Ingo Kennerknecht
Impact in
- Cognitive Neuroscience top 2%
- Face Recognition and Perception
- Autism Spectrum Disorder Research
-
- Evolutionary Psychology and Human Behavior
Papers in
- Genetics 40
- Genomic variations and chromosomal abnormalities 17
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 8
- Genetic Syndromes and Imprinting 7
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- Sexual Differentiation and Disorders 5
- Co-authors
- Gotthold Barbi (18 shared papers)M. Grueter (2 shared papers)Thomas Grueter (2 shared papers)Steve Edwards (2 shared papers)Jürgen Horst (4 shared papers)Peter Steinbach (5 shared papers)Virginia Wong (1 shared paper)R. Terinde (9 shared papers)
- Journals
- Prenatal Diagnosis (9 papers)Human Genetics (6 papers)Clinical Genetics (3 papers)European Journal of Human Genetics (3 papers)PLoS ONE (2 papers)
- Partner nations
- GermanyUnited StatesPoland
In The Last Decade
Ingo Kennerknecht
64 papers receiving 1.4k citations
Peers
Comparison fields: 5 of 93
- Cognitive Neuroscience 714
- Experimental and Cognitive Psychology 251
- Genetics 514
- Computer Vision and Pattern Recognition 300
- Neurology 158
Countries citing papers authored by Ingo Kennerknecht
This map shows the geographic impact of Ingo Kennerknecht'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 Ingo Kennerknecht with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ingo Kennerknecht more than expected).
Fields of papers citing papers by Ingo Kennerknecht
This network shows the impact of papers produced by Ingo Kennerknecht. 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 Ingo Kennerknecht. The network helps show where Ingo Kennerknecht may publish in the future.
Co-authors
The 25 scholars most cited alongside Ingo Kennerknecht, 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 66 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2006 | 194 | |
| 2 | 2007 | 92 | |
| 3 | 2008 | 81 | |
| 4 | 1995 | 74 | |
| 5 | 2006 | 58 | |
| 6 | 1992 | 54 | |
| 7 | 2010 | 49 | |
| 8 | 1997 | 48 | |
| 9 | 2011 | 43 | |
| 10 | 2006 | 36 | |
| 11 | 2010 | 35 | |
| 12 | A novel TACSTD2 gene mutation in a Turkish family with a gelatinous drop-like corneal dystrophy. | 2006 | 35 |
| 13 | 1993 | 34 | |
| 14 | 2016 | 34 | |
| 15 | 2012 | 33 | |
| 16 | 2014 | 29 | |
| 17 | 1990 | 28 | |
| 18 | 1997 | 28 | |
| 19 | 2004 | 27 | |
| 20 | 2007 | 27 |
About Ingo Kennerknecht
Ingo Kennerknecht is a scholar working on Genetics, Molecular Biology, Cognitive Neuroscience, Pediatrics, Perinatology and Child Health and Neurology, having authored 66 papers that have together received 1.5k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (17 papers), Face Recognition and Perception (14 papers), Prenatal Screening and Diagnostics (14 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (8 papers), Facial Nerve Paralysis Treatment and Research (7 papers), Genetic Syndromes and Imprinting (7 papers), Chromosomal and Genetic Variations (6 papers) and Sexual Differentiation and Disorders (5 papers). The work is most often cited by research in Cognitive Neuroscience (714 citations), Experimental and Cognitive Psychology (251 citations), Genetics (514 citations), Computer Vision and Pattern Recognition (300 citations) and Neurology (158 citations). Ingo Kennerknecht has collaborated with scholars based in Germany, United States and Poland. Frequent co-authors include Gotthold Barbi, M. Grueter, Thomas Grueter, Steve Edwards, Jürgen Horst, Peter Steinbach, Virginia Wong, R. Terinde, Walther Vogel and Sabine Schwemmle. Their work appears in journals such as Prenatal Diagnosis, Human Genetics, Clinical Genetics, European Journal of Human Genetics and PLoS ONE.
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.