Reetta Hinttala

9.6k total citations
49 papers, 653 citations indexed

About

Reetta Hinttala is a scholar working on Molecular Biology, Clinical Biochemistry and Genetics. According to data from OpenAlex, Reetta Hinttala has authored 49 papers receiving a total of 653 indexed citations (citations by other indexed papers that have themselves been cited), including 36 papers in Molecular Biology, 18 papers in Clinical Biochemistry and 8 papers in Genetics. Recurrent topics in Reetta Hinttala's work include Mitochondrial Function and Pathology (23 papers), Metabolism and Genetic Disorders (18 papers) and ATP Synthase and ATPases Research (11 papers). Reetta Hinttala is often cited by papers focused on Mitochondrial Function and Pathology (23 papers), Metabolism and Genetic Disorders (18 papers) and ATP Synthase and ATPases Research (11 papers). Reetta Hinttala collaborates with scholars based in Finland, Sweden and United States. Reetta Hinttala's co-authors include Johanna Uusimaa, Kari Majamaa, Anne M. Remes, Ilmo E. Hassinen, Heikki Rantala, Jan Smeıtınk, Matias Röyttä, Peppi Koivunen, Mika Pietilä and Jukka Hakkola and has published in prestigious journals such as Journal of Clinical Investigation, PLoS ONE and Annals of Neurology.

In The Last Decade

Reetta Hinttala

44 papers receiving 631 citations

Peers

Countries citing papers authored by Reetta Hinttala

Since Specialization

Citations

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

Fields of papers citing papers by Reetta Hinttala

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Reetta Hinttala

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

#	Work	Indexed citations
1	Phenotypic Heterogeneity in Genetic and Acquired Pediatric Cerebellar Disorders 2025 ·Movement Disorders ·(unknown), Sanna Huhtaniska, (unknown), Tytti Pokka, Salla M. Kangas, Jukka S. Moilanen, Heli Helander, (unknown), (unknown), Päivi Vieira, Elisa Rahikkala, Renzo Guerrini, (unknown), (unknown), Reetta Hinttala, Maria Suo‐Palosaari, (unknown), Johanna Uusimaa	0
2	Hyperkinetic Movement Disorder Caused by the Recurrent c. 892C >T NACC1 Variant 2024 ·Movement Disorders Clinical Practice ·(unknown), Salla M. Kangas, Estrella López‐Martín, Timothy Feyma, Fernando Scaglia, Beatriz Martı́nez-Delgado, Outi Kuismin, Maria Suo‐Palosaari, Lucinda Carr, Reetta Hinttala, Manju A. Kurian, Johanna Uusimaa	1
3	Brain MRI findings in paediatric genetic disorders associated with white matter abnormalities 2024 ·Developmental Medicine & Child Neurology ·(unknown), (unknown), Salla M. Kangas, Elisa Rahikkala, Tytti Pokka, Jukka S. Moilanen, Reetta Hinttala, Päivi Vieira, Johanna Uusimaa, Maria Suo‐Palosaari	1
4	Loss-of-function mutations of the TIE1 receptor tyrosine kinase cause late-onset primary lymphedema 2024 ·Journal of Clinical Investigation ·Pascal Brouillard, Aino Murtomäki, Veli‐Matti Leppänen, Marko Hyytiäinen, (unknown), (unknown), Laurence M. Boon, Nicole Revençu, Arin K. Greene, Andrey Anisimov, Antti M. Salo, Reetta Hinttala, Lauri Eklund, I. Quéré, Kari Alitalo, Miikka Vikkula	2
5	A novel pathogenic SLC12A5 missense variant in epilepsy of infancy with migrating focal seizures causes impaired KCC2 chloride extrusion 2024 ·Frontiers in Molecular Neuroscience ·(unknown), (unknown), (unknown), Elisa Rahikkala, (unknown), Mika Kallio, Salla M. Kangas, (unknown), Marko Huttula, Reetta Hinttala, Johanna Uusimaa, Igor Medina, (unknown)	4
6	DNA polymerase gamma variants and hepatotoxicity during maintenance therapy of childhood acute lymphoblastic leukemia: is there a causal relationship? 2023 ·The Pharmacogenomics Journal ·(unknown), (unknown), Maria Suo‐Palosaari, Stine Nygaard Nielsen, Reetta Hinttala, Kjeld Schmiegelow, Johanna Uusimaa, Arja Harila‐Saari, Riitta Niinimäki	0
7	Infantile onset encephalomyopathy, retinopathy, optic atrophy, and mitochondrial DNA depletion associated with a novel pathogenic DHX16 variant 2023 ·Clinical Genetics ·(unknown), (unknown), (unknown), Salla M. Kangas, (unknown), Päivi Vieira, Elisa Rahikkala, Katri Pylkäs, Hannu Tuominen, Hannaleena Kokkonen, Ilkka Miinalainen, Javad Nadaf, Jacek Majewski, Reetta Hinttala, Johanna Uusimaa	2
8	Analysis of human brain tissue derived from DBS surgery 2022 ·Translational Neurodegeneration ·Salla M. Kangas, (unknown), (unknown), (unknown), Bishwa Ghimire, Pirkko Mattila, Johanna Uusimaa, Markku Varjosalo, Jani Katisko, Reetta Hinttala	7
9	Modeling Rare Human Disorders in Mice: The Finnish Disease Heritage 2021 ·Cells ·(unknown), Anne Heikkinen, Salla M. Kangas, Marika Karikoski, (unknown), Antti M. Salo, Johanna Uusimaa, Reetta Vuolteenaho, Reetta Hinttala, Petra Sipilä, Satu Kuure	4
10	Transmembrane Prolyl 4-Hydroxylase is a Novel Regulator of Calcium Signaling in Astrocytes 2020 ·eNeuro ·Nadiya Byts, (unknown), (unknown), (unknown), Ilkka Miinalainen, Veli‐Pekka Ronkainen, Reetta Hinttala, Kid Törnquist, Peppi Koivunen, Johanna Myllyharju	8
11	Novel variants and phenotypes widen the phenotypic spectrum of GABRG2-related disorders 2019 ·Seizure ·(unknown), John M. Schreiber, Salla M. Kangas, Katri Pylkäs, Maria Suo‐Palosaari, Elisa Rahikkala, Johanna Liinamaa, (unknown), Ilmo E. Hassinen, Päivi Myllynen, Heikki Rantala, Reetta Hinttala, Johanna Uusimaa	20
12	Structural analysis of human NHLRC2, mutations of which are associated with FINCA disease 2018 ·PLoS ONE ·Ekaterina Biterova, (unknown), Johanna Uusimaa, Reetta Hinttala, Lloyd W. Ruddock	13
13	Case report: a novel frameshift mutation in the mitochondrial cytochrome c oxidase II gene causing mitochondrial disorder 2017 ·BMC Neurology ·(unknown), Mikko Kärppä, Hannu Tuominen, Johanna Uusimaa, Markku Saari, Reetta Hinttala, Kari Majamaa	5
14	Evaluating clinical mitochondrial respiratory chain enzymes from biopsy specimens presenting skewed probability distribution of activity data 2016 ·Mitochondrion ·(unknown), Reetta Hinttala, Heikki Rantala, Pentti Nieminen, Johanna Uusimaa, Ilmo E. Hassinen	1
15	Sodium valproate induces mitochondrial respiration dysfunction in HepG2 in vitro cell model 2015 ·Toxicology ·(unknown), (unknown), Reetta Hinttala, (unknown), Mika Pietilä, Peppi Koivunen, Jukka Hakkola, Joanna Poulton, Karl Morten, Johanna Uusimaa	78
16	Acute liver failure after valproate exposure in patients with POLG1 mutations and the prognosis after liver transplantation 2014 ·Liver Transplantation ·(unknown), (unknown), Eija Tukiainen, Arno Nordin, Johanna Arola, Reetta Kälviäinen, Leena Jutila, Matias Röyttä, Reetta Hinttala, Kari Majamaa, Heikki Mäkisalo, Johanna Uusimaa	36
17	Progressive External Ophthalmoplegia in Southwestern Finland: A Clinical and Genetic Study 2012 ·Neuroepidemiology ·Mika H. Martikainen, Reetta Hinttala, Matias Röyttä, Satu K. Jääskeläinen, Maria Wendelin‐Saarenhovi, Riitta Parkkola, Kari Majamaa	4
18	Mitochondrial DNA haplogroups in early-onset Alzheimer's disease and frontotemporal lobar degeneration 2010 ·Molecular Neurodegeneration ·Johanna Krüger, Reetta Hinttala, Kari Majamaa, Anne M. Remes	25
19	Parkinsonism associated with the homozygous W748S mutation in the POLG1 gene 2008 ·Parkinsonism & Related Disorders ·Anne M. Remes, Reetta Hinttala, Mikko Kärppä, (unknown), R. Takalo, Johanna Uusimaa, Kari Majamaa	31
20	Mutated ND2 impairs mitochondrial complex I assembly and leads to Leigh Syndrome 2006 ·Molecular Genetics and Metabolism ·Cristina Ugalde, Reetta Hinttala, Sharita Timal, Roel Smeets, Richard J. Rodenburg, Johanna Uusimaa, Lambert P. van den Heuvel, Leo Nijtmans, Kari Majamaa, Jan Smeıtınk	68

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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