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UnknownRare and Coding Region Genetic Variants Associated With Risk of Ischemic Stroke: The NHLBI Exome Sequence Project.
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S-EPMC4673986 | biostudies-literature
UnknownRare and low-frequency variants and their association with plasma levels of fibrinogen, FVII, FVIII, and vWF.
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S-EPMC4566813 | biostudies-literature
UnknownMeta-analysis identifies common and rare variants influencing blood pressure and overlapping with metabolic trait loci.
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S-EPMC5320952 | biostudies-literature
UnknownInherited causes of clonal haematopoiesis in 97,691 whole genomes.
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S-EPMC7944936 | biostudies-literature
UnknownA framework for detecting noncoding rare-variant associations of large-scale whole-genome sequencing studies.
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S-EPMC10008172 | biostudies-literature
UnknownGenome-wide association analysis identifies ancestry-specific genetic variation associated with acute response to metformin and glipizide in SUGAR-MGH.
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S-EPMC10790310 | biostudies-literature
UnknownGuidelines for the use and interpretation of assays for monitoring autophagy (3rd edition).
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S-EPMC4835977 | biostudies-literature
UnknownGlobal, regional, and national progress towards Sustainable Development Goal 3.2 for neonatal and child health: all-cause and cause-specific mortality findings from the Global Burden of Disease Study 2019.
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S-EPMC8429803 | biostudies-literature
UnknownGlobal incidence, prevalence, years lived with disability (YLDs), disability-adjusted life-years (DALYs), and healthy life expectancy (HALE) for 371 diseases and injuries in 204 countries and territories and 811 subnational locations, 1990-2021: a systematic analysis for the Global Burden of Disease Study 2021.
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S-EPMC11122111 | biostudies-literature
UnknownAnemia prevalence in women of reproductive age in low- and middle-income countries between 2000 and 2018.
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S-EPMC8516651 | biostudies-literature
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