Bert H.J. Eussen

3.2k total citations · 1 hit paper
23 papers, 2.2k citations indexed

About

Bert H.J. Eussen is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Bert H.J. Eussen has authored 23 papers receiving a total of 2.2k indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 15 papers in Genetics and 4 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Bert H.J. Eussen's work include Genomic variations and chromosomal abnormalities (6 papers), Genomics and Chromatin Dynamics (5 papers) and Prenatal Screening and Diagnostics (4 papers). Bert H.J. Eussen is often cited by papers focused on Genomic variations and chromosomal abnormalities (6 papers), Genomics and Chromatin Dynamics (5 papers) and Prenatal Screening and Diagnostics (4 papers). Bert H.J. Eussen collaborates with scholars based in Netherlands, United States and United Kingdom. Bert H.J. Eussen's co-authors include Annelies de Klein, Ludo Pagie, Lodewyk F.A. Wessels, Lars Guelen, Wouter Meuleman, Bas van Steensel, Marius B. Faza, Wendy Talhout, Wouter de Laat and Émilie Brasset and has published in prestigious journals such as Nature, The Journal of Clinical Endocrinology & Metabolism and The American Journal of Human Genetics.

In The Last Decade

Bert H.J. Eussen

23 papers receiving 2.2k citations

Hit Papers

align trajectories

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.

Domain organization of human chromosomes revealed by mapping of nuclear lamina interactions

2008 1.4k citations Lars Guelen, Ludo Pagie et al. Nature profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Bert H.J. Eussen Netherlands	12	1.7k	572	355	138	132	23	2.2k
Peter M. Kroisel Austria	16	935 0.5×	658 1.2×	172 0.5×	65 0.5×	85 0.6×	38	1.5k
Peter J. Skene United States	14	2.7k 1.5×	757 1.3×	284 0.8×	224 1.6×	95 0.7×	22	3.1k
H H Kazazian United States	32	1.7k 1.0×	857 1.5×	195 0.5×	71 0.5×	92 0.7×	64	3.2k
Willy M. Nillesen Netherlands	23	1.3k 0.7×	1.3k 2.2×	247 0.7×	135 1.0×	53 0.4×	42	2.2k
Elaine R. Levy United Kingdom	19	860 0.5×	857 1.5×	224 0.6×	93 0.7×	65 0.5×	34	1.6k
Maria Antonietta Mencarelli Italy	26	982 0.6×	1.2k 2.1×	110 0.3×	99 0.7×	71 0.5×	65	1.9k
Guy Froyen Belgium	27	1.6k 0.9×	1.6k 2.8×	266 0.7×	208 1.5×	162 1.2×	85	2.8k
Angela Maria Vianna‐Morgante Brazil	27	1.3k 0.8×	1.7k 3.0×	452 1.3×	118 0.9×	92 0.7×	108	2.3k
Giuseppe Pilia United States	23	2.0k 1.1×	1.5k 2.6×	151 0.4×	129 0.9×	321 2.4×	41	2.9k
Shutao Cai United States	9	1.5k 0.9×	556 1.0×	142 0.4×	117 0.8×	52 0.4×	12	1.8k

Countries citing papers authored by Bert H.J. Eussen

Since Specialization

Citations

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

Fields of papers citing papers by Bert H.J. Eussen

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Bert H.J. Eussen. 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 Bert H.J. Eussen. The network helps show where Bert H.J. Eussen may publish in the future.

Co-authorship network of co-authors of Bert H.J. Eussen

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

All Works

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20 of 20 papers shown

Bever, Yolande van, Katja P. Wolffenbuttel, Hennie T. Brüggenwirth, et al.. (2017). Multiparameter Investigation of a 46,XX/46,XY Tetragametic Chimeric Phenotypical Male Patient with Bilateral Scrotal Ovotestes and Ovulatory Activity. Sexual Development. 12(1-3). 145–154. 9 indexed citations

Knijnenburg, Jeroen, Rianne Oostenbrink, Bert H.J. Eussen, et al.. (2017). Postzygotic telomere capture causes segmental UPD, duplication and deletion of chromosome 8p in a patient with intellectual disability and obesity. European Journal of Medical Genetics. 60(9). 445–450. 5 indexed citations

Korpershoek, Esther, Bert H.J. Eussen, Lindsey Oudijk, et al.. (2015). Complex MAX Rearrangement in a Family With Malignant Pheochromocytoma, Renal Oncocytoma, and Erythrocytosis. The Journal of Clinical Endocrinology & Metabolism. 101(2). 453–460. 39 indexed citations

Lodder, Elisabeth M., Bert H.J. Eussen, A. Jeannette M. Hoogeboom, et al.. (2009). Implication of long-distance regulation of the HOXA cluster in a patient with postaxial polydactyly. Chromosome Research. 17(6). 737–44. 6 indexed citations

Guelen, Lars, Ludo Pagie, Émilie Brasset, et al.. (2008). Domain organization of human chromosomes revealed by mapping of nuclear lamina interactions. Nature. 453(7197). 948–951. 1418 indexed citations breakdown →

Eussen, Bert H.J., Ingrid M.B.H. van de Laar, Hannie Douben, et al.. (2006). A familial inverted duplication 2q33–q34 identified and delineated by multiple cytogenetic techniques. European Journal of Medical Genetics. 50(2). 112–119. 8 indexed citations

Nellist, Mark, Őzgür Sancak, Miriam Goedbloed, et al.. (2005). Large Deletion at the TSC1 Locus in a Family with Tuberous Sclerosis Complex. Genetic Testing. 9(3). 226–230. 8 indexed citations

Verkerk, Annemieke J.M.H., Carol A. Mathews, Marijke Joosse, et al.. (2003). Cntnap2 is disrupted in a family with gilles de la tourette syndrome and obsessive compulsive disorder. Genomics. 82(1). 1–9. 172 indexed citations

Eussen, Bert H.J., et al.. (2003). Large deletion causing the TSC2-PKD1 contiguous gene syndrome without infantile polycystic disease. Journal of Medical Genetics. 40(2). e17–e17. 12 indexed citations

10.

Galjaard, Robert‐Jan H., Herma C. van der Linde, Bert H.J. Eussen, et al.. (2003). Isolated postaxial polydactyly type B with mosaicism of a submicroscopic unbalanced translocation leading to an extended phenotype in offspring. American Journal of Medical Genetics Part A. 121A(2). 168–173. 5 indexed citations

11.

Veltman, Joris A., Eric Schoenmakers, Bert H.J. Eussen, et al.. (2002). High-Throughput Analysis of Subtelomeric Chromosome Rearrangements by Use of Array-Based Comparative Genomic Hybridization. The American Journal of Human Genetics. 70(5). 1269–1276. 167 indexed citations

12.

Preter, Katleen De, Frank Speleman, Valérie Combaret, et al.. (2002). Quantification of MYCN, DDX1, and NAG Gene Copy Number in Neuroblastoma Using a Real-Time Quantitative PCR Assay. Modern Pathology. 15(2). 159–166. 157 indexed citations

13.

Chang, G T G, Leen J. Blok, Wytske M. van Weerden, et al.. (2001). A novel gene on human chromosome 2p24 is differentially expressed between androgen-dependent and androgen-independent prostate cancer cells. European Journal of Cancer. 37(16). 2129–2134. 5 indexed citations

14.

Eussen, Bert H.J., et al.. (2000). An unbalanced submicroscopic translocation t(8;16)(q24.3;p13.3)pat associated with tuberous sclerosis complex, adult polycystic kidney disease, and hypomelanosis of Ito. Journal of Medical Genetics. 37(4). 287–291. 31 indexed citations

15.

Vries, Bert B.A. de, Bert H.J. Eussen, Otto P. van Diggelen, et al.. (1999). Submicroscopic Xpter deletion in a boy with growth and mental retardation caused by a familial t(X;14). American Journal of Medical Genetics. 87(2). 189–194. 1 indexed citations

16.

Eussen, Bert H.J., Otto P. van Diggelen, Lutgarde Govaerts, et al.. (1999). Submicroscopic Xpter deletion in a boy with growth and mental retardation caused by a familial t(X;14). American Journal of Medical Genetics. 87(2). 189–194. 12 indexed citations

17.

Chang, G T G, Leen J. Blok, Wytske M. van Weerden, et al.. (1999). Identification of a gene on human chromosome 8q11 that is differentially expressed during prostate-cancer progression. International Journal of Cancer. 83(4). 506–511. 11 indexed citations

18.

Belzen, Nico van, Winand N.M. Dinjens, Bert H.J. Eussen, & Fred T. Bosman. (1998). Expression of differentiation-related genes in colorectal cancer: possible implications for prognosis.. PubMed. 13(4). 1233–42. 54 indexed citations

19.

Opstal, Diane Van, J. O. Van Hemel, Bert H.J. Eussen, et al.. (1995). A chromosome 21‐specific cosmid cocktail for the detection of chromosome 21 aberrations in interphase nuclei. Prenatal Diagnosis. 15(8). 705–711. 8 indexed citations

20.

Verkerk, Annemieke J.M.H., Bert H.J. Eussen, J. O. Van Hemel, & Ben A. Oostra. (1992). Limited size of the fragile X site shown by fluorescence in situ hybridization. American Journal of Medical Genetics. 43(1-2). 187–191. 11 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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