A. Blankenagel

1.8k total citations
38 papers, 1.4k citations indexed

About

A. Blankenagel is a scholar working on Molecular Biology, Ophthalmology and Epidemiology. According to data from OpenAlex, A. Blankenagel has authored 38 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Molecular Biology, 12 papers in Ophthalmology and 5 papers in Epidemiology. Recurrent topics in A. Blankenagel's work include Retinal Development and Disorders (10 papers), Retinal Diseases and Treatments (7 papers) and Connexins and lens biology (5 papers). A. Blankenagel is often cited by papers focused on Retinal Development and Disorders (10 papers), Retinal Diseases and Treatments (7 papers) and Connexins and lens biology (5 papers). A. Blankenagel collaborates with scholars based in Germany, Netherlands and United States. A. Blankenagel's co-authors include Klaus Rohrschneider, Carel B. Hoyng, Frans P.M. Cremers, August F. Deutman, Han G. Brunner, B. Jeroen Klevering, Alessandra Maugeri, Ulrich Kellner, Bernhard Jurklies and Eckart Apfelstedt-Sylla and has published in prestigious journals such as The American Journal of Human Genetics, Human Molecular Genetics and The Laryngoscope.

In The Last Decade

A. Blankenagel

37 papers receiving 1.3k citations

Peers

A. Blankenagel

OPHTH

RNMI

GENET

Alan Lennon United Kingdom

Blanca Garcı́a-Sandoval Spain

Barrie Jay United Kingdom

C.F. Inglehearn United Kingdom

Mary J. van Schooneveld Netherlands

Dorien J.R. van de Pol Netherlands

Sylvain Hanein France

G. Jane Farrar Ireland

Susanne Roosing Netherlands

Almudena Ávila‐Fernández Spain

Alan Lennon United Kingdom

A. Blankenagel

1.2k ×1.0

550 ×0.7

OPHTH

151 ×0.6

RNMI

250 ×1.3

369 ×2.4

GENET

Citations per year, relative to A. Blankenagel A. Blankenagel (= 1×) peers Alan Lennon

Countries citing papers authored by A. Blankenagel

Since Specialization

Citations

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

Fields of papers citing papers by A. Blankenagel

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of A. Blankenagel

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

20 of 20 papers shown

Spandau, Ulrich, et al.. (2002). Testing Night Vision Goggles in a Dark Outside Environment. Optometry and Vision Science. 79(1). 39–45. 12 indexed citations

Rohrschneider, Klaus, et al.. (2002). Diagnostik bei Netzhauterkrankungen Vergleich von multifokalem ERG und funduskontrollierter Perimetrie – Fallstudie. Der Ophthalmologe. 99(9). 695–702. 2 indexed citations

Rohrschneider, Klaus, et al.. (2002). Nutzung und AkzeptanzÂ vonÂ vergrÃ¶Ãernden Sehhilfen. Klinische Monatsblätter für Augenheilkunde. 219(7). 507–511. 6 indexed citations

Spandau, Ulrich, et al.. (2001). A New Clinical Classification for Usher's Syndrome Based on a New Subtype of Usher's Syndrome Type I. The Laryngoscope. 111(1). 84–86. 43 indexed citations

Krämer, Franziska, Karen L. White, Daniel Pauleikhoff, et al.. (2000). Mutations in the VMD2 gene are associated with juvenile-onset vitelliform macular dystrophy (Best disease) and adult vitelliform macular dystrophy but not age-related macular degeneration. European Journal of Human Genetics. 8(4). 286–292. 169 indexed citations

Maugeri, Alessandra, B. Jeroen Klevering, Klaus Rohrschneider, et al.. (2000). Mutations in the ABCA4 (ABCR) Gene Are the Major Cause of Autosomal Recessive Cone-Rod Dystrophy. The American Journal of Human Genetics. 67(4). 960–966. 250 indexed citations

Rohrschneider, Klaus, et al.. (2000). Einsatz einer neuen Nachtsichtbrille (DAVIS)123. Klinische Monatsblätter für Augenheilkunde. 217(2). 88–93. 7 indexed citations

Maugeri, Alessandra, Marc A. van Driel, Dorien J.R. van de Pol, et al.. (1999). The 2588G→C Mutation in the ABCR Gene Is a Mild Frequent Founder Mutation in the Western European Population and Allows the Classification of ABCR Mutations in Patients with Stargardt Disease. The American Journal of Human Genetics. 64(4). 1024–1035. 213 indexed citations

Bruder, Ingo, A. Blankenagel, & Klaus Rohrschneider. (1999). Ophthalmological rehabilitation - experience at the University Eye Hospital Heidelberg. Der Ophthalmologe. 96(9). 611–616. 9 indexed citations

10.

Wolf, Matthias T. F., Bernhard Zabel, Birgit Lorenz, et al.. (1998). Analysis of aniridia patients for mutations in the PAX6 gene. Der Ophthalmologe. 95(12). 828–830. 5 indexed citations

11.

Wolf, Matthias T. F., Birgit Lorenz, Andreas Winterpacht, et al.. (1998). Ten novel mutations found in aniridia. Human Mutation. 12(5). 304–313. 5 indexed citations

12.

Rohrschneider, Klaus, et al.. (1998). Influence of image frequency of closed-circuit television systems (CCTV) on reading comfort. Der Ophthalmologe. 95(2). 110–113. 4 indexed citations

13.

Gerber, S., Jean‐Michel Rozet, T.J.R. van de Pol, et al.. (1998). Complete Exon–Intron Structure of the Retina-Specific ATP Binding Transporter Gene (ABCR) Allows the Identification of Novel Mutations Underlying Stargardt Disease. Genomics. 48(1). 139–142. 60 indexed citations

14.

Rohrschneider, Klaus, et al.. (1997). Fixationsverhalten bei Morbus Stargardt. Der Ophthalmologe. 94(9). 624–628. 22 indexed citations

15.

Rohrschneider, Klaus, et al.. (1997). Anwendungen einer neuen optoelektronischen Sehhilfe für hochgradig Sehbehinderte (LVES). Klinische Monatsblätter für Augenheilkunde. 210(2). 105–110. 5 indexed citations

16.

Auffarth, Gerd U., et al.. (1996). [Improving contrast sensitivity by cut-off filters in high adaptation luminance levels in retinitis pigmentosa].. PubMed. 93(4). 456–62. 4 indexed citations

17.

Drechsler, Matthias, E.J. Meijers-Heijboer, Susanne A. Schneider, et al.. (1994). Molecular analysis of aniridia patients for deletions involving the Wilms' tumor gene. Human Genetics. 94(4). 331–8. 24 indexed citations

18.

Carvalho, Maria Raquel Santos, Thomas Berninger, Guntram Kommerell, et al.. (1992). Leber’s Hereditary Optic Neuroretinopathy and the X-Chromosomal Susceptibility Factor: No Linkage to DXS7. Human Heredity. 42(5). 316–320. 30 indexed citations

19.

Blankenagel, A. & Wolfgang Jäeger. (1975). Television reading system. Child Care Health and Development. 1(5). 369–372.

20.

Blankenagel, A. & Wolfgang Jäeger. (1972). [Experiences with a television reading apparatus in a school for the blind].. PubMed. 161(4). 467–9. 2 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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