Neurology International

0.6(top 50%)

impact factor

150(top 50%)

papers

257(top 50%)

citations

6(top 50%)

h-index

0.6(top 50%)

impact factor

172

all documents

278

doc citations

10(top 50%)

g-index

Top Articles

#	Title	Journal	Year	Citations
1	Familial Dilated Cardiomyopathy Associated with Congenital Defects in the Setting of a Novel VCL Mutation (Lys815Arg) in Conjunction with a Known MYPBC3 Variant	Neurology International	2011	17
2	Combined Use of In Silico and In Vitro Splicing Assays for Interpretation of Genomic Variants of Unknown Significance in Cardiomyopathies and Channelopathies	Neurology International	2012	13
3	Risk factors associated with post-stroke dementia: a systematic review and meta-analysis	Neurology International	2017	12
4	The interpretation of genetic tests in inherited cardiovascular diseases	Neurology International	2011	11
5	Migraine headache in patients with idiopathic intracranial hypertension	Neurology International	2017	11
6	LQTS-associated mutation A257G in α1-syntrophin interacts with the intragenic variant P74L to modify its biophysical phenotype	Neurology International	2011	9
7	Atrioventricular Canal Defect and Associated Genetic Disorders: New Insights into Polydactyly Syndromes	Neurology International	2011	6
8	Short QT Syndrome	Neurology International	2011	6
9	Cardiovascular Characteristics of Patients with Genetic Variation in Desmoplakin (DSP)	Neurology International	2022	6
10	Sudden Infant Death Syndrome and Cardiac Channelopathies: From Mechanisms to Prevention of Avoidable Tragedies	Neurology International	2011	5
11	Matrix Metalloproteinase 9 Polymorphism and Outcome after Myocardial Infarction	Neurology International	2011	5
12	Compound Heterozygous SCN5A Gene Mutations in Aasymptomatic Brugada Syndrome Child	Neurology International	2012	5
13	Molecular basis, diagnosis and clinical management of mucopolysaccharidoses	Neurology International	2013	5
14	Pompe disease, a storage cardiomyopathy	Neurology International	2017	5
15	Biventricular Strain Imaging with Cardiac MRI in Genotyped and Histology Validated Amyloid Cardiomyopathy	Neurology International	2021	5
16	Mutations in MYBPC3 and MYH7 in Association with Brugada Type 1 ECG Pattern: Overlap between Brugada Syndrome and Hypertrophic Cardiomyopathy?	Neurology International	2021	5
17	Recent advances in the genetics of atrial fibrillation: from rare and common genetic variants to microRNA signaling	Neurology International	2011	4
18	Tafazzin Gene Mutations Are Uncommon Causes of Dilated Cardiomyopathy in Adults	Neurology International	2011	4
19	Echocardiography in Fabry disease	Neurology International	2013	4
20	Cost-Effectiveness of Genetic Studies in Inherited Heart Diseases	Neurology International	2013	4
21	Analysis of ABC Transporter Gene Expression in Atherosclerosis	Neurology International	2021	4
22	The Roles of Platelet-Activating Factor and Magnesium in Pathophysiology of Hypertension, Atherogenesis, Cardiovascular Disease, Stroke and Aging	Neurology International	2022	4
23	Genetics of Heritable Thoracic Aortic Disease	Neurology International	2022	4
24	The Novel Role of Epigenetics in Primary Prevention of Cardiovascular Diseases	Neurology International	2012	3
25	Idiopathic restrictive cardiomyopathy - perspectives from genetics studies. Is it time to redefine these disorders?	Neurology International	2012	3
26	Genetic disturbances in patients with bodily isomerism from a single center: clinical implications of affected genes and potential impact of ciliary dyskinesia	Neurology International	2016	3
27	Measurement of troponin in cardiomyopathies	Neurology International	2016	3
28	Lamin-A/C variants found in patients with cardiac conduction disease reduce sodium currents	Neurology International	2018	3
29	Reverse Takotsubo Syndrome, a Case Report of a Rare Cause for Postpartum Heart Failure	Neurology International	2018	3
30	FLNC Missense Variants in Familial Noncompaction Cardiomyopathy	Neurology International	2019	3
31	Sudden cardiac death in young athletes: Literature review of molecular basis	Neurology International	2020	3
32	The Multi-Ethnic New Zealand Study of Acute Coronary Syndromes (MENZACS): Design and Methodology	Neurology International	2021	3
33	MYH7 Genotype–Phenotype Correlation in a Cohort of Finnish Patients	Neurology International	2022	3
34	Genetic Screening of a Large Panel of Genes Associated with Cardiac Disease in a Spanish Heart Transplanted Cohort	Neurology International	2022	3
35	Time for education in cardiogenetics	Neurology International	2011	2
36	Genetics of Cardiomyopathies in Children	Neurology International	2011	2
37	Phenotypic spectrum of mutations in cardiolaminopathies	Neurology International	2011	2
38	A new era in cardiogenetics	Neurology International	2011	2
39	Catecholaminergic polymorphic ventricular tachycardia in 2012	Neurology International	2011	2
40	Ion Channels and Beating Heart: The Players and the Music	Neurology International	2011	2
41	Cardiac Electrical System Involvement in Alström Syndrome: Uncommon Causes of Dilated Cardiomyopathies	Neurology International	2012	2
42	A new clonal chromosomal aberration (47, XY, +21) in atrial myxoma from an elderly male patient	Neurology International	2012	2
43	Restrictive Cardiomyopathy and Hypertrophic Cardiomyopathy Overlap: The Importance of the Phenotype	Neurology International	2012	2
44	Lamin A/C Mutation Affecting Primarily the Right Side of the Heart	Neurology International	2013	2
45	Myocardial Deformation Imaging and Rare Cardiomyopathies with Hypertrophic Phenotype: A Review Focused on Fabry Disease, Friedreich Ataxia and Amyloidosis	Neurology International	2013	2
46	Atrial fibrillation is poorly tolerated by patients with hypertrophic concentric cardiomyopathy caused by mitochondrial tRNALeu (UUR) mutations	Neurology International	2013	2
47	Molecular Basis and Clinical Management of Gaucher Disease	Neurology International	2013	2
48	Molecular basis and clinical management of Pompe disease	Neurology International	2013	2
49	Cardiac Imaging in RASopathies/Mitogen Activated Protein Kinase Syndromes	Neurology International	2014	2
50	The impact of β 2 adrenergic receptor polymorphisms on the outcomes in cardiovascular diseases	Neurology International	2014	2

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