B Krag-Olsen
Impact in
- Genetics top 10%
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genomic variations and chromosomal abnormalities
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- Prenatal Screening and Diagnostics
Papers in
- Genetics 11
- Genomic variations and chromosomal abnormalities 6
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 3
- Genomics and Rare Diseases 2
- BRCA gene mutations in cancer 2
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- Prenatal Screening and Diagnostics 4
- Co-authors
- J. Nielsen (4 shared papers)Bent Ø. Kristensen (1 shared paper)Kaspar Sørensen (1 shared paper)Carl-Otto Gøtzsche (1 shared paper)Poul Videbech (9 shared papers)M Wohlert (7 shared papers)Lone Hvidman (6 shared papers)E. Dupont (2 shared papers)
- Journals
- Human Genetics (3 papers)Clinical Genetics (2 papers)Hereditas (2 papers)Neurology (1 paper)Acta Obstetricia Et Gynecologica Scandinavica (1 paper)
- Partner nations
- DenmarkUnited KingdomGermany
In The Last Decade
B Krag-Olsen
13 papers receiving 352 citations
Peers
Comparison fields: 5 of 60
- Genetics 199
- Pediatrics, Perinatology and Child Health 71
- Developmental Neuroscience 15
- Obstetrics and Gynecology 19
- Clinical Biochemistry 12
Countries citing papers authored by B Krag-Olsen
This map shows the geographic impact of B Krag-Olsen'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 B Krag-Olsen with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites B Krag-Olsen more than expected).
Fields of papers citing papers by B Krag-Olsen
This network shows the impact of papers produced by B Krag-Olsen. 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 B Krag-Olsen. The network helps show where B Krag-Olsen may publish in the future.
Co-authors
The 25 scholars most cited alongside B Krag-Olsen, 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 | 1994 | 185 | |
| 2 | 1982 | 41 | |
| 3 | 1987 | 32 | |
| 4 | 2003 | 26 | |
| 5 | 2004 | 21 | |
| 6 | 1980 | 19 | |
| 7 | 2003 | 18 | |
| 8 | 1981 | 15 | |
| 9 | 1980 | 4 | |
| 10 | Chromosome examination of 20,222 newborn children: results from a 7.5-year study in Arhus, Denmark. | 1986 | 4 |
| 11 | 1984 | 2 | |
| 12 | [The relation of birth weight and gestational age in a group of infants in Jutland with special reference to diagnosing infants with intrauterine growth retardation]. | 1989 | 2 |
| 13 | [Secondary pseudohypoaldosteronism in neonates due to pyelonephritis and congenital urinary tract malformations]. | 2006 | 2 |
| 14 | [Breech presentation deliveries]. | 1989 | 2 |
| 15 | [Complications of delivery following normal pregnancy in clinics]. | 1984 | 1 |
| 16 | 2008 | 0 | |
| 17 | 2009 | 0 |
About B Krag-Olsen
B Krag-Olsen is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Surgery, Molecular Biology and Pathology and Forensic Medicine, having authored 17 papers that have together received 374 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (6 papers), Prenatal Screening and Diagnostics (4 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers), Genomics and Rare Diseases (2 papers), BRCA gene mutations in cancer (2 papers), Chromosomal and Genetic Variations (2 papers), Child and Adolescent Health (2 papers) and Maternal and Perinatal Health Interventions (2 papers). The work is most often cited by research in Genetics (199 citations), Pediatrics, Perinatology and Child Health (71 citations), Developmental Neuroscience (15 citations), Obstetrics and Gynecology (19 citations) and Clinical Biochemistry (12 citations). B Krag-Olsen has collaborated with scholars based in Denmark, United Kingdom and Germany. Frequent co-authors include J. Nielsen, Bent Ø. Kristensen, Kaspar Sørensen, Carl-Otto Gøtzsche, Poul Videbech, M Wohlert, Lone Hvidman, E. Dupont, Kasper Hansen and Jens Peter Nielsen. Their work appears in journals such as Human Genetics, Clinical Genetics, Hereditas, Neurology and Acta Obstetricia Et Gynecologica Scandinavica.
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.