https://www.discovermagazine.com/interracial-sex-or-mendelian-segregation-818
Sandra Laing's extraordinary story examines being born black to white parents, raising questions about ancestry and genetic tests.
interracial sexdiscover magazinemendeliansegregation
https://www.frontiersin.org/journals/microbiology/articles/10.3389/fmicb.2023.1200937/full
Growing evidence indicates that variations in the composition of the gut microbiota are linked to the onset and progression of chronic respiratory diseases (...
gut microbiotarespiratory diseasesfrontiersassociationschronic
https://pubmed.ncbi.nlm.nih.gov/31097437/
Our study suggests lower BW within the normal range is causally associated with a more myopic refractive error. However, the impact of the causal effect was...
birth weightrefractive errorassociationadulthood
https://www.frontiersin.org/journals/medicine/articles/10.3389/fmed.2023.1191675/full
Background: We aimed to determine whether the plasma cystatin C is a causal risk factor for cardiovascular events, stroke, myocardial infarction (MI), and ca...
cystatin cfrontierscausalassociationplasma
https://www.frontiersin.org/journals/genetics/articles/10.3389/fgene.2023.1260367/full
The causation of Glycemic Traits and risks of Melanoma remains unknown. We used Mendelian Randomization (MR) to assess the links between Glycemic Traits and ...
mendelian randomizationfrontiersassociationglycemictraits
https://pubmed.ncbi.nlm.nih.gov/12520001/
Online Mendelian Inheritance in Animals (OMIA) provides up-to-date information on inherited disorders and other familial traits in non-laboratory animals. It...
mendelian inheritanceonlineanimalsomiacomparative
https://www.frontiersin.org/journals/genetics/articles/10.3389/fgene.2024.1353438/full
Background: Previous observational studies have investigated the association between sleep-related traits and male fertility; however, conclusive evidence of...
with malefrontiersassociationsleeptraits
https://pubmed.ncbi.nlm.nih.gov/27616674/
: Care must be taken to assess the NOME assumption via the IGX2 statistic before implementing standard MR-Egger regression in the two-sample summary data...
summarydatatwosamplemendelian
https://pubmed.ncbi.nlm.nih.gov/27652346/
These results provide strong evidence that low serum 25(OH)D concentration is a cause of MS, independent of established risk factors.
mendelian randomizationshowscausaleffectlow
https://pubmed.ncbi.nlm.nih.gov/37083939/
Scores of the GRCh38 genome build are highly correlated to the prior release with a performance increase due to the better coverage of features. For...
mendelian mutationregulatoryscore
https://elifesciences.org/articles/69026/figures
Harmful genetic variants at mendelian disease genes slow down adaptation, by interfering with the spread of adaptive variants in a population.
figuresdatarecentadaptationhuman
https://pubmed.ncbi.nlm.nih.gov/23819870/
Our results demonstrate the potential power gain of aggregating bioinformatics variant scores into gene-level scores and the general utility of bioinformatics...
mendelian diseasewith theidentifyinggenesvariant