Author: Robin Beaumont

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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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Biological and clinical insights from genetics of insomnia symptoms

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  • In genomics: 825
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Genome-wide association analyses in >119,000 individuals identifies thirteen morningness and two sleep duration loci

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

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  • Site-wide: 13,442
  • In genetics: 630
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Genetic studies of accelerometer-based sleep measures in 85,670 individuals yield new insights into human sleep behaviour

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

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

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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: 36,349
  • In genetics: 1,699
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Evidence that telomere length is causal for Idiopathic Pulmonary Fibrosis but not Chronic Obstructive Pulmonary Disease: A Mendelian Randomisation Study

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  • Site-wide: 38,391
  • In respiratory medicine: 88
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Evidence that low socioeconomic position accentuates genetic susceptibility to obesity

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Evidence of a common causal relationship between body mass index and inflammatory skin disease: a Mendelian Randomization study

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Variants in the fetal genome near pro-inflammatory cytokine genes on 2q13 are associated with gestational duration

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A genome wide association study of frozen shoulder identifies a common variant of WNT7B and diabetes as causal risk factors

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  • In orthopedics: 26
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Maternal and fetal genetic contribution to gestational weight gain

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Higher maternal adiposity reduces offspring birth weight if associated with a metabolically favourable profile

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  • Site-wide: 114,057
  • In genetic and genomic medicine: 565
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Common maternal and fetal genetic variants show expected polygenic effects on the probability of being born small- or large-for-gestational-age (SGA or LGA), except in the smallest 3% of babies

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A Mendelian randomisation study of smoking causality in IPF compared with COPD

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Fetal alleles predisposing to metabolically favourable adiposity are associated with higher birth weight

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  • Site-wide: 104,990

Common genetic variants with fetal effects on birth weight are enriched for proximity to genes implicated in rare developmental disorders

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