Bert H.J. Eussen

3.2k citations

23 papers · 2.5k · 1 hit paper · h-index 12

Impact in

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

Papers in

Genetics 11
- Genomic variations and chromosomal abnormalities 8
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 2
- Genetics and Neurodevelopmental Disorders 2
Developmental Biology 2
- Congenital limb and hand anomalies 2

Co-authors: Annelies de Klein (7 shared papers)Émilie Brasset (1 shared paper)Bas van Steensel (1 shared paper)Lodewyk F.A. Wessels (1 shared paper)Wendy Talhout (1 shared paper)Ludo Pagie (1 shared paper)Wouter Meuleman (1 shared paper)Wouter L. de Laat (1 shared paper)
Journals: Journal of Medical Genetics (3 papers)The American Journal of Human Genetics (2 papers)European Journal of Medical Genetics (2 papers)Genomics (2 papers)Chromosome Research (1 paper)
Partner nations: Netherlands United States United Kingdom

In The Last Decade

Bert H.J. Eussen

23 papers receiving 2.4k 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 · 1.4k citations

What are hit papers?

Paper score: A paper's citations measured against the top-1% bar of its own field and year: the square root of citations ÷ bar, so 1 means right at the bar and 2 means four times its citations. The bar blends the citation counts that enter the top 1% of the paper's subfields in its year (weighted 89.5%), of those subfields over all years (0.5%) and of its year across all fields (10%); a subfield and year with fewer than 400 papers takes its year's bar. Papers from 2026 are not scored yet: in an unfinished year, when a paper appeared matters more than how it is cited.

Hit paper: A paper cited at least 1.5× the top-1% bar of its field and year: a paper score of at least √1.5.

2008 Nature

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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20 of 20 papers shown

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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 Boulos Faza, Wendy Talhout, Bert H.J. Eussen, Annelies de Klein Hit paper breakdown →	2008	1444
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	203
3	High-Throughput Analysis of Subtelomeric Chromosome Rearrangements by Use of Array-Based Comparative Genomic Hybridization The American Journal of Human Genetics ·Joris Andre Veltman, Eric Schoenmakers, Bert H.J. Eussen, Irene M. Janssen, Gerard F. M. Merkx, Brigitte van Cleef, Conny M.A. van Ravenswaaij‐Arts, Han G. Brunner	2002	174
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, Andy D.J. Pearson	2002	161
5	Molecular Cytogenetic Analysis of Eight Inversion Duplications of Human Chromosome 13q That Each Contain a Neocentromere The American Journal of Human Genetics ·Peter E. Warburton, Marisa Dolled, Radma Mahmood, Shulan Li, Kenji Naritomi, Takaya Tohma, Toshiro Nagai, Tomonobu Hasegawa	2000	97
6	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, Frans Schoute, Bert H.J. Eussen, Samantha J.L. Knight, Kay Elizabeth Davies	1994	68
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, Carrie Ris‐Stalpers +10 others	2000	58
8	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
9	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, Frank G. Grosveld, Chris I. De Zeeuw, Niels Galjart +1 other	1998	46
10	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 G. Papathomas, Francien H. van Nederveen, Eric J.T. Belt, Gaston J H Franssen	2015	46
11	A genome-wide copy number association study of osteoporotic fractures points to the 6p25.1 locus Journal of Medical Genetics ·Ling Oei, Yi‐Hsiang Hsu, Unnur Styrkársdóttir, Bert H.J. Eussen, Annelies de Klein, Marjolein J. Peters, Bjarni V. Halldórsson, Ching-ti Liu	2013	32
12	Large deletion causing the TSC2-PKD1 contiguous gene syndrome without infantile polycystic disease Journal of Medical Genetics ·Yvo Michiel Smulders, Bert H.J. Eussen, Senno Verhoef +1 other	2003	16
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	12
14	Submicroscopic Xpter deletion in a boy with growth and mental retardation caused by a familial t(X;14) American Journal of Medical Genetics ·de Vries Bj, Bert H.J. Eussen, Otto P. van Diggelen, Annet van der Heide, Wouter H. Deelen, Lutgarde C. P. Govaerts, Dick Lindhout, J. O. Van Hemel +1 other	1999	12
15	Identification of a gene on human chromosome 8q11 that is differentially expressed during prostate-cancer progression International Journal of Cancer ·Glenn T.G. Chang, Nita Tapsi, Martine Steenbeek, Leen J. Blok, Wytske M. van Weerden, Dirk C.J.G. van Alewijk, Bert H.J. Eussen, Gert Jan van Steenbrugge	1999	11
16	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, Robert A de Man, Diane Van Opstal, Annelies de Klein	2006	11
17	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 Elisabeth Hannema	2017	11
18	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
19	Large Deletion at the TSC1 Locus in a Family with Tuberous Sclerosis Complex Genetic Testing ·Mark D. Nellist, Őzgür Sancak, Miriam Goedbloed, Monique M. van Veghel–Plandsoen, Anneke Maat‐Kievit, Dick Lindhout, Bert H.J. Eussen, Annelies de Klein	2005	9
20	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, de Vries Bj, Ben A. Oostra, Esther de Graaff, Peter Heutink +1 other	2003	7

About Bert H.J. Eussen

Bert H.J. Eussen is a scholar working on Genetics, Developmental Biology, Developmental Neuroscience, Physiology and Orthopedics and Sports Medicine, having authored 23 papers that have together received 2.5k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (8 papers), Congenital limb and hand anomalies (2 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (2 papers), Prostate Cancer Treatment and Research (2 papers), Genetics and Neurodevelopmental Disorders (2 papers), Tuberous Sclerosis Complex Research (2 papers), Adrenal and Paraganglionic Tumors (1 paper) and Bone health and osteoporosis research (1 paper). The work is most often cited by research in Molecular Biology (1.4k citations), Genetics (501 citations), Developmental Neuroscience (38 citations), Developmental Biology (15 citations) and Cell Biology (84 citations). Bert H.J. Eussen has collaborated with scholars based in Netherlands, United States and United Kingdom. Frequent co-authors include Annelies de Klein, Émilie Brasset, Bas van Steensel, Lodewyk F.A. Wessels, Wendy Talhout, Ludo Pagie, Wouter Meuleman, Wouter L. de Laat, Marius Boulos Faza and Lars Guelen. Their work appears in journals such as Journal of Medical Genetics, The American Journal of Human Genetics, European Journal of Medical Genetics, Genomics and Chromosome Research.

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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In The Last Decade

Bert H.J. Eussen

Bert H.J. Eussen's Hit Papers

Peers

Countries citing papers authored by Bert H.J. Eussen

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

All Works

About Bert H.J. Eussen

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