Joris R Vermeesch

SCAMP5, NBEA and AMISYN: three candidate genes for autism involved in secretion of large dense-core vesicles.

Jurgen Del-Favero, Kathleen Freson, Peter De Rijk, 2010, Human molecular genetics.

Hemizygous mutations in SNAP29 unmask autosomal recessive conditions and contribute to atypical findings in patients with 22q11.2DS

Stephen T Warren, Somayyeh Fahiminiya, E. Zackai, 2012, Journal of Medical Genetics.

Preimplantation genetic diagnosis guided by single-cell genomics

Thierry Voet, Masoud Zamani Esteki, J. Vermeesch, 2013, Genome Medicine.

eXtasy: variant prioritization by genomic data fusion

Bart De Moor, Yves Moreau, Ryo Sakai, 2013, Nature Methods.

Chromosome instability is common in human cleavage-stage embryos

Geert Verbeke, Yves Moreau, Miikka Vikkula, 2009, Nature Medicine.

Molecular Karyotyping: Array CGH Quality Criteria for Constitutional Genetic Diagnosis

Bart De Moor, Frank Speleman, Björn Menten, 2005, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

Concurrent whole-genome haplotyping and copy-number profiling of single cells.

Yves Moreau, Eric Legius, Masoud Zamani Esteki, 2015, American journal of human genetics.

Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies.

Leslie G Biesecker, Swaroop Aradhya, Margaret P Adam, 2010, American journal of human genetics.