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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:

SWI/SNF chromatin remodeling complexes and cancer
Jaclyn A. Biegel, Tracy Busse, Bernard E. Weissman
American Journal of Medical Genetics Part C Seminars in Medical Genetics (2014) Vol. 166, Iss. 3, pp. 350-366
Open Access | Times Cited: 171

Showing 1-25 of 171 citing articles:

Targeting the cancer epigenome for therapy
Peter A. Jones, Jean‐Pierre J. Issa, Stephen B. Baylin
Nature Reviews Genetics (2016) Vol. 17, Iss. 10, pp. 630-641
Closed Access | Times Cited: 999
Atypical teratoid/rhabdoid tumors—current concepts, advances in biology, and potential future therapies
Michael C. Frühwald, Jaclyn A. Biegel, Franck Bourdeaut, et al.
Neuro-Oncology (2016) Vol. 18, Iss. 6, pp. 764-778
Open Access | Times Cited: 211
SWI/SNF Complex–deficient Undifferentiated/Rhabdoid Carcinomas of the Gastrointestinal Tract
Abbas Agaimy, Ondřej Daum, Bruno Märkl, et al.
The American Journal of Surgical Pathology (2015) Vol. 40, Iss. 4, pp. 544-553
Closed Access | Times Cited: 204
The SWI/SNF Protein PBRM1 Restrains VHL-Loss-Driven Clear Cell Renal Cell Carcinoma
Amrita M. Nargund, Can G. Pham, Yiyu Dong, et al.
Cell Reports (2017) Vol. 18, Iss. 12, pp. 2893-2906
Open Access | Times Cited: 188
The genomic landscape of pediatric cancers: Implications for diagnosis and treatment
E. Alejandro Sweet‐Cordero, Jaclyn A. Biegel
Science (2019) Vol. 363, Iss. 6432, pp. 1170-1175
Open Access | Times Cited: 179
Oncogenic roles of SMARCB1/INI1 and its deficient tumors
Kenichi Kohashi, Yoshinao Oda
Cancer Science (2017) Vol. 108, Iss. 4, pp. 547-552
Open Access | Times Cited: 177
Lactate‐induced protein lactylation: A bridge between epigenetics and metabolic reprogramming in cancer
Ting Wang, Ye Zeng, Zheng Li, et al.
Cell Proliferation (2023) Vol. 56, Iss. 10
Open Access | Times Cited: 68
Chromatin Remodelers: From Function to Dysfunction
Gernot Längst, Laura Manelytė
Genes (2015) Vol. 6, Iss. 2, pp. 299-324
Open Access | Times Cited: 163
SMARCA4-deficient Thoracic Sarcomas
Raul Perret, Lara Chalabreysse, Sarah Watson, et al.
The American Journal of Surgical Pathology (2018) Vol. 43, Iss. 4, pp. 455-465
Closed Access | Times Cited: 156
The molecular pathogenesis of schwannomatosis, a paradigm for the co-involvement of multiple tumour suppressor genes in tumorigenesis
Hildegard Kehrer‐Sawatzki, Said Farschtschi, Victor‐Felix Mautner, et al.
Human Genetics (2016) Vol. 136, Iss. 2, pp. 129-148
Open Access | Times Cited: 134
SMARCA4-deficient pulmonary adenocarcinoma: clinicopathological, immunohistochemical, and molecular characteristics of a novel aggressive neoplasm with a consistent TTF1neg/CK7pos/HepPar-1pos immunophenotype
Abbas Agaimy, Florian Fuchs, Evgeny A. Moskalev, et al.
Virchows Archiv (2017) Vol. 471, Iss. 5, pp. 599-609
Closed Access | Times Cited: 122
Rhabdoid Tumor Predisposition Syndrome
Simone Treiger Sredni, Tadanori Tomita
Pediatric and Developmental Pathology (2014) Vol. 18, Iss. 1, pp. 49-58
Closed Access | Times Cited: 120
Role of specialized composition of SWI/SNF complexes in prostate cancer lineage plasticity
Joanna Cyrta, Anke Augspach, Maria Rosaria De Filippo, et al.
Nature Communications (2020) Vol. 11, Iss. 1
Open Access | Times Cited: 112
The ARID1B spectrum in 143 patients: from nonsyndromic intellectual disability to Coffin–Siris syndrome
Pleuntje J. van der Sluijs, Sandra Jansen, Samantha A. Schrier Vergano, et al.
Genetics in Medicine (2018) Vol. 21, Iss. 6, pp. 1295-1307
Open Access | Times Cited: 111
Coffin–Siris syndrome and related disorders involving components of the BAF (mSWI/SNF) complex: Historical review and recent advances using next generation sequencing
Tomoki Kosho, Noriko Miyake, John C. Carey
American Journal of Medical Genetics Part C Seminars in Medical Genetics (2014) Vol. 166, Iss. 3, pp. 241-251
Closed Access | Times Cited: 109
The BRG1 ATPase of Human SWI/SNF Chromatin Remodeling Enzymes as a Driver of Cancer
Qiong Wu, Jane B. Lian, Janet L. Stein, et al.
Epigenomics (2017) Vol. 9, Iss. 6, pp. 919-931
Open Access | Times Cited: 108
Snf2 controls pulcherriminic acid biosynthesis and antifungal activity of the biocontrol yeast Metschnikowia pulcherrima
Deborah Gore‐Lloyd, Inés Sumann, Alexander O. Brachmann, et al.
Molecular Microbiology (2019) Vol. 112, Iss. 1, pp. 317-332
Open Access | Times Cited: 77
Somatic mutations and single-cell transcriptomes reveal the root of malignant rhabdoid tumours
Lars Custers, Eleonora Khabirova, Tim H. H. Coorens, et al.
Nature Communications (2021) Vol. 12, Iss. 1
Open Access | Times Cited: 67
3D chromatin architecture and transcription regulation in cancer
Siwei Deng, Yuliang Feng, Siim Pauklin
Journal of Hematology & Oncology (2022) Vol. 15, Iss. 1
Open Access | Times Cited: 47
BET Bromodomain Inhibitors: Novel Design Strategies and Therapeutic Applications
Kenneth K.W. To, Enming Xing, Ross C. Larue, et al.
Molecules (2023) Vol. 28, Iss. 7, pp. 3043-3043
Open Access | Times Cited: 37
Epigenetic modifiers: activities in renal cell carcinoma
Aguirre A. de Cubas, W. Kimryn Rathmell
Nature Reviews Urology (2018) Vol. 15, Iss. 10, pp. 599-614
Open Access | Times Cited: 81
The SWI/SNF complex subunit genes: Their functions, variations, and links to risk and survival outcomes in human cancers
Sevtap Savas, Georgia Skardasi
Critical Reviews in Oncology/Hematology (2018) Vol. 123, pp. 114-131
Closed Access | Times Cited: 80
PRC2-mediated repression of SMARCA2 predicts EZH2 inhibitor activity in SWI/SNF mutant tumors
Thomas Januario, Xiaofen Ye, Russell Bainer, et al.
Proceedings of the National Academy of Sciences (2017) Vol. 114, Iss. 46, pp. 12249-12254
Open Access | Times Cited: 78
Prognostic role and implications of mutation status of tumor suppressor gene ARID1A in cancer: a systematic review and meta-analysis
Claudio Luchini, Nicola Veronese, Marco Solmi, et al.
Oncotarget (2015) Vol. 6, Iss. 36, pp. 39088-39097
Open Access | Times Cited: 75
Loss of expression of the SWI/SNF complex is a frequent event in undifferentiated/dedifferentiated urothelial carcinoma of the urinary tract
Abbas Agaimy, Simone Bertz, Liang Cheng, et al.
Virchows Archiv (2016) Vol. 469, Iss. 3, pp. 321-330
Closed Access | Times Cited: 69
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