Associated Papers
Exome sequencing reveals a rare damaging variant in GRIN2C in familial late-onset Alzheimer's disease.
Rubino E et al.
Alzheimer's Research & Therapy, 2025
39810256 (PubMed )
Supplement: 13195_2024_1661_MOESM2_ESM.xlsx › Suppl._Table_2
Relationship between APOE, PER2, PER3 and OX2R Genetic Variants and Neuropsychiatric Symptoms in Patients with Alzheimer's Disease.
Lozano-Tovar S et al.
International Journal of Environmental Research and Public Health, 2023
36901420 (PubMed )
Supplement: ijerph-20-04412-s001.zip › ijerph-2184456-supplementary.pdf
Toward a Molecular Approach to Chronotype Assessment.
Biscontin A et al.
Journal of Biological Rhythms, 2022
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 › _8773__III-7_
Whole-exome sequencing in multiplex preeclampsia families identifies novel candidate susceptibility genes.
Melton PE et al.
Journal of Hypertension, 2019
Modeling Strengthens Molecular Link between Circadian Polymorphisms and Major Mood Disorders.
Liberman AR et al.
Journal of Biological Rhythms, 2018
Circadian Clock Model Supports Molecular Link Between PER3 and Human Anxiety.
Liberman AR et al.
Scientific Reports, 2017
Circadian-relevant genes are highly polymorphic in autism spectrum disorder patients.
Yang Z et al.
Brain & Development, 2016
Screening of clock gene polymorphisms demonstrates association of a PER3 polymorphism with morningness-eveningness preference and circadian rhythm sleep disorder.
Hida A et al.
Scientific Reports, 2014
[Genetic analysis and genes relating synaptic function for autism spectrum disorder].
Yamagata T et al.
No to Hattatsu = Brain and Development, 2014
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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