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

Association of MC1R variants with melanoma risk and interaction with sun exposure: An M-SKIP project

MC1R 变异与黑色素瘤风险的关联及其与日晒的相互作用:一项 M-SKIP 项目

Stefanaki, Irene; D'Ecclesiis, Oriana; Vignati, Silvano; Gaeta, Aurora; Kypreou, Katerina; Caini, Saverio; Gandini, Sara; Nagore, Eduardo; Sera, Francesco; Botta, Francesca; Newton-Bishop, Julia; Polsky, David; Lazovich, DeAnn; Kanetsky, Peter A; Puig, Susana; Gruis, Nelleke A; Landi, Maria Teresa; Fargnoli, Maria Concetta; Stratigos, Alexander; Guida, Gabriella; Ghiorzo, Paola; Menin, Chiara; García-Borrón, José C; Little, Julian; Nan, Hongmei; Raimondi, Sara

Gene-Level Associations in Patients With and Without Pathogenic Germline Variants in CDKN2A and Pancreatic Cancer

CDKN2A致病性种系变异携带者和不携带者胰腺癌患者的基因水平关联性

Astiazaran-Symonds, Esteban; Graham, Cole; Kim, Jung; Tucker, Margaret A; Ingvar, Christian; Helgadottir, Hildur; Pastorino, Lorenza; van Doorn, Remco; Sampson, Joshua N; Zhu, Bin; Bruno, William; Queirolo, Paola; Fornarini, Giuseppe; Sciallero, Stefania; Carter, Brian; Hicks, Belynda; Hutchinson, Amy; Jones, Kristine; Stewart, Douglas R; Chanock, Stephen J; Freedman, Neal D; Landi, Maria Teresa; Höiom, Veronica; Puig, Susana; Gruis, Nelleke; Yang, Xiaohong R; Ghiorzo, Paola; Goldstein, Alisa M

MC1R variants in relation to naevi in melanoma cases and controls: a pooled analysis from the M-SKIP project

MC1R 变异与黑色素瘤病例和对照组痣的关系:来自 M-SKIP 项目的汇总分析

Stefanaki, I; Stratigos, A J; Kypreou, K P; Evangelou, E; Gandini, S; Maisonneuve, P; Polsky, D; Lazovich, D; Newton-Bishop, J; Kanetsky, P A; Puig, S; Gruis, N A; Ghiorzo, P; Pellegrini, C; De Nicolo, A; Ribas, G; Guida, G; Garcia-Borron, J C; Fargnoli, M C; Nan, H; Landi, M T; Little, J; Sera, F; Raimondi, S

Germline ATM variants predispose to melanoma: a joint analysis across the GenoMEL and MelaNostrum consortia

生殖系ATM变异易导致黑色素瘤:GenoMEL和MelaNostrum联盟的联合分析

Dalmasso, B; Pastorino, L; Nathan, V; Shah, N N; Palmer, J M; Howlie, M; Johansson, P A; Freedman, N D; Carter, B D; Beane-Freeman, L; Hicks, B; Molven, A; Helgadottir, H; Sankar, A; Tsao, H; Stratigos, A J; Helsing, P; Van Doorn, R; Gruis, N A; Visser, M; Wadt, K A W; Mann, G; Holland, E A; Nagore, E; Potrony, M; Puig, S; Menin, C; Peris, K; Fargnoli, M C; Calista, D; Soufir, N; Harland, M; Bishop, T; Kanetsky, P A; Elder, D E; Andreotti, V; Vanni, I; Bruno, W; Höiom, V; Tucker, M A; Yang, X R; Andresen, P A; Adams, D J; Landi, M T; Hayward, N K; Goldstein, A M; Ghiorzo, P

Association between a 46-SNP Polygenic Risk Score and melanoma risk in Dutch patients with familial melanoma

46个SNP多基因风险评分与荷兰家族性黑色素瘤患者黑色素瘤风险之间的关联

Thomas P Potjer ,Tara W J van der Grinten ,Inge M M Lakeman ,Sander H Bollen ,Mar Rodríguez-Girondo ,Mark M Iles ,Jennifer H Barrett ,Lambertus A Kiemeney ,Nelleke A Gruis ,Christi J van Asperen ,Nienke van der Stoep

The importance of motivation in selecting undergraduate medical students for extracurricular research programmes

在选拔本科医学生参与课外科研项目时,动机的重要性

Ommering, Belinda W C; Van Blankenstein, Floris M; van Diepen, Merel; Gruis, Nelleke A; Kool, Ada; Dekker, Friedo W

Genome-wide association meta-analyses combining multiple risk phenotypes provide insights into the genetic architecture of cutaneous melanoma susceptibility

结合多种风险表型的全基因组关联荟萃分析,为了解皮肤黑色素瘤易感性的遗传结构提供了新的视角。

Landi, Maria Teresa; Bishop, D Timothy; MacGregor, Stuart; Machiela, Mitchell J; Stratigos, Alexander J; Ghiorzo, Paola; Brossard, Myriam; Calista, Donato; Choi, Jiyeon; Fargnoli, Maria Concetta; Zhang, Tongwu; Rodolfo, Monica; Trower, Adam J; Menin, Chiara; Martinez, Jacobo; Hadjisavvas, Andreas; Song, Lei; Stefanaki, Irene; Scolyer, Richard; Yang, Rose; Goldstein, Alisa M; Potrony, Miriam; Kypreou, Katerina P; Pastorino, Lorenza; Queirolo, Paola; Pellegrini, Cristina; Cattaneo, Laura; Zawistowski, Matthew; Gimenez-Xavier, Pol; Rodriguez, Arantxa; Elefanti, Lisa; Manoukian, Siranoush; Rivoltini, Licia; Smith, Blair H; Loizidou, Maria A; Del Regno, Laura; Massi, Daniela; Mandala, Mario; Khosrotehrani, Kiarash; Akslen, Lars A; Amos, Christopher I; Andresen, Per A; Avril, Marie-Françoise; Azizi, Esther; Soyer, H Peter; Bataille, Veronique; Dalmasso, Bruna; Bowdler, Lisa M; Burdon, Kathryn P; Chen, Wei V; Codd, Veryan; Craig, Jamie E; Dębniak, Tadeusz; Falchi, Mario; Fang, Shenying; Friedman, Eitan; Simi, Sarah; Galan, Pilar; Garcia-Casado, Zaida; Gillanders, Elizabeth M; Gordon, Scott; Green, Adele; Gruis, Nelleke A; Hansson, Johan; Harland, Mark; Harris, Jessica; Helsing, Per; Henders, Anjali; Hočevar, Marko; Höiom, Veronica; Hunter, David; Ingvar, Christian; Kumar, Rajiv; Lang, Julie; Lathrop, G Mark; Lee, Jeffrey E; Li, Xin; Lubiński, Jan; Mackie, Rona M; Malt, Maryrose; Malvehy, Josep; McAloney, Kerrie; Mohamdi, Hamida; Molven, Anders; Moses, Eric K; Neale, Rachel E; Novaković, Srdjan; Nyholt, Dale R; Olsson, Håkan; Orr, Nicholas; Fritsche, Lars G; Puig-Butille, Joan Anton; Qureshi, Abrar A; Radford-Smith, Graham L; Randerson-Moor, Juliette; Requena, Celia; Rowe, Casey; Samani, Nilesh J; Sanna, Marianna; Schadendorf, Dirk; Schulze, Hans-Joachim; Simms, Lisa A; Smithers, Mark; Song, Fengju; Swerdlow, Anthony J; van der Stoep, Nienke; Kukutsch, Nicole A; Visconti, Alessia; Wallace, Leanne; Ward, Sarah V; Wheeler, Lawrie; Sturm, Richard A; Hutchinson, Amy; Jones, Kristine; Malasky, Michael; Vogt, Aurelie; Zhou, Weiyin; Pooley, Karen A; Elder, David E; Han, Jiali; Hicks, Belynda; Hayward, Nicholas K; Kanetsky, Peter A; Brummett, Chad; Montgomery, Grant W; Olsen, Catherine M; Hayward, Caroline; Dunning, Alison M; Martin, Nicholas G; Evangelou, Evangelos; Mann, Graham J; Long, Georgina; Pharoah, Paul D P; Easton, Douglas F; Barrett, Jennifer H; Cust, Anne E; Abecasis, Goncalo; Duffy, David L; Whiteman, David C; Gogas, Helen; De Nicolo, Arcangela; Tucker, Margaret A; Newton-Bishop, Julia A; Peris, Ketty; Chanock, Stephen J; Demenais, Florence; Brown, Kevin M; Puig, Susana; Nagore, Eduardo; Shi, Jianxin; Iles, Mark M; Law, Matthew H

Genome-wide analysis of constitutional DNA methylation in familial melanoma

家族性黑色素瘤中构成性DNA甲基化的全基因组分析

Salgado, Catarina; Gruis, Nelleke; Heijmans, Bastiaan T; Oosting, Jan; van Doorn, Remco

Interplay between TERT promoter mutations and methylation culminates in chromatin accessibility and TERT expression

TERT 启动子突变与甲基化之间的相互作用最终导致染色质可及性和 TERT 表达

Catarina Salgado, Celine Roelse, Rogier Nell, Nelleke Gruis, Remco van Doorn, Pieter van der Velden

Genome-wide characterization of 5-hydoxymethylcytosine in melanoma reveals major differences with nevus

对黑色素瘤中 5-羟甲基胞嘧啶的全基因组表征揭示了其与痣的主要差异

Salgado, Catarina; Oosting, Jan; Janssen, Bart; Kumar, Rajiv; Gruis, Nelleke; van Doorn, Remco