John Neidhardt

3.2k total citations · 1 hit paper
63 papers, 2.4k citations indexed

About

John Neidhardt is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Ophthalmology. According to data from OpenAlex, John Neidhardt has authored 63 papers receiving a total of 2.4k indexed citations (citations by other indexed papers that have themselves been cited), including 55 papers in Molecular Biology, 13 papers in Cellular and Molecular Neuroscience and 13 papers in Ophthalmology. Recurrent topics in John Neidhardt's work include Retinal Development and Disorders (29 papers), Retinal Diseases and Treatments (12 papers) and RNA regulation and disease (11 papers). John Neidhardt is often cited by papers focused on Retinal Development and Disorders (29 papers), Retinal Diseases and Treatments (12 papers) and RNA regulation and disease (11 papers). John Neidhardt collaborates with scholars based in Germany, Switzerland and Netherlands. John Neidhardt's co-authors include Wolfgang Berger, Barbara Kloeckener‐Gruissem, Esther Glaus, Christina Zeitz, Silke Feil, Bernd Wissinger, F Schmid, Johannes Fleischhauer, U. Förster and Eberhart Zrenner and has published in prestigious journals such as PLoS ONE, Annals of Neurology and Scientific Reports.

In The Last Decade

John Neidhardt

62 papers receiving 2.4k citations

Hit Papers

align trajectories

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.

The molecular basis of human retinal and vitreoretinal diseases

2010 439 citations Wolfgang Berger, Barbara Kloeckener‐Gruissem et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
John Neidhardt Germany	29	2.1k	677	592	572	268	63	2.4k
Pete Humphries Ireland	26	1.3k 0.6×	553 0.8×	428 0.7×	249 0.4×	126 0.5×	55	1.7k
Isabelle Perrault France	30	2.7k 1.3×	1.5k 2.3×	452 0.8×	628 1.1×	357 1.3×	71	3.0k
Ulrike Orth Germany	18	1.2k 0.6×	313 0.5×	453 0.8×	446 0.8×	233 0.9×	38	1.7k
Bernd Rautenstrauß Germany	26	747 0.4×	389 0.6×	725 1.2×	224 0.4×	330 1.2×	90	1.8k
Neena B. Haider United States	23	1.4k 0.7×	584 0.9×	383 0.6×	439 0.8×	199 0.7×	46	2.0k
Jacoline B. ten Brink Netherlands	22	1.3k 0.6×	682 1.0×	209 0.4×	608 1.1×	480 1.8×	49	2.0k
Arnold Munnich France	25	1.6k 0.8×	237 0.4×	341 0.6×	580 1.0×	196 0.7×	55	2.3k
Zhengmao Hu China	25	1000 0.5×	153 0.2×	430 0.7×	535 0.9×	207 0.8×	127	1.9k
Sylvain Hanein France	20	1.3k 0.6×	535 0.8×	305 0.5×	342 0.6×	195 0.7×	45	1.6k
G. Jane Farrar Ireland	35	3.5k 1.7×	1.1k 1.7×	1.1k 1.8×	709 1.2×	434 1.6×	93	4.1k

Countries citing papers authored by John Neidhardt

Since Specialization

Citations

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

Fields of papers citing papers by John Neidhardt

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of John Neidhardt

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

All Works

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20 of 20 papers shown

Wöhlbrand, Lars, et al.. (2023). Sensitive and selective phenol sensing in denitrifying Aromatoleum aromaticum EbN1 ^T. Microbiology Spectrum. 11(6). e0210023–e0210023. 2 indexed citations

Weissglas‐Volkov, Daphna, Guy Shapira, Yazeed Zoabi, et al.. (2023). mRNA splicing is modulated by intronic microRNAs. iScience. 26(10). 107723–107723. 1 indexed citations

Scholten, Alexander, et al.. (2021). A novel missense variant in the EML1 gene associated with bilateral ribbon-like subcortical heterotopia leads to ciliary defects. Journal of Human Genetics. 66(12). 1159–1167. 5 indexed citations

Gläser, Anne, Markus H. Gräler, Sina M. Coldewey, et al.. (2020). Identification of Brain-Specific Treatment Effects in NPC1 Disease by Focusing on Cellular and Molecular Changes of Sphingosine-1-Phosphate Metabolism. International Journal of Molecular Sciences. 21(12). 4502–4502. 8 indexed citations

Korenke, Georg Christoph, et al.. (2020). A Novel de novo Frameshift Mutation in the <b><i>BCL11A</i></b> Gene in a Patient with Intellectual Disability Syndrome and Epilepsy. Molecular Syndromology. 11(3). 135–140. 12 indexed citations

Owczarek‐Lipska, Marta, Lejla Mulahasanovic, Carolin D. Obermaier, et al.. (2019). Novel mutations in the GJC2 gene associated with Pelizaeus–Merzbacher-like disease. Molecular Biology Reports. 46(4). 4507–4516. 10 indexed citations

Bräuer, Anja U., et al.. (2019). Combining Engineered U1 snRNA and Antisense Oligonucleotides to Improve the Treatment of a BBS1 Splice Site Mutation. Molecular Therapy — Nucleic Acids. 18. 123–130. 16 indexed citations

Hoffmann, Jeremy M., B Müller, Stefan Günther, et al.. (2018). Toward genome editing in X-linked RP—development of a mouse model with specific treatment relevant features. Translational research. 203. 57–72. 6 indexed citations

Tiwari, Amit K., Johannes R. Lemke, Janine Altmueller, et al.. (2016). Identification of Novel and Recurrent Disease-Causing Mutations in Retinal Dystrophies Using Whole Exome Sequencing (WES): Benefits and Limitations. PLoS ONE. 11(7). e0158692–e0158692. 14 indexed citations

10.

Tiwari, Amit K., Angela Bahr, Johannes Fleischhauer, et al.. (2016). Next generation sequencing based identification of disease-associated mutations in Swiss patients with retinal dystrophies. Scientific Reports. 6(1). 28755–28755. 55 indexed citations

11.

Reiff, Charlotte, Marta Owczarek‐Lipska, Georg Spital, et al.. (2016). The mutation p.E113K in the Schiff base counterion of rhodopsin is associated with two distinct retinal phenotypes within the same family. Scientific Reports. 6(1). 36208–36208. 11 indexed citations

12.

Glaus, Esther, et al.. (2015). Localizing the RPGR protein along the cilium: a new method to determine efficacies to treat RPGR mutations. Gene Therapy. 22(5). 413–420. 7 indexed citations

13.

Haghighi, Alireza, Amit K. Tiwari, Niloofar Piri, et al.. (2014). Homozygosity Mapping and Whole Exome Sequencing Reveal a Novel Homozygous COL18A1 Mutation Causing Knobloch Syndrome. PLoS ONE. 9(11). e112747–e112747. 13 indexed citations

14.

Laczkó, Endre, Nancy J. Philp, John Neidhardt, et al.. (2013). The cataract and glucosuria associated monocarboxylate transporter MCT12 is a new creatine transporter. Human Molecular Genetics. 22(16). 3218–3226. 45 indexed citations

15.

Schmid, F, Esther Glaus, Daniel Barthelmes, et al.. (2011). U1 snRNA-mediated gene therapeutic correction of splice defects caused by an exceptionally mild BBS mutation. Human Mutation. 32(7). 815–824. 52 indexed citations

16.

Schmid, F, Esther Glaus, Frans P.M. Cremers, et al.. (2010). Mutation- and Tissue-Specific Alterations ofRPGRTranscripts. Investigative Ophthalmology & Visual Science. 51(3). 1628–1628. 29 indexed citations

17.

Luhmann, Ulrich F. O., John Neidhardt, Barbara Kloeckener‐Gruissem, et al.. (2008). Vascular changes in the cerebellum of Norrin /Ndph knockout mice correlate with high expression of Norrin and Frizzled‐4. European Journal of Neuroscience. 27(10). 2619–2628. 16 indexed citations

18.

Glaus, Esther, et al.. (2008). Therapeutic strategy to rescue mutation-induced exon skipping in rhodopsin by adaptation of U1 snRNA. Human Mutation. 30(2). 255–263. 51 indexed citations

19.

Neidhardt, John, et al.. (2007). Identification and characterization of a novel RPGR isoform in human retina. Human Mutation. 28(8). 797–807. 45 indexed citations

20.

Zeitz, Christina, Silke Feil, Mariana Wittmer, et al.. (2006). Mutation in the Auxiliary Calcium-Channel Subunit CACNA2D4 Causes Autosomal Recessive Cone Dystrophy. The American Journal of Human Genetics. 79(5). 973–977. 112 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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