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Times Co-cited
Similarity
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David M Berson, Felice A Dunn, Motoharu Takao. Science 2002
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Melanopsin-expressing ganglion cells in primate retina signal colour and irradiance and project to the LGN.
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Melanopsin-containing retinal ganglion cells: architecture, projections, and intrinsic photosensitivity.
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Melanopsin and rod-cone photoreceptive systems account for all major accessory visual functions in mice.
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Rod photoreceptors drive circadian photoentrainment across a wide range of light intensities.
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Diminished pupillary light reflex at high irradiances in melanopsin-knockout mice.
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Melanopsin cells are the principal conduits for rod-cone input to non-image-forming vision.
Ali D Güler, Jennifer L Ecker, Gurprit S Lall, Shafiqul Haq, Cara M Altimus, Hsi-Wen Liao, Alun R Barnard, Hugh Cahill, Tudor C Badea, Haiqing Zhao,[...]. Nature 2008
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Melanopsin is required for non-image-forming photic responses in blind mice.
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Melanopsin-expressing retinal ganglion-cell photoreceptors: cellular diversity and role in pattern vision.
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Human and macaque pupil responses driven by melanopsin-containing retinal ganglion cells.
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Characterization of an ocular photopigment capable of driving pupillary constriction in mice.
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Regulation of mammalian circadian behavior by non-rod, non-cone, ocular photoreceptors.
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M S Freedman, R J Lucas, B Soni, M von Schantz, M Muñoz, Z David-Gray, R Foster. Science 1999
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Central projections of melanopsin-expressing retinal ganglion cells in the mouse.
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Measuring and using light in the melanopsin age.
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Melanopsin (Opn4) requirement for normal light-induced circadian phase shifting.
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Colour as a signal for entraining the mammalian circadian clock.
Lauren Walmsley, Lydia Hanna, Josh Mouland, Franck Martial, Alexander West, Andrew R Smedley, David A Bechtold, Ann R Webb, Robert J Lucas, Timothy M Brown. PLoS Biol 2015
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Melanopsin-based brightness discrimination in mice and humans.
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Photoresponse diversity among the five types of intrinsically photosensitive retinal ganglion cells.
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A novel human opsin in the inner retina.
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Regulation of the mammalian pineal by non-rod, non-cone, ocular photoreceptors.
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A retinal ganglion cell that can signal irradiance continuously for 10 hours.
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Photoentrainment and pupillary light reflex are mediated by distinct populations of ipRGCs.
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Two types of melanopsin retinal ganglion cell differentially innervate the hypothalamic suprachiasmatic nucleus and the olivary pretectal nucleus.
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Role of melanopsin in circadian responses to light.
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Melanopsin: An opsin in melanophores, brain, and eye.
I Provencio, G Jiang, W J De Grip, W P Hayes, M D Rollag. Proc Natl Acad Sci U S A 1998
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Melanopsin and rod-cone photoreceptors play different roles in mediating pupillary light responses during exposure to continuous light in humans.
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Melanopsin contributions to irradiance coding in the thalamo-cortical visual system.
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Ultraviolet light provides a major input to non-image-forming light detection in mice.
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Modeling the role of mid-wavelength cones in circadian responses to light.
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Form and function of the M4 cell, an intrinsically photosensitive retinal ganglion cell type contributing to geniculocortical vision.
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Spectral responses of the human circadian system depend on the irradiance and duration of exposure to light.
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Multiple hypothalamic cell populations encoding distinct visual information.
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The influence of intrinsically-photosensitive retinal ganglion cells on the spectral sensitivity and response dynamics of the human pupillary light reflex.
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Mouse ganglion-cell photoreceptors are driven by the most sensitive rod pathway and by both types of cones.
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Photoreceptive net in the mammalian retina. This mesh of cells may explain how some blind mice can still tell day from night.
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An action spectrum for melatonin suppression: evidence for a novel non-rod, non-cone photoreceptor system in humans.
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High sensitivity of human melatonin, alertness, thermoregulation, and heart rate to short wavelength light.
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The acute light-induction of sleep is mediated by OPN4-based photoreception.
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A role for melanopsin in alpha retinal ganglion cells and contrast detection.
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Toward a clinical protocol for assessing rod, cone, and melanopsin contributions to the human pupil response.
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