A. Bardoel

1.6k total citations
14 papers, 1.3k citations indexed

About

A. Bardoel is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, A. Bardoel has authored 14 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Genetics, 6 papers in Molecular Biology and 4 papers in Surgery. Recurrent topics in A. Bardoel's work include Genomic variations and chromosomal abnormalities (3 papers), Cancer Genomics and Diagnostics (3 papers) and Connective tissue disorders research (2 papers). A. Bardoel is often cited by papers focused on Genomic variations and chromosomal abnormalities (3 papers), Cancer Genomics and Diagnostics (3 papers) and Connective tissue disorders research (2 papers). A. Bardoel collaborates with scholars based in Netherlands, France and Australia. A. Bardoel's co-authors include Cisca Wijmenga, Peter Devilee, Cees J. Cornelisse, Johan M. TeKoppele, Hans E. H. Pruijs, Ruud A. Bank, Lodewijk A. Sandkuijl, P. Pearson, Anne‐Marie Zuurmond and Jürgen Brinckmann and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Gastroenterology.

In The Last Decade

A. Bardoel

14 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
A. Bardoel Netherlands 13 466 461 326 301 169 14 1.3k
Rein P. Stulp Netherlands 14 405 0.9× 767 1.7× 544 1.7× 167 0.6× 228 1.3× 20 1.8k
José M. de Campos Spain 30 150 0.3× 985 2.1× 320 1.0× 514 1.7× 116 0.7× 77 2.3k
Michael S. Kobrin United States 29 309 0.7× 1.6k 3.4× 373 1.1× 459 1.5× 144 0.9× 37 2.8k
Naoki Maehara Japan 23 137 0.3× 780 1.7× 340 1.0× 367 1.2× 137 0.8× 85 1.8k
Jeff Stevens United States 10 154 0.3× 723 1.6× 135 0.4× 116 0.4× 209 1.2× 19 2.1k
Marja Nissinen Finland 14 358 0.8× 1.2k 2.5× 151 0.5× 49 0.2× 228 1.3× 19 2.2k
Lorin E. Olson United States 19 222 0.5× 833 1.8× 202 0.6× 156 0.5× 88 0.5× 31 1.6k
Kerry Mullaney United States 13 76 0.2× 463 1.0× 176 0.5× 362 1.2× 269 1.6× 24 1.5k
Laura Papi Italy 25 706 1.5× 1.2k 2.5× 610 1.9× 374 1.2× 641 3.8× 68 3.2k
Deborah E. Schofield United States 21 121 0.3× 822 1.8× 202 0.6× 178 0.6× 462 2.7× 46 1.6k

Countries citing papers authored by A. Bardoel

Since Specialization
Citations

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

Fields of papers citing papers by A. Bardoel

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of A. Bardoel

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

All Works

14 of 14 papers shown
1.
Hoogendoorn, Mechteld L.C., Ruben van’t Slot, A. Bardoel, et al.. (2007). An association screen of myelin-related genes implicates the chromosome 22q11 PIK4CA gene in schizophrenia. Molecular Psychiatry. 13(11). 1060–1068. 86 indexed citations
2.
Ruigrok, Ynte M., et al.. (2005). Genes and outcome after aneurysmal subarachnoid haemorrhage. Journal of Neurology. 252(4). 417–422. 30 indexed citations
3.
Belzen, Martine J. van, Bobby P. C. Koeleman, J. Bart A. Crusius, et al.. (2004). Defining the contribution of the HLA region to cis DQ2-positive coeliac disease patients. Genes and Immunity. 5(3). 215–220. 49 indexed citations
4.
5.
Zuurmond, Anne‐Marie, A. Bardoel, Cisca Wijmenga, et al.. (2003). Identification of PLOD2 as Telopeptide Lysyl Hydroxylase, an Important Enzyme in Fibrosis. Journal of Biological Chemistry. 278(42). 40967–40972. 311 indexed citations
6.
Bovée, Judith V.M.G., Martin E. van Royen, A. Bardoel, et al.. (2000). Near-Haploidy and Subsequent Polyploidization Characterize the Progression of Peripheral Chondrosarcoma. American Journal Of Pathology. 157(5). 1587–1595. 54 indexed citations
7.
Bank, Ruud A., Simon P. Robins, Cisca Wijmenga, et al.. (1999). Defective collagen crosslinking in bone, but not in ligament or cartilage, in Bruck syndrome: Indications for a bone-specific telopeptide lysyl hydroxylase on chromosome 17. Proceedings of the National Academy of Sciences. 96(3). 1054–1058. 145 indexed citations
8.
Heutink, Peter, Evert M. van Schothorst, A. Bardoel, et al.. (1994). Further Localization of the Genefor Hereditary Paragangliomasand Evidence for Linkage inUnrelated Families. European Journal of Human Genetics. 2(3). 148–158. 56 indexed citations
9.
Devilee, Peter, Evert M. van Schothorst, A. Bardoel, et al.. (1994). Allelotype of head and neck paragangliomas: Allelic imbalance is confined to the long arm of chromosome 11, the site of the predisposing locus PGL. Genes Chromosomes and Cancer. 11(2). 71–78. 53 indexed citations
10.
Gruis, Nelleke A., et al.. (1993). PCR-based microsatellite polymorphisms in the detection of loss of heterozygosity in fresh and archival tumour tissue. British Journal of Cancer. 68(2). 308–313. 59 indexed citations
11.
Devilee, Peter, et al.. (1993). Allele loss patterns on chromosome 17q in 109 breast carcinomas indicate at least two distinct target regions.. PubMed. 8(3). 781–5. 50 indexed citations
12.
Devilee, Peter, Aart H. Bootsma, A. Bardoel, et al.. (1993). Linkage to markers for the chromosome region 17q12-q21 in 13 Dutch breast cancer kindreds.. PubMed. 52(4). 730–5. 12 indexed citations
13.
Heutink, Peter, Andel G. L. van der Mey, Lodewijk A. Sandkuijl, et al.. (1992). A gene subject to genomic imprinting and responsible for hereditary paragangliomas maps to chromosome 11q23-qter. Human Molecular Genetics. 1(1). 7–10. 168 indexed citations
14.
Devilee, Peter, A. Bardoel, Tim Kievits, et al.. (1991). Frequent somatic imbalance of marker alleles for chromosome 1 in human primary breast carcinoma.. PubMed. 51(3). 1020–5. 91 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 Rein P. Stulp Breakdown of academic impact, for papers by José M. de Campos Breakdown of academic impact, for papers by Michael S. Kobrin Breakdown of academic impact, for papers by Naoki Maehara Breakdown of academic impact, for papers by Jeff Stevens Breakdown of academic impact, for papers by Marja Nissinen Breakdown of academic impact, for papers by Lorin E. Olson Breakdown of academic impact, for papers by Kerry Mullaney Breakdown of academic impact, for papers by Laura Papi Breakdown of academic impact, for papers by Deborah E. Schofield
Rankless by CCL
2026