Karin Blechschmidt
Impact in
- Genetics top 2%
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Molecular Biology top 10%
- Genomics and Chromatin Dynamics
- Genomics and Phylogenetic Studies
- RNA and protein synthesis mechanisms
Papers in
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- Neurological diseases and metabolism 2
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- Hereditary Neurological Disorders 3
- Co-authors
- Aaron Rosenthal (2 shared papers)Rebecca Gooding (2 shared papers)Frank Baas (2 shared papers)P K Thomas (1 shared paper)Rosalind H. M. King (1 shared paper)Dora Angelicheva (2 shared papers)David Gresham (2 shared papers)Luba Kalaydjieva (2 shared papers)
- Journals
- Nature (3 papers)Mammalian Genome (1 paper)Gene (1 paper)Neuromuscular Disorders (1 paper)The American Journal of Human Genetics (1 paper)
- Partner nations
- United KingdomNetherlandsUnited States
In The Last Decade
Karin Blechschmidt
10 papers receiving 2.5k citations
Karin Blechschmidt's Hit Papers
Peers
Comparison fields: 5 of 120
- Genetics 1.2k
- Molecular Biology 1.4k
- Neurology 99
- Plant Science 444
- Developmental Neuroscience 45
Countries citing papers authored by Karin Blechschmidt
This map shows the geographic impact of Karin Blechschmidt'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 Blechschmidt with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Karin Blechschmidt more than expected).
Fields of papers citing papers by Karin Blechschmidt
This network shows the impact of papers produced by Karin Blechschmidt. 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 Blechschmidt. The network helps show where Karin Blechschmidt may publish in the future.
Co-authors
The 25 scholars most cited alongside Karin Blechschmidt, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | The DNA sequence of human chromosome 21 Hit paper breakdown → | 2000 | 1102 |
| 2 | The DNA sequence of the human X chromosome Hit paper breakdown → | 2005 | 857 |
| 3 | 2000 | 309 | |
| 4 | 2001 | 125 | |
| 5 | 2006 | 96 | |
| 6 | 1997 | 61 | |
| 7 | 2000 | 21 | |
| 8 | 1997 | 18 | |
| 9 | 2001 | 4 | |
| 10 | 2005 | 1 |
About Karin Blechschmidt
Karin Blechschmidt is a scholar working on Neurology, Cellular and Molecular Neuroscience, Genetics, Cell Biology and Parasitology, having authored 10 papers that have together received 2.6k indexed citations. Recurring topics across this work include Genomics and Chromatin Dynamics (4 papers), Hereditary Neurological Disorders (3 papers), Genetic diversity and population structure (2 papers), Chromosomal and Genetic Variations (2 papers), Avian ecology and behavior (2 papers), Hippo pathway signaling and YAP/TAZ (2 papers), Neurological diseases and metabolism (2 papers) and RNA and protein synthesis mechanisms (2 papers). The work is most often cited by research in Genetics (1.2k citations), Molecular Biology (1.4k citations), Neurology (99 citations), Plant Science (444 citations) and Developmental Neuroscience (45 citations). Karin Blechschmidt has collaborated with scholars based in United Kingdom, Netherlands and United States. Frequent co-authors include Aaron Rosenthal, Rebecca Gooding, Frank Baas, P K Thomas, Rosalind H. M. King, Dora Angelicheva, David Gresham, Luba Kalaydjieva, Yoram Groner and Nili Avidan. Their work appears in journals such as Nature, Mammalian Genome, Gene, Neuromuscular Disorders and The American Journal of Human 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.