Karl Sperling
Impact in
- Cancer Research top 2%
- Carcinogens and Genotoxicity Assessment
- Molecular Biology top 1%
- DNA Repair Mechanisms
- Genomics and Chromatin Dynamics
- Epigenetics and DNA Methylation
- CRISPR and Genetic Engineering
Papers in
-
- DNA Repair Mechanisms 62
- Genomics and Chromatin Dynamics 29
- CRISPR and Genetic Engineering 15
- Genetics 60
- Genomic variations and chromosomal abnormalities 22
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 12
- Co-authors
- Martin Digweed (27 shared papers)André Reis (19 shared papers)Raymonda Varon (25 shared papers)Heidemarie Neitzel (35 shared papers)Joachim Bürger (5 shared papers)Potu N. Rao (3 shared papers)E Seemanová (10 shared papers)Krystyńa Chrzańowska (9 shared papers)
- Journals
- Human Genetics (25 papers)Chromosoma (10 papers)The American Journal of Human Genetics (6 papers)Experimental Cell Research (6 papers)Journal of Medical Genetics (6 papers)
- Partner nations
- GermanyUnited StatesPoland
In The Last Decade
Karl Sperling
182 papers receiving 7.1k citations
Karl Sperling's Hit Papers
Peers
Comparison fields: 5 of 151
- Cancer Research 1.3k
- Molecular Biology 5.1k
- Genetics 2.0k
- Cell Biology 849
- Pediatrics, Perinatology and Child Health 807
Countries citing papers authored by Karl Sperling
This map shows the geographic impact of Karl Sperling'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 Karl Sperling with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Karl Sperling more than expected).
Fields of papers citing papers by Karl Sperling
This network shows the impact of papers produced by Karl Sperling. 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 Karl Sperling. The network helps show where Karl Sperling may publish in the future.
Co-authors
The 25 scholars most cited alongside Karl Sperling, 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 193 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Nibrin, a Novel DNA Double-Strand Break Repair Protein, Is Mutated in Nijmegen Breakage Syndrome Hit paper breakdown → | 1998 | 885 |
| 2 | 2002 | 571 | |
| 3 | Arylamine N-acetyltransferase (NAT2) mutations and their allelic linkage in unrelated Caucasian individuals: correlation with phenotypic activity. | 1995 | 293 |
| 4 | 2002 | 276 | |
| 5 | 1982 | 226 | |
| 6 | 1994 | 206 | |
| 7 | 2004 | 206 | |
| 8 | 2004 | 198 | |
| 9 | 2000 | 120 | |
| 10 | 2004 | 110 | |
| 11 | 2007 | 107 | |
| 12 | 1974 | 104 | |
| 13 | Mutations in the Nijmegen Breakage Syndrome gene (NBS1) in childhood acute lymphoblastic leukemia (ALL). | 2001 | 104 |
| 14 | 1974 | 103 | |
| 15 | 1997 | 101 | |
| 16 | 2002 | 100 | |
| 17 | 2001 | 99 | |
| 18 | The gene for the ataxia-telangiectasia variant, Nijmegen breakage syndrome, maps to a 1-cM interval on chromosome 8q21. | 1997 | 95 |
| 19 | 2007 | 95 | |
| 20 | 2009 | 94 |
About Karl Sperling
Karl Sperling is a scholar working on Molecular Biology, Genetics, Cancer Research, Plant Science and Pediatrics, Perinatology and Child Health, having authored 193 papers that have together received 7.6k indexed citations. Recurring topics across this work include DNA Repair Mechanisms (62 papers), Chromosomal and Genetic Variations (38 papers), Genomics and Chromatin Dynamics (29 papers), Carcinogens and Genotoxicity Assessment (28 papers), Prenatal Screening and Diagnostics (23 papers), Genomic variations and chromosomal abnormalities (22 papers), CRISPR and Genetic Engineering (15 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (12 papers). The work is most often cited by research in Cancer Research (1.3k citations), Molecular Biology (5.1k citations), Genetics (2.0k citations), Cell Biology (849 citations) and Pediatrics, Perinatology and Child Health (807 citations). Karl Sperling has collaborated with scholars based in Germany, United States and Poland. Frequent co-authors include Martin Digweed, André Reis, Raymonda Varon, Heidemarie Neitzel, Joachim Bürger, Potu N. Rao, E Seemanová, Krystyńa Chrzańowska, Ulrike A. Mau and Gerald F. Cox. Their work appears in journals such as Human Genetics, Chromosoma, The American Journal of Human Genetics, Experimental Cell Research and Journal of Medical 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.