Modelos de enfermedades en Drosophila y análisis (epi)genéticos

Publicaciones (67)

Buscador de publicaciones

Aluja, Anton; Garcia, Luis F.; Blanch, Angel; Fibla, Joan

Association of androgen receptor gene, CAG and GGN repeat length polymorphism and impulsive-disinhibited personality traits in inmates: the role of short-long haplotype.

PSYCHIATRIC GENETICS 21 229-239. .

[doi:10.1097/YPG.0b013e328345465e]

Torres, Carmen; Sanchez-de-la-Torre, Manuel; Garcia-Moruja, Carelia; Jose Carrero, Antonio; del Monte Trujillo, Maria; Fibla, Joan; Caruz, Antonio

Immunophenotype of vitamin D receptor polymorphism associated to risk of HIV-1 infection and rate of disease progression.

CURRENT HIV RESEARCH 8 487-492. .

[doi:10.2174/157016210793499330]

Laplana, Marina; Sanchez-de-la-Torre, Manuel; Aguilo, Alicia; Casado, Ignasi; Flores, Miquel; Sanchez-Pellicer, Ramon; Fibla, Joan

Tagging long-lived individuals through vitamin-D receptor (VDR) haplotypes.

Biogerontology 11 437-446. .

[doi:10.1007/s10522-010-9273-8]

Garcia, Luis F.; Aluja, Anton; Fibla, Joan; Cuevas, Lara; Garcia, Oscar

Incremental effect for antisocial personality disorder genetic risk combining 5-HTTLPR and 5-HTTVNTR polymorphisms.

PSYCHIATRY RESEARCH 177 161-166. .

[doi:10.1016/j.psychres.2008.12.018]

Aluja, Anton; Garcia, Luis F.; Blanch, Angel; De Lorenzo, D.; Fibla, Joan

Impulsive-disinhibited personality and serotonin transporter gene polymorphisms: association study in an inmate's sample.

JOURNAL OF PSYCHIATRIC RESEARCH 43 906-914. .

[doi:10.1016/j.jpsychires.2008.11.008]

de la Torre, Manuel Sanchez; Torres, Carmen; Nieto, Gema; Vergara, Salvador; Carrero, Antonio Jose; Macias, Juan; Pineda, Juan Antonio; Caruz, Antonio; Fibla, Joan

Vitamin D receptor gene haplotypes and susceptibility to HIV-1 infection in injection drug users.

JOURNAL OF INFECTIOUS DISEASES 197 405-410. .

[doi:10.1086/525043]

Torres-Juan, Laura; Rosell, Jordi; Sanchez-de-la-Torre, Manuel; Fibla, Joan; Heine-Suner, Damia

Analysis of meiotic recombination in 22q11.2, a region that frequently undergoes deletions and duplications

BMC Medical Genetics 8 -. .

[doi:10.1186/1471-2350-8-14]