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Joris Vermeesch | Researchclopedia

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Joris Vermeesch

KU Leuven ORCID

984

Works

30,401

Citations

84

h-index

344

i10-index

Research Topics

Genomic variations and chromosomal abnormalities Prenatal Screening and Diagnostics Congenital heart defects research

Affiliations

Human Genome Sciences (United States)1995–1996

Twitter (United States)2021–2021

University of Nebraska–Lincoln1993–1994

Centre National de la Recherche Scientifique2013–2013

Albert Einstein College of Medicine2017–2017

Top Works

Consensus Statement: Chromosomal Microarray Is a First-Tier Clinical Diagnostic Test for Individuals with Developmental Disabilities or Congenital Anomalies

David T. Miller,Margaret P Adam,et al.

20102,855 citations

Chromosomal and Genetic Variations

Genetics and Neurodevelopmental Disorders

22q11.2 deletion syndrome

Donna M. McDonald‐McGinn,Kathleen E. Sullivan,et al.

20152,218 citations

Chromosome instability is common in human cleavage-stage embryos

Evelyne Vanneste,Thierry Voet,et al.

2009893 citations

Recurrent Rearrangements of Chromosome 1q21.1 and Variable Pediatric Phenotypes

Heather C. Mefford,Andrew J. Sharp,et al.

2008807 citations

Single molecule real-time (SMRT) sequencing comes of age: applications and utilities for medical diagnostics

Simon Ardui,Adam Ameur,et al.

2018755 citations

Skeletal muscle repair by adult human mesenchymal stem cells from synovial membrane

Cosimo De Bari,Francesco Dell’Accio,et al.

2003641 citations

Mosaic Copy Number Variation in Human Neurons

Michael J. McConnell,Michael Lindberg,et al.

2013561 citations

Fusion of NUP214 to ABL1 on amplified episomes in T-cell acute lymphoblastic leukemia

Carlos Graux,Jan Cools,et al.

2004421 citations

Further delineation of the 15q13 microdeletion and duplication syndromes: a clinical spectrum varying from non-pathogenic to a severe outcome

Bregje W.M. van Bon,Heather C. Mefford,et al.

2009370 citations