Stefan Coassin

5.8k total citations · 1 hit paper
52 papers, 1.6k citations indexed

About

Stefan Coassin is a scholar working on Molecular Biology, Surgery and Genetics. According to data from OpenAlex, Stefan Coassin has authored 52 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Molecular Biology, 18 papers in Surgery and 17 papers in Genetics. Recurrent topics in Stefan Coassin's work include Lipoproteins and Cardiovascular Health (15 papers), Genetic Associations and Epidemiology (15 papers) and Liver Disease Diagnosis and Treatment (5 papers). Stefan Coassin is often cited by papers focused on Lipoproteins and Cardiovascular Health (15 papers), Genetic Associations and Epidemiology (15 papers) and Liver Disease Diagnosis and Treatment (5 papers). Stefan Coassin collaborates with scholars based in Austria, Germany and United States. Stefan Coassin's co-authors include Florian Kronenberg, Barbara Kollerits, Anita Kloss‐Brandstätter, Claudia Lamina, Bernhard Paulweber, Iris M. Heid, Eva Boes, Christian Gieger, Thomas Meitinger and Angela Döring and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Nature Genetics.

In The Last Decade

Stefan Coassin

51 papers receiving 1.5k 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.

Lipoprotein(a) beyond the kringle IV repeat polymorphism: The complexity of genetic variation in the LPA gene

2022 99 citations Stefan Coassin, Florian Kronenberg Atherosclerosis profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Stefan Coassin Austria	21	486	448	339	276	275	52	1.6k
Torsten Kirsch Germany	25	759 1.6×	234 0.5×	450 1.3×	125 0.5×	210 0.8×	41	1.9k
I. Alexandru Bobulescu United States	21	725 1.5×	294 0.7×	721 2.1×	194 0.7×	231 0.8×	29	1.8k
Henning Gohlke Germany	15	397 0.8×	153 0.3×	239 0.7×	330 1.2×	179 0.7×	25	1.4k
Hiroyuki Yamada Japan	23	552 1.1×	350 0.8×	170 0.5×	139 0.5×	251 0.9×	77	2.0k
Andrzej Ciechanowicz Poland	21	411 0.8×	240 0.5×	126 0.4×	199 0.7×	164 0.6×	156	1.6k
Marcus G. Pezzolesi United States	23	590 1.2×	315 0.7×	294 0.9×	103 0.4×	295 1.1×	43	1.3k
Denise M. Sadlier Ireland	22	572 1.2×	169 0.4×	394 1.2×	97 0.4×	103 0.4×	42	1.3k
Franca Anglani Italy	24	840 1.7×	207 0.5×	501 1.5×	111 0.4×	92 0.3×	82	1.9k
Lili Chen China	20	340 0.7×	154 0.3×	103 0.3×	358 1.3×	405 1.5×	67	1.4k
Eliezer J. Holtzman Israel	25	1.2k 2.4×	305 0.7×	437 1.3×	119 0.4×	278 1.0×	69	2.1k

Countries citing papers authored by Stefan Coassin

Since Specialization

Citations

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

Fields of papers citing papers by Stefan Coassin

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Stefan Coassin

This figure shows the co-authorship network connecting the top 25 collaborators of Stefan Coassin. A scholar is included among the top collaborators of Stefan Coassin 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 Stefan Coassin. Stefan Coassin 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

Gruber, Ines, Barbara Kollerits, Lukas Forer, et al.. (2024). Lipoprotein(a) concentrations and cardiovascular disease in patients with chronic kidney disease: Results from the German Chronic Kidney Disease study. Journal of Internal Medicine. 296(6). 510–526. 4 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

Althaus, Harald, Eduardo Anglés‐Cano, Uta Ceglarek, et al.. (2023). Commutability Assessment of Candidate Reference Materials for Lipoprotein(a) by Comparison of a MS-based Candidate Reference Measurement Procedure with Immunoassays. Clinical Chemistry. 69(3). 262–272. 13 indexed citations

Noce, Damia, Luisa Foco, Dorothea Orth‐Höller, et al.. (2023). Genetic determinants of complement activation in the general population. Cell Reports. 43(1). 113611–113611. 3 indexed citations

Weißensteiner, Hansi, Claudia Lamina, Sebastian Schönherr, et al.. (2022). The kringle IV type 2 domain variant 4925G>A causes the elusive association signal of the LPA pentanucleotide repeat. Journal of Lipid Research. 63(12). 100306–100306. 4 indexed citations

Coassin, Stefan, et al.. (2021). Lysis reagents, cell numbers, and calculation method influence high-throughput measurement of HDL-mediated cholesterol efflux capacity. Journal of Lipid Research. 62. 100125–100125. 4 indexed citations

Sailer, S., Stefan Coassin, Katharina Lackner, et al.. (2021). When the genome bluffs: a tandem duplication event during generation of a novel Agmo knockout mouse model fools routine genotyping. Cell & Bioscience. 11(1). 54–54. 14 indexed citations

Werner, Ernst R., Markus A. Keller, S. Sailer, et al.. (2020). The TMEM189 gene encodes plasmanylethanolamine desaturase which introduces the characteristic vinyl ether double bond into plasmalogens. Proceedings of the National Academy of Sciences. 117(14). 7792–7798. 87 indexed citations

10.

Wunderer, Julia, Willi Salvenmoser, Birgit Lengerer, et al.. (2019). Temporary adhesion of the proseriate flatworm Minona ileanae. Philosophical Transactions of the Royal Society B Biological Sciences. 374(1784). 20190194–20190194. 16 indexed citations

11.

Erhart, Gertraud, Claudia Lamina, Terho Lehtimäki, et al.. (2018). Genetic Factors Explain a Major Fraction of the 50% Lower Lipoprotein(a) Concentrations in Finns. Arteriosclerosis Thrombosis and Vascular Biology. 38(5). 1230–1241. 32 indexed citations

12.

Fazzini, Federica, Bernd Schöpf, Michael Blatzer, et al.. (2018). Plasmid-normalized quantification of relative mitochondrial DNA copy number. Scientific Reports. 8(1). 15347–15347. 63 indexed citations

13.

Jones, Simon, et al.. (2011). Jordan’s anomaly in a case of Chanarin–Dorfman syndrome. British Journal of Haematology. 155(4). 412–412. 1 indexed citations

14.

Lamina, Claudia, Stefan Coassin, Thomas Illig, & Florian Kronenberg. (2011). Look beyond one's own nose: Combination of information from publicly available sources reveals an association of GATA4 polymorphisms with plasma triglycerides. Atherosclerosis. 219(2). 698–703. 3 indexed citations

15.

Kloss‐Brandstätter, Anita, Georg Schäfer, Gertraud Erhart, et al.. (2010). Somatic Mutations throughout the Entire Mitochondrial Genome Are Associated with Elevated PSA Levels in Prostate Cancer Patients. The American Journal of Human Genetics. 87(6). 802–812. 72 indexed citations

16.

Kloss‐Brandstätter, Anita, Claudia Lamina, Stefan Kiechl, et al.. (2009). Sex and age interaction with genetic association of atherogenic uric acid concentrations. Atherosclerosis. 210(2). 474–478. 28 indexed citations

17.

Coassin, Stefan, Anita Kloss‐Brandstätter, & Florian Kronenberg. (2008). An optimized procedure for the design and evaluation of Ecotilling assays. BMC Genomics. 9(1). 510–510. 5 indexed citations

18.

Döring, Angela, Christian Gieger, Divya Mehta, et al.. (2008). SLC2A9 influences uric acid concentrations with pronounced sex-specific effects. Nature Genetics. 40(4). 430–436. 299 indexed citations

19.

Boes, Eva, Stefan Coassin, Barbara Kollerits, Iris M. Heid, & Florian Kronenberg. (2008). Genetic-epidemiological evidence on genes associated with HDL cholesterol levels: A systematic in-depth review. Experimental Gerontology. 44(3). 136–160. 93 indexed citations

20.

Boes, Eva, Barbara Kollerits, Iris M. Heid, et al.. (2008). INSIG2 Polymorphism Is Neither Associated With BMI Nor With Phenotypes of Lipoprotein Metabolism. Obesity. 16(4). 827–833. 29 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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