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Pål Møller

As seen in: Journal of Medical Genetics (JMG), SAGE Publishing, JAMA Network, JAMA Oncology
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Articles by Pål Møller

Projected Benefit of Bilateral Salpingo-Oophorectomy by Age in BRCA Carriers

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By Vasily Giannakeas, Adriana Apostol, Nupur Dave, Jacek Gronwald, Robert Fruscio, Beth Karlan, Cezary Cybulski, Christian F. Singer, Pål Møller, Raymond Kim, Louise Bordeleau, Tuya Pal, Andrea Eisen, Fergus J. Couch, Dana Zakalik, Kelly A. Metcalfe, Nadine Tung, Amber M Aeilts, Ping Sun, Jan Lubinski, Joanne Kotsopoulos, Steven A. Narod, Kevin Sweet, Christine Elser, Seema Panchal, Georgia L. Wiesner, Susan Armel, Linda Steele, Robert Reilly, Daniel Rayson, Jeffrey Dungan, Stephanie Cohen, Susan Neuhausen, Sophie Austin Sun, Leigha Senter, Joanne L. Blum, Klaudia Stempa, Olufunmilayo Falusi Olopade, Stefania Zovato, Michelle Jacobson, Tracy Graham, Claudia Diella, Howard Saal, Kim Serfas, Carey A Cullinane, Leanne Mercer, Willam Foulkes, Edmond Lemire, Antonella Rastelli, Intan Schraeder
| JAMA Network Verified
Projected Benefit of Bilateral Salpingo-Oophorectomy by Age in BRCA Carriers Key Points Question What is the residual lifetime risk of ovarian cancer for BRCA carriers according to age at the time of bilateral salpingo-oophorectomy (BSO)? Findings In this study, we analyzed prospective data from 5713 BRCA carriers and applied the life table approach to estimate the residual ovarian cancer risk according to variant type, current age, and projected age at BSO.
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Evaluation of a combined model of Polygenic Risk Score and mismatch repair genes in the association of colorectal cancer for Norwegian cohort

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By Andrew Morris, Pål Møller, Ole A. Andreassen, Bayram C. Akdeniz
| SAGE Publishing
Get full access to this article View all access and purchase options for this article. References 1. Sung H, et al. ‘Global Cancer Statistics 2020: GLOBOCAN Estimates of Incidence and Mortality Worldwide for 36 Cancers in 185 Countries. CA Cancer J Clin 2021; 71: 209–249. 2. Ligtenberg MJL, et al. Heritable somatic methylation and inactivation of MSH2 in families with Lynch syndrome due to deletion of the 3’ exons of TACSTD1. Nat Genet 2009; 41: 112–117. 3. Dominguez-Valentin M, et al.
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Commentary on Estimating cancer risk in carriers of Lynch syndrome variants in UK Biobank

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By Pål Møller, Toni Seppälä, Mev Dominguez-Valentin, Julian Sampson
| Journal of Medical Genetics (JMG)
Footnotes Correction notice This article has been corrected since it was published online, to fix the spelling of two of the authors' last names. Contributors First author guarantee that all authors have substantially contributed to and approved submission of the comment. Funding The authors have not declared a specific grant for this research from any funding agency in the public, commercial or not-for-profit sectors.
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Commentary on Estimating cancer risk in carriers of Lynch syndrome variants in UK Biobank

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By Pål Møller, Julian Sampson, Toni T Säppäla, Mev Domiguez-Valentin
| Journal of Medical Genetics (JMG)
Footnotes Contributors First author guarantee that all authors have substantially contributed to and approved submission of the comment. Funding The authors have not declared a specific grant for this research from any funding agency in the public, commercial or not-for-profit sectors.
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