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)Antti Sajantila (3 shared papers)Matti Lukka (3 shared papers)Päivi Lahermo (2 shared papers)M.-L. Savontaus (2 shared papers)
- Journals
- Journal of Biological Chemistry (1 paper)European Journal of Human Genetics (1 paper)Biochemical Journal (1 paper)Proceedings of the National Academy of Sciences (1 paper)Journal of Inherited Metabolic Disease (1 paper)
- Partner nations
- FinlandUnited StatesGermany
In The Last Decade
P Aula
13 papers receiving 889 citations
Peers
Comparison fields: 5 of 78
- Clinical Biochemistry 198
- Genetics 283
- Molecular Biology 599
- Archeology 47
- Physiology 106
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 | 91 |
| 6 | 1998 | 25 | |
| 7 | 1989 | 20 | |
| 8 | 1983 | 17 | |
| 9 | 1984 | 16 | |
| 10 | Mapping of the gene for glutathione reductase on chromosome 8. | 1976 | 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 935 indexed citations. Recurring topics across this work include Carbohydrate Chemistry and Synthesis (3 papers), Lysosomal Storage Disorders Research (3 papers), Glycosylation and Glycoproteins Research (2 papers), Forensic and Genetic Research (2 papers), Mitochondrial Function and Pathology (2 papers), Genetic diversity and population structure (2 papers), Animal Genetics and Reproduction (1 paper) and Amino Acid Enzymes and Metabolism (1 paper). The work is most often cited by research in Clinical Biochemistry (198 citations), Genetics (283 citations), Molecular Biology (599 citations), Archeology (47 citations) and Physiology (106 citations). P Aula has collaborated with scholars based in Finland, United States and Germany. Frequent co-authors include M L Savontaus, Johanna Vilkki, Kirsi Huoponen, P. Sistonen, Antti Sajantila, Matti Lukka, Päivi Lahermo, M.-L. Savontaus, Eeva Nikoskelainen and J. Ott. Their work appears in journals such as Journal of Biological Chemistry, European Journal of Human Genetics, Biochemical Journal, Proceedings of the National Academy of Sciences and Journal of Inherited Metabolic Disease.
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.