A. Jauch
Impact in
- Hematology top 2%
- Multiple Myeloma Research and Treatments
- Genetics top 5%
- Genomic variations and chromosomal abnormalities
Papers in
-
- Genomics and Chromatin Dynamics 5
- Genetics 16
- Genomic variations and chromosomal abnormalities 10
- Co-authors
- Thomas Cremer (6 shared papers)Michael R. Speicher (5 shared papers)Peter Lichter (4 shared papers)Steffen Dietzel (3 shared papers)Evelin Schröck (2 shared papers)Stanislas du Manoir (3 shared papers)Christoph Cremer (2 shared papers)Harry Scherthan (2 shared papers)
- Journals
- Haematologica (4 papers)Oncogene (4 papers)Leukemia (3 papers)Human Genetics (3 papers)Clinical Genetics (3 papers)
- Partner nations
- GermanyUnited KingdomUnited States
In The Last Decade
A. Jauch
49 papers receiving 2.5k citations
Peers
Comparison fields: 5 of 101
- Hematology 533
- Genetics 320
- Cancer Research 437
- Molecular Biology 1.7k
- Genetics 596
Countries citing papers authored by A. Jauch
This map shows the geographic impact of A. Jauch'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 A. Jauch with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites A. Jauch more than expected).
Fields of papers citing papers by A. Jauch
This network shows the impact of papers produced by A. Jauch. 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 A. Jauch. The network helps show where A. Jauch may publish in the future.
Co-authors
The 25 scholars most cited alongside A. Jauch, 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 50 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1993 | 394 | |
| 2 | 2010 | 150 | |
| 3 | Comparative genomic hybridization of human malignant gliomas reveals multiple amplification sites and nonrandom chromosomal gains and losses. | 1994 | 149 |
| 4 | 2015 | 140 | |
| 5 | Chromosomal gains and losses in uveal melanomas detected by comparative genomic hybridization. | 1994 | 128 |
| 6 | 2005 | 126 | |
| 7 | 2003 | 115 | |
| 8 | 2010 | 112 | |
| 9 | 1996 | 100 | |
| 10 | Comparison of DNA gains and losses in primary renal clear cell carcinomas and metastatic sites: importance of 1q and 3p copy number changes in metastatic events. | 1997 | 82 |
| 11 | 2005 | 78 | |
| 12 | 2006 | 76 | |
| 13 | 1990 | 76 | |
| 14 | 2014 | 71 | |
| 15 | 2009 | 62 | |
| 16 | Correlation of microscopic phenotype with genotype in a formalin-fixed, paraffin-embedded testicular germ cell tumor with universal DNA amplification, comparative genomic hybridization, and interphase cytogenetics. | 1995 | 55 |
| 17 | 1998 | 54 | |
| 18 | A novel type of RET rearrangement (PTC8) in childhood papillary thyroid carcinomas and characterization of the involved gene (RFG8). | 2000 | 48 |
| 19 | 2007 | 46 | |
| 20 | 1998 | 46 |
About A. Jauch
A. Jauch is a scholar working on Molecular Biology, Genetics, Hematology, Plant Science and Cancer Research, having authored 50 papers that have together received 2.6k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (10 papers), Chromosomal and Genetic Variations (10 papers), Multiple Myeloma Research and Treatments (7 papers), Genomics and Chromatin Dynamics (5 papers), Cancer Genomics and Diagnostics (4 papers), Neuroendocrine Tumor Research Advances (4 papers), Acute Myeloid Leukemia Research (3 papers) and Microtubule and mitosis dynamics (3 papers). The work is most often cited by research in Hematology (533 citations), Genetics (320 citations), Cancer Research (437 citations), Molecular Biology (1.7k citations) and Genetics (596 citations). A. Jauch has collaborated with scholars based in Germany, United Kingdom and United States. Frequent co-authors include Thomas Cremer, Michael R. Speicher, Peter Lichter, Steffen Dietzel, Evelin Schröck, Stanislas du Manoir, Christoph Cremer, Harry Scherthan, Thomas Ried and Dirk Hose. Their work appears in journals such as Haematologica, Oncogene, Leukemia, Human Genetics and Clinical Genetics.
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.