about
Systems biology approach reveals genome to phenome correlation in type 2 diabetesCharacterizing genetic variants for clinical actionNew insights into behaviour using mouse ENU mutagenesisSingle nucleotide polymorphism-specific regulation of matrix metalloproteinase-9 by multiple miRNAs targeting the coding exon.Sequencing your genome: what does it mean?Genome-wide association analysis of radiation resistance in Drosophila melanogaster.The promise of whole-exome sequencing in medical genetics.Identification of rare genetic variants in novel loci associated with Paget's disease of bone.Current review of genetics of human obesity: from molecular mechanisms to an evolutionary perspective.A survey of tools for variant analysis of next-generation genome sequencing data.Gene-by-Environment Interactions in Pancreatic Cancer: Implications for Prevention.QTL mapping of leafy heads by genome resequencing in the RIL population of Brassica rapaQuantification of population benefit in evaluation of biomarkers: practical implications for disease detection and prevention.Achalasia Is Associated With eNOS4a4a, iNOS22GA, and nNOS29TT Genotypes: A Case-control Study.Case-only exome sequencing and complex disease susceptibility gene discovery: study design considerations.Verification of the Chromosome Region 9q21 Association with Pelvic Organ Prolapse Using RegulomeDB AnnotationsGenetic Influences on Physiological and Subjective Responses to an Aerobic Exercise Session among Sedentary Adults.Clinical applications of molecular genetic discoveries.Integrating optogenetic and pharmacological approaches to study neural circuit function: current applications and future directions.Genetic variants in the NOTCH4 gene influence the clinical features of migraine.A Quantitative Genomic Approach for Analysis of Fitness and Stress Related Traits in a Drosophila melanogaster Model Population.Sequence capture by hybridization to explore modern and ancient genomic diversity in model and nonmodel organisms.The need for mouse models in osteoporosis genetics research.Current and emerging technology approaches in genomicsGenetic variants in transforming growth factor-β gene (TGFB1) affect susceptibility to schizophrenia.The future for genetic studies in reproduction.The enigma of genetics etiology of atherosclerosis in the post-GWAS era.Interpreting genetic effects through models of cardiac electromechanics.Systems biology approaches to finding novel pain mediators.Pro-inflammatory genetic markers of atherosclerosis.The role and challenges of exome sequencing in studies of human diseases.Prostate cancer: from the pathophysiologic implications of some genetic risk factors to translation in personalized cancer treatments.Inherited risk factors for venous thromboembolism.A review of genome-wide association studies for multiple sclerosis: classical and hypothesis-driven approaches.An Overview of Genome-Wide Association Studies in Alzheimer's DiseaseHaplotype synthesis analysis reveals functional variants underlying known genome-wide associated susceptibility loci.High-Coverage Whole-Exome Sequencing Identifies Candidate Genes for Suicide in Victims with Major Depressive Disorder.Genetic model selection for a case-control study and a meta-analysis.Genetic Epidemiology and Public Health: The Evolution From Theory to Technology.Functional diversity of the glutathione peroxidase gene family among human populations: implications for genetic predisposition to disease and drug response.
P2860
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P2860
description
2011 nî lūn-bûn
@nan
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
2011年论文
@zh
2011年论文
@zh-cn
name
Molecular genetic studies of complex phenotypes.
@ast
Molecular genetic studies of complex phenotypes.
@en
type
label
Molecular genetic studies of complex phenotypes.
@ast
Molecular genetic studies of complex phenotypes.
@en
prefLabel
Molecular genetic studies of complex phenotypes.
@ast
Molecular genetic studies of complex phenotypes.
@en
P2860
P1476
Molecular genetic studies of complex phenotypes.
@en
P2093
Ali J Marian
P2860
P356
10.1016/J.TRSL.2011.08.001
P577
2011-08-31T00:00:00Z