Outi Vierimaa

4.9k total citations
21 papers, 1.7k citations indexed

About

Outi Vierimaa is a scholar working on Epidemiology, Molecular Biology and Oncology. According to data from OpenAlex, Outi Vierimaa has authored 21 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Epidemiology, 7 papers in Molecular Biology and 5 papers in Oncology. Recurrent topics in Outi Vierimaa's work include Neuroendocrine Tumor Research Advances (7 papers), Pituitary Gland Disorders and Treatments (4 papers) and Renal cell carcinoma treatment (2 papers). Outi Vierimaa is often cited by papers focused on Neuroendocrine Tumor Research Advances (7 papers), Pituitary Gland Disorders and Treatments (4 papers) and Renal cell carcinoma treatment (2 papers). Outi Vierimaa collaborates with scholars based in Finland, United States and Italy. Outi Vierimaa's co-authors include Lauri A. Aaltonen, Virpi Launonen, Riitta Herva, ­Eero Pukkala, Maija Kiuru, Jorma Isola, Stina Roth, Pertti Sistonen, Pasi Salmela and Auli Karhu and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and The Journal of Clinical Endocrinology & Metabolism.

In The Last Decade

Outi Vierimaa

21 papers receiving 1.7k citations

Peers

Outi Vierimaa
Trisha Dwight Australia
Rudy M. Landsvater Netherlands
Kunio Mochizuki Japan
Ludmila Matyakhina United States
Branca Cavaco Portugal
Oskar Koperek Austria
Nelly Sabbaghian Canada
Sosipatros A. Boikos United States
Christine Do Cao France
Mabel Ryder United States
Trisha Dwight Australia
Outi Vierimaa
Citations per year, relative to Outi Vierimaa Outi Vierimaa (= 1×) peers Trisha Dwight

Countries citing papers authored by Outi Vierimaa

Since Specialization
Citations

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

Fields of papers citing papers by Outi Vierimaa

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Outi Vierimaa

This figure shows the co-authorship network connecting the top 25 collaborators of Outi Vierimaa. A scholar is included among the top collaborators of Outi Vierimaa 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 Outi Vierimaa. Outi Vierimaa 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.
Raitila, Anniina, Marianthi Georgitsi, Elena Bonora, et al.. (2009). Aryl hydrocarbon receptor interacting protein mutations seem not to associate with familial non-medullary thyroid cancer. Journal of Endocrinological Investigation. 32(5). 426–429. 9 indexed citations
2.
Heliövaara, Elina, Anniina Raitila, Virpi Launonen, et al.. (2009). The Expression of AIP-Related Molecules in Elucidation of Cellular Pathways in Pituitary Adenomas. American Journal Of Pathology. 175(6). 2501–2507. 48 indexed citations
3.
Vierimaa, Outi, Andrea Villablanca, Andrei Alimov, et al.. (2009). Mutation analysis of MEN1, HRPT2, CASR, CDKN1B, and AIP genes in primary hyperparathyroidism patients with features of genetic predisposition. Journal of Endocrinological Investigation. 32(6). 512–518. 23 indexed citations
4.
Nellist, Mark, Diana van den Heuvel, Miriam Goedbloed, et al.. (2008). Missense mutations to the TSC1 gene cause tuberous sclerosis complex. European Journal of Human Genetics. 17(3). 319–328. 21 indexed citations
5.
Gylling, Annette, Maaret Ridanpää, Outi Vierimaa, et al.. (2008). Large genomic rearrangements and germline epimutations in Lynch syndrome. International Journal of Cancer. 124(10). 2333–2340. 71 indexed citations
6.
Vierimaa, Outi. (2008). Multiple Endocrine Neoplasia Type 1 (MEN1) and Pituitary Adenoma Predisposition (PAP) in Northern Finland. 6 indexed citations
7.
Georgitsi, Marianthi, Elina Heliövaara, Ralf Paschke, et al.. (2008). Large Genomic Deletions inAIPin Pituitary Adenoma Predisposition. The Journal of Clinical Endocrinology & Metabolism. 93(10). 4146–4151. 60 indexed citations
8.
Vierimaa, Outi, Tapani Ebeling, Soili Kytölä, et al.. (2007). Multiple endocrine neoplasia type 1 in Northern Finland; clinical features and genotype–phenotype correlation. European Journal of Endocrinology. 157(3). 285–294. 35 indexed citations
9.
Georgitsi, Marianthi, Anniina Raitila, Auli Karhu, et al.. (2007). Molecular diagnosis of pituitary adenoma predisposition caused by aryl hydrocarbon receptor-interacting protein gene mutations. Proceedings of the National Academy of Sciences. 104(10). 4101–4105. 123 indexed citations
10.
Vierimaa, Outi, Marianthi Georgitsi, Rainer Lehtonen, et al.. (2006). Pituitary Adenoma Predisposition Caused by Germline Mutations in the AIP Gene. Science. 312(5777). 1228–1230. 408 indexed citations
11.
Ebeling, Tapani, Outi Vierimaa, Soili Kytölä, Jaakko Leisti, & Pasi Salmela. (2004). Effect of Multiple Endocrine Neoplasia Type 1 (MEN1) Gene Mutations on Premature Mortality in Familial MEN1 Syndrome with Founder Mutations. The Journal of Clinical Endocrinology & Metabolism. 89(7). 3392–3396. 18 indexed citations
12.
Villablanca, Andrea, Thomas G. Smith, Anders Höög, et al.. (2002). Involvement of the MEN1 gene locus in familial isolated hyperparathyroidism. European Journal of Endocrinology. 147(3). 313–322. 36 indexed citations
13.
Karim, Mohammad A., Koji Suzuki, Jangsuk Oh, et al.. (2002). Apparent genotype–phenotype correlation in childhood, adolescent, and adult Chediak‐Higashi syndrome. American Journal of Medical Genetics. 108(1). 16–22. 3 indexed citations
14.
Kiuru, Maija, Virpi Launonen, Marja Hietala, et al.. (2001). Familial Cutaneous Leiomyomatosis Is a Two-Hit Condition Associated with Renal Cell Cancer of Characteristic Histopathology. American Journal Of Pathology. 159(3). 825–829. 134 indexed citations
15.
Launonen, Virpi, Outi Vierimaa, Maija Kiuru, et al.. (2001). Inherited susceptibility to uterine leiomyomas and renal cell cancer. Proceedings of the National Academy of Sciences. 98(6). 3387–3392. 454 indexed citations
16.
Tsao, Jen‐Lan, Anu Loukola, Minna Pöyhönen, et al.. (2001). Extensive somatic microsatellite mutations in normal human tissue.. PubMed. 61(11). 4541–4. 73 indexed citations
17.
Lohiniva, Jaana, Petteri Paassilta, Ulpu Seppänen, et al.. (2000). Splicing mutations in the COL3 domain of collagen IX cause multiple epiphyseal dysplasia. American Journal of Medical Genetics. 90(3). 216–216. 3 indexed citations
18.
Lohiniva, Jaana, et al.. (2000). Splicing mutations in the COL3 domain of collagen IX cause multiple epiphyseal dysplasia. American Journal of Medical Genetics. 90(3). 216–222. 42 indexed citations
19.
Juvonen, Vesa, Marja Hietala, Markku Päivärinta, et al.. (2000). Clinical and genetic findings in Finnish ataxia patients with the spinocerebellar ataxia 8 repeat expansion. Annals of Neurology. 48(3). 354–361. 56 indexed citations
20.
Juvonen, Vesa, Marja Hietala, Markku Päivärinta, et al.. (2000). Clinical and genetic findings in Finnish ataxia patients with the spinocerebellar ataxia 8 repeat expansion. Annals of Neurology. 48(3). 354–361. 3 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Trisha Dwight Breakdown of academic impact, for papers by Rudy M. Landsvater Breakdown of academic impact, for papers by Kunio Mochizuki Breakdown of academic impact, for papers by Ludmila Matyakhina Breakdown of academic impact, for papers by Branca Cavaco Breakdown of academic impact, for papers by Oskar Koperek Breakdown of academic impact, for papers by Nelly Sabbaghian Breakdown of academic impact, for papers by Sosipatros A. Boikos Breakdown of academic impact, for papers by Christine Do Cao Breakdown of academic impact, for papers by Mabel Ryder
Rankless by CCL
2026