Key publications

Evaluation of a role for NPY and NPY2R in the pathogenesis of obesity by mutation and copy number variation analysis in obese children and adolescents
Aerts Evi   Geets Ellen   Sorber Laure   Beckers Sigri   Verrijken An   Massa Guy   van Hoorenbeeck Kim   Verhulst Stijn   Van Gaal Luc   Van Hul Wim  
Annals of human genetics - ISSN 0003-4800-82:1 (2018) p. 1-10
Citatielink
Targeted search for genetic causes of the Prader Willi like phenotype
Geets Ellen  
Antwerpen, Universiteit Antwerpen, Faculteit Farmaceutische, Biomedische en Diergeneeskundige Wetenschappen, Departement Biomedische Wetenschappen, 2018,259 p.
Citatielink
Conditional mouse models support the role of SLC39A14 (ZIP14) in Hyperostosis Cranialis Interna and in bone homeostasis
Hendrickx Gretl   Borra Vere   Steenackers Ellen   Yorgan Timur A.   Hermans Christophe   Boudin Eveline   Waterval Jérôme J.   Jansen Ineke D.C.   Beker Aydemir Tolunay   Kamerling Niels   Behets Geert   Plumeyer Christine   d' Haese Patrick C.   Busse Björn   Everts Vincent   Lammens Martin   Mortier Geert   Cousins Robert J.   Schinke Thorsten   Stokroos Robert J.   Manni Johannes J.   Van Hul Wim  
PLoS genetics - ISSN 1553-7404-14:4 (2018)
Citatielink
Human genetics of sclerosing bone disorders
De Ridder Raphael   Boudin Eveline   Mortier Geert   Van Hul Wim  
CURRENT OSTEOPOROSIS REPORTS - ISSN 1544-2241-16:3 (2018) p. 256-268
Citatielink
DNA sequencing and copy number variation analysis of MCHR2 in a cohort of Prader Willi like (PWL) patients
Geets Ellen   Aerts Evi   Verrijken An   van Hoorenbeeck Kim   Verhulst Stijn   Van Gaal Luc   Van Hul Wim  
Obesity research & clinical practice - ISSN 1871-403X-12:2 (2018) p. 158-166
Citatielink

Full bibliography of this research group