Bert H.J. Eussen

3.2k citations

23 papers · 2.2k indexed · 1 hit paper · h-index 12

Molecular Biology top 5%
- Genomics and Chromatin Dynamics 5
- Congenital heart defects research 4
Genetics top 5%
- Genomic variations and chromosomal abnormalities 6
- Genetics and Neurodevelopmental Disorders 4
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 3
Aging
Plant Science top 10%
- Chromosomal and Genetic Variations 3
Cancer Research
Pediatrics, Perinatology and Child Health
- Prenatal Screening and Diagnostics 4
Physiology
- Tuberous Sclerosis Complex Research 3

Co-authors: Annelies de Klein Ludo Pagie Lodewyk F.A. Wessels Lars Guelen Wouter Meuleman Bas van Steensel Marius B. Faza Wendy Talhout
Cited by: Molecular Biology Genetics Aging
Journals: European Journal of Medical Genetics (2 papers)Journal of Medical Genetics (2 papers)Nature (2 papers)
Partner nations: Netherlands United States United Kingdom

In The Last Decade

Bert H.J. Eussen

23 papers receiving 2.2k citations

Hit Papers

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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-authorship network

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

#	Work
1	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,Guerrero Gullón,Sabine E Hannema,Arianne B. Dessens,Lambert C. J. Dorssers,Katharina Biermann,Remko Hersmus,Yolanda B. de Rijke,Leendert H. J. Looijenga	2017	9
2	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 ·Jeroen Knijnenburg,Marek Szymanowicz,Michael Beadle,Rianne Oostenbrink,Bert H.J. Eussen,Annelies de Klein,Alice S. Brooks,Laura J. C. M. van Zutven	2017	5
3	Complex MAX Rearrangement in a Family With Malignant Pheochromocytoma, Renal Oncocytoma, and Erythrocytosis The Journal of Clinical Endocrinology & Metabolism ·Esther Korpershoek,T. Yamashita,Bert H.J. Eussen,Lindsey Oudijk,Thomas Papathomas,Francien H. van Nederveen,Eric J.T. Belt,Gaston J H Franssen,David F. Restuccia,J. R. Bamberger,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	39
4	Implication of long-distance regulation of the HOXA cluster in a patient with postaxial polydactyly Chromosome Research ·Elisabeth M. Lodder,Bert H.J. Eussen,Michael Beadle,A. Jeannette M. Hoogeboom,Pino J. Poddighe,J. Henk Coert,Ben A. Oostra,Annelies de Klein,Esther de Graaff	2009	6
5	Domain organization of human chromosomes revealed by mapping of nuclear lamina interactionsbreakdown → 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	2008	1418
6	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,Willemijn Van Kol,Ron Hochstenbach,de Man,Diane Van Opstal,Annelies de Klein,Pino J. Poddighe	2006	8
7	Large Deletion at the TSC1 Locus in a Family with Tuberous Sclerosis Complex Genetic Testing ·Mark Nellist,Őzgür Sancak,Miriam Goedbloed,Xiancai Li,Anneke Maat‐Kievit,Dick Lindhout,Bert H.J. Eussen,Annelies de Klein,Dicky Halley,A.M.W. van den Ouweland	2005	8
8	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	172
9	Large deletion causing the TSC2-PKD1 contiguous gene syndrome without infantile polycystic disease Journal of Medical Genetics ·Heloísa Francini Braga,Bert H.J. Eussen,Senno Verhoef,Carine Wouters	2003	12
10	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,Carine Wouters,Ben A. Oostra,Esther de Graaff,Peter Heutink	2003	5
11	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,Yasuhiro Iwashita,Kevin Conlee,Han G. Brunner,Dominique Smeets,Ad Geurts van Kessel	2002	167
12	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,Julian Board,Andy D.J. Pearson,Anne De Paepe,Nadine Van Roy,Jo Vandesompele	2002	157
13	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,Majid Doulabi Ghorbani,Runlu Yang,Leen J. Blok,Wytske M. van Weerden,Belgrad,Bert H.J. Eussen,G.J. van Steenbrugge,Albert O. Brinkmann	2001	5
14	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	31
15	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,Nagaraj Shenoy,Amr Gadalla,Lutgarde Govaerts,Dick Lindhout,Carine Wouters,J. O. Van Hemel	1999	1
16	Submicroscopic Xpter deletion in a boy with growth and mental retardation caused by a familial t(X;14) American Journal of Medical Genetics ·Greta Celesti,Bert H.J. Eussen,Otto P. van Diggelen,Nagaraj Shenoy,Amr Gadalla,Lutgarde Govaerts,Dick Lindhout,Carine Wouters,J. O. Van Hemel	1999	12
17	Identification of a gene on human chromosome 8q11 that is differentially expressed during prostate-cancer progression International Journal of Cancer ·G T G Chang,Mantili Tania,Majid Doulabi Ghorbani,Leen J. Blok,Wytske M. van Weerden,Belgrad,Bert H.J. Eussen,G.J. van Steenbrugge,Albert O. Brinkmann	1999	11
18	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
19	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,Nagaraj Shenoy,Cardi van den Berg,Pieter In 'T Veld,Frans J. Los	1995	8
20	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

About Bert H.J. Eussen

Bert H.J. Eussen is a scholar working on Developmental Biology, Genetics, Developmental Neuroscience, Molecular Biology and Pediatrics, Perinatology and Child Health, having authored 23 papers that have together received 2.2k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (6 papers), Genomics and Chromatin Dynamics (5 papers), Prenatal Screening and Diagnostics (4 papers), Congenital heart defects research (4 papers), Genetics and Neurodevelopmental Disorders (4 papers), Tuberous Sclerosis Complex Research (3 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers) and Chromosomal and Genetic Variations (3 papers). The work is most often cited by research in Molecular Biology (1.7k citations), Genetics (572 citations), Aging (18 citations), Plant Science (355 citations) and Cancer Research (138 citations). Bert H.J. Eussen has collaborated with scholars based in Netherlands, United States and United Kingdom. Frequent 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. Their work appears in journals such as European Journal of Medical Genetics, Journal of Medical Genetics, Nature, Genomics and European Journal of Cancer.

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