Glen R. Monroe

2.0k citations

20 papers · 524 indexed · h-index 12

Equine top 5%
Genetics top 10%
- Genomics and Rare Diseases 3
- Genomic variations and chromosomal abnormalities 3
- Genetics and Neurodevelopmental Disorders 3
- Genetic Syndromes and Imprinting 2
Reproductive Medicine top 10%
- Ovarian cancer diagnosis and treatment 6
Cancer Research
- Cancer Genomics and Diagnostics 3
Molecular Biology
Pulmonary and Respiratory Medicine
- Renal cell carcinoma treatment 4
Neurology
- Neurological diseases and metabolism 2

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
Cited by: Equine Genetics Reproductive Medicine
Journals: Nature Communications (1 paper)Human Molecular Genetics (1 paper)BMC Genomics (2 papers)
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

The 25 scholars most cited alongside Glen R. Monroe, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Glen R. Monroe Line = papers co-authored together Glen R. Monroe links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	CRISPR‐Cas9 enrichment, a new strategy in microbial metagenomics to investigate complex genomic regions: The case of an environmental integron Molecular Ecology Resources ·Eva Sandoval-Quintana,Christina Stangl,Lionel Huang,Ivo Renkens,Robert Duran,Gijs van Haaften,Glen R. Monroe,Béatrice Lauga,Christine Cagnon	2023	2
2	FOXL2 and TERT promoter mutation detection in circulating tumor DNA of adult granulosa cell tumors as biomarker for disease monitoring Gynecologic Oncology ·Jolijn W. Groeneweg,Joline F. Roze,Edith Peters,Ferdinando Sereno,Anna G.J. Brink,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,Gijs W. van Haaften,Ronald P. Zweemer	2021	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 Oncotarget ·Joline F. Roze,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	2021	5
4	Familial Occurrence of Adult Granulosa Cell Tumors: Analysis of Whole-Genome Germline Variants Cancers ·Joline F. Roze,Joachim Kutzera,Wouter Koole,Margreet G.E.M. Ausems,Kristi Engelstad,Jurgen M.J. Piek,Cor D. de Kroon,René H.M. Verheijen,Gijs van Haaften,Ronald P. Zweemer,Glen R. Monroe	2021	4
5	In Vitro Systematic Drug Testing Reveals Carboplatin, Paclitaxel, and Alpelisib as a Potential Novel Combination Treatment for Adult Granulosa Cell Tumors Cancers ·Joline F. Roze,Elena Sendino Garví,Ellen Stelloo,Christina Stangl,Ferdinando Sereno,Karen Duran,Jolijn W. Groeneweg,Sterre T. Paijens,Hans W. Nijman,Hannah van Meurs,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	2021	11
6	Partner independent fusion gene detection by multiplexed CRISPR-Cas9 enrichment and long read nanopore sequencing Nature Communications ·Christina Stangl,Sam de Blank,Ivo Renkens,Liset Westera,Tamara Verbeek,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	2020	47
7	Patient engagement in research on rare gynecological tumors International Journal of Gynecological Cancer ·Joline F. Roze,Jolijn W. Groeneweg,Glen R. Monroe,Ineke Fransen,Murat Gültekin,Ronald P. Zweemer,René H.M. Verheijen	2020	2
8	Investigation of Genetic Modifiers of Copper Toxicosis in Labrador Retrievers Life ·Xiaoyan Wu,Elise R den Boer,Manon Vos‐Loohuis,Frank G. van Steenbeek,Glen R. Monroe,Isaäc J. Nijman,Peter A. J. Leegwater,Hille Fieten	2020	10
9	Whole Genome Analysis of Ovarian Granulosa Cell Tumors Reveals Tumor Heterogeneity and a High-Grade TP53-Specific Subgroup Cancers ·Joline F. Roze,Glen R. Monroe,Joachim Kutzera,Jolijn W. Groeneweg,Ellen Stelloo,Sterre T. Paijens,Hans W. Nijman,Hannah van Meurs,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	2020	30
10	Whole-exome sequencing in intellectual disability; cost before and after a diagnosis European Journal of Human Genetics ·Terry Vrijenhoek,Eline M. Middelburg,Glen R. Monroe,Koen L.I. van Gassen,Joost W. Geenen,Anke M. Hövels,Nine Knoers,Hans Kristian Ploos van Amstel,G. W. J. Frederix	2018	42
11	Dwarfism with joint laxity in Friesian horses is associated with a splice site mutation in B4GALT7 BMC Genomics ·Peter A. J. Leegwater,Manon Vos‐Loohuis,B.J. Ducro,I.J.M. Boegheim,Frank G. van Steenbeek,Isaäc J. Nijman,Glen R. Monroe,J.W.M. Bastiaansen,Bert Dibbits,Leanne Goor,Ids Hellinga,Willem Back,Anouk Schurink	2016	29
12	Effectiveness of whole-exome sequencing and costs of the traditional diagnostic trajectory in children with intellectual disability 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	2016	125
13	Compound heterozygous NEK1 variants in two siblings with oral-facial-digital syndrome type II (Mohr syndrome) European Journal of Human Genetics ·Glen R. Monroe,Isabelle Francisca Petronella Maria Kappen,Marijn F. Stokman,Pauline Terhal,Marie‐José H. van den Boogaard,Sanne M. C. Savelberg,Lars T. van der Veken,Robert JJ van Es,Susanne M.A. Lens,Rutger C.C. Hengeveld,Marijn Créton,Nard G. Janssen,Aebele B. Mink van der Molen,Michelle B. Ebbeling,Rachel H. Giles,Nine V.A.M. Knoers,Gijs van Haaften	2016	13
14	Mosaic CREBBP mutation causes overlapping clinical features of Rubinstein–Taybi and Filippi syndromes European Journal of Human Genetics ·Tamar I. de Vries,Glen R. Monroe,Martine J. van Belzen,Christian A van der Lans,Sanne M. C. Savelberg,William G. Newman,Gijs van Haaften,Rutger A. J. Nievelstein,Mieke M. van Haelst	2016	4
15	HeterozygousKIDINS220/ARMSnonsense variants cause spastic paraplegia, intellectual disability, nystagmus, and obesity 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	2016	34
16	A nonsense mutation in B3GALNT2 is concordant with hydrocephalus in Friesian horses BMC Genomics ·B.J. Ducro,Anouk Schurink,J.W.M. Bastiaansen,I.J.M. Boegheim,Frank G. van Steenbeek,Manon Vos‐Loohuis,Isaäc J. Nijman,Glen R. Monroe,Ids Hellinga,Bert Dibbits,Willem Back,Peter A. J. Leegwater	2015	25
17	Joubert syndrome: genotyping a Northern European patient cohort European Journal of Human Genetics ·Hester Y. Kroes,Glen R. Monroe,Bert van der Zwaag,Karen Duran,Carolien G. F. de Kovel,Mark J. van Roosmalen,Magdaléna Harakaľová,Isaäc J. Nijman,Wigard P. Kloosterman,Rachel H. Giles,Nine Knoers,Gijs van Haaften	2015	50
18	Familial Ehlers‐Danlos syndrome with lethal arterial events caused by a mutation in COL5A1 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,Björn I Oranen,Dennis Dooijes,Aryan Vink,Nine Knoers,Alessandra Maugeri,Gerard Pals,Isaäc J. Nijman,Gijs van Haaften,Annette F. Baas	2015	41
19	Further confirmation of the MED13L haploinsufficiency syndrome 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	2014	31
20	Whole Exome Sequencing as a Diagnostic Tool for Complex Neurological Disorders Value in Health ·G. W. J. Frederix,Glen R. Monroe,Anke M. Hövels,Gijs van Haaften	2014	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), Genomics and Rare Diseases (3 papers), Genomic variations and chromosomal abnormalities (3 papers), Genetics and Neurodevelopmental Disorders (3 papers), Cancer Genomics and Diagnostics (3 papers), Genetic Syndromes and Imprinting (2 papers) and Neurological diseases and metabolism (2 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.

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