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51. A genome-wide meta-analysis uncovers six sequence variants conferring risk of vertigo

52. Genetic variants associated with platelet count are predictive of human disease and physiological markers

53. Predicting the probability of death using proteomics

54. Lipoprotein(a) Concentration and Risks of Cardiovascular Disease and Diabetes

56. Combining Polygenic and Proteomic Risk Scores With Clinical Risk Factors to Improve Performance for Diagnosing Absence of Coronary Artery Disease in Patients With De Novo Chest Pain

57. Evaluation of Large-Scale Proteomics for Prediction of Cardiovascular Events

58. Discovery and refinement of loci associated with lipid levels

59. Common variants associated with plasma triglycerides and risk for coronary artery disease

60. Insights into imprinting from parent-of-origin phased methylomes and transcriptomes

61. Predicted loss and gain of function mutations in ACO1 are associated with erythropoiesis

62. Genome-wide association identifies seven loci for pelvic organ prolapse in Iceland and the UK Biobank

63. RANTES/CCL5 and Risk for Coronary Events: Results from the MONICA/KORA Augsburg Case-Cohort, Athero-Express and CARDIoGRAM Studies

64. Screening for Rare Coding Variants That Associate With the QTc Interval in Iceland

65. Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction

66. Genetic Variants Close to TTN , NKX2-5 , and MYH6 Associate With AVNRT

67. Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants

68. Biobank-driven genomic discovery yields new insight into atrial fibrillation biology

69. Polygenic risk score for ACE-inhibitor-associated cough based on the discovery of new genetic loci

70. Evaluation of Large-Scale Proteomics for Prediction of Cardiovascular Events

71. Genetic variants associated with syncope implicate neural and autonomic processes

73. Sequence variants with large effects on cardiac electrophysiology and disease

74. Publisher Correction: GWAS of bone size yields twelve loci that also affect height, BMD, osteoarthritis or fractures

75. GWAS of bone size yields twelve loci that also affect height, BMD, osteoarthritis or fractures

76. A PRPH splice-donor variant associates with reduced sural nerve amplitude and risk of peripheral neuropathy

77. Sequence variation at ANAPC1 accounts for 24% of the variability in corneal endothelial cell density

79. Genome-wide association meta-analysis yields 20 loci associated with gallstone disease

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

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

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

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

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

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

86. Cholesterol not particle concentration mediates the atherogenic risk conferred by apolipoprotein B particles:A Mendelian randomization analysis

87. Thirty novel sequence variants impacting human intracranial volume

89. A homozygous loss-of-function mutation leading to CYBC1 deficiency causes chronic granulomatous disease

90. Exome-chip meta-analysis identifies novel loci associated with cardiac conduction, including ADAMTS6

91. Coding variants in RPL3L and MYZAP increase risk of atrial fibrillation

92. A truncating mutation in EPOR leads to hypo-responsiveness to erythropoietin with normal haemoglobin

93. A rare missense variant in NR1H4 associates with lower cholesterol levels

94. Variant ASGR1 Associated with a Reduced Risk of Coronary Artery Disease

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

96. Symptoms, physical measures and cognitive tests after SARS-CoV-2 infection in a large population-based case-control study

97. Large-scale comparison of immunoassay- and aptamer-based plasma proteomics through genetics and disease

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

99. A genome-wide meta-analysis yields 46 new loci associating with biomarkers of iron homeostasis

100. Cohort profile: Copenhagen Hospital Biobank - Cardiovascular Disease Cohort (CHB-CVDC): Construction of a large-scale genetic cohort to facilitate a better understanding of heart diseases

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