J. Schmidtke
Impact in
- Genetics top 10%
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
- Connective tissue disorders research
- Genomic variations and chromosomal abnormalities
- Genetic diversity and population structure
- BRCA gene mutations in cancer
Papers in
- Genetics 14
- Genomics and Rare Diseases 4
- Genomic variations and chromosomal abnormalities 3
- Animal Genetics and Reproduction 3
- Forensic and Genetic Research 2
- Connective tissue disorders research 2
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- Molecular Biology Techniques and Applications 3
- CRISPR and Genetic Engineering 3
- Co-authors
- Ségolène Aymé (1 shared paper)D.N. Cooper (14 shared papers)A. Bowcock (4 shared papers)K.K. Kidd (11 shared papers)P. Pearson (11 shared papers)Willard A. Van Engel (1 shared paper)M. Tolley (9 shared papers)M. Chipperfield (9 shared papers)
- Journals
- Cytogenetic and Genome Research (11 papers)Human Genetics (2 papers)Familial Cancer (1 paper)European Journal of Human Genetics (1 paper)International Journal of Legal Medicine (1 paper)
- Partner nations
- GermanyUnited KingdomNetherlands
In The Last Decade
J. Schmidtke
31 papers receiving 439 citations
Peers
Comparison fields: 5 of 93
- Genetics 242
- Molecular Biology 192
- Cancer Research 36
- Pulmonary and Respiratory Medicine 65
- Genetics 21
Countries citing papers authored by J. Schmidtke
This map shows the geographic impact of J. Schmidtke'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 J. Schmidtke with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites J. Schmidtke more than expected).
Fields of papers citing papers by J. Schmidtke
This network shows the impact of papers produced by J. Schmidtke. 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 J. Schmidtke. The network helps show where J. Schmidtke may publish in the future.
Co-authors
The 25 scholars most cited alongside J. Schmidtke, 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 | 1991 | 91 | |
| 2 | 2007 | 82 | |
| 3 | 1990 | 49 | |
| 4 | Segregation of all four major fibrillar collagen genes in the Marfan syndrome. | 1987 | 34 |
| 5 | 1980 | 28 | |
| 6 | 2008 | 22 | |
| 7 | 1986 | 18 | |
| 8 | 1991 | 17 | |
| 9 | 1992 | 14 | |
| 10 | 1988 | 11 | |
| 11 | 1976 | 11 | |
| 12 | 2006 | 10 | |
| 13 | DNA fingerprinting for paternity and maternity in group O Cayo Santiago-derived rhesus monkeys at the German Primate Center: results of a pilot study. | 1989 | 10 |
| 14 | 1993 | 9 | |
| 15 | 1989 | 7 | |
| 16 | 2011 | 7 | |
| 17 | 1997 | 6 | |
| 18 | Genetics and biochemistry of variant human phenotypes | 1989 | 5 |
| 19 | 1992 | 5 | |
| 20 | 1997 | 3 |
About J. Schmidtke
J. Schmidtke is a scholar working on Genetics, Molecular Biology, Ecology, Cardiology and Cardiovascular Medicine and Pediatrics, Perinatology and Child Health, having authored 33 papers that have together received 455 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (4 papers), Molecular Biology Techniques and Applications (3 papers), CRISPR and Genetic Engineering (3 papers), Genomic variations and chromosomal abnormalities (3 papers), Animal Genetics and Reproduction (3 papers), Forensic and Genetic Research (2 papers), Connective tissue disorders research (2 papers) and Prenatal Screening and Diagnostics (2 papers). The work is most often cited by research in Genetics (242 citations), Molecular Biology (192 citations), Cancer Research (36 citations), Pulmonary and Respiratory Medicine (65 citations) and Genetics (21 citations). J. Schmidtke has collaborated with scholars based in Germany, United Kingdom and Netherlands. Frequent co-authors include Ségolène Aymé, D.N. Cooper, A. Bowcock, K.K. Kidd, P. Pearson, Willard A. Van Engel, M. Tolley, M. Chipperfield, B. Maidak and J. Hewitt. Their work appears in journals such as Cytogenetic and Genome Research, Human Genetics, Familial Cancer, European Journal of Human Genetics and International Journal of Legal Medicine.
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.