Associated Papers
The landscape of rare genetic variants in familial Waldenström macroglobulinemia.
Pemov A et al.
Blood Neoplasia, 2024
39036705 (PubMed )
Supplement: BNEO_NEO-2023-000111-mmc8.xlsx › Supplementary_Table_7C
Pharmacogenomics of GPCR Drug Targets.
Hauser AS et al.
Cell, 2018
29249361 (PubMed )
Supplement: mmc2.xlsx › MissenseVariants
Longrange PCR-based next-generation sequencing in pharmacokinetics and pharmacodynamics study of propofol among patients under general anaesthesia.
Zakerska-Banaszak O et al.
Scientific Reports, 2017
Polymorphic variants of adrenoceptors: pharmacology, physiology, and role in disease.
Ahles A et al.
Pharmacological Reviews, 2014
Prediction of susceptibility to major depression by a model of interactions of multiple functional genetic variants and environmental factors.
Wong ML et al.
Molecular Psychiatry, 2012
ADRA1A gene is associated with BMI in chronic schizophrenia patients exposed to antipsychotics.
Liu YR et al.
The Pharmacogenomics Journal, 2010
Cardiac signaling genes exhibit unexpected sequence diversity in sporadic cardiomyopathy, revealing HSPB7 polymorphisms associated with disease.
Matkovich SJ et al.
The Journal of Clinical Investigation, 2010
Novel human alpha1a-adrenoceptor single nucleotide polymorphisms alter receptor pharmacology and biological function.
Lei B et al.
Naunyn-schmiedeberg's Archives of Pharmacology, 2005
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