Simone Rost

3.9k total citations · 1 hit paper
66 papers, 2.8k citations indexed

About

Simone Rost is a scholar working on Molecular Biology, Hematology and Nutrition and Dietetics. According to data from OpenAlex, Simone Rost has authored 66 papers receiving a total of 2.8k indexed citations (citations by other indexed papers that have themselves been cited), including 35 papers in Molecular Biology, 16 papers in Hematology and 16 papers in Nutrition and Dietetics. Recurrent topics in Simone Rost's work include Vitamin K Research Studies (16 papers), Pharmacogenetics and Drug Metabolism (13 papers) and Hemophilia Treatment and Research (13 papers). Simone Rost is often cited by papers focused on Vitamin K Research Studies (16 papers), Pharmacogenetics and Drug Metabolism (13 papers) and Hemophilia Treatment and Research (13 papers). Simone Rost collaborates with scholars based in Germany, United Kingdom and United States. Simone Rost's co-authors include Johannes Oldenburg, Clemens R. Müller, Andreas Fregin, Hans‐Joachim Pelz, Vytautas Ivaškevičius, E. Seifried, Edward G. D. Tuddenham, Tim M. Strom, Ernst Conzelmann and Knut Tore Lappegård and has published in prestigious journals such as Nature, SHILAP Revista de lepidopterología and Blood.

In The Last Decade

Simone Rost

66 papers receiving 2.7k 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.

Mutations in VKORC1 cause warfarin resistance and multiple coagulation factor deficiency type 2

2004 857 citations Simone Rost, Andreas Fregin et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Simone Rost Germany	24	1.0k	830	612	548	439	66	2.8k
Konstanze Hörtnagel Germany	20	550 0.5×	763 0.9×	240 0.4×	286 0.5×	110 0.3×	39	2.0k
Michael P. Graziano United States	29	96 0.1×	2.1k 2.5×	406 0.7×	530 1.0×	54 0.1×	42	4.4k
Bandana Chatterjee United States	35	506 0.5×	1.8k 2.2×	118 0.2×	845 1.5×	34 0.1×	97	3.7k
Mats Gåfvels Sweden	26	158 0.2×	873 1.1×	156 0.3×	348 0.6×	11 0.0×	69	2.5k
David Pulford United Kingdom	13	356 0.4×	3.2k 3.9×	196 0.3×	76 0.1×	42 0.1×	17	4.5k
Gabriele Möller Germany	31	197 0.2×	1.2k 1.4×	152 0.2×	848 1.5×	117 0.3×	64	3.1k
K S Misono United States	25	247 0.2×	1.6k 1.9×	80 0.1×	397 0.7×	29 0.1×	34	3.3k
P. Vreken Netherlands	34	143 0.1×	3.3k 4.0×	192 0.3×	188 0.3×	27 0.1×	81	4.5k
Masaharu Sakai Japan	27	150 0.1×	2.2k 2.6×	101 0.2×	262 0.5×	32 0.1×	70	3.4k
P. Pradelles France	20	73 0.1×	671 0.8×	112 0.2×	185 0.3×	39 0.1×	41	2.1k

Countries citing papers authored by Simone Rost

Since Specialization

Citations

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

Fields of papers citing papers by Simone Rost

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Simone Rost

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

Hoffjan, Sabine, Cornelia Köhler, Thomas Lücke, et al.. (2022). Homozygous Inversion on Chromosome 13 Involving SGCG Detected by Short Read Whole Genome Sequencing in a Patient Suffering from Limb-Girdle Muscular Dystrophy. Genes. 13(10). 1752–1752. 3 indexed citations

Nanda, Indrajit, et al.. (2022). Detection of pericentric inversion with breakpoint in DMD by whole genome sequencing. Molecular Genetics & Genomic Medicine. 10(10). e2028–e2028. 12 indexed citations

Rost, Simone, Eva Klopocki, Katharina Günther, et al.. (2021). CRISPR/Cas9-edited PKP2 knock-out (JMUi001-A-2) and DSG2 knock-out (JMUi001-A-3) iPSC lines as an isogenic human model system for arrhythmogenic cardiomyopathy (ACM). Stem Cell Research. 53. 102256–102256. 2 indexed citations

Weigand, Isabel, Stefan Kircher, Barbara Altieri, et al.. (2020). Targeted Gene Expression Profile Reveals CDK4 as Therapeutic Target for Selected Patients With Adrenocortical Carcinoma. Frontiers in Endocrinology. 11. 219–219. 27 indexed citations

Chen, Ruping, Martina Regensburger, Yuichiro Ueda, et al.. (2020). Generation of two patient-derived iPSC lines from siblings (LIBUCi001-A and LIBUCi002-A) and a genetically modified iPSC line (JMUi001-A-1) to mimic dilated cardiomyopathy with ataxia (DCMA) caused by a homozygous DNAJC19 mutation. Stem Cell Research. 46. 101856–101856. 5 indexed citations

Maurus, Katja, Silke Appenzeller, Sabine Roth, et al.. (2018). Panel Sequencing Shows Recurrent Genetic FAS Alterations in Primary Cutaneous Marginal Zone Lymphoma. Journal of Investigative Dermatology. 138(7). 1573–1581. 39 indexed citations

Kreß, Wolfram, et al.. (2016). Identification of variants in MBNL1 in patients with a myotonic dystrophy-like phenotype. European Journal of Human Genetics. 24(10). 1467–1472. 5 indexed citations

Potabattula, Ramya, Marcus Dittrich, Caroline Nava, et al.. (2016). Paternal age effects on spermFOXK1andKCNA7methylation and transmission into the next generation. Human Molecular Genetics. 25(22). ddw328–ddw328. 57 indexed citations

Musacchio, Thomas, Nurcan Üçeyler, Claudia Sommer, et al.. (2016). ALS and MMN mimics in patients with BSCL2 mutations: the expanding clinical spectrum of SPG17 hereditary spastic paraplegia. Journal of Neurology. 264(1). 11–20. 14 indexed citations

10.

Oldenburg, Johannes, et al.. (2015). Identification of deep intronic variants in 15 haemophilia A patients by next generation sequencing of the whole factor VIII gene. Thrombosis and Haemostasis. 114(10). 757–767. 25 indexed citations

11.

Keller, Alexander, Gudrun Grimmer, Markus J. Ankenbrand, et al.. (2014). Evaluating multiplexed next‐generation sequencing as a method in palynology for mixed pollen samples. Plant Biology. 17(2). 558–566. 159 indexed citations

12.

Fregin, Andreas, Simone Rost, Myriam Taverna, et al.. (2013). A new cell culture-based assay quantifies vitamin K 2,3-epoxide reductase complex subunit 1 function and reveals warfarin resistance phenotypes not shown by the dithiothreitol-driven VKOR assay. Journal of Thrombosis and Haemostasis. 11(5). 872–880. 29 indexed citations

13.

Müller, C. R., Simone Rost, Matthias Watzka, Carville G. Bevans, & Johannes Oldenburg. (2013). Comparative genetics of warfarin resistance. Hämostaseologie. 34(2). 143–159. 21 indexed citations

14.

Rost, Simone, Cordula Neuner, Indrajit Nanda, et al.. (2013). Novel form of X-linked nonsyndromic hearing loss with cochlear malformation caused by a mutation in the type IV collagen gene COL4A6. European Journal of Human Genetics. 22(2). 208–215. 50 indexed citations

15.

Pezeshkpoor, Behnaz, Simone Rost, Johannes Oldenburg, & Osman El‐Maarri. (2012). Identification of a third rearrangement at Xq28 that causes severe hemophilia A as a result of homologous recombination between inverted repeats. Journal of Thrombosis and Haemostasis. 10(8). 1600–1608. 15 indexed citations

16.

Pelz, Hans‐Joachim, Simone Rost, Elisabeth Müller, et al.. (2011). Distribution and frequency of VKORC1 sequence variants conferring resistance to anticoagulants in Mus musculus. Pest Management Science. 68(2). 254–259. 45 indexed citations

17.

Watzka, Matthias, Christof Geisen, Carville G. Bevans, et al.. (2010). Thirteen novel VKORC1 mutations associated with oral anticoagulant resistance: insights into improved patient diagnosis and treatment. Journal of Thrombosis and Haemostasis. 9(1). 109–118. 79 indexed citations

18.

Rost, Simone, Hans‐Joachim Pelz, Alan D. MacNicoll, et al.. (2009). Novel mutations in the VKORC1 gene of wild rats and mice – a response to 50 years of selection pressure by warfarin?. BMC Genetics. 10(1). 4–4. 118 indexed citations

19.

Rost, Simone, Christof Geisen, Andreas Fregin, et al.. (2006). Founder mutation Arg485Pro led to recurrent compound heterozygous GGCX genotypes in two German patients with VKCFD type 1. Blood Coagulation & Fibrinolysis. 17(6). 503–507. 17 indexed citations

20.

Oldenburg, Johannes, Vytautas Ivaškevičius, Simone Rost, et al.. (2001). Evaluation of DHPLC in the analysis of hemophilia A. Journal of Biochemical and Biophysical Methods. 47(1-2). 39–51. 66 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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