de Blank, Peter M. K.; Gross, Andrea M.; Akshintala, Srivandana; Blakeley, Jaishri O.; Bollag, Gideon; Cannon, Ashley; Dombi, Eva; Fangusaro, Jason; Gelb, Bruce D.; Hargrave, Darren; Kim, AeRang; Klesse, Laura J.; Loh, Mignon; Martin, Staci; Moertel, Christopher; Packer, Roger; Payne, Jonathan M.; Rauen, Katherine A.; Rios, Jonathan J.; Robison, Nathan; Schorry, Elizabeth K.; Shannon, Kevin; Stevenson, David A.; Stieglitz, Elliot; Ullrich, Nicole J.; Walsh, Karin S.; Weiss, Brian D.; Wolters, Pamela L.; Yohay, Kaleb; Yohe, Marielle E.; Widemann, Brigitte C.; Fisher, Michael J.

Thousands of induced germline mutations affecting immune cells identified by automated meiotic mapping coupled with machine learning

通过自动减数分裂图谱和机器学习鉴定的数千种诱导的影响免疫细胞的种系突变

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

IF9.1

2021-07-0610

Xu, Darui; Lyon, Stephen; Bu, Chun Hui; Hildebrand, Sara; Choi, Jin Huk; Zhong, Xue; Liu, Aijie; Turer, Emre E.; Zhang, Zhao; Russell, Jamie; Ludwig, Sara; Mahrt, Elena; Nair-Gill, Evan; Shi, Hexin; Wang, Ying; Zhang, Duanwu; Yue, Tao; Wang, Kuan-wen; SoRelle, Jeffrey A.; Su, Lijing; Misawa, Takuma; McAlpine, William; Sun, Lei; Wang, Jianhui; Zhan, Xiaoming; Choi, Mihwa; Farokhnia, Roxana; Sakla, Andrew; Schneider, Sara; Coco, Hannah; Coolbaugh, Gabrielle; Hayse, Braden; Mazal, Sara; Medler, Dawson; Nguyen, Brandon; Rodriguez, Edward; Wadley, Andrew; Tang, Miao; Li, Xiaohong; Anderton, Priscilla; Keller, Katie; Press, Amanda; Scott, Lindsay; Quan, Jiexia; Cooper, Sydney; Collie, Tiffany; Qin, Baifang; Cardin, Jennifer; Simpson, Rochelle; Tadesse, Meron; Sun, Qihua; Wise, Carol A.; Rios, Jonathan J.; Moresco, Eva Marie Y.; Beutler, Bruce

Saturation mutagenesis defines novel mouse models of severe spine deformity

DISEASE MODELS & MECHANISMS

IF3.3

2021-06-185

OAAI

Biallelic variants in RNU12 cause CDAGS syndrome

HUMAN MUTATION

IF3.7

2021-06-158

OAAI

Germline Saturation Mutagenesis Induces Skeletal Phenotypes in Mice

JOURNAL OF BONE AND MINERAL RESEARCH

IF5.9

2021-04-278

Genomic characterization of the adolescent idiopathic scoliosis-associated transcriptome and regulome

HUMAN MOLECULAR GENETICS

IF3.2

2020-11-1214

OAAI

A molecular basis for neurofibroma-associated skeletal manifestations in NF1

GENETICS IN MEDICINE

IF6.2

2020-11-0117

OAAI

Genetic association and characterization of FSTL5 in isolated clubfoot

HUMAN MOLECULAR GENETICS

IF3.2

2020-10-266

OAAI

Diagnostic yield and clinical impact of exome sequencing in early-onset scoliosis (EOS)

JOURNAL OF MEDICAL GENETICS

IF3.7

2020-05-0744

OAAI

Zhao, Sen; Zhang, Yuanqiang; Chen, Weisheng; Li, Weiyu; Wang, Shengru; Wang, Lianlei; Zhao, Yanxue; Lin, Mao; Ye, Yongyu; Lin, Jiachen; Zheng, Yu; Liu, Jiaqi; Zhao, Hengqiang; Yan, Zihui; Yang, Yongxin; Huang, Yingzhao; Lin, Guanfeng; Chen, Zefu; Zhang, Zhen; Liu, Sen; Jin, Lichao; Wang, Zhaoyang; Chen, Jingdan; Niu, Yuchen; Li, Xiaoxin; Wu, Yong; Wang, Yipeng; Du, Renqian; Gao, Na; Zhao, Hong; Yang, Ying; Liu, Ying; Tian, Ye; Li, Wenli; Zhao, Yu; Liu, Jia; Yu, Bin; Zhang, Na; Yu, Keyi; Yang, Xu; Li, Shugang; Xu, Yuan; Hu, Jianhua; Liu, Zhe; Shen, Jianxiong; Zhang, Shuyang; Su, Jianzhong; Khanshour, Anas M.; Kidane, Yared H.; Ramo, Brandon; Rios, Jonathan J.; Liu, Pengfei; Sutton, V. Reid; Posey, Jennifer E.; Wu, Zhihong; Qiu, Guixing; Wise, Carol A.; Zhang, Feng; Lupski, James R.; Zhang, Jianguo; Wu, Nan

Jonathan J. Rios

个人简介

教育背景

工作经历

荣誉奖项

研究方向