Frank Baas

35.1k total citations · 5 hit papers
361 papers, 21.7k citations indexed

About

Frank Baas is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Neurology. According to data from OpenAlex, Frank Baas has authored 361 papers receiving a total of 21.7k indexed citations (citations by other indexed papers that have themselves been cited), including 161 papers in Molecular Biology, 90 papers in Cellular and Molecular Neuroscience and 73 papers in Neurology. Recurrent topics in Frank Baas's work include Hereditary Neurological Disorders (56 papers), RNA modifications and cancer (30 papers) and Neurological diseases and metabolism (28 papers). Frank Baas is often cited by papers focused on Hereditary Neurological Disorders (56 papers), RNA modifications and cancer (30 papers) and Neurological diseases and metabolism (28 papers). Frank Baas collaborates with scholars based in Netherlands, United States and United Kingdom. Frank Baas's co-authors include Piet Borst, Marcel Kool, Marcel de Haas, Rik J. Scheper, George L. Scheffer, Pieter A. Bolhuis, Wiep Scheper, Marianne de Visser, Antoine H. C. van Kampen and Jan J. M. de Vijlder and has published in prestigious journals such as Nature, Science and New England Journal of Medicine.

In The Last Decade

Frank Baas

356 papers receiving 21.2k citations

Hit Papers

Analysis of expression of cMOAT (MRP2), MRP3, MRP4, and M... 1994 2026 2004 2015 1997 1994 2001 1998 1999 200 400 600
What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

  1. Analysis of expression of cMOAT (MRP2), MRP3, MRP4, and MRP5, homologues of the multidrug resistance-associated protein gene (MRP1), in human cancer cell lines.
    1997 746 citations Marcel Kool, Marcel de Haas et al. PubMed profile →
  2. The human multidrug resistance-associated protein MRP is a plasma membrane drug-efflux pump.
    1994 592 citations G J Zaman, M J Flens et al. profile →
  3. The Human Transcriptome Map: Clustering of Highly Expressed Genes in Chromosomal Domains
    2001 571 citations Huib N. Caron, Barbera D. C. van Schaik et al. profile →
  4. Drug export activity of the human canalicular multispecific organic anion transporter in polarized kidney MDCK cells expressing cMOAT (MRP2) cDNA.
    1998 529 citations Marcel Kool, Frank Baas et al. profile →
  5. MRP3, an organic anion transporter able to transport anti-cancer drugs
    1999 521 citations Marcel Kool, Marcel de Haas et al. profile →

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Frank Baas Netherlands 79 9.4k 5.4k 3.9k 3.2k 2.4k 361 21.7k
Joachim Herz United States 95 15.9k 1.7× 4.3k 0.8× 5.2k 1.3× 1.9k 0.6× 576 0.2× 284 35.7k
V. Wee Yong Canada 100 10.0k 1.1× 3.7k 0.7× 4.4k 1.1× 4.4k 1.4× 596 0.3× 437 30.1k
Richard P. Lifton United States 92 20.6k 2.2× 2.1k 0.4× 1.8k 0.5× 1.1k 0.4× 1.6k 0.7× 276 35.1k
Paul van der Valk Netherlands 80 5.8k 0.6× 5.4k 1.0× 1.2k 0.3× 2.1k 0.7× 1.2k 0.5× 252 19.5k
Jeffrey Milbrandt United States 106 18.1k 1.9× 2.8k 0.5× 12.5k 3.2× 2.1k 0.7× 508 0.2× 297 34.7k
David R. Hinton United States 75 9.0k 1.0× 1.9k 0.4× 1.8k 0.5× 1.2k 0.4× 502 0.2× 386 20.8k
Ben A. Oostra Netherlands 61 6.8k 0.7× 765 0.1× 2.8k 0.7× 4.2k 1.3× 1.3k 0.6× 159 16.2k
Howard J. Federoff United States 69 8.2k 0.9× 1.6k 0.3× 4.2k 1.1× 2.6k 0.8× 266 0.1× 255 16.8k
Cedric S. Raine United States 88 8.5k 0.9× 4.2k 0.8× 4.2k 1.1× 3.3k 1.0× 469 0.2× 413 31.5k
George Kollias Greece 89 12.1k 1.3× 5.6k 1.0× 1.4k 0.4× 1.5k 0.5× 379 0.2× 306 30.3k

Countries citing papers authored by Frank Baas

Since Specialization
Citations

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

Fields of papers citing papers by Frank Baas

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Frank Baas

This figure shows the co-authorship network connecting the top 25 collaborators of Frank Baas. A scholar is included among the top collaborators of Frank Baas 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 Frank Baas. Frank Baas 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.
Harteveld, Cornelis L., Linda Vijfhuizen, Christian Babbs, et al.. (2024). Loss-of-Function Variants in SUPT5H as Modifying Factors in Beta-Thalassemia. International Journal of Molecular Sciences. 25(16). 8928–8928. 4 indexed citations
2.
Rutten, Julie W., Aat A. Mulder, Jeroen Vreijling, et al.. (2024). Bi-allelic NIT1 variants cause a brain small vessel disease characterized by movement disorders, massively dilated perivascular spaces, and intracerebral hemorrhage. Genetics in Medicine. 26(6). 101105–101105. 2 indexed citations
3.
Groot, Jurriaan H. de, Frank Baas, Marjon Stijntjes, et al.. (2023). Ankle-Foot-Orthosis “Hermes” Compensates Pathological Ankle Stiffness of Chronic Stroke—A Proof of Concept. IEEE Transactions on Neural Systems and Rehabilitation Engineering. 31. 3535–3544. 2 indexed citations
4.
Gravesteijn, Gido, Anne Hafkemeijer, Jeroen van der Grond, et al.. (2022). Effect of NOTCH3 EGFr Group, Sex, and Cardiovascular Risk Factors on CADASIL Clinical and Neuroimaging Outcomes. Stroke. 53(10). 3133–3144. 20 indexed citations
5.
Kleemann, Robert, Wim van Duyvenvoorde, Nanda Keijzer, et al.. (2022). Therapeutic Intervention with Anti-Complement Component 5 Antibody Does Not Reduce NASH but Does Attenuate Atherosclerosis and MIF Concentrations in Ldlr-/-.Leiden Mice. International Journal of Molecular Sciences. 23(18). 10736–10736. 9 indexed citations
6.
Devant, Pascal, Silvia Panizza, Tasos Gogakos, et al.. (2021). Assembly defects of human tRNA splicing endonuclease contribute to impaired pre-tRNA processing in pontocerebellar hypoplasia. Nature Communications. 12(1). 5610–5610. 29 indexed citations
7.
Kuitwaard, Krista, Pieter A. van Doorn, Wouter van Rijs, et al.. (2021). Genetic biomarkers for intravenous immunoglobulin response in chronic inflammatory demyelinating polyradiculoneuropathy. European Journal of Neurology. 28(5). 1677–1683. 8 indexed citations
8.
Gravesteijn, Gido, Johannes G. Dauwerse, Maurice Overzier, et al.. (2019). Naturally occurring NOTCH3 exon skipping attenuates NOTCH3 protein aggregation and disease severity in CADASIL patients. Human Molecular Genetics. 29(11). 1853–1863. 14 indexed citations
9.
Musters, Anne, Paul L. Klarenbeek, Marieke E. Doorenspleet, et al.. (2018). In Rheumatoid Arthritis, Synovitis at Different Inflammatory Sites Is Dominated by Shared but Patient-Specific T Cell Clones. The Journal of Immunology. 201(2). 417–422. 27 indexed citations
10.
Groen, J, Katja Ritz, Thomas T. Warner, Frank Baas, & Marina A.J. Tijssen. (2014). DRD1 rare variants associated with tardive-like dystonia: A pilot pathway sequencing study in dystonia. Parkinsonism & Related Disorders. 20(7). 782–785. 7 indexed citations
11.
Houten, Sander M., Simone Denis, Heleen te Brinke, et al.. (2014). Mitochondrial NADP(H) deficiency due to a mutation in NADK2 causes dienoyl-CoA reductase deficiency with hyperlysinemia. Human Molecular Genetics. 23(18). 5009–5016. 54 indexed citations
12.
Yick, Ching Yong, Aeilko H. Zwinderman, Peter W.A. Kunst, et al.. (2013). Transcriptome sequencing (RNA-Seq) of human endobronchial biopsies: asthmaversuscontrols. European Respiratory Journal. 42(3). 662–670. 65 indexed citations
13.
Boot, Erik, Jan Booij, Janneke Zinkstok, et al.. (2011). COMT Val158met genotype and striatal D2/3 receptor binding in adults with 22q11 deletion syndrome. Synapse. 65(9). 967–970. 16 indexed citations
14.
Nijholt, Diana A.T., Ana Osório Oliveira, Celia R. Berkers, et al.. (2011). Endoplasmic reticulum stress activates autophagy but not the proteasome in neuronal cells: implications for Alzheimer's disease. Cell Death and Differentiation. 18(6). 1071–1081. 110 indexed citations
15.
Laursen, Maria Bach, Malgorzata Maria Pakula, Shan Gao, et al.. (2010). Utilization of unlocked nucleic acid (UNA) to enhance siRNA performance in vitro and in vivo. Molecular BioSystems. 6(5). 862–870. 93 indexed citations
16.
Fluiter, Kees, Olaf R.F. Mook, Jeroen Vreijling, et al.. (2009). Filling the gap in LNAantisense oligo gapmers: the effects of unlocked nucleic acid (UNA) and 4′- C -hydroxymethyl-DNA modifications on RNase H recruitment and efficacy of an LNA gapmer. Molecular BioSystems. 5(8). 838–843. 36 indexed citations
17.
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
18.
Hasselt, Nancy E., Dirk Troost, Huib N. Caron, et al.. (2008). Molecular Risk Stratification of Medulloblastoma Patients Based on Immunohistochemical Analysis of MYC, LDHB, and CCNB1 Expression. Clinical Cancer Research. 14(13). 4154–4160. 41 indexed citations
19.
Kool, Marcel, Marcel de Haas, George L. Scheffer, et al.. (1997). Analysis of expression of cMOAT (MRP2), MRP3, MRP4, and MRP5, homologues of the multidrug resistance-associated protein gene (MRP1), in human cancer cell lines.. PubMed. 57(16). 3537–47. 746 indexed citations breakdown →
20.
Zaman, G J, Marcel de Haas, C. H. M. Versantvoort, et al.. (1995). Altered MRP is associated with multidrug resistance and reduced drug accumulation in human SW-1573 cells. British Journal of Cancer. 72(2). 298–306. 19 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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