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dr. G.W. (Gijs) van Haaften

dr. G.W. (Gijs) van Haaften

Associate Professor

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Research Output (91)

FOXL2 and TERT promoter mutation detection in circulating tumor DNA of adult granulosa cell tumors as biomarker for disease monitoring

Groeneweg Jolijn W, Roze Joline F, Peters Edith D J, Sereno Ferdinando, Brink Anna G J, Paijens Sterre T, Nijman Hans W, van Meurs Hannah S, van Lonkhuijzen Luc R C W, Piek Jurgen M J, Lok Christianne A R, Monroe Glen R, van Haaften Gijs W, Zweemer Ronald P Aug 2021, In: Gynecologic Oncology. 162 , p. 413-420 8 p.

Behavioral and cognitive functioning in individuals with Cantú syndrome

Roessler Helen I., van Der Heuvel Lieke M., Shields Kathleen, Guilliams Kristin P., Knoers Nine V. A. M., van Haaften Gijs, Grange Dorothy K., van Haelst Mieke M. Aug 2021, In: American Journal of Medical Genetics. Part A. 185 , p. 2434-2444

Young adult with Cantú syndrome:Dealing with a rare genetic skin disorder

Roessler Helen, I, van Haaften Gijs, van Haelst Mieke M. 12 Jul 2021, In: BMJ Case Reports. 14 , p. 1-3

Familial Occurrence of Adult Granulosa Cell Tumors:Analysis of Whole-Genome Germline Variants

Roze Joline F, Kutzera Joachim, Koole Wouter, Ausems Margreet G E M, Engelstad Kristi, Piek Jurgen M J, de Kroon Cor D, Verheijen René H M, van Haaften Gijs, Zweemer Ronald P, Monroe Glen R 2 May 2021, In: Cancers. 13 13 p.

Drug Repurposing for Rare Diseases

Roessler Helen I., Knoers Nine V.A.M., van Haelst Mieke M., van Haaften Gijs Apr 2021, In: Trends in Pharmacological Sciences. 42 , p. 255-267 13 p.

New insights in phenotype and treatment of lung disease immuno-deficiency and chromosome breakage syndrome (LICS)

Willemse Brigitte W M, van der Crabben Saskia N, Kerstjens-Frederikse Wilhelmina S, Timens Wim, van Montfrans Joris M, Lindemans Caroline A, Boelens Jaap Jan, Hennus Marije P, van Haaften Gijs 19 Mar 2021, In: Orphanet Journal of Rare Diseases. 16

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

Roze Joline, Sendino Garví Elena, Stelloo Ellen, Stangl Christina, Sereno Ferdinando, Duran Karen, Groeneweg Jolijn, Paijens Sterre, Nijman Hans, van Meurs Hannah, van Lonkhuijzen Luc, Piek Jurgen, Lok Christianne, Jonges Geertruida, Witteveen Petronella, Verheijen René, van Haaften Gijs, Zweemer Ronald, Monroe Glen 1 Feb 2021, In: Cancers. 13 , p. 1-18 18 p.

NAA80 bi-allelic missense variants result in high-frequency hearing loss, muscle weakness and developmental delay

Muffels Irena J J, Wiame Elsa, Fuchs Sabine A, Massink Maarten P G, Rehmann Holger, Musch Jiska L I, Van Haaften Gijs, Vertommen Didier, van Schaftingen Emile, van Hasselt Peter M 2021, In: Brain communications. 3 , p. 1-14

Whole Genome Analysis of Ovarian Granulosa Cell Tumors Reveals Tumor Heterogeneity and a High-Grade TP53-Specific Subgroup

Roze Joline, Monroe Glen, Kutzera Joachim, Groeneweg Jolijn, Stelloo Ellen, Paijens Sterre, Nijman Hans, Meurs Hannah van, Lonkhuijzen Luc van, Piek Jurgen, Lok Christianne, Jonges Geertruida, Witteveen Petronella, Verheijen René, Haaften Gijs van, Zweemer Ronald 21 May 2020, In: Cancers. 12 22 p.

A de novo variant in the human HIST1H4J gene causes a syndrome analogous to the HIST1H4C-associated neurodevelopmental disorder

Tessadori Federico, Rehman Atteeq U, Giltay Jacques C, Xia Fan, Streff Haley, Duran Karen, Bakkers Jeroen, Lalani Seema R, van Haaften Gijs May 2020, In: European Journal of Human Genetics. 28 , p. 674-678 5 p.

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