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

Single vs dual genetic disease in children with congenital anomalies and solid tumors

儿童先天性畸形和实体瘤中的单一基因疾病与双重基因疾病

Watson, Deborah J; Saeidian, Amir Hossein; Wang, Xiang; Harr, Margaret H; Liu, Yichuan; Li, Yun Rose; Terek, Shannon; de Barcelos, Isabella Peixoto; Nesbitt, Addie; Nguyen, Kenny; Chang, Xiao; Connolly, John; Hou, Cuiping; Slaby, Isabella; Wang, Fengxiang; Snyder, James; Qiu, Haijun; Qu, Huiqi; March, Michael E; Zhao, Xiaonan; Mentch, Frank; Sleiman, Patrick; Glessner, Joseph; Hakonarson, Hakon

Integration of GWAS, QTLs and keratinocyte functional assays reveals molecular mechanisms of atopic dermatitis.

GWAS、QTL 和角质形成细胞功能检测的整合揭示了特应性皮炎的分子机制

Oliva Meritxell, Sarkar Mrinal K, March Michael E, Saeidian Amir Hossein, Mentch Frank D, Hsieh Chen-Lin, Tang Fanying, Uppala Ranjitha, Patrick Matthew T, Li Qinmengge, Bogle Rachael, Kahlenberg J Michelle, Watson Deborah, Glessner Joseph T, Youssefian Leila, Vahidnezhad Hassan, Tsoi Lam C, Hakonarson Hakon, Gudjonsson Johann E, Smith Kathleen M, Riley-Gillis Bridget

Variants in BSN, encoding the presynaptic protein Bassoon, result in a distinct neurodevelopmental disorder with a broad phenotypic range

编码突触前蛋白 Bassoon 的 BSN 基因变异会导致一种独特的神经发育障碍,其表型范围很广。

Guzman, Stacy G; Ruggiero, Sarah M; Ganesan, Shiva; Ellis, Colin A; Harrison, Alicia G; Sullivan, Katie R; Stark, Zornitza; Brown, Natasha J; Kana, Sajel L; Tuttle, Anabelle; Tenorio, Jair; Lapunzina, Pablo; Nevado, Julián; McDonald, Marie T; Jensen, Courtney; Wheeler, Patricia G; Stange, Lila; Morrison, Jennifer; Keren, Boris; Heide, Solveig; Keating, Meg W; Butler, Kameryn M; Lyons, Mike A; Jain, Shailly; Yeganeh, Mehdi; Thompson, Michelle L; Schroeder, Molly; Nguyen, Hoanh; Granadillo, Jorge; Johnston, Kari M; Murali, Chaya N; Bosanko, Katie; Burrow, T Andrew; Morgan, Syreeta; Watson, Deborah J; Hakonarson, Hakon; Helbig, Ingo

Implementation of DPYD and UGT1A1 Testing in Patients With GI Cancer: A Prospective, Nonrandomized Clinical Trial

在胃肠道癌症患者中实施DPYD和UGT1A1检测:一项前瞻性、非随机临床试验

Tuteja, Sony; Cayabyab, Mari Angelica S; Hoffecker, Glenda; Varughese, Lisa A; de Dieu Ndayishimiye, Jean; Wittner, Victoria A; Wang, Xingmei; Hatch, Rachel; Capozzi, Donna; Harr, Margaret; Santani, Avni; Hakonarson, Hakon; Watson, Deborah; Gabriel, Peter; Doucette, Abigail; Massa, Ryan; Damjanov, Nevena; Reddy, Nandi; Oyer, Randall; Teitelbaum, Ursina R

Impact of Applicant Signaling for Otolaryngology Interviews

申请人信号对耳鼻喉科面试的影响

Yousef, Andrew; Nichol, Ariadne; Watson, Deborah

Virtual Versus In-Person Interviews: The Impact of Perceived Success on the Applicant Experience

虚拟面试与现场面试:感知成功对应聘者体验的影响

Moufarrej, Sacha; Yousef, Andrew; Watson, Deborah

TMIC-19. Engineered T cells against the glycoprotein EFEMP1/fibulin-3 target glioblastoma cells in vitro and in vivo

TMIC-19。经基因工程改造的T细胞可靶向糖蛋白EFEMP1/fibulin-3,并在体外和体内靶向胶质母细胞瘤细胞。

Dong, Yina; Watson, Deborah J; Veerareddy, Vaishnavi; Kundu, Somanath; Mitra, Soham; Nandhu, Mohan; Longo, John; Longo, Sharon; Viapiano, Mariano

Variants in BSN, encoding the presynaptic protein Bassoon, result in a novel neurodevelopmental disorder with a broad phenotypic range

编码突触前蛋白 Bassoon 的 BSN 基因变异会导致一种新型神经发育障碍,其表型范围很广。

Guzman, Stacy G; Ruggiero, Sarah M; Ganesan, Shiva; Ellis, Colin A; Harrison, Alicia G; Sullivan, Katie R; Stark, Zornitza; Brown, Natasha J; Kana, Sajel L; Tuttle, Anabelle; Tenorio, Jair; Lapunzina, Pablo; Nevado, Julián; McDonald, Marie T; Jensen, Courtney; Wheeler, Patricia G; Stange, Lila; Morrison, Jennifer; Keren, Boris; Heide, Solveig; Keating, Meg W; Butler, Kameryn M; Lyons, Mike A; Jain, Shailly; Yeganeh, Mehdi; Thompson, Michelle L; Schroeder, Molly; Nguyen, Hoanh; Granadillo, Jorge; Johnston, Kari M; Murali, Chaya N; Bosanko, Katie; Burrow, T Andrew; Morgan, Syreeta; Watson, Deborah J; Hakonarson, Hakon; Helbig, Ingo

A Systematic Review of Virtual Subinternships in Surgical Education: Impact on Curriculum Delivery and Learner Outcomes

外科教育中虚拟实习的系统评价:对课程实施和学习者成果的影响

Monte, Olivia La; Yousef, Andrew; Watson, Deborah

Novel insights into the phenotypic spectrum and pathogenesis of Hardikar syndrome.

对哈迪卡综合征的表型谱和发病机制的新见解

Strong Alanna, March Michael E, Cardinale Christopher J, Liu Yichuan, Battig Mark R, Finoti Livia Sertori, Matsuoka Leticia S, Watson Deborah, Sridhar Sindura, Jarrett James F, Cannon India, Li Dong, Bhoj Elizabeth, Zackai Elaine H, Rand Elizabeth B, Wenger Tara, Lerman Bruce B, Shikany Amy, Weaver K Nicole, Hakonarson Hakon