Auli Nuutila

466 total citations
9 papers, 343 citations indexed

About

Auli Nuutila is a scholar working on Molecular Biology, Genetics and Psychiatry and Mental health. According to data from OpenAlex, Auli Nuutila has authored 9 papers receiving a total of 343 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 3 papers in Genetics and 3 papers in Psychiatry and Mental health. Recurrent topics in Auli Nuutila's work include Mitochondrial Function and Pathology (3 papers), Epilepsy research and treatment (3 papers) and Metabolism and Genetic Disorders (2 papers). Auli Nuutila is often cited by papers focused on Mitochondrial Function and Pathology (3 papers), Epilepsy research and treatment (3 papers) and Metabolism and Genetic Disorders (2 papers). Auli Nuutila collaborates with scholars based in Finland, United Kingdom and United States. Auli Nuutila's co-authors include Jyrki Launes, Juhani Rapola, Raili Raininko, Pirkko Santavuori, Taina Autti, Marjatta Lappi, Kimmo Sainio, Anu Suomalainen, Anna Majander and P. Santavuori and has published in prestigious journals such as Journal of Neurology Neurosurgery & Psychiatry, Epilepsia and Pediatric Research.

In The Last Decade

Auli Nuutila

9 papers receiving 326 citations

Peers

Auli Nuutila

MB

PHYSI

PMH

CB

PPCH

M. Tardieu France

Anne Roubergue France

Christiane Kehrer Germany

Heather Cahan United States

Sabine Grønborg Denmark

Noboru Fueki Japan

Charlotte Thiels Germany

Sylvie Duthel France

M. Barth France

Dawn Cordeiro Canada

M. Tardieu France

Auli Nuutila

217 ×1.4

MB

118 ×0.8

PHYSI

33 ×0.4

PMH

110 ×1.8

CB

48 ×0.8

PPCH

Citations per year, relative to Auli Nuutila Auli Nuutila (= 1×) peers M. Tardieu

Countries citing papers authored by Auli Nuutila

Since Specialization

Citations

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

Fields of papers citing papers by Auli Nuutila

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Auli Nuutila

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

All Works

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9 of 9 papers shown

1.

Ebeling, Freja, et al.. (2003). Infant stroke and beta-2-glycoprotein 1 antibodies: six cases. European Journal of Pediatrics. 162(10). 678–681. 14 indexed citations

2.

Vanhatalo, Sampsa, Iiris Nousiainen, Kai Eriksson, et al.. (2002). Visual Field Constriction in 91 Finnish Children Treated with Vigabatrin. Epilepsia. 43(7). 748–756. 67 indexed citations

3.

Heiskala, Hannu, Raili Riikonen, Pirkko Santavuori, et al.. (1996). West syndrome: individualized ACTH therapy. Brain and Development. 18(6). 456–460. 31 indexed citations

4.

Suomalainen, Anu, Anna Majander, Juhani Rapola, et al.. (1995). Correlation between the Clinical Symptoms and the Proportion of Mitochondrial DNA Carrying the 8993 Point Mutation in the NARP Syndrome. Pediatric Research. 37(5). 634–639. 70 indexed citations

5.

Suomalainen, Anu, Anna Majander, Juhani Rapola, et al.. (1994). Infantile SPASMS as presenting symptom of mitochondrial DNA 8993 T → G point mutation. Pediatric Neurology. 11(2). 85–85. 1 indexed citations

6.

Santavuori, Pirkko, Juhani Rapola, Raili Raininko, et al.. (1993). Early juvenile neuronal ceroid‐lipofuscinosis or variant Jansky‐Bielschowsky disease: Diagnostic criteria and nomenclature. Journal of Inherited Metabolic Disease. 16(2). 230–232. 18 indexed citations

7.

Autti, Taina, Raili Raininko, Jyrki Launes, Auli Nuutila, & Pirkko Santavuori. (1992). Jansky-Bielschowsky variant disease: CT, MRI, and SPECT findings. Pediatric Neurology. 8(2). 121–126. 52 indexed citations

8.

Santavuori, P., Juhani Rapola, Auli Nuutila, et al.. (1991). The Spectrum of Jansky-Bielschowsky Disease. Neuropediatrics. 22(2). 92–96. 81 indexed citations

9.

Iivanainen, M., Lea Bergström, Auli Nuutila, & M Viukari. (1984). Psychosis-like absence status of elderly patients: successful treatment with sodium valproate.. Journal of Neurology Neurosurgery & Psychiatry. 47(9). 965–969. 9 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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