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Actas 2007

Diciembre 28 2007

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Nature Genetics

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Trends in Genetics

Advisory Board and Contents
Inferring genetic ancestry from cancer sequencing data
New tRNA-targeting transposons that hijack phage and vesicles
Why are whales big? Genes behind ocean giants
Novel functions of a retroposed gene
Unified views on variant impact across many diseases
The gut microbiota links disease to human genome evolution
Functional characterization of human genomic variation linked to polygenic diseases
Fluctuating selection and the determinants of genetic variation
ATRX, a guardian of chromatin

Plos Genetics

Evolutionary trade-off and mutational bias could favor transcriptional over translational divergence within paralog pairs
Hsp90 mutants with distinct defects provide novel insights into cochaperone regulation of the folding cycle
Arabidopsis FIN219/JAR1 interacts with phytochrome a under far-red light and jasmonates in regulating hypocotyl elongation via a functional demand manner
Pbp1 associates with Puf3 and promotes translation of its target mRNAs involved in mitochondrial biogenesis
Taste and pheromonal inputs govern the regulation of time investment for mating by sexual experience in male Drosophila melanogaster
Functional analysis of three new alpha-thalassemia deletions involving MCS-R2 reveals the presence of an additional enhancer element in the 5’ boundary region
Transcriptome-wide gene-gene interaction associations elucidate pathways and functional enrichment of complex traits
Canonical correlation analysis for multi-omics: Application to cross-cohort analysis
Correction: Suppression of class I compensated cell enlargement by xs2 mutation is mediated by salicylic acid signaling
Combining Mendelian randomization and network deconvolution for inference of causal networks with GWAS summary data

Genetics

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American Journal of Human Genetics

This month in The Journal
Kurt Hirschhorn (1926–2022)
Dissecting the polygenic basis of atherosclerosis via disease-associated cell state signatures
Fast and accurate Bayesian polygenic risk modeling with variational inference
Scalable mixed model methods for set-based association studies on large-scale categorical data analysis and its application to exome-sequencing data in UK Biobank
Bi-allelic variants in INTS11 are associated with a complex neurological disorder
SRSF1 haploinsufficiency is responsible for a syndromic developmental disorder associated with intellectual disability
POLR1A variants underlie phenotypic heterogeneity in craniofacial, neural, and cardiac anomalies
Autism-specific PTEN p.Ile135Leu variant and an autism genetic background combine to dysregulate cortical neurogenesis
De novo variants implicate chromatin modification, transcriptional regulation, and retinoic acid signaling in syndromic craniosynostosis

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