John Neidhardt

3.7k citations

67 papers · 3.0k · 1 hit paper · h-index 30

Impact in

Ophthalmology top 1%
- Retinal Diseases and Treatments
Molecular Biology top 5%
- Retinal Development and Disorders
- CRISPR and Genetic Engineering
- RNA regulation and disease
- Photosynthetic Processes and Mechanisms

Papers in

Molecular Biology 56
- Retinal Development and Disorders 30
- RNA regulation and disease 9
- CRISPR and Genetic Engineering 8
- RNA Research and Splicing 5
- Advanced biosensing and bioanalysis techniques 5
- RNA modifications and cancer 5
Genetics 10

Co-authors: Wolfgang Berger (28 shared papers)Barbara Kloeckener‐Gruissem (11 shared papers)Anastasios Melis (3 shared papers)John R. Benemann (3 shared papers)Esther Glaus (14 shared papers)Christina Zeitz (9 shared papers)Silke Feil (6 shared papers)Bernd Wissinger (5 shared papers)
Journals: Investigative Ophthalmology & Visual Science (11 papers)International Journal of Molecular Sciences (5 papers)Human Mutation (5 papers)European Journal of Human Genetics (2 papers)Scientific Reports (2 papers)
Partner nations: Germany Switzerland United States

In The Last Decade

John Neidhardt

65 papers receiving 2.9k citations

John Neidhardt's Hit Papers

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The molecular basis of human retinal and vitreoretinal diseases 2010 · 463 citations

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-authors

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

Showing the 20 most-cited of 67 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	The molecular basis of human retinal and vitreoretinal diseases Progress in Retinal and Eye Research ·Wolfgang Berger, Barbara Kloeckener‐Gruissem, John Neidhardt Hit paper breakdown →	2010	463
2	Dunaliella salina (Chlorophyta) with small chlorophyll antenna sizes exhibit higher photosynthetic productivities and photon use efficiencies than normally pigmented cells Journal of Applied Phycology ·Anastasios Melis, John Neidhardt, John R. Benemann	1998	238
3	Panel-based next generation sequencing as a reliable and efficient technique to detect mutations in unselected patients with retinal dystrophies European Journal of Human Genetics ·Nicola Glöckle, Susanne Kohl, Julia Mohr, Tim Scheurenbrand, Andrea Sprecher, Nicole Weisschuh, Antje Bernd, Günther Rudolph, Max Schubach, Charlotte M. Poloschek, Eberhart Zrenner, Saskia Biskup, Wolfgang Berger, Bernd Wissinger, John Neidhardt	2013	213
4	GRIN2B mutations in west syndrome and intellectual disability with focal epilepsy Annals of Neurology ·Johannes R. Lemke, Rik Hendrickx, Kirsten Geider, Bodo Laube, Michael Schwake, (unknown), Victoria M. James, Alex Pepler, Isabelle Steiner, Konstanze Hörtnagel, John Neidhardt, Susanne Ruf, Markus Wolff, Deborah Bartholdi, Roberto Caraballo, Konrad Platzer, Arvid Suls, Peter De Jonghe, Saskia Biskup, Sarah Weckhuysen	2013	167
5	Photosystem-II repair and chloroplast recovery from irradiance stress: relationship between chronic photoinhibition, light-harvesting chlorophyll antenna size and photosynthetic productivity in Dunaliella salina (green algae) Photosynthesis Research ·John Neidhardt, John R. Benemann, Liping Zhang, Anastasios Melis	1998	131
6	Mutation in the Auxiliary Calcium-Channel Subunit CACNA2D4 Causes Autosomal Recessive Cone Dystrophy The American Journal of Human Genetics ·Katharina Agnes Wycisk, Christina Zeitz, Silke Feil, (unknown), U. Förster, John Neidhardt, Bernd Wissinger, Eberhart Zrenner, Robert Wilke, Susanne Kohl, Wolfgang Berger	2006	128
7	Mutations inGRM6Cause Autosomal Recessive Congenital Stationary Night Blindness with a Distinctive Scotopic 15-Hz Flicker Electroretinogram Investigative Ophthalmology & Visual Science ·Christina Zeitz, Maria van Genderen, John Neidhardt, Ulrich F. O. Luhmann, Frank P. Hoeben, U. Förster, Katharina Agnes Wycisk, (unknown), Carel B. Hoyng, Frans C. C. Riemslag, Franc ̧oise Meire, Frans P.M. Cremers, Wolfgang Berger	2005	127
8	Structural and Functional Abnormalities of Retinal Ribbon Synapses due toCacna2d4Mutation Investigative Ophthalmology & Visual Science ·Katharina Agnes Wycisk, Birgit Budde, Silke Feil, Sergej Skosyrski, Francesca Buzzi, John Neidhardt, Esther Glaus, Peter Nu ̈rnberg, Klaus Rüether, Wolfgang Berger	2006	114
9	Dominant optic atrophy: Culprit mitochondria in the optic nerve Progress in Retinal and Eye Research ·Guy Lenaers, Albert Neutzner, Yannick Le Dantec, Christoph Jüschke, Ting Xiao, Sarah Decembrini, Sebastian Swirski, Sinja Kieninger, Cavit Ağca, Ungsoo Samuel Kim, Pascal Reynier, Patrick Yu‐Wai‐Man, John Neidhardt, Bernd Wissinger	2020	70
10	Gene Therapeutic Approach Using Mutation-adapted U1 snRNA to Correct a RPGR Splice Defect in Patient-derived Cells Molecular Therapy ·Esther Glaus, F Schmid, Romain Da Costa, Wolfgang Berger, John Neidhardt	2011	62
11	Short DNA sequences inserted for gene targeting can accidentally interfere with off‐target gene expression The FASEB Journal ·Ingo Meier, Christian Bernreuther, Thomas Tilling, John Neidhardt, Yong Wee Wong, Christian Schulze, Thomas Streichert, Melitta Schachner	2010	61
12	Mutation of Solute Carrier SLC16A12 Associates with a Syndrome Combining Juvenile Cataract with Microcornea and Renal Glucosuria The American Journal of Human Genetics ·Barbara Kloeckener‐Gruissem, Kristof Vandekerckhove, Gudrun Nürnberg, John Neidhardt, Christina Zeitz, Peter Nürnberg, Isaak Schipper, Wolfgang Berger	2008	61
13	Tenascin-N: characterization of a novel member of the tenascin family that mediates neurite repulsion from hippocampal explants Molecular and Cellular Neuroscience ·John Neidhardt, Susanne Fehr, Michael Kutsche, Jürgen Löhler, Melitta Schachner	2003	60
14	Next generation sequencing based identification of disease-associated mutations in Swiss patients with retinal dystrophies Scientific Reports ·Amit K. Tiwari, Angela Bahr, Luzy Bähr, Johannes Fleischhauer, Martin S. Zinkernagel, N. Winkler, Daniel Barthelmes, Lieselotte Berger, Christina Gerth‐Kahlert, John Neidhardt, Wolfgang Berger	2016	58
15	Identification of novel mutations in X-linked retinitis pigmentosa families and implications for diagnostic testing PubMed ·John Neidhardt, Esther Glaus, (unknown), (unknown)	2008	58
16	Night blindness-associated mutations in the ligand-binding, cysteine-rich, and intracellular domains of the metabotropic glutamate receptor 6 abolish protein trafficking Human Mutation ·Christina Zeitz, U. Förster, John Neidhardt, Silke Feil, Stefan Kälin, Dorothee Leifert, Peter J. Flor, Wolfgang Berger	2007	55
17	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	54
18	Identification and Functional Characterization of a Novel Rhodopsin Mutation Associated with Autosomal Dominant CSNB Investigative Ophthalmology & Visual Science ·Christina Zeitz, Alecia K. Gross, Dorothee Leifert, Barbara Kloeckener‐Gruissem, Suzanne D. McAlear, Johannes R. Lemke, John Neidhardt, Wolfgang Berger	2008	53
19	Therapeutic strategy to rescue mutation-induced exon skipping in rhodopsin by adaptation of U1 snRNA Human Mutation ·Gaby Tanner, Esther Glaus, Daniel Barthelmes, Marius Ader, Johannes Fleischhauer, (unknown), Wolfgang Berger, John Neidhardt	2008	53
20	ABCA4andROM1:Implications for Modification of thePRPH2-Associated Macular Dystrophy Phenotype Investigative Ophthalmology & Visual Science ·Charlotte M. Poloschek, Michael Bach, Wolf A. Lagrèze, Esther Glaus, Johannes R. Lemke, Wolfgang Berger, John Neidhardt	2010	53

About John Neidhardt

John Neidhardt is a scholar working on Molecular Biology, Genetics, Cellular and Molecular Neuroscience, Ophthalmology and Cell Biology, having authored 67 papers that have together received 3.0k indexed citations. Recurring topics across this work include Retinal Development and Disorders (30 papers), RNA regulation and disease (9 papers), CRISPR and Genetic Engineering (8 papers), Retinal Diseases and Treatments (7 papers), Photoreceptor and optogenetics research (6 papers), RNA Research and Splicing (5 papers), Advanced biosensing and bioanalysis techniques (5 papers) and RNA modifications and cancer (5 papers). The work is most often cited by research in Ophthalmology (452 citations), Molecular Biology (2.2k citations), Cellular and Molecular Neuroscience (563 citations), Renewable Energy, Sustainability and the Environment (314 citations) and Genetics (509 citations). John Neidhardt has collaborated with scholars based in Germany, Switzerland and United States. Frequent co-authors include Wolfgang Berger, Barbara Kloeckener‐Gruissem, Anastasios Melis, John R. Benemann, Esther Glaus, Christina Zeitz, Silke Feil, Bernd Wissinger, Liping Zhang and U. Förster. Their work appears in journals such as Investigative Ophthalmology & Visual Science, International Journal of Molecular Sciences, Human Mutation, European Journal of Human Genetics and Scientific Reports.

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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John Neidhardt

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John Neidhardt

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