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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:

Noonan syndrome and clinically related disorders
Marco Tartaglia, Bruce D. Gelb, Martin Zenker
Best Practice & Research Clinical Endocrinology & Metabolism (2011) Vol. 25, Iss. 1, pp. 161-179
Open Access | Times Cited: 363

Showing 1-25 of 363 citing articles:

2023 ESC Guidelines for the management of cardiomyopathies
Elena Arbelo, Alexandros Protonotarios, Juan R. Gimeno, et al.
European Heart Journal (2023) Vol. 44, Iss. 37, pp. 3503-3626
Open Access | Times Cited: 1038
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
Molecular genetic testing and the future of clinical genomics
Sara Huston, Nicholas Katsanis
Nature Reviews Genetics (2013) Vol. 14, Iss. 6, pp. 415-426
Open Access | Times Cited: 404
The neural crest in cardiac congenital anomalies
Anna L. Keyte, Mary Redmond Hutson
Differentiation (2012) Vol. 84, Iss. 1, pp. 25-40
Open Access | Times Cited: 239
SHP2 sails from physiology to pathology
Mylène Tajan, Audrey de Rocca Serra, Philippe Valet, et al.
European Journal of Medical Genetics (2015) Vol. 58, Iss. 10, pp. 509-525
Closed Access | Times Cited: 214
Ptpn11 deletion in a novel progenitor causes metachondromatosis by inducing hedgehog signalling
Wentian Yang, Jianguo Wang, Douglas C. Moore, et al.
Nature (2013) Vol. 499, Iss. 7459, pp. 491-495
Open Access | Times Cited: 205
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
Neurocristopathies: New insights 150 years after the neural crest discovery
Guillermo A. Vega‐López, Santiago Cerrizuela, Celeste Tríbulo, et al.
Developmental Biology (2018) Vol. 444, pp. S110-S143
Open Access | Times Cited: 179
A new genomic framework to categorize pediatric acute myeloid leukemia
Masayuki Umeda, Jing Ma, Tamara Westover, et al.
Nature Genetics (2024) Vol. 56, Iss. 2, pp. 281-293
Open Access | Times Cited: 37
The role of CRAF in cancer progression: from molecular mechanisms to precision therapies
Melody Riaud, Jennifer Maxwell, Isabel Soria‐Bretones, et al.
Nature reviews. Cancer (2024) Vol. 24, Iss. 2, pp. 105-122
Closed Access | Times Cited: 22
Effects of Raf Dimerization and Its Inhibition on Normal and Disease-Associated Raf Signaling
Alyson K. Freeman, Daniel A. Ritt, Deborah K. Morrison
Molecular Cell (2013) Vol. 49, Iss. 4, pp. 751-758
Open Access | Times Cited: 186
A comprehensive review of genetics and genetic testing in azoospermia
Alaa Hamada, Sandro C. Esteves, Ashok Agarwal
Clinics (2013) Vol. 68, pp. 39-60
Open Access | Times Cited: 182
Outcomes in children with Noonan syndrome and hypertrophic cardiomyopathy: A study from the Pediatric Cardiomyopathy Registry
James D. Wilkinson, April M. Lowe, Bonnie Anne Salbert, et al.
American Heart Journal (2012) Vol. 164, Iss. 3, pp. 442-448
Closed Access | Times Cited: 171
Ras-Mediated Activation of the Raf Family Kinases
Elizabeth M. Terrell, Deborah K. Morrison
Cold Spring Harbor Perspectives in Medicine (2018) Vol. 9, Iss. 1, pp. a033746-a033746
Open Access | Times Cited: 151
Activating mutations in RRAS underlie a phenotype within the RASopathy spectrum and contribute to leukaemogenesis
Elisabetta Flex, Mamta Jaiswal, Francesca Pantaleoni, et al.
Human Molecular Genetics (2014) Vol. 23, Iss. 16, pp. 4315-4327
Open Access | Times Cited: 134
SOS1 mutations in Noonan syndrome: molecular spectrum, structural insights on pathogenic effects, and genotype-phenotype correlations
Francesca Romana Lepri, Alessandro De Luca, Lorenzo Stella, et al.
Human Mutation (2011) Vol. 32, Iss. 7, pp. 760-772
Open Access | Times Cited: 119
Noonan syndrome-causing SHP2 mutants inhibit insulin-like growth factor 1 release via growth hormone-induced ERK hyperactivation, which contributes to short stature
Audrey De Rocca Serra-Nédélec, Thomas Édouard, Karine Tréguer, et al.
Proceedings of the National Academy of Sciences (2012) Vol. 109, Iss. 11, pp. 4257-4262
Open Access | Times Cited: 111
Congenital heart defects in Noonan syndrome: Diagnosis, management, and treatment
Léa Linglart, Bruce D. Gelb
American Journal of Medical Genetics Part C Seminars in Medical Genetics (2020) Vol. 184, Iss. 1, pp. 73-80
Open Access | Times Cited: 110
BRAF gene: From human cancers to developmental syndromes
Muhammad Ramzan Manwar Hussain, Mukhtiar Baig, Hussein S. A. Mohamoud, et al.
Saudi Journal of Biological Sciences (2014) Vol. 22, Iss. 4, pp. 359-373
Open Access | Times Cited: 109
Prenatal diagnostic testing of the Noonan syndrome genes in fetuses with abnormal ultrasound findings
Ellen A. Croonen, Willy M. Nillesen, Kyra E. Stuurman, et al.
European Journal of Human Genetics (2013) Vol. 21, Iss. 9, pp. 936-942
Open Access | Times Cited: 102
The current state of clinical interpretation of sequence variants
Derick Hoskinson, Adrian M. Dubuc, Heather Mason‐Suares
Current Opinion in Genetics & Development (2017) Vol. 42, pp. 33-39
Open Access | Times Cited: 90
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
Hypertrophic Cardiomyopathy in Children: Pathophysiology, Diagnosis, and Treatment of Non-sarcomeric Causes
Emanuele Monda, Marta Rubino, Michele Lioncino, et al.
Frontiers in Pediatrics (2021) Vol. 9
Open Access | Times Cited: 68
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
Phosphorylation of Mammalian Cytochrome c and Cytochrome c Oxidase in the Regulation of Cell Destiny: Respiration, Apoptosis, and Human Disease
Maik Hüttemann, Icksoo Lee, Lawrence I. Grossman, et al.
Advances in experimental medicine and biology (2012), pp. 237-264
Open Access | Times Cited: 105
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