Marja E. Jakobs

1.1k total citations
27 papers, 769 citations indexed

About

Marja E. Jakobs is a scholar working on Molecular Biology, Pediatrics, Perinatology and Child Health and Infectious Diseases. According to data from OpenAlex, Marja E. Jakobs has authored 27 papers receiving a total of 769 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 7 papers in Pediatrics, Perinatology and Child Health and 6 papers in Infectious Diseases. Recurrent topics in Marja E. Jakobs's work include Prenatal Screening and Diagnostics (7 papers), Parvovirus B19 Infection Studies (4 papers) and Genetic Syndromes and Imprinting (3 papers). Marja E. Jakobs is often cited by papers focused on Prenatal Screening and Diagnostics (7 papers), Parvovirus B19 Infection Studies (4 papers) and Genetic Syndromes and Imprinting (3 papers). Marja E. Jakobs collaborates with scholars based in Netherlands, Canada and Germany. Marja E. Jakobs's co-authors include Frank Baas, J.M.N. Hoovers, Lodewijk IJlst, Jos P.N. Ruiter, Ronald J. A. Wanders, Barbera D. C. van Schaik, Antoine H. C. van Kampen, Marian A. J. Weterman, Karl Seeger and Şule Ünal and has published in prestigious journals such as Journal of Clinical Investigation, Blood and PLoS ONE.

In The Last Decade

Marja E. Jakobs

27 papers receiving 756 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Marja E. Jakobs Netherlands 14 260 153 130 118 116 27 769
Carole L. Moncman United States 24 666 2.6× 82 0.5× 168 1.3× 76 0.6× 62 0.5× 44 1.4k
R. Thomas Taggart United States 12 508 2.0× 94 0.6× 140 1.1× 64 0.5× 16 0.1× 21 791
R. Adler United States 7 277 1.1× 101 0.7× 108 0.8× 37 0.3× 40 0.3× 11 609
A Meindl Germany 13 769 3.0× 166 1.1× 375 2.9× 14 0.1× 57 0.5× 33 1.4k
P. Couillin France 23 999 3.8× 141 0.9× 328 2.5× 114 1.0× 18 0.2× 60 1.5k
Erdmute Kunstmann Germany 17 430 1.7× 299 2.0× 219 1.7× 11 0.1× 21 0.2× 41 1.5k
Kenji Yoshida Japan 17 315 1.2× 331 2.2× 156 1.2× 48 0.4× 29 0.3× 32 1.1k
L. H. P. M. Rademakers Netherlands 17 165 0.6× 297 1.9× 77 0.6× 11 0.1× 52 0.4× 38 991
Brian D. Mariani United States 17 589 2.3× 57 0.4× 241 1.9× 33 0.3× 9 0.1× 27 1.2k
M. A. Ritter United Kingdom 18 270 1.0× 471 3.1× 85 0.7× 7 0.1× 47 0.4× 29 1.1k

Countries citing papers authored by Marja E. Jakobs

Since Specialization
Citations

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

Fields of papers citing papers by Marja E. Jakobs

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Marja E. Jakobs

This figure shows the co-authorship network connecting the top 25 collaborators of Marja E. Jakobs. A scholar is included among the top collaborators of Marja E. Jakobs 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 Marja E. Jakobs. Marja E. Jakobs 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.
Janes, Victoria A., Sébastien Matamoros, Patrick Munk, et al.. (2022). Metagenomic DNA sequencing for semi-quantitative pathogen detection from urine: a prospective, laboratory-based, proof-of-concept study. The Lancet Microbe. 3(8). e588–e597. 17 indexed citations
2.
Brands, Xanthe, Bastiaan W. Haak, Joe M. Butler, et al.. (2021). An epigenetic and transcriptomic signature of immune tolerance in human monocytes through multi-omics integration. Genome Medicine. 13(1). 15 indexed citations
3.
Akker, Erik B. van den, Marc Hulsman, Martijn H. Brugman, et al.. (2020). Dynamic clonal hematopoiesis and functional T-cell immunity in a supercentenarian. Leukemia. 35(7). 2125–2129. 11 indexed citations
4.
Janes, Victoria A., Daan W. Notermans, Ingrid J. B. Spijkerman, et al.. (2019). Amplified fragment length polymorphism and whole genome sequencing: a comparison of methods in the investigation of a nosocomial outbreak with vancomycin resistant enterococci. Antimicrobial Resistance and Infection Control. 8(1). 153–153. 6 indexed citations
5.
Piet, Jurgen R., Madelijn Geldhoff, Barbera D. C. van Schaik, et al.. (2013). Streptococcus pneumoniae Arginine Synthesis Genes Promote Growth and Virulence in Pneumococcal Meningitis. The Journal of Infectious Diseases. 209(11). 1781–1791. 21 indexed citations
6.
Mook, Olaf R.F., Martin A. Haagmans, Frank Baas, et al.. (2013). Targeted sequence capture and GS-FLX Titanium sequencing of 23 hypertrophic and dilated cardiomyopathy genes: implementation into diagnostics. Journal of Medical Genetics. 50(9). 614–626. 27 indexed citations
7.
Weterman, Marian A. J., Vincenzo Sorrentino, Paul R. Kasher, et al.. (2011). A frameshift mutation in LRSAM1 is responsible for a dominant hereditary polyneuropathy. Human Molecular Genetics. 21(2). 358–370. 46 indexed citations
8.
Vries, Michèl de, Martin Deijs, Marta Canuti, et al.. (2011). A Sensitive Assay for Virus Discovery in Respiratory Clinical Samples. PLoS ONE. 6(1). e16118–e16118. 64 indexed citations
9.
Ritz, Katja, Barbera D. C. van Schaik, Marja E. Jakobs, et al.. (2011). Looking ultra deep: Short identical sequences and transcriptional slippage. Genomics. 98(2). 90–95. 8 indexed citations
10.
Klarenbeek, Paul L., Paul P. Tak, Barbera D. C. van Schaik, et al.. (2010). Human T-cell memory consists mainly of unexpanded clones. Immunology Letters. 133(1). 42–48. 78 indexed citations
11.
Ritz, Katja, Barbera D. C. van Schaik, Marja E. Jakobs, et al.. (2010). SGCE isoform characterization and expression in human brain: implications for myoclonus–dystonia pathogenesis?. European Journal of Human Genetics. 19(4). 438–444. 61 indexed citations
12.
Kuijpers, Taco W., Edith van de Vijver, Marian A. J. Weterman, et al.. (2008). LAD-1/variant syndrome is caused by mutations in FERMT3. Blood. 113(19). 4740–4746. 160 indexed citations
13.
Vught, Paul W.J. van, Marja E. Jakobs, Jan H. Veldink, et al.. (2007). Ciliary neurotrophic factor null alleles are not a risk factor for Charcot-Marie-Tooth disease, hereditary neuropathy with pressure palsies and amyotrophic lateral sclerosis. Neuromuscular Disorders. 17(11-12). 964–967. 5 indexed citations
14.
Asbroek, Anneloor L.M.A. ten, et al.. (2002). Ribonuclease H1 Maps to Chromosome 2 and Has at Least Three Pseudogene Loci in the Human Genome. Genomics. 79(6). 818–823. 3 indexed citations
15.
Graaf, Irene M. de, et al.. (1999). Enrichment, identification and analysis of fetal cells from maternal blood: evaluation of a prenatal diagnosis system. Prenatal Diagnosis. 19(7). 648–652. 29 indexed citations
16.
Graaf, Irene M. de, Marja E. Jakobs, N. J. Leschot, et al.. (1999). First-trimester non-invasive prenatal diagnosis of triploidy. Prenatal Diagnosis. 19(2). 175–177. 8 indexed citations
17.
18.
Jakobs, Marja E., et al.. (1996). The application of microwave denaturation in comparative genomic hybridization. Genetic Analysis Biomolecular Engineering. 13(5). 129–133. 25 indexed citations
19.
Rens, W., Carel H. van Oven, Jan Stap, Marja E. Jakobs, & Jacob A. Aten. (1994). Slit‐scanning technique using standard cell sorter instruments for analyzing and sorting nonacrocentric human chromosomes, including small ones. Cytometry. 16(1). 80–87. 8 indexed citations
20.
Schuring‐Blom, G. Heleen, et al.. (1993). Molecular cytogenetic analysis of term placentae suspected of mosaicism using fluorescence in situ hybridization. Prenatal Diagnosis. 13(8). 671–679. 22 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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