Netta Mäkinen

3.6k total citations · 1 hit paper
26 papers, 1.9k citations indexed

About

Netta Mäkinen is a scholar working on Obstetrics and Gynecology, Reproductive Medicine and Pathology and Forensic Medicine. According to data from OpenAlex, Netta Mäkinen has authored 26 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Obstetrics and Gynecology, 19 papers in Reproductive Medicine and 4 papers in Pathology and Forensic Medicine. Recurrent topics in Netta Mäkinen's work include Uterine Myomas and Treatments (19 papers), Endometriosis Research and Treatment (14 papers) and Ovarian cancer diagnosis and treatment (7 papers). Netta Mäkinen is often cited by papers focused on Uterine Myomas and Treatments (19 papers), Endometriosis Research and Treatment (14 papers) and Ovarian cancer diagnosis and treatment (7 papers). Netta Mäkinen collaborates with scholars based in Finland, Sweden and United States. Netta Mäkinen's co-authors include Pia Vahteristo, Lauri A. Aaltonen, Hanna-Riikka Heinonen, Miika Mehine, Ralf Bützow, Kati Kämpjärvi, Jari Sjöberg, Eevi Kaasinen, Mervi Aavikko and Esa Pitkänen and has published in prestigious journals such as Science, New England Journal of Medicine and Proceedings of the National Academy of Sciences.

In The Last Decade

Netta Mäkinen

26 papers receiving 1.9k 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.

MED12 , the Mediator Complex Subunit 12 Gene, Is Mutated at High Frequency in Uterine Leiomyomas

2011 470 citations Netta Mäkinen, Miika Mehine 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
Netta Mäkinen Finland	18	1.4k	1.1k	328	302	202	26	1.9k
Heli Lehtonen Finland	15	491 0.4×	386 0.3×	429 1.3×	265 0.9×	181 0.9×	19	1.2k
Mervi Aavikko Finland	15	585 0.4×	501 0.4×	352 1.1×	209 0.7×	203 1.0×	27	1.3k
Kari L. Ring United States	20	467 0.3×	406 0.4×	269 0.8×	154 0.5×	377 1.9×	74	1.3k
Ulla‐Maria Flodérus Sweden	13	283 0.2×	275 0.2×	185 0.6×	227 0.8×	165 0.8×	14	746
Peter Lim Canada	16	1.1k 0.8×	806 0.7×	172 0.5×	145 0.5×	108 0.5×	32	1.5k
Jim Biagi Canada	10	252 0.2×	275 0.2×	238 0.7×	104 0.3×	106 0.5×	17	648
Amanda Gordon United States	7	137 0.1×	400 0.3×	191 0.6×	107 0.4×	116 0.6×	15	801
Keiji Kato Japan	17	129 0.1×	117 0.1×	352 1.1×	324 1.1×	50 0.2×	46	988
Marcella Falchetti Italy	16	231 0.2×	234 0.2×	225 0.7×	126 0.4×	39 0.2×	19	803
Pilar Fernández Machín Spain	9	262 0.2×	198 0.2×	280 0.9×	66 0.2×	279 1.4×	19	710

Countries citing papers authored by Netta Mäkinen

Since Specialization

Citations

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

Fields of papers citing papers by Netta Mäkinen

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Netta Mäkinen

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

Mäkinen, Netta, Meng Zhou, Zhouwei Zhang, et al.. (2022). Whole genome sequencing reveals the independent clonal origin of multifocal ileal neuroendocrine tumors. Genome Medicine. 14(1). 82–82. 12 indexed citations

Mäkinen, Netta, Meng Zhou, Anwesha Nag, et al.. (2021). Genomic Evolution in a Patient With Lung Adenocarcinoma With a Germline EGFR T790M Mutation. JTO Clinical and Research Reports. 2(4). 100146–100146. 3 indexed citations

Zhang, Zhouwei, Netta Mäkinen, Yosuke Kasai, et al.. (2020). Patterns of chromosome 18 loss of heterozygosity in multifocal ileal neuroendocrine tumors. Genes Chromosomes and Cancer. 59(9). 535–539. 11 indexed citations

Hänninen, Ulrika A., Erkki‐Ville Wirta, Riku Katainen, et al.. (2019). Exome and immune cell score analyses reveal great variation within synchronous primary colorectal cancers. British Journal of Cancer. 120(9). 922–930. 4 indexed citations

Hänninen, Ulrika A., Riku Katainen, Tomas Tanskanen, et al.. (2018). Exome-wide somatic mutation characterization of small bowel adenocarcinoma. PLoS Genetics. 14(3). e1007200–e1007200. 54 indexed citations

Heinonen, Hanna-Riikka, Miika Mehine, Netta Mäkinen, et al.. (2017). Global metabolomic profiling of uterine leiomyomas. British Journal of Cancer. 117(12). 1855–1864. 32 indexed citations

Mäkinen, Netta, Kati Kämpjärvi, Norma Frizzell, Ralf Bützow, & Pia Vahteristo. (2017). Characterization of MED12, HMGA2, and FH alterations reveals molecular variability in uterine smooth muscle tumors. Molecular Cancer. 16(1). 101–101. 75 indexed citations

Heinonen, Hanna-Riikka, Annukka Pasanen, Oskari Heikinheimo, et al.. (2017). Multiple clinical characteristics separate MED12-mutation-positive and -negative uterine leiomyomas. Scientific Reports. 7(1). 1015–1015. 43 indexed citations

Mehine, Miika, Eevi Kaasinen, Hanna-Riikka Heinonen, et al.. (2016). Integrated data analysis reveals uterine leiomyoma subtypes with distinct driver pathways and biomarkers. Proceedings of the National Academy of Sciences. 113(5). 1315–1320. 157 indexed citations

10.

Mäkinen, Netta, Mervi Aavikko, Tuomas Heikkinen, et al.. (2016). Exome Sequencing of Uterine Leiomyosarcomas Identifies Frequent Mutations in TP53, ATRX, and MED12. PLoS Genetics. 12(2). e1005850–e1005850. 81 indexed citations

11.

Kämpjärvi, Kati, Netta Mäkinen, Miika Mehine, et al.. (2016). MED12 mutations and FH inactivation are mutually exclusive in uterine leiomyomas. British Journal of Cancer. 114(12). 1405–1411. 36 indexed citations

12.

Mehine, Miika, Hanna-Riikka Heinonen, Nanna Sarvilinna, et al.. (2015). Clonally related uterine leiomyomas are common and display branched tumor evolution. Human Molecular Genetics. 24(15). 4407–4416. 17 indexed citations

13.

Mäkinen, Netta, Hanna-Riikka Heinonen, J Sjöberg, et al.. (2014). Mutation analysis of components of the Mediator kinase module in MED12 mutation-negative uterine leiomyomas. British Journal of Cancer. 110(9). 2246–2249. 15 indexed citations

14.

Mehine, Miika, Netta Mäkinen, Hanna-Riikka Heinonen, Lauri A. Aaltonen, & Pia Vahteristo. (2014). Genomics of uterine leiomyomas: insights from high-throughput sequencing. Fertility and Sterility. 102(3). 621–629. 149 indexed citations

15.

Heinonen, Hanna-Riikka, Nanna Sarvilinna, Jari Sjöberg, et al.. (2014). MED12 mutation frequency in unselected sporadic uterine leiomyomas. Fertility and Sterility. 102(4). 1137–1142. 58 indexed citations

16.

Mäkinen, Netta, Pia Vahteristo, Kati Kämpjärvi, et al.. (2013). MED12 exon 2 mutations in histopathological uterine leiomyoma variants. European Journal of Human Genetics. 21(11). 1300–1303. 62 indexed citations

17.

Mehine, Miika, Eevi Kaasinen, Netta Mäkinen, et al.. (2013). Characterization of Uterine Leiomyomas by Whole-Genome Sequencing. New England Journal of Medicine. 369(1). 43–53. 252 indexed citations

18.

Mäkinen, Netta, Pia Vahteristo, Ralf Bützow, Jari Sjöberg, & Lauri A. Aaltonen. (2013). Exomic landscape of MED12 mutation‐negative and ‐positive uterine leiomyomas. International Journal of Cancer. 134(4). 1008–1012. 30 indexed citations

19.

Kämpjärvi, Kati, Netta Mäkinen, Outi Kilpivaara, et al.. (2012). Somatic MED12 mutations in uterine leiomyosarcoma and colorectal cancer. British Journal of Cancer. 107(10). 1761–1765. 87 indexed citations

20.

Mäkinen, Netta, Miika Mehine, Jaana Tolvanen, et al.. (2011). MED12 , the Mediator Complex Subunit 12 Gene, Is Mutated at High Frequency in Uterine Leiomyomas. Science. 334(6053). 252–255. 470 indexed citations breakdown →

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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