HuGE Literature Finder
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The impact of NRG1 expressions and methylation on multifactorial Hirschsprung disease. BMC pediatrics 2022 4 22 (1): 216. Gunadi , Kalim Alvin Santoso, Marcellus , Budi Nova Yuli Prasetyo, Iskandar Kris |
Whole genome sequencing reveals epistasis effects within RET for Hirschsprung disease. Scientific reports 2022 11 12 (1): 20423. Wang Yanbing, Mak Timothy Shin Heng, Dattani Saloni, Garcia-Barcelo Maria-Merce, Fu Alexander Xi, Yip Kevin Y, Ngan Elly Sau-Wai, Tam Paul Kwang-Hang, Tang Clara Sze-Man, Sham Pak Chu |
Multiple, independent, common variants at RET, SEMA3 and NRG1 gut enhancers specify Hirschsprung disease risk in European ancestry subjects. Journal of pediatric surgery 2021 Apr . Kapoor Ashish, Nandakumar Priyanka, Auer Dallas R, Sosa Maria X, Ross Holly, Bollinger Juli, Yan Jia, Berrios Courtney, , Chakravarti Aravin |
Common variants of NRG1 and ITGB4 confer risk of Hirschsprung disease in Han Chinese population. Journal of pediatric surgery 2020 Apr . Wei Zhiliang, Yu Xianxian, Wu Wenjie, Bai Meirong, Lu Yanjiao, Song Huanlei, Gong Yiming, Gu Beilin, Chu Xun, Cai W |
Combined Genetic Effects of RET and NRG1 Susceptibility Variants on Multifactorial Hirschsprung Disease in Indonesia. The Journal of surgical research 2019 Jan 233 96-99. Gunadi , Iskandar Kristy, Makhmudi Akhmad, Kapoor Ashi |
Noncoding RET variants explain the strong association with Hirschsprung disease in patients without rare coding sequence variant.
![]() European journal of medical genetics 2018 Jul . Virtanen Valtter B, Salo Perttu P, Cao Jia, Löf-Granström Anna, Milani Lili, Metspalu Andres, Rintala Risto J, Saarenpää-Heikkilä Outi, Paunio Tiina, Wester Tomas, Nordenskjöld Agneta, Perola Markus, Pakarinen Mikko |
Association of NRG1 and AUTS2 genetic polymorphisms with Hirschsprung disease in a South Chinese population. Journal of cellular and molecular medicine 2018 Jan . Zhang Yan, Xie Xiaoli, Zeng Jixiao, Wu Qiang, Zhang Ruizhong, Zhu Deli, Xia Huim |
Genome-wide association study of Hirschsprung disease detects a novel low-frequency variant at the RET locus.
![]() European journal of human genetics : EJHG 2018 Jan . Fadista João, Lund Marie, Skotte Line, Geller Frank, Nandakumar Priyanka, Chatterjee Sumantra, Matsson Hans, Granström Anna Löf, Wester Tomas, Salo Perttu, Virtanen Valtter, Carstensen Lisbeth, Bybjerg-Grauholm Jonas, Hougaard David Michael, Pakarinen Mikko, Perola Markus, Nordenskjöld Agneta, Chakravarti Aravinda, Melbye Mads, Feenstra Bjar |
Effects of RET, NRG1 and NRG3 Polymorphisms in a Chinese Population with Hirschsprung Disease. Scientific reports 2017 Mar 7 43222. Yang Dehua, Yang Jun, Li Shuai, Jiang Meng, Cao Guoqing, Yang Li, Zhang Xi, Zhou Ying, Li Kang, Tang Shao-T |
Trans-ethnic meta-analysis of genome-wide association studies for Hirschsprung disease.
![]() Human molecular genetics 2016 Oct . Tang Clara Sze-Man, Gui Hongsheng, Kapoor Ashish, Kim Jeong-Hyun, Luzón-Toro Berta, Pelet Anna, Burzynski Grzegorz, Lantieri Francesca, So Man-Ting, Berrios Courtney, Shin Hyoung Doo, Fernández Raquel M, Le Thuy-Linh, Verheij Joke B G M, Matera Ivana, Cherny Stacey S, Nandakumar Priyanka, Cheong Hyun Sub, Antiñolo Guillermo, Amiel Jeanne, Seo Jeong-Meen, Kim Dae-Yeon, Oh Jung-Tak, Lyonnet Stanislas, Borrego Salud, Ceccherini Isabella, Hofstra Robert M W, Chakravarti Aravinda, Kim Hyun-Young, Sham Pak Chung, Tam Paul K H, Garcia-Barceló Maria-Mer |
Cumulative Risk Impact of RET, SEMA3, and NRG1 Polymorphisms Associated With Hirschsprung Disease in Han Chinese. Journal of pediatric gastroenterology and nutrition 2016 May . Li Qi, Zhang Zhen, Diao Mei, Gan Liang, Cheng Wei, Xiao Ping, Su Lin, Shangguan Shaofang, Jiang Qian, Li Lo |
Population variation in total genetic risk of Hirschsprung disease from common RET, SEMA3 and NRG1 susceptibility polymorphisms. Human molecular genetics 2015 May 24 (10): 2997-3003. Kapoor Ashish, Jiang Qian, Chatterjee Sumantra, Chakraborty Prakash, Sosa Maria X, Berrios Courtney, Chakravarti Aravin |
Effects of RET and NRG1 polymorphisms in Indonesian patients with Hirschsprung disease. Journal of pediatric surgery 2014 Nov 49 (11): 1614-8. Gunadi , Kapoor Ashish, Ling Albee Yun, Rochadi , Makhmudi Akhmad, Herini Elisabeth Siti, Sosa Maria X, Chatterjee Sumantra, Chakravarti Aravin |
A genome-wide association study identifies potential susceptibility loci for Hirschsprung disease.
![]() PloS one 2014 9 (10): e110292. Kim Jeong-Hyun, Cheong Hyun Sub, Sul Jae Hoon, Seo Jeong-Meen, Kim Dae-Yeon, Oh Jung-Tak, Park Kwi-Won, Kim Hyun-Young, Jung Soo-Min, Jung Kyuwhan, Cho Min Jeng, Bae Joon Seol, Shin Hyoung D |
RET and NRG1 interplay in Hirschsprung disease. Human genetics 2013 May 132 (5): 591-600. Gui Hongsheng, Tang Wai-Kiu, So Man-Ting, Proitsi Petroola, Sham Pak C, Tam Paul K, Ngan Elly Sau-Wai, Sau-Wai Ngan Elly, Cherny Stacey S, Garcia-Barceló Maria-Mer |
Association of genetic polymorphisms in the RET-protooncogene and NRG1 with Hirschsprung disease in Thai patients. Journal of human genetics 2012 May 57 (5): 286-93. Phusantisampan Theerawut, Sangkhathat Surasak, Phongdara Amornrat, Chiengkriwate Piyawan, Patrapinyokul Sakda, Mahasirimongkol Surakame |
Aberrant high expression of NRG1 gene in Hirschsprung disease. Journal of pediatric surgery 2012 9 47 (9): 1694-8. Tang Weibing, Li Bo, Xu Xiaoqun, Zhou Zhigang, Wu Wei, Tang Junwei, Qin Jingjing, Geng Qiming, Jiang Weiwei, Zhang Jie, Sha Jiahao, Xia Yankai, Wang Xin |
Genome-wide copy number analysis uncovers a new HSCR gene: NRG3. PLoS genetics 2012 8 (5): e1002687. Tang Clara Sze-Man, Cheng Guo, So Man-Ting, Yip Benjamin Hon-Kei, Miao Xiao-Ping, Wong Emily Hoi-Man, Ngan Elly Sau-Wai, Lui Vincent Chi-Hang, Song You-Qiang, Chan Danny, Cheung Kenneth, Yuan Zhen-Wei, Lei Liu, Chung Patrick Ho-Yu, Liu Xue-Lai, Wong Kenneth Kak-Yuen, Marshall Christian R, Scherer Stephen W, Scherer Steve, Cherny Stacey S, Sham Pak-Chung, Tam Paul Kwong-Hang, Garcia-Barceló Maria-Mer |
Mutations in the NRG1 gene are associated with Hirschsprung disease. Human genetics 2011 Jun . Tang CS, Ngan ES, Tang WK, So MT, Cheng G, Miao XP, Leon TY, Leung BM, Hui KJ, Lui VH, Chen Y, Chan IH, Chung PH, Liu XL, Wong KK, Sham PC, Cherny SS, Tam PK, Garcia-Barcelo MM |
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