D. Weissglas-Volkov

发表

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

Päivi Pajukanta, Marja-Riitta Taskinen, Rita M Cantor, 2013, Journal of Medical Genetics.

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

T. Lehtimäki, R. Cantor, V. Salomaa, 2014 .

Investigation of Variants Identified in Caucasian Genome-Wide Association Studies for Plasma High-Density Lipoprotein Cholesterol and Triglycerides Levels in Mexican Dyslipidemic Study Samples

R. Cantor, J. Sinsheimer, C. Aguilar-Salinas, 2010, Circulation. Cardiovascular genetics.

Relative matching using low coverage sequencing

Joseph K. Pickrell, Yaniv Erlich, S. Carmi, 2020, bioRxiv.

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

N. Shomron, N. Pillar, D. Weissglas-Volkov, 2018, Cell Death & Disease.

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

N. Shomron, E. Friedman, Y. Arbel, 2016, Coronary artery disease.

Association of Stearoyl-CoA Desaturase 1 Activity With Familial Combined Hyperlipidemia

R. Cantor, C. Plaisier, P. Pajukanta, 2008, Arteriosclerosis, thrombosis, and vascular biology.

Cancer risks in Jewish male BRCA1 and BRCA2 mutation carriers

E. Friedman, H. Schayek, Y. Laitman, 2015, Breast Cancer Research and Treatment.

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

Markus Perola, Markku Heliövaara, Bogdan Pasaniuc, 2014, Nature Communications.

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

O. Sarig, N. Shomron, E. Sprecher, 2016, Pediatric dermatology.

Mutations in LMF1 cause combined lipase deficiency and severe hypertriglyceridemia

P. Pajukanta, M. Malloy, C. Pullinger, 2007, Nature Genetics.

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

Noam Shomron, Shai Carmi, Harry Ostrer, 2017, Genetics research.

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

M. Vignuzzi, N. Shomron, S. Weaver, 2016, PLoS neglected tropical diseases.

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

E. Friedman, E. Pras, Y. Laitman, 2016, Cancer genetics.

Genetic causes of high and low serum HDL-cholesterol

Päivi Pajukanta, P. Pajukanta, Daphna Weissglas-Volkov, 2010, Journal of Lipid Research.

The WWOX Gene Modulates High-Density Lipoprotein and Lipid Metabolism

C. Croce, P. Pajukanta, R. Aqeilan, 2014, Circulation. Cardiovascular genetics.

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

N. Shomron, N. Pillar, D. Weissglas-Volkov, 2018, Cell Death and Disease.

TCF7L2 is associated with high serum triacylglycerol and differentially expressed in adipose tissue in families with familial combined hyperlipidaemia

J. Sinsheimer, C. Plaisier, M. Taskinen, 2007, Diabetologia.

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

J. Sinsheimer, C. Aguilar-Salinas, P. Pajukanta, 2011, The Journal of clinical investigation.

Exome Sequencing Identifies 2 Rare Variants for Low High-Density Lipoprotein Cholesterol in an Extended Family

J. Sinsheimer, P. Pajukanta, I. Iatan, 2012, Circulation. Cardiovascular genetics.

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

O. Sarig, N. Shomron, E. Sprecher, 2016, PLoS genetics.

Galanin Preproprotein Is Associated With Elevated Plasma Triglycerides

M. Laakso, J. Sinsheimer, C. Plaisier, 2009, Arteriosclerosis, thrombosis, and vascular biology.

Transgenic Expression and Genetic Variation of Lmf1 Affect LPL Activity in Mice and Humans

M. Taskinen, P. Pajukanta, H. Mao, 2012, Arteriosclerosis, Thrombosis and Vascular Biology.

Cholesterol Levels The ATF6-Met(67)Val Substitution Is Associated With Increased Plasma

J. Sinsheimer, J. Kuusisto, B. Wouters, 2012 .

Identification of Two Common Variants Contributing to Serum Apolipoprotein B Levels in Mexicans

R. Cantor, J. Sinsheimer, C. Plaisier, 2010, Arteriosclerosis, thrombosis, and vascular biology.

Genetic Variation at the Proprotein Convertase Subtilisin/Kexin Type 5 Gene Modulates High-Density Lipoprotein Cholesterol Levels

A. Prat, N. Seidah, M. Taskinen, 2009, Circulation. Cardiovascular genetics.

The ATF6-Met[67]Val Substitution Is Associated With Increased Plasma Cholesterol Levels

M. Laakso, E. Feskens, J. Sinsheimer, 2009, Arteriosclerosis, thrombosis, and vascular biology.

Common Hepatic Nuclear Factor-4α Variants Are Associated With High Serum Lipid Levels and the Metabolic Syndrome

C. Plaisier, M. Taskinen, C. Aguilar-Salinas, 2006, Diabetes.

USF1 Contributes to High Serum Lipid Levels in Dutch FCHL Families and U.S. Whites With Coronary Artery Disease

J. Sinsheimer, P. Pajukanta, S. Hazen, 2007, Arteriosclerosis, thrombosis, and vascular biology.

RGS2 expression predicts amyloid-β sensitivity, MCI and Alzheimer's disease: genome-wide transcriptomic profiling and bioinformatics data mining

D. Gurwitz, N. Shomron, I. Gozes, 2016, Translational psychiatry.

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

T. Lehtimäki, R. Cantor, M. Laakso, 2008, American Journal of Human Genetics.

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

O. Sarig, N. Shomron, J. McGrath, 2020, Experimental dermatology.

Clinical Perspective on P 546 Methods Study Samples

J. Sinsheimer, P. Pajukanta, I. Iatan, 2022 .

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

N. Shomron, H. Tamary, N. Orenstein, 2017, Gene.

Local microRNA delivery targets Palladin and prevents metastatic breast cancer

Noam Shomron, Nuria Oliva, Natalie Artzi, 2016, Nature Communications.

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

Steve Horvath, Johanna Kuusisto, Päivi Pajukanta, 2012, BMC Medical Genomics.

Analysis of microRNAs in familial Mediterranean fever

N. Shomron, I. Ben-Zvi, G. Amarilyo, 2018, PloS one.

Evidence of How rs7575840 Influences Apolipoprotein B–Containing Lipid Particles

M. Laakso, C. Aguilar-Salinas, P. Pajukanta, 2011, Arteriosclerosis, thrombosis, and vascular biology.

Loss of Protocadherin‐12 Leads to Diencephalic‐Mesencephalic Junction Dysplasia Syndrome

S. Gabriel, H. Per, N. Shomron, 2018, Annals of neurology.

mRNA splicing is modulated by intronic microRNAs

N. Shomron, Luba Farberov, J. Neidhardt, 2023, iScience.

Evidence of How rs7575840 Influences Apolipoprotein B–Containing Lipid Particles

M. Laakso, C. Aguilar-Salinas, P. Pajukanta, 2011, Arteriosclerosis, Thrombosis and Vascular Biology.

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

T. Lehtimäki, R. Cantor, M. Laakso, 2008, American journal of human genetics.

Thematic Review Series: Genetics of Human Lipid Diseases Genetic causes of high and low serum HDL-cholesterol

P. Pajukanta, D. Weissglas-Volkov, 2010 .

Transgenic Expression and Genetic Variation of Lmf1 Affect LPL Activity in Mice and Humans

M. Taskinen, P. Pajukanta, H. Mao, 2012, Arteriosclerosis, thrombosis, and vascular biology.