Nadja Schröder

5.5k total citations · 1 hit paper
104 papers, 4.3k citations indexed

About

Nadja Schröder is a scholar working on Cellular and Molecular Neuroscience, Cognitive Neuroscience and Molecular Biology. According to data from OpenAlex, Nadja Schröder has authored 104 papers receiving a total of 4.3k indexed citations (citations by other indexed papers that have themselves been cited), including 49 papers in Cellular and Molecular Neuroscience, 28 papers in Cognitive Neuroscience and 24 papers in Molecular Biology. Recurrent topics in Nadja Schröder's work include Neuroscience and Neuropharmacology Research (39 papers), Memory and Neural Mechanisms (25 papers) and Stress Responses and Cortisol (13 papers). Nadja Schröder is often cited by papers focused on Neuroscience and Neuropharmacology Research (39 papers), Memory and Neural Mechanisms (25 papers) and Stress Responses and Cortisol (13 papers). Nadja Schröder collaborates with scholars based in Brazil, Argentina and United States. Nadja Schröder's co-authors include Rafael Roesler, Maria Noêmia Martins de Lima, João Quevedo, Elke Bromberg, Iván Izquierdo, Vanessa Athaíde Garcia, Daniela Comparsi Laranja, Flávio Kapczinski, Antônio Waldo Zuardi and Jaime E. C. Hallak and has published in prestigious journals such as SHILAP Revista de lepidopterología, Brain Research and Neuroscience.

In The Last Decade

Nadja Schröder

104 papers receiving 4.2k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Cannabidiol Reduces the Anxiety Induced by Simulated Public Speaking in Treatment-Naïve Social Phobia Patients

2011 560 citations Flávio Kapczinski, João Quevedo et al. profile →

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Nadja Schröder Brazil	36	1.7k	1.0k	1.0k	978	539	104	4.3k
Grażyna Biała Poland	30	1.8k 1.1×	1.6k 1.5×	578 0.6×	828 0.8×	725 1.3×	117	4.2k
Tim Karl Australia	42	2.1k 1.3×	1.3k 1.3×	469 0.5×	1.6k 1.6×	985 1.8×	127	5.0k
Jae Hoon Cheong South Korea	41	1.3k 0.8×	1.7k 1.6×	1.1k 1.1×	765 0.8×	540 1.0×	242	5.9k
Colin N. Haile United States	35	2.1k 1.2×	1.3k 1.2×	581 0.6×	530 0.5×	591 1.1×	86	4.0k
Christian P. Müller Germany	44	2.5k 1.5×	2.4k 2.3×	892 0.9×	654 0.7×	777 1.4×	201	6.9k
Reinaldo Ν. Takahashi Brazil	46	3.3k 2.0×	833 0.8×	1.5k 1.5×	2.1k 2.1×	696 1.3×	126	5.9k
Elio Acquas Italy	38	3.6k 2.1×	1.7k 1.7×	1.1k 1.1×	883 0.9×	471 0.9×	105	5.0k
Nuri B. Farber United States	38	2.2k 1.3×	1.2k 1.2×	883 0.8×	643 0.7×	453 0.8×	81	5.4k
Luca Steardo Italy	42	1.8k 1.0×	1.3k 1.3×	508 0.5×	2.0k 2.0×	993 1.8×	137	5.8k
András Bilkei‐Gorzó Germany	30	1.6k 1.0×	803 0.8×	539 0.5×	1.1k 1.2×	736 1.4×	82	3.4k

Countries citing papers authored by Nadja Schröder

Since Specialization

Citations

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

Fields of papers citing papers by Nadja Schröder

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Nadja Schröder

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

Molz, Patrícia, et al.. (2021). Effects of lipoic acid supplementation on age- and iron-induced memory impairment, mitochondrial DNA damage and antioxidant responses. European Journal of Nutrition. 60(7). 3679–3690. 13 indexed citations

Freitas, Betânia Souza de, Luiza Wilges Kist, Maurı́cio Reis Bogo, et al.. (2018). Novel insights into mitochondrial molecular targets of iron-induced neurodegeneration: Reversal by cannabidiol. Brain Research Bulletin. 139. 1–8. 48 indexed citations

Freitas, Betânia Souza de, et al.. (2018). Iron chelator deferiprone rescues memory deficits, hippocampal BDNF levels and antioxidant defenses in an experimental model of memory impairment. BioMetals. 31(6). 927–940. 16 indexed citations

Azeredo, Lucas Araújo de, Luis Eduardo Wearick‐Silva, Thiago Wendt Viola, et al.. (2017). Maternal separation induces hippocampal changes in cadherin-1 (CDH-1) mRNA and recognition memory impairment in adolescent mice. Neurobiology of Learning and Memory. 141. 157–167. 20 indexed citations

Blank, Martina, et al.. (2014). Basolateral amygdala activity is required for enhancement of memory consolidation produced by histone deacetylase inhibition in the hippocampus. Neurobiology of Learning and Memory. 111. 1–8. 31 indexed citations

Lima, Maria Noêmia Martins de, et al.. (2014). Long-lasting recognition memory impairment and alterations in brain levels of cytokines and BDNF induced by maternal deprivation: effects of valproic acid and topiramate. Journal of Neural Transmission. 122(5). 709–719. 49 indexed citations

Garcia, Vanessa Athaíde, Camila Hirotsu, Gabriela Matos, et al.. (2013). Modafinil ameliorates cognitive deficits induced by maternal separation and sleep deprivation. Behavioural Brain Research. 253. 274–279. 24 indexed citations

Presti-Torres, Juliana, Vanessa Athaíde Garcia, Arethuza Dornelles, et al.. (2011). Rescue of social behavior impairment by clozapine and alterations in the expression of neuronal receptors in a rat model of neurodevelopmental impairment induced by GRPR blockade. Journal of Neural Transmission. 119(3). 319–327. 7 indexed citations

Silva, Rosane Souza da, Arethuza Dornelles, Gustavo Vedana, et al.. (2010). Iron Leads to Memory Impairment that is Associated with a Decrease in Acetylcholinesterase Pathways. Current Neurovascular Research. 7(1). 15–22. 33 indexed citations

10.

Lima, Maria Noêmia Martins de, Felipe Siciliani Scalco, Gustavo Vedana, et al.. (2010). Neonatal Iron Treatment Increases Apoptotic Markers in Hippocampal and Cortical Areas of Adult Rats. Neurotoxicity Research. 19(4). 527–535. 28 indexed citations

11.

Rech, Rafael, Maria Noêmia Martins de Lima, Arethuza Dornelles, et al.. (2010). Reversal of age-associated memory impairment by rosuvastatin in rats. Experimental Gerontology. 45(5). 351–356. 26 indexed citations

12.

Schröder, Nadja, et al.. (2007). Ferro e neurodegeneração = Iron and neurodegeneration. SHILAP Revista de lepidopterología. 1 indexed citations

13.

Agostinho, Fabiano R., Luciano K. Jornada, Nadja Schröder, et al.. (2007). Effects of Chronic Haloperidol and/or Clozapine on Oxidative Stress Parameters in Rat Brain. Neurochemical Research. 32(8). 1343–1350. 15 indexed citations

14.

Luft, Tatiana, et al.. (2006). Temporary inactivation reveals an essential role of the dorsal hippocampus in consolidation of object recognition memory. Neuroscience Letters. 405(1-2). 142–146. 99 indexed citations

15.

Roesler, Rafael, Tatiana Luft, Caroline Brunetto de Farias, et al.. (2006). Molecular mechanisms mediating gastrin-releasing peptide receptor modulation of memory consolidation in the hippocampus. Neuropharmacology. 51(2). 350–357. 59 indexed citations

16.

Laranja, Daniela Comparsi, et al.. (2005). Selegiline protects against recognition memory impairment induced by neonatal iron treatment. Experimental Neurology. 196(1). 177–183. 34 indexed citations

17.

Roesler, Rafael, Gustavo Kellermann Reolon, Tatiana Luft, et al.. (2005). NMDA Receptors Mediate Consolidation of Contextual Memory in the Hippocampus after Context Preexposure. Neurochemical Research. 30(11). 1407–1411. 17 indexed citations

18.

Fredriksson, Anders, Nadja Schröder, Per Eriksson, Iván Izquierdo, & Trevor Archer. (2000). Maze learning and motor activity deficits in adult mice induced by iron exposure during a critical postnatal period. Developmental Brain Research. 119(1). 65–74. 74 indexed citations

19.

Schröder, Nadja, et al.. (1997). The effects of behavioral tasks on the in vitro phosphorylation of intermediate filament subunits of rat hippocampus are mediated by CaMKII and PKA. Brain Research. 749(2). 275–282. 8 indexed citations

20.

Freitas, Marta Sampaio de, et al.. (1997). Methylmalonic acid reduces the in vitro phosphorylation of cytoskeletal proteins in the cerebral cortex of rats. Brain Research. 763(2). 221–231. 6 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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