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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:

Activating Mutations of RRAS2 Are a Rare Cause of Noonan Syndrome
Yline Capri, Elisabetta Flex, Oliver H.F. Krumbach, et al.
The American Journal of Human Genetics (2019) Vol. 104, Iss. 6, pp. 1223-1232
Open Access | Times Cited: 64

Showing 1-25 of 64 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
Noonan syndrome: improving recognition and diagnosis
Martin Zenker, Thomas Édouard, Joanne Blair, et al.
Archives of Disease in Childhood (2022) Vol. 107, Iss. 12, pp. 1073-1078
Open Access | Times Cited: 75
SPRED2 loss-of-function causes a recessive Noonan syndrome-like phenotype
Marialetizia Motta, Giulia Fasano, Sina Gredy, et al.
The American Journal of Human Genetics (2021) Vol. 108, Iss. 11, pp. 2112-2129
Open Access | Times Cited: 57
The molecular genetics of RASopathies: An update on novel disease genes and new disorders
Marco Tartaglia, Yoko Aoki, Bruce D. Gelb
American Journal of Medical Genetics Part C Seminars in Medical Genetics (2022) Vol. 190, Iss. 4, pp. 425-439
Open Access | Times Cited: 43
Health outcomes and drug utilisation in children with Noonan syndrome: a European cohort study
Michele Santoro, Ingeborg Barišić, Alessio Coi, et al.
Orphanet Journal of Rare Diseases (2025) Vol. 20, Iss. 1
Open Access | Times Cited: 1
Germline-Activating RRAS2 Mutations Cause Noonan Syndrome
Tetsuya Niihori, Koki Nagai, Atsushi Fujita, et al.
The American Journal of Human Genetics (2019) Vol. 104, Iss. 6, pp. 1233-1240
Open Access | Times Cited: 51
The Role of R-Ras Proteins in Normal and Pathologic Migration and Morphologic Change
Shannon M. Weber, Steven L. Carroll
American Journal Of Pathology (2021) Vol. 191, Iss. 9, pp. 1499-1510
Open Access | Times Cited: 35
Activating MRAS mutations cause Noonan syndrome associated with hypertrophic cardiomyopathy
Marialetizia Motta, Lena Sagi‐Dain, Oliver H.F. Krumbach, et al.
Human Molecular Genetics (2019) Vol. 29, Iss. 11, pp. 1772-1783
Closed Access | Times Cited: 42
When to test fetuses for RASopathies? Proposition from a systematic analysis of 352 multicenter cases and a postnatal cohort
Alexandra MS Scott, Niccolò Di Giosaffatte, Valentina Pinna, et al.
Genetics in Medicine (2021) Vol. 23, Iss. 6, pp. 1116-1124
Open Access | Times Cited: 31
Juvenile myelomonocytic leukemia in the molecular era: a clinician’s guide to diagnosis, risk stratification, and treatment
Astrid Wintering, Christopher C. Dvorak, Elliot Stieglitz, et al.
Blood Advances (2021) Vol. 5, Iss. 22, pp. 4783-4793
Open Access | Times Cited: 28
Identification of a novel frameshift variation in ANKRD11: a case report of KBG syndrome
Qing Shao, Qiang Jiang, Yuqi Luo, et al.
Frontiers in Genetics (2025) Vol. 15
Open Access
Drosophila RASopathy models identify disease subtype differences and biomarkers of drug efficacy
Tirtha K. Das, Jared Gatto, Rupa Mirmira, et al.
iScience (2021) Vol. 24, Iss. 4, pp. 102306-102306
Open Access | Times Cited: 25
The role of key biomarkers in lymphatic malformation: An updated review
Mohammad-Hadi Saeed Modaghegh, Hamid Tanzadehpanah, Mohammad Mahdi Kamyar, et al.
The Journal of Gene Medicine (2024) Vol. 26, Iss. 2
Closed Access | Times Cited: 3
The ancestral type of the R-RAS protein has oncogenic potential
Antea Talajić, Kristina Dominko, Marija Lončarić, et al.
Cellular & Molecular Biology Letters (2024) Vol. 29, Iss. 1
Open Access | Times Cited: 3
RASopathies – what they reveal about RAS/MAPK signaling in skeletal muscle development
Katherine A. Rauen, William E. Tidyman
Disease Models & Mechanisms (2024) Vol. 17, Iss. 6
Open Access | Times Cited: 3
Genome-wide association analysis provides insights into the molecular etiology of dilated cardiomyopathy
Sean L. Zheng, Albert Henry, Douglas Cannie, et al.
Nature Genetics (2024) Vol. 56, Iss. 12, pp. 2646-2658
Open Access | Times Cited: 3
A hotspot mutation targeting the R-RAS2 GTPase acts as a potent oncogenic driver in a wide spectrum of tumors
Isabel Fernández‐Pisonero, Laura Clavaín, Javier Robles‐Valero, et al.
Cell Reports (2022) Vol. 38, Iss. 11, pp. 110522-110522
Open Access | Times Cited: 15
Functional diversity in the RAS subfamily of small GTPases
Gabriela Bernal Astrain, Maya Nikolova, Matthew J. Smith
Biochemical Society Transactions (2022) Vol. 50, Iss. 2, pp. 921-933
Closed Access | Times Cited: 14
Activation of the MAPK pathway (RASopathies) and partial growth hormone insensitivity
Alexsandra C. Malaquias, Alexander A.L. Jorge
Molecular and Cellular Endocrinology (2020) Vol. 519, pp. 111040-111040
Closed Access | Times Cited: 19
Dominant ARF3 variants disrupt Golgi integrity and cause a neurodevelopmental disorder recapitulated in zebrafish
Giulia Fasano, Valentina Muto, Francesca Clementina Radio, et al.
Nature Communications (2022) Vol. 13, Iss. 1
Open Access | Times Cited: 12
Phenotypic and genotypic spectrum of noonan syndrome: A retrospective analysis of 46 consecutive pediatric patients presented at a regional cardiac center in China
Qinchang Chen, Dian Hong, Yulu Huang, et al.
Heliyon (2024) Vol. 10, Iss. 5, pp. e27038-e27038
Open Access | Times Cited: 2
Functional analysis of RRAS2 pathogenic variants with a Noonan-like phenotype
Takaya Iida, Arisa Igarashi, Kae Fukunaga, et al.
Frontiers in Genetics (2024) Vol. 15
Open Access | Times Cited: 2
Swimming toward solutions: Using fish and frogs as models for understandingRASopathies
Victoria L. Patterson, Rebecca D. Burdine
Birth Defects Research (2020) Vol. 112, Iss. 10, pp. 749-765
Open Access | Times Cited: 17
Identifying the genetic causes of phenotypically diagnosed Pakistani mucopolysaccharidoses patients by whole genome sequencing
Rutaba Gul, Sabika Firasat, Mikkel Schubert, et al.
Frontiers in Genetics (2023) Vol. 14
Open Access | Times Cited: 5
MicroRNA-23b Plays a Tumor-Suppressive Role in Cutaneous Squamous Cell Carcinoma and Targets Ras-Related Protein RRAS2
Chengxi Sun, Kunal Das Mahapatra, Jonathan Elton, et al.
Journal of Investigative Dermatology (2023) Vol. 143, Iss. 12, pp. 2386-2396
Open Access | Times Cited: 5
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