Lukas Soellner

1.3k total citations
22 papers, 609 citations indexed

About

Lukas Soellner is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Lukas Soellner has authored 22 papers receiving a total of 609 indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Genetics, 15 papers in Molecular Biology and 14 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Lukas Soellner's work include Genetic Syndromes and Imprinting (19 papers), Prenatal Screening and Diagnostics (14 papers) and Epigenetics and DNA Methylation (12 papers). Lukas Soellner is often cited by papers focused on Genetic Syndromes and Imprinting (19 papers), Prenatal Screening and Diagnostics (14 papers) and Epigenetics and DNA Methylation (12 papers). Lukas Soellner collaborates with scholars based in Germany, Hungary and United Kingdom. Lukas Soellner's co-authors include Thomas Eggermann, Matthias Begemann, Karin Buiting, Dieter Kotzot, Gerhard Binder, Elisa Wirthgen, Gijs W.E. Santen, Birgit Zirn, Roland Schweizer and Miriam Elbracht and has published in prestigious journals such as New England Journal of Medicine, The Journal of Pediatrics and Trends in Molecular Medicine.

In The Last Decade

Lukas Soellner

22 papers receiving 582 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Lukas Soellner Germany 12 480 356 348 68 58 22 609
Jonathan L A Callaway United Kingdom 6 590 1.2× 538 1.5× 432 1.2× 33 0.5× 35 0.6× 8 748
Nathalie Thibaud France 9 869 1.8× 813 2.3× 574 1.6× 76 1.1× 18 0.3× 10 969
Sabrina Spengler Germany 14 487 1.0× 396 1.1× 332 1.0× 18 0.3× 26 0.4× 31 568
Lucy Bowden United Kingdom 6 440 0.9× 562 1.6× 273 0.8× 20 0.3× 85 1.5× 9 647
Fabienne Danton France 4 537 1.1× 519 1.5× 394 1.1× 38 0.6× 12 0.2× 5 612
Antoine Kerjean France 10 377 0.8× 459 1.3× 320 0.9× 15 0.2× 126 2.2× 10 604
Barbara Delle Chiaie Belgium 7 251 0.5× 195 0.5× 136 0.4× 16 0.2× 19 0.3× 10 423
R Gracia Spain 7 250 0.5× 234 0.7× 63 0.2× 129 1.9× 19 0.3× 8 353
Jérôme Dulon France 14 214 0.4× 385 1.1× 72 0.2× 271 4.0× 258 4.4× 28 737
Ioannis Papoulidis Greece 13 251 0.5× 116 0.3× 195 0.6× 7 0.1× 33 0.6× 52 388

Countries citing papers authored by Lukas Soellner

Since Specialization
Citations

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

Fields of papers citing papers by Lukas Soellner

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Lukas Soellner

This figure shows the co-authorship network connecting the top 25 collaborators of Lukas Soellner. A scholar is included among the top collaborators of Lukas Soellner 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 Lukas Soellner. Lukas Soellner 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.
Soellner, Lukas, Florian Kraft, Matthias Begemann, et al.. (2018). Search for cis-acting factors and maternal effect variants in Silver-Russell patients with ICR1 hypomethylation and their mothers. European Journal of Human Genetics. 27(1). 42–48. 10 indexed citations
2.
3.
Meyer, Robert, Lukas Soellner, Matthias Begemann, et al.. (2017). Targeted Next Generation Sequencing Approach in Patients Referred for Silver-Russell Syndrome Testing Increases the Mutation Detection Rate and Provides Decisive Information for Clinical Management. The Journal of Pediatrics. 187. 206–212.e1. 19 indexed citations
4.
Soellner, Lukas, Matthias Begemann, Franziska Degenhardt, et al.. (2017). Maternal heterozygous NLRP7 variant results in recurrent reproductive failure and imprinting disturbances in the offspring. European Journal of Human Genetics. 25(8). 924–929. 33 indexed citations
5.
Soellner, Lukas, Robert Meyer, Matthias Begemann, et al.. (2017). NLRP genes and their role in preeclampsia and multi-locus imprinting disorders. Journal of Perinatal Medicine. 46(2). 169–173. 9 indexed citations
6.
Fekete, György, Laima Ambrozaitytė, Vaidutis Kučinskas, et al.. (2016). Examinations of maternal uniparental disomy and epimutations for chromosomes 6, 14, 16 and 20 in Silver-Russell syndrome-like phenotypes. BMC Medical Genetics. 17(1). 20–20. 17 indexed citations
7.
Soellner, Lukas, Matthias Begemann, Deborah Mackay, et al.. (2016). Recent Advances in Imprinting Disorders. Clinical Genetics. 91(1). 3–13. 83 indexed citations
8.
Begemann, Matthias, Lukas Soellner, Dieter Meschede, et al.. (2016). Maternal uniparental disomy of chromosome 16 [upd(16)mat]: clinical features are rather caused by (hidden) trisomy 16 mosaicism than by upd(16)mat itself. Clinical Genetics. 92(1). 45–51. 44 indexed citations
9.
Vals, Mari‐Anne, Tiina Kahre, Kai Muru, et al.. (2015). The Frequency of Methylation Abnormalities Among Estonian Patients Selected by Clinical Diagnostic Scoring Systems for Silver–Russell Syndrome and Beckwith–Wiedemann Syndrome. Genetic Testing and Molecular Biomarkers. 19(12). 684–691. 7 indexed citations
10.
Begemann, Matthias, et al.. (2015). Microdeletions of the 7q32.2 imprinted region are associated with Silver–Russell syndrome features. American Journal of Medical Genetics Part A. 170(3). 743–749. 27 indexed citations
11.
Begemann, Matthias, Birgit Zirn, Gijs W.E. Santen, et al.. (2015). Paternally InheritedIGF2Mutation and Growth Restriction. New England Journal of Medicine. 373(4). 349–356. 148 indexed citations
12.
Rieß, Angelika, et al.. (2015). First report on concordant monozygotic twins with Silver–Russell syndrome and ICR1 hypomethylation. European Journal of Medical Genetics. 59(1). 1–4. 10 indexed citations
13.
Soellner, Lukas, David Monk, Faisal I. Rezwan, et al.. (2015). Congenital imprinting disorders: Application of multilocus and high throughput methods to decipher new pathomechanisms and improve their management. Molecular and Cellular Probes. 29(5). 282–290. 7 indexed citations
14.
Schröder, Carmen, et al.. (2015). A familialGLI2deletion (2q14.2) not associated with the holoprosencephaly syndrome phenotype. American Journal of Medical Genetics Part A. 167(5). 1121–1124. 11 indexed citations
15.
Eggermann, Thomas, Lukas Soellner, Karin Buiting, & Dieter Kotzot. (2014). Mosaicism and uniparental disomy in prenatal diagnosis. Trends in Molecular Medicine. 21(2). 77–87. 79 indexed citations
16.
Eggermann, Thomas, Susanne Bens, Reiner Siebert, et al.. (2014). Additional molecular findings in 11p15-associated imprinting disorders: an urgent need for multi-locus testing. Journal of Molecular Medicine. 92(7). 769–777. 36 indexed citations
17.
Eggermann, Thomas, Matthias Begemann, Lukas Soellner, et al.. (2013). Molekulargenetische Diagnostik von Imprintingerkrankungen. Medizinische Genetik. 25(1). 5–14. 1 indexed citations
18.
Eggermann, Thomas, Miriam Elbracht, Carmen Schröder, et al.. (2013). Congenital Imprinting Disorders: A Novel Mechanism Linking Seemingly Unrelated Disorders. The Journal of Pediatrics. 163(4). 1202–1207. 5 indexed citations
19.
Begemann, Matthias, et al.. (2012). Genome-wide paternal uniparental disomy mosaicism in a woman with Beckwith–Wiedemann syndrome and ovarian steroid cell tumour. European Journal of Human Genetics. 21(7). 788–791. 33 indexed citations
20.
Begemann, Matthias, Isabelle Leisten, Lukas Soellner, et al.. (2012). Use of multilocus methylation-specific single nucleotide primer extension (MS-SNuPE) technology in diagnostic testing for human imprinted loci. Epigenetics. 7(5). 473–481. 23 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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