A. García-García

发表

Evaluation of clinical diagnosis criteria of familial ligand defective apoB 100 and lipoprotein phenotype comparison between LDL receptor gene mutations affecting ligand-binding domain and the R3500Q mutation of the apoB gene in patients from a South European population.

F. Chaves, S. Martínez-Hervás, J. Real, 2008, Translational research : the journal of laboratory and clinical medicine.

Influence of microsomal triglyceride transfer protein promoter polymorphism −493 GT on fasting plasma triglyceride values and interaction with treatment response to atorvastatin in subjects with heterozygous familial hypercholesterolaemia

F. Chaves, J. J. Martín de Llano, J. Real, 2005, Pharmacogenetics and genomics.

Influence of LDL receptor gene mutations and the R3500Q mutation of the apoB gene on lipoprotein phenotype of familial hypercholesterolemic patients from a South European population

F. Chaves, J. Real, R. Carmena, 2003, European Journal of Human Genetics.

Genetic diagnosis of familial hypercholesterolemia in a South European outbreed population: influence of low-density lipoprotein (LDL) receptor gene mutations on treatment response to simvastatin in total, LDL, and high-density lipoprotein cholesterol.

F. Chaves, J. Real, R. Carmena, 2001, The Journal of clinical endocrinology and metabolism.

Importance of HDL cholesterol levels and the total/ HDL cholesterol ratio as a risk factor for coronary heart disease in molecularly defined heterozygous familial hypercholesterolaemia.

F. Chaves, J. Real, R. Carmena, 2001, European heart journal.

Effects of adding fenofibrate (200 mg/day) to simvastatin (10 mg/day) in patients with combined hyperlipidemia and metabolic syndrome.

S. Grundy, G. Vega, N. Cater, 2003, The American journal of cardiology.

Developing a simple and practical decision model to predict the risk of incident type 2 diabetes among the general population: The Di@bet.es Study.

F. Chaves, Isabel Peraita-Costa, M. Morales-Suárez-Varela, 2022, European journal of internal medicine.

Are IL18RAP gene polymorphisms associated with body mass regulation? A cross-sectional study

F. Chaves, R. Cortes, S. Martínez-Hervás, 2017, BMJ Open.

A Very Rare Variant in SREBF2, a Possible Cause of Hypercholesterolemia and Increased Glycemic Levels

J. Carretero, F. Chaves, S. Martínez-Hervás, 2022, Biomedicines.

Gene expression profile following an oral unsaturated fat load in abdominal obese subjects

F. Chaves, P. Marín-García, S. Martínez-Hervás, 2019, European Journal of Nutrition.

Postprandial Changes in Chemokines Related to Early Atherosclerotic Processes in Familial Hypercholesterolemic Subjects: A Preliminary Study.

F. Chaves, R. Cortes, S. Martínez-Hervás, 2016, Archives of medical research.

Large rearrangements of the LDL receptor gene and lipid profile in a FH Spanish population

J. Ordovás, F. Chaves, J. Real, 2001, European journal of clinical investigation.

Circulating mononuclear cells nuclear factor‐kappa B activity, plasma xanthine oxidase, and low grade inflammatory markers in adult patients with familial hypercholesterolaemia

F. Pallardó, J. Viña, F. Chaves, 2010, European journal of clinical investigation.

Molecular genetics of familial hypercholesterolemia in Spain: Ten novel LDLR mutations and population analysis

F. Chaves, P. Marín-García, J. Real, 2001, Human mutation.

Analysis of sequence variations in the LDL receptor gene in Spain: general gene screening or search for specific alterations?

F. Chaves, S. Martínez-Hervás, J. Real, 2006, Clinical chemistry.

Gitelman syndrome due to p.A204T mutation in CLCNKB gene

I. Millán, A. García-García, R. Enríquez, 2010, International Urology and Nephrology.

A new PCSK9 gene promoter variant affects gene expression and causes autosomal dominant hypercholesterolemia.

F. Chaves, S. Martínez-Hervás, J. Real, 2008, The Journal of clinical endocrinology and metabolism.

Metabolomic patterns, redox-related genes and metals, and bone fragility endpoints in the Hortega Study.

J. Redón, D. Monleón, F. Chaves, 2022, Free radical biology & medicine.

Respiratory chain polymorphisms and obesity in the Spanish population, a cross-sectional study

G. Rojo-Martínez, A. Lago-Sampedro, F. Chaves, 2019, BMJ Open.

Xanthine oxidoreductase polymorphisms: influence in blood pressure and oxidative stress levels

D. Corella, J. Redón, F. Chaves, 2007, Pharmacogenetics and genomics.

Reduced penetrance of autosomal dominant hypercholesterolemia in a high percentage of families: importance of genetic testing in the entire family.

F. Chaves, S. Martínez-Hervás, J. Real, 2011, Atherosclerosis.

Easy One-Step Amplification and Labeling Procedure for Copy Number Variation Detection.

Andy S. Alic, F. Chaves, S. Martínez-Hervás, 2020, Clinical chemistry.

Gene-environment interaction analysis of redox-related metals and genetic variants with plasma metabolic patterns in a general population from Spain: The Hortega Study

Sonia Tarazona, J. Redón, D. Monleón, 2022, Redox biology.

Association of C 677 T Polymorphism in MTHFR Gene , High Homocysteine and Low HDL Cholesterol Plasma Values in Heterozygous Familial Hypercholesterolemia

F. Chaves, S. Martínez-Hervás, J. Real, 2009 .

Association of C677T polymorphism in MTHFR gene, high homocysteine and low HDL cholesterol plasma values in heterozygous familial hypercholesterolemia.

F. Chaves, S. Martínez-Hervás, J. Real, 2009, Journal of atherosclerosis and thrombosis.

Association between genetic variants in oxidative stress-related genes and osteoporotic bone fracture. The Hortega Follow-up Study.

F. Chaves, J. Martín-Vallejo, J. Pérez-Castrillón, 2021, Gene.

Responsiveness of plasma lipids and lipoproteins to plant stanol esters.

S. Grundy, G. Vega, N. Cater, 2005, The American journal of cardiology.

Oxidative stress and antioxidant enzyme values in lymphomonocytes after an oral unsaturated fat load test in familial hypercholesterolemic subjects.

F. Chaves, S. Martínez-Hervás, J. Real, 2013, Translational research : the journal of laboratory and clinical medicine.

Increased oxidative stress levels and normal antioxidant enzyme activity in circulating mononuclear cells from patients of familial hypercholesterolemia.

F. Pallardó, J. Redón, F. Chaves, 2010, Metabolism: clinical and experimental.

mRNA expression profiles obtained from microdissected pancreatic cancer cells can predict patient survival

F. Chaves, P. Marín-García, A. Cervantes, 2017, Oncotarget.

Srebf2 Locus Overexpression Reduces Body Weight, Total Cholesterol and Glucose Levels in Mice Fed with Two Different Diets

J. Carretero, F. Chaves, S. Martínez-Hervás, 2020, Nutrients.

Benchmarking different approaches for Norovirus genome assembly in metagenome samples

F. Chaves, J. Rodríguez-Díaz, Iris Manzano, 2021, BMC genomics.

Polymorphisms in genes involved in inflammation, the NF-kB pathway and the renin-angiotensin-aldosterone system are associated with the risk of osteoporotic fracture. The Hortega Follow-up Study.

F. Chaves, J. Martín-Vallejo, J. Pérez-Castrillón, 2020, Bone.

Genetic variants in obesity-related genes and the risk of osteoporotic fracture. The Hortega Follow-up Study.

F. Chaves, J. Martín-Vallejo, J. Pérez-Castrillón, 2022, Frontiers in bioscience.

Familial seborrhoeic keratosis associated with multiple ‘pure reticulated acanthomas’ and infundibulocystic basal cell carcinomas

R. González-Sarmiento, E. Jordá, C. Monteagudo, 2017, The British journal of dermatology.

High miR-126-3p levels associated with cardiovascular events in a general population

J. Redón, F. Chaves, R. Cortes, 2023, European journal of internal medicine.

Genetic interaction in the association between oxidative stress and diabetes in the Spanish population.

J. Martín-Escudero, L. Briongos-Figuero, A. García-García, 2023, Free radical biology & medicine.

Metabolic syndrome phenotype in very obese women.

S. Grundy, G. Vega, E. Hamilton, 2007, Metabolic syndrome and related disorders.

Semiquantitative multiplex PCR: a useful tool for large rearrangement screening and characterization

S. Martínez-Hervás, J. Real, R. Carmena, 2006, Human mutation.