Karin Schmitt

3.3k citations
31 papers · 1.8k · 1 hit paper · h-index 17

Impact in

  • Genetics top 2%
    • Genomic variations and chromosomal abnormalities
    • Genetic Associations and Epidemiology
    • Genetic Mapping and Diversity in Plants and Animals
    • Genetics and Neurodevelopmental Disorders
    • Molecular Biology Techniques and Applications
    • Genomics and Phylogenetic Studies

Papers in

    • Genetic Associations and Epidemiology 6
    • Genomic variations and chromosomal abnormalities 4
    • Genetics and Neurodevelopmental Disorders 3
    • Animal Genetics and Reproduction 3
    • Genetic Mapping and Diversity in Plants and Animals 3
    • Molecular Biology Techniques and Applications 4
    • 14-3-3 protein interactions 3

Karin Schmitt

30 papers receiving 1.8k citations

Karin Schmitt's Hit Papers

Whole genome amplification from a single cell: implications for genetic analysis. 1992 · 719 citations
7190+11+22Years since publication200400600

Peers

Karin Schmitt
Comparison fields: 5 of 121
  • Genetics 845
  • Molecular Biology 907
  • Cancer Research 154
  • Microbiology 51
  • Pediatrics, Perinatology and Child Health 144
Replace Yoshihiro Jinno with:
Yoshihiro Jinno Japan
Carole A. Sargent United Kingdom
Mark Hoff United States
Abdul Karim Sesay United Kingdom
Florence Bernex France
Sarah J. Campbell United Kingdom
Jeffrey Rosenfeld United States
Tim Roloff Switzerland
Fujiko Watt Australia
Sally H. Cross United Kingdom
Karin Schmitt relative to Yoshihiro Jinno Japan Yoshihiro Jinno's profile →
Citations per field
00.5×1.5×
Yoshihiro Jinno · 1×
Citations per year

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-authors

The 25 scholars most cited alongside Karin Schmitt, 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 Karin Schmitt Line = papers co-authored together Karin Schmitt links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 31 papers — load more, or switch the sort, to bring in the rest.

#Work
1
Whole genome amplification from a single cell: implications for genetic analysis.
Hit paper breakdown →
1992719
2 1998217
3 1998216
4 1997157
5 199266
6 199847
7
Multipoint linkage map of the human pseudoautosomal region, based on single-sperm typing: do double crossovers occur during male meiosis?
199441
8 200638
9 199932
10
A new source of polymorphic DNA markers for sperm typing: analysis of microsatellite repeats in single cells.
199231
11 200930
12 201030
13 199827
14
Multipoint mapping calculations for sperm-typing data.
199426
15 200225
16 199624
17 199416
18 200713
19 199813
20 199312

About Karin Schmitt

Karin Schmitt is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Plant Science and Microbiology, having authored 31 papers that have together received 1.8k indexed citations. Recurring topics across this work include Genetic Associations and Epidemiology (6 papers), Genomic variations and chromosomal abnormalities (4 papers), Molecular Biology Techniques and Applications (4 papers), Genetics and Neurodevelopmental Disorders (3 papers), Animal Genetics and Reproduction (3 papers), 14-3-3 protein interactions (3 papers), Chromosomal and Genetic Variations (3 papers) and Genetic Mapping and Diversity in Plants and Animals (3 papers). The work is most often cited by research in Genetics (845 citations), Molecular Biology (907 citations), Cancer Research (154 citations), Microbiology (51 citations) and Pediatrics, Perinatology and Child Health (144 citations). Karin Schmitt has collaborated with scholars based in United States, Germany and United Kingdom. Frequent co-authors include Norman Arnheim, Lin Zhang, Xiufang Cui, William Navidi, R Hubert, Jill Harkavy‐Friedman, Paul D. Markel, Ming T. Tsuang, Dragan M. Švrakić and Dolores Malaspina. Their work appears in journals such as Genomics, BMC Microbiology, BioTechniques, Medical Microbiology and Immunology and Proceedings of the National Academy of Sciences.

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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