Maria Suo‐Palosaari

535 total citations
30 papers, 272 citations indexed

About

Maria Suo‐Palosaari is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Maria Suo‐Palosaari has authored 30 papers receiving a total of 272 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 6 papers in Genetics and 5 papers in Surgery. Recurrent topics in Maria Suo‐Palosaari's work include Genomics and Rare Diseases (5 papers), Mitochondrial Function and Pathology (5 papers) and RNA regulation and disease (3 papers). Maria Suo‐Palosaari is often cited by papers focused on Genomics and Rare Diseases (5 papers), Mitochondrial Function and Pathology (5 papers) and RNA regulation and disease (3 papers). Maria Suo‐Palosaari collaborates with scholars based in Finland, Sweden and United Kingdom. Maria Suo‐Palosaari's co-authors include Tytti Pokka, Timo Saarela, Merja Kallio, Niina Salokorpi, Tero Kontiokari, Outi Peltoniemi, Päivi Olsén, Johanna Uusimaa, Heikki Rantala and Mikko Hallman and has published in prestigious journals such as PLoS ONE, IEEE Transactions on Biomedical Engineering and Movement Disorders.

In The Last Decade

Maria Suo‐Palosaari

26 papers receiving 270 citations

Peers

Maria Suo‐Palosaari
Andrea Müllner-Eidenböck Austria
Robert P. Gallegos United States
Leo Hochhäuser United States
Shawn E. Parnell United States
Archana Ramesh United States
Martin Hlavica Switzerland
Hideaki Kohga Japan
Anna Wędrychowicz Poland
Katelyn Shortt Canada
N. Grimoldi Italy
Andrea Müllner-Eidenböck Austria
Maria Suo‐Palosaari
Citations per year, relative to Maria Suo‐Palosaari Maria Suo‐Palosaari (= 1×) peers Andrea Müllner-Eidenböck

Countries citing papers authored by Maria Suo‐Palosaari

Since Specialization
Citations

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

Fields of papers citing papers by Maria Suo‐Palosaari

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Maria Suo‐Palosaari

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

All Works

20 of 20 papers shown
1.
Huhtaniska, Sanna, Tytti Pokka, Salla M. Kangas, et al.. (2025). Phenotypic Heterogeneity in Genetic and Acquired Pediatric Cerebellar Disorders. Movement Disorders. 40(9). 1851–1862.
2.
Kangas, Salla M., Estrella López‐Martín, Timothy Feyma, et al.. (2024). Hyperkinetic Movement Disorder Caused by the Recurrent c. 892C >T NACC1 Variant. Movement Disorders Clinical Practice. 11(6). 708–715. 1 indexed citations
3.
Kangas, Salla M., Elisa Rahikkala, Tytti Pokka, et al.. (2024). Brain MRI findings in paediatric genetic disorders associated with white matter abnormalities. Developmental Medicine & Child Neurology. 67(2). 186–194. 1 indexed citations
4.
Rahikkala, Elisa, Maria Suo‐Palosaari, Päivi Vieira, et al.. (2024). Optical Genome Mapping Identifies a Second Xq27.1 Rearrangement Associated With Charcot–Marie–Tooth Neuropathy CMTX3. Molecular Genetics & Genomic Medicine. 12(9). e70014–e70014.
5.
Suo‐Palosaari, Maria, Pekka Arikoski, Päivi Koskenkorva, et al.. (2023). Radiotherapy-induced vascular cognitive impairment 20 years after childhood brain tumor. Neuro-Oncology. 26(2). 362–373. 1 indexed citations
6.
Suo‐Palosaari, Maria, Stine Nygaard Nielsen, Reetta Hinttala, et al.. (2023). DNA polymerase gamma variants and hepatotoxicity during maintenance therapy of childhood acute lymphoblastic leukemia: is there a causal relationship?. The Pharmacogenomics Journal. 23(5). 105–111.
7.
Kivisaari, Reetta, Maria Suo‐Palosaari, Pekka Arikoski, et al.. (2023). Early disc degeneration in radiotherapy-treated childhood brain tumor survivors. BMC Musculoskeletal Disorders. 24(1). 441–441. 1 indexed citations
8.
Suo‐Palosaari, Maria, et al.. (2022). Favourable long-term recovery after decompressive craniectomy: the Northern Finland experience with a predominantly adolescent patient cohort. Child s Nervous System. 38(9). 1763–1772. 1 indexed citations
9.
Nordebo, Sven, Merja Kallio, Inéz Frerichs, et al.. (2021). Model Selection Based Algorithm in Neonatal Chest EIT. IEEE Transactions on Biomedical Engineering. 68(9). 2752–2763. 8 indexed citations
10.
Pyle, Angela, Maria Suo‐Palosaari, Jennifer Duff, et al.. (2020). Homozygous TAF1C variants are associated with a novel childhood‐onset neurological phenotype. Clinical Genetics. 98(5). 493–498. 3 indexed citations
11.
Hekkala, Anne, Outi Kuismin, Hannu Tuominen, et al.. (2020). Medulloblastoma, macrocephaly, and a pathogenic germline PTEN variant: Cause or coincidence?. Molecular Genetics & Genomic Medicine. 8(9). e1302–e1302. 4 indexed citations
12.
Olsén, Päivi, et al.. (2020). Is Brain MRI Needed in Diagnostic Evaluation of Mild Intellectual Disability?. Neuropediatrics. 52(1). 27–33. 1 indexed citations
13.
Mäkitie, Riikka E., Tuukka Niinimäki, Maria Suo‐Palosaari, et al.. (2020). PLS3 Mutations Cause Severe Age and Sex-Related Spinal Pathology. Frontiers in Endocrinology. 11. 393–393. 13 indexed citations
14.
Suo‐Palosaari, Maria, Anna Sutela, Päivi Koskenkorva, et al.. (2019). Radiation-Induced Meningiomas After Childhood Brain Tumor: A Magnetic Resonance Imaging Screening Study. Journal of Adolescent and Young Adult Oncology. 8(5). 593–601. 13 indexed citations
15.
Kallio, Merja, Outi Aikio, Maria Suo‐Palosaari, et al.. (2019). NIV NAVA versus Nasal CPAP in Premature Infants: A Randomized Clinical Trial. Neonatology. 116(4). 380–384. 28 indexed citations
16.
Schreiber, John M., Salla M. Kangas, Katri Pylkäs, et al.. (2019). Novel variants and phenotypes widen the phenotypic spectrum of GABRG2-related disorders. Seizure. 69. 99–104. 20 indexed citations
17.
Harila‐Saari, Arja, Jaakko Niinimäki, Tytti Pokka, et al.. (2018). Late vertebral side effects in long-term survivors of irradiated childhood brain tumor. PLoS ONE. 13(12). e0209193–e0209193. 11 indexed citations
18.
Kallio, Merja, Outi Peltoniemi, Tero Kontiokari, et al.. (2016). Neurally adjusted ventilatory assist (NAVA) in preterm newborn infants with respiratory distress syndrome—a randomized controlled trial. European Journal of Pediatrics. 175(9). 1175–1183. 44 indexed citations
19.
Sinikumpu, Juha‐Jaakko, et al.. (2016). [Severe trampoline injuries and their risk factors among children and the young].. PubMed. 132(11). 1061–8. 2 indexed citations
20.
Suo‐Palosaari, Maria, Balázs Sármán, Nina Hautala, et al.. (2007). Cardiac BNP gene activation by angiotensin II in vivo. Molecular and Cellular Endocrinology. 273(1-2). 59–67. 27 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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