Netta Mäkinen

3.6k citations
26 papers · 1.9k · 1 hit paper · h-index 18

Impact in

    • Uterine Myomas and Treatments
    • Gynecological conditions and treatments
    • Endometrial and Cervical Cancer Treatments
    • Endometriosis Research and Treatment
    • Ovarian cancer diagnosis and treatment

Papers in

    • Uterine Myomas and Treatments 19
    • Gynecological conditions and treatments 6
    • Endometrial and Cervical Cancer Treatments 5
    • Endometriosis Research and Treatment 14
    • Ovarian cancer diagnosis and treatment 7

Netta Mäkinen

26 papers receiving 1.9k citations

Hit Papers

MED12 , the Mediator Complex Subunit 12 Gene, Is Mutated at High Frequency in Uterine Leiomyomas 2011 · 470 citations
4700+5+10Years since publication100200300400

Peers

Netta Mäkinen
Comparison fields: 5 of 55
  • Obstetrics and Gynecology 1.4k
  • Reproductive Medicine 1.1k
  • Cancer Research 170
  • Pathology and Forensic Medicine 202
  • Gastroenterology 52
Replace Heli Lehtonen with:
Heli Lehtonen Finland
Mervi Aavikko Finland
Kari L. Ring United States
Ulla‐Maria Flodérus Sweden
Peter Lim Canada
Amanda Gordon United States
Jim Biagi Canada
Keiji Kato Japan
Malti Kshirsagar United States
Joanna Przybył United States
Netta Mäkinen relative to Heli Lehtonen Finland Heli Lehtonen's profile →
Citations per field
00.5×3.0×
Heli Lehtonen · 1×
Citations per year

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-authors

The 25 scholars most cited alongside Netta Mäkinen, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Netta Mäkinen Line = papers co-authored together Netta Mäkinen links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 26 papers — load more, or switch the sort, to bring in the rest.

#Work
1
MED12 , the Mediator Complex Subunit 12 Gene, Is Mutated at High Frequency in Uterine Leiomyomas
Hit paper breakdown →
2011470
2 2013252
3 2016157
4 2014149
5 2014123
6 201189
7 201287
8 201681
9 201775
10 201362
11 201458
12 201854
13 201743
14 201636
15 201732
16 201330
17 201825
18 201517
19 201415
20 202212

About Netta Mäkinen

Netta Mäkinen is a scholar working on Obstetrics and Gynecology, Reproductive Medicine, Pathology and Forensic Medicine, Pulmonary and Respiratory Medicine and Oncology, having authored 26 papers that have together received 1.9k indexed citations. Recurring topics across this work include Uterine Myomas and Treatments (19 papers), Endometriosis Research and Treatment (14 papers), Ovarian cancer diagnosis and treatment (7 papers), Gynecological conditions and treatments (6 papers), Endometrial and Cervical Cancer Treatments (5 papers), Genetic factors in colorectal cancer (3 papers), Cancer Genomics and Diagnostics (2 papers) and Pancreatic and Hepatic Oncology Research (2 papers). The work is most often cited by research in Obstetrics and Gynecology (1.4k citations), Reproductive Medicine (1.1k citations), Cancer Research (170 citations), Pathology and Forensic Medicine (202 citations) and Gastroenterology (52 citations). Netta Mäkinen has collaborated with scholars based in Finland, Sweden and United States. Frequent co-authors include Pia Vahteristo, Lauri A. Aaltonen, Hanna-Riikka Heinonen, Miika Mehine, Ralf Bützow, Jari Sjöberg, Kati Kämpjärvi, Eevi Kaasinen, Mervi Aavikko and Esa Pitkänen. Their work appears in journals such as British Journal of Cancer, Human Molecular Genetics, PLoS Genetics, Fertility and Sterility and Genome Medicine.

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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