Karin Buiting
Impact in
- Genetics top 0.2%
- Genetic Syndromes and Imprinting
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
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- Prenatal Screening and Diagnostics
Papers in
- Genetics 127
- Genetic Syndromes and Imprinting 116
- Genomics and Rare Diseases 7
- Genomic variations and chromosomal abnormalities 4
- Craniofacial Disorders and Treatments 2
- Genetic and rare skin diseases. 2
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- Epigenetics and DNA Methylation 2
- Genomics and Chromatin Dynamics 2
- Co-authors
- Bernhard Horsthemke (69 shared papers)Bärbel Dittrich (13 shared papers)Stephanie Groß (8 shared papers)Charles A. Williams (5 shared papers)Robert D. Nicholls (8 shared papers)Christina Lich (12 shared papers)Shinji Saitoh (6 shared papers)Gabriele Gillessen‐Kaesbach (18 shared papers)
- Journals
- European Journal of Human Genetics (21 papers)Human Molecular Genetics (11 papers)The American Journal of Human Genetics (11 papers)Clinical Genetics (7 papers)Nature Genetics (7 papers)
- Partner nations
- GermanyUnited StatesUnited Kingdom
In The Last Decade
Karin Buiting
135 papers receiving 7.9k citations
Peers
Comparison fields: 5 of 107
- Genetics 5.9k
- Pediatrics, Perinatology and Child Health 460
- Reproductive Medicine 299
- Molecular Biology 1.6k
- Endocrine and Autonomic Systems 78
Countries citing papers authored by Karin Buiting
This map shows the geographic impact of Karin Buiting'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 Buiting with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Karin Buiting more than expected).
Fields of papers citing papers by Karin Buiting
This network shows the impact of papers produced by Karin Buiting. 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 Buiting. The network helps show where Karin Buiting may publish in the future.
Co-authors
The 25 scholars most cited alongside Karin Buiting, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 136 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1995 | 488 | |
| 2 | 2000 | 481 | |
| 3 | 2003 | 290 | |
| 4 | 2016 | 281 | |
| 5 | 2003 | 265 | |
| 6 | 2010 | 254 | |
| 7 | 1999 | 225 | |
| 8 | 1998 | 220 | |
| 9 | 1996 | 211 | |
| 10 | Imprinting mutations suggested by abnormal DNA methylation patterns in familial Angelman and Prader-Willi syndromes. | 1994 | 195 |
| 11 | 1992 | 177 | |
| 12 | 2001 | 168 | |
| 13 | 1996 | 154 | |
| 14 | 1997 | 151 | |
| 15 | 1998 | 151 | |
| 16 | 2015 | 150 | |
| 17 | 2018 | 123 | |
| 18 | 2000 | 121 | |
| 19 | 2011 | 120 | |
| 20 | 2006 | 118 |
About Karin Buiting
Karin Buiting is a scholar working on Genetics, Molecular Biology, Developmental Biology, Plant Science and Genetics, having authored 136 papers that have together received 8.3k indexed citations. Recurring topics across this work include Genetic Syndromes and Imprinting (116 papers), Genomics and Rare Diseases (7 papers), Genomic variations and chromosomal abnormalities (4 papers), Chromosomal and Genetic Variations (3 papers), Craniofacial Disorders and Treatments (2 papers), Epigenetics and DNA Methylation (2 papers), Genomics and Chromatin Dynamics (2 papers) and Genetic and rare skin diseases. (2 papers). The work is most often cited by research in Genetics (5.9k citations), Pediatrics, Perinatology and Child Health (460 citations), Reproductive Medicine (299 citations), Molecular Biology (1.6k citations) and Endocrine and Autonomic Systems (78 citations). Karin Buiting has collaborated with scholars based in Germany, United States and United Kingdom. Frequent co-authors include Bernhard Horsthemke, Bärbel Dittrich, Stephanie Groß, Charles A. Williams, Robert D. Nicholls, Christina Lich, Shinji Saitoh, Gabriele Gillessen‐Kaesbach, Deniz Kanber and Camilynn I. Brannan. Their work appears in journals such as European Journal of Human Genetics, Human Molecular Genetics, The American Journal of Human Genetics, Clinical Genetics and Nature 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.