Kathrin Saar

9.1k total citations · 2 hit papers
73 papers, 4.1k citations indexed

About

Kathrin Saar is a scholar working on Molecular Biology, Genetics and Physiology. According to data from OpenAlex, Kathrin Saar has authored 73 papers receiving a total of 4.1k indexed citations (citations by other indexed papers that have themselves been cited), including 32 papers in Molecular Biology, 23 papers in Genetics and 12 papers in Physiology. Recurrent topics in Kathrin Saar's work include Spaceflight effects on biology (7 papers), DNA Repair Mechanisms (6 papers) and Bipolar Disorder and Treatment (5 papers). Kathrin Saar is often cited by papers focused on Spaceflight effects on biology (7 papers), DNA Repair Mechanisms (6 papers) and Bipolar Disorder and Treatment (5 papers). Kathrin Saar collaborates with scholars based in Germany, Netherlands and United States. Kathrin Saar's co-authors include André Reis, Norbert Hübner, Hilary A. Phillips, John C. Mulley, Samuel F. Berkovic, Ingrid E. Scheffer, Dao Wen Wang, Eric W. Johnson, Rita Singh and Robyn H. Wallace and has published in prestigious journals such as Cell, Proceedings of the National Academy of Sciences and Nucleic Acids Research.

In The Last Decade

Kathrin Saar

73 papers receiving 4.0k 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.

Nibrin, a Novel DNA Double-Strand Break Repair Protein, Is Mutated in Nijmegen Breakage Syndrome

1998 811 citations Raymonda Varon, Christine Vissinga et al. Cell profile →
Febrile seizures and generalized epilepsy associated with a mutation in the Na+-channel ß1 subunit gene SCN1B

1998 783 citations Hilary A. Phillips, Kathrin Saar et al. profile →

Peers

Countries citing papers authored by Kathrin Saar

Since Specialization

Citations

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

Fields of papers citing papers by Kathrin Saar

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Kathrin Saar

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

#	Work	Indexed citations
1	Endothelial Overexpression of TGF-β-Induced Protein Impairs Venous Thrombus Resolution 2023 ·JACC Basic to Translational Science ·Magdalena L. Bochenek, Kathrin Saar, Maliheh Nazari-Jahantigh, Rajinikanth Gogiraju, Christoph B. Wiedenroth, Thomas Münzel, Eckhard Mayer, Ludger Fink, Andreas Schober, Norbert Hübner, Stefan Guth, Stavros Konstantinides, Katrin Schäfer	6
2	In Prostate Cancer Cells Cytokines Are Early Responders to Gravitational Changes Occurring in Parabolic Flights 2022 ·International Journal of Molecular Sciences ·Herbert Schulz, (unknown), Markus Wehland, Thomas J. Corydon, Ruth Hemmersbach, (unknown), Daniela Melnik, Norbert Hübner, Kathrin Saar, Manfred Infanger, Daniela Grimm	7
3	Expression of cardiovascular-related microRNAs is altered in L-arginine:glycine amidinotransferase deficient mice 2022 ·Scientific Reports ·Märit Jensen, Christian Müller, Norbert Hübner, Giannino Patone, Kathrin Saar, Chi‐un Choe, Edzard Schwedhelm, Tanja Zeller	2
4	Transcriptional signatures regulated by TRPC1/C4-mediated Background Ca2+ entry after pressure-overload induced cardiac remodelling 2020 ·Progress in Biophysics and Molecular Biology ·Juan E. Camacho Londoño, Vladimir Kuryshev, Markus Zorn, Kathrin Saar, Xiao Yu Tian, Norbert Hübner, Peter P. Nawroth, Alexander Dietrich, Lutz Birnbaumer, Peter Lipp, Christoph Dieterich, Marc Freichel	4
5	Thyroid cancer cells in space during the TEXUS-53 sounding rocket mission – The THYROID Project 2018 ·Scientific Reports ·Sascha Kopp, Marcus Krüger, (unknown), Hergen Oltmann, Andreas Schütte, Burkhard Schmitz, Johann Bauer, Herbert Schulz, Kathrin Saar, Norbert Huebner, Markus Wehland, Mohamed Zakaria Nassef, Daniela Melnik, (unknown), Manfred Infanger, Daniela Grimm	27
6	Brain region-specific expression of genes mapped within quantitative trait loci for behavioral responsiveness to acute stress in Fisher 344 and Wistar Kyoto male rats 2018 ·PLoS ONE ·(unknown), Patrick H. Lim, (unknown), Wendy Luo, (unknown), (unknown), Ryan Jankord, Kathrin Saar, Eva E. Redei	8
7	Telmisartan prevents diet-induced obesity and preserves leptin transport across the blood-brain barrier in high-fat diet-fed mice 2018 ·Pflügers Archiv - European Journal of Physiology ·(unknown), (unknown), Ines Stölting, (unknown), Kathrin Saar, Norbert Hübner, William A. Banks, Walter Raasch	27
8	Differential gene expression of human chondrocytes cultured under short-term altered gravity conditions during parabolic flight maneuvers 2015 ·Cell Communication and Signaling ·Markus Wehland, Ganna Aleshcheva, Herbert Schulz, Kathrin Saar, Norbert Hübner, Ruth Hemmersbach, Markus Braun, Xiao Ma, Timo Frett, Elisabeth Warnke, Stefan Riwaldt, Jessica Pietsch, Thomas J. Corydon, Manfred Infanger, Daniela Grimm	33
9	Identification of Stim1 as a Candidate Gene for Exaggerated Sympathetic Response to Stress in the Stroke-Prone Spontaneously Hypertensive Rat 2014 ·PLoS ONE ·Mohammed Z. Ferdaus, Bing Xiao, (unknown), Kiyomitsu Nemoto, Yuji Harada, Kathrin Saar, Norbert Hübner, Minoru Isomura, Toru Nabika	15
10	[Primary failure of eruption (PFE). Clinical and molecular genetics analysis] Article in French 2013 ·University of Regensburg Publication Server (University of Regensburg) ·Angelika Stellzig‐Eisenhauer, Eva L. Decker, Philipp Meyer‐Marcotty, Christoph Rau, Britta Fiebig, (unknown), Kathrin Saar, Franz Rüschendorf, Norbert Hübner, T. Grimm, E. Witt, Bernhard H. F. Weber	2
11	Défaut primaire d’éruption (DPE). Analyse génétique clinique et moléculaire 2013 ·L Orthodontie Française ·Angelika Stellzig‐Eisenhauer, Eva L. Decker, Philipp Meyer‐Marcotty, (unknown), Britta Fiebig, Wolfram Kreß, Kathrin Saar, Franz Rüschendorf, Norbert Hübner, T. Grimm, E. Witt, Bernhard H. F. Weber	17
12	Genome-wide Analysis Indicates More Asian than Melanesian Ancestry of Polynesians 2008 ·The American Journal of Human Genetics ·Manfred Kayser, Óscar Lao, Kathrin Saar, Silke Brauer, Xingyu Wang, Peter Nürnberg, Ronald J. Trent, Mark Stoneking	77
13	PTHR1 Loss-of-Function Mutations in Familial, Nonsyndromic Primary Failure of Tooth Eruption 2008 ·The American Journal of Human Genetics ·Eva L. Decker, Angelika Stellzig‐Eisenhauer, Britta Fiebig, (unknown), Wolfram Kreß, Kathrin Saar, Franz Rüschendorf, Norbert Hübner, T. Grimm, Bernhard H. F. Weber	112
14	Mapping of Gene Loci for Nephronophthisis Type 4 and Senior-Løken Syndrome, to Chromosome 1p36 2002 ·The American Journal of Human Genetics ·(unknown), Edgar A. Otto, (unknown), Kathrin Saar, Franz Rüschendorf, B.C.P. Polak, Sirpa Ala‐Mello, Julia Hoefele, (unknown), Maria Haller, Heymut Omran, Peter Nürnberg, Friedhelm Hildebrandt	39
15	Familial hypomagnesaemia with hypercalciuria and nephrocalcinosis maps to chromosome 3q27 and is associated with mutations in the PCLN-1 gene 2000 ·European Journal of Human Genetics ·Stefanie Weber, Katrin Hoffmann, Nikola Jeck, Kathrin Saar, (unknown), (unknown), (unknown), Nine Knoers, Pierre Cochat, (unknown), Klaus E. Bonzel, Marianne Soergel, Friedrich Manz, (unknown), (unknown), André Reis, Martin Konrad	78
16	The Fanconi Anemia Group E Gene, FANCE, Maps to Chromosome 6p 1999 ·The American Journal of Human Genetics ·Quinten Waisfisz, Çiğdem Altay, Peter A. J. Leegwater, Johan P. de Winter, Kenshi Komatsu, D. Gareth Evans, Rolf‐Dieter Wegner, André Reis, Hans Joenje, Fré Arwert, Christopher G. Mathew, Jan C. Pronk, Kathrin Saar, Neil V. Morgan, Martin Digweed	41
17	Hereditary Isolated Renal Magnesium Loss Maps to Chromosome 11q23 1999 ·The American Journal of Human Genetics ·Iwan C. Meij, Kathrin Saar, Lambert P.W.J. van den Heuvel, (unknown), Martin Vollmer, Friedhelm Hildebrandt, André Reis, L.A.H. Monnens, Nine V.A.M. Knoers	38
18	Nibrin, a Novel DNA Double-Strand Break Repair Protein, Is Mutated in Nijmegen Breakage Syndrome breakdown → 1998 ·Cell ·Raymonda Varon, Christine Vissinga, Matthias Platzer, Karen Cerosaletti, Krystyńa Chrzańowska, Kathrin Saar, Georg Beckmann, E Seemanová, Paul R. Cooper, Norma J. Nowak, Markus Stümm, Corry M.R. Weemaes, Richard A. Gatti, Richard K. Wilson, Martin Digweed, André Rosenthal, Karl Sperling, Patrick Concannon, André Reis	811
19	Localisation of a Fanconi anaemia gene to chromosome 9p 1998 ·European Journal of Human Genetics ·Kathrin Saar, Detlev Schindler, Rolf‐Dieter Wegner, André Reis, Thomas F. Wienker, Holger Hoehn, Hans Joenje, Karl Sperling, Martin Digweed	17
20	Gene Localization for an Autosomal Dominant Familial Periodic Fever to 12p13 1998 ·The American Journal of Human Genetics ·John C. Mulley, Kathrin Saar, (unknown), Franz Rüschendorf, Hilary A. Phillips, Alison Colley, David Sillence, André Reis, Meredith Wilson	63

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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