Larissa Arning

404 total citations
3 papers, 55 citations indexed

About

Larissa Arning is a scholar working on Neurology, Molecular Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Larissa Arning has authored 3 papers receiving a total of 55 indexed citations (citations by other indexed papers that have themselves been cited), including 2 papers in Neurology, 1 paper in Molecular Biology and 1 paper in Cellular and Molecular Neuroscience. Recurrent topics in Larissa Arning's work include Neuroblastoma Research and Treatments (1 paper), Neurological disorders and treatments (1 paper) and Signaling Pathways in Disease (1 paper). Larissa Arning is often cited by papers focused on Neuroblastoma Research and Treatments (1 paper), Neurological disorders and treatments (1 paper) and Signaling Pathways in Disease (1 paper). Larissa Arning collaborates with scholars based in Germany, Australia and Denmark. Larissa Arning's co-authors include Doris Steinemann, Manfred Stuhrmann, Henrik Hasle, Charlotte M. Niemeyer, Christian Flotho, Stefan Wieczorek, Klaus Roemer, Jan Voswinkel, G. Aßmann and Florence Chang and has published in prestigious journals such as Genetics in Medicine, Haematologica and PubMed.

In The Last Decade

Larissa Arning

3 papers receiving 55 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Larissa Arning Germany	3	26	22	14	10	7	3	55
Kathleen Stabla Germany	5	30 1.2×	35 1.6×	5 0.4×	9 0.9×	13 1.9×	6	76
Zsolt Nagy Hungary	5	32 1.2×	14 0.6×	14 1.0×	13 1.3×	31 4.4×	15	85
Annabell Szymansky Germany	6	39 1.5×	10 0.5×	19 1.4×	11 1.1×	5 0.7×	13	81
Rutendo Mapeta United Kingdom	2	10 0.4×	49 2.2×	22 1.6×	19 1.9×	3 0.4×	2	85
Friederike Christen Germany	4	39 1.5×	13 0.6×	17 1.2×	9 0.9×	7 1.0×	9	80
Nelli Frank Austria	4	30 1.2×	38 1.7×	14 1.0×	17 1.7×	2 0.3×	6	90
Christopher J. Yoon United States	5	50 1.9×	19 0.9×	4 0.3×	4 0.4×	5 0.7×	8	76
Tomoya Isobe Japan	6	55 2.1×	15 0.7×	15 1.1×	6 0.6×	6 0.9×	10	90
Ellen Fraint United States	5	44 1.7×	16 0.7×	18 1.3×	11 1.1×	2 0.3×	13	89
Michael I. Barbato United States	4	53 2.0×	9 0.4×	14 1.0×	23 2.3×	7 1.0×	5	85

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

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3 of 3 papers shown

1.

Kay, Chris, Qingwen Xia, Christina M. Buchanan, et al.. (2024). The frequency and clinical impact of synonymous HTT loss-of-interruption and duplication-of-interruption variants in a diverse HD cohort. Genetics in Medicine. 26(11). 101239–101239. 2 indexed citations

2.

Steinemann, Doris, Larissa Arning, Manfred Stuhrmann, et al.. (2009). Mitotic recombination and compound-heterozygous mutations are predominant NF1-inactivating mechanisms in children with juvenile myelomonocytic leukemia and neurofibromatosis type 1. Haematologica. 95(2). 320–323. 48 indexed citations

3.

Aßmann, G., et al.. (2009). The p53 G72C and MDM2 T309G single nucleotide polymorphisms in patients with Wegener's granulomatosis.. PubMed. 26(3 Suppl 49). S72–5. 5 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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