Searching journal content for articles similar to Cassa et al. 22 (3): 421.

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  1. ...@buaa.edu.cn, coxtc@umkc.edu, stylianos.antonarakis@unige.chAbstractPathogenic coding variants have been identified in thousands of genes, yet the mechanisms underlying the incomplete penetrance in individuals carrying these variants are poorly understood. In this study, in a cohort of 2009 craniofacial microsomia...
  2. ...reference-based design—quantifying pathological shifts using only healthy reference distributions, without requiring training on condition-labeled data. Because scPSS does not require annotated disease data sets, it is uniquely applicable to rare and emerging diseases. Furthermore, it employs a low...
  3. ...authors: liuee1985@sicau.edu.cn, lingzhao.fang@qgg.au.dk, liliang@sicau.edu.cnAbstractPoultry egg production is shaped by the intertwined action of multiple physiological systems, greatly magnifying the complexity of its underlying genetic regulation. Although multitissue mapping of regulatory variants...
  4. ...involving the coordinated action of transcription factors, chromatin remodelers, and RNA polymerase, which determine where and when transcription begins. Accurately mapping and quantifying transcription start sites (TSSs) from nascently transcribed RNAs remains a key area of interest, as it provides...
  5. ...approval was given by the Ethical Review Board in Sweden approved the study (ethics permit number 2019-04746). Written consent to participate and publish was provided by the subject or their legal guardians. Patient BH16643-1 was enrolled using research protocol H-47281/Pacific Northwest Research Institute...
  6. ...). Retinopathies associated with CRX present with different phenotypes, varying in their cone versus rod predominance, severity, and age of onset. Some CRX variants have been shown to cause severe dominant disease, whereas others are pathogenic only in a recessive context (Rivolta et al. 2001; Huang et al. 2012...
  7. .../AMP) guidelines to classify genetic variants into five categories: pathogenic, likely pathogenic, benign, likely benign, and variant(s) of uncertain significance (VUS) (Richards et al. 2015). Whereas the first four classifications could be useful in interpreting rare variants that are found in genes that have...
  8. ...are limiting. While mapping functional gene/genomic annotations over from humans can theoretically be used for improving variant annotation, it is estimated that ∼13% of human pathogenic ClinVar variants are common in dogs, and thus likely benign (Gao et al. 2023). Systems such as the dog are therefore rife...
  9. ...12504, USA Corresponding author: selmecki@umn.eduAbstractThe human fungal pathogen Candida albicans poses a significant burden on global health, causing high rates of mortality and antifungal drug resistance. C. albicans is a heterozygous diploid organism that reproduces asexually. Structural variants...
  10. ...Corresponding author: jefetter@bu.eduAbstractMitochondrial DNA (mtDNA) variants cause a range of diseases from severe pediatric syndromes to aging-related conditions. The percentage of mtDNA copies carrying a pathogenic variant, variant allele frequency (VAF), must reach a threshold before a biochemical defect...
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