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:

Exome sequencing identifies recurrent mutations of the splicing factor SF3B1 gene in chronic lymphocytic leukemia
Vı́ctor Quesada, Laura Peña Conde, Neus Villamor, et al.
Nature Genetics (2011) Vol. 44, Iss. 1, pp. 47-52
Closed Access | Times Cited: 983

Showing 1-25 of 983 citing articles:

Signatures of mutational processes in human cancer
Ludmil B. Alexandrov, Serena Nik‐Zainal, David C. Wedge, et al.
Nature (2013) Vol. 500, Iss. 7463, pp. 415-421
Open Access | Times Cited: 9081

The 2016 revision of the World Health Organization classification of lymphoid neoplasms
Steven H. Swerdlow, Elı́as Campo, Stefano Pileri, et al.
Blood (2016) Vol. 127, Iss. 20, pp. 2375-2390
Open Access | Times Cited: 7013

Evolution and Impact of Subclonal Mutations in Chronic Lymphocytic Leukemia
Dan A. Landau, Scott L. Carter, Petar Stojanov, et al.
Cell (2013) Vol. 152, Iss. 4, pp. 714-726
Open Access | Times Cited: 1336

Proteomic and bioinformatic analysis of mammalian SWI/SNF complexes identifies extensive roles in human malignancy
Cigall Kadoch, Diana C. Hargreaves, H. Courtney Hodges, et al.
Nature Genetics (2013) Vol. 45, Iss. 6, pp. 592-601
Open Access | Times Cited: 1278

Lessons from the Cancer Genome
Levi A. Garraway, Eric S. Lander
Cell (2013) Vol. 153, Iss. 1, pp. 17-37
Open Access | Times Cited: 1258

Convergence of Acquired Mutations and Alternative Splicing of CD19 Enables Resistance to CART-19 Immunotherapy
Elena Sotillo, David M. Barrett, Kathryn L. Black, et al.
Cancer Discovery (2015) Vol. 5, Iss. 12, pp. 1282-1295
Open Access | Times Cited: 1088

Distinct patterns of somatic genome alterations in lung adenocarcinomas and squamous cell carcinomas
Joshua D. Campbell, Anton Alexandrov, Jaegil Kim, et al.
Nature Genetics (2016) Vol. 48, Iss. 6, pp. 607-616
Open Access | Times Cited: 1064

Targeting B cell receptor signaling with ibrutinib in diffuse large B cell lymphoma
Wyndham H. Wilson, Ryan M. Young, Roland Schmitz, et al.
Nature Medicine (2015) Vol. 21, Iss. 8, pp. 922-926
Open Access | Times Cited: 1017

Mutations driving CLL and their evolution in progression and relapse
Dan A. Landau, Eugen Tausch, Amaro Taylor‐Weiner, et al.
Nature (2015) Vol. 526, Iss. 7574, pp. 525-530
Open Access | Times Cited: 982

A Probabilistic Classification Tool for Genetic Subtypes of Diffuse Large B Cell Lymphoma with Therapeutic Implications
George W. Wright, Da Wei Huang, James D. Phelan, et al.
Cancer Cell (2020) Vol. 37, Iss. 4, pp. 551-568.e14
Open Access | Times Cited: 868

RNA in cancer
Gregory J. Goodall, Vihandha O. Wickramasinghe
Nature reviews. Cancer (2020) Vol. 21, Iss. 1, pp. 22-36
Closed Access | Times Cited: 837

RNA splicing factors as oncoproteins and tumour suppressors
Heidi Dvinge, Eun Hee Kim, Omar Abdel‐Wahab, et al.
Nature reviews. Cancer (2016) Vol. 16, Iss. 7, pp. 413-430
Open Access | Times Cited: 603

Roles and mechanisms of alternative splicing in cancer — implications for care
Sophie Bonnal, Irene López‐Oreja, Juan Valcárcel
Nature Reviews Clinical Oncology (2020) Vol. 17, Iss. 8, pp. 457-474
Closed Access | Times Cited: 565

IntOGen-mutations identifies cancer drivers across tumor types
Abel González-Pérez, Christian Perez-Llamas, Jordi Deu-Pons, et al.
Nature Methods (2013) Vol. 10, Iss. 11, pp. 1081-1082
Open Access | Times Cited: 554

Epigenomic analysis detects widespread gene-body DNA hypomethylation in chronic lymphocytic leukemia
Marta Kulis, Simon Heath, Marina Bibikova, et al.
Nature Genetics (2012) Vol. 44, Iss. 11, pp. 1236-1242
Closed Access | Times Cited: 550

The Spectrum of SWI/SNF Mutations, Ubiquitous in Human Cancers
A. Hunter Shain, Jonathan R. Pollack
PLoS ONE (2013) Vol. 8, Iss. 1, pp. e55119-e55119
Open Access | Times Cited: 535

SRSF2 Mutations Contribute to Myelodysplasia by Mutant-Specific Effects on Exon Recognition
Eun Hee Kim, Janine O. Ilagan, Yang Liang, et al.
Cancer Cell (2015) Vol. 27, Iss. 5, pp. 617-630
Open Access | Times Cited: 503

Therapeutic targeting of splicing in cancer
Stanley Chun-Wei Lee, Omar Abdel‐Wahab
Nature Medicine (2016) Vol. 22, Iss. 9, pp. 976-986
Open Access | Times Cited: 502

Exome sequencing identifies recurrent somatic mutations in EIF1AX and SF3B1 in uveal melanoma with disomy 3
Marcel Martin, Lars Maßhöfer, Petra Temming, et al.
Nature Genetics (2013) Vol. 45, Iss. 8, pp. 933-936
Open Access | Times Cited: 500

Landscape of somatic mutations and clonal evolution in mantle cell lymphoma
Sı́lvia Beà, Rafael Valdés‐Mas, Alba Navarro, et al.
Proceedings of the National Academy of Sciences (2013) Vol. 110, Iss. 45, pp. 18250-18255
Open Access | Times Cited: 494

Emerging patterns of somatic mutations in cancer
Ian R. Watson, Koichi Takahashi, P. Andrew Futreal, et al.
Nature Reviews Genetics (2013) Vol. 14, Iss. 10, pp. 703-718
Open Access | Times Cited: 484

Gene mutations and treatment outcome in chronic lymphocytic leukemia: results from the CLL8 trial
Stephan Stilgenbauer, Andrea Schnaiter, Peter Paschka, et al.
Blood (2014) Vol. 123, Iss. 21, pp. 3247-3254
Closed Access | Times Cited: 480

Mutational signatures: the patterns of somatic mutations hidden in cancer genomes
Ludmil B. Alexandrov, Michael R. Stratton
Current Opinion in Genetics & Development (2014) Vol. 24, pp. 52-60
Open Access | Times Cited: 454

Chronic lymphocytic leukemia: 2020 update on diagnosis, risk stratification and treatment
Michael Hallek
American Journal of Hematology (2019) Vol. 94, Iss. 11, pp. 1266-1287
Open Access | Times Cited: 446

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