Pertti Aula

512 total citations
8 papers, 390 citations indexed

About

Pertti Aula is a scholar working on Molecular Biology, Clinical Biochemistry and Biochemistry. According to data from OpenAlex, Pertti Aula has authored 8 papers receiving a total of 390 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 3 papers in Clinical Biochemistry and 3 papers in Biochemistry. Recurrent topics in Pertti Aula's work include Mitochondrial Function and Pathology (4 papers), Amino Acid Enzymes and Metabolism (3 papers) and Metabolism and Genetic Disorders (3 papers). Pertti Aula is often cited by papers focused on Mitochondrial Function and Pathology (4 papers), Amino Acid Enzymes and Metabolism (3 papers) and Metabolism and Genetic Disorders (3 papers). Pertti Aula collaborates with scholars based in Finland, United States and Germany. Pertti Aula's co-authors include Marja‐Liisa Savontaus, Kirsi Huoponen, Juha Mykkänen, Olli Simell, David Torrents, Pablo Sanjurjo, Arja Reinikainen, Rafael de Cid, Marta Pineda and Manuel Palacı́n and has published in prestigious journals such as Nature Genetics, FEBS Letters and The American Journal of Human Genetics.

In The Last Decade

Pertti Aula

8 papers receiving 385 citations

Peers

Pertti Aula

BIOCH

MB

CB

PFM

GENET

M I Kaiser-Kupfer United States

K Takki Finland

Claire Rea United States

Joshua Marvit United States

H. G. Terheggen Switzerland

Mónica Renedo Spain

Rzem Rim Belgium

Marie Chol France

Eveline M. Hogenhout Netherlands

Piotr Nowacki Canada

M I Kaiser-Kupfer United States

Pertti Aula

120 ×0.6

BIOCH

145 ×0.7

MB

58 ×0.3

CB

69 ×1.4

PFM

43 ×1.1

GENET

Citations per year, relative to Pertti Aula Pertti Aula (= 1×) peers M I Kaiser-Kupfer

Countries citing papers authored by Pertti Aula

Since Specialization

Citations

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

Fields of papers citing papers by Pertti Aula

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Pertti Aula

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

All Works

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8 of 8 papers shown

1.

Torrents, David, Juha Mykkänen, Marta Pineda, et al.. (1999). Identification of SLC7A7, encoding y+LAT-1, as the lysinuric protein intolerance gene. Nature Genetics. 21(3). 293–296. 232 indexed citations

2.

Lamminen, Tarja, Kirsi Huoponen, Pertti Sistonen, et al.. (1998). mtDNA haplotype analysis in Finnish families with leber hereditary optic neuroretinopathy.. PubMed. 5(5). 271–9. 50 indexed citations

3.

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

4.

Juvonen, Vesa, Eeva Nikoskelainen, Tarja Lamminen, et al.. (1997). Tissue distribution of the ND4/11778 mutation in heteroplasmic lineages with Leber hereditary optic neuropathy. Human Mutation. 9(5). 412–417. 18 indexed citations

5.

Sistonen, Pertti, et al.. (1997). Lysinuric Protein Intolerance (LPI) Gene Maps to the Long Arm of Chromosome 14. The American Journal of Human Genetics. 60(6). 1479–1486. 35 indexed citations

6.

Majander, Anna, Tarja Lamminen, Vesa Juvonen, et al.. (1997). Mutations in subunit 6 of the F₁F₀‐ATP synthase cause two entirely different diseases. FEBS Letters. 412(2). 351–354. 22 indexed citations

7.

Isosomppi, Juha, et al.. (1996). A Physical Map of the 6q14–q15 Region Harboring the Locus for the Lysosomal Membrane Sialic Acid Transport Defect. Genomics. 37(1). 62–67. 17 indexed citations

8.

Huoponen, Kirsi, et al.. (1990). Analysis of mitochondrial ND4 gene DNA sequence in Finnish families with Leber hereditary optic neuroretinopathy. Genomics. 8(3). 583–585. 10 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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