logo
CanyamAI summaries for academic research
language
MobileMobile
  • Phone FeatureWeChat Mini Program
EnglishEnglish
noticeNotice
BlogBlog
delete
arrow
Back
J

John Neidhardt

University of Oldenburg

31H-index
102Paper Count
3.2KCitation Count
Published Papers 42
Publication Date
logo
Genetic Findings in Seven Cochlear Implanted Patients with Severe-to-Profound Hearing Loss
errGenes
IF2.8
err2026-08-13
err0
errOAAI
errRieke Ollermann; Fei Song; Marta Owczarek-Lipska; Amilcar Perez-Riverol; Gregor Dombrowsky; Andreas Radeloff; John Neidhardt
errShare
errSave
A human-specific RPGR isoform and a clinically approved Rho/ROCK inhibitor represent therapeutic options to address RPGR-associated defects.
errMolecular Therapy Nucleic Acids
IF6.1
err2025-10-31
err0
errOAAI
errMuhammad Usman; Paul Atigbire; Dennis Kastrati; Julia Milena Brinkhoff; Charlotte Luise Kluth; Jannis Marticke; Christoph Jüschke; John Neidhardt
errShare
errSave
Pathogenic UNC13A variants cause a neurodevelopmental syndrome by impairing synaptic function
errNature Genetics
IF29
err2025-10-22
err0
errOAAI
errReza Asadollahi; Aisha Ahmad; Paranchai Boonsawat; Jasmine Shahanoor Hinzen; Mareike Lohse; Boris Bouazza-Arostegui; Siqi Sun; Tillmann Utesch; Jonas D. Sommer; Dragana Ilic; Murugesh Padmanarayana; Kati Fischermanns; Mrinalini Ranjan; Moritz Boll; Chandran Ka; Amélie Piton; Francesca Mattioli; Bertrand Isidor; Katrin Õunap; Karit Reinson; Monica H. Wojcik; Christian R. Marshall; Saadet Mercimek-Andrews; Naomichi Matsumoto; Noriko Miyake; Bruno de Oliveira Stephan; Rachel Sayuri Honjo; Debora R. Bertola; Chong Ae Kim; Roman Yusupov; Heather C. Mefford; John Christodoulou; Joy Lee; Oliver Heath; Natasha J. Brown; Naomi Baker; Zornitza Stark; Martin Delatycki; Nicole J. Lake; Shimriet Zeidler; Linda Zuurbier; Saskia M. Maas; Chris C. de Kruiff; Farrah Rajabi; Lance H. Rodan; Stephanie A. Coury; Konrad Platzer; Henry Oppermann; Rami Abou Jamra; Skadi Beblo; Caroline Maxton; Robert Śmigiel; Hunter Underhill; Holly Dubbs; Alyssa Rosen; Katherine L. Helbig; Ingo Helbig; Sarah McKeown Ruggiero; Mark P. Fitzgerald; Dennis Kraemer; Carlos E. Prada; Jeffrey Tenney; Parul Jayakar; Sylvia Redon; Jérémie Lefranc; Kevin Uguen; Simone Race; Stephanie Efthymiou; Reza Maroofian; Henry Houlden; Sandra Coppens; Nicolas Deconinck; Balasubramaniem Ashokkumar; Perumal Varalakshmi; Vykunta Raju Gowda K; Fatemeh Eghbal; Ehsan Ghayoor Karimiani; Morteza Heidari; John Neidhardt; Marta Owczarek-Lipska; G. Christoph Korenke; Michael J. Bamshad; Philippe M. Campeau; Anna Lehman; Laura G. Hendon; Ingrid M. Wentzensen; Kristin G. Monaghan; Yanmin Chen; Anna Szuto; Ronald D. Cohn; Ping Yee Billie Au; Christoph Hübner; Felix Boschann; Kandamurugu Manickam; Daniel C. Koboldt; Aboulfazl Rad; Gabriela Oprea; Kristine K. Bachman; Andrea H. Seeley; Emanuele Agolini; Alessandra Terracciano; Piscopo Carmelo; Caleb Bupp; Bethany Grysko; Annick Rein-Rothschild; Bruria Ben Zeev; Amy Margolin; Jennifer Morrison; Aditi Dagli; Elliot Stolerman; Raymond J. Louie; Camerun Washington; Servi J. C. Stevens; Malou Heijligers; Fowzan S. Alkuraya; Jasmin Lisfeld; Axel Neu; Fabíola Paoli Monteiro; André Luiz Santos Pessoa; Antonio Edvan Camelo-Filho; Fernando Kok; Dwight Koeberl; Kacie Riley; Lydie Burglen; Diane Doummar; Bénédicte Héron; Cyril Mignot; Boris Keren; Perrine Charles; Caroline Nava; Felix P. Bernhard; Andrea A. Kühn; Sven Thoms; Ryan D. Morrie; Shila Mekhoubad; Eric M. Green; Sami J. Barmada; Aaron D. Gitler; Olaf Jahn; Jeong Seop Rhee; Christian Rosenmund; Mišo Mitkovski; Heinrich Sticht; Han Sun; Gerald Le Gac; Holger Taschenberger; Nils Brose; Jeremy S. Dittman; Anita Rauch; Noa Lipstein
errShare
errSave
Molecular treatment options for patients carrying KIAA0586 / TALPID3 variants
errMolecular Therapy Nucleic Acids
IF6.1
err2025-08-14
err0
PREAI
errJacqueline E. Taudien; Sebastian Swirski; Maike Möller; Christoph Jüschke; Marta Owczarek-Lipska; G. Christoph Korenke; John Neidhardt
errShare
errSave
Rich microbial and depolymerising diversity in Antarctic krill gut
errMICROBIOLOGY SPECTRUM
IF3.8
err2024-04-02
err0
errOAAI
errMoeller, Lars; Vainshtein, Yevhen; Meyer, Bettina; Neidhardt, John; Eren, A. Murat; Sohn, Kai; Rabus, Ralf
errShare
errSave
Sensitive and selective phenol sensing in denitrifying Aromatoleum aromaticum EbN1T
errMICROBIOLOGY SPECTRUM
IF3.8
err2023-12-12
err1
errOAAI
errBuschen, Ramona; Lambertus, Pia; Scheve, Sabine; Horst, Simon; Song, Fei; Woehlbrand, Lars; Neidhardt, John; Winklhofer, Michael; Wagner, Tristan; Rabus, Ralf
errShare
errSave
Skewed X-inactivation is associated with retinal dystrophy in female carriers of RPGR mutations
errLIFE SCIENCE ALLIANCE
IF2.9
err2023-08-04
err1
errOAAI
errUsman, Muhammad; Jueschke, Christoph; Song, Fei; Kastrati, Dennis; Owczarek-Lipska, Marta; Eilers, Jannis; Pauleikhoff, Laurenz; Lange, Clemens; Neidhardt, John
errShare
errSave
In Vivo Efficacy and Safety Evaluations of Therapeutic Splicing Correction Using U1 snRNA in the Mouse Retina
errCELLS
IF5.2
err2023-03-21
err3
errOAAI
errSwirski, Sebastian; May, Oliver; Ahlers, Malte; Wissinger, Bernd; Greschner, Martin; Jueschke, Christoph; Neidhardt, John
errShare
errSave
Autosomal dominant optic atrophy: A novel treatment for OPA1 splice defects using U1 snRNA adaption
errMOLECULAR THERAPY-NUCLEIC ACIDS
IF0
err2021-12-01
err16
errOAAI
errJueschke, Christoph; Klopstock, Thomas; Catarino, Claudia B.; Owczarek-Lipska, Marta; Wissinger, Bernd; Neidhardt, John
errShare
errSave
Bi-allelic variants in SPATA5L1 lead to intellectual disability, spastic-dystonic cerebral palsy, epilepsy, and hearing loss
errAMERICAN JOURNAL OF HUMAN GENETICS
IF8.1
err2021-10-01
err15
errOAAI
errRichard, Elodie M.; Bakhtiari, Somayeh; Marsh, Ashley P. L.; Kaiyrzhanov, Rauan; Wagner, Matias; Shetty, Sheetal; Pagnozzi, Alex; Nordlie, Sandra M.; Guida, Brandon S.; Cornejo, Patricia; Magee, Helen; Liu, James; Norton, Bethany Y.; Webster, Richard, I; Worgan, Lisa; Hakonarson, Hakon; Li, Jiankang; Guo, Yiran; Jain, Mahim; Blesson, Alyssa; Rodan, Lance H.; Abbott, Mary-Alice; Comi, Anne; Cohen, Julie S.; Alhaddad, Bader; Meitinger, Thomas; Lenz, Dominic; Ziegler, Andreas; Kotzaeridou, Urania; Brunet, Theresa; Chassevent, Anna; Smith-Hicks, Constance; Ekstein, Joseph; Weiden, Tzvi; Hahn, Andreas; Zharkinbekova, Nazira; Turnpenny, Peter; Tucci, Arianna; Yelton, Melissa; Horvath, Rita; Gungor, Serdal; Hiz, Semra; Oktay, Yavuz; Lochmuller, Hanns; Zollino, Marcella; ManuelaMorleo; Marangi, Giuseppe; Nigro, Vincenzo; Torella, Annalaura; Pinelli, Michele; Amenta, Simona; Husain, Ralf A.; Grossmann, Benita; Rapp, Marion; Steen, Claudia; Marquardt, Iris; Grimmel, Mona; Grasshoff, Ute; Korenke, G. Christoph; Owczarek-Lipska, Marta; Neidhardt, John; Radio, Francesca Clementinac; Mancini, Cecilia; Sepulveda, Dianela Judith Claps; Mc Walter, Kirsty; Begtrup, Amber; Crunk, Amy; Sacoto, Maria J. Guillen; Person, Richard; Schnur, Rhonda E.; Mancardi, Maria Margherita; Kreuder, Florian; Striano, Pasquale; Zara, Federico; Chung, Wendy K.; Marks, Warren A.; van Eyk, Clare L.; Webber, Dani L.; Corbett, Mark A.; Harper, Kelly; Berry, Jesia G.; Mac Lennan, Alastair H.; Gecz, Jozef; Tartaglia, Marco; Salpietro, Vincenzo; Christodoulou, John; Kaslin, Jan; Padilla-Lopez, Sergio; Bilguvar, Kaya; Munchau, Alexander; Ahmed, Zubair M.; Hufnagel, Robert B.; Fahey, Michael C.; Maroofian, Reza; Houlden, Henry; Sticht, Heinrich; Mane, Shrikant M.; LRad, Aboulfaz; Vona, Barbara; Jin, Sheng Chih; Haack, Tobias B.; Makowski, Christine; Hirsch, Yoel; Riazuddin, Saima; Kruer, Michael C.
errShare
errSave
Dominant optic atrophy: Culprit mitochondria in the optic nerve
errPROGRESS IN RETINAL AND EYE RESEARCH
IF14.7
err2021-07-01
err60
errOAAI
errLenaers, Guy; Neutzner, Albert; Le Dantec, Yannick; Juschke, Christoph; Xiao, Ting; Decembrini, Sarah; Swirski, Sebastian; Kieninger, Sinja; Agca, Cavit; Kim, Ungsoo S.; Reynier, Pascal; Yu-Wai-Man, Patrick; Neidhardt, John; Wissinger, Bernd
errShare
errSave
Spectrum of Disease Severity in Patients With X-Linked Retinitis Pigmentosa Due to RPGR Mutations
errINVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE
IF4.7
err2020-12-29
err26
errOAAI
errDi Iorio, Valentina; Karali, Marianthi; Melillo, Paolo; Testa, Francesco; Brunetti-Pierri, Raffaella; Musacchia, Francesco; Condroyer, Christel; Neidhardt, John; Audo, Isabelle; Zeitz, Christina; Banfi, Sandro; Simonelli, Francesca
errShare
errSave
Compound heterozygousRPE65mutations associated with an early onset autosomal recessive retinitis pigmentosa
errJOURNAL OF GENE MEDICINE
IF2.2
err2020-06-20
err7
errOAAI
errOwczarek-Lipska, Marta; Song, Fei; Jaksic, Vesna; Neidhardt, John
errShare
errSave
Combining Engineered U1 snRNA and Antisense Oligonucleotides to Improve the Treatment of a BBS1 Splice Site Mutation
errMOLECULAR THERAPY-NUCLEIC ACIDS
IF0
err2019-12-01
err14
errOAAI
errBreuel, Saskia; Vorm, Mariann; Braeuer, Anja U.; Owczarek-Lipska, Marta; Neidhardt, John
errShare
errSave
A therapy with miglustat, 2-hydroxypropyl-β-cyclodextrin and allopregnanolone restores splenic cholesterol homeostasis in Niemann-pick disease type C1
errLIPIDS IN HEALTH AND DISEASE
IF4.2
err2019-06-28
err15
errOAAI
errNesslauer, Anna-Maria; Glaeser, Anne; Graeler, Markus; Engelmann, Robby; Mueller-Hilke, Brigitte; Frank, Marcus; Burstein, Christine; Rolfs, Arndt; Neidhardt, John; Wree, Andreas; Witt, Martin; Braeuer, Anja U.
errShare
errSave
Toward genome editing in X-linked RP-development of a mouse model with specific treatment relevant features
errTRANSLATIONAL RESEARCH
IF5.9
err2019-01-01
err6
errOAAI
errSchlegel, J.; Hoffmann, J.; Roell, D.; Mueller, B.; Guenther, S.; Zhang, W.; Janise, A.; Voessing, C.; Fuehler, B.; Neidhardt, J.; Khanna, H.; Lorenz, B.; Stieger, K.
errShare
errSave
A Novel C-Terminal Mutation in Gsdma3 (C+/H-) Leads to Alopecia and Corneal Inflammatory Response in Mice
errINVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE
IF4.7
err2018-01-25
err2
errOAAI
errSwirski, Sebastian; Roeger, Carsten; Pienkowska-Schelling, Aldona; Ihlenburg, Cynthia; Fischer, Goesta; May, Oliver; Vorm, Mariann; Owczarek-Lipska, Marta; Neidhardt, John
errShare
errSave
The mutation p. E113K in the Schiff base counterion of rhodopsin is associated with two distinct retinal phenotypes within the same family
errSCIENTIFIC REPORTS
IF3.9
err2016-11-04
err14
errOAAI
errReiff, Charlotte; Owczarek-Lipska, Marta; Spital, Georg; Roeger, Carsten; Hinz, Hebke; Jueschke, Christoph; Thiele, Holger; Altmueller, Janine; Nuernberg, Peter; Da Costa, Romain; Neidhardt, John
errShare
errSave
A Novel Method Combining Vitreous Aspiration and Intravitreal AAV2/8 Injection Results in Retina-Wide Transduction in Adult Mice
errINVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE
IF4.7
err2016-10-26
err28
errOAAI
errDa Costa, Romain; Roeger, Carsten; Segelken, Jasmin; Barben, Maya; Grimm, Christian; Neidhardt, John
errShare
errSave
Next generation sequencing based identification of disease-associated mutations in Swiss patients with retinal dystrophies
errSCIENTIFIC REPORTS
IF3.9
err2016-06-29
err62
errOAAI
errTiwari, Amit; Bahr, Angela; Bahr, Luzy; Fleischhauer, Johannes; Zinkernagel, Martin S.; Winkler, Niklas; Barthelmes, Daniel; Berger, Lieselotte; Gerth-Kahlert, Christina; Neidhardt, John; Berger, Wolfgang
errShare
errSave

Research Directions

No research directions
Co-authors
Cooperation Journals
H
Håkon Håkonarson
H-index: 177 · Papers: 1.5K
T
Thomas Meitinger
H-index: 168 · Papers: 957
H
Hölger Thiele
H-index: 134 · Papers: 1.8K
P
Peter Nürnberg
H-index: 127 · Papers: 755
W
Wendy K. Chung
H-index: 127 · Papers: 1.3K
View more