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UnknownA Recurrent De Novo Variant in NACC1 Causes a Syndrome Characterized by Infantile Epilepsy, Cataracts, and Profound Developmental Delay.
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S-EPMC5294886 | biostudies-literature
UnknownIRF2BPL Is Associated with Neurological Phenotypes.
Not available
S-EPMC6081494 | biostudies-literature
UnknownContribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects.
Not available
S-EPMC5737772 | biostudies-literature
UnknownGenome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses.
Not available
S-EPMC7808397 | biostudies-literature
UnknownGenome-wide association study of 398,238 women unveils seven loci associated with high-grade serous ovarian cancer.
Not available
S-EPMC12635163 | biostudies-literature
UnknownLarge-scale genome-wide association study of 398,238 women unveils seven novel loci associated with high-grade serous epithelial ovarian cancer risk.
Not available
S-EPMC10942532 | biostudies-literature
UnknownPredominantly Persistent Intraretinal Fluid in the Comparison of Age-related Macular Degeneration Treatments Trials.
Not available
S-EPMC10282893 | biostudies-literature
UnknownStereoacuity in children with anisometropic amblyopia.
Not available
S-EPMC3223370 | biostudies-literature
UnknownA case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers.
Not available
S-EPMC7890067 | biostudies-literature
UnknownAflibercept Monotherapy or Bevacizumab First for Diabetic Macular Edema.
Not available
S-EPMC9714135 | biostudies-literature
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