Veronica Bernard

955 total citations
40 papers, 612 citations indexed

About

Veronica Bernard is a scholar working on Pathology and Forensic Medicine, Oncology and Molecular Biology. According to data from OpenAlex, Veronica Bernard has authored 40 papers receiving a total of 612 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Pathology and Forensic Medicine, 16 papers in Oncology and 12 papers in Molecular Biology. Recurrent topics in Veronica Bernard's work include Lymphoma Diagnosis and Treatment (18 papers), Viral-associated cancers and disorders (9 papers) and Chronic Lymphocytic Leukemia Research (8 papers). Veronica Bernard is often cited by papers focused on Lymphoma Diagnosis and Treatment (18 papers), Viral-associated cancers and disorders (9 papers) and Chronic Lymphocytic Leukemia Research (8 papers). Veronica Bernard collaborates with scholars based in Germany, Saudi Arabia and United States. Veronica Bernard's co-authors include Niklas Gebauer, Alfred C. Feller, Hartmut Merz, Christoph Thorns, Christine Zühlke, Hendrik Lehnert, Gabriele Gillessen‐Kaesbach, Wolfgang Gebauer, Hanno M. Witte and Harald Biersack and has published in prestigious journals such as Blood, The Journal of Clinical Endocrinology & Metabolism and British Journal of Haematology.

In The Last Decade

Veronica Bernard

34 papers receiving 609 citations

Peers

Veronica Bernard

ONCOL

PFM

EPIDE

GENET

Eva Pros Spain

Tanya Basu United Kingdom

Elke Holinski‐Feder Germany

Gisèle Danglot France

Louise James United Kingdom

Akiyoshi Ogino Japan

Toshiko Yamochi Japan

Mareina Kudo Japan

Roy J. Reinten Netherlands

Amy Billet United States

Eva Pros Spain

Veronica Bernard

159 ×0.5

ONCOL

116 ×0.5

PFM

372 ×2.0

58 ×0.4

EPIDE

21 ×0.2

GENET

Citations per year, relative to Veronica Bernard Veronica Bernard (= 1×) peers Eva Pros

Countries citing papers authored by Veronica Bernard

Since Specialization

Citations

This map shows the geographic impact of Veronica Bernard's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Veronica Bernard with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Veronica Bernard more than expected).

Fields of papers citing papers by Veronica Bernard

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Veronica Bernard. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Veronica Bernard. The network helps show where Veronica Bernard may publish in the future.

Co-authorship network of co-authors of Veronica Bernard

This figure shows the co-authorship network connecting the top 25 collaborators of Veronica Bernard. A scholar is included among the top collaborators of Veronica Bernard based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Veronica Bernard. Veronica Bernard is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Künstner, Axel, Philipp Lohneis, Hanno M. Witte, et al.. (2025). Molecular profiling of primary renal diffuse large B-cell lymphoma unravels a proclivity for immune-privileged tropism. Blood Advances. 9(15). 3900–3904.

Künstner, Axel, Hanno M. Witte, Pengwei Xing, et al.. (2024). Genome-wide DNA methylation-analysis of blastic plasmacytoid dendritic cell neoplasm identifies distinct molecular features. Leukemia. 38(5). 1086–1098. 2 indexed citations

Witte, Hanno M., Anke Fähnrich, Axel Künstner, et al.. (2023). Primary refractory plasmablastic lymphoma: A precision oncology approach. Frontiers in Oncology. 13. 1129405–1129405. 4 indexed citations

Merz, Hartmut, Heinz‐Wolfram Bernd, Veronica Bernard, et al.. (2021). Performance of international prognostic indices in plasmablastic lymphoma: a comparative evaluation. Journal of Cancer Research and Clinical Oncology. 147(10). 3043–3050. 6 indexed citations

Gebauer, Niklas, Axel Künstner, Hanno M. Witte, et al.. (2021). Genomic insights into the pathogenesis of Epstein–Barr virus-associated diffuse large B-cell lymphoma by whole-genome and targeted amplicon sequencing. Blood Cancer Journal. 11(5). 102–102. 40 indexed citations

Kandula, Namratha R., Veronica Bernard, Swapna S. Dave, et al.. (2020). The South Asian Healthy Lifestyle Intervention (SAHELI) trial: Protocol for a mixed-methods, hybrid effectiveness implementation trial for reducing cardiovascular risk in South Asians in the United States. Contemporary Clinical Trials. 92. 105995–105995. 10 indexed citations

Gebauer, Niklas, Veronica Bernard, Wolfgang Gebauer, et al.. (2014). TP53mutations are frequent events in double-hit B-cell lymphomas withMYCandBCL2but notMYCandBCL6translocations. Leukemia & lymphoma. 56(1). 179–185. 49 indexed citations

Gebauer, Niklas, Judith Gebauer, Veronica Bernard, et al.. (2014). Prevalence of targetable oncogenic mutations and genomic alterations in Epstein–Barr virus-associated diffuse large B-cell lymphoma of the elderly. Leukemia & lymphoma. 56(4). 1100–1106. 33 indexed citations

Gebauer, Niklas, Christoph Thorns, Veronica Bernard, et al.. (2014). MicroRNA Profiling of Low-Grade and Transformed Nodal Marginal Zone Lymphoma Reveals a Similar Signature Pattern Distinct from Diffuse Large B Cell Lymphoma. Acta Haematologica. 133(2). 214–220. 4 indexed citations

10.

Gebauer, Niklas, Veronica Bernard, Janina Schemme, et al.. (2014). Oncogenic Mutations and Chromosomal Aberrations in Primary Extranodal Diffuse Large B-Cell Lymphomas of the Thyroid—A Study of 21 Cases. The Journal of Clinical Endocrinology & Metabolism. 100(2). 754–762. 9 indexed citations

11.

Gebauer, Niklas, Veronica Bernard, Christoph Thorns, Alfred C. Feller, & Hartmut Merz. (2014). Oncogenic <b><i>MYD88</i></b> Mutations Are Rare Events in Double-Hit B-Cell Lymphomas. Acta Haematologica. 133(1). 113–115. 2 indexed citations

12.

Gebauer, Niklas, Veronica Bernard, Alfred C. Feller, & Hartmut Merz. (2013). ID3 mutations are recurrent events in double-hit B-cell lymphomas.. PubMed. 33(11). 4771–8. 19 indexed citations

13.

Gebauer, Niklas, Veronica Bernard, Wolfgang Gebauer, Alfred C. Feller, & Hartmut Merz. (2013). MicroRNA Expression and JAK2 Allele Burden in Bone Marrow Trephine Biopsies of Polycythemia Vera, Essential Thrombocythemia and Early Primary Myelofibrosis. Acta Haematologica. 129(4). 251–256. 12 indexed citations

14.

Gebauer, Niklas, Veronica Bernard, Wolfgang Gebauer, Alfred C. Feller, & Hartmut Merz. (2013). miRNA Expression Correlated with Morphological Findings in Chronic Myeloid Leukemia Treated with Imatinib Mesylate. Acta Haematologica. 131(1). 11–15. 4 indexed citations

15.

Bernard, Veronica, et al.. (2011). Two dominantly inherited ataxias linked to chromosome 16q22.1: SCA4 and SCA31 are not allelic. Journal of Neurology. 258(7). 1223–1227. 7 indexed citations

16.

Hehr, Ute, Zacharias Kohl, Stefan Schilling, et al.. (2010). Early onset and slow progression of SCA28, a rare dominant ataxia in a large four-generation family with a novel AFG3L2 mutation. European Journal of Human Genetics. 18(8). 965–968. 37 indexed citations

17.

Bernard, Veronica, Martina Minnerop, Katrin Bürk, et al.. (2009). Exon deletions and intragenic insertions are not rare in ataxia with oculomotor apraxia 2. BMC Medical Genetics. 10(1). 87–87. 17 indexed citations

18.

Kurth, Ingo, Frank Hoffmann, Christian A. Hübner, et al.. (2009). Missense exchanges in the TTBK2 gene mutated in SCA11. Journal of Neurology. 256(11). 1856–1859. 15 indexed citations

19.

Bernard, Veronica, Sigmar Stricker, Friedmar R. Kreuz, et al.. (2008). Ataxia with Oculomotor Apraxia Type 2: Novel Mutations in Six Patients with Juvenile Age of Onset and Elevated Serum α-Fetoprotein. Neuropediatrics. 39(6). 347–350. 10 indexed citations

20.

Zühlke, Christine, Veronica Bernard, & Gabriele Gillessen‐Kaesbach. (2007). Investigation of Recessive Ataxia Loci in Patients with Young Age of Onset. Neuropediatrics. 38(4). 207–209. 4 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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