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))

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

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

^*Corresponding author for this work

Research output: Contribution to journal › Comment/debate › Communication

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
Journal	Genetics in Medicine
Volume	24
Issue number	10
Pages (from-to)	2208
Number of pages	1
ISSN	1098-3600
DOIs	https://doi.org/10.1016/j.gim.2022.08.005
Publication status	Published - Oct 2022

Bibliographical note

Keywords

BRCA1
BRCA2
Cancer risks
Missense variants

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10.1016/j.gim.2022.08.005

https://www.sciencedirect.com/science/article/pii/S1098360022008966?via%3Dihub

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Risks of breast and ovarian cancer for women harboring pathogenic missense variants in BRCA1 and BRCA2 compared with those harboring protein truncating variants
Li, H., Engel, C., de la Hoya, M., Peterlongo, P., Yannoukakos, D., Livraghi, L., Radice, P., Thomassen, M., Hansen, T. V. O., Gerdes, A.-M., Nielsen, H. R., Caputo, S. M., Zambelli, A., Borg, A., Solano, A., Thomas, A., Parsons, M. T., Antoniou, A. C., Leslie, G. & Yang, X. & 43 others, Chenevix-Trench, G., Caldes, T., Kwong, A., Pedersen, I. S., Lautrup, C. K., John, E. M., Terry, M. B., Hopper, J. L., Southey, M. C., Andrulis, I. L., Tischkowitz, M., Janavicius, R., Boonen, S. E., Kroeldrup, L., Varesco, L., Hamann, U., Vega, A., Palmero, E. I., Garber, J., Montagna, M., Van Asperen, C. J., Foretova, L., Greene, M. H., Selkirk, T., Moller, P., Toland, A. E., Domchek, S. M., James, P. A., Thorne, H., Eccles, D. M., Nielsen, S. M., Manoukian, S., Pasini, B., Caligo, M. A., Lazaro, C., Kirk, J., Wappenschmidt, B., Spurdle, A. B., Couch, F. J., Schmutzler, R., Goldgar, D. E., ENIGMA consortium & CIMBA Consortium, Jan 2022, In: Genetics in Medicine. 24, 1, p. 119-129 11 p.
Research output: Contribution to journal › Journal article › Research › peer-review

Open Access
19 Citations (Scopus)

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Li, H., Engel, C., de la Hoya, M., Peterlongo, P., Yannoukakos, D., Livraghi, L., Radice, P., Thomassen, M., Hansen, T. V. O., Gerdes, A.-M., Nielsen, H. R., Caputo, S. M., Zambelli, A., Borg, A., Solano, A., Thomas, A., Parsons, M. T., Antoniou, A. C., Leslie, G., ... ENIGMA 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

Li, Hongyan ; Engel, Christoph ; de la Hoya, Miguel et al. / 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.

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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.",

keywords = "BRCA1, BRCA2, Cancer risks, Missense variants",

author = "Hongyan Li and Christoph Engel and {de la Hoya}, Miguel and Paolo Peterlongo and Drakoulis Yannoukakos and Luca Livraghi and Paolo Radice and Mads Thomassen and Hansen, {Thomas V. O.} and Anne-Marie Gerdes 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 {ENIGMA consortium}",

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Li, H, Engel, C, de la Hoya, M, Peterlongo, P, Yannoukakos, D, Livraghi, L, Radice, P, Thomassen, M, Hansen, TVO, Gerdes, A-M, Nielsen, HR, Caputo, SM, Zambelli, A, Borg, A, Solano, A, Thomas, A, Parsons, MT, Antoniou, AC, Leslie, G, Yang, X, Chenevix-Trench, G, Caldes, T, Kwong, A, Pedersen, IS, Lautrup, CK, John, EM, Terry, MB, Hopper, JL, Southey, MC, Andrulis, IL, Tischkowitz, M, Janavicius, R, Boonen, SE, Kroeldrup, L, Varesco, L, Hamann, U, Vega, A, Palmero, EI, Garber, J, Montagna, M, Van Asperen, CJ, Foretova, L, Greene, MH, Selkirk, T, Moller, P, Toland, AE, Domchek, SM, James, PA, Thorne, H, Eccles, DM, Nielsen, SM, Manoukian, S, Pasini, B, Caligo, MA, Lazaro, C, Kirk, J, Wappenschmidt, B, Spurdle, AB, Couch, FJ, Schmutzler, R, Goldgar, DE & ENIGMA 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)). / Li, Hongyan; Engel, Christoph; de la Hoya, Miguel et al.
In: Genetics in Medicine, Vol. 24, No. 10, 10.2022, p. 2208.

Research output: Contribution to journal › Comment/debate › Communication

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 - de la Hoya, Miguel

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 - ENIGMA 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.

KW - BRCA1

KW - BRCA2

KW - Cancer risks

KW - Missense variants

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DO - 10.1016/j.gim.2022.08.005

M3 - Comment/debate

C2 - 36205748

AN - SCOPUS:85138480593

SN - 1098-3600

VL - 24

SP - 2208

JO - Genetics in Medicine

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IS - 10

ER -

Li H, Engel C, de la Hoya M, Peterlongo P, Yannoukakos D, Livraghi L et al. 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

Bibliographical note

Keywords

Access to Document

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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