Andreea Manole

1.8k total citations
28 papers, 428 citations indexed

About

Andreea Manole is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Neurology. According to data from OpenAlex, Andreea Manole has authored 28 papers receiving a total of 428 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 9 papers in Cellular and Molecular Neuroscience and 6 papers in Neurology. Recurrent topics in Andreea Manole's work include Mitochondrial Function and Pathology (5 papers), Metabolism and Genetic Disorders (5 papers) and Hereditary Neurological Disorders (3 papers). Andreea Manole is often cited by papers focused on Mitochondrial Function and Pathology (5 papers), Metabolism and Genetic Disorders (5 papers) and Hereditary Neurological Disorders (3 papers). Andreea Manole collaborates with scholars based in United Kingdom, United States and Spain. Andreea Manole's co-authors include Henry Houlden, Stéphanie Efthymiou, Balasubramaniem Ashokkumar, Perumal Varalakshmi, Vincenzo Salpietro, Dimitri A. Svistunenko, Evgeny Zherebtsov, Mary M. Reilly, Conceição Bettencourt and Andrey Y. Abramov and has published in prestigious journals such as SHILAP Revista de lepidopterología, Neurology and Biochemistry.

In The Last Decade

Andreea Manole

27 papers receiving 418 citations

Peers

Andreea Manole
A. Larnaout Tunisia
Asbjørn Holmgren Norway
Sachit Shah United Kingdom
Tae Hyuk Kang United States
Eliana Báez-Jurado Colombia
Gianfrancesco Goracci Italy
Hyo Min Cho South Korea
Stéphanie Gobin France
Katja Scheffler Norway
Linlin Xu China
A. Larnaout Tunisia
Andreea Manole
Citations per year, relative to Andreea Manole Andreea Manole (= 1×) peers A. Larnaout

Countries citing papers authored by Andreea Manole

Since Specialization
Citations

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

Fields of papers citing papers by Andreea Manole

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Andreea Manole

This figure shows the co-authorship network connecting the top 25 collaborators of Andreea Manole. A scholar is included among the top collaborators of Andreea Manole 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 Andreea Manole. Andreea Manole 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.
Rosh, Idan, Andreea Manole, Henry Houlden, et al.. (2024). Synaptic dysfunction and extracellular matrix dysregulation in dopaminergic neurons from sporadic and E326K-GBA1 Parkinson’s disease patients. npj Parkinson s Disease. 10(1). 38–38. 10 indexed citations
2.
Scalco, R., Jasper M. Morrow, Andreea Manole, et al.. (2024). Crossover randomized controlled trial of bumetanide to rescue an attack of exercise induced hand weakness in hypokalaemic periodic paralysis. Neuromuscular Disorders. 35. 33–38.
3.
Rosh, Idan, Ashwani Choudhary, Andreea Manole, et al.. (2024). Upregulated ECM genes and increased synaptic activity in Parkinson’s human DA neurons with PINK1/ PRKN mutations. npj Parkinson s Disease. 10(1). 103–103. 5 indexed citations
4.
5.
Manole, Andreea, et al.. (2020). Adrenaline induces calcium signal in astrocytes and vasoconstriction via activation of monoamine oxidase. Free Radical Biology and Medicine. 159. 15–22. 29 indexed citations
6.
Svistunenko, Dimitri A. & Andreea Manole. (2020). Tyrosyl radical in haemoglobin and haptoglobin-haemoglobin complex: how does haptoglobin make haemoglobin less toxic?. Journal of Biomedical Research. 34(4). 281–281. 3 indexed citations
7.
Horga, Alejandro, Isabel Pareés, Iain P. Hargreaves, et al.. (2019). Differential phenotypic expression of a novel PDHA1 mutation in a female monozygotic twin pair. Human Genetics. 138(11-12). 1313–1322. 9 indexed citations
8.
Horga, Alejandro, Enrico Bugiardini, Andreea Manole, et al.. (2019). Autosomal dominant optic atrophy and cataract “plus” phenotype including axonal neuropathy. Neurology Genetics. 5(2). e322–e322. 11 indexed citations
9.
Durigon, Romina, Alice Mitchell, Aleck W.E. Jones, et al.. (2018). LETM 1 couples mitochondrial DNA metabolism and nutrient preference. EMBO Molecular Medicine. 10(9). 29 indexed citations
10.
Desikan, M., R. Scalco, Andreea Manole, et al.. (2018). GYG1 causing progressive limb girdle myopathy with onset during teenage years (polyglucosan body myopathy 2). Neuromuscular Disorders. 28(4). 346–349. 5 indexed citations
11.
Salpietro, Vincenzo, Belén Pérez‐Dueñas, Kosuke Nakashima, et al.. (2018). A homozygous loss‐of‐function mutation in PDE2A associated to early‐onset hereditary chorea. Movement Disorders. 33(3). 482–488. 42 indexed citations
12.
Mahesh, Ayyavu, et al.. (2017). Adaptive regulation of riboflavin transport in heart: effect of dietary riboflavin deficiency in cardiovascular pathogenesis. Molecular and Cellular Biochemistry. 440(1-2). 147–156. 13 indexed citations
13.
Manole, Andreea, Alejandro Horga, Josep Gámez, et al.. (2016). SBF1 mutations associated with autosomal recessive axonal neuropathy with cranial nerve involvement. Neurogenetics. 18(1). 63–67. 10 indexed citations
14.
Mestre, Tiago, Andreea Manole, H. Robson MacDonald, et al.. (2016). A novel KCNA1 mutation in a family with episodic ataxia and malignant hyperthermia. Neurogenetics. 17(4). 245–249. 21 indexed citations
15.
Chelban, Viorica, Andreea Manole, Lasse Pihlstrøm, et al.. (2016). Analysis of the prion protein gene in multiple system atrophy. Neurobiology of Aging. 49. 216.e15–216.e18. 7 indexed citations
16.
Manole, Andreea, Viorica Chelban, Nourelhoda A. Haridy, et al.. (2016). Severe axonal neuropathy is a late manifestation of SPG11. Journal of Neurology. 263(11). 2278–2286. 12 indexed citations
17.
Manole, Andreea, Demet Kekilli, Dimitri A. Svistunenko, et al.. (2015). Conformational control of the binding of diatomic gases to cytochrome c′. JBIC Journal of Biological Inorganic Chemistry. 20(4). 675–686. 12 indexed citations
18.
Manole, Andreea & Henry Houlden. (2015). Riboflavin Transporter Deficiency Neuronopathy. 7 indexed citations
19.
Manole, Andreea, Pietro Fratta, & Henry Houlden. (2014). Recent advances in bulbar syndromes. Current Opinion in Neurology. 27(5). 506–514. 8 indexed citations
20.
Manole, Andreea, et al.. (1983). Phosphatase activity in the myenteric plexus.. PubMed. 26(3). 225–9. 2 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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