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Herbert Jägle

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K S Bonsel; K Hufendiek; I Oberacher-Velten; Herbert Jägle
[Acute bilateral loss of vision in posterior reversible encephalopathy syndrome].
Anne Kurtenbach; Hana Langrová; Andre Messias; Eberhart Zrenner; Herbert Jägle
A comparison of the performance of three visual evoked potential-based methods to estimate visual acuity.
Barbara M Braunger; Ales Cvekl; Herbert Jägle; Marcus Koch; Andreas Ohlmann; Mathias W Seeliger; Naoyuki Tanimoto; Cornelia Volz; Ying Yang; Michael R Bösl; Ernst R Tamm
Constitutive overexpression of Norrin activates Wnt/β-catenin and endothelin-2 signaling to protect photoreceptors from light damage.

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All Publications

2013: K S Bonsel; K Hufendiek; I Oberacher-Velten; Herbert Jägle
[Acute bilateral loss of vision in posterior reversible encephalopathy syndrome].
Der Ophthalmologe : Zeitschrift der Deutschen Ophthalmologischen Gesellschaft 2013;110(3):247-50.
2013: Anne Kurtenbach; Hana Langrová; Andre Messias; Eberhart Zrenner; Herbert Jägle
A comparison of the performance of three visual evoked potential-based methods to estimate visual acuity.
Documenta ophthalmologica. Advances in ophthalmology 2013;126(1):45-56.
2013: Barbara M Braunger; Ales Cvekl; Herbert Jägle; Marcus Koch; Andreas Ohlmann; Mathias W Seeliger; Naoyuki Tanimoto; Cornelia Volz; Ying Yang; Michael R Bösl; Ernst R Tamm
Constitutive overexpression of Norrin activates Wnt/β-catenin and endothelin-2 signaling to protect photoreceptors from light damage.
Neurobiology of disease 2013;50():1-12.
2013: Melanie van Waveren; Herbert Jägle; Dorothea Besch
Management of strabismus with hemianopic visual field defects.
Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv für klinische und experimentelle Ophthalmologie 2013;251(2):575-84.
2012: A B Renner; Herbert Jägle
[Hereditary macular dystrophies in differential diagnosis of AMD].
Klinische Monatsblätter für Augenheilkunde 2012;229(9):905-9.
2012: Agnes B Renner; Andreas Walter; Britta S Fiebig; Herbert Jägle
Gyrate atrophy: clinical and genetic findings in a female without arginine-restricted diet during her first 39 years of life and report of a new OAT gene mutation.
Documenta ophthalmologica. Advances in ophthalmology 2012;125(1):81-9.
2012: Dorothy A Thompson; Herbert Jägle; Alki Liasis; Ruth J Lyons; Isabelle Russell-Eggitt; Stephanie Grünewald
Retinal on-pathway deficit in congenital disorder of glycosylation due to phosphomannomutase deficiency.
Archives of ophthalmology 2012;130(6):712-9.
2011: Bernd Wissinger; Christiane Wolf; Ditta Zobor; Eberhart Zrenner; Monika Andrassi-Darida; Britta Baumann; Antje Bernd; Michael Bonin; Frans P M Cremers; Elfride De Baere; Hélène Dollfus; Enyedi Peter; Christoph Friedburg; John R Heckenlively; Carel B Hoyng; Herbert Jägle; Ulrich Kellner; Bart P Leroy; Birgit Lorenz; Astrid Plomp; Thomas Rosenberg; Günter Rudolph; Roberto Salati; Alexandra Sauer; Simone Schaich; Balázs Varsányi; Susanne Kohl
Large deletions of the KCNV2 gene are common in patients with cone dystrophy with supernormal rod response.
Human mutation 2011;32(12):1398-406.
2010: Herbert Jägle; Ditta Zobor; Thomas Brauns
Accommodation limits induced optical defocus in defocus experiments.
Documenta ophthalmologica. Advances in ophthalmology 2010;121(2):103-9.
2009: M van Waveren; Herbert Jägle
[Intermittent elevation deficiency].
Der Ophthalmologe : Zeitschrift der Deutschen Ophthalmologischen Gesellschaft 2009;106(8):746-9.
2009: Veronique B D Kitiratschky; Petra Behnen; Ulrich Kellner; John R Heckenlively; Eberhart Zrenner; Herbert Jägle; Susanne Kohl; Bernd Wissinger; Karl-Wilhelm Koch
Mutations in the GUCA1A gene involved in hereditary cone dystrophies impair calcium-mediated regulation of guanylate cyclase.
Human mutation 2009;30(8):E782-96.
2009: C Jägle; Eleni Papageorgiou; Serena Preyer; Hubert Löwenheim; Ulrich Schiefer; Herbert Jägle
[Fulminant process of an orbital Mucoracea infection].
Der Ophthalmologe : Zeitschrift der Deutschen Ophthalmologischen Gesellschaft 2009;106(6):547-50.
2008: Ditta Nagy; Birgitt Schönfisch; Eberhart Zrenner; Herbert Jägle
Long-term follow-up of retinitis pigmentosa patients with multifocal electroretinography.
Investigative ophthalmology & visual science 2008;49(10):4664-71.
2008: V B D Kitiratschky; D Nagy; T Zabel; E Zrenner; Bernd Wissinger; S Kohl; Herbert Jägle
Cone and cone-rod dystrophy segregating in the same pedigree due to the same novel CRX gene mutation.
The British journal of ophthalmology 2008;92(8):1086-91.
2008: Veronique B D Kitiratschky; Tanja Grau; Antje Bernd; Eberhart Zrenner; Herbert Jägle; Agnes B Renner; Ulrich Kellner; Günther Rudolph; Samuel G Jacobson; Artur Vahe Cideciyan; Simone Schaich; Susanne Kohl; Bernd Wissinger
ABCA4 gene analysis in patients with autosomal recessive cone and cone rod dystrophies.
European journal of human genetics : EJHG 2008;16(7):812-9.
2008: Bernd Wissinger; Susann Dangel; Herbert Jägle; Lars Hansen; Britta Baumann; Günther Rudolph; Christiane Wolf; Michael Bonin; Katja Koeppen; Thomas Ladewig; Susanne Kohl; Eberhart Zrenner; Thomas Rosenberg
Cone dystrophy with supernormal rod response is strictly associated with mutations in KCNV2.
Investigative ophthalmology & visual science 2008;49(2):751-7.
2008: Andrew Stockman; Herbert Jägle; Markus Pirzer; Lindsay T Sharpe
The dependence of luminous efficiency on chromatic adaptation.
Journal of vision 2008;8(16):1.1-26.
2007: Beate Leo-Kottler; Herbert Jägle; T Küpker; S Schimpf
[How to distinguish between autosomal dominant optic atrophy and Leber's hereditary optic neuropathy].
Der Ophthalmologe : Zeitschrift der Deutschen Ophthalmologischen Gesellschaft 2007;104(12):1060-5.
2007: Hana Langrová; Herbert Jägle; Eberhart Zrenner; Anne Kurtenbach
The multifocal pattern electroretinogram (mfPERG) and cone-isolating stimuli.
Visual neuroscience 2007;24(6):805-16.
2007: Efdal Yoeruek; Herbert Jägle; Matthias Lüke; Salvatore Grisanti; Max Warga; Ralf Krott; Martin S Spitzer; Olcay Tatar; Karl Ulrich Bartz-Schmidt; Peter Szurman
Safety profile of a taurine containing irrigation solution (AcriProTect) in pars plana vitrectomy.
Retina (Philadelphia, Pa.) 2007;27(9):1286-91.
2006: Herbert Jägle; Judith Heine; Anne Kurtenbach
L:M-cone ratio estimates of the outer and inner retina and its impact on sex differences in ERG amplitudes.
Documenta ophthalmologica. Advances in ophthalmology 2006;113(2):105-13.
2006: Anne Kurtenbach; Helmut M Mayser; Herbert Jägle; Andreas Fritsche; Eberhart Zrenner
Hyperoxia, hyperglycemia, and photoreceptor sensitivity in normal and diabetic subjects.
Visual neuroscience 2006;23(3-4):651-61.
2006: Herbert Jägle; Emanuela de Luca; Ludwig Serey; Michael Bach; Lindsay T Sharpe
Visual acuity and X-linked color blindness.
Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv für klinische und experimentelle Ophthalmologie 2006;244(4):447-53.
2006: Hendrik P N Scholl; Jan Kremers; Dorothea Besch; Eberhart Zrenner; Herbert Jägle
Progressive cone dystrophy with deutan genotype and phenotype.
Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv für klinische und experimentelle Ophthalmologie 2006;244(2):183-91.
2006: Lindsay T Sharpe; Emanuela de Luca; Thorsten Hansen; Herbert Jägle; Karl R Gegenfurtner
Advantages and disadvantages of human dichromacy.
Journal of vision 2006;6(3):213-23.
2005: A Schuster; Nicole Weisschuh; Herbert Jägle; Dorothea Besch; Andreas R Janecke; H Zierler; Sabine Tippmann; Eberhart Zrenner; Bernd Wissinger
Novel rhodopsin mutations and genotype-phenotype correlation in patients with autosomal dominant retinitis pigmentosa.
The British journal of ophthalmology 2005;89(10):1258-64.
2005: Herbert Jägle; Dorothea Besch
Glare sensitivity and professional drivers' safety: a case of rod-cone dystrophy with negative electroretinogram.
Acta ophthalmologica Scandinavica 2005;83(4):504-7.
2005: Herbert Jägle; Christine Jägle; Ludwig Sèrey; Lindsay T Sharpe
Dose-dependency and time-course of electrophysiologic short-term effects of VIAGRA: a case study.
Documenta ophthalmologica. Advances in ophthalmology 2005;110(2-3):247-54.
2005: Susanne Kohl; Balazs Varsanyi; Gesine Abadin Antunes; Britta Baumann; Carel B Hoyng; Herbert Jägle; Thomas Rosenberg; Ulrich Kellner; Birgit Lorenz; Roberto Salati; Bernhard Jurklies; Ágnes Farkas; sten andreasson; Richard G Weleber; Samuel G Jacobson; Günther Rudolph; Claudio Castellan; Hélène Dollfus; Eric Legius; Mario Anastasi; Pierre Bitoun; Dorit Lev; Paul Sieving; Francis L Munier; Eberhart Zrenner; Lindsay T Sharpe; Frans P M Cremers; Bernd Wissinger
CNGB3 mutations account for 50% of all cases with autosomal recessive achromatopsia.
European journal of human genetics : EJHG 2005;13(3):302-8.
2005: Lindsay T Sharpe; Andrew Stockman; Wolfgang Jagla; Herbert Jägle
A luminous efficiency function, V*(lambda), for daylight adaptation.
Journal of vision 2005;5(11):948-68.
2005: Herbert Jägle; Markus Pirzer; Lindsay T Sharpe
The Nagel anomaloscope: its calibration and recommendations for diagnosis and research.
Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv für klinische und experimentelle Ophthalmologie 2005;243(1):26-32.
2004: Anne Kurtenbach; Judith Heine; Herbert Jägle
Multifocal electroretinogram in trichromat and dichromat observers under cone isolating conditions.
Visual neuroscience 2004;21(3):249-55.
2004: Herbert Jägle; Christine Jägle; Ludwig Sérey; Alice Yu; Albrecht Rilk; Bettina Sadowski; Dorothea Besch; Eberhart Zrenner; Lindsay T Sharpe
Visual short-term effects of Viagra: double-blind study in healthy young subjects.
American journal of ophthalmology 2004;137(5):842-9.
2004: Dimitri Tränkner; Herbert Jägle; Susanne Kohl; Eckart Apfelstedt-Sylla; Lindsay T Sharpe; U Benjamin Kaupp; Eberhart Zrenner; Reinhard Seifert; Bernd Wissinger
Molecular basis of an inherited form of incomplete achromatopsia.
The Journal of neuroscience : the official journal of the Society for Neuroscience 2004;24(1):138-47.
2003: Dorothea Besch; Herbert Jägle; Hendrik P N Scholl; Mathias W Seeliger; Eberhart Zrenner
Inherited multifocal RPE-diseases: mechanisms for local dysfunction in global retinoid cycle gene defects.
Vision research 2003;43(28):3095-108.
2003: Herbert Jägle; Bettina Sadowski; Jan Kremers; Hendrik P N Scholl; Beate Leo-Kottler; Lindsay T Sharpe
Detecting color vision in a malingerer.
Documenta ophthalmologica. Advances in ophthalmology 2003;106(2):121-8.
2002: Heidi A Baseler; Alyssa A Brewer; Lindsay T Sharpe; Antony B Morland; Herbert Jägle; Brian A Wandell
Reorganization of human cortical maps caused by inherited photoreceptor abnormalities.
Nature neuroscience 2002;5(4):364-70.
2002: Johannes Albrecht; Herbert Jägle; Donald C Hood; Lindsay T Sharpe
The multifocal electroretinogram (mfERG) and cone isolating stimuli: variation in L- and M-cone driven signals across the retina.
Journal of vision 2002;2(8):543-58.
2002: Donald C Hood; Alice L Yu; Xian Zhang; Johannes Albrecht; Herbert Jägle; Lindsay T Sharpe
The multifocal visual evoked potential and cone-isolating stimuli: implications for L- to M-cone ratios and normalization.
Journal of vision 2002;2(2):178-89.
2002: Wolfgang M Jagla; Herbert Jägle; Takaaki Hayashi; Lindsay T Sharpe; Samir S Deeb
The molecular basis of dichromatic color vision in males with multiple red and green visual pigment genes.
Human molecular genetics 2002;11(1):23-32.
2001: Bernd Wissinger; Daphne Gamer; Herbert Jägle; R Giorda; T Marx; S Mayer; Sabine Tippmann; Martina Broghammer; Bernhard Jurklies; Thomas Rosenberg; Samuel G Jacobson; E C Sener; S Tatlipinar; Carel B Hoyng; C Castellan; Pierre Bitoun; sten andreasson; Günther Rudolph; Ulrich Kellner; Birgit Lorenz; G Wolff; C Verellen-Dumoulin; M Schwartz; Frans P M Cremers; Eckart Apfelstedt-Sylla; Eberhart Zrenner; Roberto Salati; Lindsay T Sharpe; Susanne Kohl
CNGA3 mutations in hereditary cone photoreceptor disorders.
American journal of human genetics 2001;69(4):722-37.
2000: Susanne Kohl; Britta Baumann; Martina Broghammer; Herbert Jägle; Paul Sieving; Ulrich Kellner; R Spegal; M Anastasi; Eberhart Zrenner; Lindsay T Sharpe; Bernd Wissinger
Mutations in the CNGB3 gene encoding the beta-subunit of the cone photoreceptor cGMP-gated channel are responsible for achromatopsia (ACHM3) linked to chromosome 8q21.
Human molecular genetics 2000;9(14):2107-16.
1999: Lindsay T Sharpe; Andrew Stockman; Herbert Jägle; H Knau; Jeremy Nathans
L, M and L-M hybrid cone photopigments in man: deriving lambda max from flicker photometric spectral sensitivities.
Vision research 1999;39(21):3513-25.
1998: Lindsay T Sharpe; Andrew Stockman; Herbert Jägle; H Knau; G Klausen; A Reitner; Jeremy Nathans
Red, green, and red-green hybrid pigments in the human retina: correlations between deduced protein sequences and psychophysically measured spectral sensitivities.
The Journal of neuroscience : the official journal of the Society for Neuroscience 1998;18(23):10053-69.
1998: Lindsay T Sharpe; Andrew Stockman; H Knau; Herbert Jägle
Macular pigment densities derived from central and peripheral spectral sensitivity differences.
Vision research 1998;38(21):3233-9.
1998: Bernd Wissinger; Herbert Jägle; Susanne Kohl; Martina Broghammer; Britta Baumann; D B Hanna; C Hedels; Eckart Apfelstedt-Sylla; G Randazzo; Samuel G Jacobson; Eberhart Zrenner; Lindsay T Sharpe
Human rod monochromacy: linkage analysis and mapping of a cone photoreceptor expressed candidate gene on chromosome 2q11.
Genomics 1998;51(3):325-31.
1998: Susanne Kohl; T Marx; I Giddings; Herbert Jägle; Samuel G Jacobson; Eckart Apfelstedt-Sylla; Eberhart Zrenner; Lindsay T Sharpe; Bernd Wissinger
Total colourblindness is caused by mutations in the gene encoding the alpha-subunit of the cone photoreceptor cGMP-gated cation channel.
Nature genetics 1998;19(3):257-9.