Proteome Profiling of RNF213 Depleted Cells Reveals Nitric Oxide Regulator DDAH1 Antilisterial Activity.

Martina L*, Asselman C*, Thery F*, Boucher K, Delhaye L, Maia TM, Dermaut B, Eyckerman S, Impens F.

Front Cell Infect Microbiol. 2021 Nov 3;11:735416. doi: 10.3389/fcimb.2021.735416. eCollection 2021.

PMID: 34804992 * contributed equally 

Premature termination codon mutations in ABCA7 contribute to Alzheimer's disease risk in Belgian patients.

Bossaerts L, Hens E, Hanseeuw B, Vandenberghe R, Cras P, De Deyn PP, Engelborghs S, Van Broeckhoven C; BELNEU Consortium.

Neurobiol Aging. 2021 Oct;106:307.e1-307.e7. doi: 10.1016/j.neurobiolaging.2021.04.023. Epub 2021 May 2.

PMID: 34090711

Loss of adipocyte phospholipase gene PLAAT3 causes lipodystrophy and insulin resistance due to inactivated arachidonic acid-mediated PPARγ signaling.

Schuermans N*, El  Chehadeh S*,Hemelsoet D*, Bogaert E, Debackere E, Hilbert P,  Van Doninck N, Taquet MC, Rosseel T, De Clercq G, Van Haverbeke C, Chanson JB,  Funalot B, Authier FJ, Kaya S, Terryn W, Callens S, Depypere B, Van Dorpe J, Program for Undiagnosed Diseases (UD-PrOZA), Poppe B, Depienne C, Dermaut B.
BioRXiv. 2021 April. doi: https://doi.org/10.1101/2021.04.15.439941 - online ahead of print

* contributed equally 

Ring finger protein 213 assembles into a sensor for ISGylated proteins with antimicrobial activity.
Thery F*, Martina L*, Asselman C*, Zhang Y, Vessely M, Repo H, Sedeyn K, Moschonas GD, Bredow C, Teo QW, Zhang J, Leandro K, Eggermont D, De Sutter D, Boucher K, Hochepied T, Festjens N, Callewaert N, Saelens X, Dermaut B, Knobeloch KP, Beling A, Sanyal S, Radoshevich L, Eyckerman S, Impens F.N
Nat Commun. 2021 Oct 1;12(1):5772. doi: 10.1038/s41467-021-26061-w.
PMID: 34599178 * contributed equally

Family-based exome sequencing identifies RBM45 as a possible candidate gene for frontotemporal dementia and amyotrophic lateral sclerosis.

van der Zee J, Dillen L, Baradaran-Heravi Y, Gossye H, Koçoğlu C, Cuyt I, Dermaut B, Sieben A, Baets J, De Jonghe P, Vandenberghe R, De Deyn P, Cras P, Engelborghs S, Van Broeckhoven C; BELNEU Consortium.

Neurobiol Dis. 2021 Aug;156:105421. doi: 10.1016/j.nbd.2021.105421. Epub 2021 Jun 9.

PMID: 34118419 

Adult-onset congenital central hypoventilation syndrome due to PHOX2B mutation.

Meylemans A, Depuydt P, De Baere E, Hertegonne K, Derom E, Dermaut B, Hemelsoet D.

Acta Neurol Belg. 2021 Feb;121(1):23-35. doi: 10.1007/s13760-020-01363-w. Epub 2020 Apr 25.

PMID: 32335870