Yunping Lei (Y Lei)

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 21

Top Topics

Genome Wide Association

Transcription Factor

Top Venues

Journal of medical genetics

FASEB journal : official publication of the Federation of American Societies for Experimental Biology

Molecular genetics & genomic medicine

Proceedings of the National Academy of Sciences of the United States of America

This page only lists publications with an associated author ORCID identifier.

Publications

Maayke A de Koning, Paula A Pimienta Ramirez, Monique C Haak, Xiao Han, Martina Ha Ruiterkamp-Versteeg, Nicole de Leeuw, Ulrich A Schatz, Moneef Shoukier, Esther Rieger-Fackeldey, Javier U Ortiz, Sjoerd G van Duinen, Willemijn M Klein, Ruben S G M Witlox, Richard H Finnell, Gijs W E Santen, Yunping Lei, Manon Suerink
De novo heterozygous missense variants in CELSR1 as cause of fetal pleural effusions and progressive fetal hydrops. Journal of medical genetics (2024)
Maayke A de Koning, Paula A Pimienta Ramirez, Monique C Haak, Xiao Han, Martina Ha Ruiterkamp-Versteeg, Nicole de Leeuw, Ulrich A Schatz, Moneef Shoukier, Esther Rieger-Fackeldey, Javier U Ortiz, Sjoerd G van Duinen, Willemijn M Klein, Ruben S G M Witlox, Richard H Finnell, Gijs W E Santen, Yunping Lei, Manon Suerink
De novo heterozygous missense variants in CELSR1 as cause of fetal pleural effusions and progressive fetal hydrops. Journal of medical genetics 61 (6) (2024)
Maayke A de Koning, Paula A Pimienta Ramirez, Monique C Haak, Xiao Han, Martina Ha Ruiterkamp-Versteeg, Nicole de Leeuw, Ulrich A Schatz, Moneef Shoukier, Esther Rieger-Fackeldey, Javier U Ortiz, Sjoerd G van Duinen, Willemijn M Klein, Ruben S G M Witlox, Richard H Finnell, Gijs W E Santen, Yunping Lei, Manon Suerink
De novo heterozygous missense variants in CELSR1 as cause of fetal pleural effusions and progressive fetal hydrops. Journal of medical genetics 61 (6) (2024)
Maayke A de Koning, Paula A Pimienta Ramirez, Monique C Haak, Xiao Han, Martina Ha Ruiterkamp-Versteeg, Nicole de Leeuw, Ulrich A Schatz, Moneef Shoukier, Esther Rieger-Fackeldey, Javier U Ortiz, Sjoerd G van Duinen, Willemijn M Klein, Ruben S G M Witlox, Richard H Finnell, Gijs W E Santen, Yunping Lei, Manon Suerink
De novo heterozygous missense variants in CELSR1 as cause of fetal pleural effusions and progressive fetal hydrops. Journal of medical genetics (2024)
Xiao Han, Xuanye Cao, Robert M Cabrera, Paula Andrea Pimienta Ramirez, Ying Linda Lin, Bogdan J Wlodarczyk, Cuilian Zhang, Richard H Finnell, Yunping Lei
Folate regulation of planar cell polarity pathway and F-actin through folate receptor alpha. FASEB journal : official publication of the Federation of American Societies for Experimental Biology 38 (1) (2023)
Xiao Han, Xuanye Cao, Robert M Cabrera, Paula Andrea Pimienta Ramirez, Ying Linda Lin, Bogdan J Wlodarczyk, Cuilian Zhang, Richard H Finnell, Yunping Lei
Folate regulation of planar cell polarity pathway and F-actin through folate receptor alpha. FASEB journal : official publication of the Federation of American Societies for Experimental Biology 38 (1) (2023)
Xiao Han, Xuanye Cao, Robert M Cabrera, Paula Andrea Pimienta Ramirez, Ying Linda Lin, Bogdan J Wlodarczyk, Cuilian Zhang, Richard H Finnell, Yunping Lei
Folate regulation of planar cell polarity pathway and F-actin through folate receptor alpha. FASEB journal : official publication of the Federation of American Societies for Experimental Biology 38 (1) (2023)
Pagna Sok, Aniko Sabo, Lynn M Almli, Mary M Jenkins, Wendy N Nembhard, A J Agopian, Michael J Bamshad, Elizabeth E Blue, Lawrence C Brody, Austin L Brown, Marilyn L Browne, Mark A Canfield, Suzan L Carmichael, Jessica Xiao-Ling Chong, Shannon Dugan-Perez, Marcia L Feldkamp, Richard H Finnell, Richard A Gibbs, Denise M Kay, Yunping Lei, Qingchang Meng, Cynthia A Moore, James C Mullikin, Donna Muzny, Andrew F Olshan, Faith Pangilinan, Jennita Reefhuis, Paul A Romitti, Jeremy M Schraw, Gary M Shaw, Martha M Werler, Sanjiv Harpavat, Philip J Lupo, null null
Exome-wide assessment of isolated biliary atresia: A report from the National Birth Defects Prevention Study using child-parent trios and a case-control design to identify novel rare variants. American journal of medical genetics. Part A (2023)
Xiao Han, Xuanye Cao, Robert M Cabrera, Paula Andrea Pimienta Ramirez, Ying Linda Lin, Bogdan J Wlodarczyk, Cuilian Zhang, Richard H Finnell, Yunping Lei
Folate regulation of planar cell polarity pathway and F-actin through folate receptor alpha. FASEB journal : official publication of the Federation of American Societies for Experimental Biology 38 (1) (2023)
Xiao Han, Xuanye Cao, Robert M Cabrera, Paula Andrea Pimienta Ramirez, Ying Linda Lin, Bogdan J Wlodarczyk, Cuilian Zhang, Richard H Finnell, Yunping Lei
Folate regulation of planar cell polarity pathway and F-actin through folate receptor alpha. FASEB journal : official publication of the Federation of American Societies for Experimental Biology 38 (1) (2023)
Xiao Han, Xuanye Cao, Vanessa Aguiar-Pulido, Wei Yang, Menuka Karki, Paula Andrea Pimienta Ramirez, Robert M Cabrera, Ying Linda Lin, Bogdan J Wlodarczyk, Gary M Shaw, Margaret Elizabeth Ross, Cui-Lian Zhang, Richard H Finnell, Yunping Lei
CIC missense variants contribute to susceptibility for spina bifida. Human mutation (2022)
Xiao Han, Xuanye Cao, Robert M Cabrera, Paula Andrea Pimienta Ramirez, Cuilian Zhang, Vincent T Ramaekers, Richard H Finnell, Yunping Lei
KDM6B Variants May Contribute to the Pathophysiology of Human Cerebral Folate Deficiency. Biology 12 (1) (2022)
Xiao Han, Xuanye Cao, Robert M Cabrera, Paula Andrea Pimienta Ramirez, Cuilian Zhang, Vincent T Ramaekers, Richard H Finnell, Yunping Lei
KDM6B Variants May Contribute to the Pathophysiology of Human Cerebral Folate Deficiency. Biology 12 (1) (2022)
Vanessa Aguiar-Pulido, Paul Wolujewicz, Alexander Martinez-Fundichely, Eran Elhaik, Gaurav Thareja, Alice Abdel Aleem, Nader Chalhoub, Tawny Cuykendall, Jamel Al-Zamer, Yunping Lei, Haitham El-Bashir, James M Musser, Abdulla Al-Kaabi, Gary M Shaw, Ekta Khurana, Karsten Suhre, Christopher E Mason, Olivier Elemento, Richard H Finnell, Margaret Elizabeth Ross
Systems biology analysis of human genomes points to key pathways conferring spina bifida risk. Proceedings of the National Academy of Sciences of the United States of America 118 (51) (2022)
Cristiane Sá Roriz Fonteles, Richard H Finnell, Yunping Lei, Maria E Zurita-Jimenez, A J Monteiro, T M George, R J Harshbarger
De novo ALX4 variant detected in child with non-syndromic craniosynostosis. Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologicas 54 (11) (2021)
Abdel Rahman Abdel Fattah, Brian Daza, Gregorius Rustandi, Miguel Ángel Berrocal-Rubio, Benjamin Gorissen, Suresh Poovathingal, Kristofer Davie, Jorge Barrasa-Fano, Mar Cóndor, Xuanye Cao, Derek Hadar Rosenzweig, Yunping Lei, Richard H Finnell, Catherine M Verfaillie, Maurilio Sampaolesi, Peter Dedecker, Hans Van Oosterwyck, Stein Aerts, Adrian Ranga
Actuation enhances patterning in human neural tube organoids. Nature communications 12 (1) (2021)
Xuanye Cao, Tian Tian, John W Steele, Robert M Cabrera, Vanessa Aguiar-Pulido, Shruti Wadhwa, Nikitha Bhavani, Patrick Bi, Nick H Gargurevich, Ethan N Hoffman, Chun-Quan Cai, Nicholas J Marini, Wei Yang, Gary M Shaw, Margaret Elizabeth Ross, Richard H Finnell, Yunping Lei
Loss of RAD9B impairs early neural development and contributes to the risk for human spina bifida. Human mutation 41 (4) (2020)
Xuanye Cao, Annika Wolf, Sung-Eun Kim, Robert M Cabrera, Bogdan J Wlodarczyk, Huiping Zhu, Margaret Parker, Ying Lin, John W Steele, Xiao Han, Vincent Th Ramaekers, Robert Steinfeld, Richard H Finnell, Yunping Lei
CIC de novo loss of function variants contribute to cerebral folate deficiency by downregulating FOLR1 expression. Journal of medical genetics 58 (7) (2020)
Yunping Lei, Sung-Eun Kim, Zhongzhong Chen, Xuanye Cao, Huiping Zhu, Wei Yang, Gary M Shaw, Yufang Zheng, Ting Zhang, Hong-Yan Wang, Richard H Finnell
Variants identified in PTK7 associated with neural tube defects. Molecular genetics & genomic medicine 7 (4) (2019)
Thanh T Hoang, Yunping Lei, Laura E Mitchell, Shreela V Sharma, Michael D Swartz, D Kim Waller, Richard H Finnell, Renata H Benjamin, Marilyn L Browne, Mark A Canfield, Philip J Lupo, Paige McKenzie, Gary M Shaw, A J Agopian, null null
Maternal genetic markers for risk of celiac disease and their potential association with neural tube defects in offspring. Molecular genetics & genomic medicine 7 (6) (2019)
Jimi Kim, Yunping Lei, Jin Guo, Sung-Eun Kim, Bogdan J Wlodarczyk, Robert M Cabrera, Ying Linda Lin, Torbjorn K Nilsson, Ting Zhang, Aiguo Ren, Linlin Wang, Zhengwei Yuan, Yu-Fang Zheng, Hong-Yan Wang, Richard H Finnell
Formate rescues neural tube defects caused by mutations in Slc25a32. Proceedings of the National Academy of Sciences of the United States of America 115 (18) (2018)