299/4: 30 Large - scale exome chip
association analysis identifies novel type 2 diabetes susceptibility loci and highlights candidate effector genes.
Genome - wide
association analysis identifies novel loci for chronotype in 100,420 individuals from the UK Biobank.
for article Large - scale
association analysis identifies 13 new susceptibility loci for coronary artery disease.
«Gene variants modifying Huntington's symptom onset may lead to new therapeutic strategies: Genome - wide
association analysis identifies sites associated with earlier - or later - than - expected symptom appearance in human patients.»
Not exact matches
For example, Clem Yates, sourcing and supply director of Off - Piste Wines, is going to talk about private label & bulk strategies for importers and distributors and how to meet the store brand challenge, in private label & channel conflict; Andrew Shaw, Group Wine Buying Director, Conviviality PLC will talk about bottled in market strategy and how suppliers can partner with Conviviality; Florian Ceschi, Director of Ciatti Europe will give a detailed statistical
analysis of the current bulk market and will
identify opportunities where producers and negociants can take advantage of; David Richardson, Regulatory & Commercial Affairs Director, The Wine and Spirit Trade
Association (WSTA) will speak about regulatory issues specific to bulk products compared to cased goods.
To determine whether the presence and strength of the
associations between individual risk factors and severe PPH vary among women undergoing prelabor CD or intrapartum CD, stratified
analyses are needed according to CD subtype.To
identify risk factors for severe PPH within 2 distinct CD populations, prelabor CD and intrapartum CD, we performed 2 case - control studies.
Had the aim of this
analysis been to
identify characteristics associated with PPH, clearly these covariates would have been included (as would many of the maternities excluded from the
analysis as described earlier), so it would not be appropriate to use these results to draw conclusions about the
association between PPH and covariates other than intended place of birth.
While the UniFrac
analyses we performed suggest independent
associations between microbiome composition and both delivery mode and feeding method, the substantial overlap between the communities defined by both factors suggests that there are other important drivers of microbiome community composition that remain to be
identified in future
analyses.
Meta -
analyses of genome - wide
association studies conducted in these ethnically - diverse populations
identified a total of 878 genetic variants belonging to 18 loci associated with asthma risk.
The authors
identified 68 publications meeting criteria for inclusion in the
analysis: 59 reporting the prevalence of preoperative mental health conditions (65,363 patients) and 27 reporting
associations between preoperative mental health conditions and postoperative outcomes (50,182 patients).
Although the team controlled for these factors in the
analyses, the possibility of a partial confounding effect on the
associations identified in the study can not be ruled out.
While several studies in the intervening years have investigated whether particular genes were responsible for modifying HD onset, this is the first to employ genome - wide
association (GWA)
analysis, which scans an individual's whole genome to
identify chromosomal regions containing variants that are associated with the disease traits that are being studied.
Using a genome - wide
association study (GWAS) that includes 1600 individuals living in Tanzania, Botswana, or Ethiopia, the authors
identified regions of the genome that contribute to skin color variation and carried out a series of
analyses to pinpoint the responsible genes.
GWAS meta -
analysis identified an
association between the gene TLR1 and H pylori seroprevalence, «a finding that requires replication in non-white populations,» the authors write.
Genome - wide
association analysis comparing affected and unaffected PWC with the SOD1 mutation
identified a haplotype within the gene «SP110 nuclear body protein'that was associated with increased risk of developing DM and early age of onset.
Corresponding author, Dr Seth Weinberg says «Our
analysis identified several genetic
associations with facial features not previously described in earlier genome - wide studies.
This research directly responds to a 2016 pharmacoepidemiologic
analysis conducted using a large German health insurance database, which
identified an
association between dementia and long - term PPI use; however, these findings could not illustrate that PPIs caused dementia.
The study draws on an earlier
analysis the lab conducted for the Western Governors»
Association to
identify areas where renewable resources are the strongest, most consistent, and most concentrated, and where development would avoid protected areas and minimize the overall impact on wildlife habitat.
Previous genetic studies have examined the
association of aspirin, NSAIDs, or both with colorectal cancer according to a limited number of candidate genes or pathways.6 - 10 Thus, to comprehensively
identify common genetic markers that characterize individuals who may obtain differential benefit from aspirin and NSAIDs, we conducted a discovery - based, genome - wide
analysis of gene × environment interactions between regular use of aspirin, NSAIDs, or both and single - nucleotide polymorphisms (SNPs) in relation to risk of colorectal cancer.
In this study, genes
identified as differentially expressed by SAM
analysis were examined for their biologic
association to the gene ontology (GO) categories [34] as defined by the GO Consortium [33].
In the associated paper, Vitkup, Iossifov and others use a novel form of
analysis called NETBAG (network - based
analysis of genetic
associations) to
identify «the large biological network of genes affected by rare de novo CNVs in autism.»
Comparative genomic
analysis from 82 wild and wild - derived species grouped by microhabitat - use
identified variation corresponding with one of these QTL, further supporting broad
association with habitat use across the Malawi cichlid radiation.
This issue was
identified by follow - up on likely «false - positive» genetic
associations with genome - wide statistical significance in case - control
analysis.
Therefore, mining associated molecular markers via
association analysis might be a more powerful approach for
identifying causative variation.
We show how the HapMap resource can guide the design and
analysis of genetic
association studies, shed light on structural variation and recombination, and
identify loci that may have been subject to natural selection during human evolution.
Twelve type 2 diabetes susceptibility loci
identified through large - scale
association analysis
An Italian
association study and meta -
analysis with previous GWAS confirm WNT4, CDKN2BAS and FN1 as the first
identified susceptibility loci for endometriosis.
SNP & Variation Suite offers a complete set of tools for processing raw intensity data,
identifying regions of copy number variation (CNV), visualizing copy number data, and performing
association analyses on a variety of copy number covariates.
Despite type 2 diabetes having been well studied by genome - wide
association studies in other populations,
analysis in Mexican and Latin American individuals
identified SLC16A11 as a novel candidate gene for type 2 diabetes with a possible role in triacylglycerol metabolism.
Genome - wide
association analyses in 128,266 individuals
identifies new morningness and sleep duration loci.
We
identify three loci and seven genes associated with insomnia complaints, with the
associations for one locus and five genes supported by joint
analysis with an independent sample (n = 7,565).
Veröffentlichung Q. Fan et al., Meta -
analysis of gene - environment - wide
association scans accounting for education level
identifies additional loci for refractive error, Nature communications 7, 11008, 6.
The genes were
identified through population - and genome - wide linkage scans and
association analyses of at - risk haplotypes utilizing genetic and clinical data from the 17,000 participants in deCODE's obesity program in Iceland.
The EBV genetic variants
identified here provide a basis for future more directed
analysis of
association of specific EBV variation with EBV biology and EBV associated diseases.IMPORTANCE Incidence of diseases associated with EBV varies greatly in different parts of the world.
In response to the article authored by Dr. Vladimir Kogan of Ohio State University, «Value Added vs. Similar Students» Measures: Comparing Two Methods for Holding Ohio Schools Accountable,» the California Charter Schools
Association (CCSA) has
identified significant misrepresentations and
analysis errors by Dr. Kogan.
Fisher Exact
analysis, comparing genotypes of cases to controls,
identified an
association signal on CFA16 (Figure 3) extending over 6 Mb and including 28 SNPs that exceeded the Bonferroni corrected significance threshold -LRB-- Log10 (p) range = 6.39 — 10.09, Table 5).
Whole genome
association analysis studies that utilize single nucleotide polymorphism (SNP) markers have been used to
identify the molecular causes of various traits and conditions including genetic mutations within breeds that cause coat color variations [15], hairlessness [25] and defects in spinal development [26].
Molecular genome - wide
association analyses have
identified single nucleotide polymorphisms that segregate with the boldness - shyness axis in dogs [10, 11].
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Finally, in case of redundant predictors (in comparison with the bivariate
association low β coefficient / Wald statistic), a second regression
analysis with a stepwise selection procedure was run to
identify the best independently contributing predictors.
A logistic regression
analysis was used to
identify variables having a significant independent
association with an improvement of 50 % or more in positive psychotic symptoms.
The aims of the
analyses presented in this study were 1) to explore possible
associations between the coping resources with achieved copying behaviors,... quality of life, pain - related factors and socio - demographic characteristics and 2) to
identify patients with back pain who use different coping resources and to describe their respective socio - demographic and clinical characteristics.
The fact that «parental alienation syndrome» is not
identified in the Diagnostic and Statistical Manual of the American Psychiatric
Association, Fifth Edition (DSM - V), for example, does not mean that parental alienation does not exist; as Warshak's consensus statement and other meta -
analyses have demonstrated, parental alienation is much more widespread than is commonly assumed.
Multivariate logistic regression
analyses examined parity progression by birth order, while multinomial logistic regression was used to
identify associations between sex composition and use of permanent, temporary and traditional contraceptive methods.
The main results can be summarized as follows: (1) Synchrony during early mother - child interactions has neurophysiological correlates [85] as evidenced though the study of vagal tone [78], cortisol levels [80], and skin conductance [79]; (2) Synchrony impacts infant's cognitive processing [64], school adjustment [86], learning of word - object relations [87], naming of object wholes more than object parts [88]; and IQ [67], [89]; (3) Synchrony is correlated with and / or predicts better adaptation overall (e.g., the capacity for empathy in adolescence [89]; symbolic play and internal state speech [77]; the relation between mind - related comments and attachment security [90], [91]; and mutual initiation and mutual compliance [74], [92]-RRB-; (3) Lack of synchrony is related to at risk individuals and / or temperamental difficulties such as home observation in
identifying problem dyads [93], as well as mother - reported internalizing behaviors [94]; (4) Synchrony has been observable within several behavioral or sensorial modalities: smile strength and eye constriction [52]; tonal and temporal
analysis of vocal interactions [95](although, the
association between vocal interactions and synchrony differs between immigrant (lower synchrony) and non-immigrant groups [84]-RRB-; mutual gaze [96]; and coordinated movements [37]; (5) Each partner (including the infant) appears to play a role in restoring synchrony during interactions: children have coping behaviors for repairing interactive mismatches [97]; and infants are able to communicate intent and to respond to the intent expressed by the mother at the age of 2 months [98].