Norbert Arnold

13.3k citations

126 papers · 3.7k · h-index 35

Impact in

Cancer Research top 2%
- Cancer Genomics and Diagnostics
- Cancer-related molecular mechanisms research
Genetics top 1%
- BRCA gene mutations in cancer
- Genomic variations and chromosomal abnormalities

Papers in

Molecular Biology 66
- DNA Repair Mechanisms 14
- Genomics and Chromatin Dynamics 10
Genetics 54
- BRCA gene mutations in cancer 29
- Genomic variations and chromosomal abnormalities 20

Co-authors: Marion Kiechle (25 shared papers)Johannes Wienberg (10 shared papers)Ulrike Schwarz‐Boeger (8 shared papers)Roscoe Stanyon (6 shared papers)Alfons Meindl (20 shared papers)W. Jonat (22 shared papers)Sergio Tofanelli (2 shared papers)Eva Groß (9 shared papers)
Journals: Archives of Gynecology and Obstetrics (8 papers)Human Mutation (8 papers)Genes Chromosomes and Cancer (7 papers)International Journal of Cancer (6 papers)Carcinogenesis (4 papers)
Partner nations: Germany United States Sweden

In The Last Decade

Norbert Arnold

122 papers receiving 3.6k citations

Peers

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-authors

The 25 scholars most cited alongside Norbert Arnold, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Norbert Arnold Line = papers co-authored together Norbert Arnold links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 126 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Reconstruction of genomic rearrangements in great apes and gibbons by chromosome painting. Proceedings of the National Academy of Sciences ·Anna Jauch, Johannes Wienberg, Roscoe Stanyon, Norbert Arnold, Sergio Tofanelli, Takafumi Ishida, Thomas Cremer	1992	257
2	Contralateral Breast Cancer Risk in BRCA1 and BRCA2 Mutation Carriers Journal of Clinical Oncology ·Monika Graeser, Christoph Engel, Kerstin Rhiem, Dorothea Gadzicki, Ulrich Bick, Karin Kast, Ursula G. Froster, B. Schlehe, Astrid Bechtold, Norbert Arnold, Sabine Preisler-Adams, Carolin Nestle-Kraemling, Mohammad Zaino, Markus Loeffler, Marion Kiechle, Alfons Meindl, Dominic Varga, Rita K. Schmutzler	2009	234
3	Molecular and prognostic distinction between serous ovarian carcinomas of varying grade and malignant potential Oncogene ·Ivo Meinhold‐Heerlein, Dirk Bauerschlag, Felix Hilpert, Petre Dimitrov, Lisa M. Sapinoso, Marzenna Orlowska‐Volk, Thomas Bauknecht, Tjoung‐Won Park, W. Jonat, Anja Jacobsen, Jalid Sehouli, Jütta Lüttges, Maryla Krajewski, Stan Krajewski, John C. Reed, Norbert Arnold, Garret M. Hampton	2004	162
4	A comparison of BRCA1 mutation analysis by direct sequencing, SSCP and DHPLC Human Genetics ·(unknown), Norbert Arnold, J. Goette, Ulrike Schwarz‐Boeger, Marion Kiechle	1999	150
5	A comparison of BRCA1 mutation analysis by direct sequencing, SSCP and DHPLC Human Genetics ·(unknown), Norbert Arnold, J. Goette, Ulrike Schwarz‐Boeger, Marion Kiechle	1999	112
6	Overrepresentation of 3q and 8q material and loss of 18q material are recurrent findings in advanced human ovarian cancer Genes Chromosomes and Cancer ·Norbert Arnold, Lorenz Hägele, Lioba Walz, W. Schempp, Jacobus Pfisterer, Thomas Bauknecht, Marion Kiechle	1996	112
7	A genetic variant in the pre-miR-27a oncogene is associated with a reduced familial breast cancer risk Breast Cancer Research and Treatment ·Rongxi Yang, B. Schlehe, Kari Hemminki, Christian Sutter, Peter Bugert, Barbara Wappenschmidt, (unknown), Raymonda Varon, Bernhard H. F. Weber, Dieter Niederacher, Norbert Arnold, Alfons Meindl, Claus R. Bartram, Rita K. Schmutzler, Barbara Burwinkel	2009	107
8	Identification of brain- and bone-specific breast cancer metastasis genes Cancer Letters ·Andreas Klein, Christian Olendrowitz, Rita Schmutzler, Juergen A. Hampl, Peter M. Schlag, Nicolaì Maass, Norbert Arnold, Ralf Wessel, Juliane Ramser, Alfons Meindl, Siegfried Scherneck, Susanne Seitz	2008	93
9	A highly sensitive, fast, and economical technique for mutation analysis in hereditary breast and ovarian cancers Human Mutation ·Norbert Arnold, Eva Groß, Ulrike Schwarz‐Boeger, Jacobus Pfisterer, W. Jonat, Marion Kiechle	1999	91
10	Comparative genomic hybridization detects genetic imbalances in primary ovarian carcinomas as correlated with grade of differentiation Cancer ·Marion Kiechle, Anja Jacobsen, Ulrike Schwarz‐Boeger, (unknown), Jacobus Pfisterer, Norbert Arnold	2001	89
11	Decreased expression of angiogenesis antagonist EFEMP1 in sporadic breast cancer is caused by aberrant promoter methylation and points to an impact of EFEMP1 as molecular biomarker International Journal of Cancer ·Ariane Sadr‐Nabavi, Juliane Ramser, (unknown), J. Naehrig, Frank Wiesmann, Beate Betz, Heide Hellebrand, Stefanie Engert, Susanne Seitz, Rene Kreutzfeld, Takako Sasaki, Norbert Arnold, Rita K. Schmutzler, Marion Kiechle, Dieter Niederacher, Nadia Harbeck, Edgar Dahl, Alfons Meindl	2008	79
12	A variant affecting a putative miRNA target site in estrogen receptor (ESR) 1 is associated with breast cancer risk in premenopausal women Carcinogenesis ·Sandrine Tchatchou, Anke Jung, Kari Hemminki, Christian Sutter, Barbara Wappenschmidt, Peter Bugert, Bernhard H. F. Weber, Dieter Niederacher, Norbert Arnold, Raymonda Varon-Mateeva, Nina Ditsch, Alfons Meindl, Rita K. Schmutzler, Claus R. Bartram, Barbara Burwinkel	2008	72
13	LargeBRCA1 gene deletions are found in 3% of German high-risk breast cancer families Human Mutation ·Carolin Hartmann, Anika John, R�diger Klaes, Wera Hofmann, Rainer Bielen, Rolf Koehler, Bart Janssen, Claus R. Bartram, Norbert Arnold, Johannes Zschocke	2004	71
14	Limited relevance of the CHEK2 gene in hereditary breast cancer International Journal of Cancer ·Michael R. Dufault, Beate Betz, Barbara Wappenschmidt, Wera Hofmann, Katrin Bandick, Astrid Golla, Andrea Pietschmann, C. Nestle-Krämling, Kerstin Rhiem, Christine Hüttner, Celia von Lindern, Peter Dall, Marion Kiechle, Michael Untch, W. Jonat, Alfons Meindl, Siegfried Scherneck, Dieter Niederacher, Rita K. Schmutzler, Norbert Arnold	2004	71
15	The Human Bradykinin B2 Receptor Gene: Full-Length cDNA, Genomic Organization and Identification of the Regulatory Region Biochemical and Biophysical Research Communications ·S. Kammerer, Andreas Braun, Norbert Arnold, A. Roscher	1995	66
16	Genomic reorganization and disrupted chromosomal synteny in the siamang (Hylobates syndactylus) revealed by fluorescence in situ hybridization American Journal of Physical Anthropology ·Udo Koehler, Norbert Arnold, Johannes Wienberg, Sergio Tofanelli, Roscoe Stanyon	1995	66
17	Identification of specific BRCA1 and BRCA2 variants by DHPLC Human Mutation ·Eva Groß, Norbert Arnold, Katharina Pfeifer, Katrin Bandick, Marion Kiechle	2000	66
18	Genetic Characteristics of the Human Hepatic Stellate Cell Line LX-2 PLoS ONE ·Ralf Weiskirchen, Jörg Weimer, Steffen K. Meurer, Anja Kron, B. Seipel, Inga Vater, Norbert Arnold, Reiner Siebert, Lieming Xu, Scott L. Friedman, Carsten Bergmann	2013	57
19	Simian Y Chromosomes: species-specific rearrangements of DAZ, RBM, and TSPY versus contiguity of PAR and SRY Mammalian Genome ·Birgitta Gläser, Frank Grützner, Ulrike Willmann, Roscoe Stanyon, Norbert Arnold, Kay Taylor, W. Rietschel, S. Zeitler, Roland Toder, W. Schempp	1998	50
20	Mutation analysis of p53 in ovarian tumors by DHPLC Journal of Biochemical and Biophysical Methods ·Eva Groß, Marion Kiechle, Norbert Arnold	2001	49

About Norbert Arnold

Norbert Arnold is a scholar working on Molecular Biology, Genetics, Oncology, Cancer Research and Pathology and Forensic Medicine, having authored 126 papers that have together received 3.7k indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (29 papers), Genomic variations and chromosomal abnormalities (20 papers), Ovarian cancer diagnosis and treatment (16 papers), Cancer Genomics and Diagnostics (16 papers), Chromosomal and Genetic Variations (15 papers), DNA Repair Mechanisms (14 papers), Genetic factors in colorectal cancer (12 papers) and Genomics and Chromatin Dynamics (10 papers). The work is most often cited by research in Cancer Research (752 citations), Genetics (1.4k citations), Reproductive Medicine (358 citations), Molecular Biology (1.8k citations) and Oncology (542 citations). Norbert Arnold has collaborated with scholars based in Germany, United States and Sweden. Frequent co-authors include Marion Kiechle, Johannes Wienberg, Ulrike Schwarz‐Boeger, Roscoe Stanyon, Alfons Meindl, W. Jonat, Sergio Tofanelli, Eva Groß, Jacobus Pfisterer and Dieter Niederacher. Their work appears in journals such as Archives of Gynecology and Obstetrics, Human Mutation, Genes Chromosomes and Cancer, International Journal of Cancer and Carcinogenesis.

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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