Widukind Lenz

4.8k citations
118 papers · 3.6k · 1 hit paper · h-index 31

Impact in

Papers in

    • Congenital limb and hand anomalies 28
    • Genomic variations and chromosomal abnormalities 6
    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 6
    • Genetic and rare skin diseases. 6
    • Genomics and Rare Diseases 5

Widukind Lenz

116 papers receiving 3.1k citations

Widukind Lenz's Hit Papers

A short history of thalidomide embryopathy 1988 · 330 citations
3300+12+25Years since publication100200300

Peers

Widukind Lenz
Comparison fields: 5 of 134
  • Developmental Biology 563
  • Pediatrics, Perinatology and Child Health 728
  • Hematology 430
  • Genetics 1.0k
  • Genetics 346
Replace Louis K. Diamond with:
Louis K. Diamond United States
W.M. Court Brown United Kingdom
Maurice J. Mahoney United States
JAMES G. WILSON United States
Leo P. ten Kate Netherlands
Rodney E. Harris United Kingdom
Deborah A. Driscoll United States
B. Modell United Kingdom
J. Michael Connor United Kingdom
Aubrey Milunsky United States
Widukind Lenz relative to Louis K. Diamond United States Louis K. Diamond's profile →
Citations per field
00.5×5×10×17.1×
Louis K. Diamond · 1×
Citations per year

Countries citing papers authored by Widukind Lenz

Since Specialization
Citations

This map shows the geographic impact of Widukind 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 Widukind Lenz with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Widukind Lenz more than expected).

Fields of papers citing papers by Widukind Lenz

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Widukind 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 Widukind Lenz. The network helps show where Widukind Lenz may publish in the future.

Co-authors

The 25 scholars most cited alongside Widukind Lenz, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Widukind Lenz Line = papers co-authored together Widukind Lenz links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 118 papers — load more, or switch the sort, to bring in the rest.

#Work
1
A short history of thalidomide embryopathy
Hit paper breakdown →
1988330
2 1962313
3 1962282
4 1962186
5 1980160
6 1966154
7 1966139
8 1962125
9 199479
10 198878
11
[Polysyndactyly, short limbs, and genital malformations--a new syndrome?].
197176
12 197175
13 197765
14 198056
15 198356
16 199146
17 195546
18 196546
19 199045
20 199245

About Widukind Lenz

Widukind Lenz is a scholar working on Developmental Biology, Genetics, Pediatrics, Perinatology and Child Health, Anatomy and Hematology, having authored 118 papers that have together received 3.6k indexed citations. Recurring topics across this work include Congenital limb and hand anomalies (28 papers), Congenital Anomalies and Fetal Surgery (7 papers), Prenatal Screening and Diagnostics (7 papers), Medical and Biological Sciences (7 papers), Genomic variations and chromosomal abnormalities (6 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (6 papers), Genetic and rare skin diseases. (6 papers) and Genomics and Rare Diseases (5 papers). The work is most often cited by research in Developmental Biology (563 citations), Pediatrics, Perinatology and Child Health (728 citations), Hematology (430 citations), Genetics (1.0k citations) and Genetics (346 citations). Widukind Lenz has collaborated with scholars based in Germany, Hungary and Poland. Frequent co-authors include Klaus Knapp, Denis M. Burley, Rudolf Happle, Andrew E. Czeizel, Wilhelm Kosenow, Eberhard Passarge, Asım Cenani, F. Majewski, Márta Vitéz and H. Nowakowski. 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.

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