Werner Schmid

10.1k total citations · 1 hit paper
154 papers, 6.4k citations indexed

About

Werner Schmid is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Werner Schmid has authored 154 papers receiving a total of 6.4k indexed citations (citations by other indexed papers that have themselves been cited), including 47 papers in Genetics, 40 papers in Molecular Biology and 30 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Werner Schmid's work include Genomic variations and chromosomal abnormalities (25 papers), Prenatal Screening and Diagnostics (23 papers) and Chromosomal and Genetic Variations (13 papers). Werner Schmid is often cited by papers focused on Genomic variations and chromosomal abnormalities (25 papers), Prenatal Screening and Diagnostics (23 papers) and Chromosomal and Genetic Variations (13 papers). Werner Schmid collaborates with scholars based in Switzerland, Austria and Germany. Werner Schmid's co-authors include Albert Schinzel, B.E. Matter, P. Maier, Kensuke Hayashi, Klaus Böller, W. Bär, Marco Mächler, Adelgunde Kratzer, Ivo Volf and Franz Binkert and has published in prestigious journals such as The Lancet, Gastroenterology and PLoS ONE.

In The Last Decade

Werner Schmid

150 papers receiving 5.7k citations

Hit Papers

The micronucleus test 1975 2026 1992 2009 1975 500 1000 1.5k 2.0k
What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

  1. The micronucleus test
    1975 2.0k citations Werner Schmid profile →

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Werner Schmid Switzerland 37 2.3k 2.1k 1.5k 1.5k 957 154 6.4k
Roberto Barale Italy 45 2.4k 1.0× 2.9k 1.4× 934 0.6× 473 0.3× 1.4k 1.5× 211 6.7k
Rolf Schulte‐Hermann Austria 57 6.1k 2.7× 2.5k 1.2× 905 0.6× 603 0.4× 1.2k 1.2× 202 12.2k
James M. Parry United Kingdom 36 2.5k 1.1× 2.0k 1.0× 1.0k 0.7× 362 0.2× 925 1.0× 201 5.0k
W. Robert Bruce Canada 53 2.6k 1.2× 1.7k 0.8× 671 0.4× 1.1k 0.7× 612 0.6× 169 9.3k
Igor P. Pogribny United States 66 8.1k 3.6× 3.3k 1.6× 854 0.6× 1.3k 0.8× 707 0.7× 210 13.5k
Kim Boekelheide United States 55 3.4k 1.5× 1.2k 0.6× 504 0.3× 904 0.6× 2.9k 3.1× 185 9.3k
Gary A. Boorman United States 41 1.8k 0.8× 1.8k 0.9× 544 0.4× 355 0.2× 1.8k 1.9× 200 6.8k
Matthew E. Burow United States 53 4.7k 2.1× 1.8k 0.9× 606 0.4× 1.0k 0.7× 665 0.7× 200 9.0k
Michael D. Shelby United States 41 2.0k 0.9× 3.4k 1.7× 1.5k 1.0× 624 0.4× 2.1k 2.2× 131 6.4k
Jordi Surrallés Spain 34 3.0k 1.3× 2.0k 1.0× 988 0.6× 638 0.4× 907 0.9× 109 5.3k

Countries citing papers authored by Werner Schmid

Since Specialization
Citations

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

Fields of papers citing papers by Werner Schmid

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Werner Schmid

This figure shows the co-authorship network connecting the top 25 collaborators of Werner Schmid. A scholar is included among the top collaborators of Werner Schmid based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Werner Schmid. Werner Schmid is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
2.
Marhofer, Peter, Malachy O. Columb, Philipp Opfermann, et al.. (2024). The impact of biological sex in peripheral nerve blockade: A prospective pharmacodynamic, pharmacokinetic and morphometric study in volunteers. PLoS ONE. 19(1). e0297095–e0297095. 1 indexed citations
3.
Opfermann, Philipp, et al.. (2023). Sex differences in pediatric caudal epidural anesthesia under sedation without primary airway instrumentation. PLoS ONE. 18(7). e0288431–e0288431. 2 indexed citations
4.
5.
Schmid, Werner, Peter Marhofer, Oliver Kimberger, Daniela Marhofer, & Stephan C. Kettner. (2021). Perioperative sedation requirements of infants aged 0 to 3 months subjected to lower-body surgery under caudal blockade: a randomized controlled trial. Minerva Anestesiologica. 88(1-2). 16–22. 4 indexed citations
6.
Ball, Lorenzo, Sabrine N.T. Hemmes, Ary Serpa Neto, et al.. (2018). Intraoperative ventilation settings and their associations with postoperative pulmonary complications in obese patients. British Journal of Anaesthesia. 121(4). 899–908. 61 indexed citations
7.
Volf, Ivo, et al.. (1999). Human platelets exclusively bind oxidized low density lipoprotein showing no specificity for acetylated low density lipoprotein. FEBS Letters. 449(2-3). 141–145. 30 indexed citations
8.
Spiegel, Roland, Albert R. La Spada, Wolfram Kreß, Kenneth H. Fischbeck, & Werner Schmid. (1996). Somatic stability of the expanded CAG trinucleotide repeat in X-linked spinal and bulbar muscular atrophy. Human Mutation. 8(1). 32–37. 16 indexed citations
9.
Schmid, Werner, et al.. (1995). Rapid detection of sex chromosomal aneuploidies by PCR.. PubMed. 101. 111–4. 1 indexed citations
10.
Binkert, Franz, et al.. (1993). Ultrasound screening for chromosomal anomalies in the first trimester of pregnancy. Prenatal Diagnosis. 13(6). 513–518. 55 indexed citations
11.
Schmid, Werner, et al.. (1988). Kritik des Kleinschrodischen Entwurfs zu einem peinlichen Gesetzbuche für die Chur-Pfalz-Bayrischen Staaten. Bayerische Staatsbibliothek. 2 indexed citations
12.
Schmid, Michael, et al.. (1981). Somatic pairings of the Y heterochromatin in human XYY and XYqi cells. Cytogenetic and Genome Research. 29(4). 203–214. 13 indexed citations
13.
Schmid, J., et al.. (1975). [First experiences with amniocentesis from genetic indications].. Munich Personal RePEc Archive (Ludwig Maximilian University of Munich). 105(46). 1525–32. 1 indexed citations
14.
Schmid, Werner. (1975). [Prenatal genetic diagnosis. Report on 150 cases investigated in Zurich (author's transl)].. Munich Personal RePEc Archive (Ludwig Maximilian University of Munich). 64(20). 612–9. 1 indexed citations
15.
Maier, P. & Werner Schmid. (1975). The non-induction of micronuclei by quinacrine. Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis. 30(2). 299–301. 14 indexed citations
16.
Schinzel, Albert, et al.. (1974). Structural aberrations of chromosome 18. I. The 18p-syndrome. PubMed. 47(1). 1–15. 30 indexed citations
17.
Schmid, Werner, et al.. (1973). The micronucleus test methodological aspects. Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis. 19(1). 109–117. 191 indexed citations
18.
Matter, B.E. & Werner Schmid. (1971). Trenimon-induced chromosomal damage in bone-marrow cells of six mammalian species, evaluated by the micronucleus test. Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis. 12(4). 417–425. 192 indexed citations
19.
Schmid, Werner, et al.. (1969). Chromosome studies on bone marrow from Chinese hamsters treated with benzodiazepine tranquillizers and cyclophosphamide. Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis. 7(1). 99–108. 74 indexed citations
20.
Schmid, Werner & Dolph L. Hatfield. (1962). Normal Karotype/Translocation Mosaic. Cytogenetic and Genome Research. 1(3-4). 210–216. 7 indexed citations

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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