Bernd Rösler

463 total citations
6 papers, 184 citations indexed

About

Bernd Rösler is a scholar working on Molecular Biology, Genetics and Pharmacology. According to data from OpenAlex, Bernd Rösler has authored 6 papers receiving a total of 184 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Molecular Biology, 2 papers in Genetics and 1 paper in Pharmacology. Recurrent topics in Bernd Rösler's work include Hedgehog Signaling Pathway Studies (2 papers), Genomic variations and chromosomal abnormalities (2 papers) and Renal and related cancers (2 papers). Bernd Rösler is often cited by papers focused on Hedgehog Signaling Pathway Studies (2 papers), Genomic variations and chromosomal abnormalities (2 papers) and Renal and related cancers (2 papers). Bernd Rösler collaborates with scholars based in Germany, United States and Canada. Bernd Rösler's co-authors include Jürgen Kohlhase, Serdar Ceylaner, Dieter Kotzot, Ursula G. Froster, David Chitayat, Tara Montgomery, Sigrun Fuchs, Pauline Terhal, Judith Fischer and Andreas Zimmer and has published in prestigious journals such as Human Mutation, Acta Dermato Venereologica and American Journal of Medical Genetics Part A.

In The Last Decade

Bernd Rösler

6 papers receiving 178 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Bernd Rösler Germany	5	135	63	23	20	16	6	184
Silvia Azzarello‐Burri Switzerland	8	206 1.5×	139 2.2×	27 1.2×	15 0.8×	15 0.9×	17	303
Irina Lagovsky Israel	8	122 0.9×	118 1.9×	18 0.8×	24 1.2×	16 1.0×	14	282
Ursula Giussani Italy	9	124 0.9×	90 1.4×	32 1.4×	18 0.9×	3 0.2×	16	226
V Murday United Kingdom	4	127 0.9×	45 0.7×	28 1.2×	6 0.3×	8 0.5×	5	229
Sylvia Redon France	8	139 1.0×	158 2.5×	11 0.5×	33 1.6×	4 0.3×	12	227
J.G. Dauwerse Netherlands	6	211 1.6×	129 2.0×	7 0.3×	17 0.8×	7 0.4×	7	307
Ali Awaji Saudi Arabia	4	178 1.3×	170 2.7×	19 0.8×	10 0.5×	3 0.2×	6	265
Maha Faden Saudi Arabia	6	93 0.7×	100 1.6×	20 0.9×	21 1.1×	3 0.2×	9	178
Makia J. Marafie Kuwait	11	142 1.1×	154 2.4×	10 0.4×	21 1.1×	4 0.3×	28	279
Sorath Noorani Siddiqui Pakistan	10	156 1.2×	61 1.0×	18 0.8×	4 0.2×	7 0.4×	25	245

Countries citing papers authored by Bernd Rösler

Since Specialization

Citations

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

Fields of papers citing papers by Bernd Rösler

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Bernd Rösler

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

All Works

Sort: Min cites: Since: Top N: Style:

6 of 6 papers shown

1.

Has, Cristina, Agnes Schwieger‐Briel, Nina Schlipf, et al.. (2016). Target-sequence Capture and High Throughput Sequencing Identify a De novo CARD14 Mutation in an Infant with Erythrodermic Pityriasis Rubra Pilaris. Acta Dermato Venereologica. 96(7). 989–990. 9 indexed citations

2.

Zimmer, Andreas, et al.. (2016). Whole-Exome-Sequencing Reveals Small Deletions in CASP14 in Patients with Autosomal Recessive Inherited Ichthyosis. Acta Dermato Venereologica. 97(1). 102–104. 27 indexed citations

3.

Terhal, Pauline, Bernd Rösler, & Jürgen Kohlhase. (2006). A family with features overlapping Okihiro syndrome, hemifacial microsomia and isolated Duane anomaly caused by a novel SALL4 mutation. American Journal of Medical Genetics Part A. 140A(3). 222–226. 20 indexed citations

4.

Kohlhase, Jürgen, David Chitayat, Dieter Kotzot, et al.. (2005). SALL4mutations in Okihiro syndrome (Duane-radial ray syndrome), acro-renal-ocular syndrome, and related disorders. Human Mutation. 26(3). 176–183. 79 indexed citations

5.

Botzenhart, Elke, Andrew Green, Helena G. Ilyina, et al.. (2005). SALL1 mutation analysis in Townes-Brocks syndrome: twelve novel mutations and expansion of the phenotype. Human Mutation. 26(3). 282–282. 48 indexed citations

6.

Rösler, Bernd. (1967). [Thyroxine and triiodothyronine protein complexes in serum of Mesocricetus auratus and Gerbillus pyramidum].. PubMed. 18(5). 597–606. 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.

Explore authors with similar magnitude of impact