J. Herrmann
Impact in
- Developmental Biology top 2%
- Congenital limb and hand anomalies
- Genetics top 5%
- Genomic variations and chromosomal abnormalities
- Genetic Syndromes and Imprinting
- Connective tissue disorders research
- Craniofacial Disorders and Treatments
Papers in
- Co-authors
- John M. Opitz (10 shared papers)Enid F. Gilbert (8 shared papers)JohnM. Opitz (4 shared papers)Philip D. Pallister (5 shared papers)Jürgen W. Spranger (3 shared papers)Barbara McGillivray (1 shared paper)R. Brian Lowry (1 shared paper)Li‐Wen Lai (1 shared paper)
- Journals
- European Journal of Pediatrics (11 papers)Human Genetics (2 papers)The Lancet (2 papers)Blood (2 papers)Journal of Cutaneous Pathology (1 paper)
- Partner nations
- United StatesGermanySwitzerland
In The Last Decade
J. Herrmann
49 papers receiving 1.2k citations
Peers
Comparison fields: 5 of 79
- Developmental Biology 154
- Genetics 625
- Pediatrics, Perinatology and Child Health 320
- Genetics 91
- Urology 51
Countries citing papers authored by J. Herrmann
This map shows the geographic impact of J. Herrmann'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. Herrmann with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites J. Herrmann more than expected).
Fields of papers citing papers by J. Herrmann
This network shows the impact of papers produced by J. Herrmann. 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. Herrmann. The network helps show where J. Herrmann may publish in the future.
Co-authors
The 25 scholars most cited alongside J. Herrmann, 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 50 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Trisomy 15 with loss of the paternal 15 as a cause of Prader-Willi syndrome due to maternal disomy. | 1992 | 138 |
| 2 | 1992 | 78 | |
| 3 | 1974 | 76 | |
| 4 | 1977 | 73 | |
| 5 | 1981 | 69 | |
| 6 | The Stickler syndrome (hereditary arthroophthalmopathy). | 1975 | 66 |
| 7 | 1977 | 64 | |
| 8 | 1976 | 63 | |
| 9 | 1980 | 51 | |
| 10 | 1974 | 48 | |
| 11 | 2013 | 46 | |
| 12 | 1973 | 33 | |
| 13 | 1976 | 31 | |
| 14 | 1980 | 29 | |
| 15 | 1976 | 28 | |
| 16 | 1978 | 26 | |
| 17 | 1966 | 25 | |
| 18 | Studies of malformation syndromes in man XXXXII: a pleiotropic dominant mutation affecting skeletal, sexual and apocrine-mammary development. | 1976 | 23 |
| 19 | Craniosynostosis and craniosynostosis syndromes. | 1969 | 23 |
| 20 | 1975 | 22 |
About J. Herrmann
J. Herrmann is a scholar working on Genetics, Surgery, Molecular Biology, Epidemiology and Developmental Biology, having authored 50 papers that have together received 1.2k indexed citations. Recurring topics across this work include Nail Diseases and Treatments (6 papers), Congenital limb and hand anomalies (6 papers), Genomic variations and chromosomal abnormalities (6 papers), Dermatological diseases and infestations (4 papers), Prenatal Screening and Diagnostics (4 papers), Hedgehog Signaling Pathway Studies (4 papers), Connective tissue disorders research (4 papers) and Bone health and treatments (3 papers). The work is most often cited by research in Developmental Biology (154 citations), Genetics (625 citations), Pediatrics, Perinatology and Child Health (320 citations), Genetics (91 citations) and Urology (51 citations). J. Herrmann has collaborated with scholars based in United States, Germany and Switzerland. Frequent co-authors include John M. Opitz, Enid F. Gilbert, JohnM. Opitz, Philip D. Pallister, Jürgen W. Spranger, Barbara McGillivray, R. Brian Lowry, Li‐Wen Lai, Roxanne Gendron and E.D. Thomas. Their work appears in journals such as European Journal of Pediatrics, Human Genetics, The Lancet, Blood and Journal of Cutaneous Pathology.
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.