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
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_
Whole-exome sequencing in multiplex preeclampsia families identifies novel candidate susceptibility genes.
Melton PE et al.
Journal of Hypertension, 2019
Circadian-relevant genes are highly polymorphic in autism spectrum disorder patients.
Yang Z et al.
Brain & Development, 2016
A human sleep homeostasis phenotype in mice expressing a primate-specific PER3 variable-number tandem-repeat coding-region polymorphism.
Hasan S et al.
Faseb Journal : Official Publication of the Federation of American Societies for Experimental Biology, 2014
[Genetic analysis and genes relating synaptic function for autism spectrum disorder].
Yamagata T et al.
No to Hattatsu = Brain and Development, 2014
Recurrent inactivation of STAG2 in bladder cancer is not associated with aneuploidy.
Balbás-Martínez C et al.
Nature Genetics, 2013
24121791 (PubMed )
Supplement: NIHMS525200-supplement-2.xls › Relevant_mut_discovery_screen
Chronotype and PERIOD3 variable number tandem repeat polymorphism in individual sports athletes.
Kunorozva L et al.
Chronobiology International, 2012
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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