Associated Papers
Genomic selection signatures in autism spectrum disorder identifies cognitive genomic tradeoff and its relevance in paradoxical phenotypes of deficits versus potentialities.
Prakash A et al.
Scientific Reports, 2021
33986442 (PubMed )
Supplement: 41598_2021_89798_MOESM3_ESM.xlsx › Table_S1
Frequent mutation of hypoxia-related genes in persistent pulmonary hypertension of the newborn.
Wang M et al.
Respiratory Research, 2020
32054482 (PubMed )
Supplement: 12931_2020_1314_MOESM1_ESM.xlsx › S6
Association between genetic variation in the dopamine system and motor recovery after stroke.
Kim BR et al.
Restorative Neurology and Neuroscience, 2016
Common variants of the G protein-coupled receptor type 4 are associated with human essential hypertension and predict the blood pressure response to angiotensin receptor blockade.
Sanada H et al.
The Pharmacogenomics Journal, 2016
Psychopathological aspects of dopaminergic gene polymorphisms in adolescence and young adulthood.
Nemoda Z et al.
Neuroscience and Biobehavioral Reviews, 2011
The p21 codon 31*C- and DRD2 codon 313*T-related genotypes/alleles, but not XRCC1 codon 399, hOGG1 codon 326, and DRD1-48 polymorphisms, are correlated with the presence of leiomyoma.
Hsieh YY et al.
Fertility and Sterility, 2009
Study of dopamine receptors genes polymorphisms in bipolar patients with comorbid alcohol abuse.
Szczepankiewicz A et al.
Alcohol and Alcoholism (oxford, Oxfordshire), 0
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