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CYCLOPS reveals human transcriptional rhythms in health and disease

Proceedings of the National Academy of Sciences - PNAS, 2017-05, Vol.114 (20), p.5312-5317

2017

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A database of tissue-specific rhythmically expressed human genes has potential applications in circadian medicine

Science translational medicine, 2018-09, Vol.10 (458)

2018

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Clock Regulation of Metabolites Reveals Coupling between Transcription and Metabolism

Cell metabolism, 2017-04, Vol.25 (4), p.961-974.e4

2017

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NF-κB modifies the mammalian circadian clock through interaction with the core clock protein BMAL1

PLoS genetics, 2021-11, Vol.17 (11), p.e1009933-e1009933

2021

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PSMD11 modulates circadian clock function through PER and CRY nuclear translocation

PloS one, 2023-03, Vol.18 (3), p.e0283463-e0283463

2023

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Obstructive sleep apnea in a mouse model is associated with tissue-specific transcriptomic changes in circadian rhythmicity and mean 24-hour gene expression

PLoS biology, 2023-05, Vol.21 (5), p.e3002139

2023

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The NRON complex controls circadian clock function through regulated PER and CRY nuclear translocation

Scientific reports, 2019-08, Vol.9 (1), p.11883-12, Article 11883

2019

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Role for LSM genes in the regulation of circadian rhythms

Proceedings of the National Academy of Sciences - PNAS, 2014-10, Vol.111 (42), p.15166-15171

2014

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A population-based gene expression signature of molecular clock phase from a single epidermal sample

Genome medicine, 2020-08, Vol.12 (1), p.73-73, Article 73

2020

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Short-term exposure to intermittent hypoxia leads to changes in gene expression seen in chronic pulmonary disease

eLife, 2021-02, Vol.10

2021

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KPNB1 mediates PER/CRY nuclear translocation and circadian clock function

eLife, 2015-08, Vol.4

2015

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Clock Regulation of Metabolites Reveals Coupling between Transcription and Metabolism

Cell metabolism, 2017-05, Vol.25 (5), p.1206-1206

2017

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Intermittent Hypoxia Alters the Circadian Expression of Clock Genes in Mouse Brain and Liver

Genes, 2021-10, Vol.12 (10), p.1627

2021

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Genome-wide SNP genotyping identifies the Stereocilin (STRC) gene as a major contributor to pediatric bilateral sensorineural hearing impairment

American journal of medical genetics. Part A, 2012-02, Vol.158A (2), p.298-308

2012

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Normalized coefficient of variation (nCV): a method to evaluate circadian clock robustness in population scale data

Bioinformatics, 2021-12, Vol.37 (23), p.4581-4583

2021

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Population-level rhythms in human skin with implications for circadian medicine

Proceedings of the National Academy of Sciences - PNAS, 2018-11, Vol.115 (48), p.12313-12318

2018

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Computational and experimental insights into the circadian effects of SIRT1

Proceedings of the National Academy of Sciences - PNAS, 2018-11, Vol.115 (45), p.11643-11648

2018

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HDAC8 mutations in Cornelia de Lange syndrome affect the cohesin acetylation cycle

Nature (London), 2012-09, Vol.489 (7415), p.313-317

2012

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An in silico genome-wide screen for circadian clock strength in human samples

Bioinformatics (Oxford, England), 2022-12, Vol.38 (24), p.5375-5382

2022

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A large-scale study reveals 24-h operational rhythms in hospital treatment

Proceedings of the National Academy of Sciences - PNAS, 2019-10, Vol.116 (42), p.20953-20958

2019

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CRY1‐CBS binding regulates circadian clock function and metabolism

The FEBS journal, 2021-01, Vol.288 (2), p.614-639

2021

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Integration of genome-scale data identifies candidate sleep regulators

Sleep (New York, N.Y.), 2023-02, Vol.46 (2), p.1

2023

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Mechanistic Insights into the Events That Lead to Synergistic Induction of Interleukin 6 Transcription upon Activation of the Aryl Hydrocarbon Receptor and Inflammatory Signaling

The Journal of biological chemistry, 2010-08, Vol.285 (32), p.24388-24397

2010

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duper is a null mutation of Cryptochrome 1 in Syrian hamsters

Proceedings of the National Academy of Sciences - PNAS, 2022-05, Vol.119 (18), p.e2123560119

2022

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Semaphorin 3d signaling defects are associated with anomalous pulmonary venous connections

Nature medicine, 2013-06, Vol.19 (6), p.760-765

2013

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CYCLOPS reveals human transcriptional rhythms in health and disease

A database of tissue-specific rhythmically expressed human genes has potential applications in circadian medicine

Clock Regulation of Metabolites Reveals Coupling between Transcription and Metabolism

NF-κB modifies the mammalian circadian clock through interaction with the core clock protein BMAL1

PSMD11 modulates circadian clock function through PER and CRY nuclear translocation

Obstructive sleep apnea in a mouse model is associated with tissue-specific transcriptomic changes in circadian rhythmicity and mean 24-hour gene expression

The NRON complex controls circadian clock function through regulated PER and CRY nuclear translocation

Role for LSM genes in the regulation of circadian rhythms

A population-based gene expression signature of molecular clock phase from a single epidermal sample

Short-term exposure to intermittent hypoxia leads to changes in gene expression seen in chronic pulmonary disease

KPNB1 mediates PER/CRY nuclear translocation and circadian clock function

Clock Regulation of Metabolites Reveals Coupling between Transcription and Metabolism

Intermittent Hypoxia Alters the Circadian Expression of Clock Genes in Mouse Brain and Liver

Genome-wide SNP genotyping identifies the Stereocilin (STRC) gene as a major contributor to pediatric bilateral sensorineural hearing impairment

Normalized coefficient of variation (nCV): a method to evaluate circadian clock robustness in population scale data

Population-level rhythms in human skin with implications for circadian medicine

Computational and experimental insights into the circadian effects of SIRT1

HDAC8 mutations in Cornelia de Lange syndrome affect the cohesin acetylation cycle

An in silico genome-wide screen for circadian clock strength in human samples

A large-scale study reveals 24-h operational rhythms in hospital treatment

CRY1‐CBS binding regulates circadian clock function and metabolism

Integration of genome-scale data identifies candidate sleep regulators

Mechanistic Insights into the Events That Lead to Synergistic Induction of Interleukin 6 Transcription upon Activation of the Aryl Hydrocarbon Receptor and Inflammatory Signaling

duper is a null mutation of Cryptochrome 1 in Syrian hamsters

Semaphorin 3d signaling defects are associated with anomalous pulmonary venous connections

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