Elmo Saarentaus

5.5k total citations
9 papers, 97 citations indexed

About

Elmo Saarentaus is a scholar working on Genetics, Molecular Biology and Otorhinolaryngology. According to data from OpenAlex, Elmo Saarentaus has authored 9 papers receiving a total of 97 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Genetics, 2 papers in Molecular Biology and 2 papers in Otorhinolaryngology. Recurrent topics in Elmo Saarentaus's work include Genomic variations and chromosomal abnormalities (3 papers), Genomics and Rare Diseases (2 papers) and Sinusitis and nasal conditions (2 papers). Elmo Saarentaus is often cited by papers focused on Genomic variations and chromosomal abnormalities (3 papers), Genomics and Rare Diseases (2 papers) and Sinusitis and nasal conditions (2 papers). Elmo Saarentaus collaborates with scholars based in Finland, United States and Sweden. Elmo Saarentaus's co-authors include Aarno Palotie, Mitja Kurki, Samuli Ripatti, Aki S. Havulinna, Andrea Ganna, Jukka S. Moilanen, Benjamin M. Neale, Eija Hämäläinen, Outi Kuismin and Sanna Toppila‐Salmi and has published in prestigious journals such as Nature Communications, Scientific Reports and Molecular Psychiatry.

In The Last Decade

Elmo Saarentaus

7 papers receiving 97 citations

Peers

Elmo Saarentaus

GENET

MB

CN

PMH

SURGE

J. Körber Germany

Engy A. Ashaat Egypt

Radka Kremlíková Pourová Czechia

Jennifer Tarpinian United States

Candace Muss United States

Chin Yang Shapland United Kingdom

Eva Maria C. Cutiongco–de la Paz Philippines

Billur Moghaddam United States

Virginia Clowes United Kingdom

Allan L. Naarden United States

J. Körber Germany

Elmo Saarentaus

26 ×0.5

GENET

19 ×0.8

MB

12 ×0.5

CN

10 ×0.8

PMH

12 ×1.1

SURGE

Citations per year, relative to Elmo Saarentaus Elmo Saarentaus (= 1×) peers J. Körber

Countries citing papers authored by Elmo Saarentaus

Since Specialization

Citations

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

Fields of papers citing papers by Elmo Saarentaus

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Elmo Saarentaus

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

All Works

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9 of 9 papers shown

1.

Saarentaus, Elmo, Eeva Sliz, Argyro Bizaki-Vallaskangas, et al.. (2025). 131 genetic loci highlight immunological pathways and tissues in nasal polyposis and asthma. Nature Communications. 16(1). 9879–9879.

2.

Bizaki-Vallaskangas, Argyro, Joel Rämö, Eeva Sliz, et al.. (2024). Genome-wide association study indicates novel associations of annexin A13 to secretory and GAS2L2 with mucous otitis media. Scientific Reports. 14(1). 18344–18344.

3.

Hassan, Shabbeer, Elmo Saarentaus, Sanni Ruotsalainen, et al.. (2023). Genome-wide association study of varicose veins identifies a protective missense variant in GJD3 enriched in the Finnish population. Communications Biology. 6(1). 71–71. 12 indexed citations

4.

Saarentaus, Elmo, Juha Karjalainen, Joel Rämö, et al.. (2023). Inflammatory and infectious upper respiratory diseases associate with 41 genomic loci and type 2 inflammation. Nature Communications. 14(1). 83–83. 8 indexed citations

5.

Nuutinen, Mikko, Annina Lyly, Paula Virkkula, et al.. (2022). The relative proportion of comorbidities among rhinitis and rhinosinusitis patients and their impact on visit burden. Clinical and Translational Allergy. 12(7). e12181–e12181. 11 indexed citations

6.

Saarentaus, Elmo, Aki S. Havulinna, Nina Mars, et al.. (2021). Polygenic burden has broader impact on health, cognition, and socioeconomic outcomes than most rare and high-risk copy number variants. Molecular Psychiatry. 26(9). 4884–4895. 7 indexed citations

7.

Pérez‐Palma, Eduardo, Elmo Saarentaus, Marie Ravoet, et al.. (2018). Duplications at 19q13.33 in patients with neurodevelopmental disorders. Neurology Genetics. 4(1). e210–e210. 2 indexed citations

8.

Ganna, Andrea, Mitja Kurki, Aki S. Havulinna, et al.. (2018). Quantifying the Impact of Rare and Ultra-rare Coding Variation across the Phenotypic Spectrum. Työväentutkimus Vuosikirja. 54 indexed citations

9.

Kaivola, Karri, Lilja Jansson, Elmo Saarentaus, et al.. (2017). Heterozygous TYROBP deletion (PLOSLFIN) is not a strong risk factor for cognitive impairment. Neurobiology of Aging. 64. 159.e1–159.e4. 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.

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