Raija Vanhala

3.3k total citations
46 papers, 2.1k citations indexed

About

Raija Vanhala is a scholar working on Cognitive Neuroscience, Genetics and Molecular Biology. According to data from OpenAlex, Raija Vanhala has authored 46 papers receiving a total of 2.1k indexed citations (citations by other indexed papers that have themselves been cited), including 34 papers in Cognitive Neuroscience, 31 papers in Genetics and 12 papers in Molecular Biology. Recurrent topics in Raija Vanhala's work include Autism Spectrum Disorder Research (31 papers), Genetics and Neurodevelopmental Disorders (28 papers) and Genomic variations and chromosomal abnormalities (11 papers). Raija Vanhala is often cited by papers focused on Autism Spectrum Disorder Research (31 papers), Genetics and Neurodevelopmental Disorders (28 papers) and Genomic variations and chromosomal abnormalities (11 papers). Raija Vanhala collaborates with scholars based in Finland, United States and Sweden. Raija Vanhala's co-authors include Risto Näätänen, Paavo Alku, T. Lepistö, Raili Riikonen, Irma Järvelä, Tero Ylisaukko‐oja, Taina Nieminen‐von Wendt, Leena Peltonen, Teija Kujala and Mari Auranen and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Neurology and Annals of Neurology.

In The Last Decade

Raija Vanhala

46 papers receiving 2.0k citations

Peers

Raija Vanhala

GENET

PMH

DEP

Marie Gomot France

Hower Kwon United States

Maricela Alarcón United States

Gerry A. Stefanatos United States

Amy A. Lightbody United States

Christina M. Karns United States

Taina Nieminen‐von Wendt Finland

Linda Lotspeich United States

Rachel Yeung-Courchesne United States

Andrew C. Stanfield United Kingdom

Marie Gomot France

Raija Vanhala

1.8k ×1.3

783 ×0.9

GENET

492 ×1.1

307 ×1.0

PMH

411 ×1.3

DEP

Citations per year, relative to Raija Vanhala Raija Vanhala (= 1×) peers Marie Gomot

Countries citing papers authored by Raija Vanhala

Since Specialization

Citations

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

Fields of papers citing papers by Raija Vanhala

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Raija Vanhala

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

All Works

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20 of 20 papers shown

Vanhala, Raija, Heli Malm, Susanna Hinkka‐Yli‐Salomäki, et al.. (2016). Brief Report: Syndromes in Autistic Children in a Finnish Birth Cohort. Journal of Autism and Developmental Disorders. 46(8). 2780–2784. 4 indexed citations

Lindström, Riitta, et al.. (2016). Impaired neural discrimination of emotional speech prosody in children with autism spectrum disorder and language impairment. Neuroscience Letters. 628. 47–51. 21 indexed citations

Sourander, André, Heli Malm, Susanna Hinkka‐Yli‐Salomäki, et al.. (2015). The Association Between Autism Spectrum Disorders and Congenital Anomalies by Organ Systems in a Finnish National Birth Cohort. Journal of Autism and Developmental Disorders. 45(10). 3195–3203. 11 indexed citations

Hinkka‐Yli‐Salomäki, Susanna, P. Nina Banerjee, Mika Gissler, et al.. (2013). The incidence of diagnosed autism spectrum disorders in Finland. Nordic Journal of Psychiatry. 68(7). 472–480. 22 indexed citations

Kantojärvi, Katri, Karola Rehnström, Tero Ylisaukko‐oja, et al.. (2011). Fine mapping of Xq11.1‐q21.33 and mutation screening of RPS6KA6, ZNF711, ACSL4, DLG3, and IL1RAPL2 for autism spectrum disorders (ASD). Autism Research. 4(3). 228–233. 13 indexed citations

Kantojärvi, Katri, Päivi Onkamo, Raija Vanhala, et al.. (2010). Analysis of 9p24 and 11p12-13 regions in autism spectrum disorders: rs1340513 in the JMJD2C gene is associated with ASDs in Finnish sample. Psychiatric Genetics. 20(3). 102–108. 27 indexed citations

Rehnström, Karola, Tero Ylisaukko‐oja, Pekka Ellonen, et al.. (2008). Allelic variants in HTR3C show association with autism. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 150B(5). 741–746. 14 indexed citations

Lepistö, T., Raija Vanhala, Paavo Alku, et al.. (2007). The perception of invariant speech features in children with autism. Biological Psychology. 77(1). 25–31. 86 indexed citations

Riikonen, Raili, Ismo Makkonen, Raija Vanhala, et al.. (2006). Cerebrospinal fluid insulin-like growth factors IGF-1 and IGF-2 in infantile autism. Developmental Medicine & Child Neurology. 48(9). 751–751. 79 indexed citations

10.

Ylisaukko‐oja, Tero, Karola Rehnström, Mari Auranen, et al.. (2005). Analysis of four neuroligin genes as candidates for autism. European Journal of Human Genetics. 13(12). 1285–1292. 114 indexed citations

11.

Lepistö, T., Teija Kujala, Raija Vanhala, et al.. (2005). The discrimination of and orienting to speech and non-speech sounds in children with autism. Brain Research. 1066(1-2). 147–157. 238 indexed citations

12.

Ylisaukko‐oja, Tero, Maricela Alarcón, Rita M. Cantor, et al.. (2005). Search for autism loci by combined analysis of Autism Genetic Resource Exchange and Finnish families. Annals of Neurology. 59(1). 145–155. 100 indexed citations

13.

Ylisaukko‐oja, Tero, et al.. (2004). Identification of two AGTR2 mutations in male patients with non-syndromic mental retardation. Human Genetics. 114(2). 211–213. 15 indexed citations

14.

Ylisaukko‐oja, Tero, Myriam Peyrard‐Janvid, Cecilia M. Lindgren, et al.. (2004). Family-based association study of DYX1C1 variants in autism. European Journal of Human Genetics. 13(1). 127–130. 12 indexed citations

15.

Auranen, Mari, Teppo Varilo, Reija Alén, et al.. (2003). Evidence for allelic association on chromosome 3q25–27 in families with autism spectrum disorders originating from a subisolate of Finland. Molecular Psychiatry. 8(10). 879–884. 29 indexed citations

16.

Wendt, Taina Nieminen‐von, Liisa Metsähonkala, Sargo Aalto, et al.. (2003). Changes in cerebral blood flow in Asperger syndrome during theory of mind tasks presented by the auditory route. European Child & Adolescent Psychiatry. 12(4). 178–189. 52 indexed citations

17.

Paavonen, E. Juulia, Taina Nieminen‐von Wendt, Raija Vanhala, Eeva T. Aronen, & Lennart von Wendt. (2003). Effectiveness of Melatonin in the Treatment of Sleep Disturbances in Children with Asperger Disorder. Journal of Child and Adolescent Psychopharmacology. 13(1). 83–95. 101 indexed citations

18.

Čėponiené, Rita, T. Lepistö, Анна Шестакова, et al.. (2003). Speech–sound-selective auditory impairment in children with autism: They can perceive but do not attend. Proceedings of the National Academy of Sciences. 100(9). 5567–5572. 302 indexed citations

19.

Wendt, Taina Nieminen‐von, et al.. (2002). A quantitative controlled MRI study of the brain in 28 persons with Asperger syndrome. PubMed. 61(0). 22–35. 3 indexed citations

20.

Riikonen, Raili, Stine Söderström, Raija Vanhala, Ted Ebendal, & Dan Lindholm. (1997). West syndrome: Cerebrospinal fluid nerve growth factor and effect of ACTH. Pediatric Neurology. 17(3). 224–229. 25 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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