Gijs van Haaften

14PUBLICATIONS
42CO-AUTHORS
NeonatologyCardiology (incl. cardiovascular diseases)Gene expression (incl. microarray and other genome-wide approaches)Molecular targetsPredictive and prognostic markers
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Publications (14)

|Jun 15, 2026
Cognitive Decline, Neurologic Involvement, and Neonatal Crisis in ABCC9-Related Intellectual Disability and Myopathy Syndrome.

|Nov 06, 2022
Lymphedema as first clinical presentation of Cantu Syndrome: reversed phenotyping after identification of gain-of-function variant in ABCC9.

Jian Gao, Conor McClenaghan, Imke Christiaans

|Jun 02, 2021
Familial Occurrence of Adult Granulosa Cell Tumors: Analysis of Whole-Genome Germline Variants.

Joline F Roze, Joachim Kutzera, Wouter Koole

|Jan 27, 2021
In Vitro Systematic Drug Testing Reveals Carboplatin, Paclitaxel, and Alpelisib as a Potential Novel Combination Treatment for Adult Granulosa Cell Tumors.

Joline Roze, Elena Sendino Garví, Ellen Stelloo

|Jun 07, 2020
Partner independent fusion gene detection by multiplexed CRISPR-Cas9 enrichment and long read nanopore sequencing.

Christina Stangl, Sam de Blank, Ivo Renkens

|Dec 06, 2019
A de novo variant in the human HIST1H4J gene causes a syndrome analogous to the HIST1H4C-associated neurodevelopmental disorder.

Federico Tessadori, Atteeq U Rehman, Jacques C Giltay

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Frequent Collaborators

3 joint publications

Glen R Monroe

3 joint publications

Jeroen Bakkers

2 joint publications

Mieke M van Haelst

2 joint publications

Colin G Nichols