Charlotte Forsell

6.0k total citations · 1 hit paper
35 papers, 1.7k citations indexed

About

Charlotte Forsell is a scholar working on Physiology, Molecular Biology and Neurology. According to data from OpenAlex, Charlotte Forsell has authored 35 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Physiology, 17 papers in Molecular Biology and 8 papers in Neurology. Recurrent topics in Charlotte Forsell's work include Alzheimer's disease research and treatments (23 papers), Bioinformatics and Genomic Networks (8 papers) and Prion Diseases and Protein Misfolding (6 papers). Charlotte Forsell is often cited by papers focused on Alzheimer's disease research and treatments (23 papers), Bioinformatics and Genomic Networks (8 papers) and Prion Diseases and Protein Misfolding (6 papers). Charlotte Forsell collaborates with scholars based in Sweden, Japan and United States. Charlotte Forsell's co-authors include Karin Axelman, Lars Lannfelt, Camilla Nilsberth, Margaret M. Condron, Christopher B. Eckman, David B. Teplow, Steven G. Younkin, Jan Näslund, Johan Luthman and Charlotte Stenh and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Neuroscience and PLoS ONE.

In The Last Decade

Charlotte Forsell

35 papers receiving 1.6k citations

Hit Papers

align trajectories sort by overperformance

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.

The 'Arctic' APP mutation (E693G) causes Alzheimer's disease by enhanced Aβ protofibril formation

2001 943 citations Camilla Nilsberth, Anita Westlind‐Danielsson et al. Nature Neuroscience profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Charlotte Forsell Sweden	18	1.3k	882	280	273	226	35	1.7k
Vicki Olm United States	8	1.2k 0.9×	704 0.8×	291 1.0×	146 0.5×	395 1.7×	8	1.7k
Pascal Kienlen‐Campard Belgium	27	1.4k 1.1×	1.3k 1.5×	320 1.1×	143 0.5×	503 2.2×	68	2.3k
K S Kosik United States	11	1.4k 1.0×	1.1k 1.2×	250 0.9×	207 0.8×	484 2.1×	16	2.1k
Janice Kurth United States	13	1.2k 0.9×	707 0.8×	318 1.1×	724 2.7×	498 2.2×	20	2.3k
Tsuneo Yamazaki Japan	23	1.7k 1.3×	1.0k 1.2×	292 1.0×	603 2.2×	419 1.9×	53	2.5k
Luisa Onstead United States	13	1.1k 0.8×	500 0.6×	333 1.2×	205 0.8×	249 1.1×	14	1.3k
Paul Fraser Canada	15	1.4k 1.0×	879 1.0×	348 1.2×	260 1.0×	420 1.9×	18	1.8k
Konstantinos Vekrellis United States	7	1.2k 0.9×	823 0.9×	274 1.0×	126 0.5×	348 1.5×	7	1.8k
Lena Lilius Sweden	19	1.7k 1.3×	1.1k 1.3×	366 1.3×	229 0.8×	389 1.7×	42	2.2k
Emi Hama Japan	8	1.6k 1.2×	794 0.9×	458 1.6×	150 0.5×	568 2.5×	8	2.1k

Countries citing papers authored by Charlotte Forsell

Since Specialization

Citations

This map shows the geographic impact of Charlotte Forsell'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 Charlotte Forsell with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Charlotte Forsell more than expected).

Fields of papers citing papers by Charlotte Forsell

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Charlotte Forsell. 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 Charlotte Forsell. The network helps show where Charlotte Forsell may publish in the future.

Co-authorship network of co-authors of Charlotte Forsell

This figure shows the co-authorship network connecting the top 25 collaborators of Charlotte Forsell. A scholar is included among the top collaborators of Charlotte Forsell 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 Charlotte Forsell. Charlotte Forsell 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

Samuelsson, Eva‐Britt, Kirsten Coupland, Charlotte Forsell, et al.. (2018). Differences in proliferation rate between CADASIL and control vascular smooth muscle cells are related to increased TGFβ expression. Journal of Cellular and Molecular Medicine. 22(6). 3016–3024. 13 indexed citations

Thonberg, Håkan, Huei‐Hsin Chiang, Lena Lilius, et al.. (2017). Identification and description of three families with familial Alzheimer disease that segregate variants in the SORL1 gene. Acta Neuropathologica Communications. 5(1). 43–43. 38 indexed citations

Chiang, Huei‐Hsin, Charlotte Forsell, Lena Lilius, et al.. (2016). No common founder for C9orf72 expansion mutation in Sweden. Journal of Human Genetics. 62(2). 321–324. 3 indexed citations

Chiang, Huei‐Hsin, Charlotte Forsell, Lena Lilius, et al.. (2013). Novel progranulin mutations with reduced serum-progranulin levels in frontotemporal lobar degeneration. European Journal of Human Genetics. 21(11). 1260–1265. 9 indexed citations

Sillén, Anna, Lena Lilius, Charlotte Forsell, et al.. (2011). Linkage to the 8p21.1 Region Including the CLU Gene in Age at Onset Stratified Alzheimer's Disease Families. Journal of Alzheimer s Disease. 23(1). 13–20. 4 indexed citations

Sillén, Anna, Jesper Brohede, Lena Lilius, et al.. (2010). Linkage to 20p13 including the ANGPT4 gene in families with mixed Alzheimer's disease and vascular dementia. Journal of Human Genetics. 55(10). 649–655. 7 indexed citations

Forsell, Charlotte, Lena Lilius, Karin Axelman, et al.. (2008). Genetic association to the amyloid plaque associated protein gene COL25A1 in Alzheimer's disease. Neurobiology of Aging. 31(3). 409–415. 29 indexed citations

Sillén, Anna, Charlotte Forsell, Lena Lilius, et al.. (2005). Genome scan on Swedish Alzheimer's disease families. Molecular Psychiatry. 11(2). 182–186. 26 indexed citations

Lilius, Lena, Charlotte Forsell, Karin Axelman, et al.. (2003). No association between polymorphisms in the neprilysin promoter region and Swedish Alzheimer's disease patients. Neuroscience Letters. 337(2). 111–113. 17 indexed citations

10.

Nilsberth, Camilla, Anita Westlind‐Danielsson, Christopher B. Eckman, et al.. (2001). The 'Arctic' APP mutation (E693G) causes Alzheimer's disease by enhanced Aβ protofibril formation. Nature Neuroscience. 4(9). 887–893. 943 indexed citations breakdown →

11.

Nilsberth, Camilla, Anita Westlind‐Danielsson, Christopher B. Eckman, et al.. (2000). The Arctic APP mutation (E693G) causes Alzheimer's disease through a novel mechanism: Increased amyloid βprotfibril formation and decreased amyloid βlevels in plasma and conditioned media. Neurobiology of Aging. 21. 58–58. 4 indexed citations

12.

Kowalska, Anna, et al.. (1999). A Polish pedigree with Alzheimer's disease determined by a novel mutation in exon 12 of the presenilin 1 gene: clinical and molecular characterization.. PubMed. 37(1). 57–61. 13 indexed citations

13.

Basun, Hans, Charlotte Forsell, Karin Axelman, et al.. (1999). Tau gene polymorphisms and apolipoprotein E ε4 may interact to increase risk for Alzheimer’s disease. Neuroscience Letters. 277(1). 29–32. 54 indexed citations

14.

Forsell, Charlotte, et al.. (1998). The Arg269His and Glu318Gly mutations in the presenilin-1 gene found in Swedish early-onset Alzheimer's disease families. 4 indexed citations

15.

Basun, Hans, Ove Almkvist, Karin Axelman, et al.. (1997). Clinical Characteristics of a Chromosome 17--Linked Rapidly Progressive Familial Frontotemporal Dementia. Archives of Neurology. 54(5). 539–544. 49 indexed citations

16.

Froelich, Susanne, Hans Basun, Charlotte Forsell, et al.. (1997). Mapping of a disease locus for familial rapidly progressive frontotemporal dementia to chromosome 17q12-21. American Journal of Medical Genetics. 74(4). 380–385. 68 indexed citations

17.

Forsell, Charlotte, Susanne Froelich, Karin Axelman, et al.. (1997). A novel pathogenic mutation (Leu262Phe) found in the presenilin 1 gene in early-onset Alzheimer's disease. Neuroscience Letters. 234(1). 3–6. 27 indexed citations

18.

Liu, Li, et al.. (1996). Allelic association but only weak evidence for linkage to the apolipoprotein E locus in late-onset Swedish Alzheimer families. American Journal of Medical Genetics. 67(3). 306–311. 17 indexed citations

19.

Garlind, Anita, Richard F. Cowburn, Charlotte Forsell, et al.. (1995). Diminished [3H]inositol(1,4,5)P3 but not [3H]inositol(1,3,4,5)P4 binding in Alzheimer's disease brain. Brain Research. 681(1-2). 160–166. 28 indexed citations

20.

Forsell, Charlotte & Lars Lannfelt. (1995). Amyloid precursor protein mutation at codon 713 (Ala → Val) does not cause schizophrenia: non-pathogenic variant found at codon 705 (silent). Neuroscience Letters. 184(2). 90–93. 15 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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