Sibylle Wagner

959 total citations · 1 hit paper
14 papers, 713 citations indexed

About

Sibylle Wagner is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Ophthalmology. According to data from OpenAlex, Sibylle Wagner has authored 14 papers receiving a total of 713 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 3 papers in Cellular and Molecular Neuroscience and 3 papers in Ophthalmology. Recurrent topics in Sibylle Wagner's work include Connexins and lens biology (3 papers), Pluripotent Stem Cells Research (2 papers) and Fibroblast Growth Factor Research (2 papers). Sibylle Wagner is often cited by papers focused on Connexins and lens biology (3 papers), Pluripotent Stem Cells Research (2 papers) and Fibroblast Growth Factor Research (2 papers). Sibylle Wagner collaborates with scholars based in Germany, Russia and United States. Sibylle Wagner's co-authors include Alexander Borst, Martin Heisenberg, Martin Hrabě de Angelis, Nafees Ahmad, Oliver Puk, Jochen Graw, Matthias Klaften, Birgit Rathkolb, Martina Klempt and Eckhard Wolf and has published in prestigious journals such as PLoS ONE, Genetics and Endocrinology.

In The Last Decade

Sibylle Wagner

14 papers receiving 696 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.

DrosophilaMushroom Body Mutants are Deficient in Olfactory Learning

1985 563 citations Martin Heisenberg, Alexander Borst et al. Journal of Neurogenetics profile →

Peers

Countries citing papers authored by Sibylle Wagner

Since Specialization

Citations

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

Fields of papers citing papers by Sibylle Wagner

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sibylle Wagner

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

All Works

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14 of 14 papers shown

#	Work	Indexed citations
1	Bmpr1b Splice Site Mutation Leads To Optic Nerve Head Degeneration In The Mouse 2012 ·Jochen Graw, Oliver Puk, Susanne Weber, Sibylle Wagner, Frank Thiele, Gerhard K. H. Przemeck, Martin Hrabě de Angelis	1
2	The Pathologic Effect of a Novel Neomorphic Fgf9Y162C Allele Is Restricted to Decreased Vision and Retarded Lens Growth 2011 ·PLoS ONE ·Oliver Puk, Gabriele Möller, Arie Geerlof, (unknown), Nafees Ahmad, Sibylle Wagner, Jerzy Adamski, Martin Hrabě de Angelis, Jochen Graw	5
3	Generation of N-ethyl-N-nitrosourea-induced mouse mutants with deviations in hematological parameters 2011 ·Mammalian Genome ·Bernhard Aigner, Birgit Rathkolb, Martina Klempt, Sibylle Wagner, (unknown), Matthias Klaften, Jürgen Laufs, (unknown), Reinhard Sedlmeier, Martin Hrabě de Angelis, Eckhard Wolf	17
4	Microphakia and congenital cataract formation in a novel Lim2(C51R) mutant mouse. 2011 ·PubMed ·Oliver Puk, Nafees Ahmad, Sibylle Wagner, Martin Hrabě de Angelis, Jochen Graw	6
5	First Mutation in the βA2-crystallin Encoding Gene is Associated with Small Lenses and Age-Related Cataracts 2011 ·Investigative Ophthalmology & Visual Science ·Oliver Puk, Nafees Ahmad, Sibylle Wagner, Martin Hrabě de Angelis, Jochen Graw	19
6	Utilization of a Mutagenesis Screen to Generate Mouse Models of Hyperaldosteronism 2010 ·Endocrinology ·Ariadni Spyroglou, Sibylle Wagner, Celso E. Gómez-Sánchez, Birgit Rathkolb, Eckhard Wolf, Jenny Manolopoulou, Martín Reincke, Martin Bidlingmaier, Martin Hrabě de Angelis, Felix Beuschlein	6
7	Generation of N‐ethyl‐N‐nitrosourea‐induced mouse mutants with deviations in plasma enzyme activities as novel organ‐specific disease models 2009 ·Experimental Physiology ·Bernhard Aigner, Birgit Rathkolb, Matthias Klaften, Reinhard Sedlmeier, Martina Klempt, Sibylle Wagner, (unknown), Ulríke Mayer, Thomas Klopstock, Martin Hrabě de Angelis, Eckhard Wolf	16
8	N-ethyl-N-nitrosourea mutagenesis produced a small number of mice with altered plasma electrolyte levels 2009 ·Journal of Biomedical Science ·Bernhard Aigner, Birgit Rathkolb, Martina Klempt, Sibylle Wagner, (unknown), Martin Hrabě de Angelis, Eckhard Wolf	3
9	Short term regulation of aldosterone secretion after stimulation and suppression experiments in mice 2009 ·Journal of Molecular Endocrinology ·Ariadni Spyroglou, Jenny Manolopoulou, Sibylle Wagner, Martin Bidlingmaier, Martín Reincke, Felix Beuschlein	17
10	Genome-wide search for genes that modulate inflammatory arthritis caused by Ali18 mutation in mice 2009 ·Mammalian Genome ·Koichiro Abe, Matthias Klaften, Akira Narita, Tetsuaki Kimura, Kenji Imai, Minoru Kimura, Isabel Rubio‐Aliaga, Sibylle Wagner, Thilo Jakob, Martin Hrabě de Angelis	4
11	Reduced Corneal Thickness and Enlarged Anterior Chamber in a Novel ColVIIIa2^G257DMutant Mouse 2009 ·Investigative Ophthalmology & Visual Science ·Oliver Puk, Claudia Dalke, Julia Calzada‐Wack, Nafees Ahmad, Matthias Klaften, Sibylle Wagner, Martin Hrabě de Angelis, Jochen Graw	30
12	A phenotype-driven ENU mutagenesis screen for the identification of dominant mutations involved in alcohol consumption 2008 ·Mammalian Genome ·Cornelius R. Pawlak, Carles Sanchis‐Segura, Dian Soewarto, Sibylle Wagner, Martin Hrabě de Angelis, Rainer Spanagel	6
13	A Genetic Screen for Modifiers of the Delta1-Dependent Notch Signaling Function in the Mouse 2006 ·Genetics ·Isabel Rubio‐Aliaga, Dian Soewarto, Sibylle Wagner, Matthias Klaften, Helmut Fuchs, Svetoslav Kalaydjiev, Dirk H. Busch, Martina Klempt, Birgit Rathkolb, Eckhard Wolf, Koichiro Abe, (unknown), Gerhard K. H. Przemeck, Johannes Beckers, Martin Hrabě de Angelis	20
14	DrosophilaMushroom Body Mutants are Deficient in Olfactory Learning breakdown → 1985 ·Journal of Neurogenetics ·Martin Heisenberg, Alexander Borst, Sibylle Wagner, (unknown)	563

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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