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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 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: 351

Showing 1-25 of 351 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: 774
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: 691
Realizing the promise of cancer predisposition genes
Nazneen Rahman
Nature (2014) Vol. 505, Iss. 7483, pp. 302-308
Open Access | Times Cited: 569
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: 355
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
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
The genomic landscape of juvenile myelomonocytic leukemia
Elliot Stieglitz, Amaro Taylor‐Weiner, Tiffany Chang, et al.
Nature Genetics (2015) Vol. 47, Iss. 11, pp. 1326-1333
Open Access | Times Cited: 263
Exome sequencing of desmoplastic melanoma identifies recurrent NFKBIE promoter mutations and diverse activating mutations in the MAPK pathway
A. Hunter Shain, M Garrido, Thomas Botton, et al.
Nature Genetics (2015) Vol. 47, Iss. 10, pp. 1194-1199
Open Access | Times Cited: 253
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
Childhood cancer predisposition syndromes—A concise review and recommendations by the Cancer Predisposition Working Group of the Society for Pediatric Oncology and Hematology
Tim Ripperger, Stefan Bielack, Arndt Borkhardt, et al.
American Journal of Medical Genetics Part A (2017) Vol. 173, Iss. 4, pp. 1017-1037
Closed Access | Times Cited: 244
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: 236
How I treat juvenile myelomonocytic leukemia
Franco Locatelli, Charlotte M. Niemeyer
Blood (2015) Vol. 125, Iss. 7, pp. 1083-1090
Open Access | Times Cited: 221
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 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 RING finger protein family in health and disease
Chunmei Cai, Yan‐Dong Tang, Jingbo Zhai, et al.
Signal Transduction and Targeted Therapy (2022) Vol. 7, Iss. 1
Open Access | Times Cited: 104
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: 74
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
Structural basis for autoinhibition and phosphorylation-dependent activation of c-Cbl
Hao Dou, Lori Buetow, Andreas Hock, et al.
Nature Structural & Molecular Biology (2012) Vol. 19, Iss. 2, pp. 184-192
Open Access | Times Cited: 177
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
High diagnostic yield of clinical exome sequencing in Middle Eastern patients with Mendelian disorders
Tarunashree Yavarna, Nader Al‐Dewik, Mariam Almureikhi, et al.
Human Genetics (2015) Vol. 134, Iss. 9, pp. 967-980
Closed Access | Times Cited: 175
Juvenile myelomonocytic leukemia displays mutations in components of the RAS pathway and the PRC2 network
Aurélie Caye, Marion Strullu, Fabien Guidez, et al.
Nature Genetics (2015) Vol. 47, Iss. 11, pp. 1334-1340
Closed Access | Times Cited: 171
Recent advances in the pathogenesis and treatment of juvenile myelomonocytic leukaemia
Mignon L. Loh
British Journal of Haematology (2011) Vol. 152, Iss. 6, pp. 677-687
Open Access | Times Cited: 155
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
Juvenile myelomonocytic leukemia: who’s the driver at the wheel?
Charlotte M. Niemeyer, Christian Flotho
Blood (2019) Vol. 133, Iss. 10, pp. 1060-1070
Open Access | Times Cited: 140
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