Works by Monroe, Glen

Results: 14

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

Published in:

Cancers, 2021, v. 13, n. 10, p. 2430, doi. 10.3390/cancers13102430

By:

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.;
Desouki, Mohamed Mokhtar;
Fadare, Oluwole

Publication type:

Article

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

Published in:

Cancers, 2021, v. 13, n. 3, p. 368, doi. 10.3390/cancers13030368

By:

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

Publication type:

Article

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

Published in:

Cancers, 2020, v. 12, n. 5, p. 1308, doi. 10.3390/cancers12051308

By:

Roze, Joline;
Monroe, Glen;
Kutzera, Joachim;
Groeneweg, Jolijn;
Stelloo, Ellen;
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

Publication type:

Article

A nonsensemutation in B3GALNT2 is concordant with hydrocephalus in Friesian horses.

Published in:

BMC Genomics, 2015, v. 16, n. 1, p. 1, doi. 10.1186/s12864-015-1936-z

By:

Ducro, Bart J.;
Schurink, Anouk;
Bastiaansen, John W. M.;
Boegheim, Iris J. M.;
van Steenbeek, Frank G.;
Vos-Loohuis, Manon;
Nijman, Isaac J.;
Monroe, Glen R.;
Hellinga, Ids;
Dibbits, Bert W.;
Back, Willem;
Leegwater, Peter A. J.

Publication type:

Article

De novo mutations in beta- catenin (CTNNB1) appear to be a frequent cause of intellectual disability: expanding the mutational and clinical spectrum.

Published in:

Human Genetics, 2015, v. 134, n. 1, p. 97, doi. 10.1007/s00439-014-1498-1

By:

Kuechler, Alma;
Willemsen, Marjolein;
Albrecht, Beate;
Bacino, Carlos;
Bartholomew, Dennis;
Bokhoven, Hans;
den Boogaard, Marie;
Bramswig, Nuria;
Büttner, Christian;
Cremer, Kirsten;
Czeschik, Johanna;
Engels, Hartmut;
Gassen, Koen;
Graf, Elisabeth;
Haelst, Mieke;
He, Weimin;
Hogue, Jacob;
Kempers, Marlies;
Koolen, David;
Monroe, Glen

Publication type:

Article

Identification of human D lactate dehydrogenase deficiency.

Published in:

Nature Communications, 2019, v. 10, n. 1, p. N.PAG, doi. 10.1038/s41467-019-09458-6

By:

Monroe, Glen R.;
van Eerde, Albertien M.;
Tessadori, Federico;
Duran, Karen J.;
Savelberg, Sanne M. C.;
van Alfen, Johanna C.;
Terhal, Paulien A.;
van der Crabben, Saskia N.;
Lichtenbelt, Klaske D.;
Fuchs, Sabine A.;
Gerrits, Johan;
van Roosmalen, Markus J.;
van Gassen, Koen L.;
van Aalderen, Mirjam;
Koot, Bart G.;
Oostendorp, Marlies;
Duran, Marinus;
Visser, Gepke;
de Koning, Tom J.;
Calì, Francesco

Publication type:

Article

CRISPR‐Cas9 enrichment, a new strategy in microbial metagenomics to investigate complex genomic regions: The case of an environmental integron.

Published in:

Molecular Ecology Resources, 2023, v. 23, n. 6, p. 1288, doi. 10.1111/1755-0998.13798

By:

Sandoval‐Quintana, Eva;
Stangl, Christina;
Huang, Lionel;
Renkens, Ivo;
Duran, Robert;
van Haaften, Gijs;
Monroe, Glen;
Lauga, Béatrice;
Cagnon, Christine

Publication type:

Article

Investigation of Genetic Modifiers of Copper Toxicosis in Labrador Retrievers.

Published in:

Life (2075-1729), 2020, v. 10, n. 11, p. 266, doi. 10.3390/life10110266

By:

Wu, Xiaoyan;
den Boer, Elise R.;
Vos-Loohuis, Manon;
Steenbeek, Frank G. van;
Monroe, Glen R.;
Nijman, Isaäc J.;
Leegwater, Peter. A. J.;
Fieten, Hille

Publication type:

Article

Further confirmation of the MED13L haploinsufficiency syndrome.

Published in:

European Journal of Human Genetics, 2015, v. 23, n. 1, p. 135, doi. 10.1038/ejhg.2014.69

By:

van Haelst, Mieke M;
Monroe, Glen R;
Duran, Karen;
van Binsbergen, Ellen;
Breur, Johannes M;
Giltay, Jacques C;
van Haaften, Gijs

Publication type:

Article

Heterozygous KIDINS220/ARMS nonsense variants cause spastic paraplegia, intellectual disability, nystagmus, and obesity.

Published in:

Human Molecular Genetics, 2016, v. 25, n. 11, p. 2158, doi. 10.1093/hmg/ddw082

By:

Josifova, Dragana J.;
Monroe, Glen R.;
Tessadori, Federico;
Graaff, Esther de;
van der Zwaag2, Bert;
Mehta, Sarju G.;
Harakalova, Magdalena;
Duran, Karen J.;
Savelberg, Sanne M.C.;
Nijman, Isaäc J.;
Jungbluth, Heinz;
Hoogenraad, Casper C.;
Bakkers, Jeroen;
Knoers, Nine V.;
Firth, Helen V.;
Beales, Philip L.;
Haaften, Gijs van;
van Haelst, Mieke M.

Publication type:

Article

Partner independent fusion gene detection by multiplexed CRISPR-Cas9 enrichment and long read nanopore sequencing.

Published in:

Nature Communications, 2020, v. 11, n. 1, p. 1, doi. 10.1038/s41467-020-16641-7

By:

Stangl, Christina;
de Blank, Sam;
Renkens, Ivo;
Westera, Liset;
Verbeek, Tamara;
Valle-Inclan, Jose Espejo;
González, Rocio Chamorro;
Henssen, Anton G.;
van Roosmalen, Markus J.;
Stam, Ronald W.;
Voest, Emile E.;
Kloosterman, Wigard P.;
van Haaften, Gijs;
Monroe, Glen R.

Publication type:

Article

Dwarfism with joint laxity in Friesian horses is associated with a splice site mutation in B4GALT7.

Published in:

BMC Genomics, 2016, v. 17, p. 1, doi. 10.1186/s12864-016-3186-0

By:

Leegwater, Peter A.;
Vos-Loohuis, Manon;
Ducro, Bart J.;
Boegheim, Iris J.;
van Steenbeek, Frank G.;
Nijman, Isaac J.;
Monroe, Glen R.;
Bastiaansen, John W. M.;
Dibbits, Bert W.;
van de Goor, Leanne H.;
Hellinga, Ids;
Back, Willem;
Schurink, Anouk

Publication type:

Article

Familial Ehlers-Danlos syndrome with lethal arterial events caused by a mutation in COL5A1.

Published in:

American Journal of Medical Genetics. Part A, 2015, v. 167A, n. 6, p. 1196, doi. 10.1002/ajmg.a.36997

By:

Monroe, Glen R;
Harakalova, Magdalena;
van der Crabben, Saskia N;
Majoor‐Krakauer, Danielle;
Bertoli‐Avella, Aida M;
Moll, Frans L;
Oranen, Björn I;
Dooijes, Dennis;
Vink, Aryan;
Knoers, Nine V;
Maugeri, Alessandra;
Pals, Gerard;
Nijman, Isaac J;
van Haaften, Gijs;
Baas, Annette F

Publication type:

Article

Synaptic UNC13A protein variant causes increased neurotransmission and dyskinetic movement disorder.

Published in:

2017

By:

Lipstein, Noa;
Verhoeven-Duif, Nanda M.;
Michelassi, Francesco E.;
Calloway, Nathaniel;
van Hasselt, Peter M.;
Pienkowska, Katarzyna;
van Haaften, Gijs;
van Haelst, Mieke M.;
van Empelen, Ron;
Cuppen, Inge;
van Teeseling, Heleen C.;
Evelein, Annemieke M. V.;
Vorstman, Jacob A.;
Thoms, Sven;
Jahn, Olaf;
Duran, Karen J.;
Monroe, Glen R.;
Ryan, Timothy A.;
Taschenberger, Holger;
Dittman, Jeremy S.

Publication type:

journal article