Caroline Scholz
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- Genomic variations and chromosomal abnormalities 4
- Genetic Syndromes and Imprinting 2
- BRCA gene mutations in cancer 2
- Genomics and Rare Diseases 1
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- Metabolism and Genetic Disorders 2
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- Metabolomics and Mass Spectrometry Studies 1
- CRISPR and Genetic Engineering 1
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- Amino Acid Enzymes and Metabolism 1
- Co-authors
- Doris SteinemannBrigitte SchlegelbergerBernd AuberStephanie SchubertThomas IlligGunnar SchmidtVicente A. YépezNorbert Lorenz
- Journals
- The American Journal of Human Genetics (1 paper)International Journal of Cancer (1 paper)Breast Cancer Research and Treatment (1 paper)
- Partner nations
- GermanySwitzerlandAustria
In The Last Decade
Caroline Scholz
8 papers receiving 124 citations
Peers
Comparison fields: 5 of 39
- Genetics 62
- Clinical Biochemistry 14
- Molecular Biology 86
- Cancer Research 15
- Reproductive Medicine 6
Countries citing papers authored by Caroline Scholz
This map shows the geographic impact of Caroline Scholz'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 Caroline Scholz with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Caroline Scholz more than expected).
Fields of papers citing papers by Caroline Scholz
This network shows the impact of papers produced by Caroline Scholz. 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 Caroline Scholz. The network helps show where Caroline Scholz may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Caroline Scholz, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2019 | 31 | |
| 2 | 2018 | 11 | |
| 3 | 2018 | 7 | |
| 4 | 2018 | 41 | |
| 5 | 2016 | 13 | |
| 6 | 2014 | 5 | |
| 7 | 2013 | 18 | |
| 8 | Phenylketonuria identification of a new frequent mutation in the phenylalanine hydroxylase gene | 1989 | 1 |
About Caroline Scholz
Caroline Scholz is a scholar working on Clinical Biochemistry, Genetics and Endocrine and Autonomic Systems, having authored 8 papers that have together received 127 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (4 papers), Genetic Syndromes and Imprinting (2 papers), BRCA gene mutations in cancer (2 papers), Metabolism and Genetic Disorders (2 papers), Amino Acid Enzymes and Metabolism (1 paper), Genomics and Rare Diseases (1 paper), Metabolomics and Mass Spectrometry Studies (1 paper) and CRISPR and Genetic Engineering (1 paper). The work is most often cited by research in Genetics (62 citations), Clinical Biochemistry (14 citations) and Molecular Biology (86 citations). Caroline Scholz has collaborated with scholars based in Germany, Switzerland and Austria. Frequent co-authors include Doris Steinemann, Brigitte Schlegelberger, Bernd Auber, Stephanie Schubert, Thomas Illig, Gunnar Schmidt, Vicente A. Yépez, Norbert Lorenz, Colin Davenport and Mirjana Gušić. Their work appears in journals such as The American Journal of Human Genetics, International Journal of Cancer and Breast Cancer Research and Treatment.
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.