M. L. Kwee

1.2k total citations
24 papers, 640 citations indexed

About

M. L. Kwee is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, M. L. Kwee has authored 24 papers receiving a total of 640 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 12 papers in Genetics and 4 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in M. L. Kwee's work include DNA Repair Mechanisms (5 papers), Connective tissue disorders research (4 papers) and Microtubule and mitosis dynamics (3 papers). M. L. Kwee is often cited by papers focused on DNA Repair Mechanisms (5 papers), Connective tissue disorders research (4 papers) and Microtubule and mitosis dynamics (3 papers). M. L. Kwee collaborates with scholars based in Netherlands, France and United States. M. L. Kwee's co-authors include F. Arwert, Hans Joenje, Jerome R. Lo Ten Foe, Rachel A. Gibson, A. Veerman, Anneke B. Oostra, Inderjeet Dokal, Éliane Gluckman, Dick Lindhout and P. G. Barth and has published in prestigious journals such as Journal of Bone and Mineral Research, British Journal of Dermatology and Osteoporosis International.

In The Last Decade

M. L. Kwee

23 papers receiving 620 citations

Peers

M. L. Kwee
Lydia E. McMorrow United States
M. Sagi Israel
Christine R. Bryke United States
M.M. Aronson United States
Barbara Adler‐Brecher United States
Peter C. Verlander United States
Anne Marie Ottesen Denmark
K. L. Ying United States
Teresa M. Maxwell United States
Shunsuke Kimura Japan
Lydia E. McMorrow United States
M. L. Kwee
Citations per year, relative to M. L. Kwee M. L. Kwee (= 1×) peers Lydia E. McMorrow

Countries citing papers authored by M. L. Kwee

Since Specialization
Citations

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

Fields of papers citing papers by M. L. Kwee

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by M. L. Kwee. 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 M. L. Kwee. The network helps show where M. L. Kwee may publish in the future.

Co-authorship network of co-authors of M. L. Kwee

This figure shows the co-authorship network connecting the top 25 collaborators of M. L. Kwee. A scholar is included among the top collaborators of M. L. Kwee 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 M. L. Kwee. M. L. Kwee is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Klopocki, Eva, Bianca P. Hennig, Verayuth Praphanphoj, et al.. (2010). Mesomelic dysplasia Kantaputra type is associated with duplications of the HOXD locus on chromosome 2q. European Journal of Human Genetics. 18(12). 1310–1314. 24 indexed citations
2.
Dijk, Fleur S van, et al.. (2008). Rendu-Osler-Weber disease: update of medical and dental considerations. Oral Surgery Oral Medicine Oral Pathology Oral Radiology and Endodontology. 105(2). e38–e41. 21 indexed citations
3.
Kroes, Hester Y., Marcel Nelen, D. Wittebol‐Post, et al.. (2007). DNA analysis of AHI1, NPHP1 and CYCLIN D1 in Joubert syndrome patients from the Netherlands. European Journal of Medical Genetics. 51(1). 24–34. 27 indexed citations
4.
Kwee, M. L., et al.. (2006). First case of ataxia with isolated vitamin E deficiency in the Netherlands. Parkinsonism & Related Disorders. 13(5). 315–316. 8 indexed citations
5.
Kwee, M. L., et al.. (2005). An autosomal dominant high bone mass phenotype in association with craniosynostosis in an extended family is caused by an LRP5 missense mutation. Bone and Mineral. 20(7). 3 indexed citations
6.
Şimşek, Suat, Katrien Janssens, M. L. Kwee, et al.. (2005). Camurati–Engelmann disease (progressive diaphyseal dysplasia) in a Moroccan family. Osteoporosis International. 16(9). 1167–1170. 17 indexed citations
7.
Kwee, M. L., Jacqueline A. Sluijs, J. M. G. van Vugt, Liliane C. D. Wijnaendts, & Gilles Thomas. (2004). Mesomelic dysplasia, Kantaputra type: Clinical report, prenatal diagnosis, no evidence for SHOX deletion/mutation. American Journal of Medical Genetics Part A. 128A(4). 404–409. 4 indexed citations
8.
Kluijt, Irma, D. B. van Dorp, M. L. Kwee, et al.. (2000). Kabuki syndrome ? Report of six cases and review of the literature with emphasis on ocular features. Ophthalmic Genetics. 21(1). 51–61. 25 indexed citations
9.
Foe, Jerome R. Lo Ten, M. L. Kwee, Anneke B. Oostra, et al.. (1997). Somatic mosaicism in Fanconi anemia: molecular basis and clinical significance.. PubMed. 5(3). 137–48. 149 indexed citations
10.
Kwee, M. L., A. J. van Essen, J.H. Begeer, et al.. (1997). An atypical case of Fanconi anemia in elderly sibs. American Journal of Medical Genetics. 68(3). 362–366. 10 indexed citations
11.
Kwee, M. L., Jerome R. Lo Ten Foe, F. Arwert, et al.. (1996). EARLY PRENATAL DIAGNOSIS OF FANCONI ANAEMIA IN A TWIN PREGNANCY, USING DNA ANALYSIS. Prenatal Diagnosis. 16(4). 345–348. 7 indexed citations
12.
Haring, Danny A. J. P., Martina C. Cornel, J.C. van der Linden, J. M. G. van Vugt, & M. L. Kwee. (1993). Acardius acephalus after induced ovulation: A case report. Teratology. 47(4). 257–262. 9 indexed citations
13.
Pope, F M, et al.. (1992). Clinical features of an affected father and daughter with Ehlers-Danlos syndrome type VIIB. British Journal of Dermatology. 126(1). 77–82. 12 indexed citations
14.
Dorp, D. B. van, et al.. (1991). Joubert syndrome: A clinical and pathological description of an affected male and a female fetus from the same sibship. American Journal of Medical Genetics. 40(1). 100–104. 31 indexed citations
15.
Dorp, D. B. van & M. L. Kwee. (1990). Tuberous sclerosis Diagnostic problems in a family. Ophthalmic Paediatrics and Genetics. 11(2). 95–101. 2 indexed citations
16.
Brons, Jozien T. J., Herman P. van Geijn, J. W. Wladimiroff, et al.. (1988). Prenatal ultrasound diagnosis of the Holt‐Oram syndrome. Prenatal Diagnosis. 8(3). 175–181. 18 indexed citations
17.
Menko, F. H., et al.. (1988). Van der Woude syndrome--recognition of lesser expressions: case report.. PubMed. 25(3). 318–21. 3 indexed citations
18.
Kwee, M. L., P. G. Barth, F. Arwert, & K. Madan. (1984). Mosaic tetrasomy 21 in a male child. Clinical Genetics. 26(2). 150–155. 24 indexed citations
19.
20.
Heimans, Jan J., et al.. (1982). H-reflex studies in a family with possibly X-linked neuronal Charcot-Marie-Tooth disease. Clinical Neurology and Neurosurgery. 84(3). 147–158. 1 indexed citations

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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