Perttì Aula

4.9k total citations
134 papers, 3.4k citations indexed

About

Perttì Aula is a scholar working on Molecular Biology, Physiology and Genetics. According to data from OpenAlex, Perttì Aula has authored 134 papers receiving a total of 3.4k indexed citations (citations by other indexed papers that have themselves been cited), including 49 papers in Molecular Biology, 42 papers in Physiology and 38 papers in Genetics. Recurrent topics in Perttì Aula's work include Lysosomal Storage Disorders Research (38 papers), Prenatal Screening and Diagnostics (17 papers) and Glycosylation and Glycoproteins Research (17 papers). Perttì Aula is often cited by papers focused on Lysosomal Storage Disorders Research (38 papers), Prenatal Screening and Diagnostics (17 papers) and Glycosylation and Glycoproteins Research (17 papers). Perttì Aula collaborates with scholars based in Finland, Netherlands and United States. Perttì Aula's co-authors include Harriet von Koskull, Albert de la Chapelle, Riitta Herva, Maila Koivisto, Juhani Rapola, Martin Renlund, Jaakko Leisti, S. Autio, Nina Aula and Kari O. Raivio and has published in prestigious journals such as Proceedings of the National Academy of Sciences, The Lancet and Journal of Clinical Investigation.

In The Last Decade

Perttì Aula

128 papers receiving 3.2k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Perttì Aula Finland	30	1.5k	939	888	612	437	134	3.4k
Michael M. Kaback United States	35	1.5k 1.0×	1.6k 1.7×	1.1k 1.3×	626 1.0×	302 0.7×	111	4.1k
Michele D’Urso Italy	35	2.8k 1.9×	1.4k 1.5×	309 0.3×	706 1.2×	469 1.1×	100	4.2k
H. Galjaard Netherlands	42	2.6k 1.8×	1.3k 1.3×	2.1k 2.4×	425 0.7×	985 2.3×	138	5.3k
Reijo Norio Finland	36	1.1k 0.8×	1.8k 1.9×	382 0.4×	401 0.7×	218 0.5×	69	3.6k
Gail E. Herman United States	33	3.2k 2.2×	2.6k 2.8×	517 0.6×	341 0.6×	502 1.1×	102	5.7k
Virginia Nunes Spain	42	2.1k 1.4×	555 0.6×	297 0.3×	420 0.7×	394 0.9×	137	4.8k
Brian Lake United Kingdom	38	1.9k 1.3×	278 0.3×	1.8k 2.1×	270 0.4×	861 2.0×	140	4.4k
Gerhard Baumann United States	43	1.6k 1.1×	1.1k 1.2×	905 1.0×	505 0.8×	347 0.8×	103	5.5k
Donna M. Krasnewich United States	28	1.3k 0.9×	362 0.4×	671 0.8×	179 0.3×	488 1.1×	59	2.4k
Park S. Gerald United States	34	1.8k 1.2×	1.2k 1.2×	369 0.4×	484 0.8×	321 0.7×	111	3.6k

Countries citing papers authored by Perttì Aula

Since Specialization

Citations

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

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network of co-authors of Perttì Aula

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Aula, Perttì & Leevi Kääriäinen. (2009). THE KARYOTYPE OF THE ELK (ALCES ALCES). Hereditas. 51(2-3). 274–278. 2 indexed citations

Nichols, Warren W., ALBERT LEVAN, Perttì Aula, & Erling Norrby. (2009). Extreme chromosome breakage induced by measles virus in different in vitro systems. Preliminary communication. Hereditas. 51(2-3). 380–382. 13 indexed citations

Aula, Perttì & E Saksela. (2009). EARLY MORPHOLOGY OF THE CHROMOSOME DAMAGE INDUCED BY SENDAI VIRUS. Hereditas. 55(2-3). 362–366. 5 indexed citations

Koskull, Harriet von & Perttì Aula. (2009). Distribution of chromosome breaks in measles, Fanconi's anemia and controls. Hereditas. 87(1). 1–10. 2 indexed citations

Aula, Perttì. (2009). Virus-induced premature chromosome condensation (PCC) in single cells and G-bands of PCC-chromatin. Hereditas. 74(1). 81–88. 1 indexed citations

Aula, Perttì & E Saksela. (2009). Banding characteristics of paracentric marker constrictions in human chromosomes. Hereditas. 70(2). 309–310.

Aula, Perttì. (2009). Electron-microscopic observations on Sendai virus-induced chromosome pulverization in HeLa cells. Hereditas. 65(2). 163–169. 2 indexed citations

Korhonen, Tapio, et al.. (2002). Phenotypic spectrum of Salla disease, a free sialic acid storage disorder. Pediatric Neurology. 26(4). 267–273. 41 indexed citations

Aula, Nina, Frans W. Verheijen, Grazia M.S. Mancini, et al.. (2000). The Spectrum of SLC17A5-Gene Mutations Resulting in Free Sialic Acid–Storage Diseases Indicates Some Genotype-Phenotype Correlation. The American Journal of Human Genetics. 67(4). 832–840. 85 indexed citations

10.

Silander, Kaisa, et al.. (1997). Epidemiology of hereditary neuropathy with liability to pressure palsies (HNPP) in south western Finland. Neuromuscular Disorders. 7(8). 529–532. 77 indexed citations

11.

Schleutker, Johanna, Jan‐Eric Månsson, Anders Erikson, et al.. (1995). Lysosomal free sialic acid storage disorders with different phenotypic presentations--infantile-form sialic acid storage disease and Salla disease--represent allelic disorders on 6q14-15.. Europe PMC (PubMed Central). 57(4). 893–901. 25 indexed citations

12.

Hietala, Marja, et al.. (1995). Attitudes toward genetic testing among the general population and relatives of patients with a severe genetic disease: a survey from Finland.. PubMed. 56(6). 1493–500. 93 indexed citations

13.

Palo, Pertti, et al.. (1994). Transabdominal chorionic villus sampling and amniocentesis for prenatal diagnosis: 5 years' experience at a University Centre. Prenatal Diagnosis. 14(3). 157–162. 11 indexed citations

14.

Huoponen, Kirsi, Vesa Juvonen, Antti Iitiä, et al.. (1994). Time-resolved fluorometry in the diagnosis of Leber hereditary optic neuroretinopathy. Human Mutation. 3(1). 29–36. 10 indexed citations

15.

Haataja, Leena, Johanna Schleutker, Martin Renlund, et al.. (1991). LOCALIZATION OF THE GENE DEFECT IN SALLA DISEASE - A FREE SIALIC-ACID STORAGE DISORDER. The American Journal of Human Genetics. 49(4). 358–358. 3 indexed citations

16.

Renlund, Martin, Perttì Aula, John M. Opitz, & James F. Reynolds. (1987). Prenatal detection of Salla disease based upon increased free sialic acid in amniocytes. American Journal of Medical Genetics. 28(2). 377–384. 13 indexed citations

17.

Aula, Perttì, Harriet von Koskull, Kari Teramo, et al.. (1980). Glial origin of rapidly adhering amniotic fluid cells.. BMJ. 281(6253). 1456–1457. 27 indexed citations

18.

Aula, Perttì, Juhani Rapola, S. Autio, Kari O. Raivio, & O Karjalainen. (1975). Prenatal diagnosis and fetal pathology of I-cell disease (mucolipidosis type II). The Journal of Pediatrics. 87(2). 221–226. 25 indexed citations

19.

Rapola, Juhani, S. Autio, Perttì Aula, & V. Näntö. (1974). Lymphocytic inclusions in I-cell disease. The Journal of Pediatrics. 85(1). 88–90. 19 indexed citations

20.

Simell, Olli, et al.. (1973). Enzyme defect in saccharopinuria. The Journal of Pediatrics. 82(1). 54–57. 11 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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