P Aula
Impact in
- Clinical Biochemistry top 2%
- Metabolism and Genetic Disorders
- Genetics top 10%
- Forensic and Genetic Research
- Genetic diversity and population structure
- Yersinia bacterium, plague, ectoparasites research
Papers in
-
- Glycosylation and Glycoproteins Research 2
- Mitochondrial Function and Pathology 2
-
- Carbohydrate Chemistry and Synthesis 3
- Co-authors
- M L Savontaus (2 shared papers)Johanna Vilkki (2 shared papers)Kirsi Huoponen (1 shared paper)P. Sistonen (3 shared papers)M.-L. Savontaus (2 shared papers)Matti Lukka (3 shared papers)Antti Sajantila (3 shared papers)Päivi Lahermo (2 shared papers)
- Journals
- The EMBO Journal (1 paper)Journal of Inherited Metabolic Disease (1 paper)European Journal of Human Genetics (1 paper)Biochemical Journal (1 paper)Genome Research (1 paper)
- Partner nations
- FinlandUnited StatesNorway
In The Last Decade
P Aula
13 papers receiving 889 citations
Peers
Comparison fields: 5 of 84
- Clinical Biochemistry 219
- Genetics 292
- Molecular Biology 615
- Archeology 49
- Ophthalmology 40
Countries citing papers authored by P Aula
This map shows the geographic impact of P 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 P Aula with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites P Aula more than expected).
Fields of papers citing papers by P Aula
This network shows the impact of papers produced by P 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 P Aula. The network helps show where P Aula may publish in the future.
Co-authors
The 25 scholars most cited alongside P Aula, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | A new mtDNA mutation associated with Leber hereditary optic neuroretinopathy. | 1991 | 311 |
| 2 | 1995 | 200 | |
| 3 | 1991 | 116 | |
| 4 | Optic atrophy in Leber hereditary optic neuroretinopathy is probably determined by an X-chromosomal gene closely linked to DXS7. | 1991 | 104 |
| 5 | The genetic relationship between the Finns and the Finnish Saami (Lapps): analysis of nuclear DNA and mtDNA. | 1996 | 92 |
| 6 | 1998 | 25 | |
| 7 | 1989 | 20 | |
| 8 | 1983 | 17 | |
| 9 | Mapping of the gene for glutathione reductase on chromosome 8. | 1976 | 16 |
| 10 | 1984 | 16 | |
| 11 | 1993 | 12 | |
| 12 | [Molecular genetics of aspartylglucosaminuria]. | 1991 | 4 |
| 13 | The genetic relationship between the Finns and the Finnish Saami (Lapps): analysis of nuclear DNA and mitochondrial mtDNA | 1996 | 3 |
About P Aula
P Aula is a scholar working on Molecular Biology, Organic Chemistry, Physiology, Nutrition and Dietetics and Genetics, having authored 13 papers that have together received 936 indexed citations. Recurring topics across this work include Lysosomal Storage Disorders Research (3 papers), Carbohydrate Chemistry and Synthesis (3 papers), Forensic and Genetic Research (2 papers), Glycosylation and Glycoproteins Research (2 papers), Genetic diversity and population structure (2 papers), Mitochondrial Function and Pathology (2 papers), Metabolism and Genetic Disorders (1 paper) and Microbial Metabolites in Food Biotechnology (1 paper). The work is most often cited by research in Clinical Biochemistry (219 citations), Genetics (292 citations), Molecular Biology (615 citations), Archeology (49 citations) and Ophthalmology (40 citations). P Aula has collaborated with scholars based in Finland, United States and Norway. Frequent co-authors include M L Savontaus, Johanna Vilkki, Kirsi Huoponen, P. Sistonen, M.-L. Savontaus, Matti Lukka, Antti Sajantila, Päivi Lahermo, J. Ott and Eeva Nikoskelainen. Their work appears in journals such as The EMBO Journal, Journal of Inherited Metabolic Disease, European Journal of Human Genetics, Biochemical Journal and Genome Research.
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.