Iris Bartels
Impact in
-
- 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
-
- Prenatal Screening and Diagnostics 40
- Assisted Reproductive Technology and Twin Pregnancy 10
- Genetics 37
- Genomic variations and chromosomal abnormalities 26
- 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 Reineke (1 shared paper)B. Eiben (6 shared papers)Barbara Zoll (18 shared papers)I. Hansmann (11 shared papers)R. Osmers (5 shared papers)Thomas Liehr (10 shared papers)Peter Burfeind (15 shared papers)
- Journals
- Prenatal Diagnosis (13 papers)Cytogenetic and Genome Research (5 papers)Human Genetics (3 papers)European Journal of Medical Genetics (3 papers)Clinical Genetics (3 papers)
- Partner nations
- GermanyPolandUnited States
In The Last Decade
Iris Bartels
72 papers receiving 1.5k citations
Peers
Comparison fields: 5 of 101
- Pediatrics, Perinatology and Child Health 690
- Genetics 651
- Pollution 254
- Obstetrics and Gynecology 54
- Hematology 81
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 76 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1984 | 307 | |
| 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 | 228 |
| 3 | 2008 | 86 | |
| 4 | 2006 | 58 | |
| 5 | 2012 | 55 | |
| 6 | 1992 | 53 | |
| 7 | 1988 | 44 | |
| 8 | Regional mapping of six cloned DNA sequences on human chromosome 7. | 1986 | 44 |
| 9 | 1993 | 43 | |
| 10 | 2007 | 41 | |
| 11 | 2003 | 41 | |
| 12 | 2010 | 34 | |
| 13 | 2003 | 34 | |
| 14 | 2011 | 33 | |
| 15 | 1991 | 32 | |
| 16 | 1994 | 27 | |
| 17 | 1990 | 23 | |
| 18 | 2011 | 22 | |
| 19 | 2020 | 22 | |
| 20 | 1990 | 22 |
About Iris Bartels
Iris Bartels is a scholar working on Pediatrics, Perinatology and Child Health, Genetics, Molecular Biology, Surgery and Plant Science, having authored 76 papers that have together received 1.7k indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (40 papers), Genomic variations and chromosomal abnormalities (26 papers), Chromosomal and Genetic Variations (12 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 (690 citations), Genetics (651 citations), Pollution (254 citations), Obstetrics and Gynecology (54 citations) and Hematology (81 citations). Iris Bartels has collaborated with scholars based in Germany, Poland and United States. Frequent co-authors include Hans‐Joachim Knackmuss, Walter Reineke, B. Eiben, Barbara Zoll, I. Hansmann, R. Osmers, Thomas Liehr, Peter Burfeind, Martha Hentemann and R. Goebel. Their work appears in journals such as Prenatal Diagnosis, Cytogenetic and Genome Research, Human Genetics, European Journal of Medical Genetics and Clinical Genetics.
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.