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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:

Gain-of-Function Mutations in RIT1 Cause Noonan Syndrome, a RAS/MAPK Pathway Syndrome
Yoko Aoki, Tetsuya Niihori, Toshihiro Banjo, et al.
The American Journal of Human Genetics (2013) Vol. 93, Iss. 1, pp. 173-180
Open Access | Times Cited: 313

Showing 1-25 of 313 citing articles:

A RASopathy gene commonly mutated in cancer: the neurofibromatosis type 1 tumour suppressor
Nancy Ratner, Shyra J. Miller
Nature reviews. Cancer (2015) Vol. 15, Iss. 5, pp. 290-301
Open Access | Times Cited: 419
Recent advances in RASopathies
Yoko Aoki, Tetsuya Niihori, Shinichi Inoue, et al.
Journal of Human Genetics (2015) Vol. 61, Iss. 1, pp. 33-39
Open Access | Times Cited: 336
Little Fish, Big Data: Zebrafish as a Model for Cardiovascular and Metabolic Disease
Philipp Gut, Sven Reischauer, Didier Y. R. Stainier, et al.
Physiological Reviews (2017) Vol. 97, Iss. 3, pp. 889-938
Open Access | Times Cited: 284
The usefulness of whole-exome sequencing in routine clinical practice
Alejandro Iglesias, Kwame Anyane‐Yeboa, Julia Wynn, et al.
Genetics in Medicine (2014) Vol. 16, Iss. 12, pp. 922-931
Open Access | Times Cited: 224
Rare variants inSOS2andLZTR1are associated with Noonan syndrome
Guilherme Lopes Yamamoto, Meire Aguena, Monika Goś, et al.
Journal of Medical Genetics (2015) Vol. 52, Iss. 6, pp. 413-421
Open Access | Times Cited: 216
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
Cancer spectrum and frequency among children with Noonan, Costello, and cardio-facio-cutaneous syndromes
Christian P. Kratz, Lude Franke, Harm Peters, et al.
British Journal of Cancer (2015) Vol. 112, Iss. 8, pp. 1392-1397
Open Access | Times Cited: 197
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
Insights into genetics, human biology and disease gleaned from family based genomic studies
Jennifer E. Posey, Anne O’Donnell‐Luria, Jessica X. Chong, et al.
Genetics in Medicine (2019) Vol. 21, Iss. 4, pp. 798-812
Open Access | Times Cited: 188
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
The missing link between genetic association and regulatory function
Noah J Connally, Sumaiya Nazeen, Daniel Lee, et al.
eLife (2022) Vol. 11
Open Access | Times Cited: 100
Next-generation sequencing identifies rare variants associated with Noonan syndrome
Peng‐Chieh Chen, Jiani C. Yin, Hui-Wen Yu, et al.
Proceedings of the National Academy of Sciences (2014) Vol. 111, Iss. 31, pp. 11473-11478
Open Access | Times Cited: 175
Of mice and men: molecular genetics of congenital heart disease
Troels Andersen, Karin de Linde Lind Troelsen, Lars Allan Larsen
Cellular and Molecular Life Sciences (2013) Vol. 71, Iss. 8, pp. 1327-1352
Open Access | Times Cited: 165
Functional Dysregulation of CDC42 Causes Diverse Developmental Phenotypes
Simone Martinelli, Oliver H.F. Krumbach, Francesca Pantaleoni, et al.
The American Journal of Human Genetics (2018) Vol. 102, Iss. 2, pp. 309-320
Open Access | Times Cited: 157
ClinGen’s RASopathy Expert Panel consensus methods for variant interpretation
Bruce D. Gelb, Hélène Cavé, Mitchell W. Dillon, et al.
Genetics in Medicine (2018) Vol. 20, Iss. 11, pp. 1334-1345
Open Access | Times Cited: 147
Recommendations for Cancer Surveillance in Individuals with RASopathies and Other Rare Genetic Conditions with Increased Cancer Risk
Anita Villani, Mary‐Louise C. Greer, Jennifer M. Kalish, et al.
Clinical Cancer Research (2017) Vol. 23, Iss. 12, pp. e83-e90
Open Access | Times Cited: 144
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
Integrated analysis of whole-exome sequencing and transcriptome profiling in males with autism spectrum disorders
Marta Codina‐Solà, Benjamín Rodríguez‐Santiago, Aïda Homs, et al.
Molecular Autism (2015) Vol. 6, Iss. 1
Open Access | Times Cited: 122
Cardiomyopathies in Noonan syndrome and the other RASopathies
Bruce D. Gelb, Amy E. Roberts, Marco Tartaglia
Progress in Pediatric Cardiology (2015) Vol. 39, Iss. 1, pp. 13-19
Open Access | Times Cited: 114
Pathogenetics of the RASopathies
William E. Tidyman, Katherine A. Rauen
Human Molecular Genetics (2016) Vol. 25, Iss. R2, pp. R123-R132
Open Access | Times Cited: 112
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
LZTR1 facilitates polyubiquitination and degradation of RAS-GTPases
Taiki Abe, Ikumi Umeki, Shin‐ichiro Kanno, et al.
Cell Death and Differentiation (2019) Vol. 27, Iss. 3, pp. 1023-1035
Open Access | Times Cited: 101
Expansion of the RASopathies
William E. Tidyman, Katherine A. Rauen
Current Genetic Medicine Reports (2016) Vol. 4, Iss. 3, pp. 57-64
Open Access | Times Cited: 98
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
Malformation syndromes associated with disorders of sex development
John M. Hutson, Sonia Grover, Michele A. O’Connell, et al.
Nature Reviews Endocrinology (2014) Vol. 10, Iss. 8, pp. 476-487
Closed Access | Times Cited: 95
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