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:
Molecular autopsy and clinical family screening in a case of sudden cardiac death reveals ACTN2 mutation related to hypertrophic/dilated cardiomyopathy and a novel LZTR1 variant associated with Noonan syndrome
Lilia Kraoua, Hager Jaouadi, Mohamed Allouche, et al.
Molecular Genetics & Genomic Medicine (2022) Vol. 10, Iss. 7
Open Access | Times Cited: 11
Lilia Kraoua, Hager Jaouadi, Mohamed Allouche, et al.
Molecular Genetics & Genomic Medicine (2022) Vol. 10, Iss. 7
Open Access | Times Cited: 11
Showing 11 citing articles:
Sudden Cardiac Death, Post-Mortem Investigation: A Proposing Panel of First Line and Second Line Genetic Tests
Fabio Del Duca, Alessandro Ghamlouch, A Manetti, et al.
Journal of Personalized Medicine (2024) Vol. 14, Iss. 5, pp. 544-544
Open Access | Times Cited: 5
Fabio Del Duca, Alessandro Ghamlouch, A Manetti, et al.
Journal of Personalized Medicine (2024) Vol. 14, Iss. 5, pp. 544-544
Open Access | Times Cited: 5
Mutation update for the ACTN2 gene
Johanna Ranta‐aho, Montse Olivé, Marie Vandroux, et al.
Human Mutation (2022) Vol. 43, Iss. 12, pp. 1745-1756
Open Access | Times Cited: 22
Johanna Ranta‐aho, Montse Olivé, Marie Vandroux, et al.
Human Mutation (2022) Vol. 43, Iss. 12, pp. 1745-1756
Open Access | Times Cited: 22
Morphological and Genetic Aspects for Post-Mortem Diagnosis of Hypertrophic Cardiomyopathy: A Systematic Review
Vincenzo Cianci, Elena Forzese, Daniela Sapienza, et al.
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 2, pp. 1275-1275
Open Access | Times Cited: 4
Vincenzo Cianci, Elena Forzese, Daniela Sapienza, et al.
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 2, pp. 1275-1275
Open Access | Times Cited: 4
New Insights on Molecular Autopsy in Sudden Death: A Systematic Review
Luca Tomassini, Giulia Ricchezze, Piergiorgio Fedeli, et al.
Diagnostics (2024) Vol. 14, Iss. 11, pp. 1151-1151
Open Access | Times Cited: 3
Luca Tomassini, Giulia Ricchezze, Piergiorgio Fedeli, et al.
Diagnostics (2024) Vol. 14, Iss. 11, pp. 1151-1151
Open Access | Times Cited: 3
Phenotypic Expansion of Autosomal Dominant LZTR1-Related Disorders with Special Emphasis on Adult-Onset Features
Vera Uliana, Enrico Ambrosini, Antonietta Taiani, et al.
Genes (2024) Vol. 15, Iss. 7, pp. 916-916
Open Access | Times Cited: 3
Vera Uliana, Enrico Ambrosini, Antonietta Taiani, et al.
Genes (2024) Vol. 15, Iss. 7, pp. 916-916
Open Access | Times Cited: 3
RareACTN2Frameshift Variants Resulting in Protein Extension Cause Distal Myopathy and Hypertrophic Cardiomyopathy through Protein Aggregation
Johanna Ranta‐aho, Kevin J. Felice, Per Harald Jonson, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 1
Johanna Ranta‐aho, Kevin J. Felice, Per Harald Jonson, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 1
Biventricular outflow tract obstruction due to hypertrophy related to compound heterozygous variants in LZTR1
Shuai Wang, Daoquan Peng
ESC Heart Failure (2024) Vol. 11, Iss. 6, pp. 4450-4455
Open Access | Times Cited: 1
Shuai Wang, Daoquan Peng
ESC Heart Failure (2024) Vol. 11, Iss. 6, pp. 4450-4455
Open Access | Times Cited: 1
Actn2 defects accelerates H9c2 hypertrophy via ERK phosphorylation under chronic stress
Kang Wang, Ye Wang, Hua Wan, et al.
Genes & Genomics (2024) Vol. 46, Iss. 9, pp. 1013-1022
Closed Access
Kang Wang, Ye Wang, Hua Wan, et al.
Genes & Genomics (2024) Vol. 46, Iss. 9, pp. 1013-1022
Closed Access
Exome sequencing data reanalysis of 200 hypertrophic cardiomyopathy patients: the HYPERGEN French cohort 5 years after the initial analysis
Hager Jaouadi, Victor Morel, Hélène Martel, et al.
Frontiers in Medicine (2024) Vol. 11
Open Access
Hager Jaouadi, Victor Morel, Hélène Martel, et al.
Frontiers in Medicine (2024) Vol. 11
Open Access
Biallelic LZTR1 variants in a 49‐year‐old woman with hypertrophic cardiomyopathy: A clue for considering LZTR1 in adults
Giuseppe Di Stolfo, Antonio Petracca, Ester Maria Lucia Bevere, et al.
American Journal of Medical Genetics Part A (2023) Vol. 194, Iss. 5
Open Access
Giuseppe Di Stolfo, Antonio Petracca, Ester Maria Lucia Bevere, et al.
American Journal of Medical Genetics Part A (2023) Vol. 194, Iss. 5
Open Access
