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

Role of CAMK2D in neurodevelopment and associated conditions

CAMK2D在神经发育及相关疾病中的作用

Rigter, Pomme M F; de Konink, Charlotte; Dunn, Matthew J; Proietti Onori, Martina; Humberson, Jennifer B; Thomas, Matthew; Barnes, Caitlin; Prada, Carlos E; Weaver, K Nicole; Ryan, Thomas D; Caluseriu, Oana; Conway, Jennifer; Calamaro, Emily; Fong, Chin-To; Wuyts, Wim; Meuwissen, Marije; Hordijk, Eva; Jonkers, Carsten N; Anderson, Lucas; Yuseinova, Berfin; Polonia, Sarah; Beysen, Diane; Stark, Zornitza; Savva, Elena; Poulton, Cathryn; McKenzie, Fiona; Bhoj, Elizabeth; Bupp, Caleb P; Bézieau, Stéphane; Mercier, Sandra; Blevins, Amy; Wentzensen, Ingrid M; Xia, Fan; Rosenfeld, Jill A; Hsieh, Tzung-Chien; Krawitz, Peter M; Elbracht, Miriam; Veenma, Danielle C M; Schulman, Howard; Stratton, Margaret M; Küry, Sébastien; van Woerden, Geeske M

Machine Learning-Based VO(2) Estimation Using a Wearable Multiwavelength Photoplethysmography Device

基于机器学习的可穿戴多波长光电容积脉搏波描记仪VO₂估算

Hsiao, Chin-To; Tong, Carl; Coté, Gerard L

Role of CAMK2D in neurodevelopment and associated conditions

CAMK2D在神经发育及相关疾病中的作用

Rigter, Pomme M F; de Konink, Charlotte; Dunn, Matthew J; Proietti Onori, Martina; Humberson, Jennifer B; Thomas, Matthew; Barnes, Caitlin; Prada, Carlos E; Weaver, K Nicole; Ryan, Thomas D; Caluseriu, Oana; Conway, Jennifer; Calamaro, Emily; Fong, Chin-To; Wuyts, Wim; Meuwissen, Marije; Hordijk, Eva; Jonkers, Carsten N; Anderson, Lucas; Yuseinova, Berfin; Polonia, Sarah; Beysen, Diane; Stark, Zornitza; Savva, Elena; Poulton, Cathryn; McKenzie, Fiona; Bhoj, Elizabeth; Bupp, Caleb P; Bézieau, Stéphane; Mercier, Sandra; Blevins, Amy; Wentzensen, Ingrid M; Xia, Fan; Rosenfeld, Jill A; Hsieh, Tzung-Chien; Krawitz, Peter M; Elbracht, Miriam; Veenma, Danielle C M; Schulman, Howard; Stratton, Margaret M; Küry, Sébastien; van Woerden, Geeske M

Metal-free alkyne annulation enabling π-extension of boron-doped polycyclic aromatic hydrocarbons

无金属炔烃环化反应实现硼掺杂多环芳烃的π共轭扩展

Anitha, Mandala; Chin, To-Jen; Liu, Guan-Cheng; Hsieh, Chi-Tien; Wang, Kuan-Hua; Li, Shu-Li; Cheng, Mu-Jeng; Farrell, Jeffrey M

Alternative polyadenylation alters protein dosage by switching between intronic and 3'UTR sites

选择性多聚腺苷酸化通过在内含子和3'UTR位点之间切换来改变蛋白质剂量。

Nicola de Prisco ,Caitlin Ford ,Nathan D Elrod ,Winston Lee ,Lauren C Tang ,Kai-Lieh Huang ,Ai Lin ,Ping Ji ,Venkata S Jonnakuti ,Lia Boyle ,Maximilian Cabaj ,Salvatore Botta ,Katrin Õunap ,Karit Reinson ,Monica H Wojcik ,Jill A Rosenfeld ,Weimin Bi ,Kristian Tveten ,Trine Prescott ,Thorsten Gerstner ,Audrey Schroeder ,Chin-To Fong ,Jaya K George-Abraham ,Catherine A Buchanan ,Andrea Hanson-Khan ,Jonathan A Bernstein ,Aikaterini A Nella ,Wendy K Chung ,Vicky Brandt ,Marko Jovanovic ,Kimara L Targoff ,Hari Krishna Yalamanchili ,Eric J Wagner ,Vincenzo A Gennarino

Add-on soft electronic interfaces for continuous cuffless blood pressure monitoring

用于连续无袖带血压监测的附加软电子接口

Namkoong, Myeong; Baskar, Balaji; Singh, Lakhvir; Guo, Heng; McMurray, Justin; Branan, Kimberly; Rahman, Md Saifur; Hsiao, Chin-To; Kuriakose, Josh; Hernandez, Joanna; Arikan, Arda A; Garza-Rivera, Luis E; Coté, Gerard L; Tian, Limei

Perspectives on the future of dysmorphology

畸形学的未来展望

Solomon, Benjamin D; Adam, Margaret P; Fong, Chin-To; Girisha, Katta M; Hall, Judith G; Hurst, Anna C E; Krawitz, Peter M; Moosa, Shahida; Phadke, Shubha R; Tekendo-Ngongang, Cedrik; Wenger, Tara L

Sequencing individual genomes with recurrent genomic disorder deletions: an approach to characterize genes for autosomal recessive rare disease traits

对具有复发性基因组疾病缺失的个体基因组进行测序:一种表征常染色体隐性罕见病性状基因的方法

Bo Yuan ,Katharina V Schulze ,Nurit Assia Batzir ,Jefferson Sinson ,Hongzheng Dai ,Wenmiao Zhu ,Francia Bocanegra ,Chin-To Fong ,Jimmy Holder ,Joanne Nguyen ,Christian P Schaaf ,Yaping Yang ,Weimin Bi ,Christine Eng ,Chad Shaw ,James R Lupski ,Pengfei Liu

Expanding the mutational landscape and clinical phenotype of the YIF1B related brain disorder

扩展YIF1B相关脑疾病的突变图谱和临床表型

Medico Salsench, Eva; Maroofian, Reza; Deng, Ruizhi; Lanko, Kristina; Nikoncuk, Anita; Pérez, Belén; Sánchez-Lijarcio, Obdulia; Ibáñez-Mico, Salvador; Wojcik, Antonina; Vargas, Marcelo; Abbas Al-Sannaa, Nouriya; Girgis, Marian Y; Silveira, Tainá Regina Damaceno; Bauer, Peter; Schroeder, Audrey; Fong, Chin-To; Begtrup, Amber; Babaei, Meisam; Toosi, Mehran Beiraghi; Ashrafzadeh, Farah; Imannezhad, Shima; Doosti, Mohammad; Ahangari, Najmeh; Najarzadeh Torbati, Paria; Ghayoor Karimiani, Ehsan; Murphy, David; Cali, Elisa; Kaya, Ibrahim H; AlMuhaizea, Mohammad; Colak, Dilek; Cardona-Londoño, Kelly J; Arold, Stefan T; Houlden, Henry; Bertoli-Avella, Aida; Kaya, Namik; Barakat, Tahsin Stefan

De novo variants in H3-3A and H3-3B are associated with neurodevelopmental delay, dysmorphic features, and structural brain abnormalities

H3-3A 和 H3-3B 的新生变异与神经发育迟缓、畸形特征和脑结构异常有关

Volkan Okur #, Zefu Chen #, Liesbeth Vossaert, Sandra Peacock, Jill Rosenfeld, Lina Zhao, Haowei Du, Emily Calamaro, Amanda Gerard, Sen Zhao, Jill Kelsay, Ashley Lahr, Chloe Mighton, Hillary M Porter, Amy Siemon, Josh Silver, Shayna Svihovec, Chin-To Fong, Christina L Grant, Jordan Lerner-Ellis, Kan