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:
Modeling (not so) rare developmental disorders associated with mutations in the protein-tyrosine phosphatase SHP2
Maja Šolman, Daniëlle T.J. Woutersen, Jeroen den Hertog
Frontiers in Cell and Developmental Biology (2022) Vol. 10
Open Access | Times Cited: 6
Maja Šolman, Daniëlle T.J. Woutersen, Jeroen den Hertog
Frontiers in Cell and Developmental Biology (2022) Vol. 10
Open Access | Times Cited: 6
Showing 6 citing articles:
Prion-like domain mediated phase separation of ARID1A promotes oncogenic potential of Ewing’s sarcoma
Yong Ryoul Kim, Jaegeon Joo, Hee Jung Lee, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 6
Yong Ryoul Kim, Jaegeon Joo, Hee Jung Lee, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 6
Complex Roles of PTPN11/SHP2 in Carcinogenesis and Prospect of Targeting SHP2 in Cancer Therapy
Alexander Scheiter, Li‐Chun Lu, Lilian H. Gao, et al.
Annual Review of Cancer Biology (2023) Vol. 8, Iss. 1, pp. 15-33
Closed Access | Times Cited: 3
Alexander Scheiter, Li‐Chun Lu, Lilian H. Gao, et al.
Annual Review of Cancer Biology (2023) Vol. 8, Iss. 1, pp. 15-33
Closed Access | Times Cited: 3
A retrospective analysis of phosphatase catalytic subunit gene variants in patients with rare disorders identifies novel candidate neurodevelopmental disease genes
Ekaterina Lyulcheva, Genomics England Research Consortium, Daimark Bennett
Frontiers in Cell and Developmental Biology (2023) Vol. 11
Open Access | Times Cited: 2
Ekaterina Lyulcheva, Genomics England Research Consortium, Daimark Bennett
Frontiers in Cell and Developmental Biology (2023) Vol. 11
Open Access | Times Cited: 2
Progression and perspectives in disease modeling for Juvenile myelomonocytic leukemia
Sha Fu, Yao Guo, Zhiyong Peng, et al.
Medical Oncology (2024) Vol. 42, Iss. 1
Open Access
Sha Fu, Yao Guo, Zhiyong Peng, et al.
Medical Oncology (2024) Vol. 42, Iss. 1
Open Access
Protein Tyrosine Phosphatase Studies in Zebrafish
Daniëlle T.J. Woutersen, Jisca Majolée, Jeroen den Hertog
Methods in molecular biology (2023), pp. 93-110
Closed Access | Times Cited: 1
Daniëlle T.J. Woutersen, Jisca Majolée, Jeroen den Hertog
Methods in molecular biology (2023), pp. 93-110
Closed Access | Times Cited: 1
Generation of human induced pluripotent stem cell lines derived from three Noonan syndrome patients from a single family carrying the heterozygous PTPN11 c.188 A > G (p.Y63C) mutation
Giulia Sbrini, Zaira Tomasoni, Maria Rosa Cutrì, et al.
Stem Cell Research (2023) Vol. 74, pp. 103293-103293
Open Access | Times Cited: 1
Giulia Sbrini, Zaira Tomasoni, Maria Rosa Cutrì, et al.
Stem Cell Research (2023) Vol. 74, pp. 103293-103293
Open Access | Times Cited: 1
