Bernard F. Andruss

1.9k total citations · 1 hit paper
23 papers, 1.5k citations indexed

About

Bernard F. Andruss is a scholar working on Molecular Biology, Cancer Research and Oncology. According to data from OpenAlex, Bernard F. Andruss has authored 23 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 10 papers in Cancer Research and 7 papers in Oncology. Recurrent topics in Bernard F. Andruss's work include MicroRNA in disease regulation (8 papers), Pancreatic and Hepatic Oncology Research (7 papers) and Renal and related cancers (3 papers). Bernard F. Andruss is often cited by papers focused on MicroRNA in disease regulation (8 papers), Pancreatic and Hepatic Oncology Research (7 papers) and Renal and related cancers (3 papers). Bernard F. Andruss collaborates with scholars based in United States, Switzerland and Germany. Bernard F. Andruss's co-authors include Kathy Beckingham, Ruth Böhni, Ernst Hafen, Juan R. Riesgo‐Escovar, Sean Oldham, Hugo Stocker, Dennis Wylie, Sylvie Beaudenon‐Huibregtse, Emmanuel Labourier and Alexander L. Shifrin and has published in prestigious journals such as Cell, Proceedings of the National Academy of Sciences and Journal of Clinical Oncology.

In The Last Decade

Bernard F. Andruss

22 papers receiving 1.4k citations

Hit Papers

Autonomous Control of Cel... 1999 2026 2008 2017 1999 200 400 600

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Bernard F. Andruss United States 14 701 325 309 264 224 23 1.5k
Catherine Carrière United States 18 1.5k 2.2× 104 0.3× 602 1.9× 205 0.8× 368 1.6× 23 2.4k
Dierk Ingelfinger Germany 11 2.0k 2.8× 127 0.4× 144 0.5× 157 0.6× 133 0.6× 11 2.3k
Emil Karaulanov Germany 17 1.3k 1.9× 124 0.4× 132 0.4× 184 0.7× 93 0.4× 25 1.7k
Steven C. Pruitt United States 23 1.4k 2.0× 164 0.5× 51 0.2× 203 0.8× 80 0.4× 40 1.8k
Naomi Halachmi Israel 18 1.4k 2.0× 205 0.6× 69 0.2× 252 1.0× 184 0.8× 29 2.0k
Ning‐Ai Liu United States 19 588 0.8× 73 0.2× 267 0.9× 73 0.3× 190 0.8× 29 1.2k
Kathleen M. Scully United States 14 1.4k 2.0× 98 0.3× 719 2.3× 197 0.7× 132 0.6× 17 2.1k
Dominique Daegelen France 25 1.5k 2.1× 106 0.3× 84 0.3× 130 0.5× 232 1.0× 51 1.9k
Marie Vandromme France 28 1.8k 2.5× 140 0.4× 61 0.2× 148 0.6× 142 0.6× 33 2.0k
Béatrice Durand France 22 2.4k 3.5× 388 1.2× 169 0.5× 268 1.0× 109 0.5× 31 3.2k

Countries citing papers authored by Bernard F. Andruss

Since Specialization
Citations

This map shows the geographic impact of Bernard F. Andruss'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 Bernard F. Andruss with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Bernard F. Andruss more than expected).

Fields of papers citing papers by Bernard F. Andruss

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Bernard F. Andruss. 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 Bernard F. Andruss. The network helps show where Bernard F. Andruss may publish in the future.

Co-authorship network of co-authors of Bernard F. Andruss

This figure shows the co-authorship network connecting the top 25 collaborators of Bernard F. Andruss. A scholar is included among the top collaborators of Bernard F. Andruss 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 Bernard F. Andruss. Bernard F. Andruss is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Brown, Justin T., Walairat Laosinchai-Wolf, Marie E. Fahey, et al.. (2019). Analytical Validation of a Highly Sensitive, Multiplexed Chronic Myeloid Leukemia Monitoring System Targeting BCR-ABL1 RNA. Journal of Molecular Diagnostics. 21(4). 718–733. 9 indexed citations
2.
Labourier, Emmanuel, Alexander L. Shifrin, Anne E. Busseniers, et al.. (2015). Molecular Testing for miRNA, mRNA, and DNA on Fine-Needle Aspiration Improves the Preoperative Diagnosis of Thyroid Nodules With Indeterminate Cytology. The Journal of Clinical Endocrinology & Metabolism. 100(7). 2743–2750. 208 indexed citations
3.
Beaudenon‐Huibregtse, Sylvie, Erik K. Alexander, Richard Guttler, et al.. (2014). Centralized Molecular Testing for Oncogenic Gene Mutations Complements the Local Cytopathologic Diagnosis of Thyroid Nodules. Thyroid. 24(10). 1479–1487. 95 indexed citations
4.
Lee, Linda, Anna E. Szafranska-Schwarzbach, Dennis Wylie, et al.. (2014). Investigating MicroRNA Expression Profiles in Pancreatic Cystic Neoplasms. Clinical and Translational Gastroenterology. 5(1). e47–e47. 33 indexed citations
5.
Szafranska-Schwarzbach, Anna E., Dennis Wylie, Andrew M. Bellizzi, et al.. (2013). Investigation of MicroRNA (miRNA) in pancreatic cystic tumors (IMPACT) study: Differential expression observed among pancreatic cystic neoplasms. Pancreatology. 13(2). e47–e48. 2 indexed citations
6.
Lee, Linda, Anna E. Szafranska-Schwarzbach, Bernard F. Andruss, & Darwin L. Conwell. (2013). Can miRNA Biomarkers Be Utilized to Improve the Evaluation and Management of Pancreatic Cystic Lesions?. 1(1). 1 indexed citations
7.
Matthaei, Hanno, Dennis Wylie, Marco Dal Molin, et al.. (2012). miRNA Biomarkers in Cyst Fluid Augment the Diagnosis and Management of Pancreatic Cysts. Clinical Cancer Research. 18(17). 4713–4724. 126 indexed citations
8.
Szafranska-Schwarzbach, Anna E., et al.. (2012). No miR Quirk: Dysregulation of microRNAs in Pancreatic Ductal Adenocarcinoma. MicroRNA. 1(1). 49–58. 3 indexed citations
9.
Labourier, Emmanuel, et al.. (2011). An miRNA assay for the classification of benign and neoplastic lesions in pancreatic fine-needle aspirates.. Journal of Clinical Oncology. 29(4_suppl). 163–163. 1 indexed citations
10.
Szafranska-Schwarzbach, Anna E., Alex Adai, Linda Lee, Darwin L. Conwell, & Bernard F. Andruss. (2011). Development of a miRNA-based diagnostic assay for pancreatic ductal adenocarcinoma. Expert Review of Molecular Diagnostics. 11(3). 249–257. 36 indexed citations
11.
Pappas, Todd C., Andreas G. Bader, Bernard F. Andruss, David Brown, & Lance P. Ford. (2007). Applying small RNA molecules to the directed treatment of human diseases: realizing the potential. Expert Opinion on Therapeutic Targets. 12(1). 115–127. 24 indexed citations
12.
Davison, Timothy S., Charles D. Johnson, & Bernard F. Andruss. (2006). [2] Analyzing Micro‐RNA Expression Using Microarrays. Methods in enzymology on CD-ROM/Methods in enzymology. 14–34. 67 indexed citations
13.
Madabusi, Lakshmi V, Gary J. Latham, & Bernard F. Andruss. (2006). [1] RNA Extraction for Arrays. Methods in enzymology on CD-ROM/Methods in enzymology. 411. 1–14. 35 indexed citations
14.
Hadd, Andrew G., Justin T. Brown, Bernard F. Andruss, Fei Ye, & Cindy R WalkerPeach. (2005). Adoption of array technologies into the clinical laboratory. Expert Review of Molecular Diagnostics. 5(3). 409–420. 15 indexed citations
15.
Andruss, Bernard F., Clare Bolduc, & Kathy Beckingham. (2004). Movement of calmodulin between cells in the ovary and embryo of drosophila. genesis. 38(2). 93–103. 6 indexed citations
16.
Woodside, Darren G., T. Kent Teague, Yuko Miyamoto, et al.. (2003). Control of T lymphocyte morphology by the GTPase Rho. BMC Cell Biology. 4(1). 2–2. 12 indexed citations
17.
Miyamoto, Yuko, et al.. (2003). Diverse Roles of Integrins in Human T Lymphocyte Biology. Immunologic Research. 27(1). 71–84. 15 indexed citations
18.
Böhni, Ruth, Juan R. Riesgo‐Escovar, Sean Oldham, et al.. (1999). Autonomous Control of Cell and Organ Size by CHICO, a Drosophila Homolog of Vertebrate IRS1–4. Cell. 97(7). 865–875. 691 indexed citations breakdown →
19.
Beckingham, Kathy, et al.. (1998). Calcium-binding proteins and development. BioMetals. 11(4). 359–372. 13 indexed citations
20.
Andruss, Bernard F., et al.. (1997). Expression of calmodulin in Drosophila is highly regulated in a stage- and tissue-specific manner. Development Genes and Evolution. 206(8). 541–545. 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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