Lone B. Andersen
Impact in
- Neurology top 0.5%
- Neurofibromatosis and Schwannoma Cases
- Neuroblastoma Research and Treatments
- Vascular Malformations Diagnosis and Treatment
- Rheumatology top 2%
- Soft tissue tumor case studies
Papers in
- Neurology 16
- Neurofibromatosis and Schwannoma Cases 16
- Neuroblastoma Research and Treatments 6
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- Soft tissue tumor case studies 5
- Bone Tumor Diagnosis and Treatments 2
- Co-authors
- Francis S. Collins (15 shared papers)Margaret R. Wallace (9 shared papers)Ann M. Saulino (6 shared papers)Douglas A. Marchuk (12 shared papers)Anna L. Mitchell (2 shared papers)Jane W. Fountain (3 shared papers)Thomas W. Glover (5 shared papers)Bernard H. Brownstein (2 shared papers)
- Journals
- Genomics (4 papers)Genes Chromosomes and Cancer (2 papers)Human Molecular Genetics (2 papers)Nucleic Acids Research (2 papers)Nature Genetics (1 paper)
- Partner nations
- United StatesDenmarkUnited Kingdom
In The Last Decade
Lone B. Andersen
21 papers receiving 2.5k citations
Lone B. Andersen's Hit Papers
Peers
Comparison fields: 5 of 85
- Neurology 1.6k
- Rheumatology 450
- Pulmonary and Respiratory Medicine 534
- Epidemiology 479
- Molecular Biology 944
Countries citing papers authored by Lone B. Andersen
This map shows the geographic impact of Lone B. Andersen'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 Lone B. Andersen with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Lone B. Andersen more than expected).
Fields of papers citing papers by Lone B. Andersen
This network shows the impact of papers produced by Lone B. Andersen. 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 Lone B. Andersen. The network helps show where Lone B. Andersen may publish in the future.
Co-authors
The 25 scholars most cited alongside Lone B. Andersen, 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 21 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Type 1 Neurofibromatosis Gene: Identification of a Large Transcript Disrupted in Three NF1 Patients Hit paper breakdown → | 1990 | 1155 |
| 2 | 1991 | 356 | |
| 3 | 1991 | 324 | |
| 4 | 1993 | 137 | |
| 5 | 1991 | 122 | |
| 6 | 1993 | 120 | |
| 7 | 1991 | 92 | |
| 8 | 1993 | 57 | |
| 9 | 2003 | 47 | |
| 10 | 1992 | 37 | |
| 11 | 1992 | 33 | |
| 12 | 1990 | 28 | |
| 13 | 1990 | 26 | |
| 14 | 1993 | 20 | |
| 15 | 1990 | 19 | |
| 16 | 1991 | 15 | |
| 17 | 1991 | 13 | |
| 18 | 1993 | 7 | |
| 19 | 1996 | 4 | |
| 20 | which have GTPase-activating protein activity. produces two neurofibromin isoforms, both of Recklinghausen neurofibromatosis (NF1) gene A conserved alternative splice in the von | 2012 | 1 |
About Lone B. Andersen
Lone B. Andersen is a scholar working on Neurology, Rheumatology, Pulmonary and Respiratory Medicine, Molecular Biology and Cell Biology, having authored 21 papers that have together received 2.6k indexed citations. Recurring topics across this work include Neurofibromatosis and Schwannoma Cases (16 papers), Sarcoma Diagnosis and Treatment (6 papers), Neuroblastoma Research and Treatments (6 papers), Soft tissue tumor case studies (5 papers), Hereditary Neurological Disorders (2 papers), Hippo pathway signaling and YAP/TAZ (2 papers), Chromatin Remodeling and Cancer (2 papers) and Bone Tumor Diagnosis and Treatments (2 papers). The work is most often cited by research in Neurology (1.6k citations), Rheumatology (450 citations), Pulmonary and Respiratory Medicine (534 citations), Epidemiology (479 citations) and Molecular Biology (944 citations). Lone B. Andersen has collaborated with scholars based in United States, Denmark and United Kingdom. Frequent co-authors include Francis S. Collins, Margaret R. Wallace, Ann M. Saulino, Douglas A. Marchuk, Anna L. Mitchell, Jane W. Fountain, Thomas W. Glover, Bernard H. Brownstein, Hana M. Odeh and David H. Gutmann. Their work appears in journals such as Genomics, Genes Chromosomes and Cancer, Human Molecular Genetics, Nucleic Acids Research and Nature 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.