Kuetting D, Luetkens J, Wolter K, Faron A, Kania A, Thomas D, Catheter-Directed Thrombectomy for Highly Symptomatic Patients with Iliofemoral Deep Venous Thrombosis not Responsive to Conservative Treatment. - Cardiovascular And Interventional Radiology 2020 Jan 23

Bally BP, Farmer WT, Jones EV, Jessa S, Kacerovsky JB, Mayran A, Peng H, Lefebvre JL, Drouin J, Hayer A, Ernst C, Murai KK, Human iPSC-Derived Down Syndrome Astrocytes Display Genome-Wide Perturbations in Gene Expression, an Altered Adhesion Profile, and Increased Cellular Dynamics. - Human Molecular Genetics 2020 Jan 15

Bagci H, Sriskandarajah N, Robert A, Boulais J, Elkholi IE, Tran V, Lin ZY, Thibault MP, Dubé N, Faubert D, Hipfner DR, Gingras AC, Côté JF, Mapping the proximity interaction network of the Rho-family GTPases reveals signalling pathways and regulatory mechanisms. - Nature Cell Biology 2020 Jan

Kania A, Sambak P, Gugula A, Szlaga A, Soltys Z, Blasiak T, Hess G, Rajfur Z, Blasiak A, Electrophysiology and distribution of oxytocin and vasopressin neurons in the hypothalamic paraventricular nucleus: a study in male and female rats. - Brain Structure & Function 2020 Jan

Celejewska-Wójcik N, Wójcik K, Ignacak-Popiel M, Ćmiel A, Tyrak K, Gielicz A, Kania A, Nastałek P, Sanak M, Mastalerz L, Subphenotypes of NSAID-exacerbated respiratory disease identified by latent class analysis. - Allergy 2019 Dec 5

Yam, P.T., Charron, F., 2019. Extracellular phosphorylation in axon pathfinding. Nat Chem Biol 15, 1030–1031. doi:10.1038/s41589-019-0383-6

Tamayo-Orrego L and Charron F. Recent advances in SHH medulloblastoma progression: tumor suppressor mechanisms and the tumor microenvironment [version 1; peer review: 2 approved]. F1000Research 2019, 8(F1000 Faculty Rev):1823

Kania A, Nastałek P, Celejewska-Wójcik N, Sładek K, Kosobudzki M, Bortkiewicz A, Siedlecka J, Can alveolar hypoventilation due to kyphoscoliosis be a contraindication to driving? - International Journal Of Occupational Medicine And Environmental Health 2019 Oct 16

Accogli A#, Calabretta S#, St-Onge J, Boudrahem-Addour N, Dionne-Laporte A, Joset P, Azzarello-Burri S, Rauch A, Krier J, Fieg E, Pallais JC, Undiagnosed Diseases Network, McConkie-Rosell A, McDonald M, Freedman SF, Rivière J-B, Lafond-Lapalme J, Simpson BN, Hopkin RJ, Trimouille A, Van-Gils J, Begtrup A, McWalter K, Severino M, Rouleau GA, Yam PT, Charron F*, Srour M*. De novo pathogenic variants in N-cadherin cause ACOG, a syndromic neurodevelopmental disorder with agenesis of the corpus callosum and axon pathfinding, cardiac, ocular and genital defects. American Journal of Human Genetics Volume 105, Issue 4, 3 October 2019, Pages 854-868 # Equal contribution * Co-corresponding authors

Farnik M, Brożek G, Czajkowska-Malinowska M, Krenke R, Kania A, Trzaska-Sobczak M, Połtyn B, Miszczuk M, Celejewska-Wójcik N, Kuziemski K, Barczyk A, Validation of the Polish-language version of the COPD Assessment Test. - Polish Archives Of Internal Medicine 2019 Sep 30