日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Evaluation of a cancer patient navigation program ("Onkolotse") in terms of hospitalization rates, resource use and healthcare costs: rationale and design of a randomized, controlled study

评估癌症患者导航项目(“Onkolotse”)在住院率、资源利用和医疗保健成本方面的表现:一项随机对照研究的理论基础和设计

Porzig, Ralf; Neugebauer, Sina; Heckmann, Thomas; Adolf, Daniela; Kaskel, Peter; Froster, Ursula G

A case of Brooke-Spiegler syndrome with a novel mutation in the CYLD gene in a patient with aggressive non-Hodgkin's lymphoma

一例伴有CYLD基因新突变的Brooke-Spiegler综合征患者,同时患有侵袭性非霍奇金淋巴瘤

Hunstig, F; Schulz, S; Nieten, I; Froster, U; Boltze, C; Schliemann, S; Hochhaus, A; La Rosée, P

Genetic polymorphisms and ovarian cancer risk and response to paclitaxel/cisplatin chemotherapy

遗传多态性与卵巢癌风险及对紫杉醇/顺铂化疗的反应

Gorodetska, Ielizaveta; Serga, Svitlana; Levkovich, Natalia; Lahuta, Tetiana; Ostapchenko, Ludmila; Demydov, Serhyi; Anikusko, Nikolay; Cheshuk, Valeriy; Smolanka, Ivan; Sklyar, Svitlana; Polenkov, Serhyi; Boichenko, Oleksander; Kozeretska, Iryna; Savanevich, A; Ashuryk, A; Lubinski, J; Gronwald, J; Tomys, Michalina; Skrzypczak-Zielinska, Marzena; Jasinowska, Marzena; Plawski, Andrzej; Froster, Ursula; Tecza, Karolina; Pamula-Pilat, Jolanta; Kolosza, Zofia; Radlak, Natalia; Grzybowska, Ewa; Andrzej, Plawski; Piotr, Machtel; Borun, Pawel; Skrzypczak-Zielinska, Marzena; Wojciechowska-Lacka, Arleta; Godlewski, Dariusz; Banasiewicz, Tomasz; Jablonska, Ewa; Gromadzinska, Jolanta; Wasowicz, Wojciech; Bednarek, Michal; Constantinou, Maria; Kepczynski, Lukasz; Kassassir, Agata Shiar; Sobczuk, Anna; Wieszczycka, Maria; Suzin, Jacek; Kaluzewski, Bogdan; Dymerska, Dagmara; Lubinski, Jan; Kurzawski, Grzegorz; Wong-Brown, Michelle; Avery-Kiejda, Kelly; Scott, Rodney J; Lener, Marcin; Wiechowska-Kozlowska, Anna; Scott, Rodney J; Muszynska, Magdalena; Kladny, Jozef; Waloszczyk, Piotr; Rutkowska, Anna; Sukiennicki, Grzegorz; Gromowski, Tomasz; Jaworska-Bieniek, Katarzyna; van de Wetering, Thierry; Kaczmarek, Katarzyna; Jakubowska, Anna; Lubinski, Jan; Zbigniew, Banaszkiewicz; Jarmocik, Pawel; Mrozowski, Marcin; Jawien, Arkadiusz; Elsakov, Pavel; Gajdel, Katarzyna; Kurzawski, Grzegorz; Hryhorowicz, Szymon; Ziemnicka, Katarzyna; Kaczmarek-Rys, Marta; Hoppe-Golebiewska, Justyna; Plawski, Andrzej; Skrzypczak-Zielinska, Marzena; Golab, Monika; Szkudlarek, Malgorzata; Budny, Batlomiej; Ruchala, Marek; Slomsk, Ryszard; Dubanowicz, Mariola; Gupta, Satish; Muszynska, Magdalena; Jaworska-Bieniek, Katarzyna; Sukiennicki, Grzegorz; Kaczmarek, Katarzyna; Jakubowska, Anna; Lubinski, Jan; Abramowska, Anna; Godlewski, Dariusz; Tecza, Karolina; Pamula-Pilat, Jolanta; Kolosza, Zofia; Radlak, Natalia; Grzybowska, Ewa

Evaluation of a candidate breast cancer associated SNP in ERCC4 as a risk modifier in BRCA1 and BRCA2 mutation carriers. Results from the Consortium of Investigators of Modifiers of BRCA1/BRCA2 (CIMBA)

评估ERCC4基因中与乳腺癌相关的候选SNP作为BRCA1和BRCA2突变携带者风险修饰因子的作用。来自BRCA1/BRCA2修饰因子研究联盟(CIMBA)的研究结果

Osorio, A; Milne, R L; Pita, G; Peterlongo, P; Heikkinen, T; Simard, J; Chenevix-Trench, G; Spurdle, A B; Beesley, J; Chen, X; Healey, S; Neuhausen, S L; Ding, Y C; Couch, F J; Wang, X; Lindor, N; Manoukian, S; Barile, M; Viel, A; Tizzoni, L; Szabo, C I; Foretova, L; Zikan, M; Claes, K; Greene, M H; Mai, P; Rennert, G; Lejbkowicz, F; Barnett-Griness, O; Andrulis, I L; Ozcelik, H; Weerasooriya, N; Gerdes, A-M; Thomassen, M; Cruger, D G; Caligo, M A; Friedman, E; Kaufman, B; Laitman, Y; Cohen, S; Kontorovich, T; Gershoni-Baruch, R; Dagan, E; Jernström, H; Askmalm, M S; Arver, B; Malmer, B; Domchek, S M; Nathanson, K L; Brunet, J; Ramón Y Cajal, T; Yannoukakos, D; Hamann, U; Hogervorst, F B L; Verhoef, S; Gómez García, E B; Wijnen, J T; van den Ouweland, A; Easton, D F; Peock, S; Cook, M; Oliver, C T; Frost, D; Luccarini, C; Evans, D G; Lalloo, F; Eeles, R; Pichert, G; Cook, J; Hodgson, S; Morrison, P J; Douglas, F; Godwin, A K; Sinilnikova, O M; Barjhoux, L; Stoppa-Lyonnet, D; Moncoutier, V; Giraud, S; Cassini, C; Olivier-Faivre, L; Révillion, F; Peyrat, J-P; Muller, D; Fricker, J-P; Lynch, H T; John, E M; Buys, S; Daly, M; Hopper, J L; Terry, M B; Miron, A; Yassin, Y; Goldgar, D; Singer, C F; Gschwantler-Kaulich, D; Pfeiler, G; Spiess, A-C; Hansen, Thomas V O; Johannsson, O T; Kirchhoff, T; Offit, K; Kosarin, K; Piedmonte, M; Rodriguez, G C; Wakeley, K; Boggess, J F; Basil, J; Schwartz, P E; Blank, S V; Toland, A E; Montagna, M; Casella, C; Imyanitov, E N; Allavena, A; Schmutzler, R K; Versmold, B; Engel, C; Meindl, A; Ditsch, N; Arnold, N; Niederacher, D; Deissler, H; Fiebig, B; Varon-Mateeva, R; Schaefer, D; Froster, U G; Caldes, T; de la Hoya, M; McGuffog, L; Antoniou, A C; Nevanlinna, H; Radice, P; Benítez, J

The TP53 Arg72Pro and MDM2 309G>T polymorphisms are not associated with breast cancer risk in BRCA1 and BRCA2 mutation carriers

TP53 Arg72Pro 和 MDM2 309G>T 多态性与 BRCA1 和 BRCA2 突变携带者的乳腺癌风险无关。

Sinilnikova, O M; Antoniou, A C; Simard, J; Healey, S; Léoné, M; Sinnett, D; Spurdle, A B; Beesley, J; Chen, X; Greene, M H; Loud, J T; Lejbkowicz, F; Rennert, G; Dishon, S; Andrulis, I L; Domchek, S M; Nathanson, K L; Manoukian, S; Radice, P; Konstantopoulou, I; Blanco, I; Laborde, A L; Durán, M; Osorio, A; Benitez, J; Hamann, U; Hogervorst, F B L; van Os, T A M; Gille, H J P; Peock, S; Cook, M; Luccarini, C; Evans, D G; Lalloo, F; Eeles, R; Pichert, G; Davidson, R; Cole, T; Cook, J; Paterson, J; Brewer, C; Hughes, D J; Coupier, I; Giraud, S; Coulet, F; Colas, C; Soubrier, F; Rouleau, E; Bièche, I; Lidereau, R; Demange, L; Nogues, C; Lynch, H T; Schmutzler, R K; Versmold, B; Engel, C; Meindl, A; Arnold, N; Sutter, C; Deissler, H; Schaefer, D; Froster, U G; Aittomäki, K; Nevanlinna, H; McGuffog, L; Easton, D F; Chenevix-Trench, G; Stoppa-Lyonnet, D

No association of TGFB1 L10P genotypes and breast cancer risk in BRCA1 and BRCA2 mutation carriers: a multi-center cohort study

TGFB1 L10P基因型与BRCA1和BRCA2突变携带者乳腺癌风险无相关性:一项多中心队列研究

Rebbeck, Timothy R; Antoniou, Antonis C; Llopis, Trinidad Caldes; Nevanlinna, Heli; Aittomäki, Kristiina; Simard, Jacques; Spurdle, Amanda B; Couch, Fergus J; Pereira, Lutecia H Mateus; Greene, Mark H; Andrulis, Irene L; Pasche, Boris; Kaklamani, Virginia; Hamann, Ute; Szabo, Csilla; Peock, Susan; Cook, Margaret; Harrington, Patricia A; Donaldson, Alan; Male, Allison M; Gardiner, Carol Anne; Gregory, Helen; Side, Lucy E; Robinson, Anne C; Emmerson, Louise; Ellis, Ian; Peyrat, Jean-Philippe; Fournier, Joëlle; Vennin, Philippe; Adenis, Claude; Muller, Danièle; Fricker, Jean-Pierre; Longy, Michel; Sinilnikova, Olga M; Stoppa-Lyonnet, Dominique; Schmutzler, Rita K; Versmold, Beatrix; Engel, Christoph; Meindl, Alfons; Kast, Karin; Schaefer, Dieter; Froster, Ursula G; Chenevix-Trench, Georgia; Easton, Douglas F

Functional analysis of the novel TBX5 c.1333delC mutation resulting in an extended TBX5 protein

对导致TBX5蛋白延长的新型TBX5 c.1333delC突变进行功能分析

Böhm, Johann; Heinritz, Wolfram; Craig, Alexander; Vujic, Mihailo; Ekman-Joelsson, Britt-Marie; Kohlhase, Jürgen; Froster, Ursula

MYH Gene Status in Polish FAP Patients without APC Gene Mutations

波兰FAP患者(无APC基因突变)的MYH基因状态

Skrzypczak, Marzena; Podralska, Marta; Heinritz, Wolfram; Froster, Ursula G; Lipiński, Daniel; Słomski, Ryszard; Pławski, Andrzej

Mosaic chromosomal aberrations in synovial fibroblasts of patients with rheumatoid arthritis, osteoarthritis, and other inflammatory joint diseases

类风湿关节炎、骨关节炎和其他炎性关节疾病患者滑膜成纤维细胞中的嵌合性染色体畸变

R W Kinne, T Liehr, V Beensen, E Kunisch, T Zimmermann, H Holland, R Pfeiffer, H D Stahl, W Lungershausen, G Hein, A Roth, F Emmrich, U Claussen, U G Froster

Familial pericentric inversion of chromosome 1 (p34q23) and male infertility with stage specific spermatogenic arrest

家族性1号染色体臂间倒位(p34q23)和男性不育伴阶段特异性精子发生停滞

Meschede, D; Froster, U G; Bergmann, M; Nieschlag, E