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| Title | Author(s) | Issue Date | Views | |
|---|---|---|---|---|
Genetic variants on NRG1 confer susceptibility to Hirschsprung's disease Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2008 | 2008 | 115 | ||
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 | 51 | ||
Integrating genetic analysis with phenotypes of biliary atresia Proceeding/Conference:European Human Genetics Conference, ESHG 2015 | 2015 | 61 | ||
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 | 101 | ||
Estrogen receptors genetic polymorphisms risk association and their functional roles in breast cancer risk: a study on Hong Kong Chinese women Proceeding/Conference:Cancer Research | 2007 | 140 | ||
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 | 131 | ||
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 | 71 | ||
Genetic mapping for RET-dependent modifiers in Hirschsprung disease (HSCR) Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2006 | 2006 | 119 | ||
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 | 5 | ||
Fine mapping of the NRG1 Hirschsprung's-associated gene Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2010 | 2010 | 93 | ||
The protective role of homozygous L-SIGN (CLEC4M) in SARS coronavirus infection. Proceeding/Conference:HUGO Annual Human Genome Meeting, HGM 2006 | 2006 | 124 | ||
Fine mapping of Hirschsprung’s disease loci in 9q31 Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2009 | 2009 | |||
A new machine-learning based method to accurately assess copy number variants from whole genome sequencing data and its application on the analysis of the Hirschsprung disease genome Proceeding/Conference:American Society of Human Genetics (ASHG) 2019 Annual Meeting | 2019 | 61 | ||
Cost effective assay choice for rare disease study designs Proceeding/Conference:Human Heredity | 2015 | 70 | ||
Genome-wide copy number variation in anorectal malformations Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2012 | 2012 | 90 | ||
Single-cell RNA sequencing shows the immunosuppressive landscape and tumor heterogeneity of HBV-associated hepatocellular carcinoma Proceeding/Conference:The 11th Asia-Pacific Primary Liver Cancer Expert Meeting (APPLE 2021) | 2021 | 22 | ||
Genetic study of a fami segregating Waardenburg-Shah syndrome Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2012 | 2012 | 70 | ||
Rare variants in sporadic Hirschsprung disease patients Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2015 | 2015 | 91 | ||
ATP-binding cassette (ABC) transporter recessive mutations in biliary atresia cases Proceeding/Conference:American Society of Human Genetics (ASHG) 2019 Annual Meeting | 2019 | 48 | ||
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 | 108 | ||
| 2015 | 53 | |||
A RET founder mutation in Chinese hirschsprung's patients Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2009 | 2009 | 194 | ||
Genetic profile of a multiplex Hirschsprung disease family Proceeding/Conference:American Society of Human Genetics (ASHG) 2019 Annual Meeting | 2019 | 103 | ||
Copy Number Variations (CNVs) analysis of Hirschsprung Disease (HSCR) using Whole Genome Sequencing (WGS) data Proceeding/Conference:The 5th International Symposium on Development of the Enteric Nervous System: cells, signals genes and therapy, 2018 | 2018 | 63 | ||
Exonic de novo mutations in sporadic Hirschsprung disease Proceeding/Conference:European Journal of Human Genetics | 2014 |