Norbert Arnold

13.1k total citations
125 papers, 3.6k citations indexed

About

Norbert Arnold is a scholar working on Molecular Biology, Genetics and Oncology. According to data from OpenAlex, Norbert Arnold has authored 125 papers receiving a total of 3.6k indexed citations (citations by other indexed papers that have themselves been cited), including 74 papers in Molecular Biology, 56 papers in Genetics and 28 papers in Oncology. Recurrent topics in Norbert Arnold's work include BRCA gene mutations in cancer (29 papers), Genomic variations and chromosomal abnormalities (24 papers) and Chromosomal and Genetic Variations (17 papers). Norbert Arnold is often cited by papers focused on BRCA gene mutations in cancer (29 papers), Genomic variations and chromosomal abnormalities (24 papers) and Chromosomal and Genetic Variations (17 papers). Norbert Arnold collaborates with scholars based in Germany, United States and Sweden. Norbert Arnold's co-authors include Marion Kiechle, Johannes Wienberg, Ulrike Schwarz‐Boeger, Roscoe Stanyon, Alfons Meindl, W. Jonat, Eva Groß, Sergio Tofanelli, Jacobus Pfisterer and Jörg Weimer and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Clinical Oncology and PLoS ONE.

In The Last Decade

Norbert Arnold

121 papers receiving 3.5k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Norbert Arnold Germany 35 2.0k 1.4k 905 652 550 125 3.6k
Peggy Beer‐Romero United States 15 3.2k 1.6× 1.3k 0.9× 504 0.6× 1.5k 2.3× 315 0.6× 18 4.2k
Minna Taipale Finland 21 2.7k 1.3× 483 0.3× 447 0.5× 383 0.6× 263 0.5× 32 3.9k
Ohtsura Niwa Japan 35 2.5k 1.2× 1.2k 0.8× 516 0.6× 558 0.9× 185 0.3× 106 4.2k
Johan P. de Winter Netherlands 41 5.9k 2.9× 1.6k 1.1× 1.7k 1.8× 916 1.4× 630 1.1× 69 6.5k
Aaron L. Sarver United States 36 3.0k 1.5× 1.1k 0.8× 1.6k 1.8× 488 0.7× 151 0.3× 76 4.5k
Juan Méndez Spain 39 5.5k 2.7× 1.2k 0.8× 635 0.7× 1.3k 1.9× 344 0.6× 92 6.2k
Joy Delhanty United Kingdom 36 1.6k 0.8× 1.7k 1.2× 324 0.4× 241 0.4× 475 0.9× 104 4.1k
Detlev Schindler Germany 43 5.4k 2.7× 1.8k 1.3× 1.5k 1.6× 1.1k 1.7× 652 1.2× 164 6.6k
Andrew J. Pierce United States 29 5.1k 2.5× 972 0.7× 1.1k 1.2× 1.8k 2.8× 581 1.1× 76 5.8k
D.G. Harnden United Kingdom 33 2.5k 1.3× 1.6k 1.1× 1.0k 1.1× 723 1.1× 434 0.8× 90 4.8k

Countries citing papers authored by Norbert Arnold

Since Specialization
Citations

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

Fields of papers citing papers by Norbert Arnold

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Norbert Arnold

This figure shows the co-authorship network connecting the top 25 collaborators of Norbert Arnold. A scholar is included among the top collaborators of Norbert Arnold 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 Norbert Arnold. Norbert Arnold 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.
McDevitt, Trudi, Miranda Durkie, Norbert Arnold, et al.. (2024). EMQN best practice guidelines for genetic testing in hereditary breast and ovarian cancer. European Journal of Human Genetics. 32(5). 479–488. 5 indexed citations
2.
Kraft, Florian, Anna Benet‐Pagès, Daniel Berner, et al.. (2023). Quality assurance within the context of genome diagnostics (a german perspective). Medizinische Genetik. 35(2). 91–104. 1 indexed citations
3.
Weimer, Jörg, Matthias B. Stope, Edgar Dahl, et al.. (2023). Fluorescence in situ hybridization test for detection of endometrial carcinoma cells by non‐invasive vaginal swab. Journal of Cellular and Molecular Medicine. 27(3). 379–391. 4 indexed citations
4.
Lettau, Marcus, Philipp Arnold, Franziska Theilig, et al.. (2023). Chemotherapy‐induced release of ADAM17 bearing EV as a potential resistance mechanism in ovarian cancer. Journal of Extracellular Vesicles. 12(7). e12338–e12338. 13 indexed citations
5.
Arnold, Norbert, Jörg Weimer, Nicolaì Maass, et al.. (2022). Nectin-4 as Blood-Based Biomarker Enables Detection of Early Ovarian Cancer Stages. Cancers. 14(23). 5867–5867. 10 indexed citations
6.
Kast, Karin, Pauline Wimberger, & Norbert Arnold. (2018). Changes in classification of genetic variants in BRCA1 and BRCA2. Archives of Gynecology and Obstetrics. 297(2). 279–280. 7 indexed citations
7.
Becker, Kerstin, Luisa Mackenroth, Andreas Rump, et al.. (2017). Spectrum of genetic variants of BRCA1 and BRCA2 in a German single center study. Archives of Gynecology and Obstetrics. 295(5). 1227–1238. 16 indexed citations
8.
Heidemann, Simone, et al.. (2017). CDH1 mutation screen in a BRCA1/2-negative familial breast-/ovarian cancer cohort. Archives of Gynecology and Obstetrics. 297(1). 147–152. 6 indexed citations
9.
Schmutzler, Andreas, Jörg Weimer, Ali Salmassi, et al.. (2013). Sham-controlled implantation after preimplantation genetic screening by polar body biopsy and FISH. Archives of Gynecology and Obstetrics. 289(2). 439–444. 3 indexed citations
10.
Wenners, Antonia, Keyur Mehta, Sibylle Loibl, et al.. (2012). Neutrophil Gelatinase-Associated Lipocalin (NGAL) Predicts Response to Neoadjuvant Chemotherapy and Clinical Outcome in Primary Human Breast Cancer. PLoS ONE. 7(10). e45826–e45826. 44 indexed citations
11.
Meinhold‐Heerlein, Ivo, Dirk Bauerschlag, Yingyao Zhou, et al.. (2007). An Integrated Clinical-Genomics Approach Identifies a Candidate Multi-Analyte Blood Test for Serous Ovarian Carcinoma. Clinical Cancer Research. 13(2). 458–466. 41 indexed citations
12.
Klein, Andreas, M. Graessmann, Iver Petersen, et al.. (2007). Comparison of gene expression data from human and mouse breast cancers: Identification of a conserved breast tumor gene set. International Journal of Cancer. 121(3). 683–688. 26 indexed citations
13.
14.
Hofmann, Wera, Rolf Koehler, Bart Janssen, et al.. (2004). LargeBRCA1 gene deletions are found in 3% of German high-risk breast cancer families. Human Mutation. 24(6). 534–534. 69 indexed citations
15.
Kiechle, Marion, Anja Jacobsen, Ulrike Schwarz‐Boeger, et al.. (2001). Comparative genomic hybridization detects genetic imbalances in primary ovarian carcinomas as correlated with grade of differentiation. Cancer. 91(3). 534–540. 86 indexed citations
16.
Kiechle, Marion, Anja Jacobsen, Ulrike Schwarz‐Boeger, et al.. (2001). Comparative genomic hybridization detects genetic imbalances in primary ovarian carcinomas as correlated with grade of differentiation. Cancer. 91(3). 534–540. 6 indexed citations
17.
Groß, Eva, Marion Kiechle, & Norbert Arnold. (2001). Mutation analysis of p53 in ovarian tumors by DHPLC. Journal of Biochemical and Biophysical Methods. 47(1-2). 73–81. 47 indexed citations
18.
Consigliere, Stefania, Roscoe Stanyon, Udo Koehler, Norbert Arnold, & Johannes Wienberg. (1999). In situ hybridization (FISH) maps chromosomal homologies between Alouatta belzebul (Platyrrhini, Cebidae) and other primates and reveals extensive interchromosomal rearrangements between howler monkey genomes. American Journal of Primatology. 46(2). 119–133. 39 indexed citations
19.
Arnold, Norbert, et al.. (1996). Overrepresentation of 3q and 8q material and loss of 18q material are recurrent findings in advanced human ovarian cancer. Genes Chromosomes and Cancer. 16(1). 46–54. 111 indexed citations
20.
Arnold, Norbert, Roscoe Stanyon, A. Jauch, Patricia C. O’Brien, & Johannes Wienberg. (1996). Identification of complex chromosome rearrangements in the gibbon by fluorescent in situ hybridization (FISH) of a human chromosome 2q specific microlibrary, yeast artificial chromosomes, and reciprocal chromosome painting. Cytogenetic and Genome Research. 74(1-2). 80–85. 32 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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