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

Central role of glycosylation processes in human genetic susceptibility to SARS-CoV-2 infections with Omicron variants

糖基化过程在人类对携带 Omicron 变异株的 SARS-CoV-2 感染的遗传易感性中起着核心作用

Geller, Frank; Wu, Xiaoping; Lammi, Vilma; Abner, Erik; Valliere, Jesse Tyler; Nastou, Katerina; Burns, Angus; Rasmussen, Morten; Andersson, Niklas Worm; Quinn, Liam; Aagaard, Bitten; Banasik, Karina; Bliddal, Sofie; Boding, Lasse; Brunak, Søren; Brøns, Nanna; Bybjerg-Grauholm, Jonas; Christoffersen, Lea Arregui Nordahl; Didriksen, Maria; Dinh, Khoa Manh; Erikstrup, Christian; Feldt-Rasmussen, Ulla; Grønbæk, Kirsten; Kaspersen, Kathrine Agergård; Mikkelsen, Christina; Nielsen, Claus Henrik; Nielsen, Henriette Svarre; Nielsen, Susanne Dam; Nissen, Janna; Sequeros, Celia Burgos; Tommerup, Niels; Ullum, Henrik; Spiliopoulos, Lampros; Bager, Peter; Hviid, Anders; Sørensen, Erik; Pedersen, Ole Birger; Lane, Jacqueline M; Lassaunière, Ria; Ollila, Hanna M; Ostrowski, Sisse Rye; Feenstra, Bjarke

The genetic basis of dermatophytosis skin infection susceptibility

皮肤真菌病易感性的遗传基础

Haapaniemi, Hele; Eghtedarian, Reyhane; Tervi, Anniina; Valliere, Jesse; Abner, Erik; Ollila, Hanna M

Regional immunosuppression and associated systemic markers in focally relapsed sarcomatoid mesothelioma: case report

局部复发性肉瘤样间皮瘤的区域性免疫抑制及相关系统性标志物:病例报告

Ollila, Hely; Kulkarni, Prateek; Kim, Hyojin; Ankola, Pratiti; Chintala, Navin K; Thomas, Carlos; Sauter, Jennifer L; Offin, Michael; Adusumilli, Prasad S

Outcomes of bispecific antibodies after CAR T-cell failure for large B-cell lymphoma: results from the ABC consortium

CAR-T细胞疗法治疗大B细胞淋巴瘤失败后双特异性抗体的疗效:来自ABC联盟的研究结果

Melody, Megan; Grover, Natalie; Franco, Stephanie; Romancik, Jason; Cortese, Matthew; Moyo, Tamara K; Bhansali, Rahul S; Ollila, Thomas; Kenkre, Vaishalee; Fitzgerald, Lindsey; Hess, Brian; Matasar, Matt; Shouse, Geoffrey; Annunzio, Kaitlin; Herr, Megan M; Davis, James A; Jesme, Christy; Pelcovits, Ari; Moreira, Jonathan; Ma, Shuo; Winter, Jane N; Lin, Adam; Danilov, Alexey; Roy, Ishan; Barta, Stefan K; Gordon, Leo I; Stephens, Deborah; Cohen, Jonathon B; Epperla, Narendranath; Karmali, Reem

Outcomes for CART as 2L vs 3L vs 4L or beyond in aggressive B-cell lymphoma: real-world evidence from the ABC Consortium

CAR-T方案作为侵袭性B细胞淋巴瘤二线、三线、四线及以上治疗的疗效:来自ABC联盟的真实世界证据

Wang, John S; Ellsworth, Brandon L; Melody, Megan; Epperla, Narendranath; Stephens, Deborah; Romancik, Jason; Cortese, Matthew; Bhansali, Rahul; Moyo, Tamara K; Kenkre, Vaishalee; Ollila, Thomas; Hess, Brian; Fitzgerald, Lindsey; Shouse, Geoffrey; Matasar, Matthew; Herr, Megan M; Davis, James; Jesme, Christy; Pelcovits, Ari R; Moreira, Jonathan; Lin, Adam Y; Ma, Shuo; Winter, Jane N; Danilov, Alexey V; Shah, Nirav N; Barta, Stefan K; Cohen, Jonathon B; Gordon, Leo I; Grover, Natalie; Karmali, Reem

Genetic insights of sleep apnea symptomatology and endotypes

睡眠呼吸暂停症状和内型的遗传学见解

Ollila, Hanna M

Prognostic Value of a Novel Nuclear Grading of Cutaneous Melanoma: The UNC Chapel Hill Method

新型皮肤黑色素瘤核分级方法的预后价值:北卡罗来纳大学教堂山分校方法

McAlpine, Sarah G; Srivatsa, Shantanu; Jones, Paige C; Davari, Danielle; Lei, Vivian; Melendez-Gonzalez, Maria; Conlon, Kathryn; Gebrekidan, Mahlet; Moschos, Stergios J; Collichio, Frances A; Sorah, Jonathan; Edmiston, Sharon N; Conway, Kathleen; Miedema, Jayson; Ollila, David W; Thomas, Nancy E; Googe, Paul B

The politics of health: exploring the potential and the limits of health in all policies under multilevel governance

健康政治:探索多层治理下所有政策中健康的潜力和局限性

Koivusalo, Meri; Valentine, Nicole; Williams, Carmel; Ollila, Eeva; Kokkinen, Lauri

Simultaneous Omission of Sentinel Lymph Node Biopsy and Radiation in Older Women with Early ER+ Breast Cancer

对早期ER+乳腺癌老年女性同时省略前哨淋巴结活检和放射治疗

Cox, Chase E; Schumacher, Jessica; Lillie, Margaret; Carino, Joshua; Agrawal, Yash; Selfridge, Julia M; Gallagher, Kristalyn K; Ollila, David W; Casey, Dana L; Greenberg, Caprice C; Spanheimer, Philip M

Genome-wide meta-analysis identifies genetic risk loci for mono- and polyneuropathies in 983 477 individuals

全基因组荟萃分析在983477名个体中鉴定出单神经病和多发性神经病的遗传风险位点

Broberg, Martin; Gen, Finn; Kalso, Eija; Ollila, Hanna M