Associated Papers
Divergent Roles of PI3K Isoforms in PTEN-Deficient Glioblastomas.
Xie S et al.
Cell Reports, 2020
32997991 (PubMed )
Supplement: NIHMS1633676-supplement-2.xlsx › BT179_Mutations
DRD1 rare variants associated with tardive-like dystonia: a pilot pathway sequencing study in dystonia.
Groen JL et al.
Parkinsonism & Related Disorders, 2014
Rare variants in CFI, C3 and C9 are associated with high risk of advanced age-related macular degeneration.
Seddon JM et al.
Nature Genetics, 2013
24036952 (PubMed )
Supplement: NIHMS512112-supplement-2.xlsx › Supplementary_Table_2B
A population-specific HTR2B stop codon predisposes to severe impulsivity.
Bevilacqua L et al.
Nature, 2010
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