Lone B. Andersen

3.3k total citations · 1 hit paper
21 papers, 2.6k citations indexed

About

Lone B. Andersen is a scholar working on Neurology, Rheumatology and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Lone B. Andersen has authored 21 papers receiving a total of 2.6k indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Neurology, 7 papers in Rheumatology and 6 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Lone B. Andersen's work include Neurofibromatosis and Schwannoma Cases (16 papers), Sarcoma Diagnosis and Treatment (6 papers) and Neuroblastoma Research and Treatments (6 papers). Lone B. Andersen is often cited by papers focused on Neurofibromatosis and Schwannoma Cases (16 papers), Sarcoma Diagnosis and Treatment (6 papers) and Neuroblastoma Research and Treatments (6 papers). Lone B. Andersen collaborates with scholars based in United States, Denmark and Belgium. Lone B. Andersen's co-authors include Francis S. Collins, Margaret R. Wallace, Ann M. Saulino, Douglas A. Marchuk, Anna L. Mitchell, Jane W. Fountain, Thomas W. Glover, Hana M. Odeh, Bernard H. Brownstein and David H. Gutmann and has published in prestigious journals such as Nature, Science and Nucleic Acids Research.

In The Last Decade

Lone B. Andersen

21 papers receiving 2.5k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Type 1 Neurofibromatosis Gene: Identification of a Large Transcript Disrupted in Three NF1 Patients

1990 1.2k citations Margaret R. Wallace, Douglas A. Marchuk et al. Science profile →

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Lone B. Andersen United States	16	1.6k	944	534	479	450	21	2.6k
Gangfeng Xu United States	8	1.7k 1.1×	1.0k 1.1×	482 0.9×	494 1.0×	427 0.9×	12	2.7k
Jeff Stevens United States	10	1.3k 0.8×	723 0.8×	378 0.7×	410 0.9×	384 0.9×	19	2.1k
José M. de Campos Spain	30	800 0.5×	985 1.0×	289 0.5×	705 1.5×	207 0.5×	77	2.3k
Conxi Lázaro Spain	35	1.1k 0.6×	1.5k 1.5×	649 1.2×	298 0.6×	352 0.8×	147	3.6k
T. Shane Shih United States	8	692 0.4×	690 0.7×	248 0.5×	151 0.3×	108 0.2×	9	1.4k
Mariarita Santi United States	27	565 0.3×	910 1.0×	328 0.6×	161 0.3×	87 0.2×	70	1.9k
Richard Y. Chung United States	14	389 0.2×	816 0.9×	222 0.4×	236 0.5×	78 0.2×	17	1.7k
E Wright United Kingdom	9	431 0.3×	253 0.3×	114 0.2×	184 0.4×	138 0.3×	15	824
D. Wade Clapp United States	25	1.6k 0.9×	799 0.8×	526 1.0×	429 0.9×	313 0.7×	49	2.5k
Roberta Sestini Italy	22	404 0.2×	595 0.6×	208 0.4×	279 0.6×	86 0.2×	45	1.3k

Countries citing papers authored by Lone B. Andersen

Since Specialization

Citations

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

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network of co-authors of Lone B. Andersen

This figure shows the co-authorship network connecting the top 25 collaborators of Lone B. Andersen. A scholar is included among the top collaborators of Lone B. Andersen based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Lone B. Andersen. Lone B. Andersen is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Saulino, Ann M., Jacques Camonis, Michael Wigler, et al.. (2012). which have GTPase-activating protein activity. produces two neurofibromin isoforms, both of Recklinghausen neurofibromatosis (NF1) gene A conserved alternative splice in the von. 1 indexed citations

Holmstrup, Palle, et al.. (2003). Oral infections and systemic diseases. Dental Clinics of North America. 47(3). 575–598. 47 indexed citations

Andersen, Lone B., Longqing Xia, Stefan Stoll, Xinping Zhao, & James T. Elder. (1996). Lineage-specific CaN19 expression in human skin: lack of expression in normal melanocytes. Journal of Dermatological Science. 12(1). 69–72. 4 indexed citations

Andersen, Lone B., Roymarie Ballester, Douglas A. Marchuk, et al.. (1993). A Conserved Alternative Splice in the von Recklinghausen Neurofibromatosis ( NF1 ) Gene Produces Two Neurofibromin Isoforms, Both of Which Have GTPase-Activating Protein Activity. Molecular and Cellular Biology. 13(1). 487–495. 137 indexed citations

Andersen, Lone B., Jane W. Fountain, David H. Gutmann, et al.. (1993). Mutations in the neurofibromatosis 1 gene in sporadic malignant melanoma cell lines. Nature Genetics. 3(2). 118–121. 120 indexed citations

Andersen, Lone B., Susan A. Tarlé, Douglas A. Marchuk, Eric Legius, & Francis S. Collins. (1993). A compound nucleotide repeat in the neurofibro-matosis (NF1) gene. Human Molecular Genetics. 2(7). 1083–1083. 20 indexed citations

Reyniers, Edwin, Kristel De Boulle, Douglas A. Marchuk, et al.. (1993). An EcoRI RFLP in the 5′ region of the human NF1 gene. Human Genetics. 92(6). 631–631. 7 indexed citations

Marchuk, Douglas A., Margaret R. Wallace, Bernard H. Brownstein, et al.. (1992). A yeast artificial chromosome contig encompassing the type 1 neurofibromatosis gene. Genomics. 13(3). 672–680. 37 indexed citations

Legius, Eric, Douglas A. Marchuk, Bryan K. Hall, et al.. (1992). NF1-related locus on chromosome 15. Genomics. 13(4). 1316–1318. 33 indexed citations

10.

Cawthon, Richard, Lone B. Andersen, Arthur M. Buchberg, et al.. (1991). cDNA sequence and genomic structure of EVI2B, a gene lying within an intron of the neurofibromatosis type 1 gene. Genomics. 9(3). 446–460. 92 indexed citations

11.

Glover, Thomas W., et al.. (1991). Molecular and cytogenetic analysis of tumors in von recklinghausen neurofibromatosis. Genes Chromosomes and Cancer. 3(1). 62–70. 122 indexed citations

12.

Wallace, Margaret R., Lone B. Andersen, Ann M. Saulino, et al.. (1991). A de novo Alu insertion results in neurofibromatosis type 1. Nature. 353(6347). 864–866. 356 indexed citations

13.

Andersen, Lone B., et al.. (1991). A highly polymorphic cDNA probe in theNF1gene. Nucleic Acids Research. 19(13). 3754–3754. 13 indexed citations

14.

Marchuk, Douglas A., Ann M. Saulino, Manju Swaroop, et al.. (1991). cDNA cloning of the type 1 neurofibromatosis gene: Complete sequence of the NF1 gene product. Genomics. 11(4). 931–940. 324 indexed citations

15.

Andersen, Lone B., Margaret R. Wallace, Douglas A. Marchuk, et al.. (1991). A polymorphic cDNA probe on chromosome 17q11.2 located within the NF1 gene [D17S376]. Nucleic Acids Research. 19(1). 197–197. 15 indexed citations

16.

Wallace, Margaret R., Lone B. Andersen, Jane W. Fountain, et al.. (1990). A chromosome jump crosses a translocation breakpoint in the von recklinghausen neurofibromatosis region. Genes Chromosomes and Cancer. 2(4). 271–277. 19 indexed citations

17.

Upadhyaya, Meena, Alan Fryer, Duncan J. Shaw, et al.. (1990). A 90 kb DNA deletion associated with neurofibromatosis type 1.. Journal of Medical Genetics. 27(12). 738–741. 26 indexed citations

18.

Andersen, Lone B., Niels Tommerup, & Jørn Koch. (1990). Formation of a minichromosome by excision of the proximal region of 17q in a patient with von Recklinghausen neurofibromatosis. Cytogenetic and Genome Research. 53(4). 206–210. 28 indexed citations

19.

Wallace, Margaret R., Douglas A. Marchuk, Lone B. Andersen, et al.. (1990). Type 1 Neurofibromatosis Gene: Identification of a Large Transcript Disrupted in Three NF1 Patients. Science. 249(4965). 181–186. 1155 indexed citations breakdown →

20.

Andersen, Lone B. & S. A. Sørensen. (1988). Diagnosis of von Recklinghausen neurofibromatosis and the Albright syndrome. Two case reports.. PubMed. 1(2). 120–3. 1 indexed citations

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.

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