Karin Schmitt

3.3k total citations · 1 hit paper
30 papers, 1.8k citations indexed

About

Karin Schmitt is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Karin Schmitt has authored 30 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Genetics, 15 papers in Molecular Biology and 3 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Karin Schmitt's work include Genetic Associations and Epidemiology (6 papers), Molecular Biology Techniques and Applications (4 papers) and Genomic variations and chromosomal abnormalities (4 papers). Karin Schmitt is often cited by papers focused on Genetic Associations and Epidemiology (6 papers), Molecular Biology Techniques and Applications (4 papers) and Genomic variations and chromosomal abnormalities (4 papers). Karin Schmitt collaborates with scholars based in United States, Germany and United Kingdom. Karin Schmitt's co-authors include Norman Arnheim, Lin Zhang, William Navidi, R Hubert, Xiufang Cui, Ming T. Tsuang, Dolores Malaspina, Tara C. Matise, Jill Harkavy‐Friedman and Brian K. Suarez and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Genetics and Genome Research.

In The Last Decade

Karin Schmitt

29 papers receiving 1.7k citations

Hit Papers

Whole genome amplification from a single cell: implicatio... 1992 2026 2003 2014 1992 200 400 600
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. Whole genome amplification from a single cell: implications for genetic analysis.
    1992 719 citations Lin Zhang, Xiufang Cui et al. Proceedings of the National Academy of Sciences profile →

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Karin Schmitt United States 17 973 914 204 164 164 30 1.8k
Mark Hoff United States 13 1.2k 1.2× 1.2k 1.3× 254 1.2× 91 0.6× 116 0.7× 21 2.4k
Al Edwards United States 8 1.8k 1.8× 1.3k 1.4× 226 1.1× 99 0.6× 128 0.8× 9 2.7k
Jill Platko United States 17 1.6k 1.6× 1.7k 1.8× 182 0.9× 57 0.3× 187 1.1× 19 3.5k
A Eisenberg United States 11 765 0.8× 513 0.6× 164 0.8× 61 0.4× 74 0.5× 23 1.6k
Diane I. Schroeder United States 15 1.2k 1.3× 538 0.6× 130 0.6× 211 1.3× 145 0.9× 18 1.6k
Sally H. Cross United Kingdom 26 2.3k 2.3× 844 0.9× 451 2.2× 114 0.7× 128 0.8× 49 3.0k
H H Kazazian United States 32 1.7k 1.7× 857 0.9× 195 1.0× 273 1.7× 71 0.4× 64 3.2k
Paul J. Hurd United Kingdom 15 1.5k 1.6× 558 0.6× 131 0.6× 129 0.8× 141 0.9× 25 1.9k
Holly A. Hammond United States 10 1.8k 1.9× 1.7k 1.9× 194 1.0× 116 0.7× 89 0.5× 13 2.9k
Arlene R. Wyman United States 17 1.1k 1.1× 803 0.9× 241 1.2× 82 0.5× 43 0.3× 22 1.7k

Countries citing papers authored by Karin Schmitt

Since Specialization
Citations

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

Fields of papers citing papers by Karin Schmitt

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Karin Schmitt

This figure shows the co-authorship network connecting the top 25 collaborators of Karin Schmitt. A scholar is included among the top collaborators of Karin Schmitt 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 Karin Schmitt. Karin Schmitt 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.
Leisinger, Klaus M. & Karin Schmitt. (2011). Access to Healthcare and the Pharmaceutical Sector. Cambridge Quarterly of Healthcare Ethics. 20(2). 309–325. 6 indexed citations
2.
Gross, Roy, et al.. (2010). Resemblance and divergence: the “new” members of the genus Bordetella. Medical Microbiology and Immunology. 199(3). 155–163. 30 indexed citations
3.
Schmitt, Karin, Susanne Bauer, David Hot, et al.. (2009). Genomic island excisions in Bordetella petrii. BMC Microbiology. 9(1). 141–141. 29 indexed citations
4.
Schmitt, Karin, et al.. (2007). Identification and regulation of expression of a gene encoding a filamentous hemagglutinin-related protein in Bordetella holmesii. BMC Microbiology. 7(1). 100–100. 13 indexed citations
5.
Schmitt, Karin, et al.. (2006). Vector-based RNAi approaches for stable, inducible and genome-wide screens. Drug Discovery Today. 11(21-22). 975–982. 38 indexed citations
6.
Lien, Sigbjørn, Joanna Szyda, Esther P. Leeflang, et al.. (2002). Single‐Sperm Typing. Current Protocols in Human Genetics. 32(1). 9 indexed citations
7.
Schmitt, Karin, et al.. (2001). Fish × 3. Nature Genetics. 27(1). 8–9. 7 indexed citations
8.
9.
Kwok, Cheni, Ricky Critcher, & Karin Schmitt. (1998). Chapter 16 Construction and Characterization of Zebrafish Whole Genome Radiation Hybrids. Methods in cell biology. 60. 287–302. 27 indexed citations
10.
McCarthy, Linda, Jonathan Terrett, Angela Smith, et al.. (1997). A First-Generation Whole Genome–Radiation Hybrid Map Spanning the Mouse Genome. Genome Research. 7(12). 1153–1161. 157 indexed citations
11.
Bouzyk, Mark, Stephen P. Bryant, Karin Schmitt, et al.. (1996). Construction of a Radiation Hybrid Map of Chromosome 9p. Genomics. 34(2). 187–192. 7 indexed citations
12.
Hayes, Philip D., Karin Schmitt, Hywel B. Jones, et al.. (1996). Regional assignment of human ESTs by whole-genome radiation hybrid mapping. Mammalian Genome. 7(6). 446–450. 11 indexed citations
13.
Schmitt, Karin, et al.. (1996). Construction of a Mouse Whole-Genome Radiation Hybrid Panel and Application to MMU11. Genomics. 34(2). 193–197. 24 indexed citations
14.
Schmitt, Karin, Laura C. Lazzeroni, Simon J. Foote, et al.. (1994). Multipoint linkage map of the human pseudoautosomal region, based on single-sperm typing: do double crossovers occur during male meiosis?. PubMed. 55(3). 423–30. 41 indexed citations
15.
Schmitt, Karin & Norman Arnheim. (1994). Genetic recombination analysis using sperm typing.. PubMed. 16. 157–65. 2 indexed citations
16.
Lazzeroni, Laura C., Norman Arnheim, Karin Schmitt, & Kenneth Lange. (1994). Multipoint mapping calculations for sperm-typing data.. PubMed. 55(3). 431–6. 26 indexed citations
17.
Schmitt, Karin, et al.. (1994). Frequent recombination in the human T-cell receptor beta gene complex. Immunogenetics. 39(5). 335–42. 16 indexed citations
18.
Schmitt, Karin, et al.. (1993). Four PCR-based polymorphisms in the pseudoautosomal region of the human X and Y chromosomes. Human Molecular Genetics. 2(11). 1978–1978. 12 indexed citations
19.
Lewin, Harris A., Karin Schmitt, René Hubert, Michiel J. T. van Eijk, & Norman Arnheim. (1992). Close linkage between bovine prolactin and BoLA-DRB3 genes: Genetic mapping in cattle by single sperm typing. Genomics. 13(1). 44–48. 66 indexed citations
20.
Zhang, Lin, Xiufang Cui, Karin Schmitt, et al.. (1992). Whole genome amplification from a single cell: implications for genetic analysis.. Proceedings of the National Academy of Sciences. 89(13). 5847–5851. 719 indexed citations breakdown →

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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