المؤلفون: Møller, Pål, Ahadova, Aysel, Kloor, Matthias, Seppälä, Toni T., Burn, John, Haupt, Saskia, Macrae, Finlay, Dominguez-Valentin, Mev, Möslein, Gabriela, Lindblom, Annika, sunde, Lone, Winship, Ingrid, Capella, Gabriel, Monahan, Kevin, Buchanan, Daniel D., Evans, D. Gareth, Hovig, Eivind, Sampson, Julian R.

المساهمون: Syöpäsäätiö, Sigrid Juselius Foundation, Jane and Aatos Erkko Foundation, Relander Foundation, Research Council of Finland, Finland State Research Funding through Pirha and to HUS, Manchester National Institute for Health Research (NIHR) Biomedical Research Centre

المصدر: Hereditary Cancer in Clinical Practice ; volume 23, issue 1 ; ISSN 1897-4287

الاتاحة: https://doi.org/10.1186/s13053-025-00305-y
https://link.springer.com/content/pdf/10.1186/s13053-025-00305-y.pdf
https://link.springer.com/article/10.1186/s13053-025-00305-y/fulltext.html

المؤلفون: Møller, Pål, Haupt, Saskia, Ahadova, Aysel, Kloor, Matthias, Sampson, Julian R., Sunde, Lone, Seppälä, Toni, Burn, John, Bernstein, Inge, Capella, Gabriel, Evans, D. Gareth, Lindblom, Annika, Winship, Ingrid, Macrae, Finlay, Katz, Lior, Laish, Ido, Vainer, Elez, Monahan, Kevin, Half, Elizabeth, Horisberger, Karoline, da Silva, Leandro Apolinário, Heuveline, Vincent, Therkildsen, Christina, Lautrup, Charlotte, Klarskov, Louise L, Cavestro, Giulia Martina, Möslein, Gabriela, Hovig, Eivind, Dominguez-Valentin, Mev

المساهمون: Møller, Pål, Haupt, Saskia, Ahadova, Aysel, Kloor, Matthia, Sampson, Julian R., Sunde, Lone, Seppälä, Toni, Burn, John, Bernstein, Inge, Capella, Gabriel, Evans, D. Gareth, Lindblom, Annika, Winship, Ingrid, Macrae, Finlay, Katz, Lior, Laish, Ido, Vainer, Elez, Monahan, Kevin, Half, Elizabeth, Horisberger, Karoline, da Silva, Leandro Apolinário, Heuveline, Vincent, Therkildsen, Christina, Lautrup, Charlotte, Klarskov, Louise L, Cavestro, Giulia Martina, Möslein, Gabriela, Hovig, Eivind, Dominguez-Valentin, Mev

مصطلحات موضوعية: MLH1, MSH2, MSH6, PMS2, Adenoma, Colonoscopy, Colorectal, Lynch syndromes, MSI, Sojourn time, cancer, dMMR

Relation: info:eu-repo/semantics/altIdentifier/pmid/38741120; info:eu-repo/semantics/altIdentifier/wos/WOS:001221703300001; volume:22; issue:1; numberofpages:12; journal:HEREDITARY CANCER IN CLINICAL PRACTICE; https://hdl.handle.net/20.500.11768/168463

الاتاحة: https://hdl.handle.net/20.500.11768/168463
https://doi.org/10.1186/s13053-024-00279-3
https://hccpjournal.biomedcentral.com/articles/10.1186/s13053-024-00279-3

المؤلفون: Katona, Bryson W., Lubinski, Jan, Pal, Tuya, Huzarski, Tomasz, Foulkes, William D., Moller, Pal, Eisen, Andrea, Randall Armel, Susan, Neuhausen, Susan L., Raj, Rebecca, Aeilts, Amber, Singer, Christian F., Bordeleau, Louise, Karlan, Beth, Olopade, Olufunmilayo, Tung, Nadine, Zakalik, Dana, Kotsopoulos, Joanne, Fruscio, Robert, Eng, Charis, Sun, Ping, Narod, Steven A.

المساهمون: Peter Gilgan Foundation, Canadian Institutes of Health Research

المصدر: Cancer ; volume 131, issue 1 ; ISSN 0008-543X 1097-0142

الاتاحة: https://doi.org/10.1002/cncr.35666

المؤلفون: van der Werf-'t Lam, Anne Sophie, Rodriguez-Girondo, Mar, Villasmil, Mandy, Tops, Carli M., van Hest, Liselotte, Gille, Hans J.P., Duijkers, Floor A.M., Wagner, Anja, Eikenboom, Ellis, Letteboer, Tom G.W., de Jong, Mirjam M., Bajwa-ten Broeke, Sanne W., Bleeker, Fonnet, Gomez Garcia, Encarna B., Dominguez-Valentin, Mev, Møller, Pal, Suerink, Manon, Nielsen, Maartje

المساهمون: Genetica, Genetica Klinische Genetica, Child Health

مصطلحات موضوعية: cancer risks, colorectal carcinoma, endometrial carcinoma, Lynch syndrome, Genetics, Cancer Research

وصف الملف: application/pdf

Relation: https://dspace.library.uu.nl/handle/1874/455305

الاتاحة: https://dspace.library.uu.nl/handle/1874/455305

المؤلفون: Kotsopoulos, Joanne, Gronwald, Jacek, Huzarski, Tomasz, Møller, Pål, Pal, Tuya, McCuaig, Jeanna M, Singer, Christian F, Karlan, Beth Y, Aeilts, Amber, Eng, Charis, Eisen, Andrea, Bordeleau, Louise, Foulkes, William D, Tung, Nadine, Couch, Fergus J, Fruscio, Robert, Neuhausen, Susan L, Zakalik, Dana, Cybulski, Cezary, Metcalfe, Kelly, Olopade, Olufunmilayo I, Sun, Ping, Lubinski, Jan, Narod, Steven A, Sweet, Kevin, Elser, Christine, Wiesner, Georgia, Poll, Aletta, Kim, Raymond, Armel, Susan T, Demsky, Rochelle, Steele, Linda, Saal, Howard, Serfas, Kim, Panchal, Seema, Cullinane, Carey A, Reilly, Robert E, Rayson, Daniel, Mercer, Leanne, Cajal, Teresa Ramon Y, Dungan, Jeffrey, Cohen, Stephanie, Lemire, Edmond, Zovato, Stefania, Rastelli, Antonella

المصدر: JAMA Oncology, vol 10, iss 4

مصطلحات موضوعية: Biomedical and Clinical Sciences, Oncology and Carcinogenesis, Cancer, Breast Cancer, Ovarian Cancer, Clinical Research, Prevention, Rare Diseases, Good Health and Well Being, Female, Humans, Adult, Middle Aged, Aged, Male, BRCA1 Protein, BRCA2 Protein, Cohort Studies, Longitudinal Studies, Mutation, Ovariectomy, Breast Neoplasms, Risk Management, Ovarian Neoplasms, Hereditary Breast Cancer Clinical Study Group, Public Health and Health Services

جغرافية الموضوع: 484 - 492

Relation: qt54c734r5; https://escholarship.org/uc/item/54c734r5

الاتاحة: https://escholarship.org/uc/item/54c734r5

المؤلفون: Metcalfe, Kelly, Huzarski, Tomasz, Gronwald, Jacek, Kotsopoulos, Joanne, Kim, Raymond, Moller, Pal, Pal, Tuya, Aeilts, Amber, Eisen, Andrea, Karlan, Beth, Bordeleau, Louise, Tung, Nadine, Olopade, Olufunmilayo, Zakalik, Dana, Singer, Christian F, Foulkes, William, Couch, Fergus, Neuhausen, Susan L, Eng, Charis, Sun, Ping, Lubinski, Jan, Narod, Steven A

المصدر: British Journal of Cancer, vol 130, iss 2

مصطلحات موضوعية: Biomedical and Clinical Sciences, Oncology and Carcinogenesis, Cancer, Breast Cancer, Genetics, Aetiology, 2.1 Biological and endogenous factors, Good Health and Well Being, Female, Humans, Breast Neoplasms, Mastectomy, BRCA1 Protein, BRCA2 Protein, Genes, BRCA1, Mutation, Hereditary Breast Cancer Clinical Study Group, Public Health and Health Services, Oncology & Carcinogenesis

جغرافية الموضوع: 269 - 274

Relation: qt8xf8w3qd; https://escholarship.org/uc/item/8xf8w3qd

الاتاحة: https://escholarship.org/uc/item/8xf8w3qd

المؤلفون: Lubinski, Jan, Kotsopoulos, Joanne, Moller, Pal, Pal, Tuya, Eisen, Andrea, Peck, Larissa, Karlan, Beth Y, Aeilts, Amber, Eng, Charis, Bordeleau, Louise, Foulkes, William D, Tung, Nadine, Couch, Fergus J, Fruscio, Robert, Ramon y Cajal, Teresa, Singer, Christian F, Neuhausen, Susan L, Zakalik, Dana, Cybulski, Cezary, Gronwald, Jacek, Huzarski, Tomasz, Stempa, Klaudia, Dungan, Jeffrey, Cullinane, Carey, Olopade, Olufunmilayo I, Metcalfe, Kelly, Sun, Ping, Narod, Steven A, Sweet, Kevin, Senter, Leigha, Saal, Howard, Velsher, Lea, Armel, Susan, McCuaig, Jeanna, Panchal, Seema, Poll, Aletta, Lemire, Edmond, Serfas, Kim, Reilly, Robert, Costalas, Josephine, Cohen, Stephanie, Blum, Joanne

المصدر: JAMA Oncology, vol 10, iss 4

مصطلحات موضوعية: Biomedical and Clinical Sciences, Oncology and Carcinogenesis, Clinical Research, Cancer, Prevention, Breast Cancer, 2.4 Surveillance and distribution, Aetiology, Good Health and Well Being, Female, Humans, Adult, Aged, Middle Aged, Breast Neoplasms, BRCA1 Protein, Genes, BRCA2, BRCA2 Protein, Mastectomy, Cohort Studies, BRCA1, Mutation, Risk Management, Magnetic Resonance Imaging, Hereditary Breast Cancer Clinical Study Group, Public Health and Health Services

جغرافية الموضوع: 493 - 499

Relation: qt1k92c3wj; https://escholarship.org/uc/item/1k92c3wj

الاتاحة: https://escholarship.org/uc/item/1k92c3wj

المؤلفون: Cavestro, Giulia Martina, Mannucci, Alessandro, Balaguer, Francesc, Hampel, Heather, Kupfer, Sonia S., Repici, Alessandro, Sartore-Bianchi, Andrea, Seppälä, Toni T., Valentini, Vincenzo, Boland, Clement Richard, Brand, Randall E., Buffart, Tineke E., Burke, Carol A., Caccialanza, Riccardo, Cannizzaro, Renato, Cascinu, Stefano, Cercek, Andrea, Crosbie, Emma J., Danese, Silvio, Dekker, Evelien, Daca-Alvarez, Maria, Deni, Francesco, Dominguez-Valentin, Mev, Eng, Cathy, Goel, Ajay, Guillem, Josè G., Houwen, Britt B. S. L., Kahi, Charles, Kalady, Matthew F., Kastrinos, Fay, Kühn, Florian, Laghi, Luigi, Latchford, Andrew, Liska, David, Lynch, Patrick, Malesci, Alberto, Mauri, Gianluca, Meldolesi, Elisa, Møller, Pål, Monahan, Kevin J., Möslein, Gabriela, Murphy, Caitlin C., Nass, Karlijn, Ng, Kimmie, Oliani, Cristina, Papaleo, Enrico, Patel, Swati G., Puzzono, Marta, Remo, Andrea, Ricciardiello, Luigi, Ripamonti, Carla Ida, Siena, Salvatore, Singh, Satish K., Stadler, Zsofia K., Stanich, Peter P., Syngal, Sapna, Turi, Stefano, Urso, Emanuele Damiano, Valle, Laura, Vanni, Valeria Stella, Vilar, Eduardo, Vitellaro, Marco, You, Yi-Qian Nancy, Yurgelun, Matthew B., Zuppardo, Raffaella Alessia, Stoffel, Elena M.

المساهمون: Cavestro, Giulia Martina, Mannucci, Alessandro, Balaguer, Francesc, Hampel, Heather, Kupfer, Sonia S., Repici, Alessandro, Sartore-Bianchi, Andrea, Seppälä, Toni T., Valentini, Vincenzo, Boland, Clement Richard, Brand, Randall E., Buffart, Tineke E., Burke, Carol A., Caccialanza, Riccardo, Cannizzaro, Renato, Cascinu, Stefano, Cercek, Andrea, Crosbie, Emma J., Danese, Silvio, Dekker, Evelien, Daca-Alvarez, Maria, Deni, Francesco, Dominguez-Valentin, Mev, Eng, Cathy, Goel, Ajay, Guillem, Josè G., Houwen, Britt B. S. L., Kahi, Charle, Kalady, Matthew F., Kastrinos, Fay, Kühn, Florian, Laghi, Luigi, Latchford, Andrew, Liska, David, Lynch, Patrick, Malesci, Alberto, Mauri, Gianluca, Meldolesi, Elisa, Møller, Pål, Monahan, Kevin J., Möslein, Gabriela, Murphy, Caitlin C., Nass, Karlijn, Ng, Kimmie, Oliani, Cristina, Papaleo, Enrico, Patel, Swati G., Puzzono, Marta, Remo, Andrea, Ricciardiello, Luigi, Ripamonti, Carla Ida, Siena, Salvatore, Singh, Satish K., Stadler, Zsofia K., Stanich, Peter P., Syngal, Sapna, Turi, Stefano, Urso, Emanuele Damiano, Valle, Laura, Vanni, Valeria Stella, Vilar, Eduardo, Vitellaro, Marco, You, Yi-Qian Nancy, Yurgelun, Matthew B., Zuppardo, Raffaella Alessia, Stoffel, Elena M.

مصطلحات موضوعية: 50 Years, Clinical, Colorectal Cancer, Recommendation, Young

Relation: info:eu-repo/semantics/altIdentifier/pmid/36549470; info:eu-repo/semantics/altIdentifier/wos/WOS:001086330600001; volume:21; issue:3; firstpage:581; lastpage:603; numberofpages:23; journal:CLINICAL GASTROENTEROLOGY AND HEPATOLOGY; https://hdl.handle.net/20.500.11768/168460

الاتاحة: https://hdl.handle.net/20.500.11768/168460
https://doi.org/10.1016/j.cgh.2022.12.006
https://www.cghjournal.org/article/S1542-3565(22)01171-5/fulltext

المؤلفون: Dominguez-Valentin, Mev, Haupt, Saskia, Seppälä, Toni T., Sampson, Julian R., Sunde, Lone, Bernstein, Inge, Jenkins, Mark A., Engel, Christoph, Aretz, Stefan, Nielsen, Maartje, Capella, Gabriel, Balaguer, Francesc, Evans, Dafydd Gareth, Burn, John, Holinski-Feder, Elke, Bertario, Lucio, Bonanni, Bernardo, Lindblom, Annika, Levi, Zohar, Macrae, Finlay, Winship, Ingrid, Plazzer, John Paul, Sijmons, Rolf, Laghi, Luigi, Della Valle, Adriana, Heinimann, Karl, Dębniak, Tadeusz, Fruscio, Robert, Lopez-Koestner, Francisco, Alvarez-Valenzuela, Karin, Katz, Lior H., Laish, Ido, Vainer, Elez, Vaccaro, Carlos, Carraro, Dirce Maria, Monahan, Kevin, Half, Elizabeth, Stakelum, Aine, Winter, Des, Kennelly, Rory, Gluck, Nathan, Sheth, Harsh, Abu-Freha, Naim, Greenblatt, Marc, Rossi, Benedito Mauro, Bohorquez, Mabel, Cavestro, Giulia Martina, Lino-Silva, Leonardo S., Horisberger, Karoline, Tibiletti, Maria Grazia, Nascimento, Ivana do, Thomas, Huw, Rossi, Norma Teresa, Apolinário da Silva, Leandro, Zaránd, Attila, Ruiz-Bañobre, Juan, Heuveline, Vincent, Mecklin, Jukka Pekka, Pylvänäinen, Kirsi, Renkonen-Sinisalo, Laura, Lepistö, Anna, Peltomäki, Päivi, Therkildsen, Christina, Madsen, Mia Gebauer, Burgdorf, Stefan Kobbelgaard, Hopper, John L., Win, Aung Ko, Haile, Robert W., Lindor, Noralane, Gallinger, Steven, Le Marchand, Loïc, Newcomb, Polly A., Figueiredo, Jane, Buchanan, Daniel D., Thibodeau, Stephen N., von Knebel Doeberitz, Magnus, Loeffler, Markus, Rahner, Nils, Schröck, Evelin, Steinke-Lange, Verena, Schmiegel, Wolff, Vangala, Deepak, Perne, Claudia, Hüneburg, Robert, Redler, Silke, Büttner, Reinhard, Weitz, Jürgen, Pineda, Marta, Duenas, Nuria, Vidal, Joan Brunet, Moreira, Leticia, Sánchez, Ariadna, Hovig, Eivind, Nakken, Sigve, Green, Kate, Lalloo, Fiona, Hill, James, Crosbie, Emma, Mints, Miriam, Goldberg, Yael, Tjandra, Douglas, ten Broeke, Sanne W., Kariv, Revital, Rosner, Guy, Advani, Suresh H., Thomas, Lidiya, Shah, Pankaj, Shah, Mithun, Neffa, Florencia, Esperon, Patricia, Pavicic, Walter, Torrezan, Giovana Tardin, Bassaneze, Thiago, Martin, Claudia Alejandra, Moslein, Gabriela, Moller, Pål

المساهمون: Tampere University, Clinical Medicine, TAYS Cancer Centre

مصطلحات موضوعية: 3122 Cancers

وصف الملف: fulltext

Relation: 101909; 58; ORCID: /0000-0002-4940-3498/work/133055789; https://trepo.tuni.fi/handle/10024/150138; URN:NBN:fi:tuni-202308097517

الاتاحة: https://trepo.tuni.fi/handle/10024/150138
https://doi.org/10.1016/j.eclinm.2023.101909

المؤلفون: Møller, Pal, Seppälä, Toni T., Kohut, Kelly E., Ryan, Neil, Bauerfeind, Peter, Thomas, Laura E., Evans, D. Gareth, Aretz, Stefan, Sijmons, Rolf H., Half, Elizabeth, Heinimann, Karl, Horisberger, Karoline, Ahadova, Aysel, Monahan, Kevin, Crosbie, Emma J., Holinski-Feder, Elke, Scott, Rodney, Haupt, Saskia, Möslein, Gabriela, Winship, Ingrid, Bajwa-ten Broeke, Sanne W.

المساهمون: The University of Newcastle. College of Health, Medicine & Wellbeing, School of Biomedical Sciences and Pharmacy

مصطلحات موضوعية: acetylsalicylic acid, DNA mismatch repair protein MSH2, mismatch repair protein PMS2, MutL protein homolog 1, protein MSH6, SDG 3, Sustainable Development Goals

Relation: Hereditary Cancer in Clinical Practice Vol. 21, Issue 1, no. 19; http://hdl.handle.net/1959.13/1495030; uon:53958

الاتاحة: http://hdl.handle.net/1959.13/1495030

المؤلفون: Dominguez-Valentin, Mev, Crosbie, Emma J., Engel, Christoph, Aretz, Stefan, Macrae, Finlay, Winship, Ingrid, Capella, Gabriel, Thomas, Huw, Nakken, Sigve, Hovig, Eivind, Nielsen, Maartje, Sijmons, Rolf H., Bertario, Lucio, Bonanni, Bernardo, Tibiletti, Maria Grazia, Cavestro, Giulia Martina, Mints, Miriam, Gluck, Nathan, Katz, Lior, Heinimann, Karl, Vaccaro, Carlos A., Green, Kate, Lalloo, Fiona, Hill, James, Schmiegel, Wolff, Vangala, Deepak, Perne, Claudia, Strauss, Hans-Georg, Tecklenburg, Johanna, Holinski-Feder, Elke, Steinke-Lange, Verena, Mecklin, Jukka-Pekka, Plazzer, John-Paul, Pineda, Marta, Navarro, Matilde, Brunet Vidal, Joan, Kariv, Revital, Rosner, Guy, Alejandra Pinero, Tamara, Laura Gonzalez, Maria, Kalfayan, Pablo, Ryan, Neil, Ten Broeke, Sanne W., Jenkins, Mark A., Sunde, Lone, Bernstein, Inge, Burn, John, Greenblatt, Marc, Cappel, Wouter H. de Vos tot Nederveen, Della Valle, Adriana, Lopez-Koestner, Francisco, Alvarez, Karin, Buettner, Reinhard, Goergens, Heike, Morak, Monika, Holzapfel, Stefanie, Hueneburg, Robert, Doeberitz, Magnus von Knebel, Loeffler, Markus, Rahner, Nils, Weitz, Jurgen, Pylvänäinen, Kirsi, Renkonen-Sinisalo, Laura, Lepistö, Anna, Auranen, Annika, Hopper, John L., Win, Aung Ko, Haile, Robert W., Lindor, Noralane M., Gallinger, Steven, Le Marchand, Loic, Newcomb, Polly A., Figueiredo, Jane C., Thibodeau, Stephen N., Therkildsen, Christina, Okkels, Henrik, Ketabi, Zohreh, Denton, Oliver G., Rodland, Einar Andreas, Vasen, Hans, Neffa, Florencia, Esperon, Patricia, Tjandra, Douglas, Moeslein, Gabriela, Sampson, Julian R., Evans, D. Gareth, Seppälä, Toni T., Møller, Pål

المساهمون: ATG - Applied Tumor Genomics, HUS Abdominal Center, II kirurgian klinikka, Department of Surgery, Clinicum, Helsinki University Hospital Area, University of Helsinki

مصطلحات موضوعية: HEREDITARY COLORECTAL-CANCER, ASPIRIN, CAPP2, Biomedicine, General medicine, internal medicine and other clinical medicine

وصف الملف: application/pdf

Relation: The study was supported by a Pink Ribbon grant (194751) from Den Norske Kreftforening to E.H. We express our gratitude to Heikki Jarvinen, Beatrice Alcala-Repo, Teresa Ocana, Maria Pellise, Sabela Carballal, Liseth Rivero, Lorena Moreno, Gerhard Jung, Antoni Castells, Joaquin Cubiella, Laura Rivas, Luis Bujanda, Ines Gil, Jesus Banales, Catalina Garau, Rodrigo Jover, Maria Dolores Pico, Xavier Bessa, Cristina Alvarez, Montserrat Andreu, Carmen Poves, Pedro Perez Segura, Lucia Cid, Marta Carrillo, Enrique Quintero, Angeles Pizarro, Marta Garzon, Adolfo Suarez, Inmaculada Salces, Daniel Rodriguez-Alcalde, Judith Balmana, Adria Lopez, Nuria Duenas, Gemma Llort, Carmen Yague, Teresa Ramon i Cajal, David Fisas Masferrer, Alexandra Gisbert Beamud, Consol Lopez San Martin, Maite Herraiz, Pilar Perez, Cristina Carretero, Maite Betes, Marta Ponce, Elena Aguirre, Nora Alfaro, Carlos Sarroca, and Marianne Haeusler for their efforts over many years. We also thank the Finnish Cancer Foundation, Jane and Aatos Erkko Foundation, Emil Aaltonen Foundation, Finnish Medical Foundation, Instrumentarium Science Foundation, Sigrid Juselius Foundation, and the Norwegian Cancer Society (contract 194751-2017) for funding. D.G.E. and E.J.C. are supported by the all Manchester National Institute for Health Research (NIHR) Biomedical Research Center (IS-BRC-1215-20007) and J.R.S. by Health and Care Research Wales through Wales Gene Park. N.R. was a Medical Research Council Doctoral Research Fellow (MR/M018431/1). Research reported in this publication was supported by the National Cancer Institute (NCI) of the National Institutes of Health (NIH) under award number UM1CA167551 and through cooperative agreements with the following The Colon Cancer Family Registry (CCFR) centers: Australasian Colorectal Cancer Family Registry (NCI/NIH U01 CA074778 and U01/U24 CA097735), Mayo Clinic Cooperative Family Registry for Colon Cancer Studies (NCI/NIH U01/U24 CA074800), Ontario Familial Colorectal Cancer Registry (NCI/NIH U01/U24 CA074783), Seattle Colorectal Cancer Family Registry (NCI/NIH U01/U24 CA074794), University of Hawaii Colorectal Cancer Family Registry (NCI/NIH U01/U24 CA074806 and R01 CA104132 to L.L.), USC Consortium Colorectal Cancer Family Registry (NCI/NIH U01/U24 CA074799). The German Consortium for Familial Intestinal Cancer has been supported by grants from the German Cancer Aid. Data collection from Wales, UK was supported by the Wales Gene Park. This work was cofunded by the European Regional Development Fund (ERDF). M.N. and S.W.t.B were supported by a grant from the Dutch Cancer Society (DCS), grant number UL 2017-8223. G.C., M.P., and J.B.V. were funded by the Spanish Ministry of Economy and Competitiveness and cofunded by FEDER funds (A Way to Build Europe) (grant SAF2015-68016-R), CIBERONC, the Government of Catalonia (grant 2017SGR1282).; Dominguez-Valentin , M , Crosbie , E J , Engel , C , Aretz , S , Macrae , F , Winship , I , Capella , G , Thomas , H , Nakken , S , Hovig , E , Nielsen , M , Sijmons , R H , Bertario , L , Bonanni , B , Tibiletti , M G , Cavestro , G M , Mints , M , Gluck , N , Katz , L , Heinimann , K , Vaccaro , C A , Green , K , Lalloo , F , Hill , J , Schmiegel , W , Vangala , D , Perne , C , Strauss , H-G , Tecklenburg , J , Holinski-Feder , E , Steinke-Lange , V , Mecklin , J-P , Plazzer , J-P , Pineda , M , Navarro , M , Brunet Vidal , J , Kariv , R , Rosner , G , Alejandra Pinero , T , Laura Gonzalez , M , Kalfayan , P , Ryan , N , Ten Broeke , S W , Jenkins , M A , Sunde , L , Bernstein , I , Burn , J , Greenblatt , M , Cappel , W H D V T N , Della Valle , A , Lopez-Koestner , F , Alvarez , K , Buettner , R , Goergens , H , Morak , M , Holzapfel , S , Hueneburg , R , Doeberitz , M V K , Loeffler , M , Rahner , N , Weitz , J , Pylvänäinen , K , Renkonen-Sinisalo , L , Lepistö , A , Auranen , A , Hopper , J L , Win , A K , Haile , R W , Lindor , N M , Gallinger , S , Le Marchand , L , Newcomb , P A , Figueiredo , J C , Thibodeau , S N , Therkildsen , C , Okkels , H , Ketabi , Z , Denton , O G , Rodland , E A , Vasen , H , Neffa , F , Esperon , P , Tjandra , D , Moeslein , G , Sampson , J R , Evans , D G , Seppälä , T T & Møller , P 2021 , ' Risk-reducing hysterectomy and bilateral salpingo-oophorectomy in female heterozygotes of pathogenic mismatch repair variants : a Prospective Lynch Syndrome Database report ' , Genetics In medicine , vol. 23 , no. 4 , pp. 705-712 . https://doi.org/10.1038/s41436-020-01029-1; ORCID: /0000-0002-5866-4059/work/127004131; ORCID: /0000-0002-4940-3498/work/127004783; http://hdl.handle.net/10138/353260; 053c901b-4612-4593-9ac3-efc3c63f8439; 000595283200001

الاتاحة: http://hdl.handle.net/10138/353260

المؤلفون: Ahadova, Aysel, Witt, Johannes, Haupt, Saskia, Gallon, Richard, Hüneburg, Robert, Nattermann, Jacob, ten Broeke, Sanne, Bohaumilitzky, Lena, Hernandez-Sanchez, Alejandro, Santibanez-Koref, Mauro, Jackson, Michael S., Ahtiainen, Maarit, Pylvänäinen, Kirsi, Andini, Katarina, Grolmusz, Vince Kornel, Möslein, Gabriela, Dominguez-Valentin, Mev, Møller, Pål, Fürst, Daniel, Sijmons, Rolf, Borthwick, Gillian M., Burn, John, Mecklin, Jukka Pekka, Heuveline, Vincent, von Knebel Doeberitz, Magnus, Seppälä, Toni, Kloor, Matthias

المصدر: Ahadova , A , Witt , J , Haupt , S , Gallon , R , Hüneburg , R , Nattermann , J , ten Broeke , S , Bohaumilitzky , L , Hernandez-Sanchez , A , Santibanez-Koref , M , Jackson , M S , Ahtiainen , M , Pylvänäinen , K , Andini , K , Grolmusz , V K , Möslein , G , Dominguez-Valentin , M , Møller , P , Fürst , D , Sijmons , R , Borthwick , G M , Burn , J , Mecklin , J P , Heuveline , ....

مصطلحات موضوعية: cancer immunoediting, HLA genotype, immune surveillance, Lynch syndrome, personalized cancer risk

وصف الملف: application/pdf

الاتاحة: https://hdl.handle.net/11370/a0668168-ced0-4ac9-aaa2-31ad3f087fdc
https://research.rug.nl/en/publications/a0668168-ced0-4ac9-aaa2-31ad3f087fdc
https://doi.org/10.1002/ijc.34312
https://pure.rug.nl/ws/files/250012220/Intl_Journal_of_Cancer_2022_Ahadova_Is_HLA_type_a_possible_cancer_risk_modifier_in_Lynch_syndrome.pdf

المؤلفون: Akdeniz, Bayram Cevdet, Mattingsdal, Morten, Dominguez-Valentin, Mev, Frei, Oleksandr, Shadrin, Alexey, Puustusmaa, Mikk, Saar, Regina, Sõber, Siim, Møller, Pål, Andreassen, Ole, Padrik, Peeter, Hovig, Eivind

المصدر: 2072-6694.

Relation: NFR/223273; Akdeniz, Bayram Cevdet Mattingsdal, Morten Dominguez-Valentin, Mev Frei, Oleksandr Shadrin, Alexey Puustusmaa, Mikk Saar, Regina Sõber, Siim Møller, Pål Andreassen, Ole Padrik, Peeter Hovig, Eivind . A Breast Cancer Polygenic Risk Score Is Feasible for Risk Stratification in the Norwegian Population. Cancers. 2023, 15(16); http://hdl.handle.net/10852/108638; 2185454; info:ofi/fmt:kev:mtx:ctx&ctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Cancers&rft.volume=15&rft.spage=&rft.date=2023; Cancers; 15; 16; https://doi.org/10.3390/cancers15164124

الاتاحة: http://hdl.handle.net/10852/108638
https://doi.org/10.3390/cancers15164124

المؤلفون: Møller, Pål, Seppälä, Toni, Dowty, James G, Haupt, Saskia, Dominguez-Valentin, Mev, Sunde, Lone, Bernstein, Inge, Engel, Christoph, Aretz, Stefan, Nielsen, Maartje, Capella, Gabriel, Evans, Dafydd Gareth, Burn, John, Holinski-Feder, Elke, Bertario, Lucio, Bonanni, Bernardo, Lindblom, Annika, Levi, Zohar, Macrae, Finlay, Winship, Ingrid, Plazzer, John-Paul, Sijmons, Rolf, Laghi, Luigi, Valle, Adriana Della, Heinimann, Karl, Half, Elizabeth, Lopez-Koestner, Francisco, Alvarez-Valenzuela, Karin, Scott, Rodney J, Katz, Lior, Laish, Ido, Vainer, Elez, Vaccaro, Carlos Alberto, Carraro, Dirce Maria, Gluck, Nathan, Abu-Freha, Naim, Stakelum, Aine, Kennelly, Rory, Winter, Des, Rossi, Benedito Mauro, Greenblatt, Marc, Bohorquez, Mabel, Sheth, Harsh, Tibiletti, Maria Grazia, Lino-Silva, Leonardo S, Horisberger, Karoline, Portenkirchner, Carmen, Nascimento, Ivana, Rossi, Norma Teresa, da Silva, Leandro Apolinário, Thomas, Huw, Zaránd, Attila, Mecklin, Jukka-Pekka, Pylvänäinen, Kirsi, Renkonen-Sinisalo, Laura, Lepisto, Anna, Peltomäki, Päivi, Therkildsen, Christina, Lindberg, Lars Joachim, Thorlacius-Ussing, Ole, von Knebel Doeberitz, Magnus, Loeffler, Markus, Rahner, Nils, Steinke-Lange, Verena, Schmiegel, Wolff, Vangala, Deepak, Perne, Claudia, Hüneburg, Robert, de Vargas, Aída Falcón, Latchford, Andrew, Gerdes, Anne-Marie, Backman, Ann-Sofie, Guillén-Ponce, Carmen, Snyder, Carrie, Lautrup, Charlotte K, Amor, David, Palmero, Edenir, Stoffel, Elena, Duijkers, Floor, Hall, Michael J, Hampel, Heather, Williams, Heinric, Okkels, Henrik, Lubiński, Jan, Reece, Jeanette, Ngeow, Joanne, Guillem, Jose G, Arnold, Julie, Wadt, Karin, Monahan, Kevin, Senter, Leigha, Rasmussen, Lene J, van Hest, Liselotte P, Ricciardiello, Luigi, Kohonen-Corish, Maija R J, Ligtenberg, Marjolijn J L, Southey, Melissa, Aronson, Melyssa, Zahary, Mohd N, Samadder, N Jewel, Poplawski, Nicola, Hoogerbrugge, Nicoline, Morrison, Patrick J, James, Paul, Lee, Grant, Chen-Shtoyerman, Rakefet, Ankathil, Ravindran, Pai, Rish, Ward, Robyn, Parry, Susan, Dębniak, Tadeusz, John, Thomas, van Overeem Hansen, Thomas, Caldés, Trinidad, Yamaguchi, Tatsuro, Barca-Tierno, Verónica, Garre, Pilar, Cavestro, Giulia Martina, Weitz, Jürgen, Redler, Silke, Büttner, Reinhard, Heuveline, Vincent, Hopper, John L, Win, Aung Ko, Lindor, Noralane, Gallinger, Steven, Le Marchand, Loïc, Newcomb, Polly A, Figueiredo, Jane, Buchanan, Daniel D, Thibodeau, Stephen N, Ten Broeke, Sanne W, Hovig, Eivind, Nakken, Sigve, Pineda, Marta, Dueñas, Nuria, Brunet, Joan, Green, Kate, Lalloo, Fiona, Newton, Katie, Crosbie, Emma J, Mints, Miriam, Tjandra, Douglas, Neffa, Florencia, Esperon, Patricia, Kariv, Revital, Rosner, Guy, Pavicic, Walter Hernán, Kalfayan, Pablo, Torrezan, Giovana Tardin, Bassaneze, Thiago, Martin, Claudia, Moslein, Gabriela, Ahadova, Aysel, Kloor, Matthias, Sampson, Julian R, Jenkins, Mark A

المساهمون: Møller, Pål, Seppälä, Toni, Dowty, James G, Haupt, Saskia, Dominguez-Valentin, Mev, Sunde, Lone, Bernstein, Inge, Engel, Christoph, Aretz, Stefan, Nielsen, Maartje, Capella, Gabriel, Evans, Dafydd Gareth, Burn, John, Holinski-Feder, Elke, Bertario, Lucio, Bonanni, Bernardo, Lindblom, Annika, Levi, Zohar, Macrae, Finlay, Winship, Ingrid, Plazzer, John-Paul, Sijmons, Rolf, Laghi, Luigi, Valle, Adriana Della, Heinimann, Karl, Half, Elizabeth, Lopez-Koestner, Francisco, Alvarez-Valenzuela, Karin, Scott, Rodney J, Katz, Lior, Laish, Ido, Vainer, Elez, Vaccaro, Carlos Alberto, Carraro, Dirce Maria, Gluck, Nathan, Abu-Freha, Naim, Stakelum, Aine, Kennelly, Rory, Winter, De, Rossi, Benedito Mauro, Greenblatt, Marc, Bohorquez, Mabel, Sheth, Harsh, Tibiletti, Maria Grazia, Lino-Silva, Leonardo S, Horisberger, Karoline, Portenkirchner, Carmen, Nascimento, Ivana, Rossi, Norma Teresa, da Silva, Leandro Apolinário, Thomas, Huw, Zaránd, Attila, Mecklin, Jukka-Pekka, Pylvänäinen, Kirsi, Renkonen-Sinisalo, Laura, Lepisto, Anna, Peltomäki, Päivi, Therkildsen, Christina, Lindberg, Lars Joachim, Thorlacius-Ussing, Ole, von Knebel Doeberitz, Magnu, Loeffler, Marku, Rahner, Nil, Steinke-Lange, Verena, Schmiegel, Wolff, Vangala, Deepak, Perne, Claudia, Hüneburg, Robert, de Vargas, Aída Falcón, Latchford, Andrew, Gerdes, Anne-Marie, Backman, Ann-Sofie, Guillén-Ponce, Carmen, Snyder, Carrie, Lautrup, Charlotte K, Amor, David, Palmero, Edenir, Stoffel, Elena, Duijkers, Floor, Hall, Michael J, Hampel, Heather, Williams, Heinric, Okkels, Henrik, Lubiński, Jan, Reece, Jeanette, Ngeow, Joanne, Guillem, Jose G, Arnold, Julie, Wadt, Karin, Monahan, Kevin, Senter, Leigha, Rasmussen, Lene J, van Hest, Liselotte P, Ricciardiello, Luigi, Kohonen-Corish, Maija R J, Ligtenberg, Marjolijn J L, Southey, Melissa, Aronson, Melyssa, Zahary, Mohd N, Samadder, N Jewel

مصطلحات موضوعية: Colonoscopy, Colorectal cancer, Epidemiology, Incidence, Lynch Syndrome, Over-diagnosi, Penetrance, Prevention, Prospective, Segregation analysis

وصف الملف: ELETTRONICO

Relation: info:eu-repo/semantics/altIdentifier/pmid/36182917; info:eu-repo/semantics/altIdentifier/wos/WOS:000862552700001; volume:20; issue:1; firstpage:1; lastpage:11; numberofpages:11; journal:HEREDITARY CANCER IN CLINICAL PRACTICE; https://hdl.handle.net/11585/916445; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85139440044; https://hccpjournal.biomedcentral.com/articles/10.1186/s13053-022-00241-1

الاتاحة: https://hdl.handle.net/11585/916445
https://doi.org/10.1186/s13053-022-00241-1
https://hccpjournal.biomedcentral.com/articles/10.1186/s13053-022-00241-1

المؤلفون: Genetica, Genetica Klinische Genetica, Child Health, van der Werf-'t Lam, Anne Sophie, Rodriguez-Girondo, Mar, Villasmil, Mandy, Tops, Carli M., van Hest, Liselotte, Gille, Hans J.P., Duijkers, Floor A.M., Wagner, Anja, Eikenboom, Ellis, Letteboer, Tom G.W., de Jong, Mirjam M., Bajwa-ten Broeke, Sanne W., Bleeker, Fonnet, Gomez Garcia, Encarna B., Dominguez-Valentin, Mev, Møller, Pal, Suerink, Manon, Nielsen, Maartje

URL: https://doi.org/10.1002/gcc.23237
http://hdl.handle.net/1874/455305
https://dspace.library.uu.nl/handle/1874/455305
http://www.scopus.com/inward/record.url?scp=85192824079&partnerID=8YFLogxK
1045-2257
Genes Chromosomes and Cancer
63
5
e23237

المؤلفون: Zavaleta, Elizabeth, Solis, Nelly, Palacios, Maria Isabel, Zevallos-Escobar, Liz Elva, Corales, Edison Vasquez, Bazo-Alvarez, Juan Carlos, Dominguez-Barrera, Constantino, Campos, Anthony, Wernhoff, Patrik, Ekstrøm, Per Olaf, Møller, Pål, Visnovska, Martina, Hovig, Eivind, Balazar-Palacios, Janina, Alvarez-Valenzuela, Karin, Nakken, Sigve, Dominguez-Valentin, Mev

المصدر: 2072-6694.

Relation: KF/194751; Zavaleta, Elizabeth Solis, Nelly Palacios, Maria Isabel Zevallos-Escobar, Liz Elva Corales, Edison Vasquez Bazo-Alvarez, Juan Carlos Dominguez-Barrera, Constantino Campos, Anthony Wernhoff, Patrik Ekstrøm, Per Olaf Møller, Pål Visnovska, Martina Hovig, Eivind Balazar-Palacios, Janina Alvarez-Valenzuela, Karin Nakken, Sigve Dominguez-Valentin, Mev . Genetic Characterization in High-Risk Individuals from a Low-Resource City of Peru. Cancers. 2022, 14(22), 1-13; http://hdl.handle.net/10852/100391; 2089790; info:ofi/fmt:kev:mtx:ctx&ctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Cancers&rft.volume=14&rft.spage=1&rft.date=2022; Cancers; 14; 22; https://doi.org/10.3390/cancers14225603

الاتاحة: http://hdl.handle.net/10852/100391
https://doi.org/10.3390/cancers14225603

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

وصف الملف: text

Relation: https://eprints.soton.ac.uk/454437/1/GIM_2021_Li_Goldgar.pdf; Li, Hongyan, Engel, Christoph, de la Hoya, Miguel, Peterlongo, Paolo, Yannoukakos, Drakoulis, Livraghi, Luca, Eccles, Diana M. and Goldgar, David E. , ENIGMA Consortium and CIMBA Consortium (2022) 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, 24 (1), 119-129. (doi:10.1016/j.gim.2021.08.016 ).

الاتاحة: https://eprints.soton.ac.uk/454437/
https://eprints.soton.ac.uk/454437/1/GIM_2021_Li_Goldgar.pdf

المؤلفون: Møller, Pål, Evans, Dafydd Gareth

المصدر: Møller , P & Evans , D G 2022 , ' Inherited Cancer Genetic Epidemiology to Improve Precision Medicine ' , Journal of Clinical Medicine , vol. 11 , no. 3 , pp. 879 . https://doi.org/10.3390/jcm11030879

الاتاحة: https://research.manchester.ac.uk/en/publications/70efc614-81a2-461e-8255-7491a9f3a834
https://doi.org/10.3390/jcm11030879
https://www.mdpi.com/2077-0383/11/3/879

المؤلفون: European Hereditary Tumour Grp EHT, Int Mismatch Repair Consortium IMR, Moller, Pal, Seppala, Toni, Dowty, James G., Renkonen-Sinisalo, Laura, Lepistö, Anna, Peltomäki, Päivi

المساهمون: ATG - Applied Tumor Genomics, HUS Abdominal Center, Clinicum, II kirurgian klinikka, Department of Surgery, University of Helsinki, Department of Medical and Clinical Genetics

مصطلحات موضوعية: Lynch Syndrome, Epidemiology, Prevention, Penetrance, Colorectal cancer, Segregation analysis, Prospective, Incidence, Over-diagnosis, Colonoscopy, CLINICAL MANAGEMENT, GERMLINE MUTATIONS, GUIDELINES, CARRIERS, Cancers

وصف الملف: application/pdf

Relation: Toni T. Seppala: Finnish Medical Foundation, Emil Aaltonen Foundation, Cancer Society Finland, Jane and Aatos Erkko Foundation, iCAN Digital Precision Cancer Medicine Flagship, Relander Foundation, Sigrid Juselius Foundation, and Academy of Finland. Jukka-Pekka Mecklin: Cancer Society Finland, Jane and Aatos Erkko Foundation. G Capella team: funded by the Spanish Ministry of Economy and Competitiveness and co-funded by FEDER funds -a way to build Europe-(grant PID2019-111254RB-I00) and CIBERONC (CB16/12/00234). We thank CERCA Program/Generalitat de Catalunya for institutional support. S Aretz, E Holinski-Feder, and V Steinke-Lange were supported by the European Reference Network on Genetic Tumor Risk Syndromes (ERN GENTURIS) -Project ID No 739547. ERN GENTURIS is partly co-funded by the European Union within the framework of the Third Health Programme "ERN-2016 -Framework Partnership Agreement 2017-2021". BMRossi team: we thank LA-GETH (Latin America -Grupo de Estudios de Tumores Hereditarios) for the Institutional support. DGE and EJC are supported by the all Manchester NIHR Biomedical Research Centre (IS-BRC-1215-20007). JRS thanks HCRW for its support via Wales Gene Park. MRJ Kohonen-Corish had a grant from Cancer Council NSW grant RG19-01. J Burn contributed with support from Cancer Research U.K. catalyst award: Aspirin for Cancer Prevention AsCaP CRUK A24991. ". The German Consortium for Familial Intestinal Cancer was supported by grants of the German Cancer Aid. DM Carraro and GT Torrezan: Funded by the National Institute of Science and Technology in Oncogenomics and Therapeutic Innovation (FAPESP 2014/509443-1, CNPq 465682/2014-6 and CAPES -88887.136405/2017-00).). We acknowledge funding from the Norwegian Cancer Society, contract 194751-2017.; European Hereditary Tumour Grp EHT , Int Mismatch Repair Consortium IMR , Moller , P , Seppala , T , Dowty , J G , Renkonen-Sinisalo , L , Lepistö , A & Peltomäki , P 2022 , ' Colorectal cancer incidences in Lynch syndrome : a comparison of results from the prospective lynch syndrome database and the international mismatch repair consortium ' , Hereditary Cancer in Clinical Practice , vol. 20 , no. 1 , 36 . https://doi.org/10.1186/s13053-022-00241-1; ORCID: /0000-0002-5866-4059/work/121252952; ORCID: /0000-0002-4940-3498/work/121253198; ORCID: /0000-0001-8819-2980/work/121256922; http://hdl.handle.net/10138/350020; ec09892c-58be-4988-99b4-21a26f829df1; 000862552700001

الاتاحة: http://hdl.handle.net/10138/350020

المؤلفون: Dominguez-Valentin, Mev, Sampson, Julian R., Seppälä, Toni T., Møller, Pål

وصف الملف: application/pdf

Relation: https://orca.cardiff.ac.uk/id/eprint/148937/3/SAMPSON,%20Julian%20-%20Response%20to%20Chambuso%20et%20al.pdf; Dominguez-Valentin, Mev, Sampson, Julian R. https://orca.cardiff.ac.uk/view/cardiffauthors/A0160820.html orcid:0000-0002-2902-2348 orcid:0000-0002-2902-2348, Seppälä, Toni T. and Møller, Pål 2022. Response to Chambuso et al. Genetics in Medicine 24 (5) , 1151. 10.1016/j.gim.2022.01.005 https://doi.org/10.1016/j.gim.2022.01.005 file https://orca.cardiff.ac.uk/id/eprint/148937/3/SAMPSON,%20Julian%20-%20Response%20to%20Chambuso%20et%20al.pdf

الاتاحة: https://orca.cardiff.ac.uk/id/eprint/148937/
https://doi.org/10.1016/j.gim.2022.01.005
https://orca.cardiff.ac.uk/id/eprint/148937/3/SAMPSON,%20Julian%20-%20Response%20to%20Chambuso%20et%20al.pdf