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APOL1 renal risk variants are associated with obesity and body composition in African ancestry adults: An observational genotype-phenotype association study.
Not available
S-EPMC8589256
|
biostudies-literature
Cite
Effects of Testing and Disclosing Ancestry-Specific Genetic Risk for Kidney Failure on Patients and Health Care Professionals: A Randomized Clinical Trial.
Not available
S-EPMC8897752
|
biostudies-literature
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Survival Following Relapse in Children with Acute Myeloid Leukemia: A Report from AML-BFM and COG.
Not available
S-EPMC8151466
|
biostudies-literature
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Genome-Wide Epistatic Interaction between
DEF1B
and
APOL1
High-Risk Genotypes for Chronic Kidney Disease.
Not available
S-EPMC9528279
|
biostudies-literature
Cite
Biallelic MADD variants cause a phenotypic spectrum ranging from developmental delay to a multisystem disorder.
Not available
S-EPMC7447524
|
biostudies-literature
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PURA syndrome: clinical delineation and genotype-phenotype study in 32 individuals with review of published literature.
Not available
S-EPMC5800346
|
biostudies-literature
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Trans-ethnic analysis of metabochip data identifies two new loci associated with BMI.
Not available
S-EPMC5876082
|
biostudies-literature
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Targeted deep sequencing identifies mosaicism in patients with immune dysregulation.
Not available
S-EPMC12916128
|
biostudies-literature
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CAF hierarchy driven by pancreatic cancer cell p53-status creates a pro-metastatic and chemoresistant environment via perlecan.
Not available
S-EPMC6691013
|
biostudies-literature
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Deleterious, protein-altering variants in the transcriptional coregulator ZMYM3 in 27 individuals with a neurodevelopmental delay phenotype.
Not available
S-EPMC9943726
|
biostudies-literature
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