Anders Kämpe

743 total citations
21 papers, 407 citations indexed

About

Anders Kämpe is a scholar working on Genetics, Oncology and Molecular Biology. According to data from OpenAlex, Anders Kämpe has authored 21 papers receiving a total of 407 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Genetics, 8 papers in Oncology and 7 papers in Molecular Biology. Recurrent topics in Anders Kämpe's work include Connective tissue disorders research (11 papers), Bone health and treatments (8 papers) and Bone Metabolism and Diseases (5 papers). Anders Kämpe is often cited by papers focused on Connective tissue disorders research (11 papers), Bone health and treatments (8 papers) and Bone Metabolism and Diseases (5 papers). Anders Kämpe collaborates with scholars based in Sweden, Finland and United Kingdom. Anders Kämpe's co-authors include Outi Mäkitie, Riikka E. Mäkitie, Alice Costantini, Fulya Taylan, Jessica J. Alm, Minna Pekkinen, Hong Jiao, Anna Lindstrand, Per Magnusson and Artemis Doulgeraki and has published in prestigious journals such as American Journal of Psychiatry, Journal of Bone and Mineral Research and PLoS Genetics.

In The Last Decade

Anders Kämpe

20 papers receiving 404 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Anders Kämpe Sweden 14 250 225 93 71 61 21 407
Steinunn Snorradóttir Iceland 2 142 0.6× 203 0.9× 69 0.7× 135 1.9× 33 0.5× 2 303
Tonya Fishburn United States 8 249 1.0× 338 1.5× 103 1.1× 118 1.7× 57 0.9× 8 506
Chiara Verdelli Italy 15 197 0.8× 284 1.3× 148 1.6× 25 0.4× 18 0.3× 38 563
Shino Kondoh Japan 5 100 0.4× 262 1.2× 130 1.4× 133 1.9× 17 0.3× 8 406
Kathleen A. Bishop United States 12 120 0.5× 237 1.1× 120 1.3× 43 0.6× 34 0.6× 13 528
Larisa Sereda United States 8 275 1.1× 294 1.3× 100 1.1× 246 3.5× 55 0.9× 10 538
Colette Fong-Yee Australia 9 46 0.2× 118 0.5× 144 1.5× 52 0.7× 40 0.7× 12 344
Nabil Kaci France 10 316 1.3× 355 1.6× 60 0.6× 8 0.1× 33 0.5× 18 487
Jarrod P. Skinner Australia 9 42 0.2× 225 1.0× 62 0.7× 39 0.5× 16 0.3× 12 316
Udo Schnitzbauer Switzerland 11 138 0.6× 187 0.8× 53 0.6× 11 0.2× 22 0.4× 17 396

Countries citing papers authored by Anders Kämpe

Since Specialization
Citations

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

Fields of papers citing papers by Anders Kämpe

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Anders Kämpe

This figure shows the co-authorship network connecting the top 25 collaborators of Anders Kämpe. A scholar is included among the top collaborators of Anders Kämpe 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 Anders Kämpe. Anders Kämpe is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Kvist, Anders, Anders Kämpe, Therese Törngren, et al.. (2025). Polygenic scores in Familial breast cancer cases with and without pathogenic variants and the risk of contralateral breast cancer. Breast Cancer Research. 27(1). 160–160.
2.
Partanen, Juulia, Paavo Häppölä, Anders Kämpe, et al.. (2024). High Burden of Ileus and Pneumonia in Clozapine-Treated Individuals With Schizophrenia: A Finnish 25-Year Follow-Up Register Study. American Journal of Psychiatry. 181(10). 879–892. 13 indexed citations
3.
Baliakas, Panagiotis, Arielle R. Munters, Anders Kämpe, et al.. (2023). Integrating a Polygenic Risk Score into a clinical setting would impact risk predictions in familial breast cancer. Journal of Medical Genetics. 61(2). 150–154. 4 indexed citations
4.
Mäkitie, Riikka E., Petra Henning, Yaming Jiu, et al.. (2021). An ARHGAP25 variant links aberrant Rac1 function to early‐onset skeletal fragility. JBMR Plus. 5(7). e10509–e10509. 7 indexed citations
5.
Formosa, Melissa M., Dylan J. M. Bergen, Celia L. Gregson, et al.. (2021). A Roadmap to Gene Discoveries and Novel Therapies in Monogenic Low and High Bone Mass Disorders. Frontiers in Endocrinology. 12. 709711–709711. 15 indexed citations
6.
Manousaki, Despoina, Anders Kämpe, Vincenzo Forgetta, et al.. (2020). Increased Burden of Common Risk Alleles in Children With a Significant Fracture History. Journal of Bone and Mineral Research. 35(5). 875–882. 1 indexed citations
7.
Mäkitie, Riikka E., Matthias Hackl, Moritz Weigl, et al.. (2020). Unique, Gender-Dependent Serum microRNA Profile in PLS3 Gene-Related Osteoporosis. Journal of Bone and Mineral Research. 35(10). 1962–1973. 17 indexed citations
8.
Mäkitie, Riikka E., Anders Kämpe, Alice Costantini, et al.. (2020). Biomarkers in WNT1 and PLS3 Osteoporosis: Altered Concentrations of DKK1 and FGF23. Journal of Bone and Mineral Research. 35(5). 901–912. 22 indexed citations
9.
Mäkitie, Riikka E., Heli Viljakainen, Anders Kämpe, et al.. (2020). Rare Variants in Genes Linked to Appetite Control and Hypothalamic Development in Early-Onset Severe Obesity. Frontiers in Endocrinology. 11. 81–81. 25 indexed citations
10.
Mäkitie, Riikka E., Tuukka Niinimäki, Maria Suo‐Palosaari, et al.. (2020). PLS3 Mutations Cause Severe Age and Sex-Related Spinal Pathology. Frontiers in Endocrinology. 11. 393–393. 13 indexed citations
11.
Kämpe, Anders, Maria Enlund-Cerullo, Saara Valkama, et al.. (2020). Genetic variation in GC and CYP2R1 affects 25-hydroxyvitamin D concentration and skeletal parameters: A genome-wide association study in 24-month-old Finnish children. Yearbook of pediatric endocrinology. 1 indexed citations
12.
Kämpe, Anders, Maria Enlund-Cerullo, Saara Valkama, et al.. (2019). Genetic variation in GC and CYP2R1 affects 25-hydroxyvitamin D concentration and skeletal parameters: A genome-wide association study in 24-month-old Finnish children. PLoS Genetics. 15(12). e1008530–e1008530. 14 indexed citations
13.
Mäkitie, Riikka E., Alice Costantini, Anders Kämpe, Jessica J. Alm, & Outi Mäkitie. (2019). New Insights Into Monogenic Causes of Osteoporosis. Frontiers in Endocrinology. 10. 70–70. 72 indexed citations
14.
Costantini, Alice, Sini Skarp, Anders Kämpe, et al.. (2018). Rare Copy Number Variants in Array-Based Comparative Genomic Hybridization in Early-Onset Skeletal Fragility. Frontiers in Endocrinology. 9. 380–380. 24 indexed citations
15.
Costantini, Alice, et al.. (2018). A novel frameshift deletion in PLS3 causing severe primary osteoporosis. Journal of Human Genetics. 63(8). 923–926. 17 indexed citations
16.
Kämpe, Anders, Alice Costantini, Riikka E. Mäkitie, et al.. (2017). PLS3 sequencing in childhood-onset primary osteoporosis identifies two novel disease-causing variants. Osteoporosis International. 28(10). 3023–3032. 34 indexed citations
17.
Mäkitie, Riikka E., Anders Kämpe, Fulya Taylan, & Outi Mäkitie. (2017). Recent Discoveries in Monogenic Disorders of Childhood Bone Fragility. Current Osteoporosis Reports. 15(4). 303–310. 17 indexed citations
18.
Kämpe, Anders, Alice Costantini, Yael Levy‐Shraga, et al.. (2017). PLS3 Deletions Lead to Severe Spinal Osteoporosis and Disturbed Bone Matrix Mineralization. Journal of Bone and Mineral Research. 32(12). 2394–2404. 36 indexed citations
19.
Taylan, Fulya, Alice Costantini, Minna Pekkinen, et al.. (2016). Spondyloocular Syndrome: Novel Mutations in XYLT2 Gene and Expansion of the Phenotypic Spectrum. Journal of Bone and Mineral Research. 31(8). 1577–1585. 39 indexed citations
20.
Kämpe, Anders, Riikka E. Mäkitie, & Outi Mäkitie. (2015). New Genetic Forms of Childhood-Onset Primary Osteoporosis. Hormone Research in Paediatrics. 84(6). 361–369. 26 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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