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Peer-Reviewed Research Articles (2007 - 2010)
Vidal, C., and Xuereb-Anastasi, A.
(2009) Genetics of osteoporosis in the Maltese population: A
review. Malta Medical Journal 21: 6 - 11

Vidal, C.,
and Xuereb-Anastasi, A. (2009) Frequency of the CCR5-delta 32 polymorphism in
the Maltese population. International Journal of Immunogenetics 36: 301 –
304 (PMID:
19744036) (Impact factor: 1.16)
Vidal,
C., Cachia, A., and
Xuereb-Anastasi, A. (2009) Effects of a synonymous variant in exon 9 of the CD44
gene on pre-mRNA splicing in a family with osteoporosis. Bone 45: 736 -
742 (PMID:
19580891) (Impact factor: 4.145)
Scerri, C.A., Xuereb-Anastasi, A.,
and Vidal, C. (2009) No effects of a novel synonymous variant within the
CD59 gene on its protein product in duodenal biopsies of coeliac individuals.
Tissue Antigens 74: 336 - 338 (PMID:
19686460) (Impact factor: 2.245)
Vidal, C., Borg, J., Xuereb-Anastasi, A., and Scerri, C.A.
(2009) Variants within protectin (CD59) and CD44 genes linked to an
inherited haplotype in a family with coeliac disease. Tissue Antigens 73:
225 - 235 (PMID:
19254252)
(Impact factor: 2.245)
Vidal, C., and Cassar, M. (2008) A case of
tri-allelic pattern at locus D3S1358 on chromosome 3p21 inherited from
paternal grandparent. Forensic Science
International - Genetics 2: 372 - 375 (PMID:
19083850)
Jaeckle,
Santos, L.J., Xing, C.,
Barnes, R.B., Ades, L.C.,Megarbane, A., Vidal,
C., Xuereb, A., Tarpey,
P.S., Smith, R.,Khazab, M., Shoubridge,
C., Partington, M., Futreal,
A., Stratton, M.R., Gecz,
J., and Zinn, A.R.
(2008)
Refined mapping of X-linked reticulate pigmentary disorder and
sequencing of candidate genes. Human Genetics
123: 469 - 476. (PMID:
18404279) (Impact factor: 3.974)
Cassar,
M., Farrugia, C., and Vidal, C. (2008)
Allele frequencies of 14 STR loci in the population of Malta. Legal
Medicine 10: 153 – 156. (PMID:
18039589)
Vidal, C., Galea, R., Brincat, M., and Xuereb-Anastasi, A. (2007)
Linkage to chromosome 11p12 in two Maltese families with a highly
penetrant form of osteoporosis. European Journal of Human Genetics
15: 800 – 809. (PMID:
17377523) (Impact factor: 4.003)

Xuereb-Anastasi, A., and Vidal, C. (2007) The vitamin D
receptor gene and osteoporosis. Clinical Dermatology: Retinoids and
other Treatments 23: 18 – 21.
Vidal, C., Brincat, M., and Xuereb-Anastasi, A. (2007) Effects of
polymorphisms in the collagen type 1α1 gene promoter and the C677T
variant in the methylenetetrahydrofolate reductase gene on bone
mineral density in postmenopausal women in Malta. Balkan Journal of
Medical Genetics 10: 9 – 18. (Link)
Borg,
J., Scerri, C.A., Vidal, C., and Xuereb-Anastasi, A. (2007)
There is no association between -318 (C/T) and +49 (A/G) CTLA4 gene
polymorphisms and the coeliac condition in the Maltese population.
Balkan Journal of Medical Genetics 9: 49 – 51.
(Link)
Publications 2002 - 2006
Articles in preparation or submitted for publication
Vidal, C., and Xuereb-Anastasi, A. A variant in the promoter
region of TRAF6 gene increases gene expression in murine
macrophages (submitted)
Abstracts and Poster Presentations
Vidal, C., Nanan,
B., Nanan, R., and Duque, G. (2010) Activation of the kynurenine pathway of
tryptophan degradation plays a role in osteoblastogenesis. JBMR (in
press)
Vidal, C.,
Nanan, B., Nanan, R., and Duque, G. (2010) Immune and osteogenic: The two faces
of interferon gamma.
Vidal,
C., Formosa,
R., and Xuereb-Anastasi, A. (2010) Haplotypes within the TNFRSF11B (osteoprotegerin)
gene and bone mineral density (bmd) in maltese post-menopausal women. To be
presented at the IOF-ECCEO10 Congress, Florence, Italy, May 2010)
Vidal, C.,
and Xuereb-Anastasi, A.
(2009) No effects on pre-mRNA splicing of an intronic insertion/deletion within
the TRAF-6 gene. Published abstract for the 7th International
Conference on Bone and Mineral Research and 9th International
Osteoporosis Symposium, Shangai, China: May 2009
Vidal, C., Xuereb-Anastasi,
A., and Scerri, C.A. (2009) No association of polymorphisms within the CD44 gene
and the coeliac condition. European Journal of Human Genetics (in press)
Vidal, C.,
and Xuereb-Anastasi, A. (2009) A variant within the TRAF-6 gene promoter
increases gene expression in the absence of a GATA-1 binding site. Bone
45: Sup 2, S81 - 82. Poster
presentation at the International Congress of Children's Bone Health, Cambridge
2009.
Vidal, C.,
Cachia, A., and Xuereb-Anastasi, A. (2009) A variant within the CD44 gene in a
Maltese family with osteoporosis. Bone (in press)
Xuereb-Anastasi, A., Cachia, A., Gatt, C., and Vidal, C.
(2008) Sequencing of genes in two families with high incidence of
osteoporosis. Osteoporosis International 19: Supp 2,
423
Vidal, C., Borg, J., Fenech, A.,
Xuereb-Anastasi, A., and Scerri, C.A. (2008) A silent mutation within
protectin (CD59) gene and exon skipping in a family with coeliac
disease. European Journal of Human Genetics
16: Supp 1, 243 
Vidal, C., and Xuereb-Anastasi, A. (2008) A
transversion in the tumour necrosis factor receptor associated factor
6 gene promoter increases gene expression in RAW264.7 cells.
Calcified Tissue International 82: Supp
1, S148
Vidal, C., Borg, J., Felice, A.E., Xuereb-Anastasi, A., and Scerri,
CA. (2007) A genome-wide linkage scan in an extended Maltese family
with a high incidence of coeliac disease. European Journal of Human
Genetics 15: Supp 1, 241 
Vidal, C., Galea, R., Brincat, M., and Xuereb-Anastasi, A. (2007)
TRAF6 gene variants in a family with a highly penetrant form of
osteoporosis. Calcified Tissue International 80: Supp 1, S104
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