Associated Papers
HAPLN3 p.T34A contributes to incomplete penetrance of moyamoya disease in Chinese carrying RNF213 p.R4810K.
Xu J et al.
European Journal of Neurology, 2024
39315749 (PubMed )
Supplement: ENE-31-e16473-s001.xlsx › Table_S2
Evolutionary history of adenomas to colorectal cancer in FAP families.
Yang C et al.
Frontiers in Genetics, 2024
39021676 (PubMed )
Supplement: DataSheet1.ZIP › Somatic › 18R12365.xls › SNVIndel
Circadian-relevant genes are highly polymorphic in autism spectrum disorder patients.
Yang Z et al.
Brain & Development, 2016
Circadian polymorphisms in night owls, in bipolars, and in non-24-hour sleep cycles.
Kripke DF et al.
Psychiatry Investigation, 2014
25395965 (PubMed )
Supplement: pi-11-345-s001.xlsx › BALM_Meta-Analysis
[Genetic analysis and genes relating synaptic function for autism spectrum disorder].
Yamagata T et al.
No to Hattatsu = Brain and Development, 2014
Genotyping sleep disorders patients.
Kripke DF et al.
Psychiatry Investigation, 2010
Identification of coding polymorphisms in human circadian rhythm genes PER1, PER2, PER3, CLOCK, ARNTL, CRY1, CRY2 and TIMELESS in a multi-ethnic screening panel.
Hawkins GA et al.
Dna Sequence : the Journal of Dna Sequencing and Mapping, 2008
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