Monika Andrassi

505 total citations
6 papers, 392 citations indexed

About

Monika Andrassi is a scholar working on Molecular Biology, Ophthalmology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Monika Andrassi has authored 6 papers receiving a total of 392 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 4 papers in Ophthalmology and 2 papers in Cellular and Molecular Neuroscience. Recurrent topics in Monika Andrassi's work include Retinal Development and Disorders (5 papers), Retinal Diseases and Treatments (4 papers) and Photoreceptor and optogenetics research (2 papers). Monika Andrassi is often cited by papers focused on Retinal Development and Disorders (5 papers), Retinal Diseases and Treatments (4 papers) and Photoreceptor and optogenetics research (2 papers). Monika Andrassi collaborates with scholars based in Germany and Canada. Monika Andrassi's co-authors include Birgit Lorenz, Markus N. Preising, P Gyürüs, Sumin Gu, Andreas Gal, Bernhard H. F. Weber, Andrea Gehrig, Karen L. White, Günther Rudolph and Frank G. Holz and has published in prestigious journals such as European Journal of Human Genetics, Clinical Genetics and Documenta Ophthalmologica.

In The Last Decade

Monika Andrassi

6 papers receiving 386 citations

Peers

Monika Andrassi

MB

OPHTH

CMN

RNMI

GENET

L.S. Sullivan United States

S. J. Bowne United States

T. P. Dryja United States

John R. Heckenlively United States

Regine Mühlfriedel Germany

Ruben Jauregui United States

K. R. Murthy India

Jeremy M. Hoffmann United States

Dikla Bandah‐Rozenfeld Israel

Patrícia José Spain

L.S. Sullivan United States

Monika Andrassi

431 ×1.2

MB

210 ×0.8

OPHTH

120 ×1.6

CMN

56 ×0.7

RNMI

59 ×1.3

GENET

Citations per year, relative to Monika Andrassi Monika Andrassi (= 1×) peers L.S. Sullivan

Countries citing papers authored by Monika Andrassi

Since Specialization

Citations

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

Fields of papers citing papers by Monika Andrassi

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Monika Andrassi

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

All Works

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6 of 6 papers shown

1.

Lorenz, Birgit, Monika Andrassi, & Ulf Kretschmann. (2003). Phenotype in two families with RP3 associated with RPGR mutations. Ophthalmic Genetics. 24(2). 89–101. 23 indexed citations

2.

Lorenz, Birgit, P Gyürüs, Markus N. Preising, et al.. (2000). Early-onset severe rod-cone dystrophy in young children with RPE65 mutations.. PubMed. 41(9). 2735–42. 158 indexed citations

3.

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

4.

Gehrig, Andrea, Karen L. White, Birgit Lorenz, et al.. (1999). Assessment of RS1 in X‐linked juvenile retinoschisis and sporadic senile retinoschisis. Clinical Genetics. 55(6). 461–465. 13 indexed citations

5.

Böck, Markus, et al.. (1998). A comparison of two multifocal ERG systems. Documenta Ophthalmologica. 97(2). 157–178. 21 indexed citations

6.

Lorenz, Birgit, et al.. (1996). Die inkomplette kongenitale stationäre Nachtblindheit (CSNB). Eine wichtige Differentialdiagnose des kongenitalen Nystagmus. Klinische Monatsblätter für Augenheilkunde. 208(1). 48–55. 8 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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