Sarah Duerinckx
7PUBLICATIONS
73CO-AUTHORS
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Publications (7)
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|Oct 31, 2024
Brain malformations and seizures by impaired chaperonin function of TRiC.Florian Kraft, Piere Rodriguez-Aliaga, Weimin Yuan
|Sep 04, 2021
Compound heterozygous null mutations of NOBOX in sisters with delayed puberty and primary amenorrhea.Asma Sassi, Julie Désir, Sarah Duerinckx
|Aug 17, 2021
Phenotypes and genotypes in non-consanguineous and consanguineous primary microcephaly: High incidence of epilepsy.Sarah Duerinckx, Julie Désir, Camille Perazzolo
|Nov 08, 2019
Digenic inheritance of human primary microcephaly delineates centrosomal and non-centrosomal pathways.Sarah Duerinckx, Valérie Jacquemin, Séverine Drunat
|Apr 26, 2018
Phenotypes in siblings with homozygous mutations of TRAPPC9 and/or MCPH1 support a bifunctional model of MCPH1.Sarah Duerinckx, Marije Meuwissen, Camille Perazzolo
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Frequent Collaborators
2 joint publications
Sandrine Passemard
2 joint publications
Marc Abramowicz
2 joint publications
Wim Van Paesschen
1 joint publications
Yoann Vial
1 joint publications
Isabelle Maystadt
1 joint publications
Stéphanie Moortgat
1 joint publications
Isabelle Pirson
1 joint publications
Asma Sassi
1 joint publications
Anne Delbaere
1 joint publications
Florian Kraft