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UnknownDisease characteristics of MCT8 deficiency: an international, retrospective, multicentre cohort study.
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S-EPMC7611932 | biostudies-literature
UnknownMapping variants in thyroid hormone transporter MCT8 to disease severity by genomic, phenotypic, functional, structural and deep learning integration.
Not available
S-EPMC11904026 | biostudies-literature
UnknownGWAS and meta-analysis identifies 49 genetic variants underlying critical COVID-19.
Not available
S-EPMC10208981 | biostudies-literature
UnknownGenetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits.
Not available
S-EPMC6284793 | biostudies-literature
UnknownNovel Blood Pressure Locus and Gene Discovery Using Genome-Wide Association Study and Expression Data Sets From Blood and the Kidney.
Not available
S-EPMC5783787 | biostudies-literature
UnknownLow-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility.
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S-EPMC4311266 | biostudies-literature
UnknownAssociation Between Telomere Length and Risk of Cancer and Non-Neoplastic Diseases: A Mendelian Randomization Study.
Not available
S-EPMC5638008 | biostudies-literature
UnknownMulti-ancestry genome-wide study in >2.5 million individuals reveals heterogeneity in mechanistic pathways of type 2 diabetes and complications.
Not available
S-EPMC10081410 | biostudies-literature
UnknownGenetic drivers of heterogeneity in type 2 diabetes pathophysiology.
Not available
S-EPMC10937372 | biostudies-literature
UnknownConservative Oxygen Therapy in Mechanically Ventilated Critically Ill Adult Patients: The UK-ROX Randomized Clinical Trial.
Not available
S-EPMC12163715 | biostudies-literature
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