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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:

The Noonan Syndrome Gene Lztr1 Controls Cardiovascular Function by Regulating Vesicular Trafficking
Raj Nayan Sewduth, Silvia Pandolfi, Mikhail Steklov, et al.
Circulation Research (2020) Vol. 126, Iss. 10, pp. 1379-1393
Open Access | Times Cited: 28

Showing 1-25 of 28 citing articles:

The RASopathies: from pathogenetics to therapeutics
Katie E. Hebron, Edjay R. Hernandez, Marielle E. Yohe
Disease Models & Mechanisms (2022) Vol. 15, Iss. 2
Open Access | Times Cited: 117
Multi-Omics Integration for the Design of Novel Therapies and the Identification of Novel Biomarkers
Tonči Ivanišević, Raj Nayan Sewduth
Proteomes (2023) Vol. 11, Iss. 4, pp. 34-34
Open Access | Times Cited: 44
The role of insulin/IGF1 signalling in neurodevelopmental and neuropsychiatric disorders – Evidence from human neuronal cell models
János Réthelyi, Katalin Vincze, Dorothea Schall, et al.
Neuroscience & Biobehavioral Reviews (2023) Vol. 153, pp. 105330-105330
Open Access | Times Cited: 19
Novel therapeutic perspectives in Noonan syndrome and RASopathies
Céline Saint-Laurent, Laurène Mazeyrie, Armelle Yart, et al.
European Journal of Pediatrics (2023) Vol. 183, Iss. 3, pp. 1011-1019
Open Access | Times Cited: 18
Spatial Mechano‐Signaling Regulation of GTPases through Non‐Degradative Ubiquitination
Raj Nayan Sewduth, Paolo Carai, Tonči Ivanišević, et al.
Advanced Science (2023) Vol. 10, Iss. 36
Open Access | Times Cited: 11
Cardiotoxicity of Chemotherapy: A Multi-OMIC Perspective
Yan Ma, Mandy O. J. Grootaert, Raj Nayan Sewduth
Journal of Xenobiotics (2025) Vol. 15, Iss. 1, pp. 9-9
Open Access
Roles of Cullin-RING Ubiquitin Ligases in Cardiovascular Diseases
Stephanie Diaz, Kankan Wang, Benita Sjögren, et al.
Biomolecules (2022) Vol. 12, Iss. 3, pp. 416-416
Open Access | Times Cited: 18
Cross-species analysis of LZTR1 loss-of-function mutants demonstrates dependency to RIT1 orthologs
Antonio Cuevas-Navarro, Laura Rodríguez-Muñoz, Joaquím Grego‐Bessa, et al.
eLife (2022) Vol. 11
Open Access | Times Cited: 16
Cracking the Monoubiquitin Code of Genetic Diseases
Raj Nayan Sewduth, Maria Francesca Baietti, Anna Sablina
International Journal of Molecular Sciences (2020) Vol. 21, Iss. 9, pp. 3036-3036
Open Access | Times Cited: 25
Cullin 3 and Blood Pressure Regulation: Insights From Familial Hyperkalemic Hypertension
Yujiro Maeoka, Ryan J. Cornelius, James A. McCormick
Hypertension (2023) Vol. 80, Iss. 5, pp. 912-923
Open Access | Times Cited: 7
The GSK3 kinase and LZTR1 protein regulate the stability of Ras family proteins and the proliferation of pancreatic cancer cells
Chitra Palanivel, Neha Chaudhary, Parthasarathy Seshacharyulu, et al.
Neoplasia (2022) Vol. 25, pp. 28-40
Open Access | Times Cited: 10
ESCRT-III Component CHMP4C Attenuates Cardiac Hypertrophy by Targeting the Endo-Lysosomal Degradation of EGFR
Ao Liu, Huilin Xie, Fangyan Tian, et al.
Hypertension (2023) Vol. 80, Iss. 12, pp. 2674-2686
Closed Access | Times Cited: 5
MEK inhibition in Noonan syndrome patient with severe cardiovascular and lymphatic disease
Rachel D. Török, Brian Feingold, Matthew Bochkoris, et al.
Progress in Pediatric Cardiology (2024) Vol. 72, pp. 101704-101704
Closed Access | Times Cited: 1
Increased dosage of wild-type KRAS protein drivesKRAS-mutant lung tumorigenesis and drug resistance
Tonči Ivanišević, Wout Magits, Yan Ma, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 1
Translating the Role of mTOR- and RAS-Associated Signalopathies in Autism Spectrum Disorder: Models, Mechanisms and Treatment
Verica Vasić, Mattson S. O. Jones, Denise Haslinger, et al.
Genes (2021) Vol. 12, Iss. 11, pp. 1746-1746
Open Access | Times Cited: 10
The Landscape of Point Mutations in Human Protein Coding Genes Leading to Pregnancy Loss
Evgeniia M. Maksiutenko, Yury A. Barbitoff, Yulia A. Nasykhova, et al.
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 24, pp. 17572-17572
Open Access | Times Cited: 2
An Assessment of the Therapeutic Landscape for the Treatment of Heart Disease in the RASopathies
Jae-Sung Yi, Sravan Perla, Anton M. Bennett
Cardiovascular Drugs and Therapy (2022) Vol. 37, Iss. 6, pp. 1193-1204
Closed Access | Times Cited: 4
Ventricular arrhythmia and Noonan Syndrome with LZTR1 Mutations: Expanding the Phenotype with a Case Report and Review of the Literature
Zhuyuan Liu, Yan Huang, Jinxi Wang, et al.
Research Square (Research Square) (2024)
Open Access
The Noncanonical RAS/MAPK Pathway and the RASopathies
Stephanie Mo, Pau Castel
(2024), pp. 427-456
Closed Access
Modeling the Non-NF1 RASopathies
Christine Insinna, Marielle E. Yohe
(2024), pp. 869-893
Closed Access
Integrated in silico MS-based phosphoproteomics and network enrichment analysis of RASopathy proteins
Javier‐Fernando Montero‐Bullón, Óscar González-Velasco, María Isidoro‐García, et al.
Orphanet Journal of Rare Diseases (2021) Vol. 16, Iss. 1
Open Access | Times Cited: 3
Generation of a Mouse Model to Study the Noonan Syndrome Gene Lztr1 in the Telencephalon
Mary Jo Talley, Diana Nardini, Nisha Shabbir, et al.
Frontiers in Cell and Developmental Biology (2021) Vol. 9
Open Access | Times Cited: 2
Cross-species analysis of LZTR1 loss-of-function mutants demonstrates dependency to RIT1 orthologs
Antonio Cuevas-Navarro, Laura Rodríguez-Muñoz, Joaquím Grego‐Bessa, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access | Times Cited: 1
CHMP4C Deficiency Represses Angiogenesis in Chronic Ischemia by Inhibiting Hypoxia-induced Wnt/β-catenin Signaling Activation via GSK3β
Wen Liu, Suling Ding, Zhiwei Zhang, et al.
Research Square (Research Square) (2023)
Open Access
Genotype-Phenotype Correlation in Noonan Syndrome – Focus on LZTR1 and its Substrates
Alexandra Viktoria Busley
(2023)
Open Access
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