Alexandra Erven

1.9k total citations · 1 hit paper
11 papers, 971 citations indexed

About

Alexandra Erven is a scholar working on Molecular Biology, Sensory Systems and Cellular and Molecular Neuroscience. According to data from OpenAlex, Alexandra Erven has authored 11 papers receiving a total of 971 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 6 papers in Sensory Systems and 2 papers in Cellular and Molecular Neuroscience. Recurrent topics in Alexandra Erven's work include Hearing, Cochlea, Tinnitus, Genetics (6 papers), Developmental Biology and Gene Regulation (3 papers) and Retinal Development and Disorders (2 papers). Alexandra Erven is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (6 papers), Developmental Biology and Gene Regulation (3 papers) and Retinal Development and Disorders (2 papers). Alexandra Erven collaborates with scholars based in United Kingdom, United States and Germany. Alexandra Erven's co-authors include Karen P. Steel, Corné J. Kros, Walter Marcotti, Paul F. Kenna, G. Jane Farrar, Peter Humphries, Denise M. Sheils, Ronald A. Bush, Paul A. Sieving and Marian M. Humphries and has published in prestigious journals such as Nature Genetics, The Journal of Physiology and European Journal of Neuroscience.

In The Last Decade

Alexandra Erven

11 papers receiving 960 citations

Hit Papers

Retinopathy induced in mice by targeted disruption of the... 1997 2026 2006 2016 1997 100 200 300 400
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.

  1. Retinopathy induced in mice by targeted disruption of the rhodopsin gene
    1997 451 citations Marian M. Humphries, Derrick E. Rancourt et al. Nature Genetics profile →

Peers

Alexandra Erven
Inga Ebermann Germany
Mariette Wagenaar Netherlands
Sarah Harkins‐Perry United States
Anabel Varela United Kingdom
Dominique Larget‐Piet France
Tina Märker Germany
Andrea C. Dosé United States
Jan Reiners Germany
S. M. Slapnick United States
Inga Ebermann Germany
Alexandra Erven
Citations per year, relative to Alexandra Erven Alexandra Erven (= 1×) peers Inga Ebermann

Countries citing papers authored by Alexandra Erven

Since Specialization
Citations

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

Fields of papers citing papers by Alexandra Erven

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Alexandra Erven

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

All Works

11 of 11 papers shown
1.
Marcotti, Walter, Alexandra Erven, Stuart L. Johnson, Karen P. Steel, & Corné J. Kros. (2006). Tmc1 is necessary for normal functional maturation and survival of inner and outer hair cells in the mouse cochlea. The Journal of Physiology. 574(3). 677–698. 102 indexed citations
2.
Mashimo, Tomoji, et al.. (2006). Two quantitative trait loci affecting progressive hearing loss in 101/H mice. Mammalian Genome. 17(8). 841–850. 20 indexed citations
3.
Ahituv, Nadav, Alexandra Erven, Helmut Fuchs, et al.. (2004). An ENU-induced mutation in AP-2α leads to middle earand ocular defects in Doarad mice. Mammalian Genome. 15(6). 424–432. 19 indexed citations
4.
Vreugde, Sarah, Alexandra Erven, Corné J. Kros, et al.. (2002). Beethoven, a mouse model for dominant, progressive hearing loss DFNA36. Nature Genetics. 30(3). 257–258. 214 indexed citations
5.
Hardisty, Rachel, Alexandra Erven, Susan Morse, et al.. (2002). The Deaf Mouse Mutant Jeff (Jf) is a Single Gene Model of Otitis Media. Journal of the Association for Research in Otolaryngology. 4(2). 130–138. 64 indexed citations
6.
Kiernan, Amy E., Alexandra Erven, Jo Peters, et al.. (2002). ENU mutagenesis reveals a highly mutable locus on mouse Chromosome 4 that affects ear morphogenesis. Mammalian Genome. 13(3). 142–148. 41 indexed citations
7.
Kiernan, Amy E., Alexandra Erven, Jo Peters, et al.. (2002). ENU mutagenesis reveals a highly mutable locus on mouse Chromosome 4 that affects ear morphogenesis. Mammalian Genome. 13(3). 142–148. 36 indexed citations
8.
Erven, Alexandra, Michael J. Skynner, Katsuzumi Okumura, et al.. (2002). A novel stereocilia defect in sensory hair cells of the deaf mouse mutant Tasmanian devil. European Journal of Neuroscience. 16(8). 1433–1441. 19 indexed citations
9.
Kiernan, Amy E., Alexandra Erven, Jo Peters, et al.. (2002). ENU mutagenesis reveals a highly mutable locus on mouse Chromosome 4 that affects ear morphogenesis. Mammalian Genome. 13(3). 142–148. 1 indexed citations
10.
Humphries, Marian M., Derrick E. Rancourt, G. Jane Farrar, et al.. (1997). Retinopathy induced in mice by targeted disruption of the rhodopsin gene. Nature Genetics. 15(2). 216–219. 451 indexed citations breakdown →
11.
Kenna, Paul F., Fiona C. Mansergh, Sophia Millington‐Ward, et al.. (1997). Clinical and molecular genetic characterisation of a family segregating autosomal dominant retinitis pigmentosa and sensorineural deafness. British Journal of Ophthalmology. 81(3). 207–213. 4 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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