Brith Otterud
Impact in
-
- Genetic Neurodegenerative Diseases
- Hereditary Neurological Disorders
- Neurology top 5%
- Neurological diseases and metabolism
Papers in
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- Congenital heart defects research 3
-
- Hereditary Neurological Disorders 5
- Genetic Neurodegenerative Diseases 3
- Co-authors
- Mark Leppert (17 shared papers)Mark Leppert (8 shared papers)M. Leppert (11 shared papers)Lisa Baird (5 shared papers)Tena Varvil (6 shared papers)John K. Fink (6 shared papers)Kent L. Anderson (3 shared papers)Richard A. Lewis (2 shared papers)
- Journals
- Human Genetics (3 papers)Neurology (3 papers)Blood (3 papers)Human Molecular Genetics (2 papers)Genomics (2 papers)
- Partner nations
- United StatesBelgiumPoland
In The Last Decade
Brith Otterud
40 papers receiving 2.0k citations
Peers
Comparison fields: 5 of 83
- Cellular and Molecular Neuroscience 501
- Neurology 150
- Hematology 192
- Genetics 163
- Sensory Systems 69
Countries citing papers authored by Brith Otterud
This map shows the geographic impact of Brith Otterud'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 Brith Otterud with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Brith Otterud more than expected).
Fields of papers citing papers by Brith Otterud
This network shows the impact of papers produced by Brith Otterud. 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 Brith Otterud. The network helps show where Brith Otterud may publish in the future.
Co-authors
The 25 scholars most cited alongside Brith Otterud, 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 41 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Autosomal dominant spinocerebellar ataxia with sensory axonal neuropathy (SCA4): clinical description and genetic localization to chromosome 16q22.1. | 1996 | 183 |
| 2 | 1994 | 134 | |
| 3 | 1999 | 131 | |
| 4 | 1998 | 117 | |
| 5 | 1995 | 117 | |
| 6 | 2003 | 112 | |
| 7 | Linkage of a variant or attenuated form of adenomatous polyposis coli to the adenomatous polyposis coli (APC) locus. | 1992 | 112 |
| 8 | Genetic linkage analysis in familial benign (hypocalciuric) hypercalcemia: evidence for locus heterogeneity. | 1993 | 106 |
| 9 | Autosomal dominant familial spastic paraplegia: tight linkage to chromosome 15q. | 1995 | 102 |
| 10 | 1996 | 88 | |
| 11 | Paroxysmal dystonic choreoathetosis: tight linkage to chromosome 2q. | 1996 | 83 |
| 12 | 2010 | 79 | |
| 13 | 2004 | 74 | |
| 14 | 1999 | 71 | |
| 15 | 2013 | 51 | |
| 16 | A gene for familial total anomalous pulmonary venous return maps to chromosome 4p13-q12. | 1995 | 50 |
| 17 | 2012 | 48 | |
| 18 | 2008 | 47 | |
| 19 | A YAC contig encompassing the recessive Stargardt disease gene (STGD) on chromosome 1p. | 1995 | 44 |
| 20 | 1999 | 39 |
About Brith Otterud
Brith Otterud is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience, Genetics, Immunology and Genetics, having authored 41 papers that have together received 2.1k indexed citations. Recurring topics across this work include Neurogenetic and Muscular Disorders Research (6 papers), Neurological diseases and metabolism (5 papers), Hereditary Neurological Disorders (5 papers), Immunotherapy and Immune Responses (4 papers), T-cell and B-cell Immunology (4 papers), Congenital heart defects research (3 papers), Genetic Neurodegenerative Diseases (3 papers) and Immune Cell Function and Interaction (3 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (501 citations), Neurology (150 citations), Hematology (192 citations), Genetics (163 citations) and Sensory Systems (69 citations). Brith Otterud has collaborated with scholars based in United States, Belgium and Poland. Frequent co-authors include Mark Leppert, Mark Leppert, M. Leppert, Lisa Baird, Tena Varvil, John K. Fink, Kent L. Anderson, Richard A. Lewis, Charles E. Jackson and Andy Peiffer. Their work appears in journals such as Human Genetics, Neurology, Blood, Human Molecular Genetics and Genomics.
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.