Monique Losekoot

5.2k citations

125 papers · 3.1k indexed · h-index 34

Endocrinology, Diabetes and Metabolism top 2%
- Growth Hormone and Insulin-like Growth Factors 29
Genetics top 1%
- Hemoglobinopathies and Related Disorders 21
- Genetic Syndromes and Imprinting 16
- Genomic variations and chromosomal abnormalities 14
- Genetic and Kidney Cyst Diseases 12
- Diabetes and associated disorders 10
Genetics top 2%
- Hemoglobinopathies and Related Disorders 21
- Genetic Syndromes and Imprinting 16
- Genomic variations and chromosomal abnormalities 14
- Genetic and Kidney Cyst Diseases 12
- Diabetes and associated disorders 10
Hematology top 5%
Molecular Biology top 5%
- DNA Repair Mechanisms 12
Cellular and Molecular Neuroscience
- Genetic Neurodegenerative Diseases 15

Co-authors: Riccardo Fodde Jan M. Wit Luigi F. Bernini Wilma Oostdijk Hermine A. van Duyvenvoorde Claudia Ruivenkamp Sarina G. Kant Paola Giordano
Cited by: Endocrinology, Diabetes and Metabolism Genetics
Journals: Blood (2 papers)Annals of Internal Medicine (1 paper)The Journal of Clinical Endocrinology & Metabolism (10 papers)
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

The 25 scholars most cited alongside Monique Losekoot, 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 Monique Losekoot Line = papers co-authored together Monique Losekoot links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Delayed Adrenarche may be an Additional Feature of Immunoglobulin Super Family Member 1 Deficiency Syndrome Journal of Clinical Research in Pediatric Endocrinology ·Severine Van Hulle,Margarita Craen,Bert Callewaert,Sjoerd D. Joustra,Wilma Oostdijk,Monique Losekoot,Jan M. Wit,Marc‐Olivier Turgeon,Daniel J. Bernard,Jean De Schepper	2016	18
2	Current and Best Practices of Genetic Testing for Maturity Onset Diabetes of the Young: Views of Professional Experts Public Health Genomics ·Angeli M. van der Zwaag,Stephanie S. Weinreich,Astrid Bosma,Tessel Rigter,Monique Losekoot,Lidewij Henneman,Martina C. Cornel	2014	17
3	Copy number variants in patients with short stature 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,Hedi L Claahsen-van de Grinten,Sandy A. van Gool,Martijn H. Breuning,Monique Losekoot,Jeffrey Baron,Claudia Ruivenkamp,Jan M. Wit	2013	57
4	Ten Year’s Experience in External Quality Assessment for Genetic Testing of Huntington Disease in Europe: Still Room for Improvement Clinical Genetics ·Monique Losekoot,Sara Seneca,Outi Kämäräinen,Simon Patton,S Stenhouse	2009	1
5	Hepatocyte nuclear factor (HNF)1A and HNF4A substitution occurring simultaneously in a family with maturity‐onset diabetes of the young Diabetic Medicine ·Hanneke J.B.H. Beijers,Monique Losekoot,Roelof J. Odink,Bert Bravenboer	2009	5
6	Neuronal Intranuclear and Neuropil Inclusions for Pathological Assessment of Huntington’s Disease Brain Pathology ·Marion L. C. Maat–Schieman,Raymund A.C. Roos,Monique Losekoot,Josephine C. Dorsman,Corrie Welling‐Graafland,Ingrid M. Hegeman-Kleinn,Freerk Broeyer,Martijn H. Breuning,Sjoerd G. van Duinen	2007	20
7	Increased prevalence of catecholamine excess and phaeochromocytomas in a well-defined Dutch population with SDHD-linked head and neck paragangliomas 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	2005	33
8	[From gene to disease; HD gene and Huntington disease]. PubMed ·J A Maat-Kievit,Monique Losekoot,R.A.C. Roos	2001	0
9	[From gene to disease; achondroplasia and other skeletal dysplasias due to an activating mutation in the fibroblast growth factor]. PubMed ·Conny M.A. van Ravenswaaij‐Arts,Monique Losekoot	2001	3
10	First-trimester diagnosis of late-infantile neuronal ceroid lipofuscinosis (LINCL) by tripeptidyl peptidase I assay and CLN2 mutation analysis 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	2001	6
11	A new X-linked mental retardation syndrome with distal limb defects, hearing impairment, verrucosis and immunodeficiency. Data Archiving and Networked Services (DANS) ·JC Oosterwijk,Anita Wischmeijer,Monique Losekoot,A Haraldson,G Theunissen,No Value van Gelderen	1999	2
12	Monozygotic twin brothers with the fragile X syndrome: different CGG repeats and different mental capacities Journal of Medical Genetics ·A T Helderman-van den Enden,P. D. Maaswinkel‐Mooij,E Hoogendoorn,Rob Willemsen,J A Maat-Kievit,Monique Losekoot,B. A. Oostra	1999	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. Journal of Medical Genetics ·Monique Losekoot,E Hoogendoorn,Renske Olmer,C. C. Jansen,JC Oosterwijk,A M van den Ouweland,Dicky Halley,Stephen T. Warren,Rob Willemsen,B. A. Oostra,Egbert Bakker	1997	19
14	Atypical HbH disease in a Surinamese patient resulting from a combination of the −SEA and −α^3.7 deletions with HbC heterozygosity British Journal of Haematology ·Paola Giordano,C. L. Harteveld,J. J. Michiels,W. J. Terpstra,D. Batelaan,Peter van Delft,Robert J. Plug,M. J. R. VAN DER WIELEN,Monique Losekoot,Luigi F. Bernini	1997	13
15	Huntington's disease : report on four Saudi families Saudi Medical Journal ·Saeed Bohlega,Donald R. McLean,M. Zuheir Al Kawi,S Omer,Raymund A.C. Roos,Monique Losekoot,Egbert Bakker	1996	2
16	An IVS1–116 (A→G) acceptor splice site mutation in the α₂ globin gene causing α⁺ thalassaemia in two Dutch families British Journal of Haematology ·Cornelis L. Harteveld,J. G. A. M. Heister,Paola Giordano,D. Batelaan,Peter van Delft,H. L. Haak,P. Wijermans,Monique Losekoot,Luigi F. Bernini	1996	23
17	Hb Utrecht [α₂ 129(H12)Leu → Pro], a new unstable α2‐chain variant associated with a mild α‐thalassaemic phenotype British Journal of Haematology ·Cornelis L. Harteveld,Paola Giordano,Monique Losekoot,J. G. A. M. Heister,D. Batelaan,Peter van Delft,Marrie C.A. Bruin,Luigi F. Bernini	1996	16
18	A novel polyadenylation signal mutation in the α₂‐globin gene causing α thalassaemia British Journal of Haematology ·Cornelis L. Harteveld,Monique Losekoot,H. L. Haak,J. G. A. M. Heister,Paola Giordano,L.F. Bernini	1994	55
19	Rapid identification by denaturing gradient gel electrophoresis of mutations in the γ‐globin gene promoters in non‐deletion type HPFH British Journal of Haematology ·Enrico Gottardi,Monique Losekoot,Riccardo Fodde,Giuseppe Saglio,Clara Camaschella,Luigi F. Bernini	1992	25
20	[Combined alpha and beta thalassemia in a Chinese family in The Netherlands]. PubMed ·Monique Losekoot,C Beijer,Giordano Pc,van Gemeren Ad,Oei Yb,Bernini Lf	1989	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), Genetic Syndromes and Imprinting (16 papers), Genetic Neurodegenerative Diseases (15 papers), Genomic variations and chromosomal abnormalities (14 papers), DNA Repair Mechanisms (12 papers), Genetic and Kidney Cyst Diseases (12 papers) and Diabetes and associated disorders (10 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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