Large‐scale development of cost‐effective SNP marker assays for diversity assessment and genetic mapping in chickpea and comparative mapping in legumes
Development of high-throughput SNP-based genotyping in Acacia auriculiformis x A. mangium hybrids using short-read transcriptome data
Evaluation of diagnostic molecular markers for DUS phenotypic assessment in the cereal crop, barley (Hordeum vulgare ssp. vulgare L.)
Single nucleotide polymorphisms identification, characterization and linkage mapping in Chenopodium quinoa
Impaired auxin biosynthesis in the defective endosperm18 mutant is due to mutational loss of expression in the ZmYuc1 gene encoding endosperm-specific YUCCA1 protein in maize
Interaction of a 17q12 variant with both fetal and infant smoke exposure in the development of childhood asthma‐like symptoms.
A role for PACE4 in osteoarthritis pain: evidence from human genetic association and null mutant phenotype
Effects of polymorphisms in TRAILR1 and TNFR1A on the response to anti-TNF therapies in patients with rheumatoid and psoriatic arthritis
Effets des polymorphismes des gènes< i> TRAILR1 et< i> TNFR1A sur la réponse au traitement anti-TNF chez les patients atteints de polyarthrite rhumatoïde et de rhumatisme psoriasique.
Polymorphisms in the Interleukin 4, Interleukin 13, and Corresponding Receptor Genes Are Not Associated with Systemic Sclerosis and Do Not Influence Gene Expression
TRAF Family Member-Associated NF-KB Activator (TANK) Gene Polymorphism in Chronic Periodontitis and Peri-implantitis Patients
Analysis of RANKL gene polymorphism (rs9533156 and rs2277438) in Iranian patients with chronic periodontitis and periimplantitis
Impact of Loss-of-function Mutations in the Filaggrin Gene and Atopic Dermatitis on the Development of Occupational Irritant Contact Dermatitis
Clinical course of occupational irritant contact dermatitis of the hands in relation to filaggrin genotype status and atopy
Apolipoprotein-E and hepatitis C lipoviral particles in genotype 1 infection: Evidence for an association with interferon sensitivity
Hepatitis C viral load, genotype 3 and IL28B CC genotype predict mortality in HIV and hepatitis C coinfected individuals
PWE-166 Increasing VacA toxin activity alters Helicobacter pylori colonisation density and the nature of the acquired immune response in a mouse model of infection
Stratifying type 2 diabetes cases by BMI identifies genetic risk variants in LAMA1 and enrichment for risk variants in lean compared to obese cases
The association of white matter volume in psychotic disorders with genotypic variation in NRG1, MOG and CNP: a voxel-based analysis in affected individuals and their unaffected relatives
Hirschsprung's disease and variants in genes that regulate enteric neural crest cell proliferation, migration and differentiation
The development of a validated real-time (TaqMan) PCR for detection of Stagonosporopsis andigena and S. crystalliniformis in infected leaves of potato and tomato
Genetic variation in MME in relation to neprilysin protein and enzyme activity, Aβ levels, and Alzheimer's disease risk
Identification of a Late Onset Alzheimer's Disease Candidate Risk Variant at 9q21. 33 in Polish Patients
PPAR$gamma$2 gene Pro12Ala and PPAR$alpha$ gene Leu162Val SNPs interact with dietary intake of fat in determination of plasma lipid concentrations
The Genetic Consequences of Spatially Varying Selection in the Panmictic American Eel (Anguilla rostrata)
Comparison of IKKI Gene Polymorphisms (rs1539243 and rs12728136) between Chronic Periodontitis and Peri-implantitis Patients in an Iranian Population (A Cross-Sectional Study)
From genes to phenotypes–Evaluation of two methods for the SNP analysis in archaeological remains: Pyrosequencing and competitive allele specific PCR (KASPar)
A common variant highly associated with plasma VEGFA levels also contributes to the variation of both LDL-C and HDL-C
