Andreas Laner
Impact in
-
- Genetic factors in colorectal cancer
-
- Cancer Genomics and Diagnostics
Papers in
-
- Genetic factors in colorectal cancer 15
-
- DNA Repair Mechanisms 3
- Co-authors
- Elke Holinski‐Feder (22 shared papers)Monika Morak (12 shared papers)Gisela Keller (3 shared papers)Anna Benet‐Pagès (10 shared papers)Heather Hampel (1 shared paper)Albert de la Chapelle (1 shared paper)Barbara Heidenreich (1 shared paper)Johan T. den Dunnen (1 shared paper)
- Journals
- European Journal of Human Genetics (6 papers)Familial Cancer (6 papers)Journal of Medical Genetics (4 papers)Pediatric Research (1 paper)BMC Medical Genomics (1 paper)
- Partner nations
- GermanyUnited StatesNetherlands
In The Last Decade
Andreas Laner
30 papers receiving 503 citations
Peers
Comparison fields: 5 of 58
- Pathology and Forensic Medicine 240
- Cancer Research 130
- Genetics 119
- Oncology 103
- Molecular Biology 170
Countries citing papers authored by Andreas Laner
This map shows the geographic impact of Andreas Laner'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 Laner with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Andreas Laner more than expected).
Fields of papers citing papers by Andreas Laner
This network shows the impact of papers produced by Andreas Laner. 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 Laner. The network helps show where Andreas Laner may publish in the future.
Co-authors
The 25 scholars most cited alongside Andreas Laner, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 33 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2014 | 72 | |
| 2 | 2021 | 47 | |
| 3 | 2013 | 45 | |
| 4 | 2015 | 44 | |
| 5 | 2016 | 40 | |
| 6 | 2010 | 37 | |
| 7 | 2018 | 23 | |
| 8 | 2010 | 20 | |
| 9 | 2010 | 20 | |
| 10 | 2019 | 16 | |
| 11 | 2021 | 13 | |
| 12 | 2017 | 12 | |
| 13 | 2023 | 11 | |
| 14 | 2019 | 11 | |
| 15 | 2008 | 10 | |
| 16 | 2020 | 9 | |
| 17 | 2015 | 9 | |
| 18 | 2023 | 8 | |
| 19 | 2020 | 8 | |
| 20 | 2020 | 8 |
About Andreas Laner
Andreas Laner is a scholar working on Pathology and Forensic Medicine, Molecular Biology, Genetics, Oncology and Cancer Research, having authored 33 papers that have together received 510 indexed citations. Recurring topics across this work include Genetic factors in colorectal cancer (15 papers), Genomics and Rare Diseases (6 papers), Cancer Genomics and Diagnostics (5 papers), DNA Repair Mechanisms (3 papers), Genomic variations and chromosomal abnormalities (3 papers), Colorectal Cancer Treatments and Studies (3 papers), Cardiac electrophysiology and arrhythmias (2 papers) and BRCA gene mutations in cancer (2 papers). The work is most often cited by research in Pathology and Forensic Medicine (240 citations), Cancer Research (130 citations), Genetics (119 citations), Oncology (103 citations) and Molecular Biology (170 citations). Andreas Laner has collaborated with scholars based in Germany, United States and Netherlands. Frequent co-authors include Elke Holinski‐Feder, Monika Morak, Gisela Keller, Anna Benet‐Pagès, Heather Hampel, Albert de la Chapelle, Barbara Heidenreich, Johan T. den Dunnen, Hans Scheffer and Gunnar Houge. Their work appears in journals such as European Journal of Human Genetics, Familial Cancer, Journal of Medical Genetics, Pediatric Research and BMC Medical Genomics.
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.