Three different insertion polymorphisms 3' to the human apolipoprotein A-IV gene.

od Civeira, F, Cassidy, D K, Schaefer, E J, Ordovas, J M
Wydane 1989

A common variant in the ABCA1 gene is associated with a lower risk for premature coronary heart disease in familial hypercholesterolaemia

od Cenarro, A, Artieda, M, Castillo, S, Mozas, P, Reyes, G, Tejedor, D, Alonso, R, Mata, P, Pocovi, M, Civeira, F
Wydane 2003

ANGPTL3 gene variants in subjects with familial combined hyperlipidemia

od Bea, A. M., Franco-Marín, E., Marco-Benedí, V., Jarauta, E., Gracia-Rubio, I., Cenarro, A., Civeira, F., Lamiquiz-Moneo, I.
Wydane w Sci Rep (2021)

Replacement of cysteine at position 46 in the first cysteine-rich repeat of the LDL receptor impairs apolipoprotein recognition

od Benito-Vicente, A., Uribe, K. B., Siddiqi, H., Jebari, S., Galicia-Garcia, U., Larrea-Sebal, A., Cenarro, A., Stef, M., Ostolaza, H., Civeira, F., Palacios, L., Martin, C.
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Higher incidence of mild cognitive impairment in familial hypercholesterolemia

od Zambón, D., Quintana, M., Mata, P., Alonso, R., Benavent, J., Cruz-Sánchez, F., Gich, J., Pocoví, M., Civeira, F., Capurro, S., Bachman, D., Sambamurti, K., Nicholas, J., Pappolla, M. A.
Wydane 2010

Identification and validation of seven new loci showing differential DNA methylation related to serum lipid profile: an epigenome-wide approach. The REGICOR study

od Sayols-Baixeras, S, Subirana, I, Lluis-Ganella, C, Civeira, F, Roquer, J, Do, AN, Absher, D, Cenarro, A, Muñoz, D, Soriano-Tárraga, C, Jiménez-Conde, J, Ordovas, J M, Senti, M, Aslibekyan, S, Marrugat, J, Arnett, D K, Elosua, R
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Corrigendum: Identification and validation of seven new loci showing differential DNA methylation related to serum lipid profile: an epigenome-wide approach. The REGICOR study

od Sayols-Baixeras, S, Subirana, I, Lluis-Ganella, C, Civeira, F, Roquer, J, Do, A N, Absher, D, Cenarro, A, Muñoz, D, Soriano-Tárraga, C, Jiménez-Conde, J, Ordovas, J M, Senti, M, Aslibekyan, S, Marrugat, J, Arnett, D K, Elosua, R
Wydane w Hum Mol Genet (2019)

A third major locus for autosomal dominant hypercholesterolemia maps to 1p34.1-p32.

od Varret, M, Rabès, J P, Saint-Jore, B, Cenarro, A, Marinoni, J C, Civeira, F, Devillers, M, Krempf, M, Coulon, M, Thiart, R, Kotze, M J, Schmidt, H, Buzzi, J C, Kostner, G M, Bertolini, S, Pocovi, M, Rosa, A, Farnier, M, Martinez, M, Junien, C, Boileau, C
Wydane 1999