Associated Papers
Unraveling the Genetic Architecture of Hepatoblastoma Risk: Birth Defects and Increased Burden of Germline Damaging Variants in Gastrointestinal/Renal Cancer Predisposition and DNA Repair Genes.
Aguiar T et al.
Frontiers in Genetics, 2022
35495172 (PubMed )
Supplement: DataSheet1.xlsx › Supp_table_3
Revisiting the complex architecture of ALS in Turkey: Expanding genotypes, shared phenotypes, molecular networks, and a public variant database.
Tunca C et al.
Human Mutation, 2020
The contribution of rare and common variants in 30 genes to risk nicotine dependence.
Yang J et al.
Molecular Psychiatry, 2015
Habenular expression of rare missense variants of the β4 nicotinic receptor subunit alters nicotine consumption.
Slimak MA et al.
Frontiers in Human Neuroscience, 2014
Examination of rare missense variants in the CHRNA5-A3-B4 gene cluster to level of response to alcohol in the San Diego Sibling Pair study.
Choquet H et al.
Alcoholism, Clinical and Experimental Research, 2013
Natural variation within the neuronal nicotinic acetylcholine receptor cluster on human chromosome 15q24: influence on heritable autonomic traits in twin pairs.
Rana BK et al.
The Journal of Pharmacology and Experimental Therapeutics, 2009
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