Maria Arvio

950 total citations
42 papers, 587 citations indexed

About

Maria Arvio is a scholar working on Genetics, Molecular Biology and Psychiatry and Mental health. According to data from OpenAlex, Maria Arvio has authored 42 papers receiving a total of 587 indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Genetics, 17 papers in Molecular Biology and 8 papers in Psychiatry and Mental health. Recurrent topics in Maria Arvio's work include Genetics and Neurodevelopmental Disorders (18 papers), Genomics and Rare Diseases (9 papers) and Epilepsy research and treatment (7 papers). Maria Arvio is often cited by papers focused on Genetics and Neurodevelopmental Disorders (18 papers), Genomics and Rare Diseases (9 papers) and Epilepsy research and treatment (7 papers). Maria Arvio collaborates with scholars based in Finland, United States and Germany. Maria Arvio's co-authors include Matti Sillanpää, Maarit Peippo, Jukka Peltola, Kai Lehtimäki, Suvi Liimatainen, K. O. J. Simola, Auli Sirén, Leena Haataja, Aila Tiitinen and Irma Järvelä and has published in prestigious journals such as SHILAP Revista de lepidopterología, NeuroImage and Scientific Reports.

In The Last Decade

Maria Arvio

41 papers receiving 574 citations

Peers

Maria Arvio

GENET

PMH

PHEOH

David K. Urion United States

Mary A. Murphy United States

Nicholas Craddock United Kingdom

Heidi Cope United States

Po‐Chang Hsiao Taiwan

Luke S. Heuer United States

Laura Hercher United States

Erick Sell Canada

Joan Jasien United States

Jennifer Judy United States

David K. Urion United States

Maria Arvio

114 ×0.4

GENET

120 ×0.8

203 ×1.4

PMH

108 ×0.8

99 ×0.9

PHEOH

Citations per year, relative to Maria Arvio Maria Arvio (= 1×) peers David K. Urion

Countries citing papers authored by Maria Arvio

Since Specialization

Citations

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

Fields of papers citing papers by Maria Arvio

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Maria Arvio

This figure shows the co-authorship network connecting the top 25 collaborators of Maria Arvio. A scholar is included among the top collaborators of Maria Arvio 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 Maria Arvio. Maria Arvio 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

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

Parkkola, Riitta, Anushree Acharya, Suzanne M. Leal, et al.. (2023). A novel variant in CYFIP2 in a girl with severe disabilities and bilateral perisylvian polymicrogyria. American Journal of Medical Genetics Part A. 194(4). e63478–e63478. 1 indexed citations

Arvio, Maria, et al.. (2023). Manifestations of Intellectual Disability, Dystonia, and Parkinson’s Disease in an Adult Patient with ARX Gene Mutation c.558_560dup p.(Pro187dup). SHILAP Revista de lepidopterología. 2023. 1–5.

Arvio, Maria, et al.. (2021). Report of a novel missense mutation in the MECP2 gene in a middle‐aged man with intellectual disability syndrome. SHILAP Revista de lepidopterología. 9(8). e04602–e04602. 2 indexed citations

Carroll, Renée, Marie Shaw, Maria Arvio, et al.. (2020). Two novel intragenic variants in the FMR1 gene in patients with suspect clinical diagnosis of Fragile X syndrome and no CGG repeat expansion. European Journal of Medical Genetics. 63(10). 104010–104010. 4 indexed citations

Arvio, Maria, et al.. (2016). Age at Death in Individuals with Intellectual Disabilities. Journal of Applied Research in Intellectual Disabilities. 30(4). 782–785. 25 indexed citations

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

Arvio, Maria, H Kääriäinen, Hilde Van Esch, et al.. (2013). Novel changes in the SLC16A2 gene identified by X-exome sequencing in two Finnish families with Allan-Herndon Dudley syndrome. European Journal of Human Genetics. 21. 161–162. 1 indexed citations

Lehtimäki, Kai, Suvi Liimatainen, Jukka Peltola, & Maria Arvio. (2011). The serum level of interleukin-6 in patients with intellectual disability and refractory epilepsy. Epilepsy Research. 95(1-2). 184–187. 41 indexed citations

10.

Lehtimäki, Kai, Jukka Peltola, Suvi Liimatainen, Anna‐Maija Haapala, & Maria Arvio. (2011). Cardiolipin and β2-Glycoprotein I antibodies associate with cognitive impairment and seizure frequency in developmental disorders. Seizure. 20(6). 438–441. 4 indexed citations

11.

Kerr, Mike, Mark Scheepers, Maria Arvio, et al.. (2009). Consensus guidelines into the management of epilepsy in adults with an intellectual disability. Journal of Intellectual Disability Research. 53(8). 687–694. 59 indexed citations

12.

Louhivuori, Verna, et al.. (2009). The Val66Met polymorphism in the BDNF gene is associated with epilepsy in fragile X syndrome. Epilepsy Research. 85(1). 114–117. 25 indexed citations

13.

Pekkonen, Eero, et al.. (2007). Delayed auditory processing underlying stimulus detection in Down syndrome. NeuroImage. 35(4). 1547–1550. 16 indexed citations

14.

Arvio, Maria & Matti Sillanpää. (2003). Prevalence, aetiology and comorbidity of severe and profound intellectual disability in Finland. Journal of Intellectual Disability Research. 47(2). 108–112. 93 indexed citations

15.

Arvio, Maria, et al.. (2003). Temporo-occipital spikes: a typical EEG finding in Kabuki syndrome. Pediatric Neurology. 30(1). 67–70. 13 indexed citations

16.

Arvio, Maria, Juhani Rapola, & P. Pelkonen. (1998). Chronic arthritis in patients with aspartylglucosaminuria.. PubMed. 25(6). 1131–4. 13 indexed citations

17.

Arvio, Maria, et al.. (1998). Impaired oral health in patients with aspartylglucosaminuria. Oral Surgery Oral Medicine Oral Pathology Oral Radiology and Endodontology. 86(5). 562–568. 9 indexed citations

18.

Arvio, Maria, Maarit Peippo, & K. O. J. Simola. (1997). Applicability of a checklist for clinical screening of the fragile X syndrome. Clinical Genetics. 52(4). 211–215. 31 indexed citations

19.

Arvio, Maria. (1993). Follow‐up in patients with aspartylglucosaminuria. Part II. Adaptive skills. Acta Paediatrica. 82(6-7). 590–594. 15 indexed citations

20.

Arvio, Maria. (1993). Follow‐up in patients with aspartylglucosaminuria. Part I. The course of intellectual functions. Acta Paediatrica. 82(5). 469–471. 22 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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