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Homo sapiens
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Genetic effects on liver chromatin accessibility identify disease regulatory variants.
Not available
S-EPMC8323023
|
biostudies-literature
Cite
Genetic Variants Associated With Hidradenitis Suppurativa.
Not available
S-EPMC10372759
|
biostudies-literature
Cite
Allelic Heterogeneity at the CRP Locus Identified by Whole-Genome Sequencing in Multi-ancestry Cohorts.
Not available
S-EPMC7042494
|
biostudies-literature
Cite
Genomic loci and molecular genetic mechanisms for hidradenitis suppurativa.
Not available
S-EPMC12279254
|
biostudies-literature
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Sequence data and association statistics from 12,940 type 2 diabetes cases and controls.
Not available
S-EPMC5735917
|
biostudies-literature
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Genome-wide Association Study of Platelet Count Identifies Ancestry-Specific Loci in Hispanic/Latino Americans.
Not available
S-EPMC4746331
|
biostudies-literature
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Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility.
Not available
S-EPMC4311266
|
biostudies-literature
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Population-scale skeletal muscle single-nucleus multi-omic profiling reveals extensive context specific genetic regulation.
Not available
S-EPMC10760134
|
biostudies-literature
Cite
Variants in MTNR1B influence fasting glucose levels.
Not available
S-EPMC2682768
|
biostudies-literature
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Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci.
Not available
S-EPMC8960770
|
biostudies-literature
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