Cornelia Daumer‐Haas
Impact in
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- Prenatal Screening and Diagnostics
- Fetal and Pediatric Neurological Disorders
- Genetics top 5%
- Craniofacial Disorders and Treatments
- Genomic variations and chromosomal abnormalities
- Connective tissue disorders research
- Genomics and Rare Diseases
Papers in
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- Pharmacological Effects and Toxicity Studies 1
- Fetal and Pediatric Neurological Disorders 1
- Prenatal Screening and Diagnostics 1
- Genetics 5
- Genomic variations and chromosomal abnormalities 3
- Genetics and Neurodevelopmental Disorders 1
- Co-authors
- K.-Ph. Gloning (1 shared paper)Konstanze Hörtnagel (1 shared paper)Michael L. Nerlich (1 shared paper)Boris Tutschek (1 shared paper)Thomas Schramm (1 shared paper)Ute Hehr (2 shared papers)Dorien J.M. Peters (1 shared paper)Jill Dixon (1 shared paper)
- Journals
- The American Journal of Human Genetics (2 papers)Human Genetics (2 papers)Communications Biology (1 paper)Nature Genetics (1 paper)Reproductive Toxicology (1 paper)
- Partner nations
- GermanyUnited StatesSwitzerland
In The Last Decade
Cornelia Daumer‐Haas
14 papers receiving 1.0k citations
Peers
Comparison fields: 5 of 45
- Pediatrics, Perinatology and Child Health 115
- Genetics 266
- Developmental Biology 7
- Molecular Biology 180
- Biological Psychiatry 1
Countries citing papers authored by Cornelia Daumer‐Haas
This map shows the geographic impact of Cornelia Daumer‐Haas'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 Cornelia Daumer‐Haas with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Cornelia Daumer‐Haas more than expected).
Fields of papers citing papers by Cornelia Daumer‐Haas
This network shows the impact of papers produced by Cornelia Daumer‐Haas. 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 Cornelia Daumer‐Haas. The network helps show where Cornelia Daumer‐Haas may publish in the future.
Co-authors
The 25 scholars most cited alongside Cornelia Daumer‐Haas, 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 | 2010 | 281 | |
| 2 | 2015 | 173 | |
| 3 | 2009 | 159 | |
| 4 | 2014 | 94 | |
| 5 | 1999 | 74 | |
| 6 | 2012 | 65 | |
| 7 | 2020 | 40 | |
| 8 | 2021 | 40 | |
| 9 | 2010 | 36 | |
| 10 | 2013 | 23 | |
| 11 | 1994 | 20 | |
| 12 | 2006 | 17 | |
| 13 | 1996 | 14 | |
| 14 | 2011 | 2 |
About Cornelia Daumer‐Haas
Cornelia Daumer‐Haas is a scholar working on Pediatrics, Perinatology and Child Health, Genetics, Molecular Biology, Public Health, Environmental and Occupational Health and Nuclear Energy and Engineering, having authored 14 papers that have together received 1.0k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (3 papers), Down syndrome and intellectual disability research (1 paper), Genetics and Neurodevelopmental Disorders (1 paper), Protein Tyrosine Phosphatases (1 paper), Mitochondrial Function and Pathology (1 paper), Pharmacological Effects and Toxicity Studies (1 paper), Fetal and Pediatric Neurological Disorders (1 paper) and Prenatal Screening and Diagnostics (1 paper). The work is most often cited by research in Pediatrics, Perinatology and Child Health (115 citations), Genetics (266 citations), Developmental Biology (7 citations), Molecular Biology (180 citations) and Biological Psychiatry (1 citation). Cornelia Daumer‐Haas has collaborated with scholars based in Germany, United States and Switzerland. Frequent co-authors include K.-Ph. Gloning, Konstanze Hörtnagel, Michael L. Nerlich, Boris Tutschek, Thomas Schramm, Ute Hehr, Dorien J.M. Peters, Jill Dixon, Claudia A. L. Ruivenkamp and Robert Maiwald. Their work appears in journals such as The American Journal of Human Genetics, Human Genetics, Communications Biology, Nature Genetics and Reproductive Toxicology.
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.