Sentence examples for several complex phenotypes from inspiring English sources

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This method has shown great promise in ascertaining common polymorphisms responsible for several complex phenotypes like diabetes, stroke and coronary artery disease [8].

The Neocodex Biobank and Genome Research Consortium is planning a number of genome-wide association studies (GWAS) in several complex phenotypes.

Similar(58)

Common CNVs have been reported to be associated with several complex disease phenotypes including HIV acquisition and progression [31] [33].

Several types of structured populations were used to discover the genetic architecture underlying complex phenotypes, and several QTL related to heterosis were detected.

GWAS, which are designed on the common disease-common variant hypothesis (CD-CV), identified several SNPs and loci for complex phenotypes.

Regarding beta-lactams, we observed wild type phenotype, cephalosporinase overexpression, penicillinase production, oxacillinase production, efflux pumps overexpression, porin D2 impermeability or complex phenotypes associating several of the previous resistance mechanisms.

In humans, habituation is a well-documented neural endo-phenotype of several complex behavioral disorders including schizophrenia and autism [ 18, 19].

Additional attention was drawn to CHD2 as a candidate photosensitive epilepsy gene as the only shared gene within several reported overlapping copy number variants of the chromosome 15q26.1 region associated with complex phenotypes including epilepsy with photosensitivity.

Second, it can also serve as a rapid screening tool for complex phenotypes that cannot be characterised by using only one or even several parameters.

several variants within the same region/gene are associated with the same phenotype or that variation in complex phenotypes such as height are also due to numerous relatively rare loci indirect, linkage disequilibrium-based association studies would have very limited power and linkage-based gene mapping techniques would be the preferred approach.

The molecular basis of IIMs in humans, as in many other autoimmune rheumatic diseases, is heterogeneous, involving several complex cellular components that probably contribute to differences in disease susceptibility, clinical and histopathological phenotype, and severity.

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