Erratum: Risks of breast and ovarian cancer for women harboring pathogenic missense variants in BRCA1 and BRCA2 compared with those harboring protein truncating variants (Genetics in Medicine (2022) 24(1) (119–129), (S1098360021011308), (10.1016/j.gim.2021.08.016))

on behalf of the ENIGMA Consortium and CIMBA Consortium

doi:10.1016/j.gim.2022.08.005

Erratum: Risks of breast and ovarian cancer for women harboring pathogenic missense variants in BRCA1 and BRCA2 compared with those harboring protein truncating variants (Genetics in Medicine (2022) 24(1) (119–129), (S1098360021011308), (10.1016/j.gim.2021.08.016))

on behalf of the ENIGMA Consortium and CIMBA Consortium

Medicine Monash Health

Research output: Contribution to journal › Comment / Debate › Other › peer-review

1 Citation (Scopus)

Abstract

Correction to: Genetics in Medicine 2022; https://doi.org/10.1016/j.gim.2021.08.016 In the article “Risks of breast and ovarian cancer for women harboring pathogenic missense variants in BRCA1 and BRCA2 compared with those harboring protein truncating variants” by Li H et al (Genet Med 2022;24:119-129), the affiliations for authors Siranoush Manoukian and Barbara Pasini were not listed correctly. The affiliations have been corrected online and can be accessed at https://doi.org/10.1016/j.gim.2021.08.016.

Original language	English
Pages (from-to)	2208
Number of pages	1
Journal	Genetics in Medicine
Volume	24
Issue number	10
DOIs	https://doi.org/10.1016/j.gim.2022.08.005
Publication status	Published - Oct 2022

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10.1016/j.gim.2022.08.005

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on behalf of the ENIGMA Consortium and CIMBA Consortium (2022). Erratum: Risks of breast and ovarian cancer for women harboring pathogenic missense variants in BRCA1 and BRCA2 compared with those harboring protein truncating variants (Genetics in Medicine (2022) 24(1) (119–129), (S1098360021011308), (10.1016/j.gim.2021.08.016)). Genetics in Medicine, 24(10), 2208. https://doi.org/10.1016/j.gim.2022.08.005

on behalf of the ENIGMA Consortium and CIMBA Consortium. / Erratum : Risks of breast and ovarian cancer for women harboring pathogenic missense variants in BRCA1 and BRCA2 compared with those harboring protein truncating variants (Genetics in Medicine (2022) 24(1) (119–129), (S1098360021011308), (10.1016/j.gim.2021.08.016)). In: Genetics in Medicine. 2022 ; Vol. 24, No. 10. pp. 2208.

@article{3f80d395a0254afb8f16b6d79f58218d,

title = "Erratum: Risks of breast and ovarian cancer for women harboring pathogenic missense variants in BRCA1 and BRCA2 compared with those harboring protein truncating variants (Genetics in Medicine (2022) 24(1) (119–129), (S1098360021011308), (10.1016/j.gim.2021.08.016))",

abstract = "Correction to: Genetics in Medicine 2022; https://doi.org/10.1016/j.gim.2021.08.016 In the article “Risks of breast and ovarian cancer for women harboring pathogenic missense variants in BRCA1 and BRCA2 compared with those harboring protein truncating variants” by Li H et al (Genet Med 2022;24:119-129), the affiliations for authors Siranoush Manoukian and Barbara Pasini were not listed correctly. The affiliations have been corrected online and can be accessed at https://doi.org/10.1016/j.gim.2021.08.016.",

author = "Hongyan Li and Christoph Engel and Hoya, {Miguel de la} and Paolo Peterlongo and Drakoulis Yannoukakos and Luca Livraghi and Paolo Radice and Mads Thomassen and Hansen, {Thomas V.O.} and Gerdes, {Anne Marie} and Nielsen, {Henriette R.} and Caputo, {Sandrine M.} and Alberto Zambelli and Ake Borg and Angela Solano and Abigail Thomas and Parsons, {Michael T.} and Antoniou, {Antonis C.} and Goska Leslie and Xin Yang and Georgia Chenevix-Trench and Trinidad Caldes and Ava Kwong and Pedersen, {Inge S{\o}kilde} and Lautrup, {Charlotte K.} and John, {Esther M.} and Terry, {Mary Beth} and Hopper, {John L.} and Southey, {Melissa C.} and Andrulis, {Irene L.} and Marc Tischkowitz and Ramunas Janavicius and Boonen, {Susanne E.} and Lone Kroeldrup and Liliana Varesco and Ute Hamann and Ana Vega and Palmero, {Edenir I.} and Judy Garber and Marco Montagna and {Van Asperen}, {Christi J.} and Lenka Foretova and Greene, {Mark H.} and Tina Selkirk and Pal Moller and Toland, {Amanda E.} and Domchek, {Susan M.} and James, {Paul A.} and Heather Thorne and Eccles, {Diana M.} and Nielsen, {Sarah M.} and Siranoush Manoukian and Barbara Pasini and Caligo, {Maria A.} and Conxi Lazaro and Judy Kirk and Barbara Wappenschmidt and Spurdle, {Amanda B.} and Couch, {Fergus J.} and Rita Schmutzler and Goldgar, {David E.} and {on behalf of the ENIGMA Consortium and CIMBA Consortium}",

note = "Publisher Copyright: {\textcopyright} 2021 American College of Medical Genetics and Genomics",

year = "2022",

month = oct,

doi = "10.1016/j.gim.2022.08.005",

language = "English",

volume = "24",

pages = "2208",

journal = "Genetics in Medicine",

issn = "1098-3600",

publisher = "Nature Publishing Group",

number = "10",

}

on behalf of the ENIGMA Consortium and CIMBA Consortium 2022, 'Erratum: Risks of breast and ovarian cancer for women harboring pathogenic missense variants in BRCA1 and BRCA2 compared with those harboring protein truncating variants (Genetics in Medicine (2022) 24(1) (119–129), (S1098360021011308), (10.1016/j.gim.2021.08.016))', Genetics in Medicine, vol. 24, no. 10, pp. 2208. https://doi.org/10.1016/j.gim.2022.08.005

Erratum: Risks of breast and ovarian cancer for women harboring pathogenic missense variants in BRCA1 and BRCA2 compared with those harboring protein truncating variants (Genetics in Medicine (2022) 24(1) (119–129), (S1098360021011308), (10.1016/j.gim.2021.08.016)). / on behalf of the ENIGMA Consortium and CIMBA Consortium.
In: Genetics in Medicine, Vol. 24, No. 10, 10.2022, p. 2208.

Research output: Contribution to journal › Comment / Debate › Other › peer-review

TY - JOUR

T1 - Erratum

T2 - Risks of breast and ovarian cancer for women harboring pathogenic missense variants in BRCA1 and BRCA2 compared with those harboring protein truncating variants (Genetics in Medicine (2022) 24(1) (119–129), (S1098360021011308), (10.1016/j.gim.2021.08.016))

AU - Li, Hongyan

AU - Engel, Christoph

AU - Hoya, Miguel de la

AU - Peterlongo, Paolo

AU - Yannoukakos, Drakoulis

AU - Livraghi, Luca

AU - Radice, Paolo

AU - Thomassen, Mads

AU - Hansen, Thomas V.O.

AU - Gerdes, Anne Marie

AU - Nielsen, Henriette R.

AU - Caputo, Sandrine M.

AU - Zambelli, Alberto

AU - Borg, Ake

AU - Solano, Angela

AU - Thomas, Abigail

AU - Parsons, Michael T.

AU - Antoniou, Antonis C.

AU - Leslie, Goska

AU - Yang, Xin

AU - Chenevix-Trench, Georgia

AU - Caldes, Trinidad

AU - Kwong, Ava

AU - Pedersen, Inge Søkilde

AU - Lautrup, Charlotte K.

AU - John, Esther M.

AU - Terry, Mary Beth

AU - Hopper, John L.

AU - Southey, Melissa C.

AU - Andrulis, Irene L.

AU - Tischkowitz, Marc

AU - Janavicius, Ramunas

AU - Boonen, Susanne E.

AU - Kroeldrup, Lone

AU - Varesco, Liliana

AU - Hamann, Ute

AU - Vega, Ana

AU - Palmero, Edenir I.

AU - Garber, Judy

AU - Montagna, Marco

AU - Van Asperen, Christi J.

AU - Foretova, Lenka

AU - Greene, Mark H.

AU - Selkirk, Tina

AU - Moller, Pal

AU - Toland, Amanda E.

AU - Domchek, Susan M.

AU - James, Paul A.

AU - Thorne, Heather

AU - Eccles, Diana M.

AU - Nielsen, Sarah M.

AU - Manoukian, Siranoush

AU - Pasini, Barbara

AU - Caligo, Maria A.

AU - Lazaro, Conxi

AU - Kirk, Judy

AU - Wappenschmidt, Barbara

AU - Spurdle, Amanda B.

AU - Couch, Fergus J.

AU - Schmutzler, Rita

AU - Goldgar, David E.

AU - on behalf of the ENIGMA Consortium and CIMBA Consortium

PY - 2022/10

Y1 - 2022/10

N2 - Correction to: Genetics in Medicine 2022; https://doi.org/10.1016/j.gim.2021.08.016 In the article “Risks of breast and ovarian cancer for women harboring pathogenic missense variants in BRCA1 and BRCA2 compared with those harboring protein truncating variants” by Li H et al (Genet Med 2022;24:119-129), the affiliations for authors Siranoush Manoukian and Barbara Pasini were not listed correctly. The affiliations have been corrected online and can be accessed at https://doi.org/10.1016/j.gim.2021.08.016.

AB - Correction to: Genetics in Medicine 2022; https://doi.org/10.1016/j.gim.2021.08.016 In the article “Risks of breast and ovarian cancer for women harboring pathogenic missense variants in BRCA1 and BRCA2 compared with those harboring protein truncating variants” by Li H et al (Genet Med 2022;24:119-129), the affiliations for authors Siranoush Manoukian and Barbara Pasini were not listed correctly. The affiliations have been corrected online and can be accessed at https://doi.org/10.1016/j.gim.2021.08.016.

UR - http://www.scopus.com/inward/record.url?scp=85138480593&partnerID=8YFLogxK

U2 - 10.1016/j.gim.2022.08.005

DO - 10.1016/j.gim.2022.08.005

M3 - Comment / Debate

AN - SCOPUS:85138480593

SN - 1098-3600

VL - 24

SP - 2208

JO - Genetics in Medicine

JF - Genetics in Medicine

IS - 10

ER -

on behalf of the ENIGMA Consortium and CIMBA Consortium. Erratum: Risks of breast and ovarian cancer for women harboring pathogenic missense variants in BRCA1 and BRCA2 compared with those harboring protein truncating variants (Genetics in Medicine (2022) 24(1) (119–129), (S1098360021011308), (10.1016/j.gim.2021.08.016)). Genetics in Medicine. 2022 Oct;24(10):2208. doi: 10.1016/j.gim.2022.08.005

Erratum: Risks of breast and ovarian cancer for women harboring pathogenic missense variants in BRCA1 and BRCA2 compared with those harboring protein truncating variants (Genetics in Medicine (2022) 24(1) (119–129), (S1098360021011308), (10.1016/j.gim.2021.08.016))

Abstract

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Research output

Risks of breast and ovarian cancer for women harboring pathogenic missense variants in BRCA1 and BRCA2 compared with those harboring protein truncating variants

Cite this