Andreas Berger

1.8k total citations
10 papers, 405 citations indexed

About

Andreas Berger is a scholar working on Genetics, Molecular Biology and Oncology. According to data from OpenAlex, Andreas Berger has authored 10 papers receiving a total of 405 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Genetics, 4 papers in Molecular Biology and 3 papers in Oncology. Recurrent topics in Andreas Berger's work include BRCA gene mutations in cancer (5 papers), Protein Kinase Regulation and GTPase Signaling (2 papers) and Receptor Mechanisms and Signaling (2 papers). Andreas Berger is often cited by papers focused on BRCA gene mutations in cancer (5 papers), Protein Kinase Regulation and GTPase Signaling (2 papers) and Receptor Mechanisms and Signaling (2 papers). Andreas Berger collaborates with scholars based in Austria, United States and Germany. Andreas Berger's co-authors include Marcel E. Durieux, Hans H. Goebel, Kathrin Wieczorek, Helmut Klocker, Simone Millinger, Christian Marth, Heidi Fiegl, Elisabeth Mueller‐Holzner, Martin Widschwendter and Christian Ensinger and has published in prestigious journals such as Journal of Clinical Oncology, PLoS ONE and Cancer Research.

In The Last Decade

Andreas Berger

10 papers receiving 397 citations

Peers

Andreas Berger

MB

CR

ONCOL

GENET

PFM

Tsung-Ming Chen Taiwan

Anna Sobczuk Poland

Yanlin Luo China

Darcy L. Thull United States

Margaret Cook Canada

Cristina Alvarez Spain

Masaru Ichida Japan

A. F. Wilson United States

Qingxiao Hong China

Tsung-Ming Chen Taiwan

Andreas Berger

237 ×1.2

MB

97 ×0.8

CR

65 ×0.6

ONCOL

56 ×0.7

GENET

23 ×0.5

PFM

Citations per year, relative to Andreas Berger Andreas Berger (= 1×) peers Tsung-Ming Chen

Countries citing papers authored by Andreas Berger

Since Specialization

Citations

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

Fields of papers citing papers by Andreas Berger

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Andreas Berger. 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 Andreas Berger. The network helps show where Andreas Berger may publish in the future.

Co-authorship network of co-authors of Andreas Berger

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

All Works

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10 of 10 papers shown

1.

Singer, Christian F., Yen Y. Tan, Daniela Muhr, et al.. (2019). Association between family history, mutation locations, and prevalence of BRCA1 or 2 mutations in ovarian cancer patients. Cancer Medicine. 8(4). 1875–1881. 20 indexed citations

2.

Tea, Muy‐Kheng M., Yen Y. Tan, Ella Asseryanis, et al.. (2018). Improving comprehension of genetic counseling for hereditary breast and ovarian cancer clients with a visual tool. PLoS ONE. 13(7). e0200559–e0200559. 9 indexed citations

3.

Pfeiler, Georg, et al.. (2016). Changes of Socio-demographic data of clients seeking genetic counseling for hereditary breast and ovarian cancer due to the “Angelina Jolie Effect”. BMC Cancer. 16(1). 436–436. 27 indexed citations

4.

Salama, Mohamed, Daniela Muhr, Andreas Berger, et al.. (2015). Effect of lifestyle and reproductive factors on the onset of breast cancer in female BRCA 1 and 2 mutation carriers. Molecular Genetics & Genomic Medicine. 4(2). 172–177. 18 indexed citations

5.

Singer, Christian F., Daniela Muhr, Christine Rappaport, et al.. (2013). Clinical implications of genetic testing for BRCA1 and BRCA2 mutations in Austria. Clinical Genetics. 85(1). 72–75. 6 indexed citations

6.

Pfeiler, Georg, Robert Königsberg, Peyman Hadji, et al.. (2013). The impact of estrogen depletion by aromatase inhibitors on adiponectin serum levels in postmenopausal patients with breast cancer.. Journal of Clinical Oncology. 31(15_suppl). e11601–e11601. 3 indexed citations

7.

Bartova, Lucie, Andreas Berger, & Lukas Pezawas. (2010). Is there a personalized medicine for mood disorders?. European Archives of Psychiatry and Clinical Neuroscience. 260(S2). 121–126. 23 indexed citations

8.

Fiegl, Heidi, Simone Millinger, Elisabeth Mueller‐Holzner, et al.. (2005). Circulating Tumor-Specific DNA: A Marker for Monitoring Efficacy of Adjuvant Therapy in Cancer Patients. Cancer Research. 65(4). 1141–1145. 208 indexed citations

9.

Wieczorek, Kathrin, et al.. (2001). Local Anesthetic Inhibition of G Protein-Coupled Receptor Signaling by Interference with Gαq Protein Function. Molecular Pharmacology. 59(2). 294–301. 4 indexed citations

10.

Wieczorek, Kathrin, et al.. (2001). Local Anesthetic Inhibition of G Protein-Coupled Receptor Signaling by Interference with Gα_q Protein Function. Molecular Pharmacology. 59(2). 294–301. 87 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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