Riikka E. Mäkitie

978 total citations
38 papers, 616 citations indexed

About

Riikka E. Mäkitie is a scholar working on Genetics, Molecular Biology and Oncology. According to data from OpenAlex, Riikka E. Mäkitie has authored 38 papers receiving a total of 616 indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Genetics, 23 papers in Molecular Biology and 10 papers in Oncology. Recurrent topics in Riikka E. Mäkitie's work include Connective tissue disorders research (17 papers), Bone health and treatments (10 papers) and Wnt/β-catenin signaling in development and cancer (6 papers). Riikka E. Mäkitie is often cited by papers focused on Connective tissue disorders research (17 papers), Bone health and treatments (10 papers) and Wnt/β-catenin signaling in development and cancer (6 papers). Riikka E. Mäkitie collaborates with scholars based in Finland, Sweden and United Kingdom. Riikka E. Mäkitie's co-authors include Outi Mäkitie, Anders Kämpe, Alice Costantini, Minna Pekkinen, Jessica J. Alm, Matthias Hackl, Johannes Grillari, Sakari Kakko, Riitta Niinimäki and Christine Lainé and has published in prestigious journals such as The Journal of Clinical Endocrinology & Metabolism, Journal of Bone and Mineral Research and Frontiers in Immunology.

In The Last Decade

Riikka E. Mäkitie

34 papers receiving 612 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Riikka E. Mäkitie Finland 16 386 306 134 125 114 38 616
Alice Costantini Sweden 13 255 0.7× 263 0.9× 91 0.7× 66 0.5× 42 0.4× 28 430
Els Van Hul Belgium 9 536 1.4× 251 0.8× 222 1.7× 69 0.6× 51 0.4× 15 739
María Isabel Pérez‐Núñez Spain 12 394 1.0× 107 0.3× 87 0.6× 155 1.2× 133 1.2× 42 597
Danese M. Joiner United States 10 334 0.9× 88 0.3× 111 0.8× 89 0.7× 51 0.4× 11 491
Sachi P. Deschenes United States 7 160 0.4× 259 0.8× 71 0.5× 116 0.9× 41 0.4× 7 414
Tomoo Yamate Japan 9 289 0.7× 119 0.4× 191 1.4× 82 0.7× 48 0.4× 11 547
Weiguang Zhao China 5 437 1.1× 87 0.3× 114 0.9× 162 1.3× 30 0.3× 10 581
Marta Maycas Spain 10 375 1.0× 69 0.2× 233 1.7× 176 1.4× 34 0.3× 11 560
Forest Lai United States 7 311 0.8× 56 0.2× 189 1.4× 148 1.2× 43 0.4× 7 497
Lesya Zelenchuk United States 10 176 0.5× 92 0.3× 88 0.7× 82 0.7× 20 0.2× 13 369

Countries citing papers authored by Riikka E. Mäkitie

Since Specialization
Citations

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

Fields of papers citing papers by Riikka E. Mäkitie

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Riikka E. Mäkitie. 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 Riikka E. Mäkitie. The network helps show where Riikka E. Mäkitie may publish in the future.

Co-authorship network of co-authors of Riikka E. Mäkitie

This figure shows the co-authorship network connecting the top 25 collaborators of Riikka E. Mäkitie. A scholar is included among the top collaborators of Riikka E. Mäkitie 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 Riikka E. Mäkitie. Riikka E. Mäkitie 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.
Oghabian, Ali, Kirsi Määttä, Riikka E. Mäkitie, et al.. (2025). Transcriptomic and lipidomic profiling provide novel insight into the pathogenesis of monogenic SGMS2 -related osteoporosis. JBMR Plus. 9(10). ziaf128–ziaf128.
2.
Määttä, Kirsi, Yu‐Chia Chen, Riikka E. Mäkitie, et al.. (2025). Utilizing CRISPR-Cas13d-knockdown in zebrafish to study a rare monogenic bone fragility syndrome. JBMR Plus. 9(11). ziaf153–ziaf153.
3.
Nieminen, Mikko T., et al.. (2024). Fibrous dysplasia of the head and neck in Southern Finland: a retrospective study on clinical characteristics, diagnostics, and treatment. European Archives of Oto-Rhino-Laryngology. 281(6). 3189–3195.
4.
Hauta‐alus, Helena, et al.. (2022). Lipocalin-2 is associated with FGF23 in WNT1 and PLS3 osteoporosis. Frontiers in Endocrinology. 13. 954730–954730. 3 indexed citations
5.
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
6.
Mäkitie, Riikka E., Stéphane Blouin, Ville‐Valtteri Välimäki, et al.. (2021). Abnormal Bone Tissue Organization and Osteocyte Lacunocanalicular Network in Early‐Onset Osteoporosis Due to SGMS2 Mutations. JBMR Plus. 5(11). e10537–e10537. 11 indexed citations
7.
Fratzl‐Zelman, Nadja, Katherine Wesseling‐Perry, Riikka E. Mäkitie, et al.. (2021). Bone material properties and response to teriparatide in osteoporosis due to WNT1 and PLS3 mutations. Bone. 146. 115900–115900. 10 indexed citations
8.
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
9.
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
10.
Costantini, Alice, Riikka E. Mäkitie, Markus A. Hartmann, et al.. (2020). Early-Onset Osteoporosis: Rare Monogenic Forms Elucidate the Complexity of Disease Pathogenesis Beyond Type I Collagen. Journal of Bone and Mineral Research. 37(9). 1623–1641. 18 indexed citations
11.
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
12.
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
13.
Mäkitie, Riikka E., et al.. (2018). Recessive multiple epiphyseal dysplasia – Clinical characteristics caused by rare compound heterozygous SLC26A2 genotypes. European Journal of Medical Genetics. 62(11). 103573–103573. 9 indexed citations
14.
Mäkitie, Riikka E., et al.. (2018). A novel MYT1L mutation in a patient with severe early‐onset obesity and intellectual disability. American Journal of Medical Genetics Part A. 176(9). 1972–1975. 21 indexed citations
15.
Vakkilainen, Svetlana, Riikka E. Mäkitie, Paula Klemetti, et al.. (2018). A Wide Spectrum of Autoimmune Manifestations and Other Symptoms Suggesting Immune Dysregulation in Patients With Cartilage-Hair Hypoplasia. Frontiers in Immunology. 9. 2468–2468. 14 indexed citations
16.
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
17.
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
18.
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
19.
Wesseling‐Perry, Katherine, Riikka E. Mäkitie, Ville‐Valtteri Välimäki, et al.. (2017). Osteocyte Protein Expression Is Altered in Low-Turnover Osteoporosis Caused by Mutations in WNT1 and PLS3. The Journal of Clinical Endocrinology & Metabolism. 102(7). 2340–2348. 25 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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