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UnknownYY1 Haploinsufficiency Causes an Intellectual Disability Syndrome Featuring Transcriptional and Chromatin Dysfunction.
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S-EPMC5473733 | biostudies-literature
UnknownEarly trajectories of virological and immunological biomarkers and clinical outcomes in patients admitted to hospital for COVID-19: an international, prospective cohort study.
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S-EPMC11181148 | biostudies-literature
UnknownIntegrated analysis of environmental and genetic influences on cord blood DNA methylation in new-borns.
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S-EPMC6559955 | biostudies-literature
UnknownIdentifying the Common Genetic Basis of Antidepressant Response.
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S-EPMC9117153 | biostudies-literature
UnknownLoss-of-function mutations in SLC30A8 protect against type 2 diabetes.
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S-EPMC4051628 | biostudies-literature
UnknownGenome-wide association study of borderline personality disorder identifies 11 loci and highlights shared risk with mental and somatic disorders.
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S-EPMC12363718 | biostudies-literature
UnknownAn original phylogenetic approach identified mitochondrial haplogroup T1a1 as inversely associated with breast cancer risk in BRCA2 mutation carriers.
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S-EPMC4478717 | biostudies-literature
UnknownDNA glycosylases involved in base excision repair may be associated with cancer risk in BRCA1 and BRCA2 mutation carriers.
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S-EPMC3974638 | biostudies-literature
UnknownEffect of remote ischaemic conditioning on clinical outcomes in patients with acute myocardial infarction (CONDI-2/ERIC-PPCI): a single-blind randomised controlled trial.
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S-EPMC6891239 | biostudies-literature
UnknownGenome-wide association study in BRCA1 mutation carriers identifies novel loci associated with breast and ovarian cancer risk.
Not available
S-EPMC3609646 | biostudies-literature
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