Ute Knoll
Impact in
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- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Connective tissue disorders research
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- Prenatal Screening and Diagnostics
- Fetal and Pediatric Neurological Disorders
Papers in
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- Prenatal Screening and Diagnostics 10
- Fetal and Pediatric Neurological Disorders 4
- Genetics 4
- Connective tissue disorders research 1
- Hemoglobinopathies and Related Disorders 1
- Co-authors
- Rolf Becker (8 shared papers)Rolf‐Dieter Wegner (6 shared papers)Michael Entezami (8 shared papers)Markus Stümm (5 shared papers)Ekkehart Lausch (1 shared paper)Mohandas Nair (1 shared paper)Jürgen W. Spranger (1 shared paper)Hanka Venselaar (1 shared paper)
- Journals
- Prenatal Diagnosis (3 papers)Ultrasound in Obstetrics and Gynecology (3 papers)The American Journal of Human Genetics (1 paper)Fetal Diagnosis and Therapy (1 paper)Ultraschall in der Medizin - European Journal of Ultrasound (1 paper)
- Partner nations
- GermanyUnited StatesNetherlands
In The Last Decade
Ute Knoll
12 papers receiving 138 citations
Peers
Comparison fields: 5 of 46
- Genetics 94
- Pediatrics, Perinatology and Child Health 57
- Genetics 15
- Cell Biology 18
- Developmental Biology 2
Countries citing papers authored by Ute Knoll
This map shows the geographic impact of Ute Knoll'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 Knoll with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ute Knoll more than expected).
Fields of papers citing papers by Ute Knoll
This network shows the impact of papers produced by Ute Knoll. 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 Knoll. The network helps show where Ute Knoll may publish in the future.
Co-authors
The 25 scholars most cited alongside Ute Knoll, 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 | 2011 | 66 | |
| 2 | 2014 | 23 | |
| 3 | 2003 | 21 | |
| 4 | 2009 | 14 | |
| 5 | 2004 | 13 | |
| 6 | 2010 | 11 | |
| 7 | 2007 | 10 | |
| 8 | 2010 | 4 | |
| 9 | The potential of first trimester anomaly scan and first trimester fetal echocardiography as screening procedures in a medium risk population | 2005 | 2 |
| 10 | 2006 | 1 | |
| 11 | 2019 | 1 | |
| 12 | 2006 | 1 |
About Ute Knoll
Ute Knoll is a scholar working on Pediatrics, Perinatology and Child Health, Genetics, Surgery, Infectious Diseases and Molecular Biology, having authored 12 papers that have together received 167 indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (10 papers), Fetal and Pediatric Neurological Disorders (4 papers), Congenital Anomalies and Fetal Surgery (3 papers), Parvovirus B19 Infection Studies (2 papers), Urological Disorders and Treatments (2 papers), Connective tissue disorders research (1 paper), Hemoglobinopathies and Related Disorders (1 paper) and Biochemical and Molecular Research (1 paper). The work is most often cited by research in Genetics (94 citations), Pediatrics, Perinatology and Child Health (57 citations), Genetics (15 citations), Cell Biology (18 citations) and Developmental Biology (2 citations). Ute Knoll has collaborated with scholars based in Germany, United States and Netherlands. Frequent co-authors include Rolf Becker, Rolf‐Dieter Wegner, Michael Entezami, Markus Stümm, Ekkehart Lausch, Mohandas Nair, Jürgen W. Spranger, Hanka Venselaar, Joris A. Veltman and Han G. Brunner. Their work appears in journals such as Prenatal Diagnosis, Ultrasound in Obstetrics and Gynecology, The American Journal of Human Genetics, Fetal Diagnosis and Therapy and Ultraschall in der Medizin - European Journal of Ultrasound.
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.