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

Strengthening Faculty Mentoring of Online DrPH Students: A Service-First Focus Approach

加强教师对在线公共卫生博士生的指导:以服务为先的视角

Bohn, H Joseph Jr; Petersen, Donna J

User Testing an mHealth Behavioral Health App for Hopi/Tewa Youth During the COVID-19 Pandemic: Usability Study

新冠疫情期间针对霍皮/特瓦族青年的移动健康行为健康应用程序的用户测试:可用性研究

Hagemann, Shelby; Vigil-Hayes, Morgan; Amresh, Ashish; Adams, Marissa; H Joseph, Darold; Futterman Collier, Ann

Differential impacts of parental attention deficit/hyperactivity disorder on early maternal-infant attachment

父母注意力缺陷/多动障碍对早期母婴依恋的不同影响

Mark, Elyse; Molina, Brooke S G; Wilson, Michelle A; Zeanah, Charles H; Joseph, Heather M

Nuclear Histone 3 Post-Translational Modification Profiling in Whole Cells using Spectral Flow Cytometry

利用光谱流式细胞术对全细胞中核组蛋白3的翻译后修饰进行分析

Golden, Carly S; Williams, Saylor; Sreerama, Sandeep; Blankevoort, Sophia; Yost, H Joseph; Tristani-Firouzi, Martin; Belkina, Anna; Serrano, Maria A

Assessing the contribution of rare protein-coding germline variants to prostate cancer risk and severity in 37,184 cases

评估罕见蛋白质编码种系变异对 37,184 例前列腺癌风险和严重程度的影响

Mitchell, Jonathan; Camacho, Niedzica; Shea, Patrick; Stopsack, Konrad H; Joseph, Vijai; Burren, Oliver S; Dhindsa, Ryan S; Nag, Abhishek; Berchuck, Jacob E; O'Neill, Amanda; Abbasi, Ali; Zoghbi, Anthony W; Alegre-Díaz, Jesus; Kuri-Morales, Pablo; Berumen, Jaime; Tapia-Conyer, Roberto; Emberson, Jonathan; Torres, Jason M; Collins, Rory; Wang, Quanli; Goldstein, David; Matakidou, Athena; Haefliger, Carolina; Anderson-Dring, Lauren; March, Ruth; Jobanputra, Vaidehi; Dougherty, Brian; Carss, Keren; Petrovski, Slavé; Kantoff, Philip W; Offit, Kenneth; Mucci, Lorelei A; Pomerantz, Mark; Fabre, Margarete A

Recessive genetic contribution to congenital heart disease in 5,424 probands

5424例先证者中隐性遗传因素对先天性心脏病的影响

Dong, Weilai; Jin, Sheng Chih; Sierant, Michael C; Lu, Ziyu; Li, Boyang; Lu, Qiongshi; Morton, Sarah U; Zhang, Junhui; López-Giráldez, Francesc; Nelson-Williams, Carol; Knight, James R; Zhao, Hongyu; Cao, Junyue; Mane, Shrikant; Gruber, Peter J; Lek, Monkol; Goldmuntz, Elizabeth; Deanfield, John; Giardini, Alessandro; Mital, Seema; Russell, Mark; Gaynor, J William; Cnota, James F; Wagner, Michael; Srivastava, Deepak; Bernstein, Daniel; Porter, George A Jr; Newburger, Jane; Roberts, Amy E; Yandell, Mark; Yost, H Joseph; Tristani-Firouzi, Martin; Kim, Richard; Seidman, Jonathan; Chung, Wendy K; Gelb, Bruce D; Seidman, Christine E; Lifton, Richard P; Brueckner, Martina

Genomic analysis of 11,555 probands identifies 60 dominant congenital heart disease genes

对 11,555 名先证者的基因组分析鉴定出 60 个显性先天性心脏病基因

Sierant, Michael C; Jin, Sheng Chih; Bilguvar, Kaya; Morton, Sarah U; Dong, Weilai; Jiang, Wei; Lu, Ziyu; Li, Boyang; López-Giráldez, Francesc; Tikhonova, Irina; Zeng, Xue; Lu, Qiongshi; Choi, Jungmin; Zhang, Junhui; Nelson-Williams, Carol; Knight, James R; Zhao, Hongyu; Cao, Junyue; Mane, Shrikant; Sedore, Stanley C; Gruber, Peter J; Lek, Monkol; Goldmuntz, Elizabeth; Deanfield, John; Giardini, Alessandro; Mital, Seema; Russell, Mark; Gaynor, J William; King, Eileen; Wagner, Michael; Srivastava, Deepak; Shen, Yufeng; Bernstein, Daniel; Porter, George A Jr; Newburger, Jane W; Seidman, Jonathan G; Roberts, Amy E; Yandell, Mark; Yost, H Joseph; Tristani-Firouzi, Martin; Kim, Richard; Chung, Wendy K; Gelb, Bruce D; Seidman, Christine E; Brueckner, Martina; Lifton, Richard P

The Utah NeoSeq Project: a collaborative multidisciplinary program to facilitate genomic diagnostics in the neonatal intensive care unit

犹他州NeoSeq项目:一项旨在促进新生儿重症监护病房基因组诊断的多学科合作项目

Malone Jenkins, Sabrina; Palmquist, Rachel N; Moore, Barry; Boyden, Steven E; Nicholas, Thomas J; Bayrak-Toydemir, Pinar; Mao, Rong; Farrell, J Andrew R; Holt, Carson H; Rynearson, Shawn G; Solorzano, Chelsea M; Ward, Alistair; Best, D Hunter; Al-Sweel, Najla; Bentley, Dawn L; Brunelli, Luca; Chow, Clement Y; Close, Devin W; Cormier, Michael J; Deshotel, Malia J; Durtschi, Jacob; Eide, Erik J; Floyd, Luaiva; Fredrickson, Eric K; Fulmer, Makenzie L; Hernandez, Edgar J; Kapron, Ashley L; Karren, Mary Anne; Lewis, Robert G; Miller, Christine E; Murtaugh, L Charles; Nicholson, Kelsey E; Noble, Katherine; O'Fallon, Brendan D; O'Shea, John M; Pattison, David C; Pedersen, Brent S; Petersen, Brandy J; Peterson, Bennet D; Pizzo, Lucilla; Reynolds, Hayley M; Rindler, Paul; Torr, Carrie B; Wen, Ting; Yost, H Joseph; Zhao, Jian; Yandell, Mark; Marth, Gabor T; Quinlan, Aaron R; Carey, John C; Shayota, Brian J; Tristani-Firouzi, Martin; Bonkowsky, Joshua L

Prognostic significance of serum complement activation, neutrophil extracellular traps and extracellular DNA in newly diagnosed epithelial ovarian cancer

血清补体激活、中性粒细胞胞外陷阱和细胞外DNA在初诊上皮性卵巢癌中的预后意义

Ricciuti, Jason; Liu, Qian; Khan, A N M Nazmul H; Joseph, Janine M; Veuskens, Bert; Giridharan, Thejaswini; Suzuki, Sora; Emmons, Tiffany; Yaffe, Michael; Kuijpers, Taco W; Jongerius, Ilse; Brouwer, Mieke; Pouw, Richard B; Odunsi, Kunle; Frederick, Peter; Mager, Katherine LaVigne; Lele, Shashikant; Gaulin, Nicole; Hakim, Christiane; Edwards, Robert P; Olawaiye, Alexander B; Sukamanovich, Paniti; Taylor, Sarah; Elishaev, Esther; Zsiros, Emese; Modugno, Francesmary; Moysich, Kirsten; Segal, Brahm

Efficient identification of de novo mutations in family trios: a consensus-based informatic approach

高效识别家族三联体中的新生突变:一种基于共识的信息学方法

Shadrina, Mariya; Kalay, Özem; Demirkaya-Budak, Sinem; LeDuc, Charles A; Chung, Wendy K; Turgut, Deniz; Budak, Gungor; Arslan, Elif; Semenyuk, Vladimir; Davis-Dusenbery, Brandi; Seidman, Christine E; Yost, H Joseph; Jain, Amit; Gelb, Bruce D