Antti Sajantila

19.8k total citations
198 papers, 7.2k citations indexed

About

Antti Sajantila is a scholar working on Genetics, Molecular Biology and Pharmacology. According to data from OpenAlex, Antti Sajantila has authored 198 papers receiving a total of 7.2k indexed citations (citations by other indexed papers that have themselves been cited), including 86 papers in Genetics, 61 papers in Molecular Biology and 20 papers in Pharmacology. Recurrent topics in Antti Sajantila's work include Forensic and Genetic Research (66 papers), Molecular Biology Techniques and Applications (24 papers) and Genetic diversity and population structure (23 papers). Antti Sajantila is often cited by papers focused on Forensic and Genetic Research (66 papers), Molecular Biology Techniques and Applications (24 papers) and Genetic diversity and population structure (23 papers). Antti Sajantila collaborates with scholars based in Finland, United States and United Kingdom. Antti Sajantila's co-authors include Bruce Budowle, Matti Lukka, Jukka U. Palo, Manfred Kayser, Johanna Sistonen, Svante Pääbo, Silvia Fuselli, Minttu Hedman, Philippe Lunetta and Mark Stoneking and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Nature Communications.

In The Last Decade

Antti Sajantila

193 papers receiving 6.8k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Antti Sajantila Finland 46 3.8k 2.6k 775 734 428 198 7.2k
António Amorim Portugal 48 5.5k 1.5× 3.9k 1.5× 1.1k 1.4× 103 0.1× 274 0.6× 451 9.4k
Howard M. Cann United States 31 4.0k 1.0× 3.2k 1.3× 263 0.3× 151 0.2× 230 0.5× 122 8.3k
Peter de Knijff Netherlands 58 5.8k 1.5× 4.4k 1.7× 656 0.8× 147 0.2× 148 0.3× 198 11.1k
Hua Tang United States 38 4.6k 1.2× 2.2k 0.8× 170 0.2× 139 0.2× 186 0.4× 134 7.9k
Judith R. Kidd United States 46 3.0k 0.8× 2.3k 0.9× 136 0.2× 138 0.2× 244 0.6× 103 8.9k
Michael E. Weale United Kingdom 40 2.7k 0.7× 2.0k 0.8× 127 0.2× 330 0.4× 632 1.5× 95 6.1k
Ranjan Deka United States 44 3.4k 0.9× 2.1k 0.8× 333 0.4× 108 0.1× 272 0.6× 159 6.9k
Rick A. Kittles United States 48 3.6k 1.0× 2.4k 0.9× 140 0.2× 316 0.4× 1.0k 2.4× 209 9.1k
Esteban J. Parra Canada 47 3.7k 1.0× 1.5k 0.6× 174 0.2× 211 0.3× 222 0.5× 125 7.2k
Óscar Lao Netherlands 32 1.8k 0.5× 1.0k 0.4× 428 0.6× 259 0.4× 149 0.3× 66 3.4k

Countries citing papers authored by Antti Sajantila

Since Specialization
Citations

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

Fields of papers citing papers by Antti Sajantila

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Antti Sajantila

This figure shows the co-authorship network connecting the top 25 collaborators of Antti Sajantila. A scholar is included among the top collaborators of Antti Sajantila 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 Antti Sajantila. Antti Sajantila 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.
Pratas, Diogo, Mari Toppinen, Peter Simmonds, et al.. (2024). Intra-host genomic diversity and integration landscape of human tissue-resident DNA virome. Nucleic Acids Research. 52(21). 13073–13093. 2 indexed citations
2.
Vuorio, Alpo, et al.. (2023). Commercial Aircraft-Assisted Suicide Accident Investigations Re-Visited—Agreeing to Disagree?. Safety. 9(1). 17–17. 1 indexed citations
3.
Pratas, Diogo, et al.. (2023). Unmasking the tissue-resident eukaryotic DNA virome in humans. Nucleic Acids Research. 51(7). 3223–3239. 31 indexed citations
4.
Pratas, Diogo, et al.. (2022). Detection of Low-Copy Human Virus DNA upon Prolonged Formalin Fixation. Viruses. 14(1). 133–133. 7 indexed citations
5.
Pratas, Diogo, et al.. (2020). A hybrid pipeline for reconstruction and analysis of viral genomes at multi-organ level. GigaScience. 9(8). 24 indexed citations
6.
Pett, Helmi, Jukka U. Palo, Jari Haukka, et al.. (2019). Completed suicides of citalopram users-the role of CYP genotypes and adverse drug interactions. STM:n Hallinnonalan avoin julkaisuarkisto (Julkari). 2 indexed citations
7.
Lamnidis, Thiseas C., Kerttu Majander, Choongwon Jeong, et al.. (2018). Ancient Fennoscandian genomes reveal origin and spread of Siberian ancestry in Europe. Nature Communications. 9(1). 5018–5018. 71 indexed citations
8.
Wendt, Frank R., et al.. (2018). Supervised Classification of CYP2D6 Genotype and Metabolizer Phenotype With Postmortem Tramadol-Exposed Finns. American Journal of Forensic Medicine & Pathology. 40(1). 8–18. 8 indexed citations
9.
Haukka, Jari, et al.. (2017). Serotonergic 5HTTLPR/rs25531 s-allele homozygosity associates with violent suicides in male citalopram users. STM:n Hallinnonalan avoin julkaisuarkisto (Julkari).
10.
Seo, Seung Bum, Xiangpei Zeng, Mourad Assidi, et al.. (2014). High throughput whole mitochondrial genome sequencing by two platforms of massively parallel sequencing. BMC Genomics. 15(S2). 9 indexed citations
11.
Ranta, Helena, et al.. (2011). Age assessment by the Greulich and Pyle method compared to other skeletal X-ray and dental methods in data from Finnish child victims of the Southeast Asian Tsunami. Forensic Science Medicine and Pathology. 7(4). 311–316. 25 indexed citations
12.
Sääksjärvi, Ilari E., Jukka U. Palo, Pekka Saukko, et al.. (2009). Hyönteiset oikeuslääkärin apuna. 64. 1 indexed citations
13.
Sistonen, Johanna, Silvia Fuselli, Jukka U. Palo, et al.. (2009). Pharmacogenetic variation at CYP2C9, CYP2C19, and CYP2D6 at global and microgeographic scales. Pharmacogenetics and Genomics. 19(2). 170–179. 158 indexed citations
14.
Sigurðsson, Snævar, et al.. (2006). A microarray system for genotyping 150 single nucleotide polymorphisms in the coding region of human mitochondrial DNA. Genomics. 87(4). 534–542. 19 indexed citations
15.
Hedman, Minttu, Ville N. Pimenoff, Matti Lukka, P. Sistonen, & Antti Sajantila. (2004). Analysis of 16 Y STR loci in the Finnish population reveals a local reduction in the diversity of male lineages. Forensic Science International. 142(1). 37–43. 34 indexed citations
16.
Vauhkonen, Hanna, Matti Vauhkonen, P. Sipponen, & Antti Sajantila. (2004). Correlation Between the Allelic Distribution of STRs in a Finnish Population and Phenotypically Different Gastrointestinal Tumours: A Study Using Four X‐Chromosomal Markers (DXS7423, DXS8377, ARA, DXS101). Annals of Human Genetics. 68(6). 555–562. 10 indexed citations
17.
Lunetta, Philippe, Antti Penttilä, & Antti Sajantila. (2002). Drowning in Finland: “external cause” and “injury” codes. Injury Prevention. 8(4). 342–344. 27 indexed citations
18.
Raitio, Mirja, Katarina Lindroos, Tomi Pastinen, et al.. (2001). Y-Chromosomal SNPs in Finno–Ugric-Speaking Populations Analyzed by Minisequencing on Microarrays. Genome Research. 11(3). 471–482. 65 indexed citations
19.
Syvänen, A-C, Antti Sajantila, & Matti Lukka. (1993). Forensic DNA typing by the solid-phase minisequencing method. Birkhäuser Basel eBooks. 67. 275–282. 2 indexed citations
20.
Helminen, Päivi, Antti Sajantila, V. Johnsson, et al.. (1992). Amplification of three hypervariable DNA regions by polymerase chain reaction for paternity determinations: comparison with conventional methods and DNA fingerprinting. Molecular and Cellular Probes. 6(1). 21–26. 16 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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