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UnknownUnderstanding the origin of Paris Agreement emission uncertainties.
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S-EPMC5467211 | biostudies-literature
UnknownGWAS meta-analysis of over 29,000 people with epilepsy identifies 26 risk loci and subtype-specific genetic architecture.
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S-EPMC10484785 | biostudies-literature
UnknownGain-of-function and loss-of-function variants in GRIA3 lead to distinct neurodevelopmental phenotypes.
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S-EPMC11068105 | biostudies-literature
UnknownDominant variants in major spliceosome U4 and U5 small nuclear RNA genes cause neurodevelopmental disorders through splicing disruption.
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S-EPMC12165858 | biostudies-literature
UnknownExome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypes.
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S-EPMC11646479 | biostudies-literature
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