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Scientific Reports (12)
npj Parkinson's Disease (6)
Journal of Human Genetics (1)
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Showing 1–23 of 23 results

Advanced filters: Author: Mohamed Chahine Clear advanced filters

Association of LRRK2 p.A419V with Parkinson’s Disease in East Asians and analysis of age at onset

Kai Shi Lim
Maria Teresa Periñan
Masharip Atadzhanov
ResearchOpen Access02 Feb 2026
npj Parkinson's Disease

P: 1-12
Cloning, functional expression, and pharmacological characterization of inwardly rectifying potassium channels (Kir) from Apis mellifera

Fabien Sourisseau
Chaimaa Chahine
Mohamed Chahine
ResearchOpen Access03 Apr 2024
Scientific Reports

Volume: 14, P: 1-14
Biophysical and structural insights into the SCN4A E452K variant linked to myotonia and paramyotonia congenita

Quentin Plumereau
Spencer Lile
Mohamed Chahine
ResearchOpen Access26 Sept 2025
Scientific Reports

Volume: 15, P: 1-13
Author Correction: Elucidating causative gene variants in hereditary Parkinson’s disease in the Global Parkinson’s Genetics Program (GP2)

Lara M. Lange
Micol Avenali
Masharip Atadzhanov
Amendments and CorrectionsOpen Access13 Sept 2023
npj Parkinson's Disease

Volume: 9, P: 1-3
Multi-ancestry genome-wide association meta-analysis of Parkinson’s disease

Multi-ancestry genome-wide association analyses identify new risk loci for Parkinson’s disease, and fine-mapping and co-localization analyses implicate candidate genes whose expression is associated with disease susceptibility.

Jonggeol Jeffrey Kim
Dan Vitale
Ignacio Mata
ResearchOpen Access28 Dec 2023
Nature Genetics

Volume: 56, P: 27-36
De novo Y1460C missense variant in Na_V1.1 impedes the pore region and results in epileptic encephalopathy

Quentin Plumereau
Aya Ebdalla
Mohamed Chahine
ResearchOpen Access13 Oct 2022
Scientific Reports

Volume: 12, P: 1-8
Genetic associations of protein-coding variants in human disease

A meta-analysis combining whole-exome sequencing data from UK Biobank participants and imputed genotypes from FinnGen participants enables identification of genetic associations with human disease in the rare and low-frequency allelic spectrum

Benjamin B. Sun
Mitja I. Kurki
Heiko Runz
ResearchOpen Access23 Feb 2022
Nature

Volume: 603, P: 95-102
TMEM175, SCARB2 and CTSB associations with Parkinson’s disease risk across populations

Wenhua Sun
Claudia Schulte
Masharip Atadzhanov
ResearchOpen Access02 Dec 2025
npj Parkinson's Disease

Volume: 11, P: 1-10
Substitutions of the S4DIV R2 residue (R1451) in Na_V1.4 lead to complex forms of paramyotonia congenita and periodic paralyses

Hugo Poulin
Pascal Gosselin-Badaroudine
Mohamed Chahine
ResearchOpen Access01 Feb 2018
Scientific Reports

Volume: 8, P: 1-13
iPSC-derived cardiomyocytes from patients with myotonic dystrophy type 1 have abnormal ion channel functions and slower conduction velocities

Hugo Poulin
Aurélie Mercier
Mohamed Chahine
ResearchOpen Access28 Jan 2021
Scientific Reports

Volume: 11, P: 1-13
Insights into ancestral diversity in Parkinson’s disease risk: a comparative assessment of polygenic risk scores

Paula Saffie-Awad
Spencer M. Grant
Sara Bandres-Ciga
ResearchOpen Access03 Jul 2025
npj Parkinson's Disease

Volume: 11, P: 1-13
Biophysical properties of Na_V1.5 channels from atrial-like and ventricular-like cardiomyocytes derived from human induced pluripotent stem cells

Charles-Albert Chapotte-Baldacci
Marion Pierre
Mohamed Chahine
ResearchOpen Access24 Nov 2023
Scientific Reports

Volume: 13, P: 1-15
Perinatal and Postnatal Expression of Cav1.3 α_1D Ca²⁺ Channel in the Rat Heart

Yongxia Qu
Eddy Karnabi
Mohamed Boutjdir
Research01 Jun 2011
Pediatric Research

Volume: 69, P: 479-484
Na_V1.5 knockout in iPSCs: a novel approach to study Na_V1.5 variants in a human cardiomyocyte environment

Marion Pierre
Mohammed Djemai
Mohamed Chahine
ResearchOpen Access25 Aug 2021
Scientific Reports

Volume: 11, P: 1-16
Antisense oligonucleotides as a potential treatment for brain deficits observed in myotonic dystrophy type 1

Siham Ait Benichou
Dominic Jauvin
Jack Puymirat
ResearchOpen Access25 Jan 2022
Gene Therapy

Volume: 29, P: 698-709
A leaky voltage sensor domain of cardiac sodium channels causes arrhythmias associated with dilated cardiomyopathy

Adrien Moreau
Pascal Gosselin-Badaroudine
Mohamed Chahine
ResearchOpen Access14 Sept 2018
Scientific Reports

Volume: 8, P: 1-12
Characterization of the honeybee AmNa_V1 channel and tools to assess the toxicity of insecticides

Pascal Gosselin-Badaroudine
Adrien Moreau
Mohamed Chahine
ResearchOpen Access23 Jul 2015
Scientific Reports

Volume: 5, P: 1-17
Defining the causes of sporadic Parkinson’s disease in the global Parkinson’s genetics program (GP2)

Clodagh Towns
Madeleine Richer
Masharip Atadzhanov
ResearchOpen Access12 Sept 2023
npj Parkinson's Disease

Volume: 9, P: 1-6
The LRRK2 p.L1795F variant causes Parkinson’s disease in the European population

Lara M. Lange
Kristin Levine
Masharip Atadzhanov
ResearchOpen Access25 Mar 2025
npj Parkinson's Disease

Volume: 11, P: 1-10
Genetic analysis of the cardiac sodium channel gene SCN5A in Koreans with Brugada syndrome

Dong-Jik Shin
Yangsoo Jang
Sungjoo Kim Yoon
Research01 Oct 2004
Journal of Human Genetics

Volume: 49, P: 573-578
Combining NGN2 programming and dopaminergic patterning for a rapid and efficient generation of hiPSC-derived midbrain neurons

Razan Sheta
Maxime Teixeira
Abid Oueslati
ResearchOpen Access13 Oct 2022
Scientific Reports

Volume: 12, P: 1-16
Voltage-gated sodium channels from the bees Apis mellifera and Bombus terrestris are differentially modulated by pyrethroid insecticides

Aklesso Kadala
Mercédès Charreton
Claude Collet
ResearchOpen Access31 Jan 2019
Scientific Reports

Volume: 9, P: 1-12
A204E mutation in Na_v1.4 DIS3 exerts gain- and loss-of-function effects that lead to periodic paralysis combining hyper- with hypo-kalaemic signs

Yosuke Kokunai
Carine Dalle
Sophie Nicole
ResearchOpen Access12 Nov 2018
Scientific Reports

Volume: 8, P: 1-10

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Association of LRRK2 p.A419V with Parkinson’s Disease in East Asians and analysis of age at onset

Cloning, functional expression, and pharmacological characterization of inwardly rectifying potassium channels (Kir) from Apis mellifera

Biophysical and structural insights into the SCN4A E452K variant linked to myotonia and paramyotonia congenita

Author Correction: Elucidating causative gene variants in hereditary Parkinson’s disease in the Global Parkinson’s Genetics Program (GP2)

Multi-ancestry genome-wide association meta-analysis of Parkinson’s disease

De novo Y1460C missense variant in Na_V1.1 impedes the pore region and results in epileptic encephalopathy

Genetic associations of protein-coding variants in human disease

TMEM175, SCARB2 and CTSB associations with Parkinson’s disease risk across populations

Substitutions of the S4DIV R2 residue (R1451) in Na_V1.4 lead to complex forms of paramyotonia congenita and periodic paralyses

iPSC-derived cardiomyocytes from patients with myotonic dystrophy type 1 have abnormal ion channel functions and slower conduction velocities

Insights into ancestral diversity in Parkinson’s disease risk: a comparative assessment of polygenic risk scores

Biophysical properties of Na_V1.5 channels from atrial-like and ventricular-like cardiomyocytes derived from human induced pluripotent stem cells

Perinatal and Postnatal Expression of Cav1.3 α_1D Ca²⁺ Channel in the Rat Heart

Na_V1.5 knockout in iPSCs: a novel approach to study Na_V1.5 variants in a human cardiomyocyte environment

Antisense oligonucleotides as a potential treatment for brain deficits observed in myotonic dystrophy type 1

A leaky voltage sensor domain of cardiac sodium channels causes arrhythmias associated with dilated cardiomyopathy

Characterization of the honeybee AmNa_V1 channel and tools to assess the toxicity of insecticides

Defining the causes of sporadic Parkinson’s disease in the global Parkinson’s genetics program (GP2)

The LRRK2 p.L1795F variant causes Parkinson’s disease in the European population

Genetic analysis of the cardiac sodium channel gene SCN5A in Koreans with Brugada syndrome

Combining NGN2 programming and dopaminergic patterning for a rapid and efficient generation of hiPSC-derived midbrain neurons

Voltage-gated sodium channels from the bees Apis mellifera and Bombus terrestris are differentially modulated by pyrethroid insecticides

A204E mutation in Na_v1.4 DIS3 exerts gain- and loss-of-function effects that lead to periodic paralysis combining hyper- with hypo-kalaemic signs

Search

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