Aarno Palotie

186.5k total citations · 4 hit papers
334 papers, 14.9k citations indexed

About

Aarno Palotie is a scholar working on Molecular Biology, Genetics and Psychiatry and Mental health. According to data from OpenAlex, Aarno Palotie has authored 334 papers receiving a total of 14.9k indexed citations (citations by other indexed papers that have themselves been cited), including 123 papers in Molecular Biology, 112 papers in Genetics and 37 papers in Psychiatry and Mental health. Recurrent topics in Aarno Palotie's work include Genetic Associations and Epidemiology (47 papers), Genomic variations and chromosomal abnormalities (32 papers) and Migraine and Headache Studies (31 papers). Aarno Palotie is often cited by papers focused on Genetic Associations and Epidemiology (47 papers), Genomic variations and chromosomal abnormalities (32 papers) and Migraine and Headache Studies (31 papers). Aarno Palotie collaborates with scholars based in Finland, United States and United Kingdom. Aarno Palotie's co-authors include Leena Peltonen, Samuli Ripatti, Olli Kallioniemi, David B. Seligson, Steve Horvath, Maija Wessman, Veikko Salomaa, Leena Peltonen, Markus Perola and Nina Horelli‐Kuitunen and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and The Lancet.

In The Last Decade

Aarno Palotie

323 papers receiving 14.5k citations

Hit Papers

In vivo amplification of ... 1995 2026 2005 2015 1995 1997 2003 2020 250 500 750 1000
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.

  1. In vivo amplification of the androgen receptor gene and progression of human prostate cancer
    1995 1.1k citations Aarno Palotie, Olli Kallioniemi et al. profile →
  2. An autoimmune disease, APECED, caused by mutations in a novel gene featuring two PHD-type zinc-finger domains
    1997 890 citations Nina Horelli‐Kuitunen, Aarno Palotie et al. profile →
  3. Carbonic anhydrase IX is an independent predictor of survival in advanced renal clear cell carcinoma: implications for prognosis and therapy.
    2003 514 citations Aarno Palotie et al. profile →
  4. Polygenic and clinical risk scores and their impact on age at onset and prediction of cardiometabolic diseases and common cancers
    2020 245 citations Nina Mars, Jukka Koskela et al. profile →

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Aarno Palotie Finland 63 5.7k 4.1k 2.6k 1.6k 1.4k 334 14.9k
Eitan Friedman Israel 64 6.1k 1.1× 5.1k 1.2× 1.2k 0.5× 2.4k 1.5× 949 0.7× 484 17.1k
Tom R. Gaunt United Kingdom 47 5.6k 1.0× 5.4k 1.3× 880 0.3× 1.1k 0.7× 993 0.7× 200 13.8k
Andrew D. Paterson Canada 59 5.2k 0.9× 3.9k 1.0× 947 0.4× 505 0.3× 987 0.7× 329 12.9k
Elaine Lyon United States 30 10.9k 1.9× 10.3k 2.5× 1.7k 0.7× 2.3k 1.5× 842 0.6× 102 23.2k
Juha Kere Finland 78 10.3k 1.8× 5.5k 1.3× 2.1k 0.8× 1.6k 1.0× 849 0.6× 512 22.1k
Daniel J. Schaid United States 75 5.8k 1.0× 7.6k 1.8× 2.1k 0.8× 3.4k 2.1× 693 0.5× 343 20.5k
Mark Leppert United States 65 8.0k 1.4× 4.3k 1.0× 2.0k 0.8× 2.6k 1.6× 654 0.5× 164 20.9k
Wendy K. Chung United States 72 8.6k 1.5× 7.3k 1.8× 2.7k 1.1× 1.6k 1.0× 1.0k 0.7× 567 22.7k
Aravinda Chakravarti United States 68 9.4k 1.7× 8.5k 2.1× 2.8k 1.1× 932 0.6× 826 0.6× 297 22.1k
Madhuri Hegde United States 35 11.5k 2.0× 10.7k 2.6× 1.7k 0.6× 2.6k 1.6× 824 0.6× 138 23.8k

Countries citing papers authored by Aarno Palotie

Since Specialization
Citations

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

Fields of papers citing papers by Aarno Palotie

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Aarno Palotie

This figure shows the co-authorship network connecting the top 25 collaborators of Aarno Palotie. A scholar is included among the top collaborators of Aarno Palotie 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 Aarno Palotie. Aarno Palotie 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.
Pirruccello, James P., Paolo Di Achille, Seung Hoan Choi, et al.. (2024). Deep learning of left atrial structure and function provides link to atrial fibrillation risk. Nature Communications. 15(1). 4304–4304. 10 indexed citations
2.
Kiiskinen, Tuomo, Niina Pitkänen, Hannele Laivuori, et al.. (2023). Use of electronic health record data mining for heart failure subtyping. BMC Research Notes. 16(1). 208–208. 2 indexed citations
3.
Skotte, Line, Juha Karjalainen, Erik Abner, et al.. (2022). Comprehensive genome-wide association study of different forms of hernia identifies more than 80 associated loci. Nature Communications. 13(1). 3200–3200. 12 indexed citations
4.
Strausz, Satu, Tuomo Kiiskinen, Martin Broberg, et al.. (2021). Sleep apnoea is a risk factor for severe COVID-19. BMJ Open Respiratory Research. 8(1). e000845–e000845. 74 indexed citations
5.
6.
Tanigawa, Yosuke, Michael Wainberg, Juha Karjalainen, et al.. (2020). Rare protein-altering variants in ANGPTL7 lower intraocular pressure and protect against glaucoma. PLoS Genetics. 16(5). e1008682–e1008682. 26 indexed citations
7.
McFadyen, Charles, Frederick A. Zeiler, Virginia Newcombe, et al.. (2019). Apolipoprotein E4 Polymorphism and Outcomes from Traumatic Brain Injury: A Living Systematic Review and Meta-Analysis. Journal of Neurotrauma. 38(8). 1124–1136. 54 indexed citations
8.
Kerminen, Sini, Alicia R. Martin, Jukka Koskela, et al.. (2019). Geographic Variation and Bias in the Polygenic Scores of Complex Diseases and Traits in Finland. STM:n Hallinnonalan avoin julkaisuarkisto (Julkari). 1 indexed citations
9.
Zeiler, Frederick A., Charles McFadyen, Virginia Newcombe, et al.. (2018). Genetic Influences on Patient-Oriented Outcomes in Traumatic Brain Injury: A Living Systematic Review of Non-Apolipoprotein E Single-Nucleotide Polymorphisms. Journal of Neurotrauma. 38(8). 1107–1123. 48 indexed citations
10.
Niestroj, Lisa‐Marie, Michael Nothnagel, Patrick May, et al.. (2018). Guideline‐based and bioinformatic reassessment of lesion‐associated gene and variant pathogenicity in focal human epilepsies. Epilepsia. 59(11). 2145–2152. 6 indexed citations
11.
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
12.
Kaunisto, Mari, Ritva Jokela, Minna Tallgren, et al.. (2013). Pain in 1,000 Women Treated for Breast Cancer. Anesthesiology. 119(6). 1410–1421. 86 indexed citations
13.
Lahti, Jari, Hannu Alho, Leena Kovanen, et al.. (2013). mu-Opioid Receptor Gene (OPRM1) Polymorphism A118G: Lack of Association in Finnish Populations with Alcohol Dependence or Alcohol Consumption. STM:n Hallinnonalan avoin julkaisuarkisto (Julkari). 1 indexed citations
14.
Surakka, Ida, Kati Kristiansson, Michael Inouye, et al.. (2010). Founder population-specific HapMap panel increases power in GWA studies through improved imputation accuracy and CNV tagging. STM:n Hallinnonalan avoin julkaisuarkisto (Julkari). 14 indexed citations
15.
Inouye, Michael, Kaisa Silander, Eija Hämäläinen, et al.. (2010). An Immune Response Network Associated with Blood Lipid Levels. PLoS Genetics. 6(9). e1001113–e1001113. 78 indexed citations
16.
Wartiovaara, Ulla, Petri Salvén, Hanna Mikkola, et al.. (1998). Peripheral blood platelets express VEGF-C and VEGF which are released during platelet activation. Journal of Thrombosis and Haemostasis. 80. 171–175. 2 indexed citations
17.
Horelli‐Kuitunen, Nina, Ellen I. Closs, Marja‐Liisa Savontaus, et al.. (1997). Human cationic amino acid transporter gene hCAT-2 is assigned to 8p22 but is not the causative gene in lysinuric protein intolerance. Human Genetics. 100(1). 80–83. 6 indexed citations
18.
Halila, R, Maris Laan, Mika Saksela, et al.. (1995). The human gene for xanthine dehydrogenase (XDH) is localized on chromosome band 2p22. Cytogenetic and Genome Research. 68(1-2). 61–63. 19 indexed citations
19.
20.
Palotie, Aarno, Leena Peltonen, Leila Risteli, & Juha Risteli. (1983). Effect of the structural components of basement membranes on the attachment of teratocarcinoma-derived endodermal cells. Experimental Cell Research. 144(1). 31–37. 12 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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