Jan E. Dumon

1.3k total citations
31 papers, 944 citations indexed

About

Jan E. Dumon is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Jan E. Dumon has authored 31 papers receiving a total of 944 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Genetics, 11 papers in Molecular Biology and 9 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Jan E. Dumon's work include Prenatal Screening and Diagnostics (8 papers), Genomic variations and chromosomal abnormalities (8 papers) and Connective tissue disorders research (3 papers). Jan E. Dumon is often cited by papers focused on Prenatal Screening and Diagnostics (8 papers), Genomic variations and chromosomal abnormalities (8 papers) and Connective tissue disorders research (3 papers). Jan E. Dumon collaborates with scholars based in Belgium, Netherlands and United States. Jan E. Dumon's co-authors include Patrick J. Willems, Thomas B. Friedman, Charles I. Berlín, Rachel Fisher, Bronya J.B. Keats, Robert J. Morell, Karen H. Friderici, Harry Ostrer, Linda J. Hood and Guy Van Camp and has published in prestigious journals such as Nature, New England Journal of Medicine and Human Molecular Genetics.

In The Last Decade

Jan E. Dumon

31 papers receiving 902 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Jan E. Dumon Belgium 14 498 389 240 143 140 31 944
Patricia Blanchet France 16 501 1.0× 268 0.7× 245 1.0× 84 0.6× 56 0.4× 47 828
Maria Grigoriadou Greece 18 329 0.7× 190 0.5× 191 0.8× 84 0.6× 42 0.3× 48 723
Jun Shen United States 20 807 1.6× 555 1.4× 307 1.3× 116 0.8× 190 1.4× 44 1.6k
Mary Z. Pelias United States 17 536 1.1× 375 1.0× 238 1.0× 110 0.8× 58 0.4× 35 1.1k
Hashem Shahin Palestinian Territory 15 697 1.4× 756 1.9× 171 0.7× 318 2.2× 150 1.1× 17 1.2k
L. Zelante Italy 10 316 0.6× 367 0.9× 59 0.2× 142 1.0× 92 0.7× 13 793
Saber Masmoudi Tunisia 21 625 1.3× 718 1.8× 200 0.8× 329 2.3× 140 1.0× 98 1.3k
Laurence Jonard France 15 379 0.8× 301 0.8× 102 0.4× 135 0.9× 90 0.6× 36 742
Valentina Labay Israel 10 767 1.5× 328 0.8× 96 0.4× 86 0.6× 87 0.6× 11 1.3k
Terry‐Lynn Young Canada 20 696 1.4× 196 0.5× 430 1.8× 80 0.6× 59 0.4× 43 1.6k

Countries citing papers authored by Jan E. Dumon

Since Specialization
Citations

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

Fields of papers citing papers by Jan E. Dumon

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jan E. Dumon. 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 Jan E. Dumon. The network helps show where Jan E. Dumon may publish in the future.

Co-authorship network of co-authors of Jan E. Dumon

This figure shows the co-authorship network connecting the top 25 collaborators of Jan E. Dumon. A scholar is included among the top collaborators of Jan E. Dumon 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 Jan E. Dumon. Jan E. Dumon 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.
Stinissen, Piet, Bernadette Van Roy, Guy Van Camp, et al.. (2005). Study of the origin of nondisjunction in a family with two cases of Down syndrome using cytogenetic and molecular polymorphisms. American Journal of Medical Genetics. 37(S7). 133–136. 1 indexed citations
2.
Morell, Robert J., Linda J. Hood, Karen H. Friderici, et al.. (1998). Mutations in the Connexin 26 Gene (GJB2) among Ashkenazi Jews with Nonsyndromic Recessive Deafness. New England Journal of Medicine. 339(21). 1500–1505. 432 indexed citations
3.
Bossuyt, Paul, et al.. (1995). Incidence of low-fluorescence α satellite region on chromosome 21 escaping detection of aneuploidy at interphase by FISH. Cytogenetic and Genome Research. 68(3-4). 203–206. 15 indexed citations
4.
Parizel, Paul M., et al.. (1993). Tricho‐rhino‐phalangeal syndrome type I (TRP I) due to an apparently balanced translocation involving 8q24. American Journal of Medical Genetics. 45(4). 450–455. 7 indexed citations
5.
6.
Schrander‐Stumpel, C. T. R. M., A. Spaepen, J. P. Fryns, & Jan E. Dumon. (1992). A severe case of mandibuloacral dysplasia in a girl. American Journal of Medical Genetics. 43(5). 877–881. 23 indexed citations
7.
Willems, Patrick J., Bernadette Van Roy, Kristel De Boulle, et al.. (1992). Segregation of the fragile X mutation from an affected male to his normal daughter. Human Molecular Genetics. 1(7). 511–515. 46 indexed citations
8.
Auwera, Bart Van Der, Nadine Van Roy, Anne De Paepe, et al.. (1992). Molecular cytogenetic analysis of XX males using Y-specific DNA sequences, including SRY. Human Genetics. 89(1). 23–28. 17 indexed citations
9.
10.
Wauters, J., Jan Hendrickx, Paul Coucke, et al.. (1991). Frequency of the phenylalanine deletion (ΔF508) in the CF gene of Belgian cystic fibrosis patients. Clinical Genetics. 39(2). 89–92. 2 indexed citations
11.
Buntinx, Inge, et al.. (1991). Acardiac amorphous twin with prune belly sequence in the co‐twin. American Journal of Medical Genetics. 39(4). 453–457. 11 indexed citations
12.
Willems, Patrick J., Rosanna Gatti, John Darby, et al.. (1991). Fucosidosis revisited: A review of 77 patients. American Journal of Medical Genetics. 38(1). 111–131. 115 indexed citations
13.
Willems, Patrick J., et al.. (1991). Fryns syndrome without diaphragmatic hernia?. American Journal of Medical Genetics. 41(2). 255–257. 21 indexed citations
14.
Willems, Patrick J., Bart Van Der Auwera, Lieve Vits, et al.. (1990). Assignment of X-linked hydrocephalus to Xq28 by linkage analysis. Genomics. 8(2). 367–370. 48 indexed citations
15.
Willems, Patrick J., Lieve Vits, Berten Ceulemans, et al.. (1990). Two brothers with mental retardation discordant for the Fragile‐X syndrome. American Journal of Medical Genetics. 36(1). 122–125. 3 indexed citations
16.
Willems, Patrick J., Lieve Vits, R. J. A. Wanders, et al.. (1990). Linkage of DNA Markers at Xq28 to Adrenoleukodystrophy and Adrenomyeloneuropathy Present Within the Same Family. Archives of Neurology. 47(6). 665–669. 5 indexed citations
17.
Dumon, Jan E., et al.. (1988). Karyotypic evidence for the leukemic involvement of the erythroblasts in erythroleukemia.. PubMed. 2(5). 296–9. 3 indexed citations
18.
Dumon, Jan E., et al.. (1987). Antenatal ultrasonographic diagnosis of trisomy 18 (Edwards syndrome). European Journal of Obstetrics & Gynecology and Reproductive Biology. 26(4). 353–358. 2 indexed citations
19.
Neetens, A, et al.. (1982). Chromosomal anomalies in patients with retinoblastoma.. PubMed. 203. 47–56. 1 indexed citations
20.
Leroy, J. G., et al.. (1970). Deficiency of Arylsulphatase A in Leucocytes and Skin Fibroblasts in Juvenile Metachromatic Leucodystrophy. Nature. 226(5245). 553–554. 17 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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