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Results 1-25 of 54 (Search time: 0.007 seconds).

TitleAuthor(s)Issue Date
 
2019
 
Genetic profile of a multiplex Hirschsprung disease family
Proceeding/Conference:American Society of Human Genetics (ASHG) 2019 Annual Meeting
2019
 
Genetic variants on NRG1 confer susceptibility to Hirschsprung's disease
Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2008
2008
 
Genome-wide association study identifies susceptibility loci for biliary atresia
Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2008
2008
 
Hedgehog-notch induced premature gliogenesis of neural crest: a cause of Hirschsprung disease
Proceeding/Conference:Annual Meeting of the International Society for Stem Cell Research, ISSCR 2010
2010
 
Single-cell RNA sequencing unravels the immunosuppressive landscape and tumor heterogeneity of HBV-associated hepatocellular carcinoma
Proceeding/Conference:International Liver Cancer Association (ILCA) Annual Conference 2021
2021
 
Whole exome sequencing analysis in biliary atresia: a follow-up study
Proceeding/Conference:68th Annual Meeting of the American Society of Human Genetics, 2018
2018
Unraveling the genetic basis of nasopharyngeal carcinoma using next-generation sequencing approaches
Proceeding/Conference:Annual Meeting of the American Association for Cancer Research, AACR 2015
2015
2015
 
Integrating genetic analysis with phenotypes of biliary atresia
Proceeding/Conference:European Human Genetics Conference, ESHG 2015
2015
 
Whole-exome sequencing identifies genetic susceptibility locus associated with familial nasopharyngeal carcinoma
Proceeding/Conference:International Symposium on Epstein Barr Virus & Associated Disease
2016
 
2015
 
Deciphering the genetic basis of Hirschsprung disease by whole genome sequencing
Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2016
2016
 
Whole genome sequencing implicates rare variants in sporadic Hirschsprung disease
Proceeding/Conference:European Human Genetics Conference (ESHG) 2017
2017
 
Gene network analysis of candidate loci for human anorectal malformations
Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2013
2013
 
Comprehensive comparison of copy number variations detection using Illumina Omni 2.5M and Affymetrix CytoScan® arrays
Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2013
2013
 
2012
 
Potential use of patient specific induced-pluriopotent stem cell (iPSC) to delineate the molecular pathogenesis of syndromic Hirschsprung (HSCR)
Proceeding/Conference:Annual Meeting of the International Society for Stem Cell Research, ISSCR 2013
2013
 
De novo mutations associated with sporadic cases of Caudal regresion syndrome
Proceeding/Conference:European Journal of Human Genetics
2014
 
Exonic de novo mutations in sporadic Hirschsprung disease
Proceeding/Conference:European Journal of Human Genetics
2014
 
2012
 
Dysregulation of Gli Signaling Underlies Degective Enteric Nervous System Development
Proceeding/Conference:Annual Meeting of the International Society for Stem Cell Research, ISSCR 2014
2014
 
Gli, a family of novel Hirschsprung genes: discovery and mechanisms
Proceeding/Conference:BAPS-IPEG 2014 Joint Congress
2014
 
Using next-generation whole-exome sequencing approaches to elucidate the genetic basis for nasopharyngeal carcinoma
Proceeding/Conference:Gordon Research Conference (GRC) on Genomic Instability
2014
 
Genetics of congenital megacolon in East Asians
Proceeding/Conference:Annual Meeting of the American Society of Human Genetics
2018