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Author Details
Full Name
Hao Hu
Affiliation
Aerospace Center Hospital
ORCID
Career Start Year
2011
Papers
32
H Index
20
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36439444
Four circadian rhythm-related genes predict incidence and prognosis in hepatocellular carcinoma.
Front Oncol
2022
32447321
Integrated case-control and somatic-germline interaction analyses of soft-tissue sarcoma.
J Med Genet
2021
30624610
Functionally oriented analysis of cardiometabolic traits in a trans-ethnic sample.
Hum Mol Genet
2019
29294048
XPAT: a toolkit to conduct cross-platform association studies with heterogeneous sequencing datasets.
Nucleic Acids Res
2018
29463208
The VAAST Variant Prioritizer (VVP): ultrafast, easy to use whole genome variant prioritization tool.
BMC Bioinformatics
2018
29317335
Integrated case-control and somatic-germline interaction analyses of melanoma susceptibility genes.
Biochim Biophys Acta Mol Basis Dis
2018
28036300
Evolutionary selected Tibetan variants of HIF pathway and risk of lung cancer.
Oncotarget
2017
28233034
Gain-of-function EGLN1 prolyl hydroxylase (PHD2 D4E:C127S) in combination with EPAS1 (HIF-2α) polymorphism lowers hemoglobin concentration in Tibetan highlanders.
J Mol Med (Berl)
2017
28448578
Evolutionary history of Tibetans inferred from whole-genome sequencing.
PLoS Genet
2017
27562213
VARPRISM: incorporating variant prioritization in tests of de novo mutation association.
Genome Med
2016
26501420
The Relationship between Native American Ancestry, Body Mass Index and Diabetes Risk among Mexican-Americans.
PLoS One
2015
26569114
Genome-Wide Association Study of Staphylococcus aureus Carriage in a Community-Based Sample of Mexican-Americans in Starr County, Texas.
PLoS One
2015
24497848
Relationship estimation from whole-genome sequence data.
PLoS Genet
2014
25050558
Rare mutations in RINT1 predispose carriers to breast and Lynch syndrome-spectrum cancers.
Cancer Discov
2014
24837662
A unified test of linkage analysis and rare-variant association for analysis of pedigree sequence data.
Nat Biotechnol
2014
24763993
Using VAAST to Identify Disease-Associated Variants in Next-Generation Sequencing Data.
Curr Protoc Hum Genet
2014
24675841
TBX3 regulates splicing in vivo: a novel molecular mechanism for Ulnar-mammary syndrome.
PLoS Genet
2014
24297533
Detecting statistical interaction between somatic mutational events and germline variation from next-generation sequence data.
Pac Symp Biocomput
2014
24429422
In vivo determination of direct targets of the nonsense-mediated decay pathway in Drosophila.
G3 (Bethesda)
2014
24478445
Combined proteomic and transcriptomic interrogation of the venom gland of Conus geographus uncovers novel components and functional compartmentalization.
Mol Cell Proteomics
2014
23371554
Genomic diversity and evolution of the head crest in the rock pigeon.
Science
2013
24252905
Genetic risk factors in two Utah pedigrees at high risk for suicide.
Transl Psychiatry
2013
23836555
VAAST 2.0: improved variant classification and disease-gene identification using a conservation-controlled amino acid substitution matrix.
Genet Epidemiol
2013
23994590
Characterization of the peptidylglycine α-amidating monooxygenase (PAM) from the venom ducts of neogastropods, Conus bullatus and Conus geographus.
Toxicon
2013
23410975
Modeling clear cell sarcomagenesis in the mouse: cell of origin differentiation state impacts tumor characteristics.
Cancer Cell
2013
22742208
Elucidation of the molecular envenomation strategy of the cone snail Conus geographus through transcriptome sequencing of its venom duct.
BMC Genomics
2012
21266071
Characterization of the Conus bullatus genome and its venom-duct transcriptome.
BMC Genomics
2011
21282631
Draft genome of the globally widespread and invasive Argentine ant (Linepithema humile).
Proc Natl Acad Sci U S A
2011
21282651
Draft genome of the red harvester ant Pogonomyrmex barbatus.
Proc Natl Acad Sci U S A
2011
21347285
The genome sequence of the leaf-cutter ant Atta cephalotes reveals insights into its obligate symbiotic lifestyle.
PLoS Genet
2011
21325948
Global analysis of disease-related DNA sequence variation in 10 healthy individuals: implications for whole genome-based clinical diagnostics.
Genet Med
2011
21700766
A probabilistic disease-gene finder for personal genomes.
Genome Res
2011
1 - 32 of 32
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