ZFIN Person: Callewaert, Bert

ZFIN ID: ZDB-PERS-220914-1

Callewaert, Bert

Email:	Bert.Callewaert@Ugent.be
URL:	http://www.cmgg.be/en
Affiliation:	Callewaert Lab
Address:	Center for Medical Genetics Ghent University - Department of Biomolecular Medicine C. Heymanslaan 10 B-9000 Ghent Belgium
Country:	Belgium
Phone:	+32 9 332 3603
Fax:	+32 9 332 4970
ORCID ID:	0000-0002-9743-4205

BIOGRAPHY AND RESEARCH INTERESTS

PUBLICATIONS

Pottie, L., Van Gool, W., Vanhooydonck, M., Hanisch, F.G., Goeminne, G., Rajkovic, A., Coucke, P., Sips, P., Callewaert, B. (2021) Loss of zebrafish atp6v1e1b, encoding a subunit of vacuolar ATPase, recapitulates human ARCL type 2C syndrome and identifies multiple pathobiological signatures. PLoS Genetics. 17:e1009603

Pottie, L., Adamo, C.S., Beyens, A., Lütke, S., Tapaneeyaphan, P., De Clercq, A., Salmon, P.L., De Rycke, R., Gezdirici, A., Gulec, E.Y., Khan, N., Urquhart, J.E., Newman, W.G., Metcalfe, K., Efthymiou, S., Maroofian, R., Anwar, N., Maqbool, S., Rahman, F., Altweijri, I., Alsaleh, M., Abdullah, S.M., Al-Owain, M., Hashem, M., Houlden, H., Alkuraya, F.S., Sips, P., Sengle, G., Callewaert, B. (2021) Bi-allelic premature truncating variants in LTBP1 cause cutis laxa syndrome. American journal of human genetics. 108(6):1095-1114

NON-ZEBRAFISH PUBLICATIONS