Iben Bache
Impact in
- Genetics top 10%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Diabetes and associated disorders
- Human-Computer Interaction top 10%
Papers in
- Genetics 15
- Genomic variations and chromosomal abnormalities 10
- Genetics and Neurodevelopmental Disorders 7
- Genomics and Rare Diseases 3
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 2
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- Congenital heart defects research 4
- Co-authors
- Niels Tommerup (15 shared papers)Zeynep Tümer (8 shared papers)Nete Munk Nielsen (2 shared papers)Klaus Rostgaard (2 shared papers)Morten Frisch (2 shared papers)Robert J. Biggar (1 shared paper)Kristian Tore Jørgensen (1 shared paper)Asli Silahtaroglu (2 shared papers)
- Journals
- European Journal of Human Genetics (6 papers)Genetics in Medicine (1 paper)Prenatal Diagnosis (1 paper)Diabetic Medicine (1 paper)Genes Chromosomes and Cancer (1 paper)
- Partner nations
- DenmarkGermanyUnited States
In The Last Decade
Iben Bache
27 papers receiving 711 citations
Peers
Comparison fields: 5 of 93
- Genetics 294
- Human-Computer Interaction 29
- General Dentistry 7
- Developmental and Educational Psychology 46
- Cognitive Neuroscience 59
Countries citing papers authored by Iben Bache
This map shows the geographic impact of Iben Bache'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 Iben Bache with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Iben Bache more than expected).
Fields of papers citing papers by Iben Bache
This network shows the impact of papers produced by Iben Bache. 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 Iben Bache. The network helps show where Iben Bache may publish in the future.
Co-authors
The 25 scholars most cited alongside Iben Bache, 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 29 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2010 | 123 | |
| 2 | 2016 | 118 | |
| 3 | 2010 | 73 | |
| 4 | 2007 | 63 | |
| 5 | 2016 | 53 | |
| 6 | 1999 | 33 | |
| 7 | 2010 | 31 | |
| 8 | 2012 | 25 | |
| 9 | 2017 | 25 | |
| 10 | 2000 | 22 | |
| 11 | 2007 | 22 | |
| 12 | 2014 | 19 | |
| 13 | 2006 | 19 | |
| 14 | 2016 | 16 | |
| 15 | 2008 | 14 | |
| 16 | 2010 | 14 | |
| 17 | 2019 | 12 | |
| 18 | 2005 | 11 | |
| 19 | 2006 | 9 | |
| 20 | 2007 | 8 |
About Iben Bache
Iben Bache is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Surgery and Epidemiology, having authored 29 papers that have together received 739 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (10 papers), Genetics and Neurodevelopmental Disorders (7 papers), Congenital heart defects research (4 papers), Prenatal Screening and Diagnostics (4 papers), Genomics and Rare Diseases (3 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (2 papers), Chromosomal and Genetic Variations (2 papers) and Diabetes Management and Research (1 paper). The work is most often cited by research in Genetics (294 citations), Human-Computer Interaction (29 citations), General Dentistry (7 citations), Developmental and Educational Psychology (46 citations) and Cognitive Neuroscience (59 citations). Iben Bache has collaborated with scholars based in Denmark, Germany and United States. Frequent co-authors include Niels Tommerup, Zeynep Tümer, Nete Munk Nielsen, Klaus Rostgaard, Morten Frisch, Robert J. Biggar, Kristian Tore Jørgensen, Asli Silahtaroglu, Anne Nørremølle and Karsten Buschard. Their work appears in journals such as European Journal of Human Genetics, Genetics in Medicine, Prenatal Diagnosis, Diabetic Medicine and Genes Chromosomes and Cancer.
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.