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Pilar Mozas
Observed names:
P Mozas,
P. Mozas
Institution:
Universidad de Zaragoza
Observed institutions:
Tufts University,
Universidad de Zaragoza,
Instituto de Salud Carlos III,
Jean Mayer Human Nutrition Research Center on Aging,
Centro de Investigación Biomédica en Red,
Instituto de Investigación Sanitaria Aragón,
Instituto Aragonés de Ciencias de la Salud
show all 7
OpenAlex ID:
A5032054802
Association of Polymorphisms at the SR-BI Gene Locus With Plasma Lipid Levels and Body Mass Index in a White Population
1999
·
Susan Acton
, Doreen Osgood
, et al.
·
Arteriosclerosis Thrombosis and Vascular Biology
·
213
Molecular characterization of familial hypercholesterolemia in Spain: Identification of 39 novel and 77 recurrent mutations in LDLR
2004
·
Pilar Mozas
, Sergio Castillo
, et al.
·
Human Mutation
·
84
PDF
Promoter variant −204A > C of the cholesterol 7α-hydroxylase gene: Association with response to plant sterols in humans and increased transcriptional activity in transfected HepG2 cells
2010
·
Isabel De Castro-Orós
, Sandra Pampín
, et al.
·
Clinical Nutrition
·
55
β-glucocerebrosidase gene locus as a link for Gaucher's disease and familial hypo-α-lipoproteinaemia
1998
·
Miguel Pocovi
, Ana Cenarro
, et al.
·
The Lancet
·
53
A mutation (−49C>T) in the promoter of the low density lipoprotein receptor gene associated with familial hypercholesterolemia
2002
·
Pilar Mozas
, Román Galetto
, et al.
·
Journal of Lipid Research
·
37
PDF
Mutation analysis in 36 unrelated Spanish subjects with familial hypercholesterolemia: Identification of 3 novel mutations in the LDL receptor gene
2000
·
Pilar Mozas
, Ana Cenarro
, et al.
·
Human Mutation
·
33
PDF
Assessment of plasma chitotriosidase activity, CCL18/PARC concentration and NP-C suspicion index in the diagnosis of Niemann-Pick disease type C: a prospective observational study
2017
·
on behalf of the Spanish NP-C Group
, Isabel De Castro-Orós
, et al.
·
Journal of Translational Medicine
·
30
PDF
The apolipoprotein B R3500Q gene mutation in Spanish subjects with a clinical diagnosis of familial hypercholesterolemia
2002
·
Sergio Castillo
, Diego Tejedor
, et al.
·
Atherosclerosis
·
30
Genetic Variants of LDLR and PCSK9 Associated with Variations in Response to Antihypercholesterolemic Effects of Armolipid Plus with Berberine
2016
·
Isabel De Castro-Orós
, Rosa Solà
, et al.
·
PLoS ONE
·
28
PDF
Comparison of the hypolipidemic effect of gemfibrozil versus simvastatin in patients with type III hyperlipoproteinemia
1999
·
Fernando Civeira
, Ana Cenarro
, et al.
·
American Heart Journal
·
26
A presumptive new locus for autosomal dominant hypercholesterolemia mapping to 8q24.22
2010
·
A Cenarro
, A-L García-Otín
, et al.
·
Clinical Genetics
·
25
Apolipoprotein E genotype is not associated with cardiovascular disease in heterozygous subjects with familial hypercholesterolemia
2003
·
P Mozas
, S Castillo
, et al.
·
American Heart Journal
·
19
Comparison of DNA Array Platform vs DNA Sequencing as Genetic Diagnosis Tools for Familial Hypercholesterolemia
2006
·
Diego Tejedor
, Sergio Castillo
, et al.
·
Clinical Chemistry
·
17
PDF
Screening of APOB Gene Mutations in Subjects with Clinical Diagnosis of Familial Hypercholesterolemia
2005
·
Erardo Merino-Ibarra
, Sergio Castillo
, et al.
·
Human Biology
·
15
Ampelography and microsatellite DNA analysis of autochthonous and endangered grapevine cultivars in the province of Huesca (Spain)
2011
·
J. Casanova
, P. Mozas
, et al.
·
Spanish Journal of Agricultural Research
·
12
PDF
Evaluation of two approaches to lysosomal acid lipase deficiency patient identification: An observational retrospective study
2019
·
Jorge J. Cebolla
, Pilar Irún
, et al.
·
Atherosclerosis
·
10
A double mutant [N543H+2393del9] allele in the LDL receptor gene in familial hypercholesterolemia: effect on plasma cholesterol levels and cardiovascular disease
2002
·
S. Castillo
, G. Reyes
, et al.
·
Human Mutation
·
10
PDF
SNP3 polymorphism in apo A-V gene is associated with small dense LDL particles in Type 2 diabetes
2004
·
E. Esteve
, E. Faure
, et al.
·
Diabetologia
·
9
PDF
Diferencias en la presentación clínica en sujetos con fenotipo de hipercolesterolemia familiar por defectos en el receptor LDL y por defectos de la apo B-100
2003
·
Ignacio García-Álvarez
, Sergio Castillo
, et al.
·
Revista Española de Cardiología
·
5
Transmitochondrial Cybrid Generation Using Cancer Cell Lines
2023
·
Ruth Soler-Agesta
, Joaquín Marco-Brualla
, et al.
·
Journal of Visualized Experiments
·
3
Exploring lipid biomarkers in Gaucher disease: LC-MS/MS analysis of dried blood spot samples
2024
·
Isidro Arevalo-Vargas
, Irene Serrano Gonzalo
, et al.
·
Molecular Genetics and Metabolism
·
1
The apolipoprotein B R3500Q gene mutation in Spanish subjects with a clinical diagnosis of familial hypercholesterolemia
2004
·
S. Castillo
, D. Tejedor
, et al.
·
Clínica e Investigación en Arteriosclerosis
·
1
Analysis of mutations in the LDLR gene in spanish patients with familial hypercholesterolemia by SSCP
2000
·
P. Mozas
, A. Cenarro
, et al.
·
Atherosclerosis
·
1
1.P.177 Comparison of the hypolipidemic effect of gemfibrozil versus simvastatin in patients with type III hyperlipoproteinemia
1997
·
F. Civeira
, A. Cenarro
, et al.
·
Atherosclerosis
·
1
Necrotic Core-Mediated Immune Suppression in a Patient-Derived Glioblastoma-on-Chip Model
2025
·
Clara Bayona
, Teodora Randelovic
, et al.
·
Jornadas de jóvenes investigadores del I3A
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Works count:
41
Citation count:
718
H-index:
14
I10-index:
17
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