M. Mannens

1.2k citations

30 papers · 836 · h-index 15

Impact in

Genetics top 10%
- Genetic Syndromes and Imprinting
- Genomic variations and chromosomal abnormalities
Pediatrics, Perinatology and Child Health top 5%
- Prenatal Screening and Diagnostics

Papers in

Molecular Biology 25
- Epigenetics and DNA Methylation 10
- Renal and related cancers 8
- RNA modifications and cancer 3
Genetics 17
- Genetic Syndromes and Imprinting 11
- Genomic variations and chromosomal abnormalities 4
- Genetic and Kidney Cyst Diseases 2

Co-authors: A. Westerveld (11 shared papers)Jet Bliek (8 shared papers)J.M.N. Hoovers (9 shared papers)Mariëlle Alders (8 shared papers)Marja Steenman (3 shared papers)Peter Little (5 shared papers)N. J. Leschot (3 shared papers)David J. Porteous (2 shared papers)
Journals: Genomics (6 papers)Cytogenetic and Genome Research (5 papers)Human Molecular Genetics (2 papers)European Journal of Human Genetics (2 papers)Genes Chromosomes and Cancer (2 papers)
Partner nations: Netherlands United Kingdom United States

In The Last Decade

M. Mannens

30 papers receiving 824 citations

Peers

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-authors

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

All Works

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#	Work
1	High-resolution localization of 69 potential human zinc finger protein genes: A number are clustered Genomics ·J.M.N. Hoovers, M. Mannens, Rosalind M. John, Jet Bliek, Veronica van Heyningen, David J. Porteous, N. J. Leschot, A. Westerveld, Peter Little	1992	114
2	Somatic Mosaicism for Partial Paternal Isodisomy in Wiedemann-Beckwith Syndrome: A Post-Fertilization Event European Journal of Human Genetics ·Isabelle Henry, Anne Puech, A. Riesewijk, L. Ahnine, M. Mannens, C. Beldjord, Pierre Bitoun, M F Tournade, P. Landrieu, Claudine Junien	1993	114
3	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 ·Mariëlle Alders, Matt Hodges, Anna‐Katerina Hadjantonakis, Jan Postmus, Inge van Wijk, Jet Bliek, Maurice de Meulemeester, A. Westerveld, François Guillemot, Cees B.M. Oudejans, Peter Little, M. Mannens	1997	69
4	A Dominant Negative Isoform of the Long QT Syndrome 1 Gene Product Journal of Biological Chemistry ·Sophie Demolombe, Isabelle Baró, Yann Péréon, Jet Bliek, Raha Mohammad-Panah, H. Pollard, Shabnam Morid, M. Mannens, Arthur A.M. Wilde, Jacques Barhanin, Flavien Charpentier, Denis Escande	1998	69
5	Properdin deficiency: molecular basis and disease association Molecular Immunology ·C. A. P. Fijen, R. van den Bogaard, M. Schipper, M. Mannens, M Schlesinger, Fredrikson G. Nordin, J. Dankert, Mohamed R. Daha, A.G. Sjöholm, Lennart Truedsson, Ed J. Kuijper	1999	63
6	Genetics of Beckwith‐Wiedemann syndrome‐associated tumors: Common genetic pathways Genes Chromosomes and Cancer ·Marja Steenman, A. Westerveld, M. Mannens	2000	62
7	Homozygous Premature Truncation of the HERG Protein Circulation ·Theo M. Hoorntje, Mariëlle Alders, J. Peter van Tintelen, K. Lip, Narayanswami Sreeram, Allard C. van der Wal, M. Mannens, Arthur A.M. Wilde	1999	49
8	High-Resolution Chromosomal Localization of the Human Calcitonin/CGRP/IAPP Gene Family Members Genomics ·J.M.N. Hoovers, E. Redeker, Frank Speleman, Jo W.M. Höppener, Shama L. Bhola, Jet Bliek, Nadine Van Roy, N. J. Leschot, A. Westerveld, M. Mannens	1993	29
9	Autosomal dominant aniridia linked to the chromosome 11p13 markers catalase and D11S151 in a large Dutch family Cytogenetic and Genome Research ·M. Mannens, E. M. Bleeker‐Wagemakers, Jet Bliek, J.M.N. Hoovers, Ingrid A.M. Mandjes, Simon Tol, R.R. Frants, Christa Heyting, A. Westerveld, Rosalyn Slater	1989	27
10	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 ·Peter Devilee, Maries van den Broek, M. Mannens, Rosalyn Slater, Cornelisse Cj, A. Westerveld, P. Meera Khan	1991	25
11	An Integrated Physical Map of 210 Markers Assigned to the Short Arm of Human Chromosome 11 Genomics ·E. Redeker, J.M.N. Hoovers, Mariëlle Alders, C.J.A. van Moorsel, Alasdair Ivens, Simon G. Gregory, Linda M. Kalikin, Jet Bliek, L. de Galan, R. van den Bogaard, Jenny A. Visser, Robbert van der Voort, Andrew P. Feinberg, Peter Little, A. Westerveld, M. Mannens	1994	23
12	Efficient Molecular Diagnostic Strategy for ABCC6 in Pseudoxanthoma Elasticum Genetic Testing ·Xiao Hu, Astrid S. Plomp, Theo G. M. F. Gorgels, Jacoline ten Brink, Willem J.P Loves, M. Mannens, Paulus T.V.M. de Jong, Arthur A. Bergen	2004	19
13	The distal region of 11p13 and associated genetic diseases Genomics ·M. Mannens, J.M.N. Hoovers, E. M. Bleeker‐Wagemakers, E. Redeker, Jet Bliek, M. Overbeeke-Melkert, G F Saunders, Bryan R.G. Williams, V. van Heynigen, Claudine Junien, Daniel A. Haber, Frank Speleman, Christa Heyting, Rosalyn Slater, N. J. Leschot, A. Westerveld	1991	19
14	Comparative genomic hybridization analysis of hepatoblastomas: additional evidence for a genetic link with Wilms tumor and rhabdomyosarcoma Cytogenetic and Genome Research ·Marja Steenman, Gail E. Tomlinson, A. Westerveld, M. Mannens	1999	18
15	Physical mapping of 3 candidate tumor suppressor genes relative to Beckwith-Wiedemann syndrome associated chromosomal breakpoints at 11p15.3 Cytogenetic and Genome Research ·E. Redeker, Mariëlle Alders, J.M.N. Hoovers, Charles W. Richard, A. Westerveld, M. Mannens	1995	18
16	Cytogenetic and molecular analysis of cellular atypical mesoblastic nephroma Genes Chromosomes and Cancer ·Frank Speleman, Eva van den Berg, Catharina Dhooge, Wolter Oosterhuis, B. Redeker, Christian R. De Potter, R. Y. J. Tamminga, Nadine Van Roy, M. Mannens	1998	14
17	Review Article: Genomic imprinting: concept and clinical consequences Annals of Medicine ·M. Mannens, Mariëlle Alders	1999	14
18	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 ·M. Andrew Nesbit, Matt Hodges, Louise J. Campbell, T.M.A.M.O. de Meulemeester, Mariëlle Alders, Nanda R. Rodrigues, Kevin Talbot, Aspasia Theodosiou, M. Mannens, Yoshihiko Nakamura, Peter Little, Kay E. Davies	1997	13
19	Detection of a cryptic paracentric inversion within band 11p13 in familial aniridia by fluorescence in situ hybridization Human Genetics ·Yoshimitsu Fukushima, J.M.N. Hoovers, M. Mannens, Keiko Wakui, Hirofumi Ohashi, Takuji Ohno, Yasuo Ueoka, Norio Niikawa	1993	12
20	Carrier detection by microsatellite haplotyping in 10 properdin type 1‐deficient families European Journal of Clinical Investigation ·C. A. P. Fijen, R. van den Bogaard, Mohamed R. Daha, J. Dankert, M. Mannens, Ed J. Kuijper	1996	11

About M. Mannens

M. Mannens is a scholar working on Molecular Biology, Genetics, Pediatrics, Perinatology and Child Health, Immunology and Pathology and Forensic Medicine, having authored 30 papers that have together received 836 indexed citations. Recurring topics across this work include Genetic Syndromes and Imprinting (11 papers), Epigenetics and DNA Methylation (10 papers), Renal and related cancers (8 papers), Prenatal Screening and Diagnostics (7 papers), Genomic variations and chromosomal abnormalities (4 papers), RNA modifications and cancer (3 papers), Genetic and Kidney Cyst Diseases (2 papers) and Complement system in diseases (2 papers). The work is most often cited by research in Genetics (314 citations), Pediatrics, Perinatology and Child Health (197 citations), Molecular Biology (595 citations), Cardiology and Cardiovascular Medicine (106 citations) and Cancer Research (62 citations). M. Mannens has collaborated with scholars based in Netherlands, United Kingdom and United States. Frequent 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. Their work appears in journals such as Genomics, Cytogenetic and Genome Research, Human Molecular Genetics, European Journal of Human Genetics and Genes Chromosomes and Cancer.

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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