TY - JOUR
T1 - Breast cancer polygenic risk scores derived in White European populations are not calibrated for women of Ashkenazi Jewish descent
T2 - Breast cancer polygenic risk scores derived in White European populations are not calibrated for women of Ashkenazi Jewish descent (Genetics in Medicine (2023) 25(9), (S1098360023008596), (10.1016/j.gim.2023.100846))
AU - Roberts, Eleanor
AU - van Veen, Elke M.
AU - Byers, Helen
AU - Barnett-Griness, Ofra
AU - Gronich, Naomi
AU - Lejbkowicz, Flavio
AU - Pinchev, Mila
AU - Smith, Miriam J.
AU - Howell, Anthony
AU - Newman, William G.
AU - Woodward, Emma R.
AU - Harkness, Elaine F.
AU - Brentnall, Adam R.
AU - Cuzick, Jack
AU - Rennert, Gad
AU - Howell, Sacha J.
AU - Gareth Evans, D.
N1 - Publisher Copyright:
© 2023 The Authors
PY - 2023/10
Y1 - 2023/10
N2 - Correction to: Genetics in Medicine 2023; https://doi.org/10.1016/j.gim.2023.100846, published online 12 April 2023. In the article “Breast cancer polygenic risk scores derived in White European populations are not calibrated for women of Ashkenazi Jewish descent” (Genet Med 2023;25:100846), the following updates were made. On page 4 (left-hand column, first paragraph), “2 risk alleles = p2 = 0.242 = 0.058, 1 risk allele = 2pq = 2(0.24 × 0.76) = 0.36 and 0 risk alleles = q2 = 0.762 = 0.58. The population risk for the nonrisk allele genotype q2 is (0.058 × 1.242) + (0.36 × 1.24) + (0.58 × 1) = 1.12. The risk for each genotype is homozygous risk allele (p2) = 1.242/1.12 = 1.37, heterozygous risk allele (2pq) = 1.24/1.12 = 1.11, homozygous nonrisk allele (q2) = 1/1.12 = 0.89.17,18” was changed to “Population frequencies are as follows: 2 risk alleles = p2 = 0.242 = 0.058, 1 risk allele = 2pq = 2(0.24 × 0.76) = 0.36 and 0 risk alleles = q2 = 0.762 = 0.58. The population risk for the nonrisk allele genotype q2 is (0.058 × 1.242) + (0.36 × 1.24) + (0.58 × 1) = 1.12. The risk for each genotype is homozygous risk allele (p2) = 1.242/1.12 = 1.37, heterozygous risk allele (2pq) = 1.24/1.12 = 1.11, homozygous nonrisk allele (q2) = 1/1.12 = 0.89.17,18” On page 7 (Funding section), the following sentence has been added “This work was also funded by Cancer Research UK ACED International Alliance for Cancer Early Detection C19941/A27859.” The authors would like to apologize for any inconvenience this may have caused. The article has been corrected online and can be accessed at https://doi.org/10.1016/j.gim.2023.100846.
AB - Correction to: Genetics in Medicine 2023; https://doi.org/10.1016/j.gim.2023.100846, published online 12 April 2023. In the article “Breast cancer polygenic risk scores derived in White European populations are not calibrated for women of Ashkenazi Jewish descent” (Genet Med 2023;25:100846), the following updates were made. On page 4 (left-hand column, first paragraph), “2 risk alleles = p2 = 0.242 = 0.058, 1 risk allele = 2pq = 2(0.24 × 0.76) = 0.36 and 0 risk alleles = q2 = 0.762 = 0.58. The population risk for the nonrisk allele genotype q2 is (0.058 × 1.242) + (0.36 × 1.24) + (0.58 × 1) = 1.12. The risk for each genotype is homozygous risk allele (p2) = 1.242/1.12 = 1.37, heterozygous risk allele (2pq) = 1.24/1.12 = 1.11, homozygous nonrisk allele (q2) = 1/1.12 = 0.89.17,18” was changed to “Population frequencies are as follows: 2 risk alleles = p2 = 0.242 = 0.058, 1 risk allele = 2pq = 2(0.24 × 0.76) = 0.36 and 0 risk alleles = q2 = 0.762 = 0.58. The population risk for the nonrisk allele genotype q2 is (0.058 × 1.242) + (0.36 × 1.24) + (0.58 × 1) = 1.12. The risk for each genotype is homozygous risk allele (p2) = 1.242/1.12 = 1.37, heterozygous risk allele (2pq) = 1.24/1.12 = 1.11, homozygous nonrisk allele (q2) = 1/1.12 = 0.89.17,18” On page 7 (Funding section), the following sentence has been added “This work was also funded by Cancer Research UK ACED International Alliance for Cancer Early Detection C19941/A27859.” The authors would like to apologize for any inconvenience this may have caused. The article has been corrected online and can be accessed at https://doi.org/10.1016/j.gim.2023.100846.
UR - http://www.scopus.com/inward/record.url?scp=85169585387&partnerID=8YFLogxK
U2 - 10.1016/j.gim.2023.100963
DO - 10.1016/j.gim.2023.100963
M3 - ???researchoutput.researchoutputtypes.contributiontojournal.comment???
C2 - 37650883
AN - SCOPUS:85169585387
SN - 1098-3600
VL - 25
SP - 100963
JO - Genetics in Medicine
JF - Genetics in Medicine
IS - 10
M1 - 100963
ER -