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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:

Germline mutations of the CBL gene define a new genetic syndrome with predisposition to juvenile myelomonocytic leukaemia
B. Perez, Françoise Méchinaud, Claire Galambrun, et al.
Journal of Medical Genetics (2010) Vol. 47, Iss. 10, pp. 686-691
Open Access | Times Cited: 140

Showing 1-25 of 140 citing articles:

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
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
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: 312
Exome Sequencing and the Management of Neurometabolic Disorders
Maja Tarailo‐Graovac, Casper Shyr, Colin J.D. Ross, et al.
New England Journal of Medicine (2016) Vol. 374, Iss. 23, pp. 2246-2255
Open Access | Times Cited: 265
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
How I treat juvenile myelomonocytic leukemia
Franco Locatelli, Charlotte M. Niemeyer
Blood (2015) Vol. 125, Iss. 7, pp. 1083-1090
Open Access | Times Cited: 220
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
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
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: 139
RAS diseases in children
Charlotte M. Niemeyer
Haematologica (2014) Vol. 99, Iss. 11, pp. 1653-1662
Open Access | Times Cited: 128
Bedside to bench in juvenile myelomonocytic leukemia: insights into leukemogenesis from a rare pediatric leukemia
Tiffany Chang, Christopher C. Dvorak, Mignon L. Loh
Blood (2014) Vol. 124, Iss. 16, pp. 2487-2497
Open Access | Times Cited: 103
Clinical overview on RASopathies
Martin Zenker
American Journal of Medical Genetics Part C Seminars in Medical Genetics (2022) Vol. 190, Iss. 4, pp. 414-424
Open Access | Times Cited: 49
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: 41
The International Consensus Classification (ICC) of hematologic neoplasms with germline predisposition, pediatric myelodysplastic syndrome, and juvenile myelomonocytic leukemia
Martina Rudelius, Olga K. Weinberg, Charlotte M. Niemeyer, et al.
Virchows Archiv (2022) Vol. 482, Iss. 1, pp. 113-130
Closed Access | Times Cited: 41
Review and update ofSPRED1mutations causing legius syndrome
Hilde Brems, Éric Pasmant, Rick van Minkelen, et al.
Human Mutation (2012) Vol. 33, Iss. 11, pp. 1538-1546
Open Access | Times Cited: 92
Clinical manifestations of mutations in RAS and related intracellular signal transduction factors
Martin Zenker
Current Opinion in Pediatrics (2011) Vol. 23, Iss. 4, pp. 443-451
Closed Access | Times Cited: 90
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: 89
Pediatric leukemia predisposition syndromes: clues to understanding leukemogenesis
Alix E. Seif
Cancer Genetics (2011) Vol. 204, Iss. 5, pp. 227-244
Closed Access | Times Cited: 85
Dominant Noonan syndrome-causing LZTR1 mutations specifically affect the Kelch domain substrate-recognition surface and enhance RAS-MAPK signaling
Marialetizia Motta, Miray Fidan, Emanuele Bellacchio, et al.
Human Molecular Genetics (2018) Vol. 28, Iss. 6, pp. 1007-1022
Open Access | Times Cited: 81
Myeloid Dysregulation in a Human Induced Pluripotent Stem Cell Model of PTPN11 -Associated Juvenile Myelomonocytic Leukemia
Sonia Mulero‐Navarro, Ana Sevilla, Ángel Román, et al.
Cell Reports (2015) Vol. 13, Iss. 3, pp. 504-515
Open Access | Times Cited: 78
Assessment of the ExAC data set for the presence of individuals with pathogenic genotypes implicated in severe Mendelian pediatric disorders
Maja Tarailo‐Graovac, Jing Zhu, Allison Matthews, et al.
Genetics in Medicine (2017) Vol. 19, Iss. 12, pp. 1300-1308
Open Access | Times Cited: 68
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