نتائج البحث - "Hogervorst, Frans B."

المساهمون: Dumont, Martine, 1Genomics Center, CHU de Québec-Université Laval Research Center, 2705 Laurier Boulevard, Quebec City, QC GIV 4G2, Canada, martine.dumont@crchudequebec.ulaval.ca (M.D.), charles.joly-beauparlant@crchudequebec.ulaval.ca (C.J.-B.), arnaud.droit@crchudequebec.ulaval.ca (A.D.), stephane.dubois@crchudequebec.ulaval.ca (S.D.), annie-c.c-deschesnes@crchudequebec.ulaval.ca (A.-C.C.-D.), penny.soucy@crchudequebec.ulaval.ca (P.S.), maxime.vallee@chu-lyon.fr (M.V.), frederic.fournier.4@ulaval.ca (F.F.), audrey@mims.ai (A.L.), Weber-Lassalle, Nana, 2Center for Familial Breast and Ovarian Cancer, Center for Integrated Oncology (CIO), Faculty of Medicine and University Hospital Cologne, University of Cologne, 50937 Cologne, Germany, nana.weber-lassalle@uk-koeln.de (N.W.-L.), corinna.ernst@uk-koeln.de (C.E.), rita.schmutzler@uk-koeln.de (R.K.S.), eric.hahnen@uk-koeln.de (E.H.), Joly-Beauparlant, Charles, Ernst, Corinna, Droit, Arnaud, Feng, Bing-Jian, 3Department of Dermatology, University of Utah, Salt Lake City, UT 84103, USA, bingjian.feng@hsc.utah.edu (B.-J.F.), david.goldgar@hsc.utah.edu (D.E.G.), Dubois, Stéphane, Collin-Deschesnes, Annie-Claude, Soucy, Penny, Vallée, Maxime, Fournier, Frédéric, Lemaçon, Audrey, Adank, Muriel A., 5Family Cancer Clinic, The Netherlands Cancer Institute—Antoni van Leeuwenhoek Hospital, 1066 Amsterdam, The Netherlands, m.adank@nki.nl (M.A.A.), f.hogervorst@nki.nl (F.B.L.H.), l.vd.kolk@nki.nl (L.v.d.K.), Allen, Jamie, 6Centre for Cancer Genetic Epidemiology, Department of Public Health and Primary Care, University of Cambridge, Cambridge CB1 8RN, UK, jma@ebi.ac.uk (J.A.), mkh39@medschl.cam.ac.uk (M.K.B.), sc2017@medschl.cam.ac.uk (S.C.), paul.pharoah@medschl.cam.ac.uk (P.D.P.P.), qw232@medschl.cam.ac.uk (Q.W.), dfe20@medschl.cam.ac.uk (D.F.E.), Altmüller, Janine, 7Cologne Center for Genomics (CCG), Faculty of Medicine, University Hospital Cologne, University of Cologne, 50931 Cologne, Germany, janine.altmueller@mdc-berlin.de (J.A.), holger.thiele@uni-koeln.de (H.T.), Arnold, Norbert, 8Institute of Clinical Molecular Biology, Department of Gynaecology and Obstetrics, University Hospital of Schleswig-Holstein, Campus Kiel, Christian-Albrechts University Kiel, 24105 Kiel, Germany, norbert.arnold@uksh.de, Ausems, Margreet G. E. M., 9Division Laboratories, Pharmacy and Biomedical Genetics, Department of Genetics, University Medical Center Utrecht, 3584 Utrecht, The Netherlands, m.g.e.m.ausems@umcutrecht.nl, Berutti, Riccardo, 10Institute of Human Genetics, Technische Universität München, 81675 Munich, Germany, riccardo.berutti@helmholtz-muenchen.de (R.B.), tim.strom@tum.de (T.M.S.), Bolla, Manjeet K., Bull, Shelley, 11Lunenfeld-Tanenbaum Research Institute, Sinai Health System, Toronto, ON M5G 1X5, Canada, bull@lunenfeld.ca (S.B.), jessica.green@sinaihealth.ca (J.G.), gary.bader@utoronto.ca (G.D.B.), andrulis@lunenfeld.ca (I.L.A.), Carvalho, Sara, Cornelissen, Sten, 13Division of Molecular Pathology, The Netherlands Cancer Institute—Antoni van Leeuwenhoek Hospital, 1066 Amsterdam, The Netherlands, s.cornelissen@nki.nl (S.C.), r.keeman@nki.nl (R.K.), mk.schmidt@nki.nl (M.K.S.), Dufault, Michael R., 14Precision Medicine and Computational Biology, Sanofi Genzyme, Cambridge, MA 02142, USA, michael.dufault@sanofi.com, Dunning, Alison M., 15Centre for Cancer Genetic Epidemiology, Department of Oncology, University of Cambridge, Cambridge CB1 8RN, UK, amd24@medschl.cam.ac.uk (A.M.D.), craig@srl.cam.ac.uk (C.L.), ms483@medschl.cam.ac.uk (M.S.), Engel, Christoph, 16Institute for Medical Informatics, Statistics and Epidemiology, University of Leipzig, 04107 Leipzig, Germany, christoph.engel@imise.uni-leipzig.de, Gehrig, Andrea, 17Centre of Familial Breast and Ovarian Cancer, Department of Medical Genetics, Institute of Human Genetics, University of Würzburg, 97074 Würzburg, Germany, gehrig@biozentrum.uni-wuerzburg.de, Geurts-Giele, Willemina R. R., 18Department of Clinical Genetics, Erasmus University Medical Center, 3015 Rotterdam, The Netherlands, w.geurts-giele@erasmusmc.nl, Gieger, Christian, 19Institute of Epidemiology, Helmholtz Zentrum München, German Research Center for Environmental Health, 85764 Neuherberg, Germany, christian.gieger@helmholtz-muenchen.de (C.G.), peters@helmholtz-muenchen.de (A.P.), Green, Jessica, Hackmann, Karl, 22Institute for Clinical Genetics, Faculty of Medicine Carl Gustav Carus, Technische Universität Dresden, 01307 Dresden, Germany, karl.hackmann@uniklinikum-dresden.de, Helmy, Mohamed, 23The Donnelly Centre, University of Toronto, Toronto, ON M5S 3E1, Canada, mohamed_helmy@bii.a-star.edu.sg, Hentschel, Julia, 26Institute of Human Genetics, University Leipzig, 04103 Leipzig, Germany, julia.hentschel@medizin.uni-leipzig.de, Hogervorst, Frans B. L., Hollestelle, Antoinette, 27Department of Medical Oncology, Erasmus MC Cancer Institute, 3015 Rotterdam, The Netherlands, a.hollestelle@erasmusmc.nl (A.H.), m.hooning@erasmusmc.nl (M.J.H.), j.martens@erasmusmc.nl (J.W.M.M.), Hooning, Maartje J., Horváth, Judit, 28Institute of Human Genetics, University of Münster, 48149 Münster, Germany, judit.horvath@ukmuenster.de, Ikram, M. Arfan, 29Department of Epidemiology, Erasmus MC University Medical Center, 3015 Rotterdam, The Netherlands, m.a.ikram@erasmusmc.nl, Kaulfuß, Silke, 30Institute of Human Genetics, University Medical Center Göttingen, 37075 Göttingen, Germany, silke.kaulfuss@med.uni-goettingen.de, Keeman, Renske, Kuang, Da, 21Department of Molecular Genetics, University of Toronto, Toronto, ON M5S 1A8, Canada, kvn.kuang@mail.utoronto.ca, Luccarini, Craig, Maier, Wolfgang, 31German Center for Neurodegenerative Diseases (DZNE), Department of Neurodegenerative Diseases and Geriatric Psychiatry, Medical Faculty, University Hospital Bonn, 53127 Bonn, Germany, wolfgang.maier@ukb.uni-bonn.de, Martens, John W. M., Niederacher, Dieter, 32Department of Gynecology and Obstetrics, University Hospital Düsseldorf, Heinrich-Heine University Düsseldorf, 40225 Düsseldorf, Germany, niederac@med.uni-duesseldorf.de, Nürnberg, Peter, 33Center for Molecular Medicine Cologne (CMMC), Cologne Center for Genomics (CCG), Faculty of Medicine, University Hospital Cologne, University of Cologne, 50931 Cologne, Germany, nuernberg@uni-koeln.de, Ott, Claus-Eric, 34Institute of Medical Genetics and Human Genetics, Charité-Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin, Humboldt-Universität zu Berlin and Berlin Institute of Health, 13353 Berlin, Germany, claus-eric.ott@charite.de, Peters, Annette, Pharoah, Paul D. P., Ramirez, Alfredo, 36Division for Neurogenetics and Molecular Psychiatry, Medical Faculty, University of Cologne, 50937 Cologne, Germany, alfredo.ramirez@uk-koeln.de, Ramser, Juliane, 37Division of Gynaecology and Obstetrics, Klinikum Rechts der Isar der Technischen Universität München, 81675 Munich, Germany, juliane.ramser@mri.tum.de (J.R.), alfons.meindl@gmx.de (A.M.), Riedel-Heller, Steffi, 38Institute of Social Medicine, Occupational Health and Public Health, Faculty of Medicine, University of Leipzig, 04103 Leipzig, Germany, steffi.riedel-heller@medizin.uni-leipzig.de, Schmidt, Gunnar, 39Institute of Human Genetics, Hannover Medical School, 30625 Hannover, Germany, schmidt.gunnar@mh-hannover.de, Shah, Mitul, Scherer, Martin, 40Department of Primary Medical Care, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany, m.scherer@uke.de, Stäbler, Antje, 41Institute of Medical Genetics and Applied Genomics, University of Tübingen, 72076 Tübingen, Germany, antje.staebler@med.uni-tuebingen.de, Strom, Tim M., Sutter, Christian, 42Institute of Human Genetics, University Hospital Heidelberg, 69120 Heidelberg, Germany, christian.sutter@med.uni-heidelberg.de, Thiele, Holger, van Asperen, Christi J., 43Department of Clinical Genetics, Leiden University Medical Center, 2333 Leiden, The Netherlands, c.j.van_asperen@lumc.nl (C.J.v.A.), r.b.van_der_luijt@lumc.nl (R.B.v.d.L.), van der Kolk, Lizet, van der Luijt, Rob B., Volk, Alexander E., 45Institute of Human Genetics, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany, a.volk@uke.de, Wagner, Michael, 46Department of Neurodegenerative Diseases and Geriatric Psychiatry, University Hospital Bonn, 53127 Bonn, Germany, michael.wagner@ukbonn.de, Waisfisz, Quinten, 47Department of Human Genetics, Amsterdam UMC, Vrije Universiteit Amsterdam, 1081 Amsterdam, The Netherlands, q.waisfisz@vumc.nl, Wang, Qin, Wang-Gohrke, Shan, 48Department of Gynaecology and Obstetrics, University of Ulm, 89081 Ulm, Germany, shan.wang-gohrke@uniklinik-ulm.de, Weber, Bernhard H. F., 49Institute of Human Genetics, Regensburg University, 93053 Regensburg, Germany, bweb@klinik.uni-regensburg.de, Devilee, Peter, 51Department of Pathology, Department of Human Genetics, Leiden University Medical Center, 2333 Leiden, The Netherlands, p.devilee@lumc.nl, Tavtigian, Sean, 4Huntsman Cancer Institute, University of Utah, Salt Lake City, UT 84112, USA, sean.tavtigian@hci.utah.edu, Bader, Gary D., Meindl, Alfons, Goldgar, David E., Andrulis, Irene L., Schmutzler, Rita K., Easton, Douglas F., Schmidt, Marjanka K., Hahnen, Eric, Simard, Jacques

العلاقة: https://resolver.sub.uni-goettingen.de/purl?gro-2/112620Test

الإتاحة: https://doi.org/10.3390/cancers14143363Test
https://resolver.sub.uni-goettingen.de/purl?gro-2/112620Test

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النص الكامل

5

دورية أكاديمية

BRCA2 Hypomorphic Missense Variants Confer Moderate Risks of Breast Cancer

المؤلفون: Shimelis, Hermela, Mesman, Romy LS, Von Nicolai, Catharina, Ehlen, Asa, Guidugli, Lucia, Martin, Charlotte, Calléja, Fabienne MGR, Meeks, Huong, Hallberg, Emily, Hinton, Jamie, Lilyquist, Jenna, Hu, Chunling, Aalfs, Cora M, Aittomäki, Kristiina, Andrulis, Irene, Anton-Culver, Hoda, Arndt, Volker, Beckmann, Matthias W, Benitez, Javier, Bogdanova, Natalia V, Bojesen, Stig E, Bolla, Manjeet K, Borresen-Dale, Anne-Lise, Brauch, Hiltrud, Brennan, Paul, Brenner, Hermann, Broeks, Annegien, Brouwers, Barbara, Brüning, Thomas, Burwinkel, Barbara, Chang-Claude, Jenny, Chenevix-Trench, Georgia, Cheng, Ching-Yu, Choi, Ji-Yeob, Collée, J Margriet, Cox, Angela, Cross, Simon S, Czene, Kamila, Darabi, Hatef, Dennis, Joe, Dörk, Thilo, dos-Santos-Silva, Isabel, Dunning, Alison M, Fasching, Peter A, Figueroa, Jonine, Flyger, Henrik, García-Closas, Montserrat, Giles, Graham G, Glendon, Gord, Guénel, Pascal, Haiman, Christopher A, Hall, Per, Hamann, Ute, Hartman, Mikael, Hogervorst, Frans B, Hollestelle, Antoinette, Hopper, John L, Ito, Hidemi, Jakubowska, Anna, Kang, Daehee, Kosma, Veli-Matti, Kristensen, Vessela, Lai, Kah-Nyin, Lambrechts, Diether, Le Marchand, Loic, Li, Jingmei, Lindblom, Annika, Lophatananon, Artitaya, Lubinski, Jan, Machackova, Eva, Mannermaa, Arto, Margolin, Sara, Marme, Frederik, Matsuo, Keitaro, Miao, Hui, Michailidou, Kyriaki, Milne, Roger L, Muir, Kenneth, Neuhausen, Susan L, Nevanlinna, Heli, Olson, Janet E, Olswold, Curtis, Oosterwijk, Jan JC, Osorio, Ana, Peterlongo, Paolo, Peto, Julian, Pharoah, Paul DP, Pylkäs, Katri, Radice, Paolo, Rashid, Muhammad Usman, Rhenius, Valerie, Rudolph, Anja, Sangrajrang, Suleeporn, Sawyer, Elinor J, Schmidt, Marjanka K, Schoemaker, Minouk J, Seynaeve, Caroline, Shah, Mitul, Shen, Chen-Yang, Shrubsole, Martha

المصدر: Cancer Research. 77(11)

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/3wp0r87gTest

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6

دورية أكاديمية

PALB2, CHEK2 and ATM rare variants and cancer risk: data from COGS

المؤلفون: Southey, Melissa C, Goldgar, David E, Winqvist, Robert, Pylkäs, Katri, Couch, Fergus, Tischkowitz, Marc, Foulkes, William D, Dennis, Joe, Michailidou, Kyriaki, van Rensburg, Elizabeth J, Heikkinen, Tuomas, Nevanlinna, Heli, Hopper, John L, Dörk, Thilo, Claes, Kathleen BM, Reis-Filho, Jorge, Teo, Zhi Ling, Radice, Paolo, Catucci, Irene, Peterlongo, Paolo, Tsimiklis, Helen, Odefrey, Fabrice A, Dowty, James G, Schmidt, Marjanka K, Broeks, Annegien, Hogervorst, Frans B, Verhoef, Senno, Carpenter, Jane, Clarke, Christine, Scott, Rodney J, Fasching, Peter A, Haeberle, Lothar, Ekici, Arif B, Beckmann, Matthias W, Peto, Julian, dos-Santos-Silva, Isabel, Fletcher, Olivia, Johnson, Nichola, Bolla, Manjeet K, Sawyer, Elinor J, Tomlinson, Ian, Kerin, Michael J, Miller, Nicola, Marme, Federik, Burwinkel, Barbara, Yang, Rongxi, Guénel, Pascal, Truong, Thérèse, Menegaux, Florence, Sanchez, Marie, Bojesen, Stig, Nielsen, Sune F, Flyger, Henrik, Benitez, Javier, Zamora, M Pilar, Perez, Jose Ignacio Arias, Menéndez, Primitiva, Anton-Culver, Hoda, Neuhausen, Susan, Ziogas, Argyrios, Clarke, Christina A, Brenner, Hermann, Arndt, Volker, Stegmaier, Christa, Brauch, Hiltrud, Brüning, Thomas, Ko, Yon-Dschun, Muranen, Taru A, Aittomäki, Kristiina, Blomqvist, Carl, Bogdanova, Natalia V, Antonenkova, Natalia N, Lindblom, Annika, Margolin, Sara, Mannermaa, Arto, Kataja, Vesa, Kosma, Veli-Matti, Hartikainen, Jaana M, Spurdle, Amanda B, Investigators, kConFab, Group, Australian Ovarian Cancer Study, Wauters, Els, Smeets, Dominiek, Beuselinck, Benoit, Floris, Giuseppe, Chang-Claude, Jenny, Rudolph, Anja, Seibold, Petra, Flesch-Janys, Dieter, Olson, Janet E, Vachon, Celine, Pankratz, Vernon S, McLean, Catriona, Haiman, Christopher A, Henderson, Brian E, Schumacher, Fredrick, Le Marchand, Loic, Kristensen, Vessela, Alnæs, Grethe Grenaker, Zheng, Wei

المصدر: Journal of Medical Genetics. 53(12)

مصطلحات موضوعية: Biological Sciences, Biomedical and Clinical Sciences, Genetics, Oncology and Carcinogenesis, Ovarian Cancer, Aging, Breast Cancer, Cancer, Women's Health, Rare Diseases, Prevention, Urologic Diseases, Aetiology, 2.1 Biological and endogenous factors, Ataxia Telangiectasia Mutated Proteins, Breast Neoplasms, Case-Control Studies, Checkpoint Kinase 2, Fanconi Anemia Complementation Group N Protein, Female, Genetic Association Studies, Genetic Predisposition to Disease, Humans, Male, Mutation, Nuclear Proteins, Ovarian Neoplasms, Prostatic Neoplasms, Risk, Tumor Suppressor Proteins, Australian Ovarian Cancer Study Group, Cancer: breast, Cancer: ovary, Cancer: prostate, cancer predisposition, Medical and Health Sciences, Genetics & Heredity, Clinical sciences

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/9gn7b78qTest
https://escholarship.org/content/qt9gn7b78q/qt9gn7b78q.pdfTest

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7

دورية أكاديمية

Impact of genetic counseling strategy on diagnostic yield and workload for genome-sequencing-based tumor diagnostics.

المؤلفون: Koster, Roelof, Schipper, Luuk J, Giesbertz, Noor A A, van Beek, Daphne, Mendeville, Matías, Samsom, Kris G, Rosenberg, Efraim H, Hogervorst, Frans B L, Roepman, Paul, Boelens, Mirjam C, Bosch, Linda J W, van den Berg, Jose G, Meijer, Gerrit A, Voest, Emile E, Cuppen, Edwin, Ruijs, Marielle W G, van Wezel, Tom, van der Kolk, Lizet, Monkhorst, Kim

المصدر: Genet Med ; ISSN:1530-0366 ; Volume:26 ; Issue:2

مصطلحات موضوعية: Cancer genetics, Genome sequencing, Germline, Molecular diagnostics, Validation

العلاقة: https://doi.org/10.1016/j.gim.2023.101032Test; https://pubmed.ncbi.nlm.nih.gov/38006283Test

الإتاحة: https://doi.org/10.1016/j.gim.2023.101032Test
https://pubmed.ncbi.nlm.nih.gov/38006283Test

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8

دورية أكاديمية

Optimized whole-genome sequencing workflow for tumor diagnostics in routine pathology practice

المصدر: Samsom , K G , Bosch , L J W , Schipper , L J , Schout , D , Roepman , P , Boelens , M C , Lalezari , F , Klompenhouwer , E G , de Langen , A J , Buffart , T E , van Linder , B M H , van Deventer , K , van den Burg , K , Unmehopa , U , Rosenberg , E H , Koster , R , Hogervorst , F B L , van den Berg , J G , Riethorst , I , Schoenmaker , ....

العلاقة: https://research.vumc.nl/en/publications/ff18b677-94fa-4d6c-8bc6-37540c78267dTest

الإتاحة: https://doi.org/10.1038/s41596-023-00933-5Test
https://research.vumc.nl/en/publications/ff18b677-94fa-4d6c-8bc6-37540c78267dTest
http://www.scopus.com/inward/record.url?scp=85179696140&partnerID=8YFLogxKTest

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9

دورية أكاديمية

Large-scale genome-wide association study of 398,238 women unveils seven novel loci associated with high-grade serous epithelial ovarian cancer risk.

المؤلفون: Barnes, Daniel R, Tyrer, Jonathan P, Dennis, Joe, Leslie, Goska, Bolla, Manjeet K, Lush, Michael, Aeilts, Amber M, AittomÃ¤ki, Kristiina, Andrieu, Nadine, Andrulis, Irene L, Anton-Culver, Hoda, Arason, Adalgeir, Arun, Banu K, BalmaÃ±a, Judith, Bandera, Elisa V, Barkardottir, Rosa B, Berger, Lieke P V, de Gonzalez, Amy Berrington, Berthet, Pascaline, BiaÅ‚kowska, Katarzyna, BjÃ¸rge, Line, Blanco, Amie M, Blok, Marinus J, Bobolis, Kristie A, Bogdanova, Natalia V, Brenton, James D, Butz, Henriett, Buys, Saundra S, Caligo, Maria A, Campbell, Ian, Castillo, Carmen, Claes, Kathleen B M, Colonna, Sarah V, Cook, Linda S, Daly, Mary B, Dansonka-Mieszkowska, Agnieszka, de la Hoya, Miguel, deFazio, Anna, DePersia, Allison, Ding, Yuan Chun, Domchek, Susan M, DÃ¶rk, Thilo, Einbeigi, Zakaria, Engel, Christoph, Evans, D Gareth, Foretova, Lenka, Fortner, RenÃ©e T, Fostira, Florentia, Foti, Maria Cristina, Friedman, Eitan, Frone, Megan N, Ganz, Patricia A, Gentry-Maharaj, Aleksandra, Glendon, Gord, Godwin, Andrew K, GonzÃ¡lez-Neira, Anna, Greene, Mark H, Gronwald, Jacek, Guerrieri-Gonzaga, Aliana, Hamann, Ute, Hansen, Thomas V O, Harris, Holly R, Hauke, Jan, Heitz, Florian, Hogervorst, Frans B L, Hooning, Maartje J, Hopper, John L, Huff, Chad D, Huntsman, David G, Imyanitov, Evgeny N, Izatt, Louise, Jakubowska, Anna, James, Paul A, Janavicius, Ramunas, John, Esther M, Kar, Siddhartha, Karlan, Beth Y, Kennedy, Catherine J, Kiemeney, Lambertus A L M, Konstantopoulou, Irene, Kupryjanczyk, Jolanta, Laitman, Yael, Lavie, Ofer, Lawrenson, Kate, Lester, Jenny, Lesueur, Fabienne, Lopez-Pleguezuelos, Carlos, Mai, Phuong L, Manoukian, Siranoush, May, Taymaa, McNeish, Iain A, Menon, Usha, Milne, Roger L, Modugno, Francesmary, Mongiovi, Jennifer M, Montagna, Marco, Moysich, Kirsten B, Neuhausen, Susan L, Nielsen, Finn C, NoguÃ¨s, Catherine, OlÃ¡h, Edit, Olopade, Olufunmilayo I, Osorio, Ana, Papi, Laura, Pathak, Harsh, Pearce, Celeste L, Pedersen, Inge S, Peixoto, Ana, Pejovic, Tanja, Peng, Pei-Chen, Peshkin, Beth N, Peterlongo, Paolo, Powell, C Bethan, Prokofyeva, Darya, Pujana, Miquel Angel, Radice, Paolo, Rashid, Muhammad U, Rennert, Gad, Richenberg, George, Sandler, Dale P, Sasamoto, Naoko, Setiawan, Veronica W, Sharma, Priyanka, Sieh, Weiva, Singer, Christian F, Snape, Katie, Sokolenko, Anna P, Soucy, Penny, Southey, Melissa C, Stoppa-Lyonnet, Dominique, Sutphen, Rebecca, Sutter, Christian, Teixeira, Manuel R, Terry, Kathryn L, Thomsen, Liv Cecilie V, Tischkowitz, Marc, Toland, Amanda E, Van Gorp, Toon, Vega, Ana, Velez Edwards, Digna R, Webb, Penelope M, Weitzel, Jeffrey N, Wentzensen, Nicolas, Whittemore, Alice S, Winham, Stacey J, Wu, Anna H, Yadav, Siddhartha, Yu, Yao, Ziogas, Argyrios, Berchuck, Andrew, Couch, Fergus J, Goode, Ellen L, Goodman, Marc T, Monteiro, Alvaro N, Offit, Kenneth, Ramus, Susan J, Risch, Harvey A, Schildkraut, Joellen M, Thomassen, Mads, Simard, Jacques, Easton, Douglas F, Jones, Michelle R, Chenevix-Trench, Georgia, Gayther, Simon A, Antoniou, Antonis C, Pharoah, Paul D P

المصدر: Articles, Abstracts, and Reports

مصطلحات موضوعية: oregon, medford, genomics, Epidemiology, Obstetrics and Gynecology, Oncology

العلاقة: https://digitalcommons.providence.org/publications/8634Test; https://pubmed.ncbi.nlm.nih.gov/38496424Test

الإتاحة: https://digitalcommons.providence.org/publications/8634Test
https://pubmed.ncbi.nlm.nih.gov/38496424Test

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10

دورية أكاديمية

Breast cancer risks associated with missense variants in breast cancer susceptibility genes

المؤلفون: Dorling, Leila, Carvalho, Sara, Allen, Jamie, Parsons, Michael T, Fortuno, Cristina, González-Neira, Anna, Heijl, Stephan M, Adank, Muriel A, Ahearn, Thomas U, Andrulis, Irene L, Auvinen, Päivi, Becher, Heiko, Beckmann, Matthias W, Behrens, Sabine, Bermisheva, Marina, Bogdanova, Natalia V, Bojesen, Stig E, Bolla, Manjeet K, Bremer, Michael, Briceno, Ignacio, Camp, Nicola J, Campbell, Archie, Castelao, Jose E, Chang-Claude, Jenny, Chanock, Stephen J, Chenevix-Trench, Georgia, Collée, J Margriet, Czene, Kamila, Dennis, Joe, Dörk, Thilo, Eriksson, Mikael, Evans, D Gareth, Fasching, Peter A, Figueroa, Jonine, Flyger, Henrik, Gabrielson, Marike, Gago-Dominguez, Manuela, García-Closas, Montserrat, Giles, Graham G, Glendon, Gord, Guénel, Pascal, Gündert, Melanie, Hadjisavvas, Andreas, Hahnen, Eric, Hall, Per, Hamann, Ute, Harkness, Elaine F, Hartman, Mikael, Hogervorst, Frans B L, Oosterwijk, Jan C, Easton, Douglas F.

المصدر: NBCS Collaborators , Dorling , L , Carvalho , S , Allen , J , Parsons , M T , Fortuno , C , González-Neira , A , Heijl , S M , Adank , M A , Ahearn , T U , Andrulis , I L , Auvinen , P , Becher , H , Beckmann , M W , Behrens , S , Bermisheva , M , Bogdanova , N V , Bojesen , S E , Bolla , M K , Bremer , M , Briceno , I , Camp , N J , Campbell , ....

مصطلحات موضوعية: Breast Neoplasms/genetics, Case-Control Studies, Female, Genetic Predisposition to Disease, Humans, Mutation, Missense

وصف الملف: application/pdf

العلاقة: https://research.rug.nl/en/publications/34812060-15d8-4897-b466-768783ba5cabTest

الإتاحة: https://doi.org/10.1186/s13073-022-01052-8Test
https://hdl.handle.net/11370/34812060-15d8-4897-b466-768783ba5cabTest
https://research.rug.nl/en/publications/34812060-15d8-4897-b466-768783ba5cabTest
https://pure.rug.nl/ws/files/224485198/s13073_022_01052_8.pdfTest

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