Publications by authors named "Pal Moller"

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Menopausal hormone therapy and the risk of breast cancer in women with a pathogenic variant in BRCA1 or BRCA2.
Joanne Kotsopoulos, Marta Seca, Jacek Gronwald, Tomasz Huzarski, Pål Møller

J Natl Cancer Inst· December 2025

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Treatment of infertility and risk of breast cancer among women with a BRCA pathogenic variant: a matched case-control study.
Marta Seca, Jacek Gronwald, Tomasz Huzarski, Karen Glass, Amber Aeilts, Pal Moller

BMC Cancer· November 2025

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Ovarian cancer after breast cancer in women with a BRCA1 or BRCA2 pathogenic variant.
Adriana I Apostol, Joanne Kotsopoulos, Jacek Gronwald, Raymond H Kim, Beth Y Karlan, Pal Moller

Gynecol Oncol· October 2025

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Characterization of Screening Strategies for Lynch Syndrome in Latin America.
Anthony Vladimir Campos-Segura, Karin Alvarez, Alexis German Murillo Carrasco, Benedito Mauro Rossi, Mabel Bohorquez

Clin Gastroenterol Hepatol· August 2025

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Optimizing risk-reducing surgery and aspirin decision aids for Lynch syndrome carriers using the person-based approach: A think-aloud interview study.
Kelly Kohut, Kate Morton, Lesley Turner, Rebecca Foster, Elizabeth K Bancroft, Pål Moller

J Genet Couns· August 2025

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Commentary on .
Pål Møller, Toni T Seppälä, Mev Dominguez-Valentin, Julian Sampson

J Med Genet· January 2025

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The incidence of pancreatic cancer in women with a BRCA1 or BRCA2 mutation.
Bryson W Katona, Jan Lubinski, Tuya Pal, Tomasz Huzarski, William D Foulkes, Pal Moller

Cancer· January 2025

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Colorectal carcinogenesis in the Lynch syndromes and familial adenomatous polyposis: trigger events and downstream consequences.
Pål Møller, Aysel Ahadova, Matthias Kloor, Toni T Seppälä, John Burn

Hered Cancer Clin Pract· January 2025

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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.
Bayram C Akdeniz, Andrew H Morris, Pål Møller, Ole Andreassen, Eivind Hovig

Tumori· December 2024

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Incidence of peritoneal cancer after oophorectomy among BRCA1 and BRCA2 mutation carriers.
Steven A Narod, Jacek Gronwald, Beth Karlan, Pal Moller, Tomasz Huzarski

J Natl Cancer Inst· November 2024

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Gene-based burden tests of rare germline variants identify six cancer susceptibility genes.
Erna V Ivarsdottir, Julius Gudmundsson, Vinicius Tragante, Gardar Sveinbjornsson, Snaedis Kristmundsdottir, Pal Moller, Pall H Moller

Nat Genet· November 2024

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Genetic testing for prevention and treatment of cancer.
Pål Møller, Eivind Hovig

Tidsskr Nor Laegeforen· November 2024

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Incidence of endometrial cancer in BRCA mutation carriers.
Joanne Kotsopoulos, Jan Lubinski, Tomasz Huzarski, Brittany L Bychkovsky, Pal Moller

Gynecol Oncol· October 2024

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Delineating genotype and parent-of-origin effect on the phenotype in MSH6-associated Lynch syndrome.
Anne-Sophie van der Werf-'t Lam, Mar Rodriguez-Girondo, Mandy Villasmil, Carli M Tops, Liselotte van Hest

Genes Chromosomes Cancer· May 2024

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Incidences of colorectal adenomas and cancers under colonoscopy surveillance suggest an accelerated "Big Bang" pathway to CRC in three of the four Lynch syndromes.
Pål Møller, Saskia Haupt, Aysel Ahadova, Matthias Kloor, Julian R Sampson

Hered Cancer Clin Pract· May 2024

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MRI Surveillance and Breast Cancer Mortality in Women With BRCA1 and BRCA2 Sequence Variations.
Jan Lubinski, Joanne Kotsopoulos, Pal Moller, Tuya Pal, Andrea Eisen

JAMA Oncol· April 2024

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Bilateral Oophorectomy and All-Cause Mortality in Women With BRCA1 and BRCA2 Sequence Variations.
Joanne Kotsopoulos, Jacek Gronwald, Tomasz Huzarski, Pål Møller, Tuya Pal

JAMA Oncol· April 2024

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Risk-reducing mastectomy and breast cancer mortality in women with a BRCA1 or BRCA2 pathogenic variant: an international analysis.
Kelly Metcalfe, Tomasz Huzarski, Jacek Gronwald, Joanne Kotsopoulos, Raymond Kim, Pal Moller

Br J Cancer· February 2024

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Dominantly inherited micro-satellite instable cancer - the four Lynch syndromes - an EHTG, PLSD position statement.
Pal Møller, Toni T Seppälä, Aysel Ahadova, Emma J Crosbie, Elke Holinski-Feder

Hered Cancer Clin Pract· October 2023

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A Breast Cancer Polygenic Risk Score Is Feasible for Risk Stratification in the Norwegian Population.
Bayram Cevdet Akdeniz, Morten Mattingsdal, Mev Dominguez-Valentin, Oleksandr Frei, Alexey Shadrin

Cancers (Basel)· August 2023

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Mortality by age, gene and gender in carriers of pathogenic mismatch repair gene variants receiving surveillance for early cancer diagnosis and treatment: a report from the prospective Lynch syndrome database.
Mev Dominguez-Valentin, Saskia Haupt, Toni T Seppälä, Julian R Sampson, Lone Sunde, Pål Moller

EClinicalMedicine· April 2023

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Delphi Initiative for Early-Onset Colorectal Cancer (DIRECt) International Management Guidelines.
Giulia Martina Cavestro, Alessandro Mannucci, Francesc Balaguer, Heather Hampel, Sonia S Kupfer

Clin Gastroenterol Hepatol· March 2023

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The risks of cancer in older women with BRCA pathogenic variants: How far have we come?
Kelly A Metcalfe, Jacek Gronwald, Nadine M Tung, Jeanna M McCuaig, Andrea Eisen, Pal Moller

Cancer· March 2023

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The Prospective Lynch Syndrome Database: background, design, main results and complete MySQL code.
Pål Møller

Hered Cancer Clin Pract· November 2022

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Genetic Characterization in High-Risk Individuals from a Low-Resource City of Peru.
Elizabeth Zavaleta, Nelly Solis, Maria Isabel Palacios, Liz Elva Zevallos-Escobar, Edison Vasquez Corales

Cancers (Basel)· November 2022

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