Ute Moog
Impact in
- Genetics top 1%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Genetic and rare skin diseases.
- Genomics and Rare Diseases
- BRCA gene mutations in cancer
- Cognitive Neuroscience top 5%
- Autism Spectrum Disorder Research
Papers in
- Genetics 67
- Genomic variations and chromosomal abnormalities 26
- Genetics and Neurodevelopmental Disorders 19
- Genomics and Rare Diseases 12
- Genetic and rare skin diseases. 9
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- RNA regulation and disease 7
- Hedgehog Signaling Pathway Studies 7
- Co-authors
- Hartmut Engels (4 shared papers)Peep F. M. Stalmeier (4 shared papers)W.A.J. van Daal (4 shared papers)Gudrun Rappold (4 shared papers)Mariëlle S. van Roosmalen (4 shared papers)Josette E. H. M. Hoekstra‐Weebers (4 shared papers)Jan C. Oosterwijk (4 shared papers)Lia C.G. Verhoef (4 shared papers)
- Journals
- Clinical Genetics (9 papers)European Journal of Human Genetics (7 papers)Journal of Medical Genetics (4 papers)Familial Cancer (3 papers)American Journal of Medical Genetics Part A (19 papers)
- Partner nations
- GermanyNetherlandsPoland
In The Last Decade
Ute Moog
97 papers receiving 2.7k citations
Peers
Comparison fields: 5 of 116
- Genetics 1.7k
- Cognitive Neuroscience 421
- Molecular Biology 1.2k
- Pediatrics, Perinatology and Child Health 209
- Pathology and Forensic Medicine 175
Countries citing papers authored by Ute Moog
This map shows the geographic impact of Ute Moog'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 Ute Moog with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ute Moog more than expected).
Fields of papers citing papers by Ute Moog
This network shows the impact of papers produced by Ute Moog. 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 Ute Moog. The network helps show where Ute Moog may publish in the future.
Co-authors
The 25 scholars most cited alongside Ute Moog, 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 100 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2010 | 439 | |
| 2 | 2004 | 96 | |
| 3 | 2009 | 87 | |
| 4 | 2003 | 84 | |
| 5 | 2009 | 77 | |
| 6 | 2002 | 67 | |
| 7 | 2006 | 67 | |
| 8 | 2004 | 63 | |
| 9 | 2003 | 61 | |
| 10 | 2004 | 60 | |
| 11 | 2015 | 60 | |
| 12 | 2016 | 58 | |
| 13 | 2007 | 58 | |
| 14 | 2007 | 51 | |
| 15 | 2004 | 50 | |
| 16 | 2010 | 48 | |
| 17 | 2003 | 46 | |
| 18 | 2009 | 46 | |
| 19 | 2000 | 45 | |
| 20 | 1994 | 38 |
About Ute Moog
Ute Moog is a scholar working on Genetics, Molecular Biology, Plant Science, Pathology and Forensic Medicine and Pediatrics, Perinatology and Child Health, having authored 100 papers that have together received 2.8k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (26 papers), Genetics and Neurodevelopmental Disorders (19 papers), Genomics and Rare Diseases (12 papers), Genetic and rare skin diseases. (9 papers), Chromosomal and Genetic Variations (9 papers), Autism Spectrum Disorder Research (7 papers), RNA regulation and disease (7 papers) and Hedgehog Signaling Pathway Studies (7 papers). The work is most often cited by research in Genetics (1.7k citations), Cognitive Neuroscience (421 citations), Molecular Biology (1.2k citations), Pediatrics, Perinatology and Child Health (209 citations) and Pathology and Forensic Medicine (175 citations). Ute Moog has collaborated with scholars based in Germany, Netherlands and Poland. Frequent co-authors include Hartmut Engels, Peep F. M. Stalmeier, W.A.J. van Daal, Gudrun Rappold, Mariëlle S. van Roosmalen, Josette E. H. M. Hoekstra‐Weebers, Jan C. Oosterwijk, Lia C.G. Verhoef, Michael von Bonin and Volker Endris. Their work appears in journals such as Clinical Genetics, European Journal of Human Genetics, Journal of Medical Genetics, Familial Cancer and American Journal of Medical Genetics Part A.
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.