Gijs van Haaften

ORCID

Publication Activity (10 Years)

Years Active: 2016-2023
Publications (10 Years): 13

Top Venues

European journal of human genetics : EJHG

Cancers

Nature genetics

Disease models & mechanisms

This page only lists publications with an associated author ORCID identifier.

Publications

Inge van Outersterp, Vincent H J van der Velden, Patricia G Hoogeveen, Goda E Vaitkevičienė, Edwin Sonneveld, Gijs van Haaften, Roland P Kuiper, Udo Zur Stadt, Gabriele Escherich, Judith M Boer, Monique L den Boer
ABL-class Genomic Breakpoint Q-PCR: A Patient-specific Approach for MRD Monitoring in Acute Lymphoblastic Leukemia. HemaSphere 7 (10) (2023)
Jian Gao, Conor McClenaghan, Imke Christiaans, Marielle Alders, Kirsten van Duinen, Mieke M van Haelst, Gijs van Haaften, Colin G Nichols
Lymphedema as first clinical presentation of Cantu Syndrome: reversed phenotyping after identification of gain-of-function variant in ABCC9. European journal of human genetics : EJHG (2022)
Joline Roze, Elena Sendino Garví, Ellen Stelloo, Christina Stangl, Ferdinando Sereno, Karen Duran, Jolijn W Groeneweg, Sterre Paijens, Hans Nijman, Hannah van Meurs, Luc van Lonkhuijzen, Jurgen M J Piek, Christianne A R Lok, Geertruida Jonges, Petronella Witteveen, René Verheijen, Gijs van Haaften, Ronald Zweemer, Glen R Monroe
In Vitro Systematic Drug Testing Reveals Carboplatin, Paclitaxel, and Alpelisib as a Potential Novel Combination Treatment for Adult Granulosa Cell Tumors. Cancers 13 (3) (2021)
Joline F Roze, Joachim Kutzera, Wouter Koole, Margreet G E M Ausems, Kristi Engelstad, Jurgen M J Piek, Cornelis D de Kroon, René H M Verheijen, Gijs van Haaften, Ronald P Zweemer, Glen R Monroe
Familial Occurrence of Adult Granulosa Cell Tumors: Analysis of Whole-Genome Germline Variants. Cancers 13 (10) (2021)
Christina Stangl, Sam de Blank, Ivo Renkens, Liset Westera, Tamara Verbeek, Jose Espejo Valle-Inclan, Rocio Chamorro González, Anton G Henssen, Markus J van Roosmalen, Ronald W Stam, Emile E Voest, Wigard P Kloosterman, Gijs van Haaften, Glen R Monroe
Partner independent fusion gene detection by multiplexed CRISPR-Cas9 enrichment and long read nanopore sequencing. Nature communications 11 (1) (2020)
Federico Tessadori, Atteeq U Rehman, Jacques C Giltay, Fan Xia, Haley Streff, Karen Duran, Jeroen Bakkers, Seema R Lalani, Gijs van Haaften
A de novo variant in the human HIST1H4J gene causes a syndrome analogous to the HIST1H4C-associated neurodevelopmental disorder. European journal of human genetics : EJHG 28 (5) (2019)
Anneke Kievit, Federico Tessadori, Hannie Douben, Ingrid Jordens, Madelon Maurice, Jeannette Hoogeboom, Raoul Hennekam, Sheela Nampoothiri, Hülya Kayserili, Marco Castori, Margo Whiteford, Connie Motter, Catherine Melver, Michael Cunningham, Anne Hing, Nancy M Kokitsu-Nakata, Siulan Vendramini-Pittoli, Antonio Richieri-Costa, Annette F Baas, Corstiaan C Breugem, Karen Duran, Maarten Massink, Patrick W B Derksen, Wilfred F J van IJcken, Leontine van Unen, Fernando Santos-Simarro, Pablo Lapunzina, Vera L Gil-da Silva Lopes, Elaine Lustosa-Mendes, Max Krall, Anne Slavotinek, Victor Martinez-Glez, Jeroen Bakkers, Koen L I van Gassen, Annelies de Klein, Marie-José H van den Boogaard, Gijs van Haaften
Variants in members of the cadherin-catenin complex, CDH1 and CTNND1, cause blepharocheilodontic syndrome. European journal of human genetics : EJHG 26 (2) (2018)
Federico Tessadori, Helen I Roessler, Sanne M C Savelberg, Sonja Chocron, Sarah M Kamel, Karen J Duran, Mieke M van Haelst, Gijs van Haaften, Jeroen Bakkers
Effective CRISPR/Cas9-based nucleotide editing in zebrafish to model human genetic cardiovascular disorders. Disease models & mechanisms 11 (10) (2018)
Federico Tessadori, Jacques C Giltay, Jane A Hurst, Maarten P Massink, Karen Duran, Harmjan R Vos, Robert M van Es, null null, Richard H Scott, Koen L I van Gassen, Jeroen Bakkers, Gijs van Haaften
Germline mutations affecting the histone H4 core cause a developmental syndrome by altering DNA damage response and cell cycle control. Nature genetics 49 (11) (2017)
Edwin P Kirk, Ingrid Scurr, Gijs van Haaften, Mieke M van Haelst, Colin G Nichols, Maggie Williams, Sarah F Smithson, Dorothy K Grange
Clinical utility gene card for: Cantú syndrome. European journal of human genetics : EJHG 25 (4) (2017)
Glen R Monroe, Isabelle Fpm Kappen, Marijn F Stokman, Paulien A Terhal, Marie-José H van den Boogaard, Sanne Mc Savelberg, Lars T van der Veken, Robert Jj van Es, Susanne M Lens, Rutger C Hengeveld, Marijn A Creton, Nard G Janssen, Aebele B Mink van der Molen, Michelle B Ebbeling, Rachel H Giles, Nine V Knoers, Gijs van Haaften
Compound heterozygous NEK1 variants in two siblings with oral-facial-digital syndrome type II (Mohr syndrome). European journal of human genetics : EJHG 24 (12) (2016)
Tamar I de Vries, Glen R Monroe, Martine J van Belzen, Christian A van der Lans, Sanne Mc Savelberg, William G Newman, Gijs van Haaften, Rutger A Nievelstein, Mieke M van Haelst
Mosaic CREBBP mutation causes overlapping clinical features of Rubinstein-Taybi and Filippi syndromes. European journal of human genetics : EJHG 24 (9) (2016)
Glen R Monroe, Gerardus W Frederix, Sanne M C Savelberg, Tamar I de Vries, Karen J Duran, Jasper J van der Smagt, Paulien A Terhal, Peter M van Hasselt, Hester Y Kroes, Nanda M Verhoeven-Duif, Isaäc J Nijman, Ellen C Carbo, Koen L van Gassen, Nine V Knoers, Anke M Hövels, Mieke M van Haelst, Gepke Visser, Gijs van Haaften
Effectiveness of whole-exome sequencing and costs of the traditional diagnostic trajectory in children with intellectual disability. Genetics in medicine : official journal of the American College of Medical Genetics 18 (9) (2016)

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Publication Activity (10 Years)

Top Topics

Top Venues

Gijs van Haaften