先天性巨结肠 (Chinese Wikipedia)

Analysis of information sources in references of the Wikipedia article "先天性巨结肠" in Chinese language version.

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11doi.org

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8nih.gov

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3web.archive.org

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2semanticscholar.org

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1rarediseases.org

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doi.org

Xiao J, et al. Comprehensive characterization of the genetic landscape of familial Hirschsprung’s disease. World J Pediatr. 2023; https://doi.org/10.1007/s12519-023-00686-x
Martucciello G, Ceccherini I, Lerone M, Jasonni V. Pathogenesis of Hirschsprung's disease. Journal of Pediatric Surgery. 2000, 35 (7): 1017–1025. PMID 10917288. doi:10.1053/jpsu.2000.7763.
Puri P, Shinkai T. Pathogenesis of Hirschsprung's disease and its variants: recent progress. Semin. Pediatr. Surg. 2004, 13 (1): 18–24. PMID 14765367. S2CID 11395791. doi:10.1053/j.sempedsurg.2003.09.004.
Garcia-Barcelo, Maria-Merce. Genome-wide association study identifies NRG1 as a susceptibility locus for Hirschsprung's disease. Proc. Natl. Acad. Sci. USA. 2009, 106 (8): 2694–2699. Bibcode:2009PNAS..106.2694G. PMC 2650328 . PMID 19196962. doi:10.1073/pnas.0809630105 .
Tang, Clara. Genome-wide copy number analysis uncovers a new HSCR gene: NRG3.. PLOS Genet. May 10, 2012, 8 (5): e1002687. PMC 3349728 . PMID 22589734. doi:10.1371/journal.pgen.1002687 .
Yang J, Duan S, Zhong R, Yin J, Pu J, Ke J, Lu X, Zou L, Zhang H, Zhu Z, Wang D, Xiao H, Guo A, Xia J, Miao X, Tang S, Wang G. Exome sequencing identified NRG3 as a novel susceptible gene of Hirschsprung's disease in a Chinese population. Mol. Neurobiol. 2013, 47 (3): 957–66. PMID 23315268. S2CID 16842806. doi:10.1007/s12035-012-8392-4.
Shin JG, Seo JY, Seo JM, Kim DY, Oh JT, Park KW, Kim HY, Kim JH, Shin HD. Association analysis of NOX5 polymorphisms with Hirschsprung disease. J Pediatr Surg. 2019. PMID 30732963. doi:10.1016/j.jpedsurg.2019.01.018.
Beltman L, et al. Risk factors for complications in patients with Hirschsprung disease while awaiting surgery: beware of bowel perforation. J. Pediatr. Surg. https://doi.org/10.1016/J.JPEDSURG.2022.02.022 (2022).
Mottadelli G, et al. Robotic surgery in Hirschsprung disease: a unicentric experience on 31 procedures. J. Robot. Surg. https://doi.org/10.1007/S11701-022-01488-5 (2022).
Beltman L, et al. Transition zone pull-through in patients with Hirschsprung disease: is redo surgery beneficial for the long-term outcomes? J. Pediatr. Surg. https://doi.org/ 10.1016/J.JPEDSURG.2023.02.043 (2023).
Trinidad S, et al. Long-term male sexual function and fecal incontinence outcomes for adult patients with Hirschsprung disease or anorectal malformation. J. Pediatr. Surg. https://doi.org/10.1016/J.JPEDSURG.2023.04.006 (2023).

harvard.edu

ui.adsabs.harvard.edu

Garcia-Barcelo, Maria-Merce. Genome-wide association study identifies NRG1 as a susceptibility locus for Hirschsprung's disease. Proc. Natl. Acad. Sci. USA. 2009, 106 (8): 2694–2699. Bibcode:2009PNAS..106.2694G. PMC 2650328 . PMID 19196962. doi:10.1073/pnas.0809630105 .

nature.com

Chial, H. Proto-oncogenes to Oncogenes to Cancer. Nature Education. 2008, 1: 33.

nih.gov

ncbi.nlm.nih.gov

Martucciello G, Ceccherini I, Lerone M, Jasonni V. Pathogenesis of Hirschsprung's disease. Journal of Pediatric Surgery. 2000, 35 (7): 1017–1025. PMID 10917288. doi:10.1053/jpsu.2000.7763.
Puri P, Shinkai T. Pathogenesis of Hirschsprung's disease and its variants: recent progress. Semin. Pediatr. Surg. 2004, 13 (1): 18–24. PMID 14765367. S2CID 11395791. doi:10.1053/j.sempedsurg.2003.09.004.
Garcia-Barcelo, Maria-Merce. Genome-wide association study identifies NRG1 as a susceptibility locus for Hirschsprung's disease. Proc. Natl. Acad. Sci. USA. 2009, 106 (8): 2694–2699. Bibcode:2009PNAS..106.2694G. PMC 2650328 . PMID 19196962. doi:10.1073/pnas.0809630105 .
Tang, Clara. Genome-wide copy number analysis uncovers a new HSCR gene: NRG3.. PLOS Genet. May 10, 2012, 8 (5): e1002687. PMC 3349728 . PMID 22589734. doi:10.1371/journal.pgen.1002687 .
Yang J, Duan S, Zhong R, Yin J, Pu J, Ke J, Lu X, Zou L, Zhang H, Zhu Z, Wang D, Xiao H, Guo A, Xia J, Miao X, Tang S, Wang G. Exome sequencing identified NRG3 as a novel susceptible gene of Hirschsprung's disease in a Chinese population. Mol. Neurobiol. 2013, 47 (3): 957–66. PMID 23315268. S2CID 16842806. doi:10.1007/s12035-012-8392-4.
Shin JG, Seo JY, Seo JM, Kim DY, Oh JT, Park KW, Kim HY, Kim JH, Shin HD. Association analysis of NOX5 polymorphisms with Hirschsprung disease. J Pediatr Surg. 2019. PMID 30732963. doi:10.1016/j.jpedsurg.2019.01.018.

ghr.nlm.nih.gov

Hirschsprung disease. Genetics Home Reference. August 2012 [14 December 2017]. （原始内容存档于18 November 2017）.

niddk.nih.gov

Hirschsprung Disease. NIDDK. July 2017 [14 December 2017]. （原始内容存档于24 November 2017）.

rarediseases.org

Hirschsprung's Disease. NORD (National Organization for Rare Disorders). 2017 [14 December 2017]. （原始内容存档于21 September 2017）.

semanticscholar.org

api.semanticscholar.org

Puri P, Shinkai T. Pathogenesis of Hirschsprung's disease and its variants: recent progress. Semin. Pediatr. Surg. 2004, 13 (1): 18–24. PMID 14765367. S2CID 11395791. doi:10.1053/j.sempedsurg.2003.09.004.
Yang J, Duan S, Zhong R, Yin J, Pu J, Ke J, Lu X, Zou L, Zhang H, Zhu Z, Wang D, Xiao H, Guo A, Xia J, Miao X, Tang S, Wang G. Exome sequencing identified NRG3 as a novel susceptible gene of Hirschsprung's disease in a Chinese population. Mol. Neurobiol. 2013, 47 (3): 957–66. PMID 23315268. S2CID 16842806. doi:10.1007/s12035-012-8392-4.

web.archive.org

Hirschsprung disease. Genetics Home Reference. August 2012 [14 December 2017]. （原始内容存档于18 November 2017）.
Hirschsprung Disease. NIDDK. July 2017 [14 December 2017]. （原始内容存档于24 November 2017）.
Hirschsprung's Disease. NORD (National Organization for Rare Disorders). 2017 [14 December 2017]. （原始内容存档于21 September 2017）.