Paul Coucke

发表

BATCH-GE: Analysis of NGS Data for Genome Editing Assessment.

Wouter Steyaert, Annekatrien Boel, Paul Coucke, 2018, Methods in molecular biology.

Analysing 454 amplicon resequencing experiments using the modular and database oriented Variant Identification Pipeline

Jo Vandesompele, Dieter Deforce, Sofie Bekaert, 2010, BMC Bioinformatics.

Publisher Correction: BATCH-GE: Batch analysis of Next-Generation Sequencing data for genome editing assessment

Björn Menten, Wouter Steyaert, Annekatrien Boel, 2018, Scientific Reports.

Immunohistochemical Analysis of the Cytokeratin Expression in Middle Ear Cholesteatoma and Related Epithelial Tissues

Paul Coucke, I. Leigh, F. Ramaekers, 1992, The Annals of otology, rhinology, and laryngology.

A syndrome of altered cardiovascular, craniofacial, neurocognitive and skeletal development caused by mutations in TGFBR1 or TGFBR2

Wolfram Kress, Julie De Backer, Jan Hellemans, 2005, Nature Genetics.

CRASH Syndrome: Clinical Spectrum of Corpus Callosum Hypoplasia, Retardation, Adducted Thumbs, Spastic Paraparesis and Hydrocephalus Due to Mutations in One Single Gene, L1

Vance Lemmon, Paul Coucke, Erik Fransen, 1995, European journal of human genetics : EJHG.

Novel MYH11 and ACTA2 mutations reveal a role for enhanced TGFβ signaling in FTAAD.

Paul Coucke, Marjolijn Renard, Bart Loeys, 2013, International journal of cardiology.

A mutation in CABP2, expressed in cochlear hair cells, causes autosomal-recessive hearing impairment.

Akira Inagaki, Tobias Moser, Paul Coucke, 2012, American journal of human genetics.

Aneurysm Syndromes Caused by Mutations in the TGF-β Receptor

George H. Thomas, Julie De Backer, Paul Coucke, 2006 .

A combined defect in the biosynthesis of N- and O-glycans in patients with cutis laxa and neurological involvement: the biochemical characteristics.

Ron A Wevers, Eva Morava, Paul Coucke, 2005, Biochimica et biophysica acta.

Homozygosity for a missense mutation in fibulin-5 (FBLN5) results in a severe form of cutis laxa.

Paul Coucke, Bart Loeys, Geert Mortier, 2002, Human molecular genetics.