Corrigendum to Replication of GWAS-identified neuroblastoma risk loci strengthens the role of BARD1 and affirms the cumulative effect of genetic variations on disease susceptibility [Carcinogenesis, 34, 3, 605-611] DOI:10.1093/carcin/bgs380;Replication of GWAS-identified neuroblastoma risk loci strengthens the role of BARD1 and affirms the cumulative effect of genetic variations on disease susceptibility

Carcinogenesis

Volumn 34, Issue 3, 2013, Pages 605-611

  Capasso, Mario ^a,b   Diskin, Sharon J ^c,d,e   Totaro, Francesca ^a,b   Longo, Luca ^f,g   de Mariano, Marilena ^f,g   Russo, Roberta ^a,b   Cimmino, Flora ^a,b   Hakonarson, Hakon ^c,d   Tonini, Gian Paolo ^g   Devoto, Marcella ^c,d,h   Maris, John M ^c,d,e   Iolascon, Achille ^a,b  

^a UNIVERSITY OF NAPLES FEDERICO II   (Italy)

^b CEINGE BIOTECNOLOGIE AVANZATE   (Italy)

^c CHILDREN S HOSPITAL OF PHILADELPHIA   (United States)

^d UNIVERSITY OF PENNSYLVANIA   (United States)

^e UNIVERSITY OF PENNSYLVANIA   (United States)

^f UNIVERSITY OF GENOA   (Italy)

^g Italian Neuroblastoma Foundation   (Italy)

^h SAPIENZA UNIVERSITY OF ROME   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

BRCA1 ASSOCIATED RING DOMAIN PROTEIN 1; MESSENGER RNA;

ARTICLE; CANCER RISK; CHILD; CONTROLLED STUDY; DISEASE PREDISPOSITION; EUROPEAN AMERICAN; FEMALE; GENE EXPRESSION; GENE FREQUENCY; GENE LOCUS; GENETIC ASSOCIATION; GENETIC VARIABILITY; HUMAN; LYMPHOBLASTOID CELL LINE; MAJOR CLINICAL STUDY; MALE; NEUROBLASTOMA; NEUROBLASTOMA CELL; PHENOTYPE; PRESCHOOL CHILD; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM; TUMOR SUPPRESSOR GENE;

EID: 84874789453     PISSN: 01433334     EISSN: 14602180     Source Type: Journal    
DOI: 10.1093/carcin/bgu036     Document Type: Erratum

References (20)

1. Maris, J.M. (2010) Recent advances in neuroblastoma. N. Engl. J. Med., 362, 2202-2211.
2. Cohn, S.L. et al. (2009) The International Neuroblastoma Risk Group (INRG) classification system: an INRG Task Force report. J. Clin. Oncol., 27, 289-297.
3. Maris, J.M. et al. (2008) Chromosome 6p22 locus associated with clinically aggressive neuroblastoma. N. Engl. J. Med., 358, 2585-2593.
4. Capasso, M. et al. (2009) Common variations in BARD1 influence susceptibility to high-risk neuroblastoma. Nat. Genet., 41, 718-723.
5. Wang, K. et al. (2011) Integrative genomics identifies LMO1 as a neuroblastoma oncogene. Nature, 469, 216-220.
6. Nguyen, L.B. et al. (2011) Phenotype restricted genome-wide association study using a gene-centric approach identifies three low-risk neuroblastoma susceptibility Loci. PLoS Genet., 7, e1002026.
7. Diskin, S.J. et al. (2012) Identification of a new neuroblastoma susceptibility locus at 6q16 implicating HACE1 and LIN28B. Nat. Genet., 44, 1126-1130.
8. Latorre, V. et al. (2012) Replication of neuroblastoma SNP association at the BARD1 locus in African-Americans. Cancer Epidemiol. Biomarkers Prev., 21, 658-663.
9. Price, A.L. et al. (2008) Discerning the ancestry of European Americans in genetic association studies. PLoS Genet., 4, e236.
10. Seldin, M.F. et al. (2006) European population substructure: clustering of northern and southern populations. PLoS Genet., 2, e143.
11. Bosse, K.R. et al. (2012) Common variation at BARD1 results in the expression of an oncogenic isoform that influences neuroblastoma susceptibility and oncogenicity. Cancer Res., 72, 2068-2078.
12. Holm, K. et al. (2010) SNPexp: a web tool for calculating and visualizing correlation between HapMap genotypes and gene expression levels. BMC Bioinformatics, 11, 600.
13. Yang, T.P. et al. (2010) Genevar: a database and Java application for the analysis and visualization of SNP-gene associations in eQTL studies. Bioinformatics, 26, 2474-2476.
14. Capasso, M. et al. (2007) Cytokine gene polymorphisms in Italian preterm infants: association between interleukin-10-1082 G/A polymorphism and respiratory distress syndrome. Pediatr. Res., 61, 313-317.
15. Purcell, S. et al. (2007) PLINK: a tool set for whole-genome association and population-based linkage analyses. Am. J. Hum. Genet., 81, 559-575.
16. Johnson, A.D. et al. (2008) SNAP: a web-based tool for identification and annotation of proxy SNPs using HapMap. Bioinformatics, 24, 2938-2939.
17. Barrett, J.C. et al. (2005) Haploview: analysis and visualization of LD and haplotype maps. Bioinformatics, 21, 263-265.
18. Sporn, J.C. et al. (2011) BARD1 expression predicts outcome in colon cancer. Clin. Cancer Res., 17, 5451-5462.
19. Irminger-Finger, I. et al. (2006) Is there more to BARD1 than BRCA1? Nat. Rev. Cancer, 6, 382-391.
20. Capasso, M. et al. (2010) Genetics and genomics of neuroblastoma. Cancer Treat. Res., 155, 65-84.