| A recessive Nav1.4 mutation underlies congenital myasthenic syndrome with periodic paralysis K Habbout, H Poulin, F Rivier, S Giuliano, D Sternberg, B Fontaine, ... Neurology 86 (2), 161-169, 2016 | 65 | 2016 |
| Fluoxetine blocks Nav1. 5 channels via a mechanism similar to that of class 1 antiarrhythmics H Poulin, O Theriault, MJ Beaulieu, M Chahine Biophysical Journal 106 (2), 325a-326a, 2014 | 42 | 2014 |
| Pyridoxal-5′-phosphate (MC-1), a vitamin B6 derivative, inhibits expressed P2X receptors O Thériault, H Poulin, GR Thomas, AD Friesen, WA Al-Shaqha, ... Canadian journal of physiology and pharmacology 92 (3), 189-196, 2014 | 41 | 2014 |
| Differential modulation of Nav1. 7 and Nav1. 8 channels by antidepressant drugs O Thériault, H Poulin, JM Beaulieu, M Chahine European journal of pharmacology 764, 395-403, 2015 | 23 | 2015 |
| iPSC-derived cardiomyocytes from patients with myotonic dystrophy type 1 have abnormal ion channel functions and slower conduction velocities H Poulin, A Mercier, M Djemai, V Pouliot, I Deschenes, M Boutjdir, ... Scientific reports 11 (1), 2500, 2021 | 20 | 2021 |
| Substitutions of the S4DIV R2 residue (R1451) in NaV1.4 lead to complex forms of paramyotonia congenita and periodic paralyses H Poulin, P Gosselin-Badaroudine, S Vicart, K Habbout, D Sternberg, ... Scientific reports 8 (1), 2041, 2018 | 20 | 2018 |
| The PLAGL1 gene is down-regulated in human extraskeletal myxoid chondrosarcoma tumors H Poulin, Y Labelle Cancer letters 227 (2), 185-191, 2005 | 20 | 2005 |
| Serum-and glucocorticoid-regulated kinase 1 (SGK1) induction by the EWS/NOR1 (NR4A3) fusion protein H Poulin, C Filion, M Ladanyi, Y Labelle Biochemical and biophysical research communications 346 (1), 306-313, 2006 | 14 | 2006 |
| NaV1.5 knockout in iPSCs: a novel approach to study NaV1.5 variants in a human cardiomyocyte environment M Pierre, M Djemai, H Poulin, M Chahine Scientific reports 11 (1), 17168, 2021 | 11 | 2021 |
| Differentiation of lymphoblastoid-derived iPSCs into functional cardiomyocytes, neurons and myoblasts H Poulin, L Martineau, V Racine, J Puymirat, M Chahine Biochemical and biophysical research communications 516 (1), 222-228, 2019 | 11 | 2019 |
| The variant hERG/R148W associated with LQTS is a mutation that reduces current density on co-expression with the WT A Mechakra, Y Vincent, P Chevalier, G Millat, E Ficker, M Jastrzebski, ... Gene 536 (2), 348-356, 2014 | 10 | 2014 |
| SCN2A-related epilepsy of infancy with migrating focal seizures: report of a variant with apparent gain- and loss-of-function effects XR Yang, VKM Ginjupalli, O Theriault, H Poulin, JP Appendino, PYB Au, ... Journal of Neurophysiology 127 (5), 1388-1397, 2022 | 8 | 2022 |
| R1617Q epilepsy mutation slows NaV1.6 sodium channel inactivation and increases the persistent current and neuronal firing H Poulin, M Chahine The Journal of Physiology 599 (5), 1651-1664, 2021 | 8 | 2021 |
| Modulation of peripheral Na+ channels and neuronal firing by n-butyl-p-aminobenzoate O Thériault, H Poulin, A Sculptoreanu, WC De Groat, ME O’Leary, ... European journal of pharmacology 727, 158-166, 2014 | 4 | 2014 |
| De novo Y1460C missense variant in NaV1.1 impedes the pore region and results in epileptic encephalopathy Q Plumereau, A Ebdalla, H Poulin, JP Appendino, MH Scantlebury, ... Scientific Reports 12 (1), 17182, 2022 | 1 | 2022 |
| Generation of a patient-specific iPSC cell line with cardiac arrhythmias and dilated cardiomyopathy (CBRCULi016-A), an isogenic control (CBRCULi016-A-1), and a paternal control … M Djemai, D Jauvin, H Poulin, CA Chapotte-Baldacci, M Chahine Stem Cell Research 75, 103308, 2024 | | 2024 |
