Cnnm2 | List of Frontiers open access articles

Case Report

Published on 20 Aug 2021

Case Report: CNNM2 Mutations Cause Damaged Brain Development and Intractable Epilepsy in a Patient Without Hypomagnesemia

in Genetics of Common and Rare Diseases

Xiucui Li
Shijia Bao
Wei Wang
Xulai Shi
Ying Hu
Feng Li
Qianlei Zhao
Feixia Zheng
Zhongdong Lin

Frontiers in Genetics

doi 10.3389/fgene.2021.705734

4,162 views
10 citations

Original Research

Published on 29 Jun 2022

Novel CNNM2 Mutation Responsible for Autosomal-Dominant Hypomagnesemia With Seizure

in Genetics of Common and Rare Diseases

Min-Hua Tseng
Sung-Sen Yang
Chih-Chien Sung
Jhao-Jhuang Ding
Yu-Juei Hsu
Shih-Ming Chu
Shih-Hua Lin

Frontiers in Genetics

doi 10.3389/fgene.2022.875013

4,109 views
12 citations

Original Research

Published on 19 Jun 2025

Two novel variants in CNNM2 disrupts magnesium efflux leading to neurodevelopmental disorders

in Genetics of Common and Rare Diseases

Huijuan Li
Jing Liu
Yingdi Liu
Yaning Liu
Kehui Lu
Juan Wen
Huimin Zhu
Desheng Liang
Zhuo Li
Lingqian Wu

Frontiers in Genetics

doi 10.3389/fgene.2025.1600877

2,663 views

Original Research

Published on 16 Sep 2021

CNNM2-Related Disorders: Phenotype and Its Severity Were Associated With the Mode of Inheritance

in Pediatric Neurology

Han Zhang
Ye Wu
Yuwu Jiang

Frontiers in Pediatrics

doi 10.3389/fped.2021.699568

5,766 views
10 citations

Original Research

Published on 02 Sep 2020

Studies in Zebrafish Demonstrate That CNNM2 and NT5C2 Are Most Likely the Causal Genes at the Blood Pressure-Associated Locus on Human Chromosome 10q24.32

in Hypertension

Krishan K. Vishnolia
Celine Hoene
Karim Tarhbalouti
Julian Revenstorff
Zouhair Aherrahrou
Jeanette Erdmann

Frontiers in Cardiovascular Medicine

doi 10.3389/fcvm.2020.00135

7,816 views
21 citations

Original Research

Published on 27 Oct 2017

Perinatal Asphyxia in Rat Alters Expression of Novel Schizophrenia Risk Genes

in Brain Disease Mechanisms

Alessandra Paparelli
Keiko Iwata
Tomoyasu Wakuda
Conrad Iyegbe
Robin M. Murray
Nori Takei

Frontiers in Molecular Neuroscience

doi 10.3389/fnmol.2017.00341

4,685 views
13 citations

General Commentary

Published on 19 Oct 2020

Commentary: Studies in Zebrafish Demonstrate That CNNM2 and NT5C2 Are Most Likely the Causal Genes at the Blood Pressure-Associated Locus on Human Chromosome 10q24.32

in Hypertension

Daniela Sorriento
Guido Iaccarino

Frontiers in Cardiovascular Medicine

doi 10.3389/fcvm.2020.582101

2,925 views
2 citations

Articles

Case Report: CNNM2 Mutations Cause Damaged Brain Development and Intractable Epilepsy in a Patient Without Hypomagnesemia

Novel CNNM2 Mutation Responsible for Autosomal-Dominant Hypomagnesemia With Seizure

Two novel variants in CNNM2 disrupts magnesium efflux leading to neurodevelopmental disorders

CNNM2-Related Disorders: Phenotype and Its Severity Were Associated With the Mode of Inheritance

Studies in Zebrafish Demonstrate That CNNM2 and NT5C2 Are Most Likely the Causal Genes at the Blood Pressure-Associated Locus on Human Chromosome 10q24.32

Perinatal Asphyxia in Rat Alters Expression of Novel Schizophrenia Risk Genes

Commentary: Studies in Zebrafish Demonstrate That CNNM2 and NT5C2 Are Most Likely the Causal Genes at the Blood Pressure-Associated Locus on Human Chromosome 10q24.32