Sebastian Schönherr

13.7k total citations · 1 hit paper
54 papers, 1.7k citations indexed

About

Sebastian Schönherr is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Sebastian Schönherr has authored 54 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Molecular Biology, 25 papers in Genetics and 8 papers in Surgery. Recurrent topics in Sebastian Schönherr's work include Genetic Associations and Epidemiology (18 papers), Genomics and Phylogenetic Studies (14 papers) and Mitochondrial Function and Pathology (7 papers). Sebastian Schönherr is often cited by papers focused on Genetic Associations and Epidemiology (18 papers), Genomics and Phylogenetic Studies (14 papers) and Mitochondrial Function and Pathology (7 papers). Sebastian Schönherr collaborates with scholars based in Austria, Germany and United States. Sebastian Schönherr's co-authors include Florian Kronenberg, Hansi Weißensteiner, Anita Kloss‐Brandstätter, Günther Specht, Lukas Forer, Dominic Pacher, Hans‐Jürgen Bandelt, Antonio Salas, Robert Binna and Christian Fuchsberger and has published in prestigious journals such as Nucleic Acids Research, SHILAP Revista de lepidopterología and Bioinformatics.

In The Last Decade

Sebastian Schönherr

50 papers receiving 1.7k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

HaploGrep 2: mitochondrial haplogroup classification in the era of high-throughput sequencing

2016 518 citations Hansi Weißensteiner, Dominic Pacher et al. Nucleic Acids Research profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Sebastian Schönherr Austria	17	884	768	321	194	144	54	1.7k
Hansi Weißensteiner Austria	15	848 1.0×	835 1.1×	330 1.0×	216 1.1×	148 1.0×	40	1.6k
Lukas Forer Austria	19	1.1k 1.3×	879 1.1×	208 0.6×	180 0.9×	102 0.7×	58	2.2k
Albert Min‐Shan Ko Taiwan	24	493 0.6×	461 0.6×	254 0.8×	39 0.2×	154 1.1×	47	1.8k
María Cerezo Spain	13	1.1k 1.2×	917 1.2×	127 0.4×	25 0.1×	20 0.1×	19	1.8k
Aisha Mohyuddin Pakistan	18	909 1.0×	548 0.7×	265 0.8×	20 0.1×	25 0.2×	32	1.6k
Marı́a Brión Spain	27	1.1k 1.3×	869 1.1×	154 0.5×	16 0.1×	31 0.2×	90	2.1k
Estella S. Poloni Switzerland	18	633 0.7×	293 0.4×	170 0.5×	24 0.1×	31 0.2×	33	1.1k
Ewelina Pośpiech Poland	27	650 0.7×	1.2k 1.5×	162 0.5×	15 0.1×	11 0.1×	58	1.9k
Matti Lukka Finland	19	709 0.8×	497 0.6×	58 0.2×	31 0.2×	15 0.1×	42	1.7k
K Omoto Japan	18	461 0.5×	306 0.4×	149 0.5×	47 0.2×	20 0.1×	50	1.0k

Countries citing papers authored by Sebastian Schönherr

Since Specialization

Citations

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

Fields of papers citing papers by Sebastian Schönherr

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sebastian Schönherr

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

All Works

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20 of 20 papers shown

Forer, Lukas, Daniel Taliun, Jonathon LeFaive, et al.. (2024). Imputation Server PGS: an automated approach to calculate polygenic risk scores on imputation servers. Nucleic Acids Research. 52(W1). W70–W77. 4 indexed citations

Kollerits, Barbara, Fruzsina Kotsis, Markus P. Schneider, et al.. (2024). Association of Serum Afamin Concentrations With Kidney Failure in Patients With CKD: Findings From the German CKD Cohort Study. American Journal of Kidney Diseases. 85(4). 432–441.e1.

Koller, Á., Michele Filosi, Hansi Weißensteiner, et al.. (2024). Nuclear and mitochondrial genetic variants associated with mitochondrial DNA copy number. Scientific Reports. 14(1). 2083–2083. 3 indexed citations

Maio, Silvia Di, Hansi Weißensteiner, Bernhard Paulweber, et al.. (2024). Nanopore sequencing with unique molecular identifiers enables accurate mutation analysis and haplotyping in the complex lipoprotein(a) KIV-2 VNTR. Genome Medicine. 16(1). 117–117. 2 indexed citations

Schönherr, Sebastian, Hansi Weißensteiner, Florian Kronenberg, & Lukas Forer. (2023). Haplogrep 3 - an interactive haplogroup classification and analysis platform. Nucleic Acids Research. 51(W1). W263–W268. 43 indexed citations

Schönherr, Sebastian, Claudia Lamina, Lukas Forer, et al.. (2023). KLKB1 and CLSTN2 are associated with HDL-mediated cholesterol efflux capacity in a genome-wide association study. Atherosclerosis. 368. 1–11. 3 indexed citations

Forer, Lukas, Sebastian Schönherr, Christian Gieger, et al.. (2023). A polygenic and family risk score are both independently associated with risk of type 2 diabetes in a population-based study. Scientific Reports. 13(1). 4805–4805. 7 indexed citations

Schönherr, Sebastian, Laura Jung, & Henning Trawinski. (2023). Klimawandel und vektorübertragene Infektionen in EuropaTeil 1: Überblick und mückenübertragene Infektionen. 30(5). 233–244. 2 indexed citations

Forer, Lukas, Sebastian Schönherr, Annette Peters, et al.. (2022). A Family and a Genome-Wide Polygenic Risk Score Are Independently Associated With Stroke in a Population-Based Study. Stroke. 53(7). 2331–2339. 6 indexed citations

10.

Lamina, Claudia, Silvia Di Maio, Sebastian Schönherr, et al.. (2022). The effect of LPA Thr3888Pro on lipoprotein(a) and coronary artery disease is modified by the LPA KIV-2 variant 4925G>A. Atherosclerosis. 349. 151–159. 5 indexed citations

11.

Forer, Lukas, Sebastian Schönherr, Jonathon LeFaive, et al.. (2022). Extent to which array genotyping and imputation with large reference panels approximate deep whole-genome sequencing. The American Journal of Human Genetics. 109(9). 1653–1666. 15 indexed citations

12.

Carvalho, Filipa S., Ana Catarina Fonseca, Friedemann Paul, et al.. (2021). From Forensics to Clinical Research: Expanding the Variant Calling Pipeline for the Precision ID mtDNA Whole Genome Panel. International Journal of Molecular Sciences. 22(21). 12031–12031. 5 indexed citations

13.

Fazzini, Federica, Claudia Lamina, Á. Koller, et al.. (2021). Association of mitochondrial DNA copy number with metabolic syndrome and type 2 diabetes in 14 176 individuals. Journal of Internal Medicine. 290(1). 190–202. 69 indexed citations

14.

Borena, Wegene, Zoltán Bánki, Katie Bates, et al.. (2021). Persistence of immunity to SARS-CoV-2 over time in the ski resort Ischgl. EBioMedicine. 70. 103534–103534. 12 indexed citations

15.

Schönherr, Sebastian, et al.. (2020). Assessing the impact of institution-specific guidelines for antimicrobials on doctors’ prescribing behavior at a German tertiary-care center and the additional benefits of providing a mobile application. PLoS ONE. 15(11). e0241642–e0241642. 4 indexed citations

16.

Weißensteiner, Hansi, Dominic Pacher, Anita Kloss‐Brandstätter, et al.. (2016). HaploGrep 2: mitochondrial haplogroup classification in the era of high-throughput sequencing. Nucleic Acids Research. 44(W1). W58–W63. 518 indexed citations breakdown →

17.

Forer, Lukas, Enis Afgan, Hansi Weißensteiner, et al.. (2015). Cloudflow – A Framework for MapReduce Pipeline Development in Biomedical Research. Figshare. 3 indexed citations

18.

Spjuth, Ola, Erik Bongcam‐Rudloff, Lukas Forer, et al.. (2015). Experiences with workflows for automating data-intensive bioinformatics. Biology Direct. 10(1). 43–43. 41 indexed citations

19.

Schönherr, Sebastian, Lukas Forer, Hansi Weißensteiner, et al.. (2012). Cloudgene: A graphical execution platform for MapReduce programs on private and public clouds. BMC Bioinformatics. 13(1). 200–200. 34 indexed citations

20.

Schönherr, Sebastian, et al.. (2010). Synchronous metadata management of large storage systems. 1–6. 1 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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