Britta Belitz
Impact in
-
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
- Congenital Ear and Nasal Anomalies
-
- Prenatal Screening and Diagnostics
Papers in
- Genetics 5
- Genomic variations and chromosomal abnormalities 5
-
- Genomics and Chromatin Dynamics 3
- Congenital heart defects research 1
- Co-authors
- Lutz Pfeiffer (3 shared papers)Vera M. Kalscheuer (1 shared paper)Anna Latos‐Bieleńska (1 shared paper)Fikret Erdogan (1 shared paper)Joanna Walczak‐Sztulpa (1 shared paper)Andreas W. Kuß (1 shared paper)Marzena Wiśniewska (1 shared paper)Christina Kelbova (1 shared paper)
- Journals
- Journal of Histochemistry & Cytochemistry (3 papers)European Journal of Human Genetics (1 paper)Archives of Gynecology and Obstetrics (1 paper)American Journal of Medical Genetics Part A (1 paper)
- Partner nations
- GermanyPolandUnited Kingdom
In The Last Decade
Britta Belitz
6 papers receiving 110 citations
Peers
Comparison fields: 5 of 25
- Genetics 85
- Pediatrics, Perinatology and Child Health 29
- Plant Science 32
- Genetics 7
- Molecular Biology 47
Countries citing papers authored by Britta Belitz
This map shows the geographic impact of Britta Belitz'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 Britta Belitz with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Britta Belitz more than expected).
Fields of papers citing papers by Britta Belitz
This network shows the impact of papers produced by Britta Belitz. 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 Britta Belitz. The network helps show where Britta Belitz may publish in the future.
Co-authors
The 25 scholars most cited alongside Britta Belitz, 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 | 2008 | 72 | |
| 2 | 2004 | 21 | |
| 3 | 2007 | 11 | |
| 4 | 2012 | 10 | |
| 5 | 2005 | 5 | |
| 6 | 2013 | 5 |
About Britta Belitz
Britta Belitz is a scholar working on Genetics, Molecular Biology, Plant Science, Surgery and Pediatrics, Perinatology and Child Health, having authored 6 papers that have together received 124 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (5 papers), Chromosomal and Genetic Variations (4 papers), Genomics and Chromatin Dynamics (3 papers), Pancreatic function and diabetes (1 paper), Prenatal Screening and Diagnostics (1 paper) and Congenital heart defects research (1 paper). The work is most often cited by research in Genetics (85 citations), Pediatrics, Perinatology and Child Health (29 citations), Plant Science (32 citations), Genetics (7 citations) and Molecular Biology (47 citations). Britta Belitz has collaborated with scholars based in Germany, Poland and United Kingdom. Frequent co-authors include Lutz Pfeiffer, Vera M. Kalscheuer, Anna Latos‐Bieleńska, Fikret Erdogan, Joanna Walczak‐Sztulpa, Andreas W. Kuß, Marzena Wiśniewska, Christina Kelbova, Hans‐Hilger Ropers and Reinhard Ullmann. Their work appears in journals such as Journal of Histochemistry & Cytochemistry, European Journal of Human Genetics, Archives of Gynecology and Obstetrics 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.