Auli Sirén

772 total citations
14 papers, 238 citations indexed

About

Auli Sirén is a scholar working on Genetics, Psychiatry and Mental health and Cellular and Molecular Neuroscience. According to data from OpenAlex, Auli Sirén has authored 14 papers receiving a total of 238 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Genetics, 6 papers in Psychiatry and Mental health and 5 papers in Cellular and Molecular Neuroscience. Recurrent topics in Auli Sirén's work include Genetics and Neurodevelopmental Disorders (6 papers), Epilepsy research and treatment (5 papers) and Neuroscience and Neuropharmacology Research (5 papers). Auli Sirén is often cited by papers focused on Genetics and Neurodevelopmental Disorders (6 papers), Epilepsy research and treatment (5 papers) and Neuroscience and Neuropharmacology Research (5 papers). Auli Sirén collaborates with scholars based in Finland, Belgium and United States. Auli Sirén's co-authors include Maria Arvio, Kari Hirvonen, M. Tenhunen, Anneli Kylliäinen, M Koivikko, Irma Järvelä, Kristiina Avela, Massimo Pandolfo, Eva Andermann and Hao Hu and has published in prestigious journals such as Neurology, Scientific Reports and Movement Disorders.

In The Last Decade

Auli Sirén

14 papers receiving 234 citations

Peers

Auli Sirén
Viola Doccini Italy
V. Sgrò Italy
Matthew J. Gazzellone Canada
Valentina Marchiani Italy
Theresa Scattergood United States
Ahmed Abdelmoity United States
Seok Kyu Kang United States
Anne Hempelmann Germany
Trine Bjørg Hammer Denmark
Estelle Fédirko France
Viola Doccini Italy
Auli Sirén
Citations per year, relative to Auli Sirén Auli Sirén (= 1×) peers Viola Doccini

Countries citing papers authored by Auli Sirén

Since Specialization
Citations

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

Fields of papers citing papers by Auli Sirén

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Auli Sirén

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

All Works

14 of 14 papers shown
1.
Schrauwen, Isabelle, Anushree Acharya, Susanna Öhman, et al.. (2024). Optical genome mapping unveils hidden structural variants in neurodevelopmental disorders. Scientific Reports. 14(1). 11239–11239. 7 indexed citations
2.
Häppölä, Paavo, Ville Artto, Heidi Hautakangas, et al.. (2022). NCOR2 is a novel candidate gene for migraine-epilepsy phenotype. Cephalalgia. 42(7). 631–644. 5 indexed citations
3.
Kokkonen, Hannaleena, Auli Sirén, Tuomo Määttä, et al.. (2021). Identification of microduplications at Xp21.2 and Xq13.1 in neurodevelopmental disorders. Molecular Genetics & Genomic Medicine. 9(12). e1703–e1703. 7 indexed citations
4.
Sirén, Auli, et al.. (2019). Cognition in adults with Williams syndrome—A 20‐year follow‐up study. Molecular Genetics & Genomic Medicine. 7(6). e695–e695. 8 indexed citations
5.
Sirén, Auli, et al.. (2018). Signs indicating dementia in Down, Williams and Fragile X syndromes. Molecular Genetics & Genomic Medicine. 6(5). 855–860. 15 indexed citations
6.
Sirén, Auli, Kristiina Avela, Mirja Somer, et al.. (2014). X-exome sequencing in Finnish families with Intellectual Disability - four novel mutations and two novel syndromic phenotypes. Orphanet Journal of Rare Diseases. 9(1). 49–49. 52 indexed citations
7.
Abou‐Khalil, Bassel, Auli Sirén, Frédérick Andermann, et al.. (2013). A new locus for familial temporal lobe epilepsy on chromosome 3q. Epilepsy Research. 106(3). 338–344. 14 indexed citations
8.
Kovel, Carolien G. F. de, Dalila Pinto, Ulrike Tauer, et al.. (2010). Whole-genome linkage scan for epilepsy-related photosensitivity: A mega-analysis. Epilepsy Research. 89(2-3). 286–294. 33 indexed citations
9.
Sirén, Auli, Anne Polvi, Malgorzata Labuda, et al.. (2009). Suggestive evidence for a new locus for epilepsy with heterogeneous phenotypes on chromosome 17q. Epilepsy Research. 88(1). 65–75. 14 indexed citations
10.
Sirén, Auli, et al.. (2007). Beneficial effects of antiepileptic medication on absence seizures and cognitive functioning in children. Epilepsy & Behavior. 11(1). 85–91. 37 indexed citations
11.
Sirén, Auli, et al.. (2006). Hyperekplexia in Kurdish families: A possible GLRA1 founder mutation. Neurology. 67(1). 137–139. 7 indexed citations
12.
13.
Badhwar, AmanPreet, Auli Sirén, Eva Andermann, & Frédérick Andermann. (2002). Myoclonic status epilepticus: Video presentation. Movement Disorders. 17(2). 409–411. 6 indexed citations
14.
Robinson, Robert, Nichole Taske, Thomas Sander, et al.. (2002). Linkage analysis between childhood absence epilepsy and genes encoding GABAA and GABAB receptors, voltage-dependent calcium channels, and the ECA1 region on chromosome 8q. Epilepsy Research. 48(3). 169–179. 23 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

Breakdown of academic impact, for papers by Viola Doccini Breakdown of academic impact, for papers by V. Sgrò Breakdown of academic impact, for papers by Matthew J. Gazzellone Breakdown of academic impact, for papers by Valentina Marchiani Breakdown of academic impact, for papers by Theresa Scattergood Breakdown of academic impact, for papers by Ahmed Abdelmoity Breakdown of academic impact, for papers by Seok Kyu Kang Breakdown of academic impact, for papers by Anne Hempelmann Breakdown of academic impact, for papers by Trine Bjørg Hammer Breakdown of academic impact, for papers by Estelle Fédirko
Rankless by CCL
2026