Lisbeth Tranebjærg
Impact in
- Sensory Systems top 0.5%
- Hearing, Cochlea, Tinnitus, Genetics
- Neurology top 1%
- Neuroinflammation and Neurodegeneration Mechanisms
Papers in
-
- Congenital heart defects research 14
- RNA regulation and disease 14
- Mitochondrial Function and Pathology 13
- Genetics 56
- Genetics and Neurodevelopmental Disorders 25
- Genomic variations and chromosomal abnormalities 15
- Co-authors
- Nanna Dahl Rendtorff (35 shared papers)Claes Möller (9 shared papers)Herbert A. Lubs (7 shared papers)Martina C. Cornel (5 shared papers)Niels Tommerup (10 shared papers)Charles E. Schwartz (6 shared papers)Thomas Rosenberg (6 shared papers)Øivind Nilssen (7 shared papers)
- Journals
- European Journal of Human Genetics (19 papers)Journal of Medical Genetics (7 papers)Clinical Genetics (7 papers)The American Journal of Human Genetics (7 papers)Human Molecular Genetics (6 papers)
- Partner nations
- DenmarkNorwayUnited States
In The Last Decade
Lisbeth Tranebjærg
160 papers receiving 6.5k citations
Lisbeth Tranebjærg's Hit Papers
Peers
Comparison fields: 5 of 149
- Sensory Systems 792
- Neurology 637
- Genetics 2.1k
- Clinical Biochemistry 316
- Molecular Biology 3.1k
Countries citing papers authored by Lisbeth Tranebjærg
This map shows the geographic impact of Lisbeth Tranebjærg'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 Lisbeth Tranebjærg with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Lisbeth Tranebjærg more than expected).
Fields of papers citing papers by Lisbeth Tranebjærg
This network shows the impact of papers produced by Lisbeth Tranebjærg. 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 Lisbeth Tranebjærg. The network helps show where Lisbeth Tranebjærg may publish in the future.
Co-authors
The 25 scholars most cited alongside Lisbeth Tranebjærg, 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 162 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Mutations in Two Genes Encoding Different Subunits of a Receptor Signaling Complex Result in an Identical Disease Phenotype Hit paper breakdown → | 2002 | 530 |
| 2 | 1991 | 286 | |
| 3 | Whole-genome sequencing in health care. Recommendations of the European Society of Human Genetics. | 2013 | 272 |
| 4 | 1994 | 259 | |
| 5 | 2013 | 259 | |
| 6 | 1997 | 233 | |
| 7 | 1995 | 200 | |
| 8 | 1996 | 199 | |
| 9 | 2012 | 179 | |
| 10 | 2005 | 161 | |
| 11 | A new gene (DYX3) for dyslexia is located on chromosome 2. | 1999 | 159 |
| 12 | 2007 | 141 | |
| 13 | 1995 | 136 | |
| 14 | 2006 | 113 | |
| 15 | 2009 | 92 | |
| 16 | 2008 | 92 | |
| 17 | 1997 | 91 | |
| 18 | 2011 | 90 | |
| 19 | 2001 | 85 | |
| 20 | 1996 | 79 |
About Lisbeth Tranebjærg
Lisbeth Tranebjærg is a scholar working on Molecular Biology, Genetics, Sensory Systems, Cell Biology and Cellular and Molecular Neuroscience, having authored 162 papers that have together received 6.8k indexed citations. Recurring topics across this work include Hearing, Cochlea, Tinnitus, Genetics (28 papers), Genetics and Neurodevelopmental Disorders (25 papers), Genomic variations and chromosomal abnormalities (15 papers), Congenital heart defects research (14 papers), RNA regulation and disease (14 papers), Mitochondrial Function and Pathology (13 papers), Genetic Neurodegenerative Diseases (13 papers) and Endoplasmic Reticulum Stress and Disease (11 papers). The work is most often cited by research in Sensory Systems (792 citations), Neurology (637 citations), Genetics (2.1k citations), Clinical Biochemistry (316 citations) and Molecular Biology (3.1k citations). Lisbeth Tranebjærg has collaborated with scholars based in Denmark, Norway and United States. Frequent co-authors include Nanna Dahl Rendtorff, Claes Möller, Herbert A. Lubs, Martina C. Cornel, Niels Tommerup, Charles E. Schwartz, Thomas Rosenberg, Øivind Nilssen, Rolf Adolfsson and Leena Peltonen. Their work appears in journals such as European Journal of Human Genetics, Journal of Medical Genetics, Clinical Genetics, The American Journal of Human Genetics and Human Molecular 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.