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2014
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2025
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2024
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A syndromic neurodevelopmental disorder caused by rare variants in PPFIA3.
Not available
S-EPMC10806447
|
biostudies-literature
Cite
A large-scale assessment of two-way SNP interactions in breast cancer susceptibility using 46,450 cases and 42,461 controls from the breast cancer association consortium.
Not available
S-EPMC3943524
|
biostudies-literature
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The somatic genomic landscape of chromophobe renal cell carcinoma.
Not available
S-EPMC4160352
|
biostudies-literature
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Common non-synonymous SNPs associated with breast cancer susceptibility: findings from the Breast Cancer Association Consortium.
Not available
S-EPMC4204770
|
biostudies-literature
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Identification of independent association signals and putative functional variants for breast cancer risk through fine-scale mapping of the 12p11 locus.
Not available
S-EPMC4962376
|
biostudies-literature
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Partial Loss of USP9X Function Leads to a Male Neurodevelopmental and Behavioral Disorder Converging on Transforming Growth Factor β Signaling.
Not available
S-EPMC6925349
|
biostudies-literature
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A second update on mapping the human genetic architecture of COVID-19.
Not available
S-EPMC10482689
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biostudies-literature
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Elliptic anisotropy measurement of the f<sub>0</sub>(980) hadron in proton-lead collisions and evidence for its quark-antiquark composition.
Not available
S-EPMC12391314
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biostudies-literature
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Search for heavy neutrinos and [Formula: see text] bosons with right-handed couplings in proton-proton collisions at [Formula: see text].
Not available
S-EPMC4371073
|
biostudies-literature
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Measurement of the differential cross section for top quark pair production in pp collisions at [Formula: see text].
Not available
S-EPMC4657759
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biostudies-literature
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