Literature DB >> 30086163

Correction: Inherited variants in genes somatically mutated in thyroid cancer.

Chiara Campo, Aleksandra Köhler, Gisella Figlioli, Rossella Elisei, Cristina Romei, Monica Cipollini, Franco Bambi, Kari Hemminki, Federica Gemignani, Stefano Landi, Asta Försti.   

Abstract

[This corrects the article DOI: 10.1371/journal.pone.0174995.].

Entities:  

Year:  2018        PMID: 30086163      PMCID: PMC6080776          DOI: 10.1371/journal.pone.0202208

Source DB:  PubMed          Journal:  PLoS One        ISSN: 1932-6203            Impact factor:   3.240


There is an error in the email address listed for corresponding author Chiara Campo. The email address should be chiaracampo28@gmail.com. Table 3, “Association of the 8 top SNPs in the two Italian sets with WDTC risk (Part II),” does not appear correctly. Please view Table 3 here.
Table 3

Association of the 8 top SNPs in the two Italian sets with WDTC risk (Part II).

Italian1*Italian2*Combined
Gene/SNPCaseControlOR [95% CI]pValueCaseControlOR [95% CI]pValueOR [95% CI]pValue
TSHR (rs2268477) 
CC121012361.0 [reference]5663951.0 [reference] 
AC2483040.79[0.64–0.98]0.03115761.19[0.86–1.65]0.300.95[0.64–1.42]0.81
AA10270.42[0.18–0.95]0.04961.30[0.44–3.85]0.630.64[0.33–1.23]0.18 
AC + AA2583310.76[0.62–0.94]0.01124821.20[0.87–1.65]0.270.94[0.60–1.47]0.78 
Per allele0.75[0.62–0.91]3.96 × 10−31.18[0.88–1.58]0.260.93[0.59–1.44]0.74
SMAD4 (rs7229678)           
GG5665421.0 [reference]2511871.0 [reference] 
CG6517290.84[0.70–1.01]0.073372291.05[0.81–1.37]0.700.94[0.78–1.05]0.19 
CC2252580.75[0.58–0.96]0.02103820.99[0.69–1.41]0.930.82[0.67–1.01]0.06
CG + CC8769870.82[0.69–0.97]0.024403111.04[0.81–1.33]0.770.88[0.77–1.02]0.09 
Per allele0.86[0.76–0.97]0.011.01[0.85–1.20]0.940.91[0.82–1.00]0.06
GNAS (rs7121)           
TT5716781.0 [reference]2691661.0 [reference] 
CT6516791.19[0.99–1.42]0.063222370.81[0.62–1.06]0.120.99[0.68–1.45]0.98 
CC2402021.51[1.18–1.95]1.28 × 10−3100950.63[0.44–0.89]9.63 × 10−30.98[0.42–2.32]0.97
CT + CC8918811.26[1.06–1.49]7.12 × 10−34223320.76[0.59–0.97]0.030.99[0.60–1.62]0.96
Per allele1.23[1.09–1.39]7.90 × 10−40.79[0.66–0.94]7.26 × 10−30.99[0.64–1.53]0.97
GNAS (rs1800900)           
GG4474911.0 [reference]1901481.0 [reference] 
AG6587441.03[0.85–1.25 ]0.763542601.04[0.79–1.37]0.771.03[0.88–1.21]0.69 
AA3603091.36[1.08–1.70]8.82 × 10−3144901.27[0.90–1.81]0.171.33[1.10–1.61]3.00 × 10−3
AG + AA101810531.13[0.94–1.34]0.194983501.10[0.84–1.43]0.491.12[0.97–1.30]0.13 
Per allele1.17[1.04–1.31]0.011.11[0.94–1.32]0.221.15[1.05–1.27]4.00 × 10−3

SNP: single nucleotide polymorphism, OR: odd ratio, CI: confidence interval

(*) The analysis was conducted adjusting for the covariates of sex and age

SNP: single nucleotide polymorphism, OR: odd ratio, CI: confidence interval (*) The analysis was conducted adjusting for the covariates of sex and age
  1 in total

1.  Inherited variants in genes somatically mutated in thyroid cancer.

Authors:  Chiara Campo; Aleksandra Köhler; Gisella Figlioli; Rossella Elisei; Cristina Romei; Monica Cipollini; Franco Bambi; Kari Hemminki; Federica Gemignani; Stefano Landi; Asta Försti
Journal:  PLoS One       Date:  2017-04-14       Impact factor: 3.240

  1 in total

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