H. J. Eussen

635 total citations
10 papers, 415 citations indexed

About

H. J. Eussen is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, H. J. Eussen has authored 10 papers receiving a total of 415 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Genetics, 4 papers in Molecular Biology and 3 papers in Surgery. Recurrent topics in H. J. Eussen's work include Genomic variations and chromosomal abnormalities (5 papers), Prenatal Screening and Diagnostics (3 papers) and RNA modifications and cancer (2 papers). H. J. Eussen is often cited by papers focused on Genomic variations and chromosomal abnormalities (5 papers), Prenatal Screening and Diagnostics (3 papers) and RNA modifications and cancer (2 papers). H. J. Eussen collaborates with scholars based in Netherlands, United States and Belgium. H. J. Eussen's co-authors include J. O. Van Hemel, Carine Wouters, Annelies de Klein, Dick Tibboel, Merel Klaassens, R. J. H. Galjaard, Marieke van Dooren, Hannie Douben, Alexander T. den Dekker and Ronald R. de Krijger and has published in prestigious journals such as The American Journal of Human Genetics, Neurobiology of Disease and Human Genetics.

In The Last Decade

H. J. Eussen

10 papers receiving 391 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
H. J. Eussen Netherlands	8	159	157	155	101	97	10	415
Susan J. Kirkpatrick United States	10	154 1.0×	211 1.3×	122 0.8×	120 1.2×	31 0.3×	13	430
Roy Wadey United Kingdom	9	413 2.6×	216 1.4×	182 1.2×	37 0.4×	71 0.7×	9	582
Carole Brewer United Kingdom	8	191 1.2×	301 1.9×	50 0.3×	49 0.5×	27 0.3×	9	484
April M. Hacker United States	9	432 2.7×	361 2.3×	49 0.3×	52 0.5×	86 0.9×	11	560
Birsen Karaman Türkiye	12	180 1.1×	157 1.0×	64 0.4×	57 0.6×	33 0.3×	58	345
Daniele De Brasi Italy	14	224 1.4×	256 1.6×	73 0.5×	86 0.9×	38 0.4×	44	478
I. López Pajares Spain	12	286 1.8×	316 2.0×	76 0.5×	106 1.0×	48 0.5×	27	493
Marie‐Pierre Cordier France	11	168 1.1×	189 1.2×	82 0.5×	119 1.2×	24 0.2×	34	438
Nicole Chia Australia	7	122 0.8×	202 1.3×	137 0.9×	93 0.9×	12 0.1×	11	373
Ken L. Jones United States	6	154 1.0×	96 0.6×	38 0.2×	26 0.3×	39 0.4×	7	284

Countries citing papers authored by H. J. Eussen

Since Specialization

Citations

This map shows the geographic impact of 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 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 H. J. Eussen more than expected).

Fields of papers citing papers by H. J. Eussen

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

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

This figure shows the co-authorship network connecting the top 25 collaborators of H. J. Eussen. A scholar is included among the top collaborators of 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 H. J. Eussen. 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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10 of 10 papers shown

Brosens, Erwin, H. J. Eussen, Yolande van Bever, et al.. (2012). VACTERL Association Etiology: The Impact of de novo and Rare Copy Number Variations. Molecular Syndromology. 4(1-2). 20–26. 22 indexed citations

Hes, Frederik J., et al.. (2007). Frequency of Von Hippel‐Lindau germline mutations in classic and non‐classic Von Hippel‐Lindau disease identified by DNA sequencing, Southern blot analysis and multiplex ligation‐dependent probe amplification. Clinical Genetics. 72(2). 122–129. 50 indexed citations

Hagen, Johanna M. van, Jos N. van der Geest, Ruben S. van der Giessen, et al.. (2006). Contribution of CYLN2 and GTF2IRD1 to neurological and cognitive symptoms in Williams Syndrome. Neurobiology of Disease. 26(1). 112–124. 56 indexed citations

Klaassens, Merel, Daryl A. Scott, Marieke van Dooren, et al.. (2006). Congenital diaphragmatic hernia associated with duplication of 11q23‐qter. American Journal of Medical Genetics Part A. 140A(14). 1580–1586. 41 indexed citations

Baart, Esther B., Irene van den Berg, Elena Martini, et al.. (2006). FISH analysis of 15 chromosomes in human day 4 and 5 preimplantation embryos: the added value of extended aneuploidy detection. Prenatal Diagnosis. 27(1). 55–63. 32 indexed citations

Klaassens, Merel, Marieke van Dooren, H. J. Eussen, et al.. (2005). Congenital Diaphragmatic Hernia and Chromosome 15q26: Determination of a Candidate Region by Use of Fluorescent In Situ Hybridization and Array-Based Comparative Genomic Hybridization. The American Journal of Human Genetics. 76(5). 877–882. 113 indexed citations

Eussen, H. J., et al.. (2004). Deletion of the TWIST gene in a large five‐generation family. Clinical Genetics. 65(5). 396–399. 6 indexed citations

Hemel, J. O. Van & H. J. Eussen. (2000). Interchromosomal insertions. Human Genetics. 107(5). 415–432. 78 indexed citations

Opstal, Diane Van, H. J. Eussen, J. O. Van Hemel, & E. S. Sachs. (1993). Application of fluorescent in situ hybridization for ‘de novo’ anomalies in prenatal diagnosis. Prenatal Diagnosis. 13(9). 825–832. 12 indexed citations

10.

Oostra, B. A., J.F. de Rijk-van Andel, H. J. Eussen, et al.. (1991). DNA analysis in patients with lissencephaly type I and other cortical dysplasias. American Journal of Medical Genetics. 40(3). 383–386. 5 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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