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

CTNNB1-related disorders: clinical and radiological contributions from a French cohort

CTNNB1相关疾病:来自法国队列的临床和放射学研究

Chauvet-Piat, Eline; François-Heude, Marie-Céline; Manes, Gaël; Coget, Arthur; Leboucq, Nicolas; Lecardonnel, Bérénice; Baide-Mairena, Heidy; Allais, Marine; Touati, Souad; Sanchez, Stéphanie; Khalil, Mirna; Chevassus, Hugues; Willems, Marjolaines; Geneviève, David; Serrand, Marion; Mazzola, Laure; Dubard, Vincent; Renaud, Mathilde; Le Camus, Caroline; More, Rebecca; Milh, Mathieu; Paris, Caroline; Cécile, Ians-Bouteiller; Roubertie, Agathe

Ultra-deep duplex sequencing reveals unique features of somatic evolution in the normal tissues of a family with Li-Fraumeni syndrome

超深度双链测序揭示了李-弗劳梅尼综合征家族正常组织中体细胞进化的独特特征

Colegrove, Hunter L; Dubard-Gault, Marianne E; Marshall, Henry; Kohrn, Brendan F; Smith, Thomas H; Norgaard, Zachary K; Lo, Fang Yin; Schmidt, Elizabeth K; Higgins, Jacob E; Valentine, Charles C 3rd; Marshall, Desiree A; Clark, John I; Konnick, Eric Q; Salk, Jesse J; Horwitz, Marshall S; Rahbari, Raheleh; Feder, Alison F; Risques, Rosa Ana

Long-Term Survival Following Chemoradiation in Locoregional Recurrent Germline ATM Mutated Pancreatic Ductal Adenocarcinoma

局部复发性生殖系ATM突变胰腺导管腺癌患者接受放化疗后的长期生存率

Safyan, Rachael A; Zhang, Keven; Apisarnthanarax, Smith; Sham, Jonathan G; Pillarisetty, Venu G; Kugel, Sita; Dubard-Gault, Marianne; Pritchard, Colin C; Konnick, Eric Q; Sahani, Dushyant; Chiorean, E Gabriela

Does paired genetic testing improve targeted therapy choices and screening recommendations for patients with upper gastrointestinal cancers and their families? A prospective cohort of 42 patients

配对基因检测能否改善上消化道癌症患者及其家属的靶向治疗选择和筛查建议?一项纳入 42 名患者的前瞻性队列研究

Tatunay, Kevin; Cohen, Stacey; Naylor, Lorraine V; Handford, Cynthia L; Jacobson, Angela; Shankaran, Veena; Oelschlager, Brant; Grady, William M; Sjoding, Britta; Lally, Everett; Facchini, Lauren; Sun, Qin; Laurino, Mercy Y; Pritchard, Colin; Konnick, Eric Q; Dubard-Gault, Marianne E

Lessons learned in migrating from one commercial genetics clinical decision-making tool to another: Assessment of data integrity and utilization

从一种商业遗传学临床决策工具迁移到另一种工具的过程中汲取的经验教训:数据完整性和利用率的评估

Le, Calvin; Tatunay, Kevin; Liu, Wayne; Lu, Haibo; Rodis, Nicole-Ann; Nam, Thomas; Laurino, Mercy Y; Dubard-Gault, Marianne E

Combined Germline and Mosaic SDHA Mutation Is Associated With a Multicancer Syndrome Including Neuroblastoma, Renal Cancer, and Multifocal GI Tumor

生殖系和嵌合型SDHA突变相结合与多种癌症综合征相关,包括神经母细胞瘤、肾癌和多灶性胃肠道肿瘤。

Cranmer, Lee D; Konnick, Eric Q; Yoshida, Jennifer R; Jacobson, Angela L; Malik, Bilal A; Mogal, Harveshp; Sullivan, Lucas B; Handfrod, Cynthia L; Pritchard, Colin C; Dubard-Gault, Marianne E

Assessment of a Peer Physician Coaching Partnership Between a Designated Cancer Center Genetics Service and a Community Cancer Network Hospital

对指定癌症中心遗传服务部门与社区癌症网络医院之间同侪医师辅导合作关系的评估

Santos, Lauren G; Buzdnitskaya, Tatyana; Rolf, Bradley A; Souza, William; Sienko, Mark; Ruiz-Bonilla, Jose Alberto; Shah, Binay; Jewell, Patrick; Jensen, Lindsay; Horike-Pyne, Martha; Elrod, Jo Ann; Crews, Jennie; Laurino, Mercy; Weeks, Kevin Austin; Dubard-Gault, Marianne E

Multiple Primary Cancers in Patients Undergoing Tumor-Normal Sequencing Define Novel Associations

接受肿瘤-正常组织测序的患者中发现多种原发性癌症,揭示了新的关联

Liu, Ying L; Cadoo, Karen A; Mukherjee, Semanti; Khurram, Aliya; Tkachuk, Kaitlyn; Kemel, Yelena; Maio, Anna; Belhadj, Sami; Carlo, Maria I; Latham, Alicia; Walsh, Michael F; Dubard-Gault, Marianne E; Wang, Yuhan; Brannon, A Rose; Salo-Mullen, Erin; Sheehan, Margaret; Fiala, Elise; Devolder, Bryan; Dandiker, Sita; Mandelker, Diana; Zehir, Ahmet; Ladanyi, Marc; Berger, Michael F; Solit, David B; Bandlamudi, Chaitanya; Ravichandran, Vignesh; Bajorin, Dean F; Stadler, Zsofia K; Robson, Mark E; Vijai, Joseph; Seshan, Venkatraman; Offit, Kenneth

Leveraging Accountable Care Organization infrastructure for rapid pandemic response in independent primary care practices

利用责任医疗组织(ACO)的基础设施,在独立基层医疗机构中快速应对疫情

Amon, Carly; King, Jennifer; Colclasure, Jordan; Hodge, Kim; DuBard, C Annette

Inherited TP53 Variants and Risk of Prostate Cancer

遗传性TP53变异与前列腺癌风险

Maxwell, Kara N; Cheng, Heather H; Powers, Jacquelyn; Gulati, Roman; Ledet, Elisa M; Morrison, Casey; Le, Anh; Hausler, Ryan; Stopfer, Jill; Hyman, Sophie; Kohlmann, Wendy; Naumer, Anne; Vagher, Jennie; Greenberg, Samantha E; Naylor, Lorraine; Laurino, Mercy; Konnick, Eric Q; Shirts, Brian H; AlDubayan, Saud H; Van Allen, Eliezer M; Nguyen, Bastien; Vijai, Joseph; Abida, Wassim; Carlo, Maria I; Dubard-Gault, Marianne; Lee, Daniel J; Maese, Luke D; Mandelker, Diana; Montgomery, Bruce; Morris, Michael J; Nicolosi, Piper; Nussbaum, Robert L; Schwartz, Lauren E; Stadler, Zsofia; Garber, Judy E; Offit, Kenneth; Schiffman, Joshua D; Nelson, Peter S; Sartor, Oliver; Walsh, Michael F; Pritchard, Colin C