نتائج البحث - "Alnaes, G.I.G."

1

دورية أكاديمية

Germline HOXB13 mutations p.G84E and p.R217C do not confer an increased breast cancer risk

المؤلفون: Liu, J., Prager - van der Smissen, W.J.C., Collée, J.M., Bolla, M.K., Wang, Q., Michailidou, K., Dennis, J., Ahearn, T.U., Aittomäki, K., Ambrosone, C.B., Andrulis, I.L., Truong, T., Untch, M., Vachon, C.M., van Asperen, C.J., Wolk, A., Yamaji, T., Zheng, W., Ziogas, A., Ziv, E., Beckmann, M.W., Hou, M.-F., Torres-Mejía, G., Dörk, T., Swerdlow, A.J., Hamann, U., Schmidt, M.K., Dunning, A.M., Pharoah, P.D.P., Easton, D.F., Behrens, S., Bermisheva, M., Hunter, D.J., Bernstein, L., Bogdanova, N.V., Bogdanova-Markov, N., Bojesen, S.E., Brauch, H., Brenner, H., Briceno, I., Brucker, S.Y., Brüning, T., Burwinkel, B., Huo, D., Cai, Q., Cai, H., Campa, D., Canzian, F., Castelao, J.E., Chang-Claude, J., Chanock, S.J., Choi, J.-Y., Christiaens, M., Clarke, C.L., Clarke, C., Sahlberg, K.K., Børresen-Dale, A.-L., Ottestad, L., Kåresen, R., Schlichting, E., Holmen, M.M., Sauer, T., Haakensen, V., Engebråten, O., Naume, B., Marsh, D., Fosså, A., Kiserud, C.E., Reinertsen, K.V., Helland, Å., Riis, M., Geisler, J., Bathen, T.F., Borgen, E., Fritzman, B., Garred, Ø., Scott, R., Geitvik, G.A., Hofvind, S., Langerød, A., Lingjærde, O.C., Mælandsmo, G.M., Russnes, H.G., Skjerven, H.K., Sørlie, T., Alnæs, G.I.G., Couch, F.J., Baxter, R., Czene, K., Daly, M.B., Devilee, P., dos-Santos-Silva, I., Dwek, M., Eccles, D.M., Eliassen, A.H., Fasching, P.A., Figueroa, J., Flyger, H., Yip, D., Fritschi, L., Gago-Dominguez, M., Gapstur, S.M., García-Closas, M., García-Sáenz, J.A., Gaudet, M.M., Giles, G.G., Goldberg, M.S., Goldgar, D.E., Guénel, P., Carpenter, J., Haiman, C.A., Håkansson, N., Hall, P., Harrington, P.A., Hart, S.N., Hartman, M., Hillemanns, P., Hopper, J.L., Davis, A., Anton-Culver, H., Pathmanathan, N., Simpson, P., Graham, D., Sachchithananthan, M., Ito, H., Iwasaki, M., Jakimovska, M., Jakubowska, A., John, E.M., Kaaks, R., Antonenkova, N.N., Kang, D., Keeman, R., Khusnutdinova, E., Kim, S.-W., Kraft, P., Kristensen, V.N., Kurian, A.W., Le Marchand, L., Li, J., Lindblom, A., Arndt, V., Lophatananon, A., Luben, R.N., Lubi?ski, J., Mannermaa, A., Manoochehri, M., Manoukian, S., Margolin, S., Mariapun, S., Matsuo, K., Maurer, T., Arnold, N., Mavroudis, D., Meindl, A., Menon, U., Milne, R.L., Muir, K., Mulligan, A.M., Neuhausen, S.L., Nevanlinna, H., Offit, K., Olopade, O.I., Aronson, K.J., Olson, J.E., Olsson, H., Orr, N., Park, S.K., Peterlongo, P., Peto, J., Plaseska-Karanfilska, D., Presneau, N., Rack, B., Rau-Murthy, R., Augustinsson, A., Rennert, G., Rennert, H.S., Rhenius, V., Romero, A., Ruebner, M., Saloustros, E., Schmutzler, R.K., Schneeweiss, A., Scott, C., Shah, M., Auvinen, P., Shen, C.-Y., Shu, X.-O., Simard, J., Sohn, C., Southey, M.C., Spinelli, J.J., Tamimi, R.M., Tapper, W.J., Teo, S.H., Terry, M.B., Becher, H., Torres, D.

المساهمون: DEPT OF SURGERY

المصدر: Scopus OA2020

العلاقة: Liu, J., Prager - van der Smissen, W.J.C., Collée, J.M., Bolla, M.K., Wang, Q., Michailidou, K., Dennis, J., Ahearn, T.U., Aittomäki, K., Ambrosone, C.B., Andrulis, I.L., Truong, T., Untch, M., Vachon, C.M., van Asperen, C.J., Wolk, A., Yamaji, T., Zheng, W., Ziogas, A., Ziv, E., Beckmann, M.W., Hou, M.-F., Torres-Mejía, G., Dörk, T., Swerdlow, A.J., Hamann, U., Schmidt, M.K., Dunning, A.M., Pharoah, P.D.P., Easton, D.F., Behrens, S., Bermisheva, M., Hunter, D.J., Bernstein, L., Bogdanova, N.V., Bogdanova-Markov, N., Bojesen, S.E., Brauch, H., Brenner, H., Briceno, I., Brucker, S.Y., Brüning, T., Burwinkel, B., Huo, D., Cai, Q., Cai, H., Campa, D., Canzian, F., Castelao, J.E., Chang-Claude, J., Chanock, S.J., Choi, J.-Y., Christiaens, M., Clarke, C.L., Clarke, C., Sahlberg, K.K., Børresen-Dale, A.-L., Ottestad, L., Kåresen, R., Schlichting, E., Holmen, M.M., Sauer, T., Haakensen, V., Engebråten, O., Naume, B., Marsh, D., Fosså, A., Kiserud, C.E., Reinertsen, K.V., Helland, Å., Riis, M., Geisler, J., Bathen, T.F., Borgen, E., Fritzman, B., Garred, Ø., Scott, R., Geitvik, G.A., Hofvind, S., Langerød, A., Lingjærde, O.C., Mælandsmo, G.M., Russnes, H.G., Skjerven, H.K., Sørlie, T., Alnæs, G.I.G., Couch, F.J., Baxter, R., Czene, K., Daly, M.B., Devilee, P., dos-Santos-Silva, I., Dwek, M., Eccles, D.M., Eliassen, A.H., Fasching, P.A., Figueroa, J., Flyger, H., Yip, D., Fritschi, L., Gago-Dominguez, M., Gapstur, S.M., García-Closas, M., García-Sáenz, J.A., Gaudet, M.M., Giles, G.G., Goldberg, M.S., Goldgar, D.E., Guénel, P., Carpenter, J., Haiman, C.A., Håkansson, N., Hall, P., Harrington, P.A., Hart, S.N., Hartman, M., Hillemanns, P., Hopper, J.L., Davis, A., Anton-Culver, H., Pathmanathan, N., Simpson, P., Graham, D., Sachchithananthan, M., Ito, H., Iwasaki, M., Jakimovska, M., Jakubowska, A., John, E.M., Kaaks, R., Antonenkova, N.N., Kang, D., Keeman, R., Khusnutdinova, E., Kim, S.-W., Kraft, P., Kristensen, V.N., Kurian, A.W., Le Marchand, L., Li, J., Lindblom, A., Arndt, V., Lophatananon, A., Luben, R.N., Lubi?ski, J., Mannermaa, A., Manoochehri, M., Manoukian, S., Margolin, S., Mariapun, S., Matsuo, K., Maurer, T., Arnold, N., Mavroudis, D., Meindl, A., Menon, U., Milne, R.L., Muir, K., Mulligan, A.M., Neuhausen, S.L., Nevanlinna, H., Offit, K., Olopade, O.I., Aronson, K.J., Olson, J.E., Olsson, H., Orr, N., Park, S.K., Peterlongo, P., Peto, J., Plaseska-Karanfilska, D., Presneau, N., Rack, B., Rau-Murthy, R., Augustinsson, A., Rennert, G., Rennert, H.S., Rhenius, V., Romero, A., Ruebner, M., Saloustros, E., Schmutzler, R.K., Schneeweiss, A., Scott, C., Shah, M., Auvinen, P., Shen, C.-Y., Shu, X.-O., Simard, J., Sohn, C., Southey, M.C., Spinelli, J.J., Tamimi, R.M., Tapper, W.J., Teo, S.H., Terry, M.B., Becher, H., Torres, D. (2020). Germline HOXB13 mutations p.G84E and p.R217C do not confer an increased breast cancer risk. Scientific Reports 10 (1) : 9688. ScholarBank@NUS Repository. https://doi.org/10.1038/s41598-020-65665-yTest; https://scholarbank.nus.edu.sg/handle/10635/199341Test

الإتاحة: https://scholarbank.nus.edu.sg/handle/10635/199341Test

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2

دورية أكاديمية

Genome-wide association study of germline variants and breast cancer-specific mortality

المؤلفون: Escala-Garcia, M., Guo, Q., Dörk, T., Canisius, S., Keeman, R., Dennis, J., Beesley, J., Lecarpentier, J., Bolla, M.K., Wang, Q., Abraham, J., Andrulis, I.L., Anton-Culver, H., Arndt, V., Auer, P.L., Beckmann, M.W., Behrens, S., Benitez, J., Bermisheva, M., Bernstein, L., Blomqvist, C., Boeckx, B., Bojesen, S.E., Bonanni, B., Børresen-Dale, A.-L., Brauch, H., Brenner, H., Brentnall, A., Brinton, L., Broberg, P., Brock, I.W., Brucker, S.Y., Burwinkel, B., Caldas, C., Caldés, T., Campa, D., Canzian, F., Carracedo, A., Carter, B.D., Castelao, J.E., Chang-Claude, J., Chanock, S.J., Chenevix-Trench, G., Cheng, T.-Y.D., Chin, S.-F., Clarke, C.L., NBCS Collaborators, Cordina-Duverger, E., Couch, F.J., Cox, D.G., Cox, A., Cross, S.S., Czene, K., Daly, M.B., Devilee, P., Dunn, J.A., Dunning, A.M., Durcan, L., Dwek, M., Earl, H.M., Ekici, A.B., Eliassen, A.H., Ellberg, C., Engel, C., Eriksson, M., Evans, D.G., Figueroa, J., Flesch-Janys, D., Flyger, H., Gabrielson, M., Gago-Dominguez, M., Galle, E., Gapstur, S.M., García-Closas, M., García-Sáenz, J.A., Gaudet, M.M., George, A., Georgoulias, V., Giles, G.G., Glendon, G., Goldgar, D.E., González-Neira, A., Alnæs, G.I.G., Grip, M., Guénel, P., Haeberle, L., Hahnen, E., Haiman, C.A., Håkansson, N., Hall, P., Hamann, U., Hankinson, S., Harkness, E.F., Harrington, P.A., Hart, S.N., Hartikainen, J.M., Hein, A., Hillemanns, P., Hiller, L., Holleczek, B., Hollestelle, A., Hooning, M.J., Hoover, R.N., Hopper, J.L., Howell, A., Huang, G., Humphreys, K., Hunter, D.J., Janni, W., John, E.M., Jones, M.E., Jukkola-Vuorinen, A., Jung, A., Kaaks, R., Kabisch, M., Kaczmarek, K., Kerin, M.J., Khan, S., Khusnutdinova, E., Kiiski, J.I., Kitahara, C.M., Knight, J.A., Ko, Y.-D., Koppert, L.B., Kosma, V.-M., Kraft, P., Kristensen, V.N., Krüger, U., Kühl, T., Lambrechts, D., Le Marchand, L., Lee, E., Lejbkowicz, F., Li, L., Lindblom, A., Lindström, S., Linet, M., Lissowska, J., Lo, W.-Y., Loibl, S., Lubiński, J., Lux, M.P., MacInnis, R.J., Maierthaler, M., Maishman, T., Makalic, E., Mannermaa, A., Manoochehri, M., Manoukian, S., Margolin, S., Martinez, M.E., Mavroudis, D., McLean, C., Meindl, A., Middha, P., Miller, N., Milne, R.L., Moreno, F., Mulligan, A.M., Mulot, C., Nassir, R., Neuhausen, S.L., Newman, W.T., Nielsen, S.F., Nordestgaard, B.G., Norman, A., Olsson, H., Orr, N., Pankratz, V.S., Park-Simon, T.-W., Perez, J.I.A., Pérez-Barrios, C., Peterlongo, P., Petridis, C., Pinchev, M., Prajzendanc, K., Prentice, R., Presneau, N., Prokofieva, D., Pylkäs, K., Rack, B., Radice, P., Ramachandran, D., Rennert, G., Rennert, H.S., Rhenius, V., Romero, A., Roylance, R., Saloustros, E., Sawyer, E.J., Schmidt, D.F., Schmutzler, R.K., Schneeweiss, A., Schoemaker, M.J., Schumacher, F., Schwentner, L., Scott, R.J., Scott, C., Seynaeve, C., Shah, M., Simard, J., Smeets, A., Sohn, C., Southey, M.C., Swerdlow, A.J., Talhouk, A., Tamimi, R.M., Tapper, W.J., Teixeira, M.R., Tengström, M., Terry, M.B., Thöne, K., Tollenaar, R.A.E.M., Tomlinson, I., Torres, D., Truong, T., Turman, C., Turnbull, C., Ulmer, H.-U., Untch, M., Vachon, C., van Asperen, C.J., van den Ouweland, A.M.W., van Veen, E.M., Wendt, C., Whittemore, A.S., Willett, W., Winqvist, R., Wolk, A., Yang, X.R., Zhang, Y., Easton, D.F., Fasching, P.A., Nevanlinna, H., Eccles, D.M., Pharoah, P.D.P., Schmidt, M.K.

وصف الملف: text

العلاقة: https://eprints.whiterose.ac.uk/143034/2/s41416-019-0393-x.pdfTest; Escala-Garcia, M., Guo, Q., Dörk, T. et al. (234 more authors) (2019) Genome-wide association study of germline variants and breast cancer-specific mortality. British Journal of Cancer, 120. pp. 647-657. ISSN 0007-0920

الإتاحة: https://eprints.whiterose.ac.uk/143034Test/
https://eprints.whiterose.ac.uk/143034/2/s41416-019-0393-x.pdfTest

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3

Breast Cancer Risk Genes — Association Analysis in More than 113,000 Women

المؤلفون: Dorling, L., Carvalho, S., Allen, J., Gonzalez-Neira, A., Luccarini, C., Wahlstrom, C., Pooley, K.A., Parsons, M.T., Fortuno, C., Wang, Q., Bolla, M.K., Dennis, J., Keeman, R., Alonso, M.R., Alvarez, N., Herraez, B., Fernandez, V., Nunez-Torres, R., Osorio, A., Valcich, J., Li, M., Torngren, T., Harrington, P.A., Baynes, C., Conroy, D.M., Decker, B., Fachal, L., Mavaddat, N., Ahearn, T., Aittomaki, K., Antonenkova, N.N., Arnold, N., Arveux, P., Ausems, M.G.E.M., Auvinen, P., Becher, H., Beckmann, M.W., Behrens, S., Bermisheva, M., Bialkowska, K., Blomqvist, C., Bogdanova, N.V., Bogdanova-Markov, N., Bojesen, S.E., Bonanni, B., Borresen-Dale, A.L., Brauch, H., Bremer, M., Briceno, I., Bruning, T., Burwinkel, B., Cameron, D.A., Camp, N.J., Campbell, A., Carracedo, A., Castelao, J.E., Cessna, M.H., Chanock, S.J., Christiansen, H., Collee, J.M., Cordina-Duverger, E., Cornelissen, S., Czene, K., Dork, T., Ekici, A.B., Engel, C., Eriksson, M., Fasching, P.A., Figueroa, J., Flyger, H., Forsti, A., Gabrielson, M., Gago-Dominguez, M., Georgoulias, V., Gil, F., Giles, G.G., Glendon, G., Garcia, E.B.G., Alnaes, G.I.G., Guenel, P., Hadjisavvas, A., Haeberle, L., Hahnen, E., Hall, P., Hamann, U., Harkness, E.F., Hartikainen, J.M., Hartman, M., He, W., Heemskerk-Gerritsen, B.A.M., Hillemanns, P., Hogervorst, F.B.L., Hollestelle, A., Ho, W.K., Hooning, M.J., Howell, A., Humphreys, K., Idris, F., Jakubowska, A., Jung, A., Kapoor, P.M., Kerin, M.J., Khusnutdinova, E., Kim, S.W., Ko, Y.D., Kosma, V.M., Kristensen, V.N., Kyriacou, K., Lakeman, I.M.M., Lee, J.W., Lee, M.H., Li, J.M., Lindblom, A., W.Y. lo, Loizidou, M.A., Lophatananon, A., Lubinski, J., MacInnis, R.J., Madsen, M.J., Mannermaa, A., Manoochehri, M., Manoukian, S., Margolin, S., Martinez, M.E., Maurer, T., Mavroudis, D., McLean, C., Meindl, A., Mensenkamp, A.R., Michailidou, K., Miller, N., Taib, N.A.M., Muir, K., Mulligan, A.M., Nevanlinna, H., Newman, W.G., Nordestgaard, B.G., Ng, P.S., Oosterwijk, J.C., Park, S.K., Park-Simon, T.W., Perez, J.I.A., Peterlongo, P., Porteous, D.J., Prajzendanc, K., Prokofyeva, D., Radice, P., Rashid, M.U., Rhenius, V., Rookus, M.A., Rudiger, T., Saloustros, E., Sawyer, E.J., Schmutzler, R.K., Schneeweiss, A., Schurmann, P., Shah, M., Sohn, C., Southey, M.C., Surowy, H., Suvanto, M., Thanasitthichai, S., Tomlinson, I., Torres, D., Truong, T., Tzardi, M., Valova, Y., Asperen, C.J. van, Dam, R.M. van, Ouweland, A.M.W. van den, Kolk, L.E. van der, Veen, E.M. van, Wendt, C., Williams, J.A., Yang, X.H.R., Yoon, S.Y., Zamora, M.P., Evans, D.G., Hoya, M. de la, Simard, J., Antoniou, A.C., Borg, A., Andrulis, I.L., Chang-Claude, J., Garcia-Closas, M., Chenevix-Trench, G., Milne, R.L., Pharoah, P.D.P., Schmidt, M.K., Spurdle, A.B., Vreeswijk, M.P.G., Benitez, J., Dunning, A.M., Kvist, A., Teo, S.H., Devilee, P., Easton, D.F., Breast Canc Assoc Consortium

المساهمون: Erasmus MC other, Medical Oncology, Clinical Genetics, Keeman, Renske [0000-0002-5452-9933], Decker, Brennan [0000-0003-4516-7421], Eriksson, Mikael [0000-0001-8135-4270], Martinez, Maria Elena [0000-0002-6728-1834], Surowy, Harald [0000-0002-3595-9188], Pharoah, Paul DP [0000-0001-8494-732X], Apollo - University of Cambridge Repository, Damage and Repair in Cancer Development and Cancer Treatment (DARE), Targeted Gynaecologic Oncology (TARGON), RS: GROW - R4 - Reproductive and Perinatal Medicine, MUMC+: DA KG Polikliniek (9), Klinische Genetica

المصدر: New England Journal of Medicine, 384(5), 428-439. MASSACHUSETTS MEDICAL SOC
Dorling, L, Carvalho, S, Allen, J, González-Neira, A, Luccarini, C, Wahlström, C, A. Pooley, K, T. Parsons, M, Fortuno, C, Wang, Q, K. Bolla, M, Dennis, J, Keeman, R, Alonso, M R, Álvarez, N, Herraez, B, Fernandez, V, Núñez-Torres, R, Osario, A, Valchich, J, Li, M, Törngren, T, A. Harrington, P, Baynes, C, M. Conroy, D, Decker, B, Fachal, L, Mavaddat, N, Ahearn, T, Aittomäki, K, N. Antonenkova, N, Arnold, N, Arveux, P, G.E.M Ausems, M, Auvinen, P, Becher, H, W. Beckmann, M, Behrens, S, Bermisheva, M, Białkowska, K, Blomqvist, C, V. Bogdanova, N, Bogdanova-Markov, N, E. Bojesen, S, Bonanni, B, Børresen-Dale, A-L, Brauch, H, Bremer, M, Briceno, I, Brüning, T, Burwinkel, B & Cameron, D A 2021, ' Breast cancer risk genes: association analysis in more than 113,000 women ', New England Journal of Medicine . https://doi.org/10.1056/NEJMoa1913948Test
N Engl J Med
New England Journal of Medicine, 384(5), 428-439. Massachussetts Medical Society
Breast Cancer Association Consortium 2021, ' Breast Cancer Risk Genes — Association Analysis in More than 113,000 Women ', New England Journal of Medicine, vol. 384, no. 5, pp. 428-439 . https://doi.org/10.1056/NEJMoa1913948Test
The New England Journal of Medicine, 384, 5, pp. 428-439
New England Journal of Medicine
New England Journal of Medicine, 384(5), 428-439. MASSACHUSETTS MEDICAL SOCIETY
The New England Journal of Medicine, 384, 428-439

مصطلحات موضوعية: Adult, Risk, Oncology, medicine.medical_specialty, Adolescent, PALB2, Genetic counseling, Genes, BRCA2, Mutation, Missense, Genes, BRCA1, Estrogen receptor, Breast Neoplasms, 030204 cardiovascular system & hematology, OVARIAN-CANCER, Article, Young Adult, 03 medical and health sciences, 0302 clinical medicine, Breast cancer, SDG 3 - Good Health and Well-being, Internal medicine, Odds Ratio, medicine, Humans, Genetic Predisposition to Disease, 030212 general & internal medicine, skin and connective tissue diseases, CHEK2, Aged, Genetic testing, Genetic association, Aged, 80 and over, Women's cancers Radboud Institute for Molecular Life Sciences [Radboudumc 17], medicine.diagnostic_test, MUTATIONS, business.industry, Age Factors, Genetic Variation, Sequence Analysis, DNA, General Medicine, Odds ratio, Middle Aged, BRCA1, medicine.disease, 3. Good health, Logistic Models, Female, business

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::853c9edad5e502a334ea18615af80eeaTest
https://doi.org/10.1056/nejmoa1913948Test

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دورية أكاديمية

Serum concentrations of active tamoxifen metabolites predict long-term survival in adjuvantly treated breast cancer patients

المؤلفون: Helland, T. (Thomas), Henne, N. (Nina), Bifulco, E. (Ersilia), Naume, B. (Bjorn), Borgen, E. (Elin), Kristensen, V.N. (Vessela N.), Kvaløy, J.T. (Jan T.), Lash, T.L. (Timothy L.), Alnæs, G.I.G. (Grethe I.G.), Schaik, R.H.N. (Ron) van, Janssen, E.A.M. (Emiel A.M.), Hustad, S. (Steinar), Lien, E.A. (Ernst A.), Mellgren, G. (Gunnar), Søiland, H. (Håvard)

المصدر: Breast Cancer Research (Print) vol. 19 no. 1

مصطلحات موضوعية: 4OHtam, Adjuvant, Breast cancer, CYP2D6, Endoxifen, Metabolism, Prognosis, Survival, Tamoxifen

وصف الملف: application/pdf

العلاقة: http://repub.eur.nl/pub/103232Test; urn:hdl:1765/103232

الإتاحة: https://doi.org/10.1186/s13058-017-0916-4Test
http://repub.eur.nl/pub/103232Test

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5

دورية أكاديمية

Common variants in breast cancer risk loci predispose to distinct tumor subtypes

المؤلفون: Ahearn, T.U., Zhang, H.Y., Michailidou, K., Milne, R.L., Bolla, M.K., Dennis, J., Dunning, A.M., Lush, M., Wang, Q., Andrulis, I.L., Anton-Culver, H., Arndt, V., Aronson, K.J., Auer, P.L., Augustinsson, A., Baten, A., Becher, H., Behrens, S., Benitez, J., Bermisheva, M., Blomqvist, C., Bojesen, S.E., Bonanni, B., Borresen-Dale, A.L., Brauch, H., Brenner, H., Brooks-Wilson, A., Bruning, T., Burwinkel, B., Buys, S.S., Canzian, F., Castelao, J.E., Chang-Claude, J., Chanock, S.J., Chenevix-Trench, G., Clarke, C.L., Collee, J.M., Cox, A., Cross, S.S., Czene, K., Daly, M.B., Devilee, P., Dork, T., Dwek, M., Eccles, D.M., Evans, D.G., Fasching, P.A., Figueroa, J., Floris, G., Gago-Dominguez, M., Gapstur, S.M., Garcia-Saenz, J.A., Gaudet, M.M., Giles, G.G., Goldberg, M.S., Gonzalez-Neira, A., Alnaes, G.I.G., Grip, M., Guenel, P., Haiman, C.A., Hall, P., Hamann, U., Harkness, E.F., Heemskerk-Gerritsen, B.A.M., Holleczek, B., Hollestelle, A., Hooning, M.J., Hoover, R.N., Hopper, J.L., Howell, A., Jakimovska, M., Jakubowska, A., John, E.M., Jones, M.E., Jung, A., Kaaks, R., Kauppila, S., Keeman, R., Khusnutdinova, E., Kitahara, C.M., Ko, Y.D., Koutros, S., Kristensen, V.N., Kruger, U., Kubelka-Sabit, K., Kurian, A.W., Kyriacou, K., Lambrechts, D., Lee, D.G., Lindblom, A., Linet, M., Lissowska, J., Llaneza, A., W.Y. lo, MacInnis, R.J., Mannermaa, A., Manoochehri, M., Margolin, S., Martinez, M.E., McLean, C., Meindl, A., Menon, U., Nevanlinna, H., Newman, W.G., Nodora, J., Offit, K., Olsson, H., Orr, N., Park-Simon, T.W., Patel, A.V., Peto, J., Pita, G., Plaseska-Karanfilska, D., Prentice, R., Punie, K., Pylkas, K., Radice, P., Rennert, G., Romero, A., Rudiger, T., Saloustros, E., Sampson, S., Sandler, D.P., Sawyer, E.J., Schmutzler, R.K., Schoemaker, M.J., Schottker, B., Sherman, M.E., Shu, X.O., Smichkoska, S., Southey, M.C., Spinelli, J.J., Swerdlow, A.J., Tamimi, R.M., Tapper, W.J., Taylor, J.A., Teras, L.R., Terry, M.B., Torres, D., Troester, M.A., Vachon, C.M., Deurzen, C.H.M. van, Veen, E.M. van, Wagner, P., Weinberg, C.R., Wendt, C., Wesseling, J., Winqvist, R., Wolk, A., Yang, X.H.R., Zheng, W., Couch, F.J., Simard, J., Kraft, P., Easton, D.F., Pharoah, P.D.P., Schmidt, M.K., Garcia-Closas, M., Chatterjee, N., NBCS Collaborators, ABCTB Investigators, KConFab AOCS Investigators

المصدر: Breast Cancer Research

مصطلحات موضوعية: Breast cancer, Etiologic heterogeneity, Genetic predisposition, Common breast cancer susceptibility variants

وصف الملف: application/pdf

العلاقة: https://breast-cancer-research.biomedcentral.com/articles/10.1186/s13058-021-01484-xTest; lumc-id: 122276974; https://hdl.handle.net/1887/3563986Test

الإتاحة: https://doi.org/10.1186/s13058-021-01484-xTest
https://hdl.handle.net/1887/3563986Test

View record in BASE

6

Two truncating variants in FANCC and breast cancer risk

المؤلفون: Dork, T., Peterlongo, P., Mannermaa, A., Bolla, M.K., Wang, Q., Dennis, J., Ahearn, T., Andrulis, I.L., Anton-Culver, H., Arndt, V., Aronson, K.J., Augustinsson, A., Freeman, L.E.B., Beckmann, M.W., Beeghly-Fadiel, A., Behrens, S., Bermisheva, M., Blomqvist, C., Bogdanova, N., Bojesen, S.E., Brauch, H., Brenner, H., Burwinkel, B., Canzian, F., Chan, T.L., Chang-Claude, J., Chanock, S.J., Choi, J.Y., Christiansen, H., Clarke, C.L., Couch, F.J., Czene, K., Daly, M.B., dos-Santos-Silva, I., Dwek, M., Eccles, D.M., Ekici, A.B., Eriksson, M., Evans, D.G., Fasching, P.A., Figueroa, J., Flyger, H., Fritschisl, L., Gabrielson, M., Gago-Dominguez, M., Gao, C., Gapstur, S.M., Garcia-Closas, M., Garcia-Saenz, J.A., Gaudet, M.M., Giles, G.G., Goldberg, M.S., Goldgar, D.E., Guenel, P., Haeberle, L., Haiman, C.A., Hakansson, N., Hall, P., Hamann, U., Hartman, M., Hauke, J., Hein, A., Hillemanns, P., Hogervorst, F.B.L., Hooning, M.J., Hopper, J.L., Howell, T., Huo, D.Z., Ito, H., Iwasaki, M., Jakubowska, A., Janni, W., John, E.M., Jung, A., Kaaks, R., Kang, D., Kapoor, P.M., Khusnutdinova, E., Kim, S.W., Kitahara, C.M., Koutros, S., Kraft, P., Kristensen, V.N., Kwon, A., Lambrechts, D., Marchand, L. le, Li, J.M., Lindstrom, S., Linet, M., W.Y. lo, Long, J.R., Lophatananon, A., Lubinski, J., Manoochehri, M., Manoukian, S., Margolin, S., Martinez, E., Matsuo, K., Mavroudis, D., Meindl, A., Menon, U., Milne, R.L., Taib, N.A.M., Muir, K., Mulligan, A.M., Neuhausen, S.L., Nevanlinna, H., Neven, P., Newman, W.G., Offit, K., Olopade, O.I., Olshan, A.F., Olson, J.E., Olsson, H., Park, S.K., Park-Simon, T.W., Peto, J., Plaseska-Karanfilska, D., Pohl-Rescigno, E., Presneau, N., Rack, B., Radice, P., Rashid, M.U., Rennert, G., Rennert, H.S., Romero, A., Ruebner, M., Saloustros, E., Schmidt, M.K., Schmutzler, R.K., Schneider, M.O., Schoemaker, M.J., Scott, C., Shen, C.Y., Shu, X.O., Simard, J., Slager, S., Smichkoska, S., Southey, M.C., Spinelli, J.J., Stone, J., Surowy, H., Swerdlow, A.J., Tamimi, R.M., Tapper, W.J., Teo, S.H., Terry, M.B., Toland, A.E., Tollenaar, R.A.E.M., Torres, D., Torres-Mejia, G., Troester, M.A., Truong, T., Tsugane, S., Untch, M., Vachon, C.M., Ouweland, A.M.W. van den, Veen, E.M. van, Vijai, J., Wendt, C., Wolk, A., Yu, J.C., Zheng, W., Ziogas, A., Ziv, E., Dunning, A.M., Pharoah, P.D.P., Schindler, D., Devilee, P., Easton, D.F., Balleine, R., Baxter, R., Braye, S., Carpenter, J., Dahlstrom, J., Forbes, J., Lee, C.S., Marsh, D., Morey, A., Pathmanathan, N., Scott, R., Simpson, P., Spigelman, A., Wilcken, N., Yip, D., Zeps, N., Borresen-Dale, A.L., Alnaes, G.I.G., Sahlberg, K.K., Ottestad, L., Karesen, R., Schlichting, E., Holmen, M.M., Sauer, T., Haakensen, V., Engebraten, O., Naume, B., Fossa, A., Kiserud, C.E., Reinertsen, K.V., Helland, A., Riis, M., Geisler, J., ABCTB Investigators, NBCS Collaborators

المساهمون: Andrulis, Irene L [0000-0002-4226-6435], Arndt, Volker [0000-0001-9320-8684], Brauch, Hiltrud [0000-0001-7531-2736], Dwek, Miriam [0000-0001-7184-2932], Ekici, Arif B [0000-0001-6099-7066], Fasching, Peter A [0000-0003-4885-8471], Figueroa, Jonine [0000-0002-5100-623X], Hein, Alexander [0000-0003-2601-3398], Ito, Hidemi [0000-0002-8023-4581], Matsuo, Keitaro [0000-0003-1761-6314], Menon, Usha [0000-0003-3708-1732], Milne, Roger L [0000-0001-5764-7268], Muir, Kenneth [0000-0001-6429-988X], Nevanlinna, Heli [0000-0002-0916-2976], Newman, William G [0000-0002-6382-4678], Peto, Julian [0000-0002-1685-8912], Rennert, Gad [0000-0002-8512-068X], Romero, Atocha [0000-0002-1634-7397], Schmidt, Marjanka K [0000-0002-2228-429X], Scott, Christopher [0000-0003-1340-0647], Stone, Jennifer [0000-0001-5077-0124], Truong, Thérèse [0000-0002-2943-6786], Tsugane, Shoichiro [0000-0003-4105-2774], Ziogas, Argyrios [0000-0003-4529-3727], Dunning, Alison M [0000-0001-6651-7166], Pharoah, Paul DP [0000-0001-8494-732X], Devilee, Peter [0000-0002-8023-2009], Easton, Douglas F [0000-0003-2444-3247], Apollo - University of Cambridge Repository, Andrulis, Irene L. [0000-0002-4226-6435], Ekici, Arif B. [0000-0001-6099-7066], Fasching, Peter A. [0000-0003-4885-8471], Milne, Roger L. [0000-0001-5764-7268], Newman, William G. [0000-0002-6382-4678], Schmidt, Marjanka K. [0000-0002-2228-429X], Dunning, Alison M. [0000-0001-6651-7166], Pharoah, Paul D. P. [0000-0001-8494-732X], Easton, Douglas F. [0000-0003-2444-3247], HUS Comprehensive Cancer Center, Clinicum, University Management, Department of Oncology, University of Helsinki, Department of Obstetrics and Gynecology, HUS Gynecology and Obstetrics, Medical Oncology, Clinical Genetics

المصدر: 2019, ' Two truncating variants in FANCC and breast cancer risk ', Scientific Reports, vol. 9, no. 1 . https://doi.org/10.1038/s41598-019-48804-yTest
ABCTB Investigators & NBCS Collaborators 2019, ' Two truncating variants in FANCC and breast cancer risk ', Scientific Reports, vol. 9, no. 1, 12524 . https://doi.org/10.1038/s41598-019-48804-yTest
Scientific Reports, 9. NATURE PUBLISHING GROUP
Scientific Reports
Scientific Reports, Vol 9, Iss 1, Pp 1-14 (2019)
Scientific Reports, 9:12524. Nature Publishing Group

مصطلحات موضوعية: 0301 basic medicine, Oncology, PROTEIN, lcsh:Medicine, 45/47, 0302 clinical medicine, Fanconi anemia, Genotype, lcsh:Science, Sequence Deletion, Multidisciplinary, BRCA1 Protein, Fanconi Anemia Complementation Group C Protein, 1184 Genetics, developmental biology, physiology, BRCA2 Protein, 3. Good health, BIALLELIC MUTATIONS, DNA-REPAIR, Female, 692/499, Medical Genetics, medicine.medical_specialty, PALB2, 3122 Cancers, ABCTB Investigators, Breast Neoplasms, FANCONIS ANEMIA, Article, 692/4028, NBCS Collaborators, 03 medical and health sciences, Breast cancer, SDG 3 - Good Health and Well-being, Internal medicine, medicine, Humans, NONSENSE MUTATION, Genetic Predisposition to Disease, Medicinsk genetik, 45, business.industry, Genetic heterogeneity, lcsh:R, Case-control study, Genetic Variation, Odds ratio, medicine.disease, GENE, Fanconi Anemia, 030104 developmental biology, Risk factors, Case-Control Studies, lcsh:Q, 3111 Biomedicine, business, 030217 neurology & neurosurgery