List of works - Daphna Weissglas-Volkov

Actionable clinical decisions based on comprehensive genomic evaluation in asymptomatic adults

scientific article

Adipose co-expression networks across Finns and Mexicans identify novel triglyceride-associated genes

scientific article

Amerindian-specific regions under positive selection harbour new lipid variants in Latinos

scientific article

Analysis of microRNAs in familial Mediterranean fever.

scientific article

Association of stearoyl-CoA desaturase 1 activity with familial combined hyperlipidemia

scientific article

Cancer risks in Jewish male BRCA1 and BRCA2 mutation carriers

scientific article published on 19 March 2015

Common hepatic nuclear factor-4alpha variants are associated with high serum lipid levels and the metabolic syndrome

scientific article published on July 2006

Comparison of breast cancer metastasis models reveals a possible mechanism of tumor aggressiveness

scholarly article by Nir Pillar et al published 10 October 2018 in Cell Death and Disease

Corrigendum to "X-linked elliptocytosis with impaired growth is related to mutated AMMECR1" [Gene 606C (2017) 47-52].

scientific article published on 23 November 2017

Differential analysis of mutations in the Jewish population and their implications for diseases.

scientific article published on 15 May 2017

Evidence of how rs7575840 influences apolipoprotein B-containing lipid particles

scientific article

Exome sequencing identifies 2 rare variants for low high-density lipoprotein cholesterol in an extended family

scientific article

Galanin preproprotein is associated with elevated plasma triglycerides

scientific article

Genetic causes of high and low serum HDL-cholesterol

scientific article

Genetic variation at the proprotein convertase subtilisin/kexin type 5 gene modulates high-density lipoprotein cholesterol levels

scientific article

Genomic study in Mexicans identifies a new locus for triglycerides and refines European lipid loci

scientific article published on 15 March 2013

Identification of two common variants contributing to serum apolipoprotein B levels in Mexicans

scientific article

Investigation of variants identified in caucasian genome-wide association studies for plasma high-density lipoprotein cholesterol and triglycerides levels in Mexican dyslipidemic study samples

scientific article

Local microRNA delivery targets Palladin and prevents metastatic breast cancer.

scientific article published on 19 September 2016

Loss of Protocadherin-12 Leads to Diencephalic-Mesencephalic Junction Dysplasia Syndrome.

scientific article published on 4 October 2018

Mutations in LMF1 cause combined lipase deficiency and severe hypertriglyceridemia

scientific journal article

Mutations in TSPEAR, Encoding a Regulator of Notch Signaling, Affect Tooth and Hair Follicle Morphogenesis.

scientific article

Phenotypic suppression of acral peeling skin syndrome in a patient with autosomal recessive congenital ichthyosis

scientific article published on 02 July 2020

Somatic Mosaicism for a "Lethal" GJB2 Mutation Results in a Patterned Form of Spiny Hyperkeratosis without Eccrine Involvement

scientific article published on 18 April 2016

The ATF6-Met[67]Val substitution is associated with increased plasma cholesterol levels

scientific article published on 10 August 2009

The N342S MYLIP polymorphism is associated with high total cholesterol and increased LDL receptor degradation in humans

scientific article

The WWOX gene modulates high-density lipoprotein and lipid metabolism

scientific article

The risk for developing cancer in Israeli ATM, BLM, and FANCC heterozygous mutation carriers.

scientific article published on 22 December 2015

Transgenic expression and genetic variation of Lmf1 affect LPL activity in mice and humans

scientific article published on 16 February 2012

USF1 contributes to high serum lipid levels in Dutch FCHL families and U.S. whites with coronary artery disease

scientific article published on 02 August 2007

WW-domain-containing oxidoreductase is associated with low plasma HDL-C levels

scientific article published on August 2008

Whole-Genome Sequencing Analysis from the Chikungunya Virus Caribbean Outbreak Reveals Novel Evolutionary Genomic Elements

scientific article published on 25 January 2016

Whole-exome sequencing in individuals with multiple cardiovascular risk factors and normal coronary arteries

scientific article published on 01 June 2016

X-linked elliptocytosis with impaired growth is related to mutated AMMECR1.

scientific article published on 9 January 2017

List of works by Daphna Weissglas-Volkov

Actionable clinical decisions based on comprehensive genomic evaluation in asymptomatic adults

Adipose co-expression networks across Finns and Mexicans identify novel triglyceride-associated genes

Amerindian-specific regions under positive selection harbour new lipid variants in Latinos

Analysis of microRNAs in familial Mediterranean fever.

Association of stearoyl-CoA desaturase 1 activity with familial combined hyperlipidemia

Cancer risks in Jewish male BRCA1 and BRCA2 mutation carriers

Common hepatic nuclear factor-4alpha variants are associated with high serum lipid levels and the metabolic syndrome

Comparison of breast cancer metastasis models reveals a possible mechanism of tumor aggressiveness

Corrigendum to "X-linked elliptocytosis with impaired growth is related to mutated AMMECR1" [Gene 606C (2017) 47-52].

Differential analysis of mutations in the Jewish population and their implications for diseases.

Evidence of how rs7575840 influences apolipoprotein B-containing lipid particles

Exome sequencing identifies 2 rare variants for low high-density lipoprotein cholesterol in an extended family

Galanin preproprotein is associated with elevated plasma triglycerides

Genetic causes of high and low serum HDL-cholesterol

Genetic variation at the proprotein convertase subtilisin/kexin type 5 gene modulates high-density lipoprotein cholesterol levels

Genomic study in Mexicans identifies a new locus for triglycerides and refines European lipid loci

Identification of two common variants contributing to serum apolipoprotein B levels in Mexicans

Investigation of variants identified in caucasian genome-wide association studies for plasma high-density lipoprotein cholesterol and triglycerides levels in Mexican dyslipidemic study samples

Local microRNA delivery targets Palladin and prevents metastatic breast cancer.

Loss of Protocadherin-12 Leads to Diencephalic-Mesencephalic Junction Dysplasia Syndrome.

Mutations in LMF1 cause combined lipase deficiency and severe hypertriglyceridemia

Mutations in TSPEAR, Encoding a Regulator of Notch Signaling, Affect Tooth and Hair Follicle Morphogenesis.

Phenotypic suppression of acral peeling skin syndrome in a patient with autosomal recessive congenital ichthyosis

Somatic Mosaicism for a "Lethal" GJB2 Mutation Results in a Patterned Form of Spiny Hyperkeratosis without Eccrine Involvement

The ATF6-Met[67]Val substitution is associated with increased plasma cholesterol levels

The N342S MYLIP polymorphism is associated with high total cholesterol and increased LDL receptor degradation in humans

The WWOX gene modulates high-density lipoprotein and lipid metabolism

The risk for developing cancer in Israeli ATM, BLM, and FANCC heterozygous mutation carriers.

Transgenic expression and genetic variation of Lmf1 affect LPL activity in mice and humans

USF1 contributes to high serum lipid levels in Dutch FCHL families and U.S. whites with coronary artery disease

WW-domain-containing oxidoreductase is associated with low plasma HDL-C levels

Whole-Genome Sequencing Analysis from the Chikungunya Virus Caribbean Outbreak Reveals Novel Evolutionary Genomic Elements

Whole-exome sequencing in individuals with multiple cardiovascular risk factors and normal coronary arteries

X-linked elliptocytosis with impaired growth is related to mutated AMMECR1.