Brecht Guillemyn

5PUBLICATIONS
30CO-AUTHORS
Aerospace structuresMaterials engineering not elsewhere classifiedInfant and child healthCell and nuclear divisionCancer genetics
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Publications (5)

|Sep 18, 2023
Syntaxin 18 Defects in Human and Zebrafish Unravel Key Roles in Early Cartilage and Bone Development.

Brecht Guillemyn, Hanna De Saffel, Jan Willem Bek

|Mar 29, 2021
Loss of TANGO1 Leads to Absence of Bone Mineralization.

Brecht Guillemyn, Sheela Nampoothiri, Delfien Syx

|Feb 01, 2021
Aberrant binding of mutant HSP47 affects posttranslational modification of type I collagen and leads to osteogenesis imperfecta.

Delfien Syx, Yoshihiro Ishikawa, Jan Gebauer

|Jan 31, 2020
Functional characterization of the first missense variant in CEP78, a founder allele associated with cone-rod dystrophy, hearing loss, and reduced male fertility.

Giulia Ascari, Frank Peelman, Pietro Farinelli

|Mar 22, 2019
Ptosis as a unique hallmark for autosomal recessive WNT1-associated osteogenesis imperfecta.

Sheela Nampoothiri, Brecht Guillemyn, Nursel Elcioglu

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Frequent Collaborators

2 joint publications

Sofie Symoens

1 joint publications

Giulia Ascari

1 joint publications

Frank Peelman

1 joint publications

Pietro Farinelli