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Current Opinion in Neurology|September 5, 2014
Muscle channelopathies: recent advances in genetics, pathophysiology and therapyKaren Suetterlin, Roope Männikkö, Michael G Hanna
Nature|October 25, 2002
Voltage-sensing mechanism is conserved among ion channels gated by opposite voltagesRoope Männikkö, Fredrik Elinder, H Peter Larsson
The Journal of Physiology|June 17, 2006
Mode shifts in the voltage gating of the mouse and human HCN2 and HCN4 channelsFredrik Elinder, Roope Männikkö, Shilpi Pandey, et al.
Expert Review of Molecular Diagnostics|July 14, 2020
Improving genetic diagnostics of skeletal muscle channelopathiesVinojini Vivekanandam, Roope Männikkö, Emma Matthews, et al.
The Journal of General Physiology|November 12, 2003
Molecular movement of the voltage sensor in a K channelAmir Broomand, Roope Männikkö, H Peter Larsson, et al.
The Journal of General Physiology|February 16, 2005
Hysteresis in the voltage dependence of HCN channels: conversion between two modes affects pacemaker propertiesRoope Männikkö, Shilpi Pandey, H Peter Larsson, et al.
Brain : a Journal of Neurology|November 16, 2022
In silico versus functional characterization of genetic variants: lessons from muscle channelopathiesVinojini Vivekanandam, Rebecca Ellmers, Dipa Jayaseelan, et al.
Neurology|March 24, 2017
Predominantly myalgic phenotype caused by the c.3466G>A p.A1156T mutation in SCN4A geneJohanna Palmio, Satu Sandell, Michael G Hanna, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|February 18, 2020
In vivo assessment of interictal sarcolemmal membrane properties in hypokalaemic and hyperkalaemic periodic paralysisS Veronica Tan, Karen Suetterlin, Roope Männikkö, et al.
Human Molecular Genetics|December 22, 2009
Interaction between mutations in the slide helix of Kir6.2 associated with neonatal diabetes and neurological symptomsRoope Männikkö, Craig Jefferies, Sarah E Flanagan, et al.
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