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The incidence of pancreatic cancer in BRCA1 and BRCA2 mutation carriers
The incidence of pancreatic cancer in BRCA1 and BRCA2 mutation carriers
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The incidence of pancreatic cancer in BRCA1 and BRCA2 mutation carriers

IQBAL, J ; RAGONE, A ; SENTER, L ; SINGER, C. F ; AINSWORTH, P ; KIM-SING, C ; TUNG, N ; FRIEDMAN, E ; LLACUACHAQUI, M ; PING, S ; NAROD, S. A ; LUBINSKI, J ; LYNCH, H. T ; MOLLER, P ; GHADIRIAN, P ; FOULKES, W. D ; ARMEL, S ; EISEN, A ; NEUHAUSEN, S. L

British journal of cancer, 2012-12, Vol.107 (12), p.2005-2009 [Periódico revisado por pares]

Basingstoke: Nature Publishing Group

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2
Incidence of colorectal cancer in BRCA1 and BRCA2 mutation carriers: results from a follow-up study
Incidence of colorectal cancer in BRCA1 and BRCA2 mutation carriers: results from a follow-up study
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Incidence of colorectal cancer in BRCA1 and BRCA2 mutation carriers: results from a follow-up study

PHELAN, C. M ; IQBAL, J ; NEUHAUSEN, S. L ; SENTER, L ; SINGER, C. F ; AINSWORTH, P ; KIM-SING, C ; TUNG, N ; LLACUACHAQUI, M ; CHORNOKUR, G ; PING, S ; NAROD, S. A ; LYNCH, H. T ; LUBINSKI, J ; GRONWALD, J ; MOLLER, P ; GHADIRIAN, P ; FOULKES, W. D ; ARMEL, S ; EISEN, A

British journal of cancer, 2014-01, Vol.110 (2), p.530-534 [Periódico revisado por pares]

Basingstoke: Nature Publishing Group

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3
BRCA1 and BRCA2 genetic testing—pitfalls and recommendations for managing variants of uncertain clinical significance
BRCA1 and BRCA2 genetic testing—pitfalls and recommendations for managing variants of uncertain clinical significance
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BRCA1 and BRCA2 genetic testing—pitfalls and recommendations for managing variants of uncertain clinical significance

Eccles, D.M. ; Mitchell, G. ; Monteiro, A.N.A. ; Schmutzler, R. ; Couch, F.J. ; Spurdle, A.B. ; Gómez-García, E.B. ; Driessen, R. ; Lindor, N.M. ; Blok, M.J. ; Moller, P. ; de la Hoya, M. ; Pal, T. ; Domchek, S. ; Nathanson, K. ; Van Asperen, C. ; Diez, O. ; Rheim, K. ; Stoppa-Lyonnet, D. ; Parsons, M. ; Goldgar, D.

Annals of oncology, 2015-10, Vol.26 (10), p.2057-2065 [Periódico revisado por pares]

England: Elsevier Ltd

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4
Hormone Therapy and the Risk of Breast Cancer in BRCA1 Mutation Carriers
Hormone Therapy and the Risk of Breast Cancer in BRCA1 Mutation Carriers
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Hormone Therapy and the Risk of Breast Cancer in BRCA1 Mutation Carriers

Eisen, Andrea ; Lubinski, Jan ; Gronwald, Jacek ; Moller, Pal ; Lynch, Henry T. ; Klijn, Jan ; Kim-Sing, Charmaine ; Neuhausen, Susan L. ; Gilbert, Lucy ; Ghadirian, Parviz ; Manoukian, Siranoush ; Rennert, Gad ; Friedman, Eitan ; Isaacs, Claudine ; Rosen, Eliot ; Rosen, Barry ; Daly, Mary ; Sun, Ping ; Narod, Steven A.

JNCI : Journal of the National Cancer Institute, 2008-10, Vol.100 (19), p.1361-1367 [Periódico revisado por pares]

Cary, NC: Oxford University Press

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5
MSH2 Mutation Carriers Are at Higher Risk of Cancer Than MLH1 Mutation Carriers: A Study of Hereditary Nonpolyposis Colorectal Cancer Families
MSH2 Mutation Carriers Are at Higher Risk of Cancer Than MLH1 Mutation Carriers: A Study of Hereditary Nonpolyposis Colorectal Cancer Families
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MSH2 Mutation Carriers Are at Higher Risk of Cancer Than MLH1 Mutation Carriers: A Study of Hereditary Nonpolyposis Colorectal Cancer Families

VASEN, H. F. A ; STORMORKEN, A ; MENKO, F. H ; NAGENGAST, F. M ; KLEIBEUKER, J. H ; GRIFFIOEN, G ; TAAL, B. G ; MOLLER, P ; WIJNEN, J. T

Journal of clinical oncology, 2001-10, Vol.19 (20), p.4074-4080 [Periódico revisado por pares]

Baltimore, MD: American Society of Clinical Oncology

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6
The Comet Assay as a Rapid Test in Biomonitoring Occupational Exposure to DNA-damaging Agents and Effect of Confounding Factors
The Comet Assay as a Rapid Test in Biomonitoring Occupational Exposure to DNA-damaging Agents and Effect of Confounding Factors
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The Comet Assay as a Rapid Test in Biomonitoring Occupational Exposure to DNA-damaging Agents and Effect of Confounding Factors

Møller, P ; Knudsen, L E ; Loft, S ; Wallin, H

Cancer epidemiology, biomarkers & prevention, 2000-10, Vol.9 (10), p.1005-1015 [Periódico revisado por pares]

Philadelphia, PA: American Association for Cancer Research

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7
Recommendations to improve identification of hereditary and familial colorectal cancer in Europe
Recommendations to improve identification of hereditary and familial colorectal cancer in Europe
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Recommendations to improve identification of hereditary and familial colorectal cancer in Europe

Vasen, H. F. A. ; Möslein, G. ; Alonso, A. ; Aretz, S. ; Bernstein, I. ; Bertario, L. ; Blanco, I. ; Bulow, S. ; Burn, J. ; Capella, G. ; Colas, C. ; Engel, C. ; Frayling, I. ; Rahner, N. ; Hes, F. J. ; Hodgson, S. ; Mecklin, J.-P. ; Møller, P. ; Myrhøj, T. ; Nagengast, F. M. ; Parc, Y. ; Ponz de Leon, M. ; Renkonen-Sinisalo, L. ; Sampson, J. R. ; Stormorken, A. ; Tejpar, S. ; Thomas, H. J. W. ; Wijnen, J. ; Lubinski, J. ; Järvinen, H. ; Claes, E. ; Heinimann, K. ; Karagiannis, J. A. ; Lindblom, A. ; Dove-Edwin, I. ; Müller, H.

Familial cancer, 2010-06, Vol.9 (2), p.109-115 [Periódico revisado por pares]

Dordrecht: Springer Netherlands

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8
Human papillomavirus immunization uptake among girls with a refugee background compared with Danish-born girls: a national register-based cohort study
Human papillomavirus immunization uptake among girls with a refugee background compared with Danish-born girls: a national register-based cohort study
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Human papillomavirus immunization uptake among girls with a refugee background compared with Danish-born girls: a national register-based cohort study

Møller, Sanne P ; Kristiansen, Maria ; Norredam, Marie

European journal of cancer prevention, 2018-01, Vol.27 (1), p.42-45 [Periódico revisado por pares]

England

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9
Mutations of the tumor suppressor gene SOCS-1 in classical hodgkin lymphoma are frequent and associated with nuclear phospho-STAT5 accumulation
Mutations of the tumor suppressor gene SOCS-1 in classical hodgkin lymphoma are frequent and associated with nuclear phospho-STAT5 accumulation
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Mutations of the tumor suppressor gene SOCS-1 in classical hodgkin lymphoma are frequent and associated with nuclear phospho-STAT5 accumulation

WENIGER, M. A ; MELZNER, I ; MENZ, C. K ; WEGENER, S ; BUCUR, A. J ; DORSCH, K ; MATTFELDT, T ; BARTH, T. F. E ; MÖLLER, P

Oncogene, 2006-04, Vol.25 (18), p.2679-2684 [Periódico revisado por pares]

Basingstoke: Nature Publishing

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10
Lynch syndrome caused by germline PMS2 mutations: delineating the cancer risk
Lynch syndrome caused by germline PMS2 mutations: delineating the cancer risk
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Lynch syndrome caused by germline PMS2 mutations: delineating the cancer risk

ten Broeke, Sanne W ; Brohet, Richard M ; Tops, Carli M ; van der Klift, Heleen M ; Velthuizen, Mary E ; Bernstein, Inge ; Capellá Munar, Gabriel ; Gomez Garcia, Encarna ; Hoogerbrugge, Nicoline ; Letteboer, Tom G W ; Menko, Fred H ; Lindblom, Annika ; Mensenkamp, Arjen R ; Moller, Pal ; van Os, Theo A ; Rahner, Nils ; Redeker, Bert J W ; Sijmons, Rolf H ; Spruijt, Liesbeth ; Suerink, Manon ; Vos, Yvonne J ; Wagner, Anja ; Hes, Frederik J ; Vasen, Hans F ; Nielsen, Maartje ; Wijnen, Juul T

Journal of clinical oncology, 2015-02, Vol.33 (4), p.319-325 [Periódico revisado por pares]

United States

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