Anaïs Begemann

635 total citations
4 papers, 108 citations indexed

About

Anaïs Begemann is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Anaïs Begemann has authored 4 papers receiving a total of 108 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Genetics, 1 paper in Molecular Biology and 1 paper in Pediatrics, Perinatology and Child Health. Recurrent topics in Anaïs Begemann's work include Genetics and Neurodevelopmental Disorders (3 papers), Genomics and Rare Diseases (2 papers) and Epilepsy research and treatment (1 paper). Anaïs Begemann is often cited by papers focused on Genetics and Neurodevelopmental Disorders (3 papers), Genomics and Rare Diseases (2 papers) and Epilepsy research and treatment (1 paper). Anaïs Begemann collaborates with scholars based in Switzerland, Germany and Austria. Anaïs Begemann's co-authors include Anita Rauch, Markus Zweier, Heinrich Sticht, Barbara Plecko, Pascal Joset, Pasquale Striano, Martina Baethmann, Sorina Mihaela Papuc, Lisa M. Crowther and Federico Zara and has published in prestigious journals such as Journal of Medical Genetics, Molecular Medicine and European Journal of Medical Genetics.

In The Last Decade

Anaïs Begemann

4 papers receiving 106 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Anaïs Begemann Switzerland	3	51	47	36	26	20	4	108
G. Pitelet France	3	33 0.6×	21 0.4×	42 1.2×	11 0.4×	17 0.8×	4	93
Kamer Tezcan United States	5	35 0.7×	33 0.7×	43 1.2×	18 0.7×	36 1.8×	5	126
C. Whitehouse United Kingdom	5	67 1.3×	21 0.4×	38 1.1×	59 2.3×	56 2.8×	17	276
Marie‐Aude Spitz France	7	99 1.9×	53 1.1×	29 0.8×	16 0.6×	7 0.3×	11	136
Ahlam A. Hamed Sudan	7	33 0.6×	19 0.4×	17 0.5×	24 0.9×	3 0.1×	15	102
Amy Kritzer United States	7	45 0.9×	41 0.9×	60 1.7×	4 0.2×	17 0.8×	16	122
Iglika Yordanova Bulgaria	6	35 0.7×	39 0.8×	18 0.5×	48 1.8×	6 0.3×	7	85
C. Rauscher Austria	6	50 1.0×	28 0.6×	24 0.7×	15 0.6×	5 0.3×	12	112
Gretchen K. Von Allmen United States	3	50 1.0×	27 0.6×	25 0.7×	21 0.8×	2 0.1×	4	86
Chontelle King New Zealand	6	48 0.9×	51 1.1×	9 0.3×	35 1.3×	9 0.5×	6	109

Countries citing papers authored by Anaïs Begemann

Since Specialization

Citations

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

Fields of papers citing papers by Anaïs Begemann

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Anaïs Begemann

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

All Works

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4 of 4 papers shown

1.

Ivanovski, Ivan, Anaïs Begemann, Katharina Steindl, et al.. (2023). The current benefit of genome sequencing compared to exome sequencing in patients with developmental or epileptic encephalopathies. Molecular Genetics & Genomic Medicine. 11(5). e2148–e2148. 10 indexed citations

2.

Begemann, Anaïs, et al.. (2022). A Xp22.11-p21.3 microdeletion in a three-generation family supports male lethality of POLA1 nullisomy resulting in reduced fertility of female carriers. European Journal of Medical Genetics. 65(12). 104628–104628. 1 indexed citations

3.

Begemann, Anaïs, Mario A. Acuña, Markus Zweier, et al.. (2019). Further corroboration of distinct functional features in SCN2A variants causing intellectual disability or epileptic phenotypes. Molecular Medicine. 25(1). 6–6. 39 indexed citations

4.

Plecko, Barbara, Markus Zweier, Anaïs Begemann, et al.. (2017). Confirmation of mutations in PROSC as a novel cause of vitamin B_₆-dependent epilepsy. Journal of Medical Genetics. 54(12). 809–814. 58 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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