Nina Aula

857 total citations
10 papers, 616 citations indexed

About

Nina Aula is a scholar working on Physiology, Pediatrics, Perinatology and Child Health and Cell Biology. According to data from OpenAlex, Nina Aula has authored 10 papers receiving a total of 616 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Physiology, 4 papers in Pediatrics, Perinatology and Child Health and 4 papers in Cell Biology. Recurrent topics in Nina Aula's work include Lysosomal Storage Disorders Research (9 papers), Cellular transport and secretion (4 papers) and Neonatal Health and Biochemistry (4 papers). Nina Aula is often cited by papers focused on Lysosomal Storage Disorders Research (9 papers), Cellular transport and secretion (4 papers) and Neonatal Health and Biochemistry (4 papers). Nina Aula collaborates with scholars based in Finland, United States and Netherlands. Nina Aula's co-authors include Perttì Aula, Frans W. Verheijen, Leena Peltonen, Cecile Beerens, Marijke Joosse, Grazia M.S. Mancini, H. Galjaard, Adrie C. Havelaar, Elly Verbeek and Peter J. van der Spek and has published in prestigious journals such as Nature Genetics, The American Journal of Human Genetics and Neurobiology of Disease.

In The Last Decade

Nina Aula

10 papers receiving 604 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Nina Aula Finland	8	353	258	208	93	74	10	616
Roscoe O. Brady United States	10	426 1.2×	317 1.2×	164 0.8×	100 1.1×	27 0.4×	10	713
Marie‐Thérèse Vanier France	11	361 1.0×	335 1.3×	169 0.8×	31 0.3×	27 0.4×	17	641
Maja Di Rocco Italy	12	131 0.4×	212 0.8×	71 0.3×	39 0.4×	56 0.8×	20	459
J Jaeken Belgium	11	162 0.5×	421 1.6×	58 0.3×	116 1.2×	92 1.2×	19	760
O. Thomas Mueller United States	16	221 0.6×	313 1.2×	107 0.5×	41 0.4×	96 1.3×	30	743
Susanna Lualdi Italy	19	371 1.1×	376 1.5×	106 0.5×	48 0.5×	21 0.3×	25	690
Kyle Peake Canada	11	355 1.0×	173 0.7×	106 0.5×	40 0.4×	20 0.3×	15	582
J. Vesa Finland	11	173 0.5×	349 1.4×	131 0.6×	28 0.3×	14 0.2×	12	563
Lúcia Lacerda Portugal	16	745 2.1×	286 1.1×	294 1.4×	149 1.6×	28 0.4×	39	936
Robert L. Conway United States	13	147 0.4×	338 1.3×	82 0.4×	66 0.7×	119 1.6×	23	723

Countries citing papers authored by Nina Aula

Since Specialization

Citations

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

Fields of papers citing papers by Nina Aula

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Nina Aula

This figure shows the co-authorship network connecting the top 25 collaborators of Nina Aula. A scholar is included among the top collaborators of Nina 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 Nina Aula. Nina 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:

10 of 10 papers shown

1.

Siintola, Eija, Meral Topçu, Nina Aula, et al.. (2007). The Novel Neuronal Ceroid Lipofuscinosis Gene MFSD8 Encodes a Putative Lysosomal Transporter. The American Journal of Human Genetics. 81(1). 136–146. 166 indexed citations

2.

Joensuu, Tarja, Mervi Kuronen, Kirsi Alakurtti, et al.. (2006). Cystatin B: mutation detection, alternative splicing and expression in progressive myclonus epilepsy of Unverricht-Lundborg type (EPM1) patients. European Journal of Human Genetics. 15(2). 185–193. 61 indexed citations

3.

Aula, Nina & Perttì Aula. (2006). Prenatal diagnosis of free sialic acid storage disorders (SASD). Prenatal Diagnosis. 26(8). 655–658. 9 indexed citations

4.

Aula, Nina, Outi Kopra, Anu Jalanko, & Leena Peltonen. (2004). Sialin expression in the CNS implicates extralysosomal function in neurons. Neurobiology of Disease. 15(2). 251–261. 29 indexed citations

5.

Aula, Nina. (2003). Molecular pathogenesis of Salla disease. Työväentutkimus Vuosikirja. 4 indexed citations

6.

Aula, Nina, Anu Jalanko, Perttì Aula, & Leena Peltonen. (2002). Unraveling the molecular pathogenesis of free sialic acid storage disorders: altered targeting of mutant sialin. Molecular Genetics and Metabolism. 77(1-2). 99–107. 25 indexed citations

7.

Aula, Nina, et al.. (2001). Prenatal detection of free sialic acid storage disease: genetic and biochemical studies in nine families. Prenatal Diagnosis. 21(5). 354–358. 7 indexed citations

8.

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

9.

Verheijen, Frans W., Elly Verbeek, Nina Aula, et al.. (2000). A new gene, encoding an anion transporter, is mutated in sialic acid storage diseases. Nat Genet. 7 indexed citations

10.

Verheijen, Frans W., Elly Verbeek, Nina Aula, et al.. (1999). A new gene, encoding an anion transporter, is mutated in sialic acid storage diseases. Nature Genetics. 23(4). 462–465. 223 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.

Explore authors with similar magnitude of impact