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UnknownChildhood intelligence is heritable, highly polygenic and associated with FNBP1L.
Not available
S-EPMC3935975 | biostudies-literature
UnknownAustralian Genomics: Outcomes of a 5-year national program to accelerate the integration of genomics in healthcare.
Not available
S-EPMC10027474 | biostudies-literature
UnknownGenetic variation in the 15q25 nicotinic acetylcholine receptor gene cluster (CHRNA5-CHRNA3-CHRNB4) interacts with maternal self-reported smoking status during pregnancy to influence birth weight.
Not available
S-EPMC3516066 | biostudies-literature
UnknownShariant platform: Enabling evidence sharing across Australian clinical genetic-testing laboratories to support variant interpretation.
Not available
S-EPMC9674965 | biostudies-literature
UnknownNovel risk loci for COVID-19 hospitalization among admixed American populations.
Not available
S-EPMC11449485 | biostudies-literature
UnknownEstimation and partitioning of (co)heritability of inflammatory bowel disease from GWAS and immunochip data.
Not available
S-EPMC4119411 | biostudies-literature
UnknownA multitiered analysis platform for genome sequencing: Design and initial findings of the Australian Genomics Cardiovascular Disorders Flagship.
Not available
S-EPMC11613726 | biostudies-literature
UnknownTCTEX1D2 mutations underlie Jeune asphyxiating thoracic dystrophy with impaired retrograde intraflagellar transport.
Not available
S-EPMC4468853 | biostudies-literature
UnknownTiming, rates and spectra of human germline mutation.
Not available
S-EPMC4731925 | biostudies-literature
UnknownMutations in GDP-mannose pyrophosphorylase B cause congenital and limb-girdle muscular dystrophies associated with hypoglycosylation of α-dystroglycan.
Not available
S-EPMC3710768 | biostudies-literature
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