G.A.P. Bruns
Impact in
- Molecular Biology top 1%
- Renal and related cancers
- Genomics and Chromatin Dynamics
- Epigenetics and DNA Methylation
- Prion Diseases and Protein Misfolding
- Hematology top 1%
Papers in
-
- Renal and related cancers 13
- RNA modifications and cancer 8
- Ubiquitin and proteasome pathways 7
- CRISPR and Genetic Engineering 7
- Biochemical and Molecular Research 7
- Genetics 33
- Genetics and Neurodevelopmental Disorders 9
- Genomic variations and chromosomal abnormalities 8
- Co-authors
- Stuart H. Orkin (9 shared papers)Rachael L. Neve (11 shared papers)Manfred Gessler (11 shared papers)Webster K. Cavenee (3 shared papers)Annemarie Poustka (1 shared paper)James F. Gusella (6 shared papers)David M. Kurnit (9 shared papers)Paul C. Watkins (3 shared papers)
- Journals
- Proceedings of the National Academy of Sciences (9 papers)Science (9 papers)Human Genetics (9 papers)Journal of Biological Chemistry (9 papers)Genomics (9 papers)
- Partner nations
- United StatesCanadaUnited Kingdom
In The Last Decade
G.A.P. Bruns
110 papers receiving 9.7k citations
G.A.P. Bruns's Hit Papers
Peers
Comparison fields: 5 of 137
- Molecular Biology 6.2k
- Hematology 834
- Physiology 1.8k
- Genetics 2.0k
- Immunology 1.4k
Countries citing papers authored by G.A.P. Bruns
This map shows the geographic impact of G.A.P. Bruns'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 G.A.P. Bruns with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites G.A.P. Bruns more than expected).
Fields of papers citing papers by G.A.P. Bruns
This network shows the impact of papers produced by G.A.P. Bruns. 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 G.A.P. Bruns. The network helps show where G.A.P. Bruns may publish in the future.
Co-authors
The 25 scholars most cited alongside G.A.P. Bruns, 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 114 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Amyloid β Protein Gene: cDNA, mRNA Distribution, and Genetic Linkage Near the Alzheimer Locus Hit paper breakdown → | 1987 | 1396 |
| 2 | Homozygous deletion in Wilms tumours of a zinc-finger gene identified by chromosome jumping Hit paper breakdown → | 1990 | 1164 |
| 3 | Transposition and amplification of oncogene-related sequences in human neuroblastomas Hit paper breakdown → | 1983 | 641 |
| 4 | 1985 | 356 | |
| 5 | A strategy to reveal high-frequency RFLPs along the human X chromosome. | 1984 | 346 |
| 6 | 1985 | 303 | |
| 7 | 1990 | 283 | |
| 8 | 1992 | 271 | |
| 9 | 1992 | 269 | |
| 10 | 1990 | 266 | |
| 11 | 1984 | 251 | |
| 12 | 1989 | 233 | |
| 13 | 1984 | 186 | |
| 14 | 1973 | 183 | |
| 15 | 2003 | 167 | |
| 16 | 1996 | 145 | |
| 17 | 1990 | 141 | |
| 18 | 1986 | 140 | |
| 19 | 1989 | 124 | |
| 20 | 1987 | 123 |
About G.A.P. Bruns
G.A.P. Bruns is a scholar working on Molecular Biology, Genetics, Ophthalmology, Immunology and Genetics, having authored 114 papers that have together received 10.3k indexed citations. Recurring topics across this work include Renal and related cancers (13 papers), Genetics and Neurodevelopmental Disorders (9 papers), Genomic variations and chromosomal abnormalities (8 papers), RNA modifications and cancer (8 papers), Ubiquitin and proteasome pathways (7 papers), CRISPR and Genetic Engineering (7 papers), Chromosomal and Genetic Variations (7 papers) and Biochemical and Molecular Research (7 papers). The work is most often cited by research in Molecular Biology (6.2k citations), Hematology (834 citations), Physiology (1.8k citations), Genetics (2.0k citations) and Immunology (1.4k citations). G.A.P. Bruns has collaborated with scholars based in United States, Canada and United Kingdom. Frequent co-authors include Stuart H. Orkin, Rachael L. Neve, Manfred Gessler, Webster K. Cavenee, Annemarie Poustka, James F. Gusella, David M. Kurnit, Paul C. Watkins, Samuel A. Latt and David W. Patterson. Their work appears in journals such as Proceedings of the National Academy of Sciences, Science, Human Genetics, Journal of Biological Chemistry and 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.