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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:

Heterozygous Germline Mutations in the CBL Tumor-Suppressor Gene Cause a Noonan Syndrome-like Phenotype
Simone Martinelli, Alessandro De Luca, Emilia Stellacci, et al.
The American Journal of Human Genetics (2010) Vol. 87, Iss. 2, pp. 250-257
Open Access | Times Cited: 248

Showing 1-25 of 248 citing articles:

The RASopathies
Katherine A. Rauen
Annual Review of Genomics and Human Genetics (2013) Vol. 14, Iss. 1, pp. 355-369
Open Access | Times Cited: 773
Noonan syndrome
Amy E. Roberts, Judith Allanson, Marco Tartaglia, et al.
The Lancet (2013) Vol. 381, Iss. 9863, pp. 333-342
Open Access | Times Cited: 690
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
Factors influencing success of clinical genome sequencing across a broad spectrum of disorders
Jenny C. Taylor, Hilary C. Martin, Stefano Lise, et al.
Nature Genetics (2015) Vol. 47, Iss. 7, pp. 717-726
Open Access | Times Cited: 354
Germline CBL mutations cause developmental abnormalities and predispose to juvenile myelomonocytic leukemia
Charlotte M. Niemeyer, Michelle Kang, Danielle H. Shin, et al.
Nature Genetics (2010) Vol. 42, Iss. 9, pp. 794-800
Open Access | Times Cited: 350
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: 333
Endocytosis and Signaling: Cell Logistics Shape the Eukaryotic Cell Plan
Sara Sigismund, Stefano Confalonieri, Andrea Ciliberto, et al.
Physiological Reviews (2012) Vol. 92, Iss. 1, pp. 273-366
Open Access | Times Cited: 321
Clinical whole-genome sequencing in severe early-onset epilepsy reveals new genes and improves molecular diagnosis
H. Christian Martin, Grace Kim, A. T. Pagnamenta, et al.
Human Molecular Genetics (2014) Vol. 23, Iss. 12, pp. 3200-3211
Open Access | Times Cited: 250
Ultra-sensitive Sequencing Identifies High Prevalence of Clonal Hematopoiesis-Associated Mutations throughout Adult Life
Rocío Acuña‐Hidalgo, Hilal Sengül, Marloes Steehouwer, et al.
The American Journal of Human Genetics (2017) Vol. 101, Iss. 1, pp. 50-64
Open Access | Times Cited: 234
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: 196
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: 115
Integrated multi-omics for rapid rare disease diagnosis on a national scale
Sebastian Lunke, Sophie E. Bouffler, Chirag Patel, et al.
Nature Medicine (2023) Vol. 29, Iss. 7, pp. 1681-1691
Open Access | Times Cited: 73
Cancer in Noonan, Costello, cardiofaciocutaneous and LEOPARD syndromes
Christian P. Kratz, Suthee Rapisuwon, Helen E. Reed, et al.
American Journal of Medical Genetics Part C Seminars in Medical Genetics (2011) Vol. 157, Iss. 2, pp. 83-89
Open Access | Times Cited: 209
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
Self-domestication in Homo sapiens: Insights from comparative genomics
Constantina Theofanopoulou, Simone Gastaldon, Thomas O’Rourke, et al.
PLoS ONE (2017) Vol. 12, Iss. 10, pp. e0185306-e0185306
Open Access | Times Cited: 168
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
Autism traits in the RASopathies
Brigid Adviento, Iris L Corbin, Felicia Widjaja, et al.
Journal of Medical Genetics (2013) Vol. 51, Iss. 1, pp. 10-20
Open Access | Times Cited: 158
Atlas of Genetics and Cytogenetics in Oncology and Haematology

Atlas of Genetics and Cytogenetics in Oncology and Haematology (2011)
Open Access | Times Cited: 145
RAS diseases in children
Charlotte M. Niemeyer
Haematologica (2014) Vol. 99, Iss. 11, pp. 1653-1662
Open Access | Times Cited: 128
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
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
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
Genotype and phenotype in patients with Noonan syndrome and a RIT1 mutation
Karim Kouz, Christina Lißewski, Stephanie Spranger, et al.
Genetics in Medicine (2016) Vol. 18, Iss. 12, pp. 1226-1234
Open Access | Times Cited: 91
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
RASopathies: From germline mutations to somatic and multigenic diseases
Quentin Riller, Frédéric Rieux‐Laucat
Biomedical Journal (2021) Vol. 44, Iss. 4, pp. 422-432
Open Access | Times Cited: 56
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