Iris Bartels
Impact in
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- Prenatal Screening and Diagnostics
- Assisted Reproductive Technology and Twin Pregnancy
- Genetics top 5%
- Genomic variations and chromosomal abnormalities
- Genetic Syndromes and Imprinting
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
Papers in
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- Prenatal Screening and Diagnostics 42
- Assisted Reproductive Technology and Twin Pregnancy 10
- Genetics 39
- Genomic variations and chromosomal abnormalities 28
- Genetic Syndromes and Imprinting 9
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 4
- Co-authors
- Hans‐Joachim Knackmuss (2 shared papers)Walter F. Reineke (1 shared paper)Barbara Zoll (19 shared papers)Ingo Hansmann (12 shared papers)B. Eiben (6 shared papers)R. Osmers (5 shared papers)Peter Burfeind (16 shared papers)Thomas Liehr (11 shared papers)
In The Last Decade
Iris Bartels
72 papers receiving 1.7k citations
Peers
Comparison fields: 5 of 99
- Pediatrics, Perinatology and Child Health 788
- Genetics 843
- Pollution 253
- Obstetrics and Gynecology 59
- Hematology 92
Countries citing papers authored by Iris Bartels
This map shows the geographic impact of Iris Bartels'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 Iris Bartels with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Iris Bartels more than expected).
Fields of papers citing papers by Iris Bartels
This network shows the impact of papers produced by Iris Bartels. 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 Iris Bartels. The network helps show where Iris Bartels may publish in the future.
Co-authors
The 25 scholars most cited alongside Iris Bartels, 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 75 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1984 | 306 | |
| 2 | Cytogenetic analysis of 750 spontaneous abortions with the direct-preparation method of chorionic villi and its implications for studying genetic causes of pregnancy wastage. | 1990 | 227 |
| 3 | 2003 | 145 | |
| 4 | 2008 | 94 | |
| 5 | 2012 | 59 | |
| 6 | 2006 | 57 | |
| 7 | 1992 | 54 | |
| 8 | 1988 | 47 | |
| 9 | Regional mapping of six cloned DNA sequences on human chromosome 7. | 1986 | 45 |
| 10 | 1993 | 44 | |
| 11 | 2003 | 42 | |
| 12 | 2007 | 41 | |
| 13 | 2011 | 35 | |
| 14 | 2010 | 34 | |
| 15 | 2003 | 33 | |
| 16 | 1991 | 32 | |
| 17 | 2007 | 30 | |
| 18 | 1994 | 28 | |
| 19 | 2020 | 26 | |
| 20 | 2000 | 25 |
About Iris Bartels
Iris Bartels is a scholar working on Pediatrics, Perinatology and Child Health, Genetics, Plant Science, Public Health, Environmental and Occupational Health and Surgery, having authored 75 papers that have together received 1.9k indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (42 papers), Genomic variations and chromosomal abnormalities (28 papers), Chromosomal and Genetic Variations (14 papers), Assisted Reproductive Technology and Twin Pregnancy (10 papers), Genetic Syndromes and Imprinting (9 papers), Congenital Anomalies and Fetal Surgery (7 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (4 papers) and Reproductive Biology and Fertility (4 papers). The work is most often cited by research in Pediatrics, Perinatology and Child Health (788 citations), Genetics (843 citations), Pollution (253 citations), Obstetrics and Gynecology (59 citations) and Hematology (92 citations). Iris Bartels has collaborated with scholars based in Germany, Poland and Austria. Frequent co-authors include Hans‐Joachim Knackmuss, Walter F. Reineke, Barbara Zoll, Ingo Hansmann, B. Eiben, R. Osmers, Peter Burfeind, Thomas Liehr, Martha Agnes Hentemann and A Lindemann. Their work appears in journals such as Prenatal Diagnosis, Human Genetics, Cytogenetic and Genome Research, Clinical Genetics and Molecular Cytogenetics.
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.