I. Hansmann
- Genetics top 1%
- Genomic variations and chromosomal abnormalities 23
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 16
- Animal Genetics and Reproduction 15
- Genetic Syndromes and Imprinting 12
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- Prenatal Screening and Diagnostics 20
- Reproductive Medicine top 5%
- Sperm and Testicular Function 11
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- Reproductive Biology and Fertility 30
- Molecular Biology top 10%
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- Chromosomal and Genetic Variations 28
- Co-authors
- V.V.N. Gopal RaoH. -D. ProbeckSusanne SchnittgerEdith HümmlerFriedrich BeermannG. RöhrbornIris BartelsJ. Jenderny
- Journals
- Human Genetics (29 papers)Cytogenetic and Genome Research (16 papers)Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis (10 papers)
- Partner nations
- GermanyUnited StatesPoland
In The Last Decade
I. Hansmann
127 papers receiving 2.4k citations
Peers
Comparison fields: 5 of 114
- Genetics 1.2k
- Pediatrics, Perinatology and Child Health 628
- Reproductive Medicine 169
- Public Health, Environmental and Occupational Health 497
- Molecular Biology 1.0k
Countries citing papers authored by I. Hansmann
This map shows the geographic impact of I. Hansmann'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 I. Hansmann with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites I. Hansmann more than expected).
Fields of papers citing papers by I. Hansmann
This network shows the impact of papers produced by I. Hansmann. 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 I. Hansmann. The network helps show where I. Hansmann may publish in the future.
Co-authorship network
The 25 scholars most cited alongside I. Hansmann, 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 | 2005 | 15 | |
| 2 | 2004 | 28 | |
| 3 | 2001 | 33 | |
| 4 | 2001 | 18 | |
| 5 | Towards positional cloning of the locus for benign neonatal epilepsy (EBN1) on chromosome 20 | 1994 | 1 |
| 6 | A genetic map of chromosome 20q12-q13.1: multiple highly polymorphic microsatellite and RFLP markers linked to the maturity-onset diabetes of the young (MODY) locus. | 1993 | 26 |
| 7 | 1993 | 57 | |
| 8 | 1992 | 13 | |
| 9 | 1992 | 1 | |
| 10 | 1990 | 20 | |
| 11 | 1983 | 13 | |
| 12 | 1983 | 15 | |
| 13 | 1979 | 13 | |
| 14 | 1975 | 2 | |
| 15 | 1975 | 1 | |
| 16 | 1975 | 2 | |
| 17 | 1974 | 15 | |
| 18 | 1974 | 65 | |
| 19 | 1974 | 21 | |
| 20 | 1973 | 29 |
About I. Hansmann
I. Hansmann is a scholar working on Genetics, Reproductive Medicine, Pediatrics, Perinatology and Child Health, Public Health, Environmental and Occupational Health and Developmental Biology, having authored 129 papers that have together received 2.7k indexed citations. Recurring topics across this work include Reproductive Biology and Fertility (30 papers), Chromosomal and Genetic Variations (28 papers), Genomic variations and chromosomal abnormalities (23 papers), Prenatal Screening and Diagnostics (20 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (16 papers), Animal Genetics and Reproduction (15 papers), Genetic Syndromes and Imprinting (12 papers) and Sperm and Testicular Function (11 papers). The work is most often cited by research in Genetics (1.2k citations), Pediatrics, Perinatology and Child Health (628 citations), Reproductive Medicine (169 citations), Public Health, Environmental and Occupational Health (497 citations) and Molecular Biology (1.0k citations). I. Hansmann has collaborated with scholars based in Germany, United States and Poland. Frequent co-authors include V.V.N. Gopal Rao, H. -D. Probeck, Susanne Schnittger, Edith Hümmler, Friedrich Beermann, G. Röhrborn, Iris Bartels, J. Jenderny, B. Eiben and B. Hinney. Their work appears in journals such as Human Genetics, Cytogenetic and Genome Research, Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis, Genomics 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.