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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:

Genetic variants of genes in the NER pathway associated with risk of breast cancer: A large‐scale analysis of 14 published GWAS datasets in the DRIVE study
Jie Ge, Hongliang Liu, Danwen Qian, et al.
International Journal of Cancer (2019) Vol. 145, Iss. 5, pp. 1270-1279
Open Access | Times Cited: 21

Showing 21 citing articles:

Genetic variations in DNA excision repair pathway contribute to the chemosensitivity and prognosis of acute myeloid leukemia
Amin Zhang, Wancheng Liu, Xiaodong Guo, et al.
Clinica Chimica Acta (2024) Vol. 558, pp. 117899-117899
Closed Access | Times Cited: 4
Interplay between BRCA1 and GADD45A and Its Potential for Nucleotide Excision Repair in Breast Cancer Pathogenesis
Sylwia Pietrasik, Gabriela Zajac, Jan Morawiec, et al.
International Journal of Molecular Sciences (2020) Vol. 21, Iss. 3, pp. 870-870
Open Access | Times Cited: 36
Evolving insights: how DNA repair pathways impact cancer evolution
Jiadong Zhou, Xiao Albert Zhou, Ning Zhang, et al.
Cancer Biology and Medicine (2020) Vol. 17, Iss. 4, pp. 805-827
Open Access | Times Cited: 25
Genetic variations in nucleotide excision repair pathway genes and hepatoblastoma susceptibility
Zhenjian Zhuo, Lei Miao, Wenfeng Hua, et al.
International Journal of Cancer (2021) Vol. 149, Iss. 9, pp. 1649-1658
Open Access | Times Cited: 17
Regulatory roles of Osteopontin in lung epithelial inflammation and epithelial‐telocyte interaction
Huirong Fu, Xuanqi Liu, Lin Shi, et al.
Clinical and Translational Medicine (2023) Vol. 13, Iss. 8
Open Access | Times Cited: 6
Variants in SNAI1, AMDHD1 and CUBN in vitamin D pathway genes are associated with breast cancer risk: a large-scale analysis of 14 GWASs in the DRIVE study.
Haijiao Wang, Lingling Zhao, Hongliang Liu, et al.
PubMed (2020) Vol. 10, Iss. 7, pp. 2160-2173
Closed Access | Times Cited: 11
Association of IL-8 -251T>A and IL-18 -607C>A polymorphisms with susceptibility to breast cancer – a meta-analysis
Meraj Farbod, Seyed Alireza Dastgheib, Fatemeh Asadian, et al.
Klinicka onkologie (2022) Vol. 35, Iss. 3
Open Access | Times Cited: 7
MMP-8 C-799 T, Lys460Thr, and Lys87Glu variants are not related to risk of cancer
Li‐Feng Zhang, Lijie Zhu, Wei Zhang, et al.
BMC Medical Genetics (2019) Vol. 20, Iss. 1
Open Access | Times Cited: 9
Personalized analysis of breast cancer using sample-specific networks
Ke Zhu, Cong Pian, Qiong Xiang, et al.
PeerJ (2020) Vol. 8, pp. e9161-e9161
Open Access | Times Cited: 7
Genetic variants in Ras/Raf/MEK/ERK pathway are associated with gastric cancer risk in Chinese Han population
Xiaowei Wang, Xu Wu, Junyi Xin, et al.
Archives of Toxicology (2020) Vol. 94, Iss. 8, pp. 2683-2690
Closed Access | Times Cited: 5
Association of genetic variants of FBXO32 and FOXO6 in the FOXO pathway with breast cancer risk
Haijiao Wang, Hongliang Liu, Lingling Zhao, et al.
Molecular Carcinogenesis (2021) Vol. 60, Iss. 10, pp. 661-670
Open Access | Times Cited: 5
Prognostic Model and Immune Response of Clear Cell Renal Cell Carcinoma Based on Co-Expression Genes Signature
Dong‐Sheng Yang
Clinical Genitourinary Cancer (2024) Vol. 22, Iss. 5, pp. 102167-102167
Closed Access
Genotype and haplotype analysis between ESR1 variants and breast cancer in the Bangladeshi patients: A PCR-RFLP-based genetic association study
Md. Shafiul Hossen, Md. Abdul Aziz, Md Abdul Barek, et al.
Research Square (Research Square) (2023)
Open Access | Times Cited: 1
Association of polymorphisms in nucleotide excision repair pathway genes with susceptibility to cutaneous melanoma
Ahmad Hashemzehi, Mohammadamin Ghadyani, Fatemeh Asadian, et al.
Klinicka onkologie (2021) Vol. 34, Iss. 5
Open Access | Times Cited: 2
Integrative bioinformatic analyses of genome-wide association studies for understanding the genetic bases of human height
Tingxue Wang, Rao Jiang, Juanjuan Bai, et al.
Biologia (2020) Vol. 75, Iss. 12, pp. 2413-2420
Closed Access | Times Cited: 1
The Prognostic Value and Biological Functions of HFM1 in Breast Cancer
Yingxia Ying, Yiling Meng, Lei Bian, et al.
Epigenomics (2023) Vol. 15, Iss. 3, pp. 147-166
Closed Access
THE ROLE OF SINGLE-NUCLEOTIDE POLYMORPHISMS IN DETERMINING THE TACTICS OF TREATMENT, PROGNOSIS AND AT RISK OF DEVELOPING BREAST CANCER
Valery V. Benberin, Nasrulla Shanazarov, Г О Арипжанова, et al.
Современные проблемы науки и образования (Modern Problems of Science and Education) (2020), Iss. №4 2020, pp. 9-9
Open Access
Peer Review #2 of "Personalized analysis of breast cancer using sample-specific networks (v0.1)"

(2020)
Open Access
Peer Review #1 of "Personalized analysis of breast cancer using sample-specific networks (v0.2)"

(2020)
Open Access
Peer Review #1 of "Personalized analysis of breast cancer using sample-specific networks (v0.1)"

(2020)
Open Access
Data Integration for Big Data analytics to identify the gaps in Rheumatoid Arthritis Genomics in a Post-GWAS era
Sidrah Jahangir, Peter John, Attya Bhatti, et al.
2022 2nd International Conference on Advance Computing and Innovative Technologies in Engineering (ICACITE) (2022), pp. 956-964
Closed Access
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