arrow
返回
W

Won Chan Jeong

seegene medical foundation

5H指数
19论文数
46被引数
收录论文 7
发表时间
Identification of recurrent MYH7 variant hypertrophic cardiomyopathy patients in Korea: a case series韩国复发性MYH7变异肥厚型心肌病患者的识别:一个病例系列
err2025-12-31
err0
PREAI
errRyu, Seung Woo; Jang, Seokhui; Son, Jang-Won; Lee, Sun Hwa; Kim, Yisik; Lee, Soo Yong; Hong, Geu-Ru; Lee, Sang Chol; Ko, Kyu-Yong; Hwang, Ji-won; Seo, Go Hun; Jeong, Won Chan; Kim, Kyung-Hee
err分享
err收藏
A programmed decline in ribosome levels governs human early neurodevelopment程序性核糖体水平下降调控人类早期神经发育
err2025-08-04
err0
errOAAI
errChunyang Ni; Yudong Wei; Barbara Vona; Dayea Park; Yulei Wei; Daniel A. Schmitz; Yi Ding; Masahiro Sakurai; Emily Ballard; Leijie Li; Yan Liu; Ashwani Kumar; Chao Xing; Shenlu Qin; Sangin Kim; Martina Foglizzo; Jianchao Zhao; Hyung-Goo Kim; Cumhur Ekmekci; Ehsan Ghayoor Karimiani; Shima Imannezhad; Fatemeh Eghbal; Reza Shervin Badv; Eva Maria Christina Schwaibold; Mohammadreza Dehghani; Mohammad Yahya Vahidi Mehrjardi; Zahra Metanat; Hosein Eslamiyeh; Ebtissal Khouj; Saleh Mohammed Nasser Alhajj; Aziza Chedrawi; Khushnooda Ramzan; Jamil A. Hashmi; Majed M. Alluqmani; Sulman Basit; Danai Veltra; Nikolaos M. Marinakis; Georgios Niotakis; Pelagia Vorgia; Christalena Sofocleous; Hane Lee; Won Chan Jeong; Muhammad Umair; Muhammad Bilal; César Augusto Pinheiro Ferreira Alves; Matthew Sieber; Michael Kruer; Henry Houlden; Fowzan S. Alkuraya; Elton Zeqiraj; Roger A. Greenberg; Can Cenik; Leqian Yu; Reza Maroofian; Jun Wu; Michael Buszczak
err分享
err收藏
Exome sequencing of 18,994 ethnically diverse patients with suspected rare Mendelian disorders对18,994名怀疑患有罕见孟德尔疾病的具有不同族裔背景的患者进行外显子测序
err2025-01-22
err0
errOAAI
errHan, Heonjong; Seo, Go Hun; Hyun, Seong-In; Kwon, Kisang; Ryu, Seung Woo; Khang, Rin; Lee, Eugene; Kim, Jihye; Song, Yongjun; Jeong, Won Chan; Han, Joohyun; Kim, Dong-wook; Yang, Soyeon; Lee, Sohyun; Jang, Sohyun; Lee, Jungsul; Lee, Hane
err分享
err收藏
Clinical and neuroradiological spectrum of biallelic variants in NOTCH3
err2024-09-01
err0
errOAAI
errIruzubieta, Pablo; Alves, Cesar Augusto Pinheiro Ferreira; Al Shamsi, Aisha M.; Elghazali, Gehad; Zaki, Maha S.; Pinelli, Lorenzo; Lopergolo, Diego; Cho, Bernard P. H.; Jolly, Amy A.; Al Futaisi, Amna; Al-Amrani, Fatema; Galli, Jessica; Fazzi, Elisa; Vulin, Katarina; Barajas-Olmos, Francisco; Hengel, Holger; Aljamal, Bayan Mohammed; Nasr, Vahideh; Assarzadegan, Farhad; Ragno, Michele; Trojano, Luigi; Ojeda, Naomi Meave; Cakar, Arman; Bianchi, Silvia; Pescini, Francesca; Poggesi, Anna; Al Tenalji, Amal; Aziz, Majid; Mohammad, Rahema; Chedrawi, Aziza; De Stefano, Nicola; Zifarelli, Giovanni; Schoels, Ludger; Haack, Tobias B.; Rebelo, Adriana; Zuchner, Stephan; Koc, Filiz; Griffiths, Lyn R.; Orozco, Lorena; Helmes, Karla Garcia; Babaei, Meisam; Bauer, Peter; Jeong, Won Chan; Karimiani, Ehsan Ghayoor; Schmidts, Miriam; Gleeson, Joseph G.; Chung, Wendy K.; Alkuraya, Fowzan Sami; Shalbafan, Bita; Markus, Hugh S.; Houlden, Henry; Maroofian, Reza
err分享
err收藏
Bi-allelic loss-of-function variants in WBP4, encoding a spliceosome protein, result in a variable neurodevelopmental syndrome
err2023-12-01
err6
errOAAI
errEngal, Eden; Oja, Kaisa Teele; Maroofian, Reza; Geminder, Ophir; Le, Thuy-Linh; Marzin, Pauline; Guimier, Anne; Mor, Evyatar; Zvi, Naama; Elefant, Naama; Zaki, Maha S.; Gleeson, Joseph G.; Muru, Kai; Pajusalu, Sander; Wojcik, Monica H.; Pachat, Divya; Elmaksoud, Marwa Abd; Jeong, Won Chan; Lee, Hane; Bauer, Peter; Zifarelli, Giovanni; Houlden, Henry; Daana, Muhannad; Elpeleg, Orly; Amiel, Jeanne; Lyonnet, Stanislas; Gordon, Christopher T.; Harel, Tamar; Ounap, Katrin; Salton, Maayan; Mor-Shaked, Hagar
err分享
err收藏