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UnknownLIN28A loss-of-function is associated with Parkinson's disease pathogenesis
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S-SCDT-EMBOJ-2018-101196 | biostudies-other
UnknownThe Type 2 Diabetes Knowledge Portal: An open access genetic resource dedicated to type 2 diabetes and related traits.
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S-EPMC10231654 | biostudies-literature
UnknownDe novo mutations across 1,465 diverse genomes reveal mutational insights and reductions in the Amish founder population.
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S-EPMC7007577 | biostudies-literature
UnknownThe Surface-Topography Challenge: A Multi-Laboratory Benchmark Study to Advance the Characterization of Topography.
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S-EPMC12296861 | biostudies-literature
UnknownMulti-ancestry polygenic risk scores for the prediction of type 2 diabetes and complications in diverse ancestries.
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S-EPMC12330429 | biostudies-literature
UnknownMulti-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation.
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S-EPMC9179018 | biostudies-literature
UnknownMulti-ancestry genome-wide study in >2.5 million individuals reveals heterogeneity in mechanistic pathways of type 2 diabetes and complications.
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S-EPMC10081410 | biostudies-literature
UnknownGuidelines for the use and interpretation of assays for monitoring autophagy (3rd edition).
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S-EPMC4835977 | biostudies-literature
UnknownGenetic drivers of heterogeneity in type 2 diabetes pathophysiology.
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S-EPMC10937372 | biostudies-literature
UnknownImplicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis.
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S-EPMC9793579 | biostudies-literature
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