H.‐D. Rott
Impact in
- Developmental Biology top 10%
- Genetics top 5%
- Genomic variations and chromosomal abnormalities
- Genetic and rare skin diseases.
- Genetic and Kidney Cyst Diseases
Papers in
- Genetics 17
- Genomic variations and chromosomal abnormalities 6
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 3
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- RNA regulation and disease 3
- Co-authors
- R. A. Pfeiffer (3 shared papers)Raimund Fahsold (3 shared papers)Gesa Schwanitz (7 shared papers)Gabriele E. Lang (2 shared papers)Peter Lorenz (1 shared paper)Thomas Liehr (1 shared paper)Udo Trautmann (1 shared paper)Anita Rauch (1 shared paper)
- Journals
- Human Genetics (7 papers)European Journal of Pediatrics (4 papers)Clinical Genetics (4 papers)Ultraschall in der Medizin - European Journal of Ultrasound (3 papers)The Pediatric Infectious Disease Journal (1 paper)
- Partner nations
- GermanyNetherlandsEstonia
In The Last Decade
H.‐D. Rott
39 papers receiving 588 citations
Peers
Comparison fields: 5 of 72
- Developmental Biology 32
- Genetics 342
- Pediatrics, Perinatology and Child Health 127
- Cell Biology 63
- Microbiology 23
Countries citing papers authored by H.‐D. Rott
This map shows the geographic impact of H.‐D. Rott'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 H.‐D. Rott with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites H.‐D. Rott more than expected).
Fields of papers citing papers by H.‐D. Rott
This network shows the impact of papers produced by H.‐D. Rott. 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 H.‐D. Rott. The network helps show where H.‐D. Rott may publish in the future.
Co-authors
The 25 scholars most cited alongside H.‐D. Rott, 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 40 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1979 | 87 | |
| 2 | 1992 | 74 | |
| 3 | 1973 | 67 | |
| 4 | 1991 | 41 | |
| 5 | 2004 | 36 | |
| 6 | 1990 | 35 | |
| 7 | 1998 | 35 | |
| 8 | Genetics of Kartagener's syndrome. | 1983 | 31 |
| 9 | 1972 | 25 | |
| 10 | 1971 | 25 | |
| 11 | 1990 | 24 | |
| 12 | 1974 | 18 | |
| 13 | 1973 | 13 | |
| 14 | 1972 | 10 | |
| 15 | 1988 | 10 | |
| 16 | 1984 | 10 | |
| 17 | 1991 | 9 | |
| 18 | An autosomal dominant facio-audio symphalangism syndrome with Klippel-Feil anomaly: a new variant of multiple synostoses. | 1990 | 9 |
| 19 | 1991 | 8 | |
| 20 | 1982 | 8 |
About H.‐D. Rott
H.‐D. Rott is a scholar working on Genetics, Molecular Biology, Cell Biology, Pediatrics, Perinatology and Child Health and Pulmonary and Respiratory Medicine, having authored 40 papers that have together received 639 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (6 papers), Prenatal Screening and Diagnostics (4 papers), Chromosomal and Genetic Variations (4 papers), Tuberous Sclerosis Complex Research (4 papers), Neonatal Respiratory Health Research (4 papers), Congenital limb and hand anomalies (3 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers) and RNA regulation and disease (3 papers). The work is most often cited by research in Developmental Biology (32 citations), Genetics (342 citations), Pediatrics, Perinatology and Child Health (127 citations), Cell Biology (63 citations) and Microbiology (23 citations). H.‐D. Rott has collaborated with scholars based in Germany, Netherlands and Estonia. Frequent co-authors include R. A. Pfeiffer, Raimund Fahsold, Gesa Schwanitz, Gabriele E. Lang, Peter Lorenz, Thomas Liehr, Udo Trautmann, Anita Rauch, J Lejeune and J Couturier. Their work appears in journals such as Human Genetics, European Journal of Pediatrics, Clinical Genetics, Ultraschall in der Medizin - European Journal of Ultrasound and The Pediatric Infectious Disease Journal.
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.