Hongzhe Li

发表

Phenotype Restricted Genome-Wide Association Study Using a Gene-Centric Approach Identifies Three Low-Risk Neuroblastoma Susceptibility Loci

Joseph T. Glessner, J. Glessner, H. Hakonarson, 2011, PLoS genetics.

Copy number variation at 1q21.1 associated with neuroblastoma

Sharon J. Diskin, John M. Maris, Struan F. A. Grant, 2009, Nature.

Chromosome 6p22 locus associated with clinically aggressive neuroblastoma.

Nazneen Rahman, Joseph T. Glessner, Hakon Hakonarson, 2008, The New England journal of medicine.

SPARSE SEGMENT IDENTIFICATIONS WITH APPLICATIONS TO DNA COPY NUMBER VARIATION ANALYSIS

T. Cai, Hongzhe Li, X. J. Jeng, 2015 .

Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseases

Constantin Polychronakos, Yiran Guo, Dong Li, 2016 .

A change-point model for identifying 3′UTR switching by next-generation RNA sequencing

Hongzhe Li, Zhi Wei, Wei Wang, 2014, Bioinform..

Common variations in BARD1 influence susceptibility to high-risk neuroblastoma

Nazneen Rahman, Sharon J. Diskin, John M. Maris, 2009, Nature Genetics.

Chromosomal Instability and Copy Number Alterations in Barrett's Esophagus and Esophageal Adenocarcinoma

Carissa A. Sanchez, Patricia L. Blount, C. Maley, 2009, Clinical Cancer Research.

Integrative genomics identifies LMO1 as a neuroblastoma oncogene

Nazneen Rahman, Sharon J. Diskin, John M. Maris, 2011, Nature.

Variants of DENND1B associated with asthma in children.

Ingo Ruczinski, James Flory, Terri H Beaty, 2010, The New England journal of medicine.

A Statistical Method for Identifying Trait-Associated Copy Number Variants

Qian Wu, Hongzhe Li, Hongzhe Li, 2015, Human Heredity.

Functional methylome analysis of human diabetic kidney disease.

A. Verma, Chengxiang Qiu, K. Suszták, 2019, JCI insight.

HLA-A amino acid polymorphism and delayed kidney allograft function

A. Israni, M. Joffe, H. Feldman, 2008, Proceedings of the National Academy of Sciences.

17q12-21 variants interact with smoke exposure as a risk factor for pediatric asthma but are equally associated with early-onset versus late-onset asthma in North Americans of European ancestry.

Joseph T. Glessner, Ryan M. Smith, J. Glessner, 2009, The Journal of allergy and clinical immunology.

A Statistical Method for Identifying Trait-Associated Copy Number Variants

Hongzhe Li, Qian Wu, Jessie Jeng, 2015, Human Heredity.

Functional methylome analysis of human diabetic kidney disease.

A. Verma, Chengxiang Qiu, K. Suszták, 2019, JCI insight.