Associated Papers
Rare coding variants in CHRNB3 associate with reduced daily cigarette smoking across ancestries.
Rajagopal VM et al.
Nature Communications, 2026
41735279 (PubMed )
Supplement: 41467_2026_68825_MOESM9_ESM.xlsx › Table_8
De novo mutations in moderate or severe intellectual disability.
Hamdan FF et al.
Plos Genetics, 2014
25356899 (PubMed )
Supplement: pgen.1004772.s004.xlsx › 115.81
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