John Neidhardt

3.2k citations

63 papers · 2.4k indexed · 1 hit paper · h-index 29

Ophthalmology top 0.5%
- Retinal Diseases and Treatments 12
Cellular and Molecular Neuroscience top 5%
- Photoreceptor and optogenetics research 10
Molecular Biology top 5%
- Retinal Development and Disorders 29
- RNA regulation and disease 11
- CRISPR and Genetic Engineering 8
- Advanced biosensing and bioanalysis techniques 7
- RNA Research and Splicing 6
- RNA modifications and cancer 5
Genetics top 5%
Cell Biology top 5%

Co-authors: Wolfgang Berger Barbara Kloeckener‐Gruissem Esther Glaus Christina Zeitz Silke Feil Bernd Wissinger F Schmid Johannes Fleischhauer
Cited by: Ophthalmology Cellular and Molecular Neuroscience Molecular Biology
Journals: Investigative Ophthalmology & Visual Science (11 papers)International Journal of Molecular Sciences (5 papers)Human Mutation (5 papers)
Partner nations: Germany Switzerland Netherlands

In The Last Decade

John Neidhardt

62 papers receiving 2.4k citations

Hit Papers

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Peers

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

The 25 scholars most cited alongside John Neidhardt, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with John Neidhardt Line = papers co-authored together John Neidhardt links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Sensitive and selective phenol sensing in denitrifying Aromatoleum aromaticum EbN1 ^T Microbiology Spectrum ·Cristina dos Santos Hack,Anne-Emmanuelle Rault,M. El Faydy,B NEUSCHWANDERTETRI,Antonio Sergio Gomes,Lars Wöhlbrand,John Neidhardt,Michael Winklhofer,Tristan Wagner,Ralf Rabus	2023	2
2	mRNA splicing is modulated by intronic microRNAs iScience ·Woranittha Kritsarikan,Daphna Weissglas‐Volkov,Guy Shapira,Yazeed Zoabi,N.. Compositeur. Parolier Alonso,Barbara Kloeckener‐Gruissem,John Neidhardt,Noam Shomron	2023	1
3	A novel missense variant in the EML1 gene associated with bilateral ribbon-like subcortical heterotopia leads to ciliary defects Journal of Human Genetics ·Muhamad Aliff Haikal Kamaruzzaman,Marcy Z Chavez,Sangita Majhi,R. J. MacW.,Alexander Scholten,Indra Neffi Ridwan,Eva Bültmann,Martine Vercelletto,Marta Owczarek‐Lipska,John Neidhardt	2021	5
4	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 ·Anne Gläser,Bavantha Gamage,Markus H. Gräler,Sina M. Coldewey,Guillermo Gaviria Correa,Moritz J. Frech,Fan Yang,Jiankai Luo,Viviane de Azevedo Araújo,Bruno da Silva Schwarstzhoupt,Nicola Brandt,Diana Heimes,祐史高野,Georg Christoph Korenke,Marta Owczarek‐Lipska,John Neidhardt,Arndt Rolfs,Andreas Wree,Martin Witt,Anja U. Bräuer	2020	8
5	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 ·Georg Christoph Korenke,R. Endro Wibisono,Saskia Biskup,John Neidhardt,Marta Owczarek‐Lipska	2020	12
6	Novel mutations in the GJC2 gene associated with Pelizaeus–Merzbacher-like disease Molecular Biology Reports ·Marta Owczarek‐Lipska,Lejla Mulahasanovic,Carolin D. Obermaier,Konstanze Hörtnagel,Bernd A. Neubauer,Elvira O G van Vliet,Saskia Biskup,John Neidhardt	2019	10
7	Combining Engineered U1 snRNA and Antisense Oligonucleotides to Improve the Treatment of a BBS1 Splice Site Mutation Molecular Therapy — Nucleic Acids ·Vinicius Cavarzani,Gong Hongyu,Anja U. Bräuer,Marta Owczarek‐Lipska,John Neidhardt	2019	16
8	Toward genome editing in X-linked RP—development of a mouse model with specific treatment relevant features Translational research ·Li Yang-han,Jeremy M. Hoffmann,BRENNA MENEZES MARQUES PEREIRA,B Müller,Stefan Günther,Wei Zhang,P. M. Hamilton,Indra Neffi Ridwan,Lucille Richards Lane,John Neidhardt,Vera Holder,Birgit Lorenz,Knut Stieger	2018	6
9	Identification of Novel and Recurrent Disease-Causing Mutations in Retinal Dystrophies Using Whole Exome Sequencing (WES): Benefits and Limitations PLoS ONE ·Amit K. Tiwari,Johannes R. Lemke,Janine Altmueller,Hölger Thiele,Esther Glaus,Johannes Fleischhauer,Peter Nürnberg,John Neidhardt,Wolfgang Berger	2016	14
10	Next generation sequencing based identification of disease-associated mutations in Swiss patients with retinal dystrophies Scientific Reports ·Amit K. Tiwari,Angela Bahr,Gerundium,Johannes Fleischhauer,Martin S. Zinkernagel,Syamrurrijal,Daniel Barthelmes,Lieselotte Berger,Christina Gerth‐Kahlert,John Neidhardt,Wolfgang Berger	2016	55
11	The mutation p.E113K in the Schiff base counterion of rhodopsin is associated with two distinct retinal phenotypes within the same family Scientific Reports ·Charlotte Reiff,Marta Owczarek‐Lipska,Georg Spital,José P Otero,谢鹏强李玲,Christoph Jüschke,Hölger Thiele,Janine Altmüller,Peter Nürnberg,Nikola Tesla,John Neidhardt	2016	11
12	Localizing the RPGR protein along the cilium: a new method to determine efficacies to treat RPGR mutations Gene Therapy ·Nikola Tesla,Esther Glaus,Amit K. Tiwari,Barbara Kloeckener‐Gruissem,Wolfgang Berger,John Neidhardt	2015	7
13	Homozygosity Mapping and Whole Exome Sequencing Reveal a Novel Homozygous COL18A1 Mutation Causing Knobloch Syndrome PLoS ONE ·Alireza Haghighi,Amit K. Tiwari,Niloofar Piri,Gudrun Nürnberg,Nasrollah Saleh-Gohari,(unknown),(unknown),John Neidhardt,Peter Nürnberg,Wolfgang Berger	2014	13
14	The cataract and glucosuria associated monocarboxylate transporter MCT12 is a new creatine transporter Human Molecular Genetics ·G Jóźwiak,Endre Laczkó,Nancy J. Philp,John Neidhardt,J Marcos Ercilla,Larissa Campagna Martini,Daniel F. Schorderet,Francis L. Munier,François Verrey,Wolfgang Berger,Simone M. R. Camargo,Barbara Kloeckener‐Gruissem	2013	45
15	U1 snRNA-mediated gene therapeutic correction of splice defects caused by an exceptionally mild BBS mutation Human Mutation ·F Schmid,Esther Glaus,Daniel Barthelmes,Manfred Fliegauf,Harald Gaspar,Gudrun Nürnberg,Peter Nürnberg,Heymut Omran,Wolfgang Berger,John Neidhardt	2011	52
16	Mutation- and Tissue-Specific Alterations ofRPGRTranscripts Investigative Ophthalmology & Visual Science ·F Schmid,Esther Glaus,Frans P.M. Cremers,Barbara Kloeckener‐Gruissem,Wolfgang Berger,John Neidhardt	2010	29
17	Vascular changes in the cerebellum of Norrin /Ndph knockout mice correlate with high expression of Norrin and Frizzled‐4 European Journal of Neuroscience ·Ulrich F. O. Luhmann,John Neidhardt,Barbara Kloeckener‐Gruissem,Anita Baklund,Esther Glaus,Silke Feil,Wolfgang Berger	2008	16
18	Therapeutic strategy to rescue mutation-induced exon skipping in rhodopsin by adaptation of U1 snRNA Human Mutation ·曾华平,Esther Glaus,Lauren B. Moja,Marius Ader,Johannes Fleischhauer,(unknown),Wolfgang Berger,John Neidhardt	2008	51
19	Identification and characterization of a novel RPGR isoform in human retina Human Mutation ·John Neidhardt,Esther Glaus,Lauren B. Moja,Christina Zeitz,Johannes Fleischhauer,Wolfgang Berger	2007	45
20	Mutation in the Auxiliary Calcium-Channel Subunit CACNA2D4 Causes Autosomal Recessive Cone Dystrophy The American Journal of Human Genetics ·Goutham Potharlanka,Christina Zeitz,Silke Feil,Mariana Wittmer,U. Förster,John Neidhardt,Bernd Wissinger,Eberhart Zrenner,Robert Wilke,Susanne Kohl,Wolfgang Berger	2006	112

About John Neidhardt

John Neidhardt is a scholar working on Ophthalmology, Molecular Biology, Cellular and Molecular Neuroscience, Cell Biology and Genetics, having authored 63 papers that have together received 2.4k indexed citations. Recurring topics across this work include Retinal Development and Disorders (29 papers), Retinal Diseases and Treatments (12 papers), RNA regulation and disease (11 papers), Photoreceptor and optogenetics research (10 papers), CRISPR and Genetic Engineering (8 papers), Advanced biosensing and bioanalysis techniques (7 papers), RNA Research and Splicing (6 papers) and RNA modifications and cancer (5 papers). The work is most often cited by research in Ophthalmology (677 citations), Cellular and Molecular Neuroscience (592 citations), Molecular Biology (2.1k citations), Genetics (572 citations) and Cell Biology (268 citations). John Neidhardt has collaborated with scholars based in Germany, Switzerland and Netherlands. Frequent 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. Their work appears in journals such as Investigative Ophthalmology & Visual Science, International Journal of Molecular Sciences, Human Mutation, Scientific Reports and European Journal of Human Genetics.

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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