Associated Papers
Whole-exome sequencing identified recurrent and novel variants in benzene-induced leukemia.
Lin D et al.
Bmc Medical Genomics, 2023
36703207 (PubMed )
Supplement: 12920_2023_1442_MOESM3_ESM.xlsx › Sheet1
Prioritization of candidate genes for a South African family with Parkinson's disease using in-silico tools.
Sebate B et al.
Plos One, 2021
33770142 (PubMed )
Supplement: pone.0249324.s003.xlsx › 8774__IV-2_
Phenotyping of PER3 variants reveals widespread effects on circadian preference, sleep regulation, and health.
Archer SN et al.
Sleep Medicine Reviews, 2018
Mutation of the Human Circadian Clock Gene CRY1 in Familial Delayed Sleep Phase Disorder.
Patke A et al.
Cell, 2017
Circadian-relevant genes are highly polymorphic in autism spectrum disorder patients.
Yang Z et al.
Brain & Development, 2016
[Genetic analysis and genes relating synaptic function for autism spectrum disorder].
Yamagata T et al.
No to Hattatsu = Brain and Development, 2014
Polymorphism in the PER3 promoter associates with diurnal preference and delayed sleep phase disorder.
Archer SN et al.
Sleep, 2010
[Functional polymorphisms in clock genes and circadian rhythm sleep disorders].
Ebisawa T
Nihon Shinkei Seishin Yakurigaku Zasshi = Japanese Journal of Psychopharmacology, 2007
Circadian rhythms in the CNS and peripheral clock disorders: human sleep disorders and clock genes.
Ebisawa T
Journal of Pharmacological Sciences, 2007
The casein kinase 1 family: participation in multiple cellular processes in eukaryotes.
Knippschild U et al.
Cellular Signalling, 2005
Association of structural polymorphisms in the human period3 gene with delayed sleep phase syndrome.
Ebisawa T et al.
Embo Reports, 2001
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