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51. Loci for insulin processing and secretion provide insight into type 2 diabetes risk.

52. Loci for insulin processing and secretion provide insight into type 2 diabetes risk

53. Using Mendelian Randomisation methods to understand whether diurnal preference is causally related to mental health

54. Genome-wide association analysis of self-reported daytime sleepiness identifies 42 loci that suggest biological subtypes

55. Genetic studies of accelerometer-based sleep measures yield new insights into human sleep behaviour

56. Genome-wide association study identifies genetic loci for self-reported habitual sleep duration supported by accelerometer-derived estimates

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

58. Loci for insulin processing and secretion provide insight into type 2 diabetes risk

60. Additional file 26 of Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis

61. Additional file 34 of Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis

62. Additional file 16 of Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis

63. Author Correction : The power of genetic diversity in genome-wide association studies of lipids

64. Additional file 6 of Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis

65. Additional file 9 of Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis

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

67. Reduced penetrance of MODY-associated HNF1A/HNF4A variants but not GCK variants in clinically unselected cohorts

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

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

70. Recurrent 17q12 microduplications contribute to renal disease but not diabetes

71. Detection and characterization of male sex chromosome abnormalities in the UK Biobank study

72. Identification and single-base gene-editing functional validation of a cis-EPO variant as a genetic predictor for EPO-increasing therapies

74. Response to Prakash et al.

75. Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity

76. The genetic architecture of type 2 diabetes

79. Identification and single-base gene-editing functional validation of a cis-EPO variant as a genetic predictor for EPO-increasing therapies

80. Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis

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

82. Association of maternal circulating 25(OH)D and calcium with birth weight: A mendelian randomisation analysis

83. Evidence of a causal relationship between body mass index and psoriasis: A mendelian randomization study

84. Recurrent 17q12 microduplications contribute to renal disease but not diabetes.

85. Prevalence of Fabry disease-causing variants in the UK Biobank.

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

87. Assessing the Causal Role of Sleep Traits on Glycated Hemoglobin: A Mendelian Randomization Study

89. Corrigendum to: A genome-wide association study implicates multiple mechanisms influencing raised urinary albumin–creatinine ratio

91. Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity

92. Babies of South Asian and European Ancestry Show Similar Associations with Genetic Risk Score for Birth Weight Despite the Smaller Size of South Asian Newborns

93. Babies of South Asian and European Ancestry Show Similar Associations With Genetic Risk Score for Birth Weight Despite the Smaller Size of South Asian Newborns

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

96. Fetal alleles predisposing to metabolically favorable adiposity are associated with higher birth weight

97. Author response: Disease consequences of higher adiposity uncoupled from its adverse metabolic effects using Mendelian randomisation

98. Another explanation for apparent epistasis

99. Genetic Evidence for Causal Relationships Between Maternal Obesity-Related Traits and Birth Weight

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