about
Investigation of variants identified in caucasian genome-wide association studies for plasma high-density lipoprotein cholesterol and triglycerides levels in Mexican dyslipidemic study samplesMutations in LMF1 cause combined lipase deficiency and severe hypertriglyceridemiaIdentification of two common variants contributing to serum apolipoprotein B levels in Mexicans.Amerindian-specific regions under positive selection harbour new lipid variants in Latinos.Genetic variation at the proprotein convertase subtilisin/kexin type 5 gene modulates high-density lipoprotein cholesterol levelsGenetic causes of high and low serum HDL-cholesterol.Adipose co-expression networks across Finns and Mexicans identify novel triglyceride-associated genes.Association of stearoyl-CoA desaturase 1 activity with familial combined hyperlipidemia.Evidence of how rs7575840 influences apolipoprotein B-containing lipid particles.The WWOX gene modulates high-density lipoprotein and lipid metabolism.The N342S MYLIP polymorphism is associated with high total cholesterol and increased LDL receptor degradation in humans.Whole-Genome Sequencing Analysis from the Chikungunya Virus Caribbean Outbreak Reveals Novel Evolutionary Genomic ElementsTransgenic expression and genetic variation of Lmf1 affect LPL activity in mice and humansActionable clinical decisions based on comprehensive genomic evaluation in asymptomatic adults.Exome sequencing identifies 2 rare variants for low high-density lipoprotein cholesterol in an extended familyWW-domain-containing oxidoreductase is associated with low plasma HDL-C levelsGalanin preproprotein is associated with elevated plasma triglycerides.Genomic study in Mexicans identifies a new locus for triglycerides and refines European lipid loci.Differential analysis of mutations in the Jewish population and their implications for diseases.Somatic Mosaicism for a "Lethal" GJB2 Mutation Results in a Patterned Form of Spiny Hyperkeratosis without Eccrine Involvement.Cancer risks in Jewish male BRCA1 and BRCA2 mutation carriers.The ATF6-Met[67]Val substitution is associated with increased plasma cholesterol levels.Common hepatic nuclear factor-4alpha variants are associated with high serum lipid levels and the metabolic syndrome.X-linked elliptocytosis with impaired growth is related to mutated AMMECR1.Corrigendum to "X-linked elliptocytosis with impaired growth is related to mutated AMMECR1" [Gene 606C (2017) 47-52].
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P50
name
Daphna Weissglas-Volkov
@ast
Daphna Weissglas-Volkov
@en
Daphna Weissglas-Volkov
@es
Daphna Weissglas-Volkov
@nl
type
label
Daphna Weissglas-Volkov
@ast
Daphna Weissglas-Volkov
@en
Daphna Weissglas-Volkov
@es
Daphna Weissglas-Volkov
@nl
prefLabel
Daphna Weissglas-Volkov
@ast
Daphna Weissglas-Volkov
@en
Daphna Weissglas-Volkov
@es
Daphna Weissglas-Volkov
@nl