Glen R. Monroe

2.0k citations

20 papers · 524 indexed · h-index 12

Co-authors: Gijs van Haaften Isaäc J. Nijman Nine Knoers Karen Duran Mieke M. van Haelst Koen L.I. van Gassen G. W. J. Frederix Anke M. Hövels
Topics: Ovarian cancer diagnosis and treatment (6 papers)Renal cell carcinoma treatment (4 papers)Genomics and Rare Diseases (3 papers)
Cited by: Equine Genetics Reproductive Medicine
Journals: Nature Communications Human Molecular Genetics BMC Genomics
Partner nations: Netherlands United Kingdom Belgium

In The Last Decade

Glen R. Monroe

20 papers receiving 517 citations

Peers

Countries citing papers authored by Glen R. Monroe

Since Specialization

Citations

This map shows the geographic impact of Glen R. Monroe's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Glen R. Monroe with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Glen R. Monroe more than expected).

Fields of papers citing papers by Glen R. Monroe

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Glen R. Monroe. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Glen R. Monroe. The network helps show where Glen R. Monroe may publish in the future.

Co-authorship network of co-authors of Glen R. Monroe

This figure shows the co-authorship network connecting the top 25 collaborators of Glen R. Monroe. A scholar is included among the top collaborators of Glen R. Monroe based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Glen R. Monroe. Glen R. Monroe is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	CRISPR‐Cas9 enrichment, a new strategy in microbial metagenomics to investigate complex genomic regions: The case of an environmental integron 2023 ·Molecular Ecology Resources ·(unknown),(unknown),(unknown),Ivo Renkens,Robert Duran,Gijs van Haaften,Glen R. Monroe,Béatrice Lauga,Christine Cagnon	2
2	FOXL2 and TERT promoter mutation detection in circulating tumor DNA of adult granulosa cell tumors as biomarker for disease monitoring 2021 ·Gynecologic Oncology ·Jolijn W. Groeneweg,(unknown),Edith Peters,(unknown),(unknown),Sterre T. Paijens,Hans W. Nijman,Hannah S. van Meurs,Luc R.C.W. van Lonkhuijzen,Jurgen M.J. Piek,Christianne Lok,Glen R. Monroe,(unknown),Ronald P. Zweemer	18
3	[18F]FDG and [18F]FES positron emission tomography for disease monitoring and assessment of anti-hormonal treatment eligibility in granulosa cell tumors of the ovary 2021 ·Oncotarget ·(unknown),Hannah S. van Meurs,Glen R. Monroe,Wouter B. Veldhuis,Luc R.C.W. van Lonkhuijzen,Roel J. Bennink,Jolijn W. Groeneweg,Petronella O. Witteveen,Geertruida N. Jonges,Ronald P. Zweemer,Arthur J. A. T. Braat	5
4	Familial Occurrence of Adult Granulosa Cell Tumors: Analysis of Whole-Genome Germline Variants 2021 ·Cancers ·(unknown),Joachim Kutzera,Wouter Koole,Margreet G.E.M. Ausems,(unknown),Jurgen M.J. Piek,Cor D. de Kroon,René H.M. Verheijen,Gijs van Haaften,Ronald P. Zweemer,Glen R. Monroe	4
5	In Vitro Systematic Drug Testing Reveals Carboplatin, Paclitaxel, and Alpelisib as a Potential Novel Combination Treatment for Adult Granulosa Cell Tumors 2021 ·Cancers ·(unknown),(unknown),Ellen Stelloo,(unknown),(unknown),Karen Duran,Jolijn W. Groeneweg,Sterre T. Paijens,Hans W. Nijman,(unknown),Luc R.C.W. van Lonkhuijzen,Jurgen M.J. Piek,Christianne Lok,Geertruida N. Jonges,Petronella O. Witteveen,René H.M. Verheijen,Gijs van Haaften,Ronald P. Zweemer,Glen R. Monroe	11
6	Partner independent fusion gene detection by multiplexed CRISPR-Cas9 enrichment and long read nanopore sequencing 2020 ·Nature Communications ·(unknown),Sam de Blank,Ivo Renkens,Liset Westera,(unknown),Jose Espejo Valle-Inclán,Rocío Chamorro González,Anton G. Henssen,Markus J. van Roosmalen,Ronald W. Stam,Emile E. Voest,Wigard P. Kloosterman,Gijs van Haaften,Glen R. Monroe	47
7	Patient engagement in research on rare gynecological tumors 2020 ·International Journal of Gynecological Cancer ·(unknown),Jolijn W. Groeneweg,Glen R. Monroe,(unknown),Murat Gültekin,Ronald P. Zweemer,René H.M. Verheijen	2
8	Investigation of Genetic Modifiers of Copper Toxicosis in Labrador Retrievers 2020 ·Life ·(unknown),(unknown),(unknown),Frank G. van Steenbeek,Glen R. Monroe,Isaäc J. Nijman,Peter A. J. Leegwater,Hille Fieten	10
9	Whole Genome Analysis of Ovarian Granulosa Cell Tumors Reveals Tumor Heterogeneity and a High-Grade TP53-Specific Subgroup 2020 ·Cancers ·(unknown),Glen R. Monroe,Joachim Kutzera,Jolijn W. Groeneweg,Ellen Stelloo,Sterre T. Paijens,Hans W. Nijman,(unknown),Luc R.C.W. van Lonkhuijzen,Jurgen M.J. Piek,Christianne Lok,Geertruida N. Jonges,Petronella O. Witteveen,René H.M. Verheijen,Gijs van Haaften,Ronald P. Zweemer	30
10	Whole-exome sequencing in intellectual disability; cost before and after a diagnosis 2018 ·European Journal of Human Genetics ·Terry Vrijenhoek,(unknown),Glen R. Monroe,Koen L.I. van Gassen,(unknown),Anke M. Hövels,Nine Knoers,Hans Kristian Ploos van Amstel,G. W. J. Frederix	42
11	Dwarfism with joint laxity in Friesian horses is associated with a splice site mutation in B4GALT7 2016 ·BMC Genomics ·Peter A. J. Leegwater,(unknown),B.J. Ducro,(unknown),Frank G. van Steenbeek,Isaäc J. Nijman,Glen R. Monroe,J.W.M. Bastiaansen,Bert Dibbits,(unknown),(unknown),Willem Back,Anouk Schurink	29
12	Effectiveness of whole-exome sequencing and costs of the traditional diagnostic trajectory in children with intellectual disability 2016 ·Genetics in Medicine ·Glen R. Monroe,G. W. J. Frederix,Sanne M. C. Savelberg,Tamar I. de Vries,Karen Duran,Jasper J. van der Smagt,Pauline Terhal,Peter M. van Hasselt,Hester Y. Kroes,Nanda M. Verhoeven‐Duif,Isaäc J. Nijman,Ellen C. Carbo,Koen L.I. van Gassen,Nine Knoers,Anke M. Hövels,Mieke M. van Haelst,Gepke Visser,Gijs van Haaften	125
13	Compound heterozygous NEK1 variants in two siblings with oral-facial-digital syndrome type II (Mohr syndrome) 2016 ·European Journal of Human Genetics ·Glen R. Monroe,(unknown),Marijn F. Stokman,Pauline Terhal,Marie‐José H. van den Boogaard,Sanne M. C. Savelberg,Lars T. van der Veken,(unknown),Susanne M.A. Lens,Rutger C.C. Hengeveld,Marijn Créton,Nard G. Janssen,Aebele B. Mink van der Molen,(unknown),Rachel H. Giles,Nine V.A.M. Knoers,Gijs van Haaften	13
14	Mosaic CREBBP mutation causes overlapping clinical features of Rubinstein–Taybi and Filippi syndromes 2016 ·European Journal of Human Genetics ·Tamar I. de Vries,Glen R. Monroe,Martine J. van Belzen,(unknown),Sanne M. C. Savelberg,William G. Newman,Gijs van Haaften,Rutger A. J. Nievelstein,Mieke M. van Haelst	4
15	HeterozygousKIDINS220/ARMSnonsense variants cause spastic paraplegia, intellectual disability, nystagmus, and obesity 2016 ·Human Molecular Genetics ·Dragana Josifova,Glen R. Monroe,Federico Tessadori,Esther de Graaff,Bert van der Zwaag,Sarju Mehta,(unknown),Magdaléna Harakaľová,Karen Duran,Sanne M. C. Savelberg,Isaäc J. Nijman,Heinz Jungbluth,Casper C. Hoogenraad,Jeroen Bakkers,Nine Knoers,Helen V. Firth,Philip L. Beales,Gijs van Haaften,Mieke M. van Haelst	34
16	A nonsense mutation in B3GALNT2 is concordant with hydrocephalus in Friesian horses 2015 ·BMC Genomics ·B.J. Ducro,Anouk Schurink,J.W.M. Bastiaansen,(unknown),Frank G. van Steenbeek,(unknown),Isaäc J. Nijman,Glen R. Monroe,(unknown),Bert Dibbits,Willem Back,Peter A. J. Leegwater	25
17	Joubert syndrome: genotyping a Northern European patient cohort 2015 ·European Journal of Human Genetics ·Hester Y. Kroes,Glen R. Monroe,Bert van der Zwaag,Karen Duran,Carolien G. F. de Kovel,(unknown),Magdaléna Harakaľová,Isaäc J. Nijman,Wigard P. Kloosterman,Rachel H. Giles,Nine Knoers,Gijs van Haaften	50
18	Familial Ehlers‐Danlos syndrome with lethal arterial events caused by a mutation in COL5A1 2015 ·American Journal of Medical Genetics Part A ·Glen R. Monroe,Magdaléna Harakaľová,Saskia N. van der Crabben,Daniëlle Majoor‐Krakauer,Aida M. Bertoli‐Avella,Frans L. Moll,(unknown),Dennis Dooijes,Aryan Vink,Nine Knoers,Alessandra Maugeri,Gerard Pals,Isaäc J. Nijman,Gijs van Haaften,Annette F. Baas	41
19	Further confirmation of the MED13L haploinsufficiency syndrome 2014 ·European Journal of Human Genetics ·Mieke M. van Haelst,Glen R. Monroe,Karen Duran,Ellen van Binsbergen,Johannes M. P. J. Breur,Jacques C. Giltay,Gijs van Haaften	31
20	Whole Exome Sequencing as a Diagnostic Tool for Complex Neurological Disorders 2014 ·Value in Health ·G. W. J. Frederix,Glen R. Monroe,Anke M. Hövels,Gijs van Haaften	1

About Glen R. Monroe

Glen R. Monroe is a scholar working on Equine, Reproductive Medicine and Developmental Biology, having authored 20 papers that have together received 524 indexed citations. Recurring topics across this work include Ovarian cancer diagnosis and treatment (6 papers), Renal cell carcinoma treatment (4 papers) and Genomics and Rare Diseases (3 papers). The work is most often cited by research in Equine (26 citations), Genetics (313 citations) and Reproductive Medicine (54 citations). Glen R. Monroe has collaborated with scholars based in Netherlands, United Kingdom and Belgium. Frequent co-authors include Gijs van Haaften, Isaäc J. Nijman, Nine Knoers, Karen Duran, Mieke M. van Haelst, Koen L.I. van Gassen, G. W. J. Frederix, Anke M. Hövels, Hester Y. Kroes and Sanne M. C. Savelberg. Their work appears in journals such as Nature Communications, Human Molecular Genetics and BMC Genomics.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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