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Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk
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Genetic associations and architecture of asthma-chronic obstructive pulmonary disease overlap
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Lrp5 mutant and crispant zebrafish faithfully model human osteoporosis, establishing the zebrafish as a platform for CRISPR‐based functional screening of osteoporosis candidate genes
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Winter activity unrelated to introgression in British bumblebee Bombus terrestris audax
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Rare and low-frequency exonic variants and gene-by-smoking interactions in pulmonary function
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Deep scoping : a breeding strategy to preserve, reintroduce and exploit genetic variation
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A cross-omics integrative study of metabolic signatures of chronic obstructive pulmonary disease
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Chronic obstructive pulmonary disease and related phenotypes : polygenic risk scores in population-based and case-control cohorts
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Genetic and environmental influences on human height from infancy through adulthood at different levels of parental education
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Exploiting natural variation in root system architecture via genome wide association studies
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Comparative performances of machine learning methods for classifying Crohn Disease patients using genome-wide genotyping data
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Trait mapping in diverse arthropods by bulked segregant analysis
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Height and body mass index as modifiers of breast cancer risk in BRCA1/2 mutation carriers : a Mendelian randomization study
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Limited overlap in significant hits between genome-wide association studies on two airflow obstruction definitions in the same population
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Heritability and genome-wide association study of diffusing capacity of the lung
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Influence of genetic variants on childhood lung function : the Generation R study
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An intronic VNTR affects splicing of ABCA7 and increases risk of Alzheimer's disease
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A transcriptome-wide association study among 97,898 women to identify candidate susceptibility genes for epithelial ovarian cancer risk
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COPD GWAS variant at 19q13.2 in relation with DNA methylation and gene expression
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Malignant testicular germ cell tumors in postpubertal individuals with androgen insensitivity : prevalence, pathology and relevance of single nucleotide polymorphism-based susceptibility profiling
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BRCA2 polymorphic stop codon K3326X and the risk of breast, prostate, and ovarian cancers
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Genetic and environmental influences on adult human height across birth cohorts from 1886 to 1994
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Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways
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Effect of multiple allelic drop-outs in forensic RMNE calculations
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ERAP2 is associated with ankylosing spondylitis in HLA-B27-positive and HLA-B27-negative patients
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A 22-single nucleotide polymorphism Alzheimer's disease risk score correlates with family history, onset age, and cerebrospinal fluid Aβ42
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Involvement of toxin-antitoxin modules in Burkholderia cenocepacia biofilm persistence
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Comparative genomics of the Campylobacter lari group
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Associations of common breast cancer susceptibility alleles with risk of breast cancer subtypes in BRCA1 and BRCA2 mutation carriers
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Genetic and microbial factors modulating the ubiquitin proteasome system in inflammatory bowel disease
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A comparison of multivariate genome-wide association methods
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Rapid genetic adaptation precedes the spread of an exotic plant species
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The heterothallic sugarbeet pathogen Cercospora beticola contains exon fragments of both MAT genes that are homogenized by concerted evolution
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Genetic and QTL analyses of yield and a set of physiological traits in pepper
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Large sample size, wide variant spectrum, and advanced machine-learning technique boost risk prediction for inflammatory bowel disease
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Polymorphisms of matrix metalloproteinase gene and adiposity indices in European children: results of the IDEFICS study
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Genetic and molecular insights into the role of PROX1 in glucose metabolism
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BBS1 mutations in a wide spectrum of phenotypes ranging from nonsyndromic retinitis pigmentosa to Bardet-Biedl syndrome
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Mapping of the ms8 male sterility gene in sweet pepper (Capsicum annuum L.) on the chromosome P4 using PCR-based markers useful for breeding programmes
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Effects of haptoglobin polymorphisms and deficiency on susceptibility to inflammatory bowel disease and on severity of murine colitis
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FADS1 genetic variability interacts with dietary α-linolenic acid intake to affect serum non-HDL-cholesterol concentrations in European adolescents
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Common breast cancer susceptibility alleles and the risk of breast cancer for BRCA1 and BRCA2 mutation carriers: implications for risk prediction
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A screening methodology based on Random Forests to improve the detection of gene-gene interactions
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Cross-species microsatellite amplification in Vasconcellea and related genera and their use in germplasm classification
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Microsatellite conservation and Bayesian individual assignment in four Anguilla species
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Permutation based methods for comparing quality of life between observed treatments
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Revisiting recent challenges to the ancient fish-specific genome duplication hypothesis
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T-DNA vector backbone sequences are frequently integrated into the genome of transgenic plants obtained by Agrobacterium-mediated transformation
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ABI3 emerges from the seed
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Separation and characterization of needle and xylem maritime pine proteins
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Gene silencing results in instability of antibody production in transgenic plants
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AFLP analysis of genetic diversity within and between Arabidopsis thaliana ecotypes
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Post-transcriptional gene silencing in plants
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Post-transcriptional silencing of a neomycin phosphotransferase II transgene correlates with the accumulation of unproductive RNAs and with increased cytosine methylation of 3' flanking regions