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41 results on '"Wood, Andrew R."'

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1. Colorectal cancer risk stratification using a polygenic risk score in symptomatic patients presenting to primary care — a UK Biobank retrospective cohort study

3. Identification and analysis of individuals who deviate from their genetically-predicted phenotype

4. Monogenic causes of Premature Ovarian Insufficiency are rare and mostly recessive

5. The causal role of accelerometer-derived sleep traits on glycated haemoglobin: a Mendelian randomization study

6. Study of the associations between short telomeres, sex hormones and pulmonary fibrosis

7. Genomic insights into the mechanism of NK3R antagonists for treatment of menopausal vasomotor symptoms

8. The impact of Mendelian sleep and circadian genetic variants in a population setting

10. The penetrance of age-related monogenic disease depends on ascertainment context

11. Associations of genetic scores for birth weight with newborn size and later Anthropometric traits and cardiometabolic risk markers in South Asians

12. Assessing the causal role of sleep traits on glycated haemoglobin: a Mendelian randomization study

15. Differentially expressed genes reflect disease-induced rather than disease-causing changes in the transcriptome

16. The Trans-Ancestral Genomic Architecture of Glycaemic Traits

17. 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

19. Evidence that Telomere Length is Causal for Idiopathic Pulmonary Fibrosis but not Chronic Obstructive Pulmonary Disease: A Mendelian Randomisation Study

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

22. Is disrupted sleep a risk factor for Alzheimer’s disease? Evidence from a two-sample Mendelian randomization analysis

24. Investigating causal relationships between sleep traits and risk of breast cancer: a Mendelian randomization study

25. Genome-wide association analysis of excessive daytime sleepiness identifies 42 loci that suggest phenotypic subgroups

26. Assessing the pathogenicity, penetrance and expressivity of putative disease-causing variants in a population setting

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

28. GWAS in 446,118 European adults identifies 78 genetic loci for self-reported habitual sleep duration supported by accelerometer-derived estimates

29. Meta-analysis of genome-wide association studies for body fat distribution in 694,649 individuals of European ancestry

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

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

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

33. Mosaic Turner syndrome shows reduced phenotypic penetrance in an adult population study compared to clinically ascertained cases

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

35. Evidence that lower socioeconomic position accentuates genetic susceptibility to obesity

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

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

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

39. A reference panel of 64,976 haplotypes for genotype imputation

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

41. A reference panel of 64,976 haplotypes for genotype imputation

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