Perttu Salo

9.5k total citations
18 papers, 603 citations indexed

About

Perttu Salo is a scholar working on Molecular Biology, Surgery and Genetics. According to data from OpenAlex, Perttu Salo has authored 18 papers receiving a total of 603 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 4 papers in Surgery and 4 papers in Genetics. Recurrent topics in Perttu Salo's work include Metabolomics and Mass Spectrometry Studies (3 papers), Congenital gastrointestinal and neural anomalies (3 papers) and Gene expression and cancer classification (3 papers). Perttu Salo is often cited by papers focused on Metabolomics and Mass Spectrometry Studies (3 papers), Congenital gastrointestinal and neural anomalies (3 papers) and Gene expression and cancer classification (3 papers). Perttu Salo collaborates with scholars based in Finland, Estonia and United States. Perttu Salo's co-authors include Markus Perola, Jeanine J. Houwing‐Duistermaat, Hae‐Won Uh, Geurt Jongbloed, Said el Bouhaddani, Taneli Raivio, Henrikki Almusa, Samuli Eldfors, Anu Suomalainen and Pekka Ellonen and has published in prestigious journals such as PLoS ONE, Scientific Reports and Genome biology.

In The Last Decade

Perttu Salo

18 papers receiving 598 citations

Peers

Countries citing papers authored by Perttu Salo

Since Specialization

Citations

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

Fields of papers citing papers by Perttu Salo

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Perttu Salo

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

All Works

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18 of 18 papers shown

#	Work	Indexed citations
1	A distinctive DNA methylation pattern in insufficient sleep 2019 ·Scientific Reports ·Alexandra Lahtinen, Sampsa Puttonen, Päivi Vanttola, Katriina Viitasalo, Sonja Sulkava, Natalia Pervjakova, Anni Joensuu, Perttu Salo, Auli Toivola, Mikko Härmä, Lili Milani, Markus Perola, Tiina Paunio	35
2	Sequential double cross-validation for assessment of added predictive ability in high-dimensional omic applications 2018 ·Archivio istituzionale della ricerca (Alma Mater Studiorum Università di Bologna) ·Mar Rodríguez‐Girondo, Perttu Salo, Tomasz Burzykowski, Markus Perola, Jeanine J. Houwing‐Duistermaat, Bart Mertens	2
3	Genome-wide association study of Hirschsprung disease detects a novel low-frequency variant at the RET locus 2018 ·European Journal of Human Genetics ·João Fadista, Marie Lund, Line Skotte, Frank Geller, Priyanka Nandakumar, Sumantra Chatterjee, Hans Matsson, Anna Löf Granström, Tomas Wester, Perttu Salo, (unknown), Lisbeth Carstensen, Jonas Bybjerg‐Grauholm, David M. Hougaard, Mikko P. Pakarinen, Markus Perola, Agneta Nordenskjöld, Aravinda Chakravarti, Mads Melbye, Bjarke Feenstra	22
4	Low galactosylation of IgG associates with higher risk for future diagnosis of rheumatoid arthritis during 10 years of follow-up 2018 ·STM:n Hallinnonalan avoin julkaisuarkisto (Julkari) ·Ivan Gudelj, Perttu Salo, Irena Trbojević‐Akmačić, (unknown), Dragan Primorac, Markus Perola, Gordan Lauc	2
5	Noncoding RET variants explain the strong association with Hirschsprung disease in patients without rare coding sequence variant 2018 ·European Journal of Medical Genetics ·(unknown), Perttu Salo, Jia Cao, (unknown), Lili Milani, Andres Metspalu, Risto Rintala, Outi Saarenpää‐Heikkilä, Tiina Paunio, Tomas Wester, Agneta Nordenskjöld, Markus Perola, Mikko P. Pakarinen	13
6	Low galactosylation of IgG associates with higher risk for future diagnosis of rheumatoid arthritis during 10 years of follow-up 2018 ·Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease ·Ivan Gudelj, Perttu Salo, Irena Trbojević‐Akmačić, (unknown), Dragan Primorac, Markus Perola, Gordan Lauc	69
7	Genome-Wide Association Study Implicates Atrial Natriuretic Peptide Rather Than B-Type Natriuretic Peptide in the Regulation of Blood Pressure in the General Population 2017 ·Circulation Cardiovascular Genetics ·Perttu Salo, Aki S. Havulinna, Taru Tukiainen, Olli T. Raitakari, Terho Lehtimäki, Mika Kähönen, Johannes Kettunen, Minna Männikkö, Johan G. Eriksson, Antti Jula, Stefan Blankenberg, Tanja Zeller, Veikko Salomaa, Kati Kristiansson, Markus Perola	25
8	Apolipoproteins and HDL cholesterol do not associate with the risk of future dementia and Alzheimer’s disease: the National Finnish population study (FINRISK) 2016 ·AGE ·Juho Tynkkynen, Jussi Hernesniemi, Tiina Laatikainen, Aki S. Havulinna, Jouko Sundvall, Jaana Leiviskä, Perttu Salo, Veikko Salomaa	24
9	Evaluation of O2PLS in Omics data integration 2016 ·BMC Bioinformatics ·Said el Bouhaddani, Jeanine J. Houwing‐Duistermaat, Perttu Salo, Markus Perola, Geurt Jongbloed, Hae‐Won Uh	127
10	High-sensitivity cardiac troponin I and NT-proBNP as predictors of incident dementia and Alzheimer’s disease: the FINRISK Study 2016 ·Journal of Neurology ·Juho Tynkkynen, Jussi Hernesniemi, Tiina Laatikainen, Aki S. Havulinna, Perttu Salo, Stefan Blankenberg, Tanja Zeller, Veikko Salomaa	22
11	The Detection of Metabolite-Mediated Gene Module Co-Expression Using Multivariate Linear Models 2016 ·PLoS ONE ·(unknown), Tatsiana Khamiakova, Ziv Shkedy, Markus Perola, Perttu Salo, Tomasz Burzykowski	3
12	Genetic Variants on Chromosome 1p13.3 Are Associated with Non-ST Elevation Myocardial Infarction and the Expression of DRAM2 in the Finnish Population 2015 ·PLoS ONE ·Perttu Salo, (unknown), Johannes Kettunen, Matti Pirinen, Antti‐Pekka Sarin, Heikki V. Huikuri, Pekka J. Karhunen, Markku Eskola, Kjell Nikus, Marja‐Liisa Lokki, Samuli Ripatti, Aki S. Havulinna, Veikko Salomaa, Aarno Palotie, Markku S. Nieminen, Juha Sinisalo, Markus Perola	6
13	Evaluation of HLA‐DRB1 imputation using a Finnish dataset 2014 ·Tissue Antigens ·Efthymia Vlachopoulou, Elisa Lahtela, Annika Wennerström, Aki S. Havulinna, Perttu Salo, Markus Perola, Veikko Salomaa, Markku S. Nieminen, Juha Sinisalo, Marja‐Liisa Lokki	15
14	Type II antithrombin deficiency caused by a founder mutation Pro73Leu in the Finnish population: clinical picture 2013 ·Journal of Thrombosis and Haemostasis ·Marja Puurunen, Perttu Salo, (unknown), Kaija Javela, Markus Perola	32
15	A polymorphism in the protein kinase C gene PRKCB is associated with α2-adrenoceptor-mediated vasoconstriction 2013 ·Pharmacogenetics and Genomics ·Jussi P. Posti, Perttu Salo, Saku Ruohonen, (unknown), Mordechai Muszkat, Gbenga G. Sofowora, Daniel Kurnik, Charles Stein, Markus Perola, Mika Scheinin, Amir Snapir	4
16	Thyroid cancer and co-occurring RET mutations in Hirschsprung disease 2013 ·Endocrine Related Cancer ·(unknown), Eero Pukkala, Reetta Kivisaari, Perttu Salo, Antti Koivusalo, Johanna Arola, Päivi J. Miettinen, Risto Rintala, Markus Perola, Mikko P. Pakarinen	13
17	Comparison of solution-based exome capture methods for next generation sequencing 2011 ·STM:n Hallinnonalan avoin julkaisuarkisto (Julkari) ·Anna-Maija Sulonen, Pekka Ellonen, Henrikki Almusa, Maija Lepistö, Samuli Eldfors, Sari Hannula, Timo Miettinen, Henna Tyynismaa, Perttu Salo, Caroline A. Heckman, Heikki Joensuu, Taneli Raivio, Anu Suomalainen, Janna Saarela	1
18	Comparison of solution-based exome capture methods for next generation sequencing 2011 ·Genome biology ·Anna-Maija Sulonen, Pekka Ellonen, Henrikki Almusa, Maija Lepistö, Samuli Eldfors, Sari Hannula, Timo Miettinen, Henna Tyynismaa, Perttu Salo, Caroline A. Heckman, Heikki Joensuu, Taneli Raivio, Anu Suomalainen, Janna Saarela	188

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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