Monique Losekoot

5.2k citations

125 papers · 3.1k indexed · h-index 34

Molecular Biology top 5%
Genetics top 1%
Endocrinology, Diabetes and Metabolism top 2%
Genetics top 2%
Pathology and Forensic Medicine top 5%

Co-authors: Riccardo Fodde Jan M. Wit Luigi F. Bernini Wilma Oostdijk Hermine A. van Duyvenvoorde Claudia Ruivenkamp Sarina G. Kant Paola Giordano
Topics: Growth Hormone and Insulin-like Growth Factors (29 papers)Hemoglobinopathies and Related Disorders (21 papers)Genetic Syndromes and Imprinting (16 papers)
Cited by: Endocrinology, Diabetes and Metabolism Genetics
Journals: Blood Annals of Internal Medicine The Journal of Clinical Endocrinology & Metabolism
Partner nations: Netherlands United States United Kingdom

In The Last Decade

Monique Losekoot

122 papers receiving 3.0k citations

Peers

Countries citing papers authored by Monique Losekoot

Since Specialization

Citations

This map shows the geographic impact of Monique Losekoot'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 Monique Losekoot with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Monique Losekoot more than expected).

Fields of papers citing papers by Monique Losekoot

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Monique Losekoot. 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 Monique Losekoot. The network helps show where Monique Losekoot may publish in the future.

Co-authorship network of co-authors of Monique Losekoot

This figure shows the co-authorship network connecting the top 25 collaborators of Monique Losekoot. A scholar is included among the top collaborators of Monique Losekoot 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 Monique Losekoot. Monique Losekoot 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	Delayed Adrenarche may be an Additional Feature of Immunoglobulin Super Family Member 1 Deficiency Syndrome 2016 ·Journal of Clinical Research in Pediatric Endocrinology ·(unknown),Margarita Craen,Bert Callewaert,Sjoerd D. Joustra,Wilma Oostdijk,Monique Losekoot,Jan M. Wit,Marc‐Olivier Turgeon,Daniel J. Bernard,Jean De Schepper	18
2	Current and Best Practices of Genetic Testing for Maturity Onset Diabetes of the Young: Views of Professional Experts 2014 ·Public Health Genomics ·(unknown),Stephanie S. Weinreich,Astrid Bosma,Tessel Rigter,Monique Losekoot,Lidewij Henneman,Martina C. Cornel	17
3	Copy number variants in patients with short stature 2013 ·European Journal of Human Genetics ·Hermine A. van Duyvenvoorde,Julian C. Lui,Sarina G. Kant,Wilma Oostdijk,Antoinet C.J. Gijsbers,Mariëtte J.V. Hoffer,Marcel Karperien,M.J.E. Walenkamp,C. Noordam,Paul G. Voorhoeve,Verónica Mericq,Alberto M. Pereira,(unknown),(unknown),Martijn H. Breuning,Monique Losekoot,Jeffrey Baron,Claudia Ruivenkamp,Jan M. Wit	57
4	Ten Year’s Experience in External Quality Assessment for Genetic Testing of Huntington Disease in Europe: Still Room for Improvement 2009 ·Clinical Genetics ·Monique Losekoot,Sara Seneca,Outi Kämäräinen,Simon Patton,(unknown)	1
5	Hepatocyte nuclear factor (HNF)1A and HNF4A substitution occurring simultaneously in a family with maturity‐onset diabetes of the young 2009 ·Diabetic Medicine ·(unknown),Monique Losekoot,Roelof J. Odink,Bert Bravenboer	5
6	Neuronal Intranuclear and Neuropil Inclusions for Pathological Assessment of Huntington’s Disease 2007 ·Brain Pathology ·Marion L. C. Maat–Schieman,Raymund A.C. Roos,Monique Losekoot,Josephine C. Dorsman,(unknown),(unknown),(unknown),Martijn H. Breuning,Sjoerd G. van Duinen	20
7	Increased prevalence of catecholamine excess and phaeochromocytomas in a well-defined Dutch population with SDHD-linked head and neck paragangliomas 2005 ·European Journal of Endocrinology ·William H. van Houtum,Eleonora P.M. Corssmit,Pim Dekker,Jeroen C. Jansen,Andel G. L. van der Mey,A Bröcker-Vriends,Peter E.M. Taschner,Monique Losekoot,Michael A. Frölich,Marcel P. M. Stokkel,Cees J. Cornelisse,Johannes A. Romijn	33
8	[From gene to disease; HD gene and Huntington disease]. 2001 ·PubMed ·J A Maat-Kievit,Monique Losekoot,R.A.C. Roos	0
9	[From gene to disease; achondroplasia and other skeletal dysplasias due to an activating mutation in the fibroblast growth factor]. 2001 ·PubMed ·Conny M.A. van Ravenswaaij‐Arts,Monique Losekoot	3
10	First-trimester diagnosis of late-infantile neuronal ceroid lipofuscinosis (LINCL) by tripeptidyl peptidase I assay and CLN2 mutation analysis 2001 ·Prenatal Diagnosis ·W. J. Kleijer,O. P. van Diggelen,J. L. M. Keulemans,Monique Losekoot,Victor H. Garritsen,Hans Stroink,Daniëlle Majoor‐Krakauer,Patrick Franken,Marcel Eurlings,Peter E.M. Taschner,Frans J. Los,R. J. H. Galjaard	6
11	A new X-linked mental retardation syndrome with distal limb defects, hearing impairment, verrucosis and immunodeficiency. 1999 ·Data Archiving and Networked Services (DANS) ·JC Oosterwijk,Anita Wischmeijer,Monique Losekoot,(unknown),(unknown),(unknown)	2
12	Monozygotic twin brothers with the fragile X syndrome: different CGG repeats and different mental capacities 1999 ·Journal of Medical Genetics ·(unknown),P. D. Maaswinkel‐Mooij,E Hoogendoorn,Rob Willemsen,J A Maat-Kievit,Monique Losekoot,B. A. Oostra	37
13	Prenatal diagnosis of the fragile X syndrome: loss of mutation owing to a double recombinant or gene conversion event at the FMR1 locus. 1997 ·Journal of Medical Genetics ·Monique Losekoot,E Hoogendoorn,Renske Olmer,(unknown),JC Oosterwijk,A M van den Ouweland,Dicky Halley,Stephen T. Warren,Rob Willemsen,B. A. Oostra,Egbert Bakker	19
14	Atypical HbH disease in a Surinamese patient resulting from a combination of the −SEA and −α^3.7 deletions with HbC heterozygosity 1997 ·British Journal of Haematology ·Paola Giordano,(unknown),J. J. Michiels,W. J. Terpstra,(unknown),Peter van Delft,(unknown),(unknown),Monique Losekoot,Luigi F. Bernini	13
15	Huntington's disease : report on four Saudi families 1996 ·Saudi Medical Journal ·Saeed Bohlega,(unknown),(unknown),(unknown),Raymund A.C. Roos,Monique Losekoot,Egbert Bakker	2
16	An IVS1–116 (A→G) acceptor splice site mutation in the α₂ globin gene causing α⁺ thalassaemia in two Dutch families 1996 ·British Journal of Haematology ·Cornelis L. Harteveld,J. G. A. M. Heister,Paola Giordano,(unknown),Peter van Delft,H. L. Haak,P. Wijermans,Monique Losekoot,Luigi F. Bernini	23
17	Hb Utrecht [α₂ 129(H12)Leu → Pro], a new unstable α2‐chain variant associated with a mild α‐thalassaemic phenotype 1996 ·British Journal of Haematology ·Cornelis L. Harteveld,Paola Giordano,Monique Losekoot,J. G. A. M. Heister,(unknown),Peter van Delft,Marrie C.A. Bruin,Luigi F. Bernini	16
18	A novel polyadenylation signal mutation in the α₂‐globin gene causing α thalassaemia 1994 ·British Journal of Haematology ·Cornelis L. Harteveld,Monique Losekoot,H. L. Haak,J. G. A. M. Heister,Paola Giordano,L.F. Bernini	55
19	Rapid identification by denaturing gradient gel electrophoresis of mutations in the γ‐globin gene promoters in non‐deletion type HPFH 1992 ·British Journal of Haematology ·Enrico Gottardi,Monique Losekoot,Riccardo Fodde,Giuseppe Saglio,Clara Camaschella,Luigi F. Bernini	25
20	[Combined alpha and beta thalassemia in a Chinese family in The Netherlands]. 1989 ·PubMed ·Monique Losekoot,(unknown),(unknown),(unknown),(unknown),(unknown)	2

About Monique Losekoot

Monique Losekoot is a scholar working on Endocrinology, Diabetes and Metabolism, Genetics and Genetics, having authored 125 papers that have together received 3.1k indexed citations. Recurring topics across this work include Growth Hormone and Insulin-like Growth Factors (29 papers), Hemoglobinopathies and Related Disorders (21 papers) and Genetic Syndromes and Imprinting (16 papers). The work is most often cited by research in Endocrinology, Diabetes and Metabolism (762 citations), Genetics (1.3k citations) and Genetics (483 citations). Monique Losekoot has collaborated with scholars based in Netherlands, United States and United Kingdom. Frequent co-authors include Riccardo Fodde, Jan M. Wit, Luigi F. Bernini, Wilma Oostdijk, Hermine A. van Duyvenvoorde, Claudia Ruivenkamp, Sarina G. Kant, Paola Giordano, Egbert Bakker and Dorien J.M. Peters. Their work appears in journals such as Blood, Annals of Internal Medicine and The Journal of Clinical Endocrinology & Metabolism.

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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