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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:

Identification of MNDA as a new marker for nodal marginal zone lymphoma
George Kanellis, Giovanna Roncador, Alberto J. Arribas, et al.
Leukemia (2009) Vol. 23, Iss. 10, pp. 1847-1857
Closed Access | Times Cited: 82

Showing 1-25 of 82 citing articles:

Clonal B cells in patients with hepatitis C virus–associated mixed cryoglobulinemia contain an expanded anergic CD21low B-cell subset
Edgar D. Charles, Claudia Brunetti, Svetlana Marukian, et al.
Blood (2011) Vol. 117, Iss. 20, pp. 5425-5437
Open Access | Times Cited: 188
Recognizing nodal marginal zone lymphoma: recent advances and pitfalls. A systematic review
Michiel van den Brand, J. Han van Krieken
Haematologica (2013) Vol. 98, Iss. 7, pp. 1003-1013
Open Access | Times Cited: 102
Nodal marginal zone lymphoma: gene expression and miRNA profiling identify diagnostic markers and potential therapeutic targets
Alberto J. Arribas, Yolanda Campos‐Martín, Cristina Gómez‐Abad, et al.
Blood (2011) Vol. 119, Iss. 3, pp. e9-e21
Open Access | Times Cited: 99
Chronic inflammation and extra-nodal marginal-zone lymphomas of MALT-type
Catherine Thiéblemont, Francesco Bertoni, Christiane Copie‐Bergman, et al.
Seminars in Cancer Biology (2013) Vol. 24, pp. 33-42
Closed Access | Times Cited: 89
Machine Learning-based Classification of Diffuse Large B-cell Lymphoma Patients by Their Protein Expression Profiles
Sally J. Deeb, Stefka Tyanova, Michael Hummel, et al.
Molecular & Cellular Proteomics (2015) Vol. 14, Iss. 11, pp. 2947-2960
Open Access | Times Cited: 83
The relative contribution of DNA methylation and genetic variants on protein biomarkers for human diseases
Muhammad Ahsan, Weronica E. Ek, Mathias Rask‐Andersen, et al.
PLoS Genetics (2017) Vol. 13, Iss. 9, pp. e1007005-e1007005
Open Access | Times Cited: 71
Optimizing therapy for nodal marginal zone lymphoma
Catherine Thiéblemont, Thierry Jo Molina, Frédéric Davi
Blood (2016) Vol. 127, Iss. 17, pp. 2064-2071
Open Access | Times Cited: 69
Follicular lymphoma and marginal zone lymphoma: how many diseases?
Camille Laurent, James R. Cook, Tadashi Yoshino, et al.
Virchows Archiv (2022) Vol. 482, Iss. 1, pp. 149-162
Open Access | Times Cited: 28
Novel developments in the pathogenesis and diagnosis of extranodal marginal zone lymphoma
Max I. Schreuder, Michiel van den Brand, Konnie M. Hebeda, et al.
Journal of Hematopathology (2017) Vol. 10, Iss. 3-4, pp. 91-107
Open Access | Times Cited: 61
Splenic marginal zone lymphoma
Miguel Á. Piris, Arantza Onaindía, Manuela Mollejo
Best Practice & Research Clinical Haematology (2016) Vol. 30, Iss. 1-2, pp. 56-64
Closed Access | Times Cited: 49
How I diagnose B-cell lymphoproliferative disorders with plasmacytic differentiation
Jonathan H. Young, Olga Pozdnyakova
American Journal of Clinical Pathology (2025)
Closed Access
Selective Immunophenotyping for Diagnosis of B-cell Neoplasms
Scott D. Boyd, Yasodha Natkunam, John R. Allen, et al.
Applied immunohistochemistry & molecular morphology (2012) Vol. 21, Iss. 2, pp. 116-131
Open Access | Times Cited: 47
IRTA1 and MNDA Expression in Marginal Zone Lymphoma
Zhen Wang, James R. Cook
American Journal of Clinical Pathology (2018) Vol. 151, Iss. 3, pp. 337-343
Open Access | Times Cited: 41
Marginal zone B-cell lymphoma: lessons from Western and Eastern diagnostic approaches
Shigeo Nakamura, Maurilio Ponzoni
Pathology (2019) Vol. 52, Iss. 1, pp. 15-29
Closed Access | Times Cited: 41
Myeloid cell nuclear differentiation antigen is expressed in a subset of marginal zone lymphomas and is useful in the differential diagnosis with follicular lymphoma
Ryan A. Metcalf, Ahmad Monabati, Monika Vyas, et al.
Human Pathology (2014) Vol. 45, Iss. 8, pp. 1730-1736
Closed Access | Times Cited: 38
Histiocytoid Sweet syndrome is infiltrated predominantly by M2-like macrophages
Anna Peroni, Chiara Colato, Donatella Schena, et al.
Journal of the American Academy of Dermatology (2014) Vol. 72, Iss. 1, pp. 131-139
Closed Access | Times Cited: 31
New Immunohistochemistry for B-Cell Lymphoma and Hodgkin Lymphoma
Xiaohong Zhang, Nadine S. Aguilera
Archives of Pathology & Laboratory Medicine (2014) Vol. 138, Iss. 12, pp. 1666-1672
Closed Access | Times Cited: 29
Clinicopathologic Features of CD5-Positive Nodal Marginal Zone Lymphoma
Jesse Jaso, C. Cameron Yin, Sa A. Wang, et al.
American Journal of Clinical Pathology (2013) Vol. 140, Iss. 5, pp. 693-700
Open Access | Times Cited: 29
Nodal marginal zone B-cell lymphoma: a diagnostic and therapeutic dilemma.
Alexandra Traverse‐Glehen, Francesco Bertoni, Catherine Thiéblemont, et al.
PubMed (2012) Vol. 26, Iss. 1, pp. 92-4
Closed Access | Times Cited: 28
Altered Spectrum of Lymphoid Neoplasms in a Single-Center Cohort of Common Variable Immunodeficiency with Immune Dysregulation
Claudia Wehr, Leonora Houet, Susanne Unger, et al.
Journal of Clinical Immunology (2021) Vol. 41, Iss. 6, pp. 1250-1265
Open Access | Times Cited: 20
MNDA, a PYHIN factor involved in transcriptional regulation and apoptosis control in leukocytes
Stefania Bottardi, Taylorjade Layne, Ailyn C. Ramòn, et al.
Frontiers in Immunology (2024) Vol. 15
Open Access | Times Cited: 2
Marginal zone lymphoma of extranodal sites: A review with an emphasis on diagnostic pitfalls and differential diagnosis with reactive conditions
Román Segura-Rivera, Sergio Piña‐Oviedo
Human Pathology (2024), pp. 105683-105683
Closed Access | Times Cited: 2
Recurrent mutations in genes involved in nuclear factor‐κB signalling in nodal marginal zone lymphoma—diagnostic and therapeutic implications
Michiel van den Brand, Jos Rijntjes, Konnie M. Hebeda, et al.
Histopathology (2016) Vol. 70, Iss. 2, pp. 174-184
Open Access | Times Cited: 22
Immunohistochemical differentiation between follicular lymphoma and nodal marginal zone lymphoma - combined performance of multiple markers
Michiel van den Brand, Janneke J.M. Mathijssen, M. García García, et al.
Haematologica (2015) Vol. 100, Iss. 9, pp. e358-e360
Open Access | Times Cited: 21
Genomic analysis of Non‐Splenic Marginal Zone Lymphomas (MZL) indicates similarities between nodal and extranodal MZL and supports their derivation from Memory B‐cells
Urban Novak, Katia Basso, Laura Pasqualucci, et al.
British Journal of Haematology (2011) Vol. 155, Iss. 3, pp. 362-365
Open Access | Times Cited: 24
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