KDM6B Variants May Contribute to the Pathophysiology of Human Cerebral Folate Deficiency

por Han, Xiao, Cao, Xuanye, Cabrera, Robert M., Pimienta Ramirez, Paula Andrea, Zhang, Cuilian, Ramaekers, Vincent T., Finnell, Richard H., Lei, Yunping
Publicado 2022

Genetic analysis of Wnt/PCP genes in neural tube defects

por Chen, Zhongzhong, Lei, Yunping, Cao, Xuanye, Zheng, Yufang, Wang, Fang, Bao, Yihua, Peng, Rui, Finnell, Richard H., Zhang, Ting, Wang, Hongyan
Publicado 2018

Correction to: Genetic analysis of Wnt/PCP genes in neural tube defects

por Chen, Zhongzhong, Lei, Yunping, Cao, Xuanye, Zheng, Yufang, Wang, Fang, Bao, Yihua, Peng, Rui, Finnell, Richard H., Zhang, Ting, Wang, Hongyan
Publicado 2021

Whole-Exome Sequencing Identifies Damaging de novo Variants in Anencephalic Cases

por Wang, Linlin, Ren, Aiguo, Tian, Tian, Li, Nan, Cao, Xuanye, Zhang, Peng, Jin, Lei, Li, Zhiwen, Shen, Yan, Zhang, Bo, Finnell, Richard H., Lei, Yunping
Publicado 2019

Wnt1 Lineage Specific Deletion of Gpr161 Results in Embryonic Midbrain Malformation and Failure of Craniofacial Skeletal Development

por Kim, Sung-Eun, Robles-Lopez, Karla, Cao, Xuanye, Liu, Kristyn, Chothani, Pooja J., Bhavani, Nikitha, Rahman, Lauren, Mukhopadhyay, Saikat, Wlodarczyk, Bogdan J., Finnell, Richard H.
Publicado 2021

Variants identified in PTK7 associated with neural tube defects

por Lei, Yunping, Kim, Sung‐Eun, Chen, Zhongzhong, Cao, Xuanye, Zhu, Huiping, Yang, Wei, Shaw, Gary M., Zheng, Yufang, Zhang, Ting, Wang, Hong‐Yan, Finnell, Richard H.
Publicado 2019

Gene Environment Interactions in the Etiology of Neural Tube Defects

por Finnell, Richard H., Caiaffa, Carlo Donato, Kim, Sung-Eun, Lei, Yunping, Steele, John, Cao, Xuanye, Tukeman, Gabriel, Lin, Ying Linda, Cabrera, Robert M., Wlodarczyk, Bogdan J.
Publicado 2021

Somatic and de novo Germline Variants of MEDs in Human Neural Tube Defects

por Tian, Tian, Cao, Xuanye, Chen, Yongyan, Jin, Lei, Li, Zhiwen, Han, Xiao, Lin, Ying, Wlodarczyk, Bogdan J., Finnell, Richard H., Yuan, Zhengwei, Wang, Linlin, Ren, Aiguo, Lei, Yunping
Publicado 2021

CIC de novo loss of function variants contribute to cerebral folate deficiency by downregulating FOLR1 expression

por Cao, Xuanye, Wolf, Annika, Kim, Sung-Eun, Cabrera, Robert M., Wlodarczyk, Bogdan J., Zhu, Huiping, Parker, Margaret, Lin, Ying, Steele, John W., Han, Xiao, Ramaekers, Vincent Th, Steinfeld, Robert, Finnell, Richard H., Lei, Yunping
Publicado 2021

Excess folic acid intake increases DNA de novo point mutations

por Cao, Xuanye, Xu, Jianfeng, Lin, Ying L., Cabrera, Robert M., Chen, Qiuying, Zhang, Chaofan, Steele, John W., Han, Xiao, Gross, Steven S., Wlodarczyk, Bogdan J., Lupski, James R., Li, Wei, Wang, Hongyan, Finnell, Richard H., Lei, Yunping
Publicado 2023

Actuation enhances patterning in human neural tube organoids

por Abdel Fattah, Abdel Rahman, Daza, Brian, Rustandi, Gregorius, Berrocal-Rubio, Miguel Ángel, Gorissen, Benjamin, Poovathingal, Suresh, Davie, Kristofer, Barrasa-Fano, Jorge, Cóndor, Mar, Cao, Xuanye, Rosenzweig, Derek Hadar, Lei, Yunping, Finnell, Richard, Verfaillie, Catherine, Sampaolesi, Maurilio, Dedecker, Peter, Van Oosterwyck, Hans, Aerts, Stein, Ranga, Adrian
Publicado 2021