H. J. Eussen - Concepedia

Author

H. J. Eussen

Erasmus University Rotterdam

Also Known As

H Eussen, H J Eussen, H. Eussen, H. J. Eussen, H.J. Eussen, H.J.F.M.M. Eussen, HJ Eussen

Publications

632

Citations

H-Index

Concepts

All Affiliations

Erasmus University Rotterdam Erasmus MC University Medical Center Utrecht

About

H. J. Eussen is an author at Erasmus University Rotterdam specializing in medicine, genetics, and genomics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	4	4	316
2	Health Sciences	1	1	33
3	Social Sciences	1	1	85
4	Epidemiology	1	1	33
5	Microbiology	1	1	33

H. J. Eussen

Publications

456

Citations

H-Index

Page 1

	Year	Citations
Congenital Diaphragmatic Hernia and Chromosome 15q26: Determination of a Candidate Region by Use of Fluorescent In Situ Hybridization and Array-Based Comparative Genomic Hybridization Merel Klaassens, Marieke van Dooren, H. J. Eussen, The American Journal of Human Genetics Developmental BiologyCongenital Diaphragmatic HerniaCytogeneticsGeneticsCandidate Region	2005	144
Contribution of CYLN2 and GTF2IRD1 to neurological and cognitive symptoms in Williams Syndrome Johanna M. van Hagen, Jos N. van der Geest, Ruben S. van der Giessen, Neurobiology of Disease Neurodegenerative DiseasesNeuropsychologyMendelian DisorderCognitive SymptomsNeurological Disorder	2006	85
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 Rob B. van der Luijt, ALW Janssen, RA Zewald, Clinical Genetics	2007	70
Congenital diaphragmatic hernia associated with duplication of 11q23‐qter Merel Klaassens, Daryl A. Scott, Marieke van Dooren, American Journal of Medical Genetics Part A Developmental AnomalyDevelopmental BiologyHernia SurgeryCongenital Diaphragmatic HerniaCytogenetics	2006	54
FISH analysis of 15 chromosomes in human day 4 and 5 preimplantation embryos: the added value of extended aneuploidy detection Esther B. Baart, Irene van den Berg, Elena Martini, Prenatal Diagnosis	2006	44
VACTERL Association Etiology: The Impact of de novo and Rare Copy Number Variations Erwin Brosens, H. J. Eussen, Yolande van Bever, Molecular Syndromology Recurrent Rare CnvsMolecular EpidemiologyGeneticsPathologyDisease Gene Identification	2012	33
Application of fluorescent <i>in situ</i> hybridization for ‘<i>de novo</i>’ anomalies in prenatal diagnosis Diane Van Opstal, H. J. Eussen, J. O. Van Hemel, Prenatal Diagnosis	1993	14
Deletion of the <i>TWIST</i> gene in a large five‐generation family IM De Heer, AJM Hoogeboom, H. J. Eussen, Clinical Genetics	2004	12

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