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A Recurrent De Novo Variant in NACC1 Causes a Syndrome Characterized by Infantile Epilepsy, Cataracts, and Profound Developmental Delay.
Not available
S-EPMC5294886
|
biostudies-literature
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Results of the two incidence screenings in the National Lung Screening Trial.
Not available
S-EPMC4307922
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biostudies-literature
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Comparative host-coronavirus protein interaction networks reveal pan-viral disease mechanisms.
Not available
S-EPMC7808408
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biostudies-literature
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The predictive ability of the 313 variant-based polygenic risk score for contralateral breast cancer risk prediction in women of European ancestry with a heterozygous BRCA1 or BRCA2 pathogenic variant.
Not available
S-EPMC8460445
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biostudies-literature
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Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses.
Not available
S-EPMC7808397
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biostudies-literature
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Fine-mapping of 150 breast cancer risk regions identifies 191 likely target genes.
Not available
S-EPMC6974400
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biostudies-literature
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A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers.
Not available
S-EPMC7890067
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biostudies-literature
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Transcriptome-wide association study of breast cancer risk by estrogen-receptor status.
Not available
S-EPMC7987299
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biostudies-literature
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Identification of six new susceptibility loci for invasive epithelial ovarian cancer.
Not available
S-EPMC4445140
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biostudies-literature
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Genome-wide association and transcriptome studies identify target genes and risk loci for breast cancer.
Not available
S-EPMC6465407
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biostudies-literature
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