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Human Genetics
Genomic signatures of the unjamming transition in compressed human bronchial epithelial cells
Article
Year: 2021
Pages: 1
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Characterizing dedifferentiation of thyroid cancer by integrated analysis
Article
Year: 2021
Pages: 1
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Using the PhenX Toolkit to Select Standard Measurement Protocols for Your Research Study
Article
Year: 2021
Pages: 1
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The PhenX Toolkit: Establishing Standard Measures for COVID‐19 Research
Article
Year: 2021
Pages: 1
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Cardiac cell type–specific gene regulatory programs and disease risk association
Article
Year: 2021
Pages: 1
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Pathogenic variants in
SMARCA5
, a chromatin remodeler, cause a range of syndromic neurodevelopmental features
Article
Year: 2021
Pages: 1
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Nuclear genome-wide associations with mitochondrial heteroplasmy
Article
Year: 2021
Pages: 1
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A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation
Article
Year: 2021
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Estimating
F
ST
and kinship for arbitrary population structures
Article
Year: 2021
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Genome-wide association analysis of Mexican bread wheat landraces for resistance to yellow and stem rust
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Year: 2021
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Molecular diversity of
Giardia duodenalis
in children under 5 years from the Manhiça district, Southern Mozambique enrolled in a matched case-control study on the aetiology of diarrhoea
Article
Year: 2021
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Human genome diversity data reveal that L564P is the predominant TPC2 variant and a prerequisite for the blond hair associated M484L gain-of-function effect
Article
Year: 2021
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The correlation of salivary telomere length and single nucleotide polymorphisms of the
ADIPOQ
,
SIRT1
and
FOXO3A
genes with lifestyle-related diseases in a Japanese population
Article
Year: 2021
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Influence of single nucleotide polymorphisms among cigarette smoking and non-smoking patients with coronary artery disease, urinary bladder cancer and lung cancer
Article
Year: 2021
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Copy number variants and fixed duplications among 198 rhesus macaques (
Macaca mulatta
)
Article
Year: 2020
Pages: 1
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ASEP: Gene-based detection of allele-specific expression across individuals in a population by RNA sequencing
Article
Year: 2020
Pages: 1
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Variants in
IL23R
-
C1orf141
and
ADO
-
ZNF365
-
EGR2
are associated with susceptibility to Vogt-Koyanagi-Harada disease in Japanese population
Article
Year: 2020
Pages: 1
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