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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:

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

Showing 1-25 of 51 citing articles:

Zebrafish disease models in drug discovery: from preclinical modelling to clinical trials
E. Elizabeth Patton, Leonard I. Zon, David M. Langenau
Nature Reviews Drug Discovery (2021) Vol. 20, Iss. 8, pp. 611-628
Open Access | Times Cited: 361
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
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
Six years’ accomplishment of the Initiative on Rare and Undiagnosed Diseases: nationwide project in Japan to discover causes, mechanisms, and cures
Yūji Takahashi, Hidetoshi Date, Hideki Oi, et al.
Journal of Human Genetics (2022) Vol. 67, Iss. 9, pp. 505-513
Open Access | Times Cited: 29
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
Inflammatory response in hematopoietic stem and progenitor cells triggered by activating SHP2 mutations evokes blood defects
Maja Šolman, Sasja Blokzijl-Franke, Florian Piques, et al.
eLife (2022) Vol. 11
Open Access | Times Cited: 20
Functional and structural insights into RAS effector proteins
Alessandro M. Mozzarelli, Dhirendra K. Simanshu, Pau Castel
Molecular Cell (2024) Vol. 84, Iss. 15, pp. 2807-2821
Closed Access | Times Cited: 4
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
Structural insights into isoform-specific RAS-PI3Kα interactions and the role of RAS in PI3Kα activation
Daniel J. Czyzyk, Wupeng Yan, Simon Messing, et al.
Nature Communications (2025) Vol. 16, Iss. 1
Open Access
Active R-RAS2/TC21 prevents cell cycle arrest and morphological alterations in mouse embryonic fibroblasts lacking RAS proteins
Isabel Fernández‐Pisonero, L. Francisco Lorenzo‐Martín, Matthias Drosten, et al.
Oncogene (2025)
Open Access
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
Long-term efficacy and safety of two doses of Norditropin<sup>®</sup> (somatropin) in Noonan syndrome: a 4-year randomized, double-blind, multicenter trial in Japanese patients
Reiko Horikawa, Tsutomu Ogata, Yoichi Matsubara, et al.
Endocrine Journal (2020) Vol. 67, Iss. 8, pp. 803-818
Open Access | Times Cited: 21
Clinical and molecular spectra of BRAF-associated RASopathy
Yena Lee, Yunha Choi, Go Hun Seo, et al.
Journal of Human Genetics (2020) Vol. 66, Iss. 4, pp. 389-399
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
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
Identification of Novel Autoantibodies Based on the Human Proteomic Chips and Evaluation of Their Performance in the Detection of Gastric Cancer
Chi Cui, Yaru Duan, Cuipeng Qiu, et al.
Frontiers in Oncology (2021) Vol. 11
Open Access | Times Cited: 15
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
Genome-wide association analysis reveals insights into the molecular etiology underlying dilated cardiomyopathy
Sean Zheng, Albert Henry, Douglas Cannie, et al.
medRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 5
SHP2 mutations induce precocious gliogenesis of Noonan syndrome-derived iPSCs during neural development in vitro
Younghee Ju, Jun Sung Park, Daejeong Kim, et al.
Stem Cell Research & Therapy (2020) Vol. 11, Iss. 1
Open Access | Times Cited: 14
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