W. Lenz
Impact in
- Developmental Biology top 0.5%
- Congenital limb and hand anomalies
- Hematology top 2%
- Multiple Myeloma Research and Treatments
Papers in
- Genetics 35
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 5
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- Congenital limb and hand anomalies 26
- Co-authors
- Klaus Knapp (4 shared papers)D. M. Burley (1 shared paper)Rudolf Happle (2 shared papers)W Kosenow (1 shared paper)Andrew E. Czeizel (10 shared papers)Eberhard Passarge (1 shared paper)Asım Cenani (2 shared papers)F. Majewski (4 shared papers)
- Journals
- European Journal of Pediatrics (12 papers)Human Genetics (6 papers)The Lancet (5 papers)Journal of Molecular Medicine (4 papers)Journal of Medical Genetics (3 papers)
- Partner nations
- GermanyHungaryUnited States
In The Last Decade
W. Lenz
104 papers receiving 2.7k citations
W. Lenz's Hit Papers
Peers
Comparison fields: 5 of 129
- Developmental Biology 472
- Hematology 375
- Pediatrics, Perinatology and Child Health 548
- Genetics 867
- Genetics 284
Countries citing papers authored by W. Lenz
This map shows the geographic impact of W. Lenz'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 W. Lenz with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites W. Lenz more than expected).
Fields of papers citing papers by W. Lenz
This network shows the impact of papers produced by W. Lenz. 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 W. Lenz. The network helps show where W. Lenz may publish in the future.
Co-authors
The 25 scholars most cited alongside W. Lenz, 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 105 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | A short history of thalidomide embryopathy Hit paper breakdown → | 1988 | 271 |
| 2 | 1962 | 263 | |
| 3 | 1962 | 250 | |
| 4 | 1962 | 156 | |
| 5 | 1980 | 126 | |
| 6 | 1966 | 124 | |
| 7 | 1966 | 118 | |
| 8 | 1962 | 115 | |
| 9 | 1994 | 74 | |
| 10 | 1988 | 68 | |
| 11 | [Polysyndactyly, short limbs, and genital malformations--a new syndrome?]. | 1971 | 68 |
| 12 | 1971 | 62 | |
| 13 | 1977 | 49 | |
| 14 | 1983 | 47 | |
| 15 | 1980 | 46 | |
| 16 | [Total syndactylia and total radioulnar synostosis in 2 brothers. A contribution on the genetics of syndactylia]. | 1967 | 41 |
| 17 | 1955 | 40 | |
| 18 | 1992 | 39 | |
| 19 | 1990 | 38 | |
| 20 | 1967 | 38 |
About W. Lenz
W. Lenz is a scholar working on Genetics, Developmental Biology, Molecular Biology, Surgery and Pediatrics, Perinatology and Child Health, having authored 105 papers that have together received 2.9k indexed citations. Recurring topics across this work include Congenital limb and hand anomalies (26 papers), Congenital Anomalies and Fetal Surgery (7 papers), Prenatal Screening and Diagnostics (7 papers), Bone fractures and treatments (5 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers), Multiple Myeloma Research and Treatments (5 papers), Medical and Biological Sciences (5 papers) and Hedgehog Signaling Pathway Studies (5 papers). The work is most often cited by research in Developmental Biology (472 citations), Hematology (375 citations), Pediatrics, Perinatology and Child Health (548 citations), Genetics (867 citations) and Genetics (284 citations). W. Lenz has collaborated with scholars based in Germany, Hungary and United States. Frequent co-authors include Klaus Knapp, D. M. Burley, Rudolf Happle, W Kosenow, Andrew E. Czeizel, Eberhard Passarge, Asım Cenani, F. Majewski, H. Nowakowski and R. A. Pfeiffer. Their work appears in journals such as European Journal of Pediatrics, Human Genetics, The Lancet, Journal of Molecular Medicine 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.