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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:

Targeted RNA sequencing: A routine ancillary technique in the diagnosis of bone and soft tissue neoplasms
Brendan C. Dickson, David Swanson
Genes Chromosomes and Cancer (2018) Vol. 58, Iss. 2, pp. 75-87
Closed Access | Times Cited: 43

Showing 1-25 of 43 citing articles:

Mesenchymal tumors of the gastrointestinal tract with NTRK rearrangements: a clinicopathological, immunophenotypic, and molecular study of eight cases, emphasizing their distinction from gastrointestinal stromal tumor (GIST)
Mazen A. Atiq, Jessica L. Davis, Jason L. Hornick, et al.
Modern Pathology (2020) Vol. 34, Iss. 1, pp. 95-103
Open Access | Times Cited: 67
YAP1-TFE3-fused hemangioendothelioma: a multi-institutional clinicopathologic study of 24 genetically-confirmed cases
Josephine K. Dermawan, Elizabeth M. Azzato, Steven D. Billings, et al.
Modern Pathology (2021) Vol. 34, Iss. 12, pp. 2211-2221
Open Access | Times Cited: 50
Salivary Gland Cancer in the Era of Routine Next-Generation Sequencing
Emilija Todorovic, Brendan C. Dickson, Ilan Weinreb
Head and Neck Pathology (2020) Vol. 14, Iss. 2, pp. 311-320
Open Access | Times Cited: 41
Adenoid Cystic Carcinoma With Striking Tubular Hypereosinophilia
Ilan Weinreb, Lisa M. Rooper, Brendan C. Dickson, et al.
The American Journal of Surgical Pathology (2023) Vol. 47, Iss. 4, pp. 497-503
Closed Access | Times Cited: 16
Identification of Novel/Rare EWSR1 Fusion Partners in Undifferentiated Mesenchymal Neoplasms
Carmen Salguero‐Aranda, Elena Di Blasi, L. Alfaro Galán, et al.
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 3, pp. 1735-1735
Open Access | Times Cited: 6
Optical Genome Mapping for Comprehensive Cytogenetic Analysis of Soft-Tissue and Bone Tumors for Diagnostic Purposes
Jef Baelen, Barbara Dewaele, Maria Dębiec‐Rychter, et al.
Journal of Molecular Diagnostics (2024) Vol. 26, Iss. 5, pp. 374-386
Open Access | Times Cited: 6
Xanthogranulomatous epithelial tumors and keratin-positive giant cell-rich soft tissue tumors: two aspects of a single entity with frequent HMGA2-NCOR2 fusions
Carina Dehner, Jonathan C. Baker, Robert S. Bell, et al.
Modern Pathology (2022) Vol. 35, Iss. 11, pp. 1656-1666
Open Access | Times Cited: 21
Recurrent VGLL3 fusions define a distinctive subset of spindle cell rhabdomyosarcoma with an indolent clinical course and striking predilection for the head and neck
Abbas Agaimy, Josephine K. Dermawan, Iona Leong, et al.
Genes Chromosomes and Cancer (2022) Vol. 61, Iss. 12, pp. 701-709
Open Access | Times Cited: 21
Expanding the spectrum of tyrosine kinase fusions in calcified chondroid mesenchymal neoplasms: Identification of a novel PDGFRA::USP8 gene fusion
Yael Fisher, Maribel D. Lacambra, Shahd S. Almohsen, et al.
Genes Chromosomes and Cancer (2023) Vol. 63, Iss. 1
Closed Access | Times Cited: 12
Molecular correlates of male germ cell tumors with overgrowth of components resembling somatic malignancies
Nicolas Wyvekens, Lynette M. Sholl, Yiying Yang, et al.
Modern Pathology (2022) Vol. 35, Iss. 12, pp. 1966-1973
Open Access | Times Cited: 17
ALK‐rearranged Mesenchymal Neoplasms: A Report of 9 cases Further Expanding the Clinicopathologic Spectrum of Emerging Kinase Fusion Positive Group of Tumors
Josephine K. Dermawan, Sara DiNapoli, Kerry Mullaney, et al.
Genes Chromosomes and Cancer (2022) Vol. 62, Iss. 2, pp. 75-84
Open Access | Times Cited: 17
Renal epithelioid angiomyolipomas overexpress TFE3 and the TFE3-regulated gene TRIM63 in the absence of TFE3 rearrangement
Katrina Collins, Julia A. Bridge, Rohit Mehra, et al.
Virchows Archiv (2024) Vol. 485, Iss. 3, pp. 471-478
Closed Access | Times Cited: 4
Targeted RNA sequencing in the routine clinical detection of fusion genes in salivary gland tumors
Justin Bubola, Christina MacMillan, Elizabeth G. Demicco, et al.
Genes Chromosomes and Cancer (2021) Vol. 60, Iss. 10, pp. 695-708
Open Access | Times Cited: 23
Advances in sarcoma molecular diagnostics
Xue Q. Wang, Angela Goytain, Brendan C. Dickson, et al.
Genes Chromosomes and Cancer (2022) Vol. 61, Iss. 6, pp. 332-345
Closed Access | Times Cited: 15
Microcribriform Adenocarcinoma of Salivary Glands
Ilan Weinreb, Elan Hahn, Brendan C. Dickson, et al.
The American Journal of Surgical Pathology (2022) Vol. 47, Iss. 2, pp. 194-201
Closed Access | Times Cited: 15
Acral fibrochondromyxoid tumor: a clinicopathologic and molecular genetic study of 37 cases
Carina Dehner, Hadley Pearson, Shahd S. Almohsen, et al.
Modern Pathology (2024) Vol. 37, Iss. 12, pp. 100599-100599
Open Access | Times Cited: 3
Clear cell stromal tumour of the lung with YAP1::TFE3 fusion: four cases including a case with highly aggressive clinical course
Carina Dehner, David Sadegh, Fouad Boulos, et al.
Histopathology (2022) Vol. 81, Iss. 2, pp. 239-245
Closed Access | Times Cited: 14
Sarcomatoid Yolk Sac Tumor Harbors Somatic Mutations That Are Otherwise Rare in Testicular Germ Cell Tumors
Andrés Acosta, Khaleel I. Al‐Obaidy, Lynette M. Sholl, et al.
The American Journal of Surgical Pathology (2022) Vol. 46, Iss. 5, pp. 701-712
Closed Access | Times Cited: 13
Recurrent EWSR1::COLCA2 Fusions Define a Novel Sarcoma With Spindle/Round Cell Morphology and Strong Predilection for the Sinonasal Tract
Abbas Agaimy, Martina Baněčková, John R. de Almeida, et al.
The American Journal of Surgical Pathology (2022) Vol. 47, Iss. 3, pp. 361-369
Closed Access | Times Cited: 13
Malignant undifferentiated epithelioid neoplasms with MAML2 rearrangements: A clinicopathologic study of seven cases demonstrating a heterogenous entity
Josephine K. Dermawan, Sara DiNapoli, Purvil Sukhadia, et al.
Genes Chromosomes and Cancer (2022) Vol. 62, Iss. 4, pp. 191-201
Open Access | Times Cited: 12
GAB1::ABL1 fusions define a distinctive soft tissue neoplasm, with variable perineurial differentiation, and a predilection for children and young adults
Abbas Agaimy, Raul Perret, Elizabeth G. Demicco, et al.
Genes Chromosomes and Cancer (2023) Vol. 62, Iss. 8, pp. 449-459
Open Access | Times Cited: 7
Testicular Juvenile Granulosa Cell Tumors Demonstrate Recurrent Loss of Chromosome 10 and Absence of Molecular Alterations Described in Ovarian Counterparts
Katrina Collins, Lynette M. Sholl, Sara O. Vargas, et al.
Modern Pathology (2023) Vol. 36, Iss. 6, pp. 100142-100142
Open Access | Times Cited: 7
Targeted next generation sequencing (NGS) to classify melanocytic neoplasms
Samaneh K. Zarabi, Elizabeth M. Azzato, Zheng Jin Tu, et al.
Journal of Cutaneous Pathology (2020) Vol. 47, Iss. 8, pp. 691-704
Open Access | Times Cited: 18
Re-evaluating tumors of purported specialized prostatic stromal origin reveals molecular heterogeneity, including non-recurring gene fusions characteristic of uterine and soft tissue sarcoma subtypes
Andrés Acosta, Lynette M. Sholl, Brendan C. Dickson, et al.
Modern Pathology (2021) Vol. 34, Iss. 9, pp. 1763-1779
Open Access | Times Cited: 13
Myoid gonadal stromal tumours are characterised by recurrent chromosome‐level copy number gains: molecular assessment of a multi‐institutional series
Katrina Collins, Lynette M. Sholl, Stephanie Siegmund, et al.
Histopathology (2022) Vol. 82, Iss. 3, pp. 431-438
Closed Access | Times Cited: 9
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