Rxivist combines preprints from bioRxiv with data from Twitter to help you find the papers being discussed in your field. Currently indexing 63,068 bioRxiv papers from 279,747 authors.

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Preprints

Genome-wide association analyses of chronotype in 697,828 individuals provides new insights into circadian rhythms in humans and links to disease

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  • In genetics: 231 out of 3,574
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  • Site-wide: 4,104 out of 63,068
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  • Site-wide: 14,134 out of 63,068

Genome-wide association analyses in >119,000 individuals identifies thirteen morningness and two sleep duration loci

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  • In genetics: 328 out of 3,574
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Mosaic Turner syndrome shows reduced phenotypic penetrance in an adult population study compared to clinically ascertained cases

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  • In genetics: 459 out of 3,574
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  • Site-wide: 6,213 out of 63,068
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  • Site-wide: 8,932 out of 63,068

HUMAN LONGEVITY IS INFLUENCED BY MANY GENETIC VARIANTS: EVIDENCE FROM 75,000 UK BIOBANK PARTICIPANTS

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  • In genomics: 982 out of 4,328
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Genomic analyses for age at menarche identify 389 independent signals and indicate BMI-independent effects of puberty timing on cancer susceptibility

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  • In genomics: 1,015 out of 4,328
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  • Site-wide: 40,498 out of 63,068
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  • Site-wide: 38,513 out of 63,068

Genome-wide association study of offspring birth weight in 86,577 women highlights maternal genetic effects that are independent of fetal genetics

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  • In genetics: 545 out of 3,574
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  • Site-wide: 40,237 out of 63,068
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  • Site-wide: 31,185 out of 63,068

Genetic studies of accelerometer-based sleep measures in 85,670 individuals yield new insights into human sleep behaviour

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  • In genetics: 548 out of 3,574
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  • Site-wide: 10,656 out of 63,068
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  • Site-wide: 16,218 out of 63,068

Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors

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  • In genetics: 565 out of 3,574
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Genetic predisposition to mosaic Y chromosome loss in blood is associated with genomic instability in other tissues and susceptibility to non-haematological cancers

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  • In genetics: 594 out of 3,574
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  • Site-wide: 1,609 out of 63,068
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  • Site-wide: 4,503 out of 63,068

GWAS identifies novel risk locus for erectile dysfunction and implicates hypothalamic neurobiology and diabetes in etiology

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  • In genomics: 1,480 out of 4,328
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  • Site-wide: 14,692 out of 63,068
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  • Site-wide: 58,190 out of 63,068

Red Blood Cell Distribution Width: genetic evidence for aging pathways in 116,666 volunteers

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  • In genomics: 1,485 out of 4,328
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  • Site-wide: 50,310 out of 63,068

A common allele in FGF21 associated with preference for sugar consumption lowers body fat in the lower body and increases blood pressure

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  • In genetics: 838 out of 3,574
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  • Site-wide: 27,936 out of 63,068
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  • Site-wide: 35,893 out of 63,068

Quantifying the extent to which index event biases influence large genetic association studies

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  • In genetics: 1,052 out of 3,574
• Year to date:
  • Site-wide: 54,633 out of 63,068
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  • Site-wide: 42,813 out of 63,068

Evidence that low socioeconomic position accentuates genetic susceptibility to obesity

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  • In genetics: 1,177 out of 3,574
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  • Site-wide: 58,013 out of 63,068
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  • Site-wide: 48,459 out of 63,068

Genetic evidence that lower circulating FSH levels lengthen menstrual cycle, increase age at menopause, and impact reproductive health: a UK Biobank study

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  • Site-wide: 19,023 out of 63,068
  • In genetics: 1,272 out of 3,574
• Year to date:
  • Site-wide: 45,483 out of 63,068
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  • Site-wide: 42,246 out of 63,068

Variants in the FTO and CDKAL1 loci have recessive effects on risk of obesity and type 2 diabetes respectively

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  • In genetics: 1,678 out of 3,574
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  • Site-wide: 50,299 out of 63,068
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  • Site-wide: 53,021 out of 63,068

Genome-wide association study of anti-Mullerian hormone levels in pre-menopausal women of late reproductive age and relationship with genetic determinants of reproductive lifespan

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  • Site-wide: 37,355 out of 63,068
  • In genomics: 3,341 out of 4,328
• Year to date:
  • Site-wide: 23,505 out of 63,068
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  • Site-wide: 22,277 out of 63,068