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Methods and software to analyze gene-environment interactions under a case-mother - control-mother design with partially missing child genotype
Methods and software to analyze gene-environment interactions under a case-mother - control-mother design with partially missing child genotype
Introduction: The case-mother - control-mother design allows to study fetal and maternal genetic factors together with env...
A common variant of ARRB2 promoter region Associated with the Prognosis of Heart Failure
A common variant of ARRB2 promoter region Associated with the Prognosis of Heart Failure
Introduction The role of ARRB2 in cardiovascular disease has recently gained increasing attention. However, the associatio...
Polymorphisms of placental iodothyronine deiodinase genes in a rural area of Northern China with high prevalence of neural tube defects
Polymorphisms of placental iodothyronine deiodinase genes in a rural area of Northern China with high prevalence of neural tube defects
Introduction: We have reported that high total homocysteine (tHCY), and the coexistence of inadequate thyroid hormones in ...
Identification of a hypoxia-related signature as candidate detector for schizophrenia based on genome-wide gene expression
Identification of a hypoxia-related signature as candidate detector for schizophrenia based on genome-wide gene expression
Introduction: Schizophrenia (SCZ), a severe neuropsychiatric disorder with high genetic susceptibility, has high rates of ...
A Comprehensive Study of Disease-Causing Variants in PAH, QDPR, PTS, and PCD Genes in Iranian Patients with Hyperphenylalaninemia: A Systematic Review
A Comprehensive Study of Disease-Causing Variants in PAH, QDPR, PTS, and PCD Genes in Iranian Patients with Hyperphenylalaninemia: A Systematic Review
<b><i>Background:</i></b> Hyperphenylalaninemia (HPA) is an autosomal recessive disorder that resu...
A comprehensive study of mutations in PAH, QDPR, PTS, and PCD genes in Iranian patients with Hyperphenylalaninemia; A systematic review
A comprehensive study of mutations in PAH, QDPR, PTS, and PCD genes in Iranian patients with Hyperphenylalaninemia; A systematic review
Background: Hyperphenylalaninemia (HPA) is an autosomal recessive disorder that results from a deficiency in the phenylala...
Reduction of Missed Diagnosis of G6PD Deficiency in Heterozygous Females by G6PD/6PGD Ratio Assay Combined with Amplification Refractory Mutation System PCR
Reduction of Missed Diagnosis of G6PD Deficiency in Heterozygous Females by G6PD/6PGD Ratio Assay Combined with Amplification Refractory Mutation System PCR
<b><i>Objective:</i></b> Glucose-6-phosphate dehydrogenase (G6PD) deficiency is an X-linked geneti...
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