosisGene mapping
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Publications (8)

|Aug 21, 2025
Prenatal Variants of Uncertain Significance (VUS): to report or not to report?

Maayke A de Koning, Malgorzata I Srebniak, Esther J Oldekamp

|Feb 06, 2023
The neurodevelopmental and facial phenotype in individuals with a TRIP12 variant.

Mio Aerden, Anne-Sophie Denommé-Pichon, Dominique Bonneau

|Nov 26, 2022
Episignature Mapping of TRIP12 Provides Functional Insight into Clark-Baraitser Syndrome.

Liselot van der Laan, Kathleen Rooney, Mariëlle Alders

|Apr 08, 2022
Noninvasive Prenatal Test Results Indicative of Maternal Malignancies: A Nationwide Genetic and Clinical Follow-Up Study.

Catharina J Heesterbeek, Sietse M Aukema, Robert-Jan H Galjaard

|Oct 22, 2020
Author Correction: Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders.

Tianyun Wang, Kendra Hoekzema, Davide Vecchio

|Oct 02, 2020
Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders.

Tianyun Wang, Kendra Hoekzema, Davide Vecchio

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