Larissa Arning

4.1k total citations
92 papers, 2.6k citations indexed

About

Larissa Arning is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Cognitive Neuroscience. According to data from OpenAlex, Larissa Arning has authored 92 papers receiving a total of 2.6k indexed citations (citations by other indexed papers that have themselves been cited), including 46 papers in Cellular and Molecular Neuroscience, 37 papers in Molecular Biology and 29 papers in Cognitive Neuroscience. Recurrent topics in Larissa Arning's work include Genetic Neurodegenerative Diseases (32 papers), Mitochondrial Function and Pathology (18 papers) and Hemispheric Asymmetry in Neuroscience (13 papers). Larissa Arning is often cited by papers focused on Genetic Neurodegenerative Diseases (32 papers), Mitochondrial Function and Pathology (18 papers) and Hemispheric Asymmetry in Neuroscience (13 papers). Larissa Arning collaborates with scholars based in Germany, United Kingdom and Netherlands. Larissa Arning's co-authors include Jörg T. Epplen, Christian Beste, Carsten Saft, Stefan Wieczorek, Sebastian Ocklenburg, Onur Güntürkün, Peter Jagiello, Wolfgang L. Gross, Ann‐Kathrin Stock and Jürgen Andrich and has published in prestigious journals such as Journal of Neuroscience, SHILAP Revista de lepidopterología and PLoS ONE.

In The Last Decade

Larissa Arning

91 papers receiving 2.5k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Larissa Arning Germany 30 1.0k 772 638 328 316 92 2.6k
Catarina Freitas Portugal 23 1.6k 1.5× 670 0.9× 638 1.0× 181 0.6× 335 1.1× 48 3.7k
Erin M. Gibson United States 18 626 0.6× 724 0.9× 354 0.6× 351 1.1× 187 0.6× 32 3.1k
Maarten Loos Netherlands 35 1.1k 1.1× 913 1.2× 496 0.8× 210 0.6× 108 0.3× 89 3.1k
Zhengang Yang China 29 1.5k 1.5× 1.1k 1.5× 309 0.5× 217 0.7× 153 0.5× 84 3.9k
Danielle A. Simmons United States 23 1.2k 1.1× 1.3k 1.7× 192 0.3× 227 0.7× 320 1.0× 35 3.0k
Maria K. Lehtinen United States 30 2.5k 2.4× 1.2k 1.5× 181 0.3× 128 0.4× 313 1.0× 63 4.5k
Timothy W. Yu United States 26 1.7k 1.6× 1.8k 2.3× 394 0.6× 197 0.6× 178 0.6× 64 4.4k
Kathy Keyvani Germany 35 1.1k 1.0× 536 0.7× 245 0.4× 271 0.8× 433 1.4× 103 3.3k

Countries citing papers authored by Larissa Arning

Since Specialization
Citations

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

Fields of papers citing papers by Larissa Arning

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Larissa Arning

This figure shows the co-authorship network connecting the top 25 collaborators of Larissa Arning. A scholar is included among the top collaborators of Larissa Arning 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 Larissa Arning. Larissa Arning 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.
Fisse, Anna Lena, Thomas Grüter, Christiane Schneider‐Gold, et al.. (2024). Association of the neonatal Fc receptor promoter variable number of tandem repeat polymorphism with immunoglobulin response in patients with chronic inflammatory demyelinating polyneuropathy. European Journal of Neurology. 31(4). e16205–e16205. 2 indexed citations
2.
Genç, Erhan, Christoph Fraenz, Caroline Schlüter, et al.. (2023). Structural architecture and brain network efficiency link polygenic scores to intelligence. Human Brain Mapping. 44(8). 3359–3376. 3 indexed citations
3.
Berretz, Gesa, Larissa Arning, Wanda M. Gerding, et al.. (2019). Structural Asymmetry in the Frontal and Temporal Lobes Is Associated with PCSK6 VNTR Polymorphism. Molecular Neurobiology. 56(11). 7765–7773. 7 indexed citations
4.
Zink, Nicolas, et al.. (2019). Dopamine D1, but not D2, signaling protects mental representations from distracting bottom-up influences. NeuroImage. 204. 116243–116243. 12 indexed citations
5.
Zink, Nicolas, et al.. (2019). CHRM2 Genotype Affects Inhibitory Control Mechanisms During Cognitive Flexibility. Molecular Neurobiology. 56(9). 6134–6141. 9 indexed citations
6.
Gerding, Wanda M., Christoph Fraenz, Patrick Friedrich, et al.. (2018). PLP1 and CNTN1 gene variation modulates the microstructure of human white matter in the corpus callosum. Brain Structure and Function. 223(8). 3875–3887. 8 indexed citations
7.
Ocklenburg, Sebastian, Larissa Arning, Wanda M. Gerding, et al.. (2015). Left-Right Axis Differentiation and Functional Lateralization: a Haplotype in the Methyltransferase Encoding Gene SETDB2 Might Mediate Handedness in Healthy Adults. Molecular Neurobiology. 53(9). 6355–6361. 15 indexed citations
8.
Arning, Larissa, Sebastian Ocklenburg, Stefanie Schulz, et al.. (2015). Handedness and the X chromosome: The role of androgen receptor CAG-repeat length. Scientific Reports. 5(1). 8325–8325. 40 indexed citations
9.
Stock, Ann‐Kathrin, Larissa Arning, Jörg T. Epplen, & Christian Beste. (2014). DRD1andDRD2Genotypes Modulate Processing Modes of Goal Activation Processes during Action Cascading. Journal of Neuroscience. 34(15). 5335–5341. 58 indexed citations
10.
Saft, Carsten, et al.. (2013). CNR1 variation is associated with the age at onset in Huntington disease. European Journal of Medical Genetics. 56(8). 416–419. 15 indexed citations
11.
Arning, Larissa, Sebastian Ocklenburg, Stefanie Schulz, et al.. (2013). PCSK6 VNTR Polymorphism Is Associated with Degree of Handedness but Not Direction of Handedness. PLoS ONE. 8(6). e67251–e67251. 74 indexed citations
12.
Ocklenburg, Sebastian, Larissa Arning, Wanda M. Gerding, et al.. (2013). Cholecystokinin A Receptor (CCKAR) Gene Variation Is Associated with Language Lateralization. PLoS ONE. 8(1). e53643–e53643. 32 indexed citations
13.
Schulz, Stefanie, Larissa Arning, Marlies Pinnow, Jörg T. Epplen, & Christian Beste. (2012). N-methyl-d-aspartate receptor 2B subunit (GRIN2B) gene variation is associated with alerting, but not with orienting and conflicting in the Attention Network Test. Neuropharmacology. 63(2). 259–265. 7 indexed citations
14.
Saft, Carsten, Denis A. Akkad, Stefan Wieczorek, et al.. (2011). PGC-1alpha downstream transcription factors NRF-1 and TFAM are genetic modifiers of Huntington disease. Molecular Neurodegeneration. 6(1). 32–32. 111 indexed citations
15.
Ness, Vanessa, et al.. (2011). Variations in the GRIN2B gene are associated with risky decision-making. Neuropharmacology. 61(5-6). 950–956. 22 indexed citations
16.
Arning, Larissa & Jörg T. Epplen. (2011). Genetic Modifiers of Huntington‘s Disease: Beyond Cag. Future Neurology. 7(1). 93–109. 19 indexed citations
17.
Arning, Larissa, Aiden Haghikia, Carsten Saft, et al.. (2010). Mitochondrial haplogroup H correlates with ATP levels and age at onset in Huntington disease. Journal of Molecular Medicine. 88(4). 431–436. 54 indexed citations
18.
Heckmann, Matthias, Julia U. Holle, Larissa Arning, et al.. (2007). The Wegener’s granulomatosis quantitative trait locus on chromosome 6p21.3 as characterised by tagSNP genotyping. Annals of the Rheumatic Diseases. 67(7). 972–979. 62 indexed citations
19.
Wieczorek, Stefan, Carsten Saft, Jürgen Andrich, et al.. (2006). No association between polymorphisms in the BDNF gene and age at onset in Huntington disease. BMC Medical Genetics. 7(1). 79–79. 15 indexed citations
20.
Wieczorek, Stefan, et al.. (2006). Mutations of the puratrophin-1 (PLEKHG4) gene on chromosome 16q22.1 are not a common genetic cause of cerebellar ataxia in a European population. Journal of Human Genetics. 51(4). 363–367. 11 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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