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1.
Obstructive sleep apnea in a mouse model is associated with tissue-specific transcriptomic changes in circadian rhythmicity and mean 24-hour gene expression.
PLoS Biol
; 21(5): e3002139, 2023 05.
Article
in English
| MEDLINE | ID: mdl-37252926
2.
duper is a null mutation of Cryptochrome 1 in Syrian hamsters.
Proc Natl Acad Sci U S A
; 119(18): e2123560119, 2022 05 03.
Article
in English
| MEDLINE | ID: mdl-35471909
3.
NF-κB modifies the mammalian circadian clock through interaction with the core clock protein BMAL1.
PLoS Genet
; 17(11): e1009933, 2021 11.
Article
in English
| MEDLINE | ID: mdl-34807912
4.
An in silico genome-wide screen for circadian clock strength in human samples.
Bioinformatics
; 38(24): 5375-5382, 2022 12 13.
Article
in English
| MEDLINE | ID: mdl-36321857
5.
Normalized coefficient of variation (nCV): a method to evaluate circadian clock robustness in population scale data.
Bioinformatics
; 37(23): 4581-4583, 2021 12 07.
Article
in English
| MEDLINE | ID: mdl-34726689
6.
A large-scale study reveals 24-h operational rhythms in hospital treatment.
Proc Natl Acad Sci U S A
; 116(42): 20953-20958, 2019 10 15.
Article
in English
| MEDLINE | ID: mdl-31575744
7.
Computational and experimental insights into the circadian effects of SIRT1.
Proc Natl Acad Sci U S A
; 115(45): 11643-11648, 2018 11 06.
Article
in English
| MEDLINE | ID: mdl-30348778
8.
Population-level rhythms in human skin with implications for circadian medicine.
Proc Natl Acad Sci U S A
; 115(48): 12313-12318, 2018 11 27.
Article
in English
| MEDLINE | ID: mdl-30377266
9.
CYCLOPS reveals human transcriptional rhythms in health and disease.
Proc Natl Acad Sci U S A
; 114(20): 5312-5317, 2017 05 16.
Article
in English
| MEDLINE | ID: mdl-28439010
10.
HDAC8 mutations in Cornelia de Lange syndrome affect the cohesin acetylation cycle.
Nature
; 489(7415): 313-7, 2012 Sep 13.
Article
in English
| MEDLINE | ID: mdl-22885700
11.
Role for LSM genes in the regulation of circadian rhythms.
Proc Natl Acad Sci U S A
; 111(42): 15166-71, 2014 Oct 21.
Article
in English
| MEDLINE | ID: mdl-25288739
12.
Reply to Furlan et al.: The role of SIRT1 in cell autonomous clock function.
Proc Natl Acad Sci U S A
; 116(27): 13173, 2019 07 02.
Article
in English
| MEDLINE | ID: mdl-31239349
13.
Loss-of-function HDAC8 mutations cause a phenotypic spectrum of Cornelia de Lange syndrome-like features, ocular hypertelorism, large fontanelle and X-linked inheritance.
Hum Mol Genet
; 23(11): 2888-900, 2014 Jun 01.
Article
in English
| MEDLINE | ID: mdl-24403048
14.
PECONPI: a novel software for uncovering pathogenic copy number variations in non-syndromic sensorineural hearing loss and other genetically heterogeneous disorders.
Am J Med Genet A
; 161A(9): 2134-47, 2013 Sep.
Article
in English
| MEDLINE | ID: mdl-23897863
15.
PSMD11 modulates circadian clock function through PER and CRY nuclear translocation.
PLoS One
; 18(3): e0283463, 2023.
Article
in English
| MEDLINE | ID: mdl-36961772
16.
Integration of genome-scale data identifies candidate sleep regulators.
Sleep
; 46(2)2023 02 08.
Article
in English
| MEDLINE | ID: mdl-36462188
17.
Genome-wide SNP genotyping identifies the Stereocilin (STRC) gene as a major contributor to pediatric bilateral sensorineural hearing impairment.
Am J Med Genet A
; 158A(2): 298-308, 2012 Feb.
Article
in English
| MEDLINE | ID: mdl-22147502
18.
Mechanistic insights into the events that lead to synergistic induction of interleukin 6 transcription upon activation of the aryl hydrocarbon receptor and inflammatory signaling.
J Biol Chem
; 285(32): 24388-97, 2010 Aug 06.
Article
in English
| MEDLINE | ID: mdl-20511231
19.
Intermittent Hypoxia Alters the Circadian Expression of Clock Genes in Mouse Brain and Liver.
Genes (Basel)
; 12(10)2021 10 16.
Article
in English
| MEDLINE | ID: mdl-34681021
20.
Short-term exposure to intermittent hypoxia leads to changes in gene expression seen in chronic pulmonary disease.
Elife
; 102021 02 18.
Article
in English
| MEDLINE | ID: mdl-33599610