ZFIN Person: Sips, Patrick

ZFIN ID: ZDB-PERS-220914-2

Sips, Patrick

Email:	Patrick.Sips@Ugent.be
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Affiliation:	Callewaert Lab
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BIOGRAPHY AND RESEARCH INTERESTS

PUBLICATIONS

Van Impe, M., Caboor, L., Deleeuw, V., De Rycke, K., Vanhooydonck, M., De Backer, J., Segers, P., Sips, P. (2023) Application of an automated analysis framework for pulsed wave Doppler cardiac ultrasound measurements to generate reference data in adult zebrafish. American journal of physiology. Regulatory, integrative and comparative physiology. 325(6):R782-R796

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