Valentin Sander

2.0k total citations
5 papers, 58 citations indexed

About

Valentin Sander is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Valentin Sander has authored 5 papers receiving a total of 58 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Molecular Biology, 2 papers in Genetics and 1 paper in Cellular and Molecular Neuroscience. Recurrent topics in Valentin Sander's work include Muscle Physiology and Disorders (3 papers), Neurogenetic and Muscular Disorders Research (2 papers) and Genomics and Rare Diseases (1 paper). Valentin Sander is often cited by papers focused on Muscle Physiology and Disorders (3 papers), Neurogenetic and Muscular Disorders Research (2 papers) and Genomics and Rare Diseases (1 paper). Valentin Sander collaborates with scholars based in Estonia and United States. Valentin Sander's co-authors include Tiina Talvik, Inga Talvik, Pilvi Ilves, Tiiu Tomberg, Anneli Kolk, Rael Laugesaar, Tiina Kahre, Andres Piirsoo, Tiia Reimand and Katrin Õunap and has published in prestigious journals such as Clinical Neurophysiology, Pediatric Neurology and Brain and Development.

In The Last Decade

Valentin Sander

5 papers receiving 56 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Valentin Sander Estonia	4	23	18	14	13	12	5	58
Anatol Mickielewicz Poland	4	35 1.5×	10 0.6×	16 1.1×	13 1.0×	10 0.8×	7	83
Susan Maillard United Kingdom	5	14 0.6×	12 0.7×	65 4.6×	5 0.4×	2 0.2×	6	115
Rodica Tălmaci Romania	6	59 2.6×	7 0.4×	4 0.3×	4 0.3×	5 0.4×	16	88
Andrew Han United States	5	22 1.0×	17 0.9×	11 0.8×	4 0.3×	11 0.9×	15	72
Nicholas Whipple United States	4	17 0.7×	4 0.2×	13 0.9×	17 1.3×	6 0.5×	9	52
Senthil Raghunathan United Kingdom	3	5 0.2×	10 0.6×	11 0.8×	16 1.2×	5 0.4×	5	43
Poh Sim Low Singapore	5	18 0.8×	78 4.3×	7 0.5×	2 0.2×	11 0.9×	5	116
Christina M. Klais United States	10	14 0.6×	25 1.4×	16 1.1×	40 3.1×	2 0.2×	17	337
Nicolas Pangaud France	4	10 0.4×	8 0.4×	19 1.4×	1 0.1×	6 0.5×	7	52
C. Cancès France	6	2 0.1×	20 1.1×	20 1.4×	36 2.8×	4 0.3×	14	82

Countries citing papers authored by Valentin Sander

Since Specialization

Citations

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

Fields of papers citing papers by Valentin Sander

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Valentin Sander

This figure shows the co-authorship network connecting the top 25 collaborators of Valentin Sander. A scholar is included among the top collaborators of Valentin Sander 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 Valentin Sander. Valentin Sander is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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5 of 5 papers shown

1.

Sander, Valentin, et al.. (2019). P76-F DYNC1H1 gene mutation in an Estonian family. Clinical Neurophysiology. 130(7). e89–e89. 1 indexed citations

2.

Talvik, Inga, Ulvi Vaher, Katrin Õunap, et al.. (2016). CDKL5 Gene-Related Epileptic Encephalopathy in Estonia: Four Cases, One Novel Mutation Causing Severe Phenotype in a Boy, and Overview of the Literature. Neuropediatrics. 47(6). 361–367. 10 indexed citations

3.

Laugesaar, Rael, Anneli Kolk, Pilvi Ilves, et al.. (2010). Epidemiology of Childhood Stroke in Estonia. Pediatric Neurology. 42(2). 93–100. 28 indexed citations

4.

Kahre, Tiina, et al.. (2003). A descriptive epidemiological study of Duchenne muscular dystrophy in childhood in Estonia. European Journal of Paediatric Neurology. 7(5). 221–226. 13 indexed citations

5.

Piirsoo, Andres, et al.. (1999). Duchenne and Becker muscular dystrophies: an Estonian experience. Brain and Development. 21(4). 244–247. 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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