Eric Legius

Supervised Classification of Array CGH Data with HMM-Based Feature Selection

Bart De Moor, Olivier Gevaert, Anneleen Daemen, 2008, Pacific Symposium on Biocomputing.

Classification of Sporadic and BRCA1 Ovarian Cancer Based on a Genome-Wide Study of Copy Number Variations

Bart De Moor, Olivier Gevaert, Anneleen Daemen, 2008, KES.

PRC2 loss amplifies Ras-driven transcription and confers sensitivity to BRD4-based therapies

Eric Legius, Kristian Helin, Hildegard Kehrer-Sawatzki, 2014, Nature.

SOX10 mutations in patients with Waardenburg-Hirschsprung disease

Giovanni Romeo, Gert Matthijs, Eric Legius, 1998, Nature Genetics.

High Incidence of Noonan Syndrome Features Including Short Stature and Pulmonic Stenosis in Patients carrying NF1 Missense Mutations Affecting p.Arg1809: Genotype–Phenotype Correlation

Ying Liu, Jing Xie, Eric Legius, 2015, Human mutation.

Spred1 Is Required for Synaptic Plasticity and Hippocampus-Dependent Learning

Nils Z. Borgesius, Eric Legius, Rudi D'Hooge, 2008, The Journal of Neuroscience.

Comparative PRKAR1A genotype-phenotype analyses in humans with Carney complex and prkar1a haploinsufficient mice.

Kimberly Burton, Tsuneo Imai, Yan Song, 2004, Proceedings of the National Academy of Sciences of the United States of America.

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

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

Mutation analysis in Costello syndrome: functional and structural characterization of the HRAS p.Lys117Arg mutation

Eric Legius, Jan Cools, Kevin Shannon, 2008, Human mutation.