H. Telenius
Impact in
-
- Genetic Neurodegenerative Diseases
- Genetics top 2%
- Genomic variations and chromosomal abnormalities
Papers in
-
- Genetic Neurodegenerative Diseases 8
-
- Mitochondrial Function and Pathology 5
- DNA Repair Mechanisms 4
- Co-authors
- Nigel P. Carter (2 shared papers)Charlotte Bebb (1 shared paper)Bruce A.J. Ponder (1 shared paper)Alan Tunnacliffe (1 shared paper)Michael R. Hayden (7 shared papers)Y. Paul Goldberg (7 shared papers)Elisabeth W. Almqvist (5 shared papers)B. P. H. Kremer (6 shared papers)
- Journals
- Human Molecular Genetics (4 papers)Journal of Medical Genetics (3 papers)Nucleic Acids Research (1 paper)Nature (1 paper)Journal of Molecular Medicine (1 paper)
- Partner nations
- SwedenUnited KingdomCanada
In The Last Decade
H. Telenius
18 papers receiving 2.6k citations
H. Telenius's Hit Papers
Peers
Comparison fields: 5 of 103
- Cellular and Molecular Neuroscience 749
- Genetics 1.0k
- Neurology 426
- Molecular Biology 1.6k
- Cancer Research 277
Countries citing papers authored by H. Telenius
This map shows the geographic impact of H. Telenius'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 H. Telenius with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites H. Telenius more than expected).
Fields of papers citing papers by H. Telenius
This network shows the impact of papers produced by H. Telenius. 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 H. Telenius. The network helps show where H. Telenius may publish in the future.
Co-authors
The 25 scholars most cited alongside H. Telenius, 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 | Degenerate oligonucleotide-primed PCR: General amplification of target DNA by a single degenerate primer Hit paper breakdown → | 1992 | 1218 |
| 2 | 1987 | 394 | |
| 3 | 1992 | 189 | |
| 4 | 1993 | 170 | |
| 5 | 1994 | 164 | |
| 6 | Sex-dependent mechanisms for expansions and contractions of the CAG repeat on affected Huntington disease chromosomes. | 1995 | 120 |
| 7 | 1997 | 98 | |
| 8 | Huntington disease without CAG expansion: phenocopies or errors in assignment? | 1994 | 94 |
| 9 | Tetrasomy 15q: two marker chromosomes with no detectable alpha-satellite DNA. | 1994 | 73 |
| 10 | 1995 | 68 | |
| 11 | 1993 | 53 | |
| 12 | 1993 | 33 | |
| 13 | 1993 | 23 | |
| 14 | Application of linked DNA markers to screening families with multiple endocrine neoplasia type 2A. | 1990 | 6 |
| 15 | 1988 | 3 | |
| 16 | 1989 | 2 | |
| 17 | 2008 | 2 | |
| 18 | 1993 | 1 | |
| 19 | 2008 | 0 |
About H. Telenius
H. Telenius is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology, Genetics, Neurology and Oncology, having authored 19 papers that have together received 2.7k indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (8 papers), Chromosomal and Genetic Variations (5 papers), Mitochondrial Function and Pathology (5 papers), Neuroendocrine Tumor Research Advances (4 papers), DNA Repair Mechanisms (4 papers), Lung Cancer Research Studies (3 papers), Genomic variations and chromosomal abnormalities (3 papers) and Animal Genetics and Reproduction (2 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (749 citations), Genetics (1.0k citations), Neurology (426 citations), Molecular Biology (1.6k citations) and Cancer Research (277 citations). H. Telenius has collaborated with scholars based in Sweden, United Kingdom and Canada. Frequent co-authors include Nigel P. Carter, Charlotte Bebb, Bruce A.J. Ponder, Alan Tunnacliffe, Michael R. Hayden, Y. Paul Goldberg, Elisabeth W. Almqvist, B. P. H. Kremer, Susan E. Andrew and Niamh Spence. Their work appears in journals such as Human Molecular Genetics, Journal of Medical Genetics, Nucleic Acids Research, Nature and Journal of Molecular Medicine.
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.