Dongliang Ge
Dongliang Ge
CEO & President, Apostle Inc
Verified email at - Homepage
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Genetic variation in IL28B predicts hepatitis C treatment-induced viral clearance
D Ge, J Fellay, AJ Thompson, JS Simon, KV Shianna, TJ Urban, ...
Nature 461 (7262), 399-401, 2009
Large recurrent microdeletions associated with schizophrenia
H Stefansson, D Rujescu, S Cichon, OPH Pietilšinen, A Ingason, ...
nature 455 (7210), 232-236, 2008
Genetic variation in IL28B and spontaneous clearance of hepatitis C virus
DL Thomas, CL Thio, MP Martin, Y Qi, D Ge, C O’hUigin, J Kidd, K Kidd, ...
Nature 461 (7265), 798-801, 2009
A whole-genome association study of major determinants for host control of HIV-1
J Fellay, KV Shianna, D Ge, S Colombo, B Ledergerber, M Weale, ...
science 317 (5840), 944-947, 2007
Interleukin-28B polymorphism improves viral kinetics and is the strongest pretreatment predictor of sustained virologic response in genotype 1 hepatitis C virus
AJ Thompson, AJ Muir, MS Sulkowski, D Ge, J Fellay, KV Shianna, ...
Gastroenterology 139 (1), 120-129. e18, 2010
A genome-wide association study in chronic obstructive pulmonary disease (COPD): identification of two major susceptibility loci
SG Pillai, D Ge, G Zhu, X Kong, KV Shianna, AC Need, S Feng, CP Hersh, ...
PLoS Genet 5 (3), e1000421, 2009
A genome-wide investigation of SNPs and CNVs in schizophrenia
AC Need, D Ge, ME Weale, J Maia, S Feng, EL Heinzen, KV Shianna, ...
PLoS Genet 5 (2), e1000373, 2009
ITPA gene variants protect against anaemia in patients treated for chronic hepatitis C
J Fellay, AJ Thompson, D Ge, CE Gumbs, TJ Urban, KV Shianna, LD Little, ...
Nature 464 (7287), 405-408, 2010
Common genetic variation and the control of HIV-1 in humans
J Fellay, D Ge, KV Shianna, S Colombo, B Ledergerber, ET Cirulli, ...
PLoS Genet 5 (12), e1000791, 2009
Tissue-specific genetic control of splicing: implications for the study of complex traits
EL Heinzen, D Ge, KD Cronin, JM Maia, KV Shianna, WN Gabriel, ...
PLoS Biol 6 (12), e1000001, 2008
Long-range LD can confound genome scans in admixed populations
AL Price, ME Weale, N Patterson, SR Myers, AC Need, KV Shianna, D Ge, ...
The American Journal of Human Genetics 83 (1), 132-135, 2008
HLA-C cell surface expression and control of HIV/AIDS correlate with a variant upstream of HLA-C
R Thomas, R Apps, Y Qi, X Gao, V Male, C O'huigin, G O'Connor, D Ge, ...
Nature genetics 41 (12), 1290-1294, 2009
Genome-wide association study in Han Chinese identifies four new susceptibility loci for coronary artery disease
X Lu, L Wang, S Chen, L He, X Yang, Y Shi, J Cheng, L Zhang, CC Gu, ...
Nature genetics 44 (8), 890-894, 2012
Rare deletions at 16p13. 11 predispose to a diverse spectrum of sporadic epilepsy syndromes
EL Heinzen, RA Radtke, TJ Urban, GL Cavalleri, C Depondt, AC Need, ...
The American Journal of Human Genetics 86 (5), 707-718, 2010
Whole-genome sequencing of a single proband together with linkage analysis identifies a Mendelian disease gene
NLM Sobreira, ET Cirulli, D Avramopoulos, E Wohler, GL Oswald, ...
PLoS Genet 6 (6), e1000991, 2010
Waist‐to‐height ratio is an accurate and easier index for evaluating obesity in children and adolescents
W Yan, H Bingxian, Y Hua, D Jianghong, C Jun, G Dongliang, Z Yujian, ...
Obesity 15 (3), 748-752, 2007
Multicentre search for genetic susceptibility loci in sporadic epilepsy syndrome and seizure types: a case-control study
GL Cavalleri, ME Weale, KV Shianna, R Singh, JM Lynch, B Grinton, ...
The Lancet Neurology 6 (11), 970-980, 2007
Variants in the ITPA gene protect against ribavirin-induced hemolytic anemia and decrease the need for ribavirin dose reduction
AJ Thompson, J Fellay, K Patel, HL Tillmann, S Naggie, D Ge, TJ Urban, ...
Gastroenterology 139 (4), 1181-1189. e2, 2010
WGAViewer: software for genomic annotation of whole genome association studies
D Ge, K Zhang, AC Need, O Martin, J Fellay, TJ Urban, A Telenti, ...
Genome Research 18 (4), 640-643, 2008
The characterization of twenty sequenced human genomes
K Pelak, KV Shianna, D Ge, JM Maia, M Zhu, JP Smith, ET Cirulli, J Fellay, ...
PLoS Genet 6 (9), e1001111, 2010
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