Associated Papers
De novo mutations in moderate or severe intellectual disability.
Hamdan FF et al.
Plos Genetics, 2014
25356899 (PubMed )
Supplement: pgen.1004772.s004.xlsx › 820.316
Rare missense variants in CHRNB3 and CHRNA3 are associated with risk of alcohol and cocaine dependence.
Haller G et al.
Human Molecular Genetics, 2014
Introduction to deep sequencing and its application to drug addiction research with a focus on rare variants.
Wang S et al.
Molecular Neurobiology, 2014
Habenular expression of rare missense variants of the β4 nicotinic receptor subunit alters nicotine consumption.
Slimak MA et al.
Frontiers in Human Neuroscience, 2014
Functional characterization improves associations between rare non-synonymous variants in CHRNB4 and smoking behavior.
Haller G et al.
Plos One, 2014
Rare missense variants in CHRNB4 are associated with reduced risk of nicotine dependence.
Haller G et al.
Human Molecular Genetics, 2012
The genetics of substance dependence.
Wang JC et al.
Annual Review of Genomics and Human Genetics, 2012
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