Associated Papers
Overactive PKA signaling underlies the hyperalgesia in an ADHD mouse model.
Kerosi DO et al.
Iscience, 2024
Cry1Δ11 mutation induces ADHD-like symptoms through hyperactive dopamine D1 receptor signaling.
Liu D et al.
Jci Insight, 2023
Whole Exome Sequencing to Find Candidate Variants for the Prediction of Kidney Transplantation Efficacy.
Aghamir SMK et al.
Genes, 2023
37372431 (PubMed )
Supplement: genes-14-01251-s001.zip › HGV__3.xlsx › _3
The impact of Mendelian sleep and circadian genetic variants in a population setting.
Weedon MN et al.
Plos Genetics, 2022
duper is a null mutation of Cryptochrome 1 in Syrian hamsters.
Lee YY et al.
Proceedings of the National Academy of Sciences of the United States of America, 2022
Over-Mutated Mitochondrial, Lysosomal and TFEB-Regulated Genes in Parkinson's Disease.
Segur-Bailach E et al.
Journal of Clinical Medicine, 2022
35330074 (PubMed )
Supplement: jcm-11-01749-s001.zip › Supl_Table_S1.pdf
An observational study investigating the CRY1Δ11 variant associated with delayed sleep-wake patterns and circadian metabolic output.
Smieszek SP et al.
Scientific Reports, 2021
Human CRY1 variants associate with attention deficit/hyperactivity disorder.
Onat OE et al.
The Journal of Clinical Investigation, 2020
The molecular genetics of human sleep.
Zhang L et al.
The European Journal of Neuroscience, 2020
Mutation of the Human Circadian Clock Gene CRY1 in Familial Delayed Sleep Phase Disorder.
Patke A et al.
Cell, 2017
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