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OpenAlex Citation Counts

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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:

Mechanisms of Congenital Heart Disease Caused by NAA15 Haploinsufficiency
Tarsha Ward, Warren Tai, Sarah U. Morton, et al.
Circulation Research (2021) Vol. 128, Iss. 8, pp. 1156-1169
Open Access | Times Cited: 46

Showing 1-25 of 46 citing articles:

Biallelic NAA60 variants with impaired N-terminal acetylation capacity cause autosomal recessive primary familial brain calcifications
Viorica Chelban, Henriette Aksnes, Reza Maroofian, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 18
Illuminating the impact of N-terminal acetylation: from protein to physiology
Nina McTiernan, Ine Kjosås, Thomas Arnesen
Nature Communications (2025) Vol. 16, Iss. 1
Open Access | Times Cited: 3
Expanding the phenotypic spectrum of NAA10-related neurodevelopmental syndrome and NAA15-related neurodevelopmental syndrome
Gholson J. Lyon, Marall Vedaie, Travis Beisheim, et al.
European Journal of Human Genetics (2023) Vol. 31, Iss. 7, pp. 824-833
Open Access | Times Cited: 42
N-terminal acetylation shields proteins from degradation and promotes age-dependent motility and longevity
Sylvia Varland, Rui D. Silva, Ine Kjosås, et al.
Nature Communications (2023) Vol. 14, Iss. 1
Open Access | Times Cited: 31
The Cardiovascular Manifestations and Management Recommendations for Ogden Syndrome
Rikhil Makwana, Rahi Patel, Rosemary O’Neill, et al.
medRxiv (Cold Spring Harbor Laboratory) (2025)
Open Access | Times Cited: 1
Longitudinal adaptive behavioral outcomes in Ogden syndrome by seizure status and therapeutic intervention
Rikhil Makwana, Carolina Christ, Elaine Marchi, et al.
American Journal of Medical Genetics Part A (2024) Vol. 194, Iss. 9
Open Access | Times Cited: 7
A Natural History ofNAA15-related Neurodevelopmental Disorder Through Adolescence
Rikhil Makwana, Carolina Christ, Rahi Patel, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 6
Molecular genetic mechanisms of congenital heart disease
Talita Zahin Choudhury, Vidu Garg
Current Opinion in Genetics & Development (2022) Vol. 75, pp. 101949-101949
Open Access | Times Cited: 20
Loss of N-terminal acetyltransferase A activity induces thermally unstable ribosomal proteins and increases their turnover in Saccharomyces cerevisiae
Ulises H. Guzmán, Henriette Aksnes, Rasmus Ree, et al.
Nature Communications (2023) Vol. 14, Iss. 1
Open Access | Times Cited: 13
NATs at a glance
Henriette Aksnes, Nina McTiernan, Thomas Arnesen
Journal of Cell Science (2023) Vol. 136, Iss. 14
Open Access | Times Cited: 12
Neuroanatomical Features of NAA10- and NAA15-Related Neurodevelopmental Syndromes
Rahi Patel, Rikhil Makwana, Carolina Christ, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 4
Natural History of NAA15‐Related Neurodevelopmental Disorder Through Adolescence
Rikhil Makwana, Carolina Christ, Rahi Patel, et al.
American Journal of Medical Genetics Part A (2025)
Open Access
Modeling SMAD2 Mutations in Induced Pluripotent Stem Cells Provides Insights Into Cardiovascular Disease Pathogenesis
Tarsha Ward, Sarah U. Morton, Gabriela Venturini, et al.
Journal of the American Heart Association (2025)
Closed Access
Neuroanatomical Features of NAA10 and NAA15-Related Neurodevelopmental Syndromes
Rahi Patel, Rikhil Makwana, Carolina Christ, et al.
Journal of Neuroradiology (2025), pp. 101339-101339
Open Access
Dysregulation of N-terminal acetylation causes cardiac arrhythmia and cardiomyopathy
Daisuke Yoshinaga, Isabel Craven, Rui Feng, et al.
Nature Communications (2025) Vol. 16, Iss. 1
Open Access
The Cardiovascular Manifestations and Management Recommendations for Ogden Syndrome
Rikhil Makwana, Rahi Patel, Rosemary O’Neill, et al.
Pediatric Cardiology (2025)
Open Access
Novel biallelic variants expand the phenotype of NAA20‐related syndrome
Gianluca D’Onofrio, Claudia Cuccurullo, Silje Kathrine Larsen, et al.
Clinical Genetics (2023) Vol. 104, Iss. 3, pp. 371-376
Closed Access | Times Cited: 7
Diverging co-translational protein complex assembly pathways are governed by interface energy distribution
Johannes Venezian, Hagit Bar-Yosef, Hila Zilberman, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 2
Longitudinal Adaptive Behavioral Outcomes in Ogden Syndrome by Seizure Status and Therapeutic Intervention
Rikhil Makwana, Carolina Christ, Elaine Marchi, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 2
Dysregulation of N-terminal acetylation causes cardiac arrhythmia and cardiomyopathy
Vassilios J. Bezzerides, Daisuke Yoshinaga, Rui Feng, et al.
Research Square (Research Square) (2024)
Open Access | Times Cited: 2
Acetyltransferase in cardiovascular disease and aging
Mariko Aoyagi Keller, Michinari Nakamura
The Journal of Cardiovascular Aging (2024) Vol. 4, Iss. 4
Open Access | Times Cited: 2
Missense NAA20 variantsimpairing the NatB protein N-terminal acetyltransferase cause autosomal recessivedevelopmental delay, intellectual disability, and microcephaly
Jennifer Morrison, Norah K. Altuwaijri, Kirsten Brønstad, et al.
Genetics in Medicine (2021) Vol. 23, Iss. 11, pp. 2213-2218
Open Access | Times Cited: 16
A nonsense variant in the N‐terminal acetyltransferase NAA30 may be associated with global developmental delay and tracheal cleft
Sylvia Varland, Kirsten Brønstad, Stephanie Skinner, et al.
American Journal of Medical Genetics Part A (2023) Vol. 191, Iss. 9, pp. 2402-2410
Open Access | Times Cited: 5
Naa12 compensates for Naa10 in mice in the amino-terminal acetylation pathway
Hyae Yon Kweon, Mi-Ni Lee, Max J. Dörfel, et al.
eLife (2021) Vol. 10
Open Access | Times Cited: 11
Network assisted analysis of de novo variants using protein-protein interaction information identified 46 candidate genes for congenital heart disease
Yuhan Xie, Wei Jiang, Weilai Dong, et al.
PLoS Genetics (2022) Vol. 18, Iss. 6, pp. e1010252-e1010252
Open Access | Times Cited: 7
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