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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:

Spectrum of mutations and genotype–phenotype analysis in Noonan syndrome patients with RIT1 mutations
Masako Yaoita, Tetsuya Niihori, Seiji Mizuno, et al.
Human Genetics (2015) Vol. 135, Iss. 2, pp. 209-222
Closed Access | Times Cited: 90

Showing 1-25 of 90 citing articles:

Genetic Basis for Congenital Heart Disease: Revisited: A Scientific Statement From the American Heart Association
Mary Ella Pierpont, Martina Brueckner, Wendy K. Chung, et al.
Circulation (2018) Vol. 138, Iss. 21
Open Access | Times Cited: 525
The RASopathy Family: Consequences of Germline Activation of the RAS/MAPK Pathway
Mylène Tajan, Romain Paccoud, Sophie Branka, et al.
Endocrine Reviews (2018) Vol. 39, Iss. 5, pp. 676-700
Open Access | Times Cited: 196
ARAF recurrent mutation causes central conducting lymphatic anomaly treatable with a MEK inhibitor
Dong Li, Michael March, Álvaro Gutiérrez-Uzquiza, et al.
Nature Medicine (2019) Vol. 25, Iss. 7, pp. 1116-1122
Closed Access | Times Cited: 182
Whole Genome Sequencing Improves Outcomes of Genetic Testing in Patients With Hypertrophic Cardiomyopathy
Richard D. Bagnall, Jodie Ingles, Marcel E. Dinger, et al.
Journal of the American College of Cardiology (2018) Vol. 72, Iss. 4, pp. 419-429
Open Access | Times Cited: 167
A novel rasopathy caused by recurrent de novo missense mutations in PPP1CB closely resembles Noonan syndrome with loose anagen hair
Karen W. Gripp, Kimberly A. Aldinger, James T. Bennett, et al.
American Journal of Medical Genetics Part A (2016) Vol. 170, Iss. 9, pp. 2237-2247
Open Access | Times Cited: 138
RIT1 oncoproteins escape LZTR1-mediated proteolysis
Pau Castel, Alice Cheng, Antonio Cuevas-Navarro, et al.
Science (2019) Vol. 363, Iss. 6432, pp. 1226-1230
Open Access | Times Cited: 96
The Ras Superfamily of Small GTPases in Non-neoplastic Cerebral Diseases
Liang Qu, Chao Pan, Shiming He, et al.
Frontiers in Molecular Neuroscience (2019) Vol. 12
Open Access | Times Cited: 76
Primary lymphoedema
Pascal Brouillard, Marlys H. Witte, Robert P. Erickson, et al.
Nature Reviews Disease Primers (2021) Vol. 7, Iss. 1
Closed Access | Times Cited: 62
Noonan syndrome in diverse populations
Paul Kruszka, Antonio R. Porras, Yonit A. Addissie, et al.
American Journal of Medical Genetics Part A (2017) Vol. 173, Iss. 9, pp. 2323-2334
Open Access | Times Cited: 82
Delineation of LZTR1 mutation-positive patients with Noonan syndrome and identification of LZTR1 binding to RAF1–PPP1CB complexes
Ikumi Umeki, Tetsuya Niihori, Taiki Abe, et al.
Human Genetics (2018) Vol. 138, Iss. 1, pp. 21-35
Closed Access | Times Cited: 71
Williams–Beuren syndrome in diverse populations
Paul Kruszka, Antonio R. Porras, Deise Helena de Souza, et al.
American Journal of Medical Genetics Part A (2018) Vol. 176, Iss. 5, pp. 1128-1136
Open Access | Times Cited: 64
Hypertrophic Cardiomyopathy in RASopathies
Michele Lioncino, Emanuele Monda, Federica Verrillo, et al.
Heart Failure Clinics (2021) Vol. 18, Iss. 1, pp. 19-29
Open Access | Times Cited: 52
Genotype‐cardiac phenotype correlations in a large single‐center cohort of patients affected by RASopathies: Clinical implications and literature review
Chiara Leoni, Rita Blandino, Angelica Bibiana Delogu, et al.
American Journal of Medical Genetics Part A (2021) Vol. 188, Iss. 2, pp. 431-445
Closed Access | Times Cited: 43
Cardiovascular disease in Noonan syndrome
Mary Ella Pierpont, M. Cristina Digilio
Current Opinion in Pediatrics (2018) Vol. 30, Iss. 5, pp. 601-608
Closed Access | Times Cited: 59
Genetic tests in lymphatic vascular malformations and lymphedema
Sandro Michelini, Stefano Paolacci, Elena Manara, et al.
Journal of Medical Genetics (2018) Vol. 55, Iss. 4, pp. 222-232
Closed Access | Times Cited: 50
Lymphatic Abnormalities in Noonan Syndrome Spectrum Disorders: A Systematic Review
Julia Sleutjes, Lotte E. R. Kleimeier, Erika Leenders, et al.
Molecular Syndromology (2021) Vol. 13, Iss. 1, pp. 1-11
Open Access | Times Cited: 34
RAS-dependent RAF-MAPK hyperactivation by pathogenic RIT1 is a therapeutic target in Noonan syndrome–associated cardiac hypertrophy
Antonio Cuevas-Navarro, Morgan E. Wagner, Richard Van, et al.
Science Advances (2023) Vol. 9, Iss. 28
Open Access | Times Cited: 13
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
Clinical and mutation profile of pediatric patients with RASopathy-associated hypertrophic cardiomyopathy: results from a Chinese cohort
Hao Chen, Xin Li, Xiaoliang Liu, et al.
Orphanet Journal of Rare Diseases (2019) Vol. 14, Iss. 1
Open Access | Times Cited: 40
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
Cognitive Phenotype and Psychopathology in Noonan Syndrome Spectrum Disorders through Various Ras/MAPK Pathway Associated Gene Variants
Ellen Wingbermühle, Renée L. Roelofs, Wouter Oomens, et al.
Journal of Clinical Medicine (2022) Vol. 11, Iss. 16, pp. 4735-4735
Open Access | Times Cited: 19
The heart in RASopathies
Angelica Bibiana Delogu, Giuseppe Limongelli, Paolo Versacci, et al.
American Journal of Medical Genetics Part C Seminars in Medical Genetics (2022) Vol. 190, Iss. 4, pp. 440-451
Closed Access | Times Cited: 19
Modulating PAK1: Accessory Proteins as Promising Therapeutic Targets
Amin Mirzaiebadizi, Rana Shafabakhsh, Mohammad Reza Ahmadian
Biomolecules (2025) Vol. 15, Iss. 2, pp. 242-242
Open Access
Update on the Clinical and Molecular Characterization of Noonan Syndrome and Other RASopathies: A Retrospective Study and Systematic Review
G.J. Reynolds, Andrea Gazzin, Diana Carli, et al.
International Journal of Molecular Sciences (2025) Vol. 26, Iss. 8, pp. 3515-3515
Open Access
Structural fingerprints, interactions, and signaling networks of RAS family proteins beyond RAS isoforms
Saeideh Nakhaei‐Rad, Fereshteh Haghighi, Parivash Nouri, et al.
Critical Reviews in Biochemistry and Molecular Biology (2018) Vol. 53, Iss. 2, pp. 130-156
Closed Access | Times Cited: 38
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