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UnknownMosaic epigenetic dysregulation of ectodermal cells in autism spectrum disorder.
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S-EPMC4038484 | biostudies-literature
UnknownLRRTM1 on chromosome 2p12 is a maternally suppressed gene that is associated paternally with handedness and schizophrenia.
Not available
S-EPMC2990633 | biostudies-literature
UnknownValidation of a host blood transcriptomic biomarker for pulmonary tuberculosis in people living with HIV: a prospective diagnostic and prognostic accuracy study.
Not available
S-EPMC8131200 | biostudies-literature
UnknownDesign features of the Diabetes and Periodontal Therapy Trial (DPTT): a multicenter randomized single-masked clinical trial testing the effect of nonsurgical periodontal therapy on glycosylated hemoglobin (HbA1c) levels in subjects with type 2 diabetes and chronic periodontitis.
Not available
S-EPMC3885354 | biostudies-literature
UnknownA genome-wide scan for common alleles affecting risk for autism.
Not available
S-EPMC2947401 | biostudies-literature
UnknownRationale and design of the Renal Lifecycle trial assessing the effect of dapagliflozin on cardiorenal outcomes in severe chronic kidney disease.
Not available
S-EPMC12394133 | biostudies-literature
UnknownA novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder.
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S-EPMC3303079 | biostudies-literature
UnknownGene-ontology enrichment analysis in two independent family-based samples highlights biologically plausible processes for autism spectrum disorders.
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S-EPMC3190264 | biostudies-literature
UnknownPrehospital use of magnesium sulfate as neuroprotection in acute stroke.
Not available
S-EPMC4920545 | biostudies-literature
UnknownCharacterizing prostate cancer risk through multi-ancestry genome-wide discovery of 187 novel risk variants.
Not available
S-EPMC10841479 | biostudies-literature
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