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Melanopsin Regulates Both Sleep-Promoting and Arousal-Promoting Responses to Light

PLoS biology, 2016-06, Vol.14 (6), p.e1002482-e1002482

2016

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Overexpression of Fto leads to increased food intake and results in obesity

Nature genetics, 2010-12, Vol.42 (12), p.1086-1092

2010

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Reciprocal interactions between circadian clocks and aging

Mammalian Genome, 2016-08, Vol.27 (7-8), p.332-340

2016

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The Regulatory Factor ZFHX3 Modifies Circadian Function in SCN via an AT Motif-Driven Axis

Cell, 2015-07, Vol.162 (3), p.607-621

2015

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When clocks go bad: neurobehavioural consequences of disrupted circadian timing

PLoS genetics, 2008-05, Vol.4 (5), p.e1000040-e1000040

2008

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Genetic background influences age-related decline in visual and nonvisual retinal responses, circadian rhythms, and sleep

Neurobiology of aging, 2015-01, Vol.36 (1), p.380-393

2015

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After-Hours Mutant Reveals a Role for Fbxl3 in Determining Mammalian Circadian Period

Science (American Association for the Advancement of Science), 2007-05, Vol.316 (5826), p.897-900

2007

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Analysis of Individual Mouse Activity in Group Housed Animals of Different Inbred Strains using a Novel Automated Home Cage Analysis System

Frontiers in behavioral neuroscience, 2016-06, Vol.10, p.106-106

2016

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The Zfhx3-Mediated Axis Regulates Sleep and Interval Timing in Mice

Cell reports (Cambridge), 2016-07, Vol.16 (3), p.615-621

2016

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Shift work-like patterns effect on female and male mouse behavior

Neurobiology of sleep and circadian rhythms, 2022-11, Vol.13, p.100082-100082, Article 100082

2022

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point mutation in TRPC3 causes abnormal Purkinje cell development and cerebellar ataxia in moonwalker mice

Proceedings of the National Academy of Sciences - PNAS, 2009-04, Vol.106 (16), p.6706-6711

2009

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Loss of Bardet-Biedl syndrome proteins causes synaptic aberrations in principal neurons

PLoS biology, 2019-09, Vol.17 (9), p.e3000414-e3000414

2019

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Harvesting mouse suprachiasmatic nucleus by vibrating microtome for diurnal transcriptome analysis

STAR protocols, 2023-12, Vol.4 (4), p.102618, Article 102618

2023

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Longitudinal home-cage automated assessment of climbing behavior shows sexual dimorphism and aging-related decrease in C57BL/6J healthy mice and allows early detection of motor impairment in the N171-82Q mouse model of Huntington's disease

Frontiers in behavioral neuroscience, 2023-03, Vol.17, p.1148172-1148172

2023

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Loss-of-Function Mutations in FRRS1L Lead to an Epileptic-Dyskinetic Encephalopathy

American journal of human genetics, 2016-06, Vol.98 (6), p.1249-1255

2016

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Reliability, robustness, and reproducibility in mouse behavioral phenotyping: a cross-laboratory study

Physiological genomics, 2008-08, Vol.34 (3), p.243-255

2008

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Replication of Genome-Wide association studies (GWAS) loci for sleep in the British G1219 cohort

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2013-07, Vol.162B (5), p.431-438

2013

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Mutation of Celsr1 Disrupts Planar Polarity of Inner Ear Hair Cells and Causes Severe Neural Tube Defects in the Mouse

Current biology, 2003-07, Vol.13 (13), p.1129-1133

2003

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Reduced anxiety and depression-like behaviours in the circadian period mutant mouse afterhours

PloS one, 2012-06, Vol.7 (6), p.e38263-e38263

2012

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Comprehensive phenotypic analysis of the Dp1Tyb mouse strain reveals a broad range of Down syndrome-related phenotypes

Disease models & mechanisms, 2021-10, Vol.14 (10)

2021

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A novel SOD1-ALS mutation separates central and peripheral effects of mutant SOD1 toxicity

Human molecular genetics, 2015-04, Vol.24 (7), p.1883-1897

2015

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Loss of Frrs1l disrupts synaptic AMPA receptor function, and results in neurodevelopmental, motor, cognitive and electrographical abnormalities

Disease models & mechanisms, 2019-02, Vol.12 (2)

2019

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Correction: Loss of Bardet-Biedl syndrome proteins causes synaptic aberrations in principal neurons

PLoS biology, 2019-10, Vol.17 (10), p.e3000520-e3000520

2019

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Early doors (Edo) mutant mouse reveals the importance of period 2 (PER2) PAS domain structure for circadian pacemaking

Proceedings of the National Academy of Sciences - PNAS, 2016-03, Vol.113 (10), p.2756-2761

2016

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Dynamic modulation of genomic enhancer elements in the suprachiasmatic nucleus, the site of the mammalian circadian clock

Genome research, 2023-05, Vol.33 (5), p.673-688

2023

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Melanopsin Regulates Both Sleep-Promoting and Arousal-Promoting Responses to Light

Overexpression of Fto leads to increased food intake and results in obesity

Reciprocal interactions between circadian clocks and aging

The Regulatory Factor ZFHX3 Modifies Circadian Function in SCN via an AT Motif-Driven Axis

When clocks go bad: neurobehavioural consequences of disrupted circadian timing

Genetic background influences age-related decline in visual and nonvisual retinal responses, circadian rhythms, and sleep

After-Hours Mutant Reveals a Role for Fbxl3 in Determining Mammalian Circadian Period

Analysis of Individual Mouse Activity in Group Housed Animals of Different Inbred Strains using a Novel Automated Home Cage Analysis System

The Zfhx3-Mediated Axis Regulates Sleep and Interval Timing in Mice

Shift work-like patterns effect on female and male mouse behavior

point mutation in TRPC3 causes abnormal Purkinje cell development and cerebellar ataxia in moonwalker mice

Loss of Bardet-Biedl syndrome proteins causes synaptic aberrations in principal neurons

Harvesting mouse suprachiasmatic nucleus by vibrating microtome for diurnal transcriptome analysis

Longitudinal home-cage automated assessment of climbing behavior shows sexual dimorphism and aging-related decrease in C57BL/6J healthy mice and allows early detection of motor impairment in the N171-82Q mouse model of Huntington's disease

Loss-of-Function Mutations in FRRS1L Lead to an Epileptic-Dyskinetic Encephalopathy

Reliability, robustness, and reproducibility in mouse behavioral phenotyping: a cross-laboratory study

Replication of Genome-Wide association studies (GWAS) loci for sleep in the British G1219 cohort

Mutation of Celsr1 Disrupts Planar Polarity of Inner Ear Hair Cells and Causes Severe Neural Tube Defects in the Mouse

Reduced anxiety and depression-like behaviours in the circadian period mutant mouse afterhours

Comprehensive phenotypic analysis of the Dp1Tyb mouse strain reveals a broad range of Down syndrome-related phenotypes

A novel SOD1-ALS mutation separates central and peripheral effects of mutant SOD1 toxicity

Loss of Frrs1l disrupts synaptic AMPA receptor function, and results in neurodevelopmental, motor, cognitive and electrographical abnormalities

Correction: Loss of Bardet-Biedl syndrome proteins causes synaptic aberrations in principal neurons

Early doors (Edo) mutant mouse reveals the importance of period 2 (PER2) PAS domain structure for circadian pacemaking

Dynamic modulation of genomic enhancer elements in the suprachiasmatic nucleus, the site of the mammalian circadian clock

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