Open Access Helper

OpenAlex Citation Counts

OpenAlex Citations Logo

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:

Genome and transcriptome sequencing of lung cancers reveal diverse mutational and splicing events
Jinfeng Liu, William Lee, Zhaoshi Jiang, et al.
Genome Research (2012) Vol. 22, Iss. 12, pp. 2315-2327
Open Access | Times Cited: 205

Showing 1-25 of 205 citing articles:

Genetic landscape of esophageal squamous cell carcinoma
Yibo Gao, Zhao-Li Chen, Jia-Gen Li, et al.
Nature Genetics (2014) Vol. 46, Iss. 10, pp. 1097-1102
Closed Access | Times Cited: 646
A comprehensive transcriptional portrait of human cancer cell lines
Christiaan Klijn, Steffen Durinck, Eric Stawiski, et al.
Nature Biotechnology (2014) Vol. 33, Iss. 3, pp. 306-312
Closed Access | Times Cited: 628
Long non-coding RNAs and complex diseases: from experimental results to computational models
Xing Chen, Chenggang Yan, Xu Zhang, et al.
Briefings in Bioinformatics (2016), pp. bbw060-bbw060
Open Access | Times Cited: 546
Functions of bromodomain-containing proteins and their roles in homeostasis and cancer
Takao Fujisawa, P. Filippakopoulos
Nature Reviews Molecular Cell Biology (2017) Vol. 18, Iss. 4, pp. 246-262
Open Access | Times Cited: 525
Aberrant RNA splicing in cancer; expression changes and driver mutations of splicing factor genes
Anita Sveen, Sami Kilpinen, Anja Ruusulehto, et al.
Oncogene (2015) Vol. 35, Iss. 19, pp. 2413-2427
Open Access | Times Cited: 444
GMAP and GSNAP for Genomic Sequence Alignment: Enhancements to Speed, Accuracy, and Functionality
Thomas D. Wu, Jens Reeder, Michael Lawrence, et al.
Methods in molecular biology (2016), pp. 283-334
Closed Access | Times Cited: 435
Genomic alterations in lung adenocarcinoma
Siddhartha Devarakonda, Daniel Morgensztern, Ramaswamy Govindan
The Lancet Oncology (2015) Vol. 16, Iss. 7, pp. e342-e351
Closed Access | Times Cited: 364
Reliable Identification of Genomic Variants from RNA-Seq Data
Robert Piskol, Gokul Ramaswami, Jin Billy Li
The American Journal of Human Genetics (2013) Vol. 93, Iss. 4, pp. 641-651
Open Access | Times Cited: 359
Intron retention is a widespread mechanism of tumor-suppressor inactivation
Hyunchul Jung, Donghoon Lee, Jongkeun Lee, et al.
Nature Genetics (2015) Vol. 47, Iss. 11, pp. 1242-1248
Closed Access | Times Cited: 340
Genetic alterations defining NSCLC subtypes and their therapeutic implications
Larissa A. Pikor, Varune Rohan Ramnarine, Stephen Lam, et al.
Lung Cancer (2013) Vol. 82, Iss. 2, pp. 179-189
Open Access | Times Cited: 325
Polyclonal RB1 mutations and acquired resistance to CDK 4/6 inhibitors in patients with metastatic breast cancer
Rosaria Condorelli, Laura M. Spring, Joyce O’Shaughnessy, et al.
Annals of Oncology (2017) Vol. 29, Iss. 3, pp. 640-645
Open Access | Times Cited: 317
Genomic Profiling of Hepatocellular Adenomas Reveals Recurrent FRK-Activating Mutations and the Mechanisms of Malignant Transformation
Camilla Pilati, Éric Letouzé, Jean–Charles Nault, et al.
Cancer Cell (2014) Vol. 25, Iss. 4, pp. 428-441
Open Access | Times Cited: 257
Uncovering novel mutational signatures by de novo extraction with SigProfilerExtractor
S. M. Ashiqul Islam, Marcos Díaz‐Gay, Yang Wu, et al.
Cell Genomics (2022) Vol. 2, Iss. 11, pp. 100179-100179
Open Access | Times Cited: 233
Alternative mRNA splicing in cancer immunotherapy
Luke Frankiw, David Baltimore, Guideng Li
Nature reviews. Immunology (2019) Vol. 19, Iss. 11, pp. 675-687
Closed Access | Times Cited: 223
Predicting lncRNA-disease associations and constructing lncRNA functional similarity network based on the information of miRNA
Xing Chen
Scientific Reports (2015) Vol. 5, Iss. 1
Open Access | Times Cited: 211
The cancer driver genes IDH1/2, JARID1C/ KDM5C, and UTX/ KDM6A: crosstalk between histone demethylation and hypoxic reprogramming in cancer metabolism
Soojeong Chang, Sujin Yim, Hyunsung Park
Experimental & Molecular Medicine (2019) Vol. 51, Iss. 6, pp. 1-17
Open Access | Times Cited: 190
A Pharmacogenomic Landscape in Human Liver Cancers
Zhixin Qiu, Hong Li, Zhengtao Zhang, et al.
Cancer Cell (2019) Vol. 36, Iss. 2, pp. 179-193.e11
Open Access | Times Cited: 167
Detection of recurrent alternative splicing switches in tumor samples reveals novel signatures of cancer
Endre Sebestyén, Michał Zawisza-Álvarez, Eduardo Eyras
Nucleic Acids Research (2015) Vol. 43, Iss. 3, pp. 1345-1356
Open Access | Times Cited: 178
Alternative splicing of intrinsically disordered regions and rewiring of protein interactions
Marija Buljan, Guilhem Chalancon, A. Keith Dunker, et al.
Current Opinion in Structural Biology (2013) Vol. 23, Iss. 3, pp. 443-450
Closed Access | Times Cited: 177
ROS-induced epithelial-mesenchymal transition in mammary epithelial cells is mediated by NF-κB-dependent activation of Snail
Magdalena A. Cichon, Derek C. Radisky
Oncotarget (2014) Vol. 5, Iss. 9, pp. 2827-2838
Open Access | Times Cited: 169
Histone Methyltransferase Ash1l Suppresses Interleukin-6 Production and Inflammatory Autoimmune Diseases by Inducing the Ubiquitin-Editing Enzyme A20
Xia Meng, Juan Liu, Xiaohui Wu, et al.
Immunity (2013) Vol. 39, Iss. 3, pp. 470-481
Open Access | Times Cited: 150
SAMHD1-dependent retroviral control and escape in mice
Jan Rehwinkel, Jonathan Maelfait, Anne Bridgeman, et al.
The EMBO Journal (2013) Vol. 32, Iss. 18, pp. 2454-2462
Open Access | Times Cited: 150
MBASED: allele-specific expression detection in cancer tissues and cell lines
Oleg Mayba, Houston Gilbert, Jinfeng Liu, et al.
Genome biology (2014) Vol. 15, Iss. 8
Open Access | Times Cited: 141
Comprehensive Analysis of Transcriptome Variation Uncovers Known and Novel Driver Events in T-Cell Acute Lymphoblastic Leukemia
Zeynep Kalender Atak, Valentina Gianfelici, Gert Hulselmans, et al.
PLoS Genetics (2013) Vol. 9, Iss. 12, pp. e1003997-e1003997
Open Access | Times Cited: 135
Inactivating CUX1 mutations promote tumorigenesis
Chi Chun Wong, Sancha Martin, Alistair G. Rust, et al.
Nature Genetics (2013) Vol. 46, Iss. 1, pp. 33-38
Open Access | Times Cited: 128
Page 1 - Next Page

Scroll to top