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For: Wallace AS, Anderson RB. Genetic interactions and modifier genes in Hirschsprung's disease. World J Gastroenterol 2011; 17(45): 4937-4944 [PMID: 22174542 DOI: 10.3748/wjg.v17.i45.4937]
URL: https://www.wjgnet.com/1007-9327/full/v17/i45/4937.htm
Number Citing Articles
1
Yuli Watanabe, Florence Broders-Bondon, Viviane Baral, Perrine Paul-Gilloteaux, Veronique Pingault, Sylvie Dufour, Nadege Bondurand. Sox10 and Itgb1 interaction in enteric neural crest cell migrationDevelopmental Biology 2013; 379(1): 92 doi: 10.1016/j.ydbio.2013.04.013
2
Qiyang Shen, Hua Zhang, Yang Su, Zechao Wen, Zhongxian Zhu, Guanglin Chen, Lei Peng, Chunxia Du, Hua Xie, Hongxing Li, Xiaofeng Lv, Changgui Lu, Yankai Xia, Weibing Tang. Identification of two novel PCDHA9 mutations associated with Hirschsprung's diseaseGene 2018; 658: 96 doi: 10.1016/j.gene.2018.02.054
3
Keisuke Sugimoto, Tomoki Miyazawa, Hitomi Nishi, Kohei Miyazaki, Takuji Enya, Mitsuru Okada, Tsukasa Takemura. Heterozygous p.S811F RET gene mutation associated with renal agenesis, oligomeganephronia and total colonic aganglionosis: a case reportBMC Nephrology 2016; 17(1) doi: 10.1186/s12882-016-0354-z
4
A. J. Barlow, J. Dixon, M. Dixon, P. A. Trainor. Tcof1 acts as a modifier of Pax3 during enteric nervous system development and in the pathogenesis of colonic aganglionosisHuman Molecular Genetics 2013; 22(6): 1206 doi: 10.1093/hmg/dds528
5
D. Henderson, J. Zimmer, H. Nakamura, Prem Puri. Hirschsprung’s disease in twins: a systematic review and meta-analysisPediatric Surgery International 2017; 33(8): 855 doi: 10.1007/s00383-017-4110-7
6
Jean-Marie Gasc, Maud Clemessy, Pierre Corvol, Hervé Kempf. A chicken model of pharmacologically-induced Hirschsprung disease reveals an unexpected role of glucocorticoids in enteric aganglionosisBiology Open 2015; 4(5): 666 doi: 10.1242/bio.201410454
7
Toshiki Takenouchi, Hiroshi Yoshihashi, Yuri Sakaguchi, Tomoko Uehara, Masataka Honda, Takao Takahashi, Kenjiro Kosaki, Sahoko Miyama. Hirschsprung disease as a yet undescribed phenotype in a patient withARID1BmutationAmerican Journal of Medical Genetics Part A 2016; 170(12): 3249 doi: 10.1002/ajmg.a.37861
8
Yang Su, Zechao Wen, Qiyang Shen, Hua Zhang, Lei Peng, Guanglin Chen, Zhongxian Zhu, Chunxia Du, Hua Xie, Hongxing Li, Yankai Xia, Weibing Tang. Long non-coding RNA LOC100507600 functions as a competitive endogenous RNA to regulate BMI1 expression by sponging miR128-1-3p in Hirschsprung's diseaseCell Cycle 2018; 17(4): 459 doi: 10.1080/15384101.2017.1403688
9
I. Zaitoun, C. S. Erickson, A. J. Barlow, T. R. Klein, A. F. Heneghan, J. F. Pierre, M. L. Epstein, A. Gosain. Altered neuronal density and neurotransmitter expression in the ganglionated region ofEdnrbnull mice: implications for Hirschsprung's diseaseNeurogastroenterology & Motility 2013; 25(3): e233 doi: 10.1111/nmo.12083
10
Ellen Merrick Schill, Jonathan I. Lake, Olga A. Tusheva, Nandor Nagy, Saya K. Bery, Lynne Foster, Marina Avetisyan, Stephen L. Johnson, William F. Stenson, Allan M. Goldstein, Robert O. Heuckeroth. Ibuprofen slows migration and inhibits bowel colonization by enteric nervous system precursors in zebrafish, chick and mouseDevelopmental Biology 2016; 409(2): 473 doi: 10.1016/j.ydbio.2015.09.023
11
Yuli Watanabe, Laure Stanchina, Laure Lecerf, Nadjet Gacem, Andrea Conidi, Viviane Baral, Veronique Pingault, Danny Huylebroeck, Nadege Bondurand. Differentiation of Mouse Enteric Nervous System Progenitor Cells Is Controlled by Endothelin 3 and Requires Regulation of Ednrb by SOX10 and ZEB2Gastroenterology 2017; 152(5): 1139 doi: 10.1053/j.gastro.2016.12.034
12
Berta Luzón‐Toro, Leticia Villalba‐Benito, Ana Torroglosa, Raquel M. Fernández, Guillermo Antiñolo, Salud Borrego. What is new about the genetic background of Hirschsprung disease?Clinical Genetics 2020; 97(1): 114 doi: 10.1111/cge.13615
13
Yunmin Li, Tatsuo Kido, Maria M. Garcia-Barcelo, Paul K. H. Tam, Z. Laura Tabatabai, Yun-Fai Chris Lau. SRY interference of normal regulation of the RET gene suggests a potential role of the Y-chromosome gene in sexual dimorphism in Hirschsprung diseaseHuman Molecular Genetics 2015; 24(3): 685 doi: 10.1093/hmg/ddu488
14
C. Tomuschat, P. Puri. RET gene is a major risk factor for Hirschsprung’s disease: a meta-analysisPediatric Surgery International 2015; 31(8): 701 doi: 10.1007/s00383-015-3731-y
15
Marta Lorente-Ros, Ane Miren Andrés, Alba Sánchez-Galán, Cinthia Amiñoso, Sixto García, Pablo Lapunzina, Jesús Solera-García. New mutations associated with Hirschsprung diseaseAnales de Pediatría (English Edition) 2020; 93(4): 222 doi: 10.1016/j.anpede.2019.05.007
16
Raj P Kapur, Lusine Ambartsumyan, Caitlin Smith. Are We Underdiagnosing Hirschsprung Disease?Pediatric and Developmental Pathology 2020; 23(1): 60 doi: 10.1177/1093526619889434
17
K-F Bergeron, DW Silversides, N Pilon. The developmental genetics of Hirschsprung's diseaseClinical Genetics 2013; 83(1): 15 doi: 10.1111/cge.12032
18
David R. Blair, Christopher S. Lyttle, Jonathan M. Mortensen, Charles F. Bearden, Anders Boeck Jensen, Hossein Khiabanian, Rachel Melamed, Raul Rabadan, Elmer V. Bernstam, Søren Brunak, Lars Juhl Jensen, Dan Nicolae, Nigam H. Shah, Robert L. Grossman, Nancy J. Cox, Kevin P. White, Andrey Rzhetsky. A Nondegenerate Code of Deleterious Variants in Mendelian Loci Contributes to Complex Disease RiskCell 2013; 155(1): 70 doi: 10.1016/j.cell.2013.08.030
19
Prem Puri, Florian Friedmacher. Rickham's Neonatal Surgery2018; : 809 doi: 10.1007/978-1-4471-4721-3_40
20
L. Lauriina Porokuokka, Heikki T. Virtanen, Jere Lindén, Yulia Sidorova, Tatiana Danilova, Maria Lindahl, Mart Saarma, Jaan-Olle Andressoo. Gfra1 Underexpression Causes Hirschsprung’s Disease and Associated Enterocolitis in MiceCellular and Molecular Gastroenterology and Hepatology 2019; 7(3): 655 doi: 10.1016/j.jcmgh.2018.12.007
21
Julia Ganz. Gut feelings: Studying enteric nervous system development, function, and disease in the zebrafish model systemDevelopmental Dynamics 2018; 247(2): 268 doi: 10.1002/dvdy.24597
22
Amanda J. Barlow. Neural Crest Cells2014; : 231 doi: 10.1016/B978-0-12-401730-6.00013-2
23
Hilary Schenck Eidam, John Russell, Kaushik Raha, Michael DeMartino, Donghui Qin, Huiping Amy Guan, Zhiliu Zhang, Gong Zhen, Haiyu Yu, Chengde Wu, Yan Pan, Gerard Joberty, Nico Zinn, Sylvie Laquerre, Sharon Robinson, Angela White, Amanda Giddings, Ehsan Mohammadi, Beverly Greenwood-Van Meerveld, Allen Oliff, Sanjay Kumar, Mui Cheung. Discovery of a First-in-Class Gut-Restricted RET Kinase Inhibitor as a Clinical Candidate for the Treatment of IBSACS Medicinal Chemistry Letters 2018; 9(7): 623 doi: 10.1021/acsmedchemlett.8b00035
24
Florian Obermayr, Ryo Hotta, Hideki Enomoto, Heather M. Young. Development and developmental disorders of the enteric nervous systemNature Reviews Gastroenterology & Hepatology 2013; 10(1): 43 doi: 10.1038/nrgastro.2012.234
25
Naho Fujiwara, Katsumi Miyahara, Nana Nakazawa-Tanaka, Chihiro Akazawa, Atsuyuki Yamataka. Increased expression of Semaphorin 3A in the endothelin receptor-B null mouse model of Hirschsprung diseaseJournal of Pediatric Surgery 2018; 53(2): 326 doi: 10.1016/j.jpedsurg.2017.11.034
26
Juntao Ke, Ying Zhu, Xiaoping Miao. The advances of genetics research on Hirschsprung's diseasePEDIATRIC INVESTIGATION 2018; 2(3): 189 doi: 10.1002/ped4.12062
27
J. M. Darlow, M. G. Dobson, R. Darlay, C. M. Molony, M. Hunziker, A. J. Green, H. J. Cordell, P. Puri, D. E. Barton. A new genome scan for primary nonsyndromic vesicoureteric reflux emphasizes high genetic heterogeneity and shows linkage and association with various genes already implicated in urinary tract developmentMolecular Genetics & Genomic Medicine 2014; 2(1): 7 doi: 10.1002/mgg3.22
28
Jiarui Pu, Shaotao Tang, Qiangsong Tong, Guobin Wang, Haibo Jia, Qiong Jia, Kang Li, Dan Li, Dehua Yang, Jun Yang, Hang Li, Shuai Li, Hong Mei. Neuregulin 1 is involved in enteric nervous system development in zebrafishJournal of Pediatric Surgery 2017; 52(7): 1182 doi: 10.1016/j.jpedsurg.2017.01.005
29
Wei-Bo Niu, Mei-Rong Bai, Huan-Lei Song, Yan-Jiao Lu, Wen-Jie Wu, Yi-Ming Gong, Xian-Xian Yu, Zhi-Liang Wei, Wen-Wen Yu, Bei-Lin Gu, Wei Cai, Xun Chu. Association of Variants in PLD1, 3p24.1, and 10q11.21 Regions With Hirschsprung’s Disease in Han Chinese PopulationFrontiers in Genetics 2020; 11 doi: 10.3389/fgene.2020.00738
30
Yang Wang, Qian Jiang, Aravinda Chakravarti, Hao Cai, Ze Xu, Wenjie Wu, Beilin Gu, Long Li, Wei Cai. MicroRNA-4516-mediated regulation of MAPK10 relies on 3′ UTR cis-acting variants and contributes to the altered risk of Hirschsprung diseaseJournal of Medical Genetics 2020; 57(9): 634 doi: 10.1136/jmedgenet-2019-106615
31
Maria M. Alves, Yunia Sribudiani, Rutger W.W. Brouwer, Jeanne Amiel, Guillermo Antiñolo, Salud Borrego, Isabella Ceccherini, Aravinda Chakravarti, Raquel M. Fernández, Maria-Mercè Garcia-Barcelo, Paola Griseri, Stanislas Lyonnet, Paul K. Tam, Wilfred F.J. van IJcken, Bart J.L. Eggen, Gerard J. te Meerman, Robert M.W. Hofstra. Contribution of rare and common variants determine complex diseases—Hirschsprung disease as a modelDevelopmental Biology 2013; 382(1): 320 doi: 10.1016/j.ydbio.2013.05.019
32
Heather M. Young, Lincon A. Stamp, Toshihiro Uesaka, Marlene M. Hao, Donald F. Newgreen, Hideki Enomoto. Physiology of the Gastrointestinal Tract2018; : 273 doi: 10.1016/B978-0-12-809954-4.00011-6
33
Jieping Huang, Ruihua Dang, Daisuke Torigoe, Anqi Li, Chuzhao Lei, Nobuya Sasaki, Jinxi Wang, Takashi Agui. Genetic variation in the GDNF promoter affects its expression and modifies the severity of Hirschsprung's disease (HSCR) in rats carrying Ednrbsl mutationsGene 2016; 575(1): 144 doi: 10.1016/j.gene.2015.08.051
34
Liina Kiho. Keeling’s Fetal and Neonatal Pathology2015; : 561 doi: 10.1007/978-3-319-19207-9_21
35
Naomi E. Butler Tjaden, Paul A. Trainor. The developmental etiology and pathogenesis of Hirschsprung diseaseTranslational Research 2013; 162(1): 1 doi: 10.1016/j.trsl.2013.03.001
36
P. N. Plowman, C. E. Plowman. Onco-ontogeny recapitulates phylogeny – a considerationOncogene 2021; 40(8): 1542 doi: 10.1038/s41388-020-01624-1
37
Allan M. Goldstein, Nikhil Thapar, Tennekoon Buddhika Karunaratne, Roberto De Giorgio. Clinical aspects of neurointestinal disease: Pathophysiology, diagnosis, and treatmentDevelopmental Biology 2016; 417(2): 217 doi: 10.1016/j.ydbio.2016.03.032
38
Tanja Mederer, Stefanie Schmitteckert, Julia Volz, Cristina Martínez, Ralph Röth, Thomas Thumberger, Volker Eckstein, Jutta Scheuerer, Cornelia Thöni, Felix Lasitschka, Leonie Carstensen, Patrick Günther, Stefan Holland-Cunz, Robert Hofstra, Erwin Brosens, Jill A. Rosenfeld, Christian P. Schaaf, Duco Schriemer, Isabella Ceccherini, Marta Rusmini, Joseph Tilghman, Berta Luzón-Toro, Ana Torroglosa, Salud Borrego, Clara Sze-man Tang, Mercè Garcia-Barceló, Paul Tam, Nagarajan Paramasivam, Melanie Bewerunge-Hudler, Carolina De La Torre, Norbert Gretz, Gudrun A. Rappold, Philipp Romero, Beate Niesler, Andrew S. McCallion. A complementary study approach unravels novel players in the pathoetiology of Hirschsprung diseasePLOS Genetics 2020; 16(11): e1009106 doi: 10.1371/journal.pgen.1009106
39
Donald F. Newgreen, Sylvie Dufour, Marthe J. Howard, Kerry A. Landman. Simple rules for a “simple” nervous system? Molecular and biomathematical approaches to enteric nervous system formation and malformationDevelopmental Biology 2013; 382(1): 305 doi: 10.1016/j.ydbio.2013.06.029
40
Benjamin J. Binder, Kerry A. Landman, Donald F. Newgreen, Joshua V. Ross. Incomplete penetrance: The role of stochasticity in developmental cell colonizationJournal of Theoretical Biology 2015; 380: 309 doi: 10.1016/j.jtbi.2015.05.028
41
Marta Lorente-Ros, Ane Miren Andrés, Alba Sánchez-Galán, Cinthia Amiñoso, Sixto García, Pablo Lapunzina, Jesús Solera García. Nuevas mutaciones asociadas a la enfermedad de HirschsprungAnales de Pediatría 2020; 93(4): 222 doi: 10.1016/j.anpedi.2019.05.019
42
Maggie L. Westfal, Allan M. Goldstein. Diagnosing and Managing Hirschsprung Disease in the NewbornNeoReviews 2018; 19(10): e577 doi: 10.1542/neo.19-10-e577
43
Yang Wang, Weihui Yan, Jun Wang, Ying Zhou, Jie Chen, Beilin Gu, Wei Cai. Common genetic variants in GAL , GAP 43 and NRSN 1 and interaction networks confer susceptibility to Hirschsprung disease Journal of Cellular and Molecular Medicine 2018; 22(7): 3377 doi: 10.1111/jcmm.13612
44
Yu-Rong Liu, Fang Ba, Lan-Jie Cheng, Xu Li, Shi-Wei Zhang, Shu-Cheng Zhang. Efficacy of Sox10 Promoter Methylation in the Diagnosis of Intestinal Neuronal Dysplasia From the Peripheral BloodClinical and Translational Gastroenterology 2019; 10(12): e00093 doi: 10.14309/ctg.0000000000000093
45
M. Barrenschee, M. Böttner, I. Hellwig, J. Harde, J. H. Egberts, T. Becker, T. Wedel. Site-specific gene expression and localization of growth factor ligand receptors RET, GFRα1 and GFRα2 in human adult colonCell and Tissue Research 2013; 354(2): 371 doi: 10.1007/s00441-013-1690-y
46
Soo-Min Jung, Suhg Namgoong, Jeong-Meen Seo, Dae-Yeon Kim, Jung-Tak Oh, Hyun-Young Kim, Jeong-Hyun Kim. Potential association between TSGA13 variants and risk of total colonic aganglionosis in Hirschsprung diseaseGene 2019; 710: 240 doi: 10.1016/j.gene.2019.06.007