M.R. Verschraegen-Spae

462 total citations
18 papers, 328 citations indexed

About

M.R. Verschraegen-Spae is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology. According to data from OpenAlex, M.R. Verschraegen-Spae has authored 18 papers receiving a total of 328 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Genetics, 10 papers in Pediatrics, Perinatology and Child Health and 5 papers in Molecular Biology. Recurrent topics in M.R. Verschraegen-Spae's work include Prenatal Screening and Diagnostics (10 papers), Genomic variations and chromosomal abnormalities (8 papers) and Chromosomal and Genetic Variations (4 papers). M.R. Verschraegen-Spae is often cited by papers focused on Prenatal Screening and Diagnostics (10 papers), Genomic variations and chromosomal abnormalities (8 papers) and Chromosomal and Genetic Variations (4 papers). M.R. Verschraegen-Spae collaborates with scholars based in Belgium, France and Germany. M.R. Verschraegen-Spae's co-authors include Marc Dhont, Nadine Van Roy, Petra De Sutter, H Laverge, Anne De Paepe, Frank Speleman, Anne De Paepe, Jules G. Leroy, Franz Klein and B Quack and has published in prestigious journals such as American Journal of Obstetrics and Gynecology, Human Reproduction and Journal of Medical Genetics.

In The Last Decade

M.R. Verschraegen-Spae

18 papers receiving 311 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
M.R. Verschraegen-Spae Belgium 11 209 176 104 86 83 18 328
N. Gregson United Kingdom 7 229 1.1× 185 1.1× 93 0.9× 76 0.9× 72 0.9× 12 360
Michael Freidine United States 9 169 0.8× 292 1.7× 80 0.8× 44 0.5× 84 1.0× 10 396
D A Couzin United Kingdom 12 226 1.1× 124 0.7× 135 1.3× 117 1.4× 26 0.3× 23 367
Sorrell H. Waxman United States 13 217 1.0× 143 0.8× 132 1.3× 50 0.6× 50 0.6× 19 387
Stéphane Serero France 8 188 0.9× 110 0.6× 133 1.3× 46 0.5× 59 0.7× 15 328
Geneviève Lefort France 13 262 1.3× 160 0.9× 148 1.4× 105 1.2× 34 0.4× 29 375
Amelia Villa Spain 9 176 0.8× 75 0.4× 83 0.8× 50 0.6× 25 0.3× 12 241
Nicoletta Villa Italy 10 259 1.2× 123 0.7× 121 1.2× 63 0.7× 92 1.1× 30 344
M. Neil Macintyre United States 12 179 0.9× 103 0.6× 89 0.9× 55 0.6× 36 0.4× 17 338
Nicole Joyé France 10 118 0.6× 105 0.6× 74 0.7× 32 0.4× 63 0.8× 17 223

Countries citing papers authored by M.R. Verschraegen-Spae

Since Specialization
Citations

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

Fields of papers citing papers by M.R. Verschraegen-Spae

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by M.R. Verschraegen-Spae. 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.R. Verschraegen-Spae. The network helps show where M.R. Verschraegen-Spae may publish in the future.

Co-authorship network of co-authors of M.R. Verschraegen-Spae

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

All Works

18 of 18 papers shown
1.
Speleman, Frank, Nadine Van Roy, Sharon W. Horsley, et al.. (2000). Subtelomeric familial translocation t(2;7)(q37;q35) leading to partial trisomy 7q35?qter: Molecular cytogenetic analysis and clinical phenotype in two generations. American Journal of Medical Genetics. 93(5). 349–354. 20 indexed citations
2.
Verschraegen-Spae, M.R., B Quack, Sophie Rousseaux, et al.. (1998). Application of fluorescence in situ hybridization to the identification of different marker chromosomes.. PubMed. 41(1). 5–10. 1 indexed citations
3.
Laverge, H, Josiane Van Der Elst, Petra De Sutter, et al.. (1998). Fluorescent in-situ hybridization on human embryos showing cleavage arrest after freezing and thawing. Human Reproduction. 13(2). 425–429. 31 indexed citations
4.
Laverge, H, Petra De Sutter, M.R. Verschraegen-Spae, Anne De Paepe, & Marc Dhont. (1997). Triple colour fluorescent in-situ hybridization for chromosomes X,Y and 1 on spare human embryos. Human Reproduction. 12(4). 809–814. 71 indexed citations
5.
Verschraegen-Spae, M.R., et al.. (1996). Mosaic tetrasomy 15q25→qter in a newborn infant with multiple anomalies. American Journal of Medical Genetics. 63(3). 482–485. 27 indexed citations
6.
Courtens, Winnie, Michael B. Petersen, J.C. Noël, et al.. (1994). Proximal deletion of chromosome 21 confirmed by in situ hybridization and molecular studies. American Journal of Medical Genetics. 51(3). 260–265. 32 indexed citations
7.
Depypere, Herman, et al.. (1993). Tubal hydatidiform mole. American Journal of Obstetrics and Gynecology. 169(1). 209–210. 15 indexed citations
8.
Verschraegen-Spae, M.R., et al.. (1993). Molecular cytogenetic characterization of marker chromosomes found at prenatal diagnosis. Prenatal Diagnosis. 13(5). 385–394. 14 indexed citations
9.
Speleman, Frank, Nadine Van Roy, M.R. Verschraegen-Spae, et al.. (1992). Detection of subtle reciprocal translocations by fluorescence in situ hybridization. Clinical Genetics. 41(4). 169–174. 33 indexed citations
10.
Quack, B, Nadine Van Roy, M.R. Verschraegen-Spae, & Franz Klein. (1992). Interstitial deletion and ring chromosome derived from 19q. Proximal 19q trisomy phenotype.. PubMed. 35(4). 241–4. 22 indexed citations
11.
12.
Farber, Claire‐Michèle, Michel Georges, Geertruida H. de Bock, et al.. (1989). Demonstration of spontaneous XX/XY chimerism by DNA fingerprinting. Human Genetics. 82(2). 197–198. 9 indexed citations
13.
Paepe, A. De, et al.. (1988). Familial meningioma. Clinical Neurology and Neurosurgery. 90(1). 61–63. 4 indexed citations
14.
Keyser, Filip De, et al.. (1988). Trisomy 3 mosaicism in a patient with Bartter syndrome.. Journal of Medical Genetics. 25(5). 358–358. 11 indexed citations
15.
Djalali, Mahmoud, et al.. (1986). The significance of pericentric inversions of chromosome 2. Human Genetics. 72(1). 32–36. 21 indexed citations
16.
Verschraegen-Spae, M.R., et al.. (1979). An immature stillbirth with lymphangiectasis and gonadal agenesis. European Journal of Obstetrics & Gynecology and Reproductive Biology. 9(5). 317–320. 1 indexed citations
17.
François, J., et al.. (1971). Tissue Culture Study of the Retinal Pigment Epithelium ofthe Adult Pig. Ophthalmic Research. 2(2). 86–95. 4 indexed citations
18.
François, J., et al.. (1971). Tissue Culture Studies of the Adult Pig Retina. Ophthalmic Research. 2(1). 25–36. 2 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by N. Gregson Breakdown of academic impact, for papers by Michael Freidine Breakdown of academic impact, for papers by D A Couzin Breakdown of academic impact, for papers by Sorrell H. Waxman Breakdown of academic impact, for papers by Stéphane Serero Breakdown of academic impact, for papers by Geneviève Lefort Breakdown of academic impact, for papers by Amelia Villa Breakdown of academic impact, for papers by Nicoletta Villa Breakdown of academic impact, for papers by M. Neil Macintyre Breakdown of academic impact, for papers by Nicole Joyé
Rankless by CCL
2026