Ana Cenarro - Concepedia

Author

Ana Cenarro

Hospital Universitario Miguel Servet ORCID

Also Known As

A Cenarro, A. Cenarro, Ana Cenarro, Lucia Baila-Rueda

272

Publications

4.1K

Citations

H-Index

100

Concepts

All Affiliations

Hospital Universitario Miguel Servet Universidad de Zaragoza Instituto de Investigación Sanitaria Aragón Instituto Aragonés de Ciencias de la Salud Instituto de Salud Carlos III

About

Ana Cenarro is an author at Hospital Universitario Miguel Servet specializing in medicine, metabolic syndrome, and atherosclerosis.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	25	51	1.6K
2	Public Health	17	24	664
3	Health Sciences	10	11	306
4	Biochemistry	10	10	225
5	Natural Sciences	2	2	49

Ana Cenarro

Publications

3.4K

Citations

H-Index

Page 1

	Year	Citations
Impaired Sensitivity to Thyroid Hormones Is Associated With Diabetes and Metabolic Syndrome Martín Laclaustra, Belén Moreno‐Franco, José Manuel Lou-Bonafonte, Diabetes Care	2018	284
A Third Major Locus for Autosomal Dominant Hypercholesterolemia Maps to 1p34.1-p32 Mathilde Varret, Jean‐Pierre Rabès, Bruno Saint-Jore, The American Journal of Human Genetics Metabolic SyndromeLipid DisorderGeneticsHuman PolymorphismPathology	1999	170
Serum Chitotriosidase Activity Is Increased in Subjects With Atherosclerosis Disease Marta Artieda, Ana Cenarro, Alberto Gañán, Arteriosclerosis Thrombosis and Vascular Biology	2003	127
Tendon Xanthomas in Familial Hypercholesterolemia Are Associated With Cardiovascular Risk Independently of the Low-Density Lipoprotein Receptor Gene Mutation Fernando Civeira, Sergio Castillo, Rodrigo Alonso, Arteriosclerosis Thrombosis and Vascular Biology	2005	120
The p.Leu167del Mutation in APOE Gene Causes Autosomal Dominant Hypercholesterolemia by Down-regulation of LDL Receptor Expression in Hepatocytes Ana Cenarro, Aitor Etxebarria, Isabel de Castro-Orós, The Journal of Clinical Endocrinology & Metabolism	2016	96
A common variant in the <i>ABCA1</i> gene is associated with a lower risk for premature coronary heart disease in familial hypercholesterolaemia Ana Cenarro Journal of Medical Genetics	2003	93
STARD1 promotes NASH-driven HCC by sustaining the generation of bile acids through the alternative mitochondrial pathway Laura Conde de la Rosa, Carmen García‐Ruiz, Carmen G. Vallejo, Journal of Hepatology	2021	92
Frequency of Low-Density Lipoprotein Receptor Gene Mutations in Patients With a Clinical Diagnosis of Familial Combined Hyperlipidemia in a Clinical Setting Fernando Civeira, Estíbaliz Jarauta, Ana Cenarro, Journal of the American College of Cardiology Metabolic SyndromeEpidemiologyMetabolic DisorderCardiovascular DiseaseGenetic Epidemiology	2008	85
Individual Variation of Scavenger Receptor Expression in Human Macrophages with Oxidized Low-Density Lipoprotein Is Associated with a Differential Inflammatory Response Paula Martín‐Fuentes, Fernando Civeira, D. Recalde, The Journal of Immunology	2007	78
Apolipoprotein E gene mutations in subjects with mixed hyperlipidemia and a clinical diagnosis of familial combined hyperlipidemia María Solanas-Barca, Isabel de Castro-Orós, Rocío Mateo‐Gállego, Atherosclerosis Metabolic SyndromeMixed HyperlipidemiaGenetic DisorderGeneticsPathology	2012	74

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