OpenAlex Citation Counts

OpenAlex Citations Logo

OpenAlex is a bibliographic catalogue of scientific papers, authors and institutions accessible in open access mode, named after the Library of Alexandria. It's citation coverage is excellent and I hope you will find utility in this listing of citing articles!

If you click the article title, you'll navigate to the article, as listed in CrossRef. If you click the Open Access links, you'll navigate to the "best Open Access location". Clicking the citation count will open this listing for that article. Lastly at the bottom of the page, you'll find basic pagination options.

Requested Article:

Left ventricular noncompaction − Risk stratification and genetic consideration −
Fukiko Ichida
Journal of Cardiology (2019) Vol. 75, Iss. 1, pp. 1-9
Open Access | Times Cited: 54

Showing 1-25 of 54 citing articles:

Noncompaction Cardiomyopathy—History and Current Knowledge for Clinical Practice
Birgit Gerecke, Rolf Engberding
Journal of Clinical Medicine (2021) Vol. 10, Iss. 11, pp. 2457-2457
Open Access | Times Cited: 37

Ventricular non-compaction review
Shaurya Srivastava, Majid Yavari, Abdullah Al‐Abcha, et al.
Heart Failure Reviews (2021) Vol. 27, Iss. 4, pp. 1063-1076
Closed Access | Times Cited: 35

Lack of morphometric evidence for ventricular compaction in humans
Jaeike W. Faber, Andrew D’Silva, Vincent M. Christoffels, et al.
Journal of Cardiology (2021) Vol. 78, Iss. 5, pp. 397-405
Open Access | Times Cited: 34

Left Ventricular Noncompaction and Congenital Heart Disease Increases the Risk of Congestive Heart Failure
Keiichi Hirono, Yukiko Hata, Nariaki Miyao, et al.
Journal of Clinical Medicine (2020) Vol. 9, Iss. 3, pp. 785-785
Open Access | Times Cited: 33

Genetic landscape in Russian patients with familial left ventricular noncompaction
А. Н. Мешков, R. P. Myasnikov, А. В. Киселева, et al.
Frontiers in Cardiovascular Medicine (2023) Vol. 10
Open Access | Times Cited: 11

How to Approach Left Ventricular Hypertrabeculation: A Practical Guide and Literature Review
Michele Alfieri, Samuele Principi, Alessandro Barbarossa, et al.
Journal of Clinical Medicine (2025) Vol. 14, Iss. 3, pp. 695-695
Open Access

Understanding the molecular basis of cardiomyopathy
Marie‐Louise Bang, Julius Bogomolovas, Ju Chen
AJP Heart and Circulatory Physiology (2021) Vol. 322, Iss. 2, pp. H181-H233
Open Access | Times Cited: 25

Genetic, clinical and imaging implications of a noncompaction phenotype population with preserved ejection fraction
Kinga Grebur, Balázs Mester, Bálint András Fekete, et al.
Frontiers in Cardiovascular Medicine (2024) Vol. 11
Open Access | Times Cited: 3

Elevated myocardial SORBS2 and the underlying implications in left ventricular noncompaction cardiomyopathy
Chunyan Li, Fan Liu, Shenghua Liu, et al.
EBioMedicine (2020) Vol. 53, pp. 102695-102695
Open Access | Times Cited: 27

Genetic Factors Underlying Sudden Infant Death Syndrome
Christine Keywan, Annapurna Poduri, Richard D. Goldstein, et al.
The Application of Clinical Genetics (2021) Vol. Volume 14, pp. 61-76
Open Access | Times Cited: 21

Genetic Profile of Left Ventricular Noncompaction Cardiomyopathy in Children—A Single Reference Center Experience
Dorota Piekutowska‐Abramczuk, Agata Paszkowska, Elżbieta Ciara, et al.
Genes (2022) Vol. 13, Iss. 8, pp. 1334-1334
Open Access | Times Cited: 10

Unusual Evolution of Hypertrophic Cardiomyopathy in Non-Compaction Myocardium in a Pompe Disease Patient
Vincenza Gragnaniello, Caterina Rizzardi, Anna Commone, et al.
Journal of Clinical Medicine (2023) Vol. 12, Iss. 6, pp. 2365-2365
Open Access | Times Cited: 4

Differences in phenotypes, symptoms, and survival in patients with cardiomyopathy—a prospective observational study from the Sahlgrenska CardioMyoPathy Centre
Charlotta Ljungman, Entela Bollano, Araz Rawshani, et al.
Frontiers in Cardiovascular Medicine (2023) Vol. 10
Open Access | Times Cited: 4

Case Report: Novel Likely Pathogenic ACTN2 Variant Causing Heterogeneous Phenotype in a Korean Family With Left Ventricular Non-compaction
Joonhong Park, Yong Gon Cho, Ha Wook Park, et al.
Frontiers in Pediatrics (2021) Vol. 9
Open Access | Times Cited: 10

Splicing factor Srsf5 deletion disrupts alternative splicing and causes noncompaction of ventricular myocardium
Xiaoli Zhang, Ze Wang, Qing Xu, et al.
iScience (2021) Vol. 24, Iss. 10, pp. 103097-103097
Open Access | Times Cited: 8

RBM20 nucleotide sequence variant in a family with a dilated phenotype of left ventricular non-compaction
О. В. Куликова, R. P. Myasnikov, А. Н. Мешков, et al.
CARDIOVASCULAR THERAPY AND PREVENTION (2023) Vol. 21, Iss. 12, pp. 3470-3470
Open Access | Times Cited: 3

Diverse cardiac phenotypes among different carriers of the same MYH7 splicing variant allele (c.732+1G>A) from a family
Peng Tu, Hairui Sun, Xiaohang Zhang, et al.
BMC Medical Genomics (2022) Vol. 15, Iss. 1
Open Access | Times Cited: 5

The Feline Cardiomyopathies: 3. Cardiomyopathies other than HCM
Mark D. Kittleson, Étienne Côté
Journal of Feline Medicine and Surgery (2021) Vol. 23, Iss. 11, pp. 1053-1067
Open Access | Times Cited: 6

The mitral regurgitation effects of cardiac structure and function in left ventricular noncompaction
Qing Zou, Rong Xu, Xiao Li, et al.
Scientific Reports (2021) Vol. 11, Iss. 1
Open Access | Times Cited: 5

Left Ventricular Noncompaction as a Rare Cause of Syncope
Pius Ojemolon, Endurance O Evbayekha, Jesse Odion, et al.
Cureus (2021)
Open Access | Times Cited: 4

Clinical profile and outcome of cardiomyopathies in infants and children seen at a tertiary centre
Monica B. Pagano, Carlo Fumagalli, Francesca Girolami, et al.
International Journal of Cardiology (2022) Vol. 371, pp. 516-522
Closed Access | Times Cited: 3

Page 1 - Next Page

Scroll to top