Gunnar Houge
Impact in
- Physiology top 2%
- Lysosomal Storage Disorders Research
- Genetics top 2%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
Papers in
- Genetics 53
- Genomic variations and chromosomal abnormalities 22
- Genetics and Neurodevelopmental Disorders 16
- Genomics and Rare Diseases 10
- Genetic Syndromes and Imprinting 7
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- RNA modifications and cancer 10
- Co-authors
- Stein Ove DøskelandMichel LanotteBjørn Tore GjertsenOlav Karsten VintermyrRoald BøeAsle HirthCamilla TøndelEinar Svarstad
- Journals
- European Journal of Human Genetics (14 papers)European Journal of Medical Genetics (5 papers)Molecular Case Studies (3 papers)FEBS Letters (3 papers)Journal of Medical Genetics (3 papers)
- Partner nations
- NorwayUnited KingdomNetherlands
In The Last Decade
Gunnar Houge
104 papers receiving 3.2k citations
Peers
Comparison fields: 5 of 120
- Physiology 899
- Genetics 812
- Molecular Biology 1.8k
- Cell Biology 407
- Rheumatology 273
Countries citing papers authored by Gunnar Houge
This map shows the geographic impact of Gunnar Houge'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 Gunnar Houge with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Gunnar Houge more than expected).
Fields of papers citing papers by Gunnar Houge
This network shows the impact of papers produced by Gunnar Houge. 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 Gunnar Houge. The network helps show where Gunnar Houge may publish in the future.
Co-authors
The 25 scholars most cited alongside Gunnar Houge, 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 | 2023 | 0 | |
| 2 | 2020 | 5 | |
| 3 | 2018 | 24 | |
| 4 | 2018 | 18 | |
| 5 | 2017 | 9 | |
| 6 | 2014 | 19 | |
| 7 | 2011 | 39 | |
| 8 | 2010 | 11 | |
| 9 | 2009 | 8 | |
| 10 | Fabrys sykdom – en diagnostisk og terapeutisk utfordring | 2005 | 1 |
| 11 | 2005 | 25 | |
| 12 | 2004 | 171 | |
| 13 | Diagnostikk av medfødte kryptiske kromosomavvik | 2003 | 1 |
| 14 | 2002 | 43 | |
| 15 | Ataksi på grunn av vitamin E-mangel | 1998 | 1 |
| 16 | 1997 | 25 | |
| 17 | 1996 | 4 | |
| 18 | 1993 | 7 | |
| 19 | 1992 | 10 | |
| 20 | 1990 | 60 |
About Gunnar Houge
Gunnar Houge is a scholar working on Genetics, Molecular Biology, Genetics, Pediatrics, Perinatology and Child Health and Physiology, having authored 112 papers that have together received 3.3k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (22 papers), Genetics and Neurodevelopmental Disorders (16 papers), Lysosomal Storage Disorders Research (15 papers), Genomics and Rare Diseases (10 papers), RNA modifications and cancer (10 papers), Prenatal Screening and Diagnostics (9 papers), Genetic Syndromes and Imprinting (7 papers) and Biomedical Research and Pathophysiology (7 papers). The work is most often cited by research in Physiology (899 citations), Genetics (812 citations), Molecular Biology (1.8k citations), Cell Biology (407 citations) and Rheumatology (273 citations). Gunnar Houge has collaborated with scholars based in Norway, United Kingdom and Netherlands. Frequent co-authors include Stein Ove Døskeland, Michel Lanotte, Bjørn Tore Gjertsen, Olav Karsten Vintermyr, Roald Bøe, Asle Hirth, Camilla Tøndel, Einar Svarstad, Helle Lybæk and Sandrine Ruchaud. Their work appears in journals such as European Journal of Human Genetics, European Journal of Medical Genetics, Molecular Case Studies, FEBS Letters and Journal of Medical 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.