M. Mannens

1.2k total citations
30 papers, 836 citations indexed

About

M. Mannens is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, M. Mannens has authored 30 papers receiving a total of 836 indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Molecular Biology, 17 papers in Genetics and 7 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in M. Mannens's work include Genetic Syndromes and Imprinting (11 papers), Epigenetics and DNA Methylation (10 papers) and Renal and related cancers (8 papers). M. Mannens is often cited by papers focused on Genetic Syndromes and Imprinting (11 papers), Epigenetics and DNA Methylation (10 papers) and Renal and related cancers (8 papers). M. Mannens collaborates with scholars based in Netherlands, United Kingdom and United States. M. Mannens's co-authors include A. Westerveld, Jet Bliek, J.M.N. Hoovers, Mariëlle Alders, Marja Steenman, Peter Little, N. J. Leschot, David J. Porteous, Veronica van Heyningen and Claudine Junien and has published in prestigious journals such as Journal of Biological Chemistry, Circulation and Human Molecular Genetics.

In The Last Decade

M. Mannens

30 papers receiving 824 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. Mannens Netherlands 15 595 314 197 106 78 30 836
Georg Klaus Hinkel Germany 17 498 0.8× 528 1.7× 107 0.5× 60 0.6× 167 2.1× 41 933
Cathy Holding United Kingdom 12 599 1.0× 180 0.6× 147 0.7× 44 0.4× 37 0.5× 38 878
Francesca Romana Lepri Italy 18 608 1.0× 429 1.4× 64 0.3× 58 0.5× 142 1.8× 62 972
Maia V. Ouspenskaia United States 14 622 1.0× 267 0.9× 99 0.5× 18 0.2× 45 0.6× 16 876
M. E. Robertson United Kingdom 9 457 0.8× 206 0.7× 68 0.3× 43 0.4× 56 0.7× 13 712
Anita Wischmeijer Italy 16 260 0.4× 333 1.1× 96 0.5× 50 0.5× 34 0.4× 29 622
K Imaizumi Japan 15 566 1.0× 404 1.3× 88 0.4× 26 0.2× 25 0.3× 27 885
Loydie A. Jerome‐Majewska Canada 17 979 1.6× 319 1.0× 144 0.7× 33 0.3× 60 0.8× 40 1.3k
Nicolette S. den Hollander Netherlands 21 510 0.9× 499 1.6× 409 2.1× 82 0.8× 469 6.0× 43 1.6k
Vincent Marion France 22 853 1.4× 876 2.8× 56 0.3× 89 0.8× 52 0.7× 42 1.5k

Countries citing papers authored by M. Mannens

Since Specialization
Citations

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

Fields of papers citing papers by M. Mannens

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of M. Mannens

This figure shows the co-authorship network connecting the top 25 collaborators of M. Mannens. A scholar is included among the top collaborators of M. Mannens 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. Mannens. M. Mannens 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.
Hu, Xiao, Astrid S. Plomp, Theo G. M. F. Gorgels, et al.. (2004). Efficient Molecular Diagnostic Strategy for ABCC6 in Pseudoxanthoma Elasticum. Genetic Testing. 8(3). 292–300. 19 indexed citations
2.
Steenman, Marja, Gail E. Tomlinson, A. Westerveld, & M. Mannens. (1999). Comparative genomic hybridization analysis of hepatoblastomas: additional evidence for a genetic link with Wilms tumor and rhabdomyosarcoma. Cytogenetic and Genome Research. 86(2). 157–161. 18 indexed citations
3.
Hoorntje, Theo M., Mariëlle Alders, J. Peter van Tintelen, et al.. (1999). Homozygous Premature Truncation of the HERG Protein. Circulation. 100(12). 1264–1267. 49 indexed citations
4.
Mannens, M. & Mariëlle Alders. (1999). Review Article: Genomic imprinting: concept and clinical consequences. Annals of Medicine. 31(1). 4–11. 14 indexed citations
5.
Fijen, C. A. P., M. Mannens, M Schlesinger, et al.. (1999). Properdin deficiency: molecular basis and disease association. Molecular Immunology. 36(13-14). 863–867. 63 indexed citations
6.
Demolombe, Sophie, Isabelle Baró, Yann Péréon, et al.. (1998). A Dominant Negative Isoform of the Long QT Syndrome 1 Gene Product. Journal of Biological Chemistry. 273(12). 6837–6843. 69 indexed citations
7.
Oudejans, Cees B.M., Bart A. Westerman, Andrea A.M. Könst, et al.. (1997). Growth regulation of extraembryonic tissues. European Journal of Obstetrics & Gynecology and Reproductive Biology. 75(1). 29–32. 2 indexed citations
8.
Alders, Mariëlle, Matt Hodges, Anna‐Katerina Hadjantonakis, et al.. (1997). The Human Achaete-Scute Homologue 2 (ASCL2, HASH2) Maps to Chromosome 11p15.5, Close to IGF2 and is Expressed in Extravillus Trophoblasts. Human Molecular Genetics. 6(6). 859–867. 69 indexed citations
9.
Nesbit, M. Andrew, Matt Hodges, Louise J. Campbell, et al.. (1997). Genomic Organization and Chromosomal Localization of a Member of the MAP Kinase Phosphatase Gene Family to Human Chromosome 11p15.5 and a Pseudogene to 10q11.2. Genomics. 42(2). 284–294. 13 indexed citations
10.
Fijen, C. A. P., et al.. (1996). Carrier detection by microsatellite haplotyping in 10 properdin type 1‐deficient families. European Journal of Clinical Investigation. 26(10). 902–906. 11 indexed citations
11.
Redeker, E., Mariëlle Alders, J.M.N. Hoovers, et al.. (1995). Physical mapping of 3 candidate tumor suppressor genes relative to Beckwith-Wiedemann syndrome associated chromosomal breakpoints at 11p15.3. Cytogenetic and Genome Research. 68(3-4). 222–225. 18 indexed citations
12.
Redeker, E., J.M.N. Hoovers, Mariëlle Alders, et al.. (1994). An Integrated Physical Map of 210 Markers Assigned to the Short Arm of Human Chromosome 11. Genomics. 21(3). 538–550. 23 indexed citations
13.
Henry, Isabelle, Veronica van Heyningen, Anne Puech, et al.. (1993). Reassessment of breakpoints in chromosome 11p15. Cytogenetic and Genome Research. 62(1). 52–53. 3 indexed citations
14.
Henry, Isabelle, Anne Puech, A. Riesewijk, et al.. (1993). Somatic Mosaicism for Partial Paternal Isodisomy in Wiedemann-Beckwith Syndrome: A Post-Fertilization Event. European Journal of Human Genetics. 1(1). 19–29. 114 indexed citations
15.
Hoovers, J.M.N., M. Mannens, Rosalind M. John, et al.. (1992). High-resolution localization of 69 potential human zinc finger protein genes: A number are clustered. Genomics. 12(2). 254–263. 114 indexed citations
16.
Ivens, Alasdair, J. D. Wilson, Simon G. Gregory, et al.. (1992). The generation of ordered sets of cosmid DNA clones from human chromosome region 11p. Genomics. 13(1). 89–94. 10 indexed citations
17.
Mannens, M., J.M.N. Hoovers, E. M. Bleeker‐Wagemakers, et al.. (1991). The distal region of 11p13 and associated genetic diseases. Genomics. 11(2). 284–293. 19 indexed citations
18.
Speleman, Frank, M. Mannens, B. Redeker, et al.. (1991). Characterization of a de novo duplication of 11p14→p13, using fluorescent in situ hybridization and Southern hybridization. Cytogenetic and Genome Research. 56(3-4). 129–131. 10 indexed citations
19.
Devilee, Peter, Maries van den Broek, M. Mannens, et al.. (1991). Differences in patterns of allelic loss between two common types of adult cancer, breast and colon carcinoma, and Wilms' tumor of childhood. International Journal of Cancer. 47(6). 817–821. 25 indexed citations
20.
Mannens, M., E. M. Bleeker‐Wagemakers, Jet Bliek, et al.. (1989). Autosomal dominant aniridia linked to the chromosome 11p13 markers catalase and D11S151 in a large Dutch family. Cytogenetic and Genome Research. 52(1-2). 32–36. 27 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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