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Genome-wide association study of 40,000 individuals identifies two novel loci associated with bipolar disorder
Oxford University Press | 2016| -
Effect of genetic background on the dystrophic phenotype in mdx mice
Oxford University Press | 2016| -
Landscape of DNA methylation on the X chromosome reflects CpG density, functional chromatin state and X-chromosome inactivation
Oxford University Press | 2015| -
Shorter telomere length in Europeans than in Africans due to polygenetic adaptation
Oxford University Press | 2016| -
Whole exome sequencing identifies lncRNA GAS8-AS1 and LPAR4 as novel papillary thyroid carcinoma driver alternations
Oxford University Press | 2016| -
Two classes of ovarian primordial follicles exhibit distinct developmental dynamics and physiological functions
Oxford University Press | 2014| -
Poly-dipeptides encoded by the C9ORF72 repeats block global protein translation
Oxford University Press | 2016| -
TRIO loss of function is associated with mild intellectual disability and affects dendritic branching and synapse function
Oxford University Press | 2016| -
Nucleolar stress and impaired stress granule formation contribute to C9orf72 RAN translation-induced cytotoxicity
Oxford University Press | 2015| -
The Werner syndrome RECQ helicase targets G4 DNA in human cells to modulate transcription
Oxford University Press | 2016| -
PARK2 enhancement is able to compensate mitophagy alterations found in sporadic Alzheimer's disease
Oxford University Press | 2016| -
Reduced cholesterol levels impair Smoothened activation in Smith-Lemli-Opitz syndrome
Oxford University Press | 2016| -
Deleterious mutations in the essential mRNA metabolism factor, hGle1, in amyotrophic lateral sclerosis
Oxford University Press | 2015| -
A recurrent p.Arg92Trp variant in steroidogenic factor-1 (NR5A1) can act as a molecular switch in human sex development
Oxford University Press | 2016| -
Genome-wide association study in Chinese identifies novel loci for blood pressure and hypertension
Oxford University Press | 2015| -
Haploinsufficiency of RCBTB1 is associated with Coats disease and familial exudative vitreoretinopathy
Oxford University Press | 2016| -
A novel missense variant in PRKCB segregates low-frequency hearing loss in an autosomal dominant family with Menieres disease
Oxford University Press | 2016| -
The PINK1, synphilin-1 and SIAH-1 complex constitutes a novel mitophagy pathway
Oxford University Press | 2016|
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