Johanna Pass

713 total citations
6 papers, 125 citations indexed

About

Johanna Pass is a scholar working on Sensory Systems, Cell Biology and Molecular Biology. According to data from OpenAlex, Johanna Pass has authored 6 papers receiving a total of 125 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Sensory Systems, 4 papers in Cell Biology and 3 papers in Molecular Biology. Recurrent topics in Johanna Pass's work include Hearing, Cochlea, Tinnitus, Genetics (3 papers), Cellular transport and secretion (3 papers) and Vestibular and auditory disorders (2 papers). Johanna Pass is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (3 papers), Cellular transport and secretion (3 papers) and Vestibular and auditory disorders (2 papers). Johanna Pass collaborates with scholars based in United Kingdom, United States and Belgium. Johanna Pass's co-authors include Karen P. Steel, Neil J. Ingham, Jing Chen, Morag A. Lewis, Jacqueline K. White, Shalini Jadeja, Annalisa Buniello, John J. Kelly, David Goulding and Ian J. Jackson and has published in prestigious journals such as PLoS ONE, Scientific Reports and PLoS Genetics.

In The Last Decade

Johanna Pass

6 papers receiving 125 citations

Peers

Johanna Pass

MB

SS

CB

NEURO

CR

Lana M. Pollock United States

Anne B.S. Giersch United States

Aisha Al‐Khayat Oman

Souad Gherbi France

Orit Dagan‐Rosenfeld United States

Soumya Korrapati United States

Eva L. Morozko United States

Thomas Jaworek United States

Felix D. Weiss United Kingdom

Carol A. Carney Spain

Lana M. Pollock United States

Johanna Pass

150 ×1.8

MB

74 ×1.2

SS

40 ×1.4

CB

32 ×1.2

NEURO

20 ×1.3

CR

Citations per year, relative to Johanna Pass Johanna Pass (= 1×) peers Lana M. Pollock

Countries citing papers authored by Johanna Pass

Since Specialization

Citations

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

Fields of papers citing papers by Johanna Pass

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Johanna Pass

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

Lewis, Morag A., Neil J. Ingham, Jing Chen, et al.. (2022). Identification and characterisation of spontaneous mutations causing deafness from a targeted knockout programme. BMC Biology. 20(1). 67–67. 2 indexed citations

2.

Ingham, Neil J., et al.. (2020). Synaptojanin2 Mutation Causes Progressive High-frequency Hearing Loss in Mice. Frontiers in Cellular Neuroscience. 14. 561857–561857. 9 indexed citations

3.

Ingham, Neil J., Selina Pearson, Morag A. Lewis, et al.. (2016). S1PR2 variants associated with auditory function in humans and endocochlear potential decline in mouse. Scientific Reports. 6(1). 28964–28964. 27 indexed citations

4.

Ebrahim, Seham, Neil J. Ingham, Morag A. Lewis, et al.. (2016). Alternative Splice Forms Influence Functions of Whirlin in Mechanosensory Hair Cell Stereocilia. Cell Reports. 15(5). 935–943. 28 indexed citations

5.

Chen, Jing, Neil J. Ingham, John J. Kelly, et al.. (2014). Spinster Homolog 2 (Spns2) Deficiency Causes Early Onset Progressive Hearing Loss. PLoS Genetics. 10(10). e1004688–e1004688. 52 indexed citations

6.

Buniello, Annalisa, Rachel E. Hardisty-Hughes, Johanna Pass, et al.. (2013). Headbobber: A Combined Morphogenetic and Cochleosaccular Mouse Model to Study 10qter Deletions in Human Deafness. PLoS ONE. 8(2). e56274–e56274. 7 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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