Concepedia

Author

Megumi Fukuyama

Shiga University of Medical ScienceORCID

Also Known As

Chiyohiko Shindoh, M Fukuyama, M. Fukuyama, MEGUMI FUKUYAMA, Megumi Fukuyama

62

Publications

666

Citations

16

H-Index

14

Concepts

All Affiliations

Shiga University of Medical ScienceKyoto UniversityNational Cerebral and Cardiovascular CenterOsaka Women's and Children's HospitalNiigata University
MF

About

Megumi Fukuyama is an author at Shiga University of Medical Science specializing in molecular genetics, genetics, and medicine.

Top Concepts

#ConceptH-IndexPublicationsCitations

1

Medicine

2

2

42

2

Molecular Genetics

2

2

42

3

Natural Sciences

1

1

26

4

Public Health

1

1

16

5

Molecular Biology

1

1

26

Megumi Fukuyama

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20

Publications

605

Citations

16

H-Index

YearCitations

Long QT syndrome type 8: novel CACNA1C mutations causing QT prolongation and variant phenotypes

Megumi Fukuyama, Qi Wang, Koichi Kato,

EP Europace

2014

93

Brugada syndrome in spinal and bulbar muscular atrophy

Amane Araki, Masahisa Katsuno, Keisuke Suzuki,

Neurology

2014

55

Clinical presentation of calmodulin mutations: the International Calmodulinopathy Registry

Lia Crotti, Carla Spazzolini, Mette Nyegaard,

European Heart Journal

2023

52

Gain‐of‐Function <i>KCNH2</i> Mutations in Patients with Brugada Syndrome

Qi Wang, Seiko Ohno, Wei-Guang Ding,

Journal of Cardiovascular Electrophysiology

2014

43

L-Type Calcium Channel Mutations in Japanese Patients With Inherited Arrhythmias

Megumi Fukuyama, Seiko Ohno, Qi Wang,

Circulation Journal

2013

43

Age-Dependent Clinical and Genetic Characteristics in Japanese Patients With Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia

Seiko Ohno, Iori Nagaoka, Megumi Fukuyama,

Circulation Journal

2013

40

Novel<i>SCN10A</i>variants associated with Brugada syndrome

Megumi Fukuyama, Seiko Ohno, Takeru Makiyama,

EP Europace

2015

32

Loss-of-function mutations in cardiac ryanodine receptor channel cause various types of arrhythmias including long QT syndrome

Sayako Hirose, Takashi Murayama, Naoyuki Tetsuo,

EP Europace

2021

31

Nonsense-mediated mRNA decay due to a CACNA1C splicing mutation in a patient with Brugada syndrome

Megumi Fukuyama, Seiko Ohno, Qi Wang,

Heart Rhythm

2013

26

Phenotypic Variability of &lt;i&gt;ANK2&lt;/i&gt; Mutations in Patients With Inherited Primary Arrhythmia Syndromes

Mari Ichikawa, Takeshi Aiba, Seiko Ohno,

Circulation Journal

2016

26

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