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

Mapping chromatin interactions at melanoma susceptibility loci uncovers distant cis-regulatory gene targets.

通过绘制黑色素瘤易感基因位点的染色质相互作用图谱,可以发现远端顺式调控基因靶点

Thakur Rohit, Xu Mai, Sowards Hayley, Yon Joshuah, Jessop Lea, Myers Timothy, Zhang Tongwu, Chari Raj, Long Erping, Rehling Thomas, Hennessey Rebecca, Funderburk Karen, Yin Jinhu, Machiela Mitchell J, Johnson Matthew E, Wells Andrew D, Chesi Alessandra, Grant Struan F A, Iles Mark M, Landi Maria Teresa, Law Matthew H, Choi Jiyeon, Brown Kevin M

Pathogenic germline IKZF1 variant alters hematopoietic gene expression profiles

致病性种系IKZF1变异体改变造血基因表达谱

Brodie, Seth A; Khincha, Payal P; Giri, Neelam; Bouk, Aaron J; Steinberg, Mia; Dai, Jieqiong; Jessop, Lea; Donovan, Frank X; Chandrasekharappa, Settara C; de Andrade, Kelvin C; Maric, Irina; Ellis, Steven R; Mirabello, Lisa; Alter, Blanche P; Savage, Sharon A

Landscape of Combination Immunotherapy and Targeted Therapy to Improve Cancer Management

联合免疫疗法和靶向疗法在改善癌症治疗中的应用现状

Colli, Leandro M; Machiela, Mitchell J; Zhang, Han; Myers, Timothy A; Jessop, Lea; Delattre, Olivier; Yu, Kai; Chanock, Stephen J

Characterization of breakpoint regions of large structural autosomal mosaic events

对大型常染色体结构嵌合事件的断点区域进行表征

Machiela, Mitchell J; Jessop, Lea; Zhou, Weiyin; Yeager, Meredith; Chanock, Stephen J

Burden of Nonsynonymous Mutations among TCGA Cancers and Candidate Immune Checkpoint Inhibitor Responses

TCGA癌症中非同义突变的负担及候选免疫检查点抑制剂反应

Colli, Leandro M; Machiela, Mitchell J; Myers, Timothy A; Jessop, Lea; Yu, Kai; Chanock, Stephen J

Characterization of large structural genetic mosaicism in human autosomes

人类常染色体中大型结构遗传嵌合现象的特征分析

Machiela, Mitchell J; Zhou, Weiyin; Sampson, Joshua N; Dean, Michael C; Jacobs, Kevin B; Black, Amanda; Brinton, Louise A; Chang, I-Shou; Chen, Chu; Chen, Constance; Chen, Kexin; Cook, Linda S; Crous Bou, Marta; De Vivo, Immaculata; Doherty, Jennifer; Friedenreich, Christine M; Gaudet, Mia M; Haiman, Christopher A; Hankinson, Susan E; Hartge, Patricia; Henderson, Brian E; Hong, Yun-Chul; Hosgood, H Dean 3rd; Hsiung, Chao A; Hu, Wei; Hunter, David J; Jessop, Lea; Kim, Hee Nam; Kim, Yeul Hong; Kim, Young Tae; Klein, Robert; Kraft, Peter; Lan, Qing; Lin, Dongxin; Liu, Jianjun; Le Marchand, Loic; Liang, Xiaolin; Lissowska, Jolanta; Lu, Lingeng; Magliocco, Anthony M; Matsuo, Keitaro; Olson, Sara H; Orlow, Irene; Park, Jae Yong; Pooler, Loreall; Prescott, Jennifer; Rastogi, Radhai; Risch, Harvey A; Schumacher, Fredrick; Seow, Adeline; Setiawan, Veronica Wendy; Shen, Hongbing; Sheng, Xin; Shin, Min-Ho; Shu, Xiao-Ou; VanDen Berg, David; Wang, Jiu-Cun; Wentzensen, Nicolas; Wong, Maria Pik; Wu, Chen; Wu, Tangchun; Wu, Yi-Long; Xia, Lucy; Yang, Hannah P; Yang, Pan-Chyr; Zheng, Wei; Zhou, Baosen; Abnet, Christian C; Albanes, Demetrius; Aldrich, Melinda C; Amos, Christopher; Amundadottir, Laufey T; Berndt, Sonja I; Blot, William J; Bock, Cathryn H; Bracci, Paige M; Burdett, Laurie; Buring, Julie E; Butler, Mary A; Carreón, Tania; Chatterjee, Nilanjan; Chung, Charles C; Cook, Michael B; Cullen, Michael; Davis, Faith G; Ding, Ti; Duell, Eric J; Epstein, Caroline G; Fan, Jin-Hu; Figueroa, Jonine D; Fraumeni, Joseph F Jr; Freedman, Neal D; Fuchs, Charles S; Gao, Yu-Tang; Gapstur, Susan M; Patiño-Garcia, Ana; Garcia-Closas, Montserrat; Gaziano, J Michael; Giles, Graham G; Gillanders, Elizabeth M; Giovannucci, Edward L; Goldin, Lynn; Goldstein, Alisa M; Greene, Mark H; Hallmans, Goran; Harris, Curtis C; Henriksson, Roger; Holly, Elizabeth A; Hoover, Robert N; Hu, Nan; Hutchinson, Amy; Jenab, Mazda; Johansen, Christoffer; Khaw, Kay-Tee; Koh, Woon-Puay; Kolonel, Laurence N; Kooperberg, Charles; Krogh, Vittorio; Kurtz, Robert C; LaCroix, Andrea; Landgren, Annelie; Landi, Maria Teresa; Li, Donghui; Liao, Linda M; Malats, Nuria; McGlynn, Katherine A; McNeill, Lorna H; McWilliams, Robert R; Melin, Beatrice S; Mirabello, Lisa; Peplonska, Beata; Peters, Ulrike; Petersen, Gloria M; Prokunina-Olsson, Ludmila; Purdue, Mark; Qiao, You-Lin; Rabe, Kari G; Rajaraman, Preetha; Real, Francisco X; Riboli, Elio; Rodríguez-Santiago, Benjamín; Rothman, Nathaniel; Ruder, Avima M; Savage, Sharon A; Schwartz, Ann G; Schwartz, Kendra L; Sesso, Howard D; Severi, Gianluca; Silverman, Debra T; Spitz, Margaret R; Stevens, Victoria L; Stolzenberg-Solomon, Rachael; Stram, Daniel; Tang, Ze-Zhong; Taylor, Philip R; Teras, Lauren R; Tobias, Geoffrey S; Viswanathan, Kala; Wacholder, Sholom; Wang, Zhaoming; Weinstein, Stephanie J; Wheeler, William; White, Emily; Wiencke, John K; Wolpin, Brian M; Wu, Xifeng; Wunder, Jay S; Yu, Kai; Zanetti, Krista A; Zeleniuch-Jacquotte, Anne; Ziegler, Regina G; de Andrade, Mariza; Barnes, Kathleen C; Beaty, Terri H; Bierut, Laura J; Desch, Karl C; Doheny, Kimberly F; Feenstra, Bjarke; Ginsburg, David; Heit, John A; Kang, Jae H; Laurie, Cecilia A; Li, Jun Z; Lowe, William L; Marazita, Mary L; Melbye, Mads; Mirel, Daniel B; Murray, Jeffrey C; Nelson, Sarah C; Pasquale, Louis R; Rice, Kenneth; Wiggs, Janey L; Wise, Anastasia; Tucker, Margaret; Pérez-Jurado, Luis A; Laurie, Cathy C; Caporaso, Neil E; Yeager, Meredith; Chanock, Stephen J

Whole-exome sequencing and functional studies identify RPS29 as a novel gene mutated in multicase Diamond-Blackfan anemia families

全外显子组测序和功能研究发现,RPS29 是多例 Diamond-Blackfan 贫血家族中一种新的突变基因。

Mirabello, Lisa; Macari, Elizabeth R; Jessop, Lea; Ellis, Steven R; Myers, Timothy; Giri, Neelam; Taylor, Alison M; McGrath, Katherine E; Humphries, Jessica M; Ballew, Bari J; Yeager, Meredith; Boland, Joseph F; He, Ji; Hicks, Belynda D; Burdett, Laurie; Alter, Blanche P; Zon, Leonard; Savage, Sharon A

RAD51B Activity and Cell Cycle Regulation in Response to DNA Damage in Breast Cancer Cell Lines.

RAD51B活性和细胞周期调控在乳腺癌细胞系DNA损伤反应中的作用

Lee Phoebe S, Fang Jun, Jessop Lea, Myers Timothy, Raj Preethi, Hu Nan, Wang Chaoyu, Taylor Philip R, Wang Jianjun, Khan Javed, Jasin Maria, Chanock Stephen J

BLM helicase ortholog Sgs1 is a central regulator of meiotic recombination intermediate metabolism

BLM解旋酶同源物Sgs1是减数分裂重组中间代谢的核心调控因子

De Muyt, Arnaud; Jessop, Lea; Kolar, Elizabeth; Sourirajan, Anuradha; Chen, Jianhong; Dayani, Yaron; Lichten, Michael

Disruption of telomerase trafficking by TCAB1 mutation causes dyskeratosis congenita

TCAB1基因突变导致端粒酶运输受阻,进而引起先天性角化不良。

Zhong, Franklin; Savage, Sharon A; Shkreli, Marina; Giri, Neelam; Jessop, Lea; Myers, Timothy; Chen, Renee; Alter, Blanche P; Artandi, Steven E