Bert H.J. Eussen

3.3k citations

23 papers · 2.4k · 1 hit paper · h-index 12

Impact in

Molecular Biology top 5%
- Genomics and Chromatin Dynamics
- RNA Research and Splicing
- Nuclear Structure and Function
- Epigenetics and DNA Methylation
- RNA modifications and cancer
Genetics top 5%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders

Papers in

Molecular Biology 15
- Genomics and Chromatin Dynamics 5
- Congenital heart defects research 4
Genetics 15
- Genomic variations and chromosomal abnormalities 6
- Genetics and Neurodevelopmental Disorders 4
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 3

Co-authors: Annelies de Klein (8 shared papers)Marius B. Faza (2 shared papers)Wouter Meuleman (2 shared papers)Ludo Pagie (2 shared papers)Émilie Brasset (2 shared papers)Wouter de Laat (2 shared papers)Lars Guelen (2 shared papers)Bas van Steensel (2 shared papers)
Journals: Genomics (2 papers)Journal of Medical Genetics (2 papers)Nature (2 papers)European Journal of Medical Genetics (2 papers)The American Journal of Human Genetics (1 paper)
Partner nations: Netherlands United States United Kingdom

In The Last Decade

Bert H.J. Eussen

23 papers receiving 2.3k citations

Bert H.J. Eussen's Hit Papers

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Domain organization of human chromosomes revealed by mapping of nuclear lamina interactions 2008 · 1.5k citations

Peers

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-authors

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

All Works

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#	Work
1	Domain organization of human chromosomes revealed by mapping of nuclear lamina interactions Nature ·Lars Guelen, Ludo Pagie, Émilie Brasset, Wouter Meuleman, Marius B. Faza, Wendy Talhout, Bert H.J. Eussen, Annelies de Klein, Lodewyk F.A. Wessels, Wouter de Laat, Bas van Steensel Hit paper breakdown →	2008	1474
2	Cntnap2 is disrupted in a family with gilles de la tourette syndrome and obsessive compulsive disorder Genomics ·Annemieke J.M.H. Verkerk, Carol A. Mathews, Marijke Joosse, Bert H.J. Eussen, Peter Heutink, Ben A. Oostra	2003	191
3	High-Throughput Analysis of Subtelomeric Chromosome Rearrangements by Use of Array-Based Comparative Genomic Hybridization The American Journal of Human Genetics ·Joris A. Veltman, Eric Schoenmakers, Bert H.J. Eussen, Irene M. Janssen, Gerard Merkx, Brigitte van Cleef, Conny Ma van Ravenswaaij, Han G. Brunner, Dominique Smeets, Ad Geurts van Kessel	2002	173
4	Quantification of MYCN, DDX1, and NAG Gene Copy Number in Neuroblastoma Using a Real-Time Quantitative PCR Assay Modern Pathology ·Katleen De Preter, Frank Speleman, Valérie Combaret, John Lunec, Geneviève Laureys, Bert H.J. Eussen, Nadine Francotte, (unknown), Andy D.J. Pearson, Anne De Paepe, Nadine Van Roy, Jo Vandesompele	2002	158
5	Segregation of FRAXE in a large family: clinical, psychometric, cytogenetic, and molecular data. PubMed ·Ben C.J. Hamel, Apt Smits, Esther de Graaff, D F Smeets, F. Schoute, Bert H.J. Eussen, Samantha J.L. Knight, Kay E. Davies, Claire F.C.H. Assman‐Hulsmans, B. A. Oostra	1994	67
6	Expression of differentiation-related genes in colorectal cancer: possible implications for prognosis. PubMed ·Nico van Belzen, Winand N.M. Dinjens, Bert H.J. Eussen, Fred T. Bosman	1998	54
7	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 ·Bert H.J. Eussen, (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown)	2000	48
8	The MurineCYLN2Gene: Genomic Organization, Chromosome Localization, and Comparison to the Human Gene That Is Located within the 7q11.23 Williams Syndrome Critical Region Genomics ·Casper C. Hoogenraad, Bert H.J. Eussen, An Langeveld, Rien van Haperen, Suzanne Winterberg, (unknown), Frank Grosveld, Chris I. De Zeeuw, Niels Galjart	1998	41
9	Complex MAX Rearrangement in a Family With Malignant Pheochromocytoma, Renal Oncocytoma, and Erythrocytosis The Journal of Clinical Endocrinology & Metabolism ·Esther Korpershoek, Djamailys Koffy, Bert H.J. Eussen, Lindsey Oudijk, Thomas Papathomas, Francien H. van Nederveen, Eric J.T. Belt, Gaston J H Franssen, David F. Restuccia, Niels M. G. Krol, Rob B. van der Luijt, Richard A. Feelders, Rogier A. Oldenburg, Wilfred F. J. van IJcken, Annelies de Klein, Wouter W. de Herder, Ronald R. de Krijger, Winand N.M. Dinjens	2015	40
10	Large deletion causing the TSC2-PKD1 contiguous gene syndrome without infantile polycystic disease Journal of Medical Genetics ·Y.M. Smulders, Bert H.J. Eussen, Senno Verhoef, Carine Wouters	2003	13
11	Submicroscopic Xpter deletion in a boy with growth and mental retardation caused by a familial t(X;14) American Journal of Medical Genetics ·Bert B.A. de Vries, Bert H.J. Eussen, Otto P. van Diggelen, Annet van der Heide, Wouter H. Deelen, Lutgarde Govaerts, Dick Lindhout, (unknown), J. O. Van Hemel	1999	12
12	Multiparameter Investigation of a 46,XX/46,XY Tetragametic Chimeric Phenotypical Male Patient with Bilateral Scrotal Ovotestes and Ovulatory Activity Sexual Development ·Yolande van Bever, Katja P. Wolffenbuttel, Hennie T. Brüggenwirth, Eric Blom, Annelies de Klein, Bert H.J. Eussen, Florijn van der Windt, Sabine E Hannema, Arianne B. Dessens, Lambert C. J. Dorssers, Katharina Biermann, Remko Hersmus, Yolanda B. de Rijke, Leendert H. J. Looijenga	2017	11
13	Limited size of the fragile X site shown by fluorescence in situ hybridization American Journal of Medical Genetics ·Annemieke J.M.H. Verkerk, Bert H.J. Eussen, J. O. Van Hemel, Ben A. Oostra	1992	11
14	Identification of a gene on human chromosome 8q11 that is differentially expressed during prostate-cancer progression International Journal of Cancer ·G T G Chang, Nita Tapsi, Martine Steenbeek, Leen J. Blok, Wytske M. van Weerden, Dirk C.J.G. van Alewijk, Bert H.J. Eussen, G.J. van Steenbrugge, Albert O. Brinkmann	1999	11
15	Large Deletion at the TSC1 Locus in a Family with Tuberous Sclerosis Complex Genetic Testing ·Mark Nellist, Őzgür Sancak, Miriam Goedbloed, Monique van Veghel‐Plandsoen, Anneke Maat‐Kievit, Dick Lindhout, Bert H.J. Eussen, Annelies de Klein, Dicky Halley, A.M.W. van den Ouweland	2005	9
16	A chromosome 21‐specific cosmid cocktail for the detection of chromosome 21 aberrations in interphase nuclei Prenatal Diagnosis ·Diane Van Opstal, J. O. Van Hemel, Bert H.J. Eussen, Annet van der Heide, Cardi van den Berg, Pieter In 'T Veld, Frans J. Los	1995	9
17	A familial inverted duplication 2q33–q34 identified and delineated by multiple cytogenetic techniques European Journal of Medical Genetics ·Bert H.J. Eussen, Ingrid M.B.H. van de Laar, Hannie Douben, Leo van Kempen, Ron Hochstenbach, de Man, Diane Van Opstal, Annelies de Klein, Pino J. Poddighe	2006	9
18	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 ·Robert‐Jan H. Galjaard, Herma C. van der Linde, Bert H.J. Eussen, Bert B.A. de Vries, (unknown), Ben A. Oostra, Esther de Graaff, Peter Heutink	2003	7
19	Implication of long-distance regulation of the HOXA cluster in a patient with postaxial polydactyly Chromosome Research ·Elisabeth M. Lodder, Bert H.J. Eussen, Daniella A.C.M. van Hassel, A. Jeannette M. Hoogeboom, Pino J. Poddighe, J. Henk Coert, Ben A. Oostra, Annelies de Klein, Esther de Graaff	2009	6
20	A novel gene on human chromosome 2p24 is differentially expressed between androgen-dependent and androgen-independent prostate cancer cells European Journal of Cancer ·G T G Chang, Martine Steenbeek, Esther C. F. Schippers, Leen J. Blok, Wytske M. van Weerden, Dirk C.J.G. van Alewijk, Bert H.J. Eussen, G.J. van Steenbrugge, Albert O. Brinkmann	2001	5

About Bert H.J. Eussen

Bert H.J. Eussen is a scholar working on Molecular Biology, Genetics, Pediatrics, Perinatology and Child Health, Physiology and Plant Science, having authored 23 papers that have together received 2.4k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (6 papers), Genomics and Chromatin Dynamics (5 papers), Genetics and Neurodevelopmental Disorders (4 papers), Congenital heart defects research (4 papers), Prenatal Screening and Diagnostics (4 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers), Chromosomal and Genetic Variations (3 papers) and Tuberous Sclerosis Complex Research (3 papers). The work is most often cited by research in Molecular Biology (1.7k citations), Genetics (567 citations), Aging (18 citations), Developmental Neuroscience (38 citations) and Developmental Biology (20 citations). Bert H.J. Eussen has collaborated with scholars based in Netherlands, United States and United Kingdom. Frequent co-authors include Annelies de Klein, Marius B. Faza, Wouter Meuleman, Ludo Pagie, Émilie Brasset, Wouter de Laat, Lars Guelen, Bas van Steensel, Lodewyk F.A. Wessels and Wendy Talhout. Their work appears in journals such as Genomics, Journal of Medical Genetics, Nature, European Journal of Medical Genetics and The American Journal of Human Genetics.

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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Bert H.J. Eussen

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