Perttì Aula
Impact in
- Physiology top 2%
- Lysosomal Storage Disorders Research
- Clinical Biochemistry top 2%
- Metabolism and Genetic Disorders
Papers in
-
- Glycosylation and Glycoproteins Research 17
- Physiology 42
- Lysosomal Storage Disorders Research 39
- Erythrocyte Function and Pathophysiology 11
- Co-authors
- Albert de la Chapelle (4 shared papers)Harriet von Koskull (13 shared papers)Maila Koivisto (1 shared paper)Riitta Herva (1 shared paper)Juhani Rapola (12 shared papers)Martin Renlund (16 shared papers)S. Autio (9 shared papers)Jaakko Leisti (12 shared papers)
- Journals
- Human Genetics (11 papers)Clinical Genetics (10 papers)Human Mutation (9 papers)Hereditas (9 papers)Prenatal Diagnosis (6 papers)
- Partner nations
- FinlandUnited StatesNetherlands
In The Last Decade
Perttì Aula
128 papers receiving 3.2k citations
Peers
Comparison fields: 5 of 125
- Physiology 866
- Clinical Biochemistry 230
- Genetics 877
- Pediatrics, Perinatology and Child Health 546
- Cell Biology 413
Countries citing papers authored by Perttì Aula
This map shows the geographic impact of Perttì 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 Perttì Aula with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Perttì Aula more than expected).
Fields of papers citing papers by Perttì Aula
This network shows the impact of papers produced by Perttì 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 Perttì Aula. The network helps show where Perttì Aula may publish in the future.
Co-authors
The 25 scholars most cited alongside Perttì 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
Showing the 20 most-cited of 134 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1981 | 270 | |
| 2 | 1999 | 224 | |
| 3 | 1979 | 110 | |
| 4 | 1991 | 105 | |
| 5 | Attitudes toward genetic testing among the general population and relatives of patients with a severe genetic disease: a survey from Finland. | 1995 | 93 |
| 6 | 2000 | 85 | |
| 7 | 1997 | 77 | |
| 8 | 1993 | 76 | |
| 9 | 1983 | 74 | |
| 10 | 1997 | 71 | |
| 11 | 1998 | 69 | |
| 12 | 1985 | 67 | |
| 13 | 1998 | 65 | |
| 14 | 1991 | 61 | |
| 15 | 1981 | 59 | |
| 16 | 1973 | 56 | |
| 17 | 1999 | 55 | |
| 18 | 1991 | 54 | |
| 19 | 1976 | 44 | |
| 20 | 1967 | 41 |
About Perttì Aula
Perttì Aula is a scholar working on Molecular Biology, Physiology, Genetics, Pediatrics, Perinatology and Child Health and Rheumatology, having authored 134 papers that have together received 3.3k indexed citations. Recurring topics across this work include Lysosomal Storage Disorders Research (39 papers), Glycosylation and Glycoproteins Research (17 papers), Prenatal Screening and Diagnostics (17 papers), Genomic variations and chromosomal abnormalities (15 papers), Glycogen Storage Diseases and Myoclonus (12 papers), Metabolism and Genetic Disorders (12 papers), Erythrocyte Function and Pathophysiology (11 papers) and Chromosomal and Genetic Variations (10 papers). The work is most often cited by research in Physiology (866 citations), Clinical Biochemistry (230 citations), Genetics (877 citations), Pediatrics, Perinatology and Child Health (546 citations) and Cell Biology (413 citations). Perttì Aula has collaborated with scholars based in Finland, United States and Netherlands. Frequent co-authors include Albert de la Chapelle, Harriet von Koskull, Maila Koivisto, Riitta Herva, Juhani Rapola, Martin Renlund, S. Autio, Jaakko Leisti, Nina Aula and Kari O. Raivio. Their work appears in journals such as Human Genetics, Clinical Genetics, Human Mutation, Hereditas and Prenatal Diagnosis.
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.