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Author Details

Biao Li
The Buck Institute for Research on Aging
1997
45
19
PMIDPaper TitleJournal TitlePublished Year
30590647Tau/MAPT disease-associated variant A152T alters tau function and toxicity via impaired retrograde axonal transport.Hum Mol Genet2019
28065470The Rare-Variant Generalized Disequilibrium Test for Association Analysis of Nuclear and Extended Pedigrees with Application to Alzheimer Disease WGS Data.Am J Hum Genet2017
28157542Erratum: The Rare-Variant Generalized Disequilibrium Test for Association Analysis of Nuclear and Extended Pedigrees with Application to Alzheimer Disease WGS Data.Am J Hum Genet2017
28984196Multitype Bellman-Harris branching model provides biological predictors of early stages of adult hippocampal neurogenesis.BMC Syst Biol2017
28669402SEQSpark: A Complete Analysis Tool for Large-Scale Rare Variant Association Studies Using Whole-Genome and Exome Sequence Data.Am J Hum Genet2017
28634997Working toward precision medicine: Predicting phenotypes from exomes in the Critical Assessment of Genome Interpretation (CAGI) challenges.Hum Mutat2017
28544481Matching phenotypes to whole genomes: Lessons learned from four iterations of the personal genome project community challenges.Hum Mutat2017
26757982Rare variant associations with waist-to-hip ratio in European-American and African-American women from the NHLBI-Exome Sequencing Project.Eur J Hum Genet2016
27604469An expanded evaluation of protein function prediction methods shows an improvement in accuracy.Genome Biol2016
26880286Mitral regurgitation as a phenotypic manifestation of nonphotosensitive trichothiodystrophy due to a splice variant in MPLKIP.BMC Med Genet2016
25545067Optimizing the molecular diagnosis of GALNS: novel methods to define and characterize Morquio-A syndrome-associated mutations.Hum Mutat2015
26177964Generation of sequence-based data for pedigree-segregating Mendelian or Complex traits.Bioinformatics2015
26121085Rare A2ML1 variants confer susceptibility to otitis media.Nat Genet2015
25873013Collapsed haplotype pattern method for linkage analysis of next-generation sequence data.Eur J Hum Genet2015
24407293A large scale Huntingtin protein interaction network implicates Rho GTPase signaling pathways in Huntington disease.J Biol Chem2014
25412673Global human frequencies of predicted nuclear pathogenic variants and the role played by protein hydrophobicity in pathogenicity potential.Sci Rep2014
25057096In silico comparative characterization of pharmacogenomic missense variants.BMC Genomics2014
25188385A probabilistic model to predict clinical phenotypic traits from genome sequencing.PLoS Comput Biol2014
24778108Power analysis and sample size estimation for sequence-based association studies.Bioinformatics2014
24894899Different rates of DNA replication at early versus late S-phase sections: multiscale modeling of stochastic events related to DNA content/EdU (5-ethynyl-2'deoxyuridine) incorporation distributions.Cytometry A2014
24336645PhenoMan: phenotypic data exploration, selection, management and quality control for association studies of rare and common variants.Bioinformatics2014
24360806Rare-variant extensions of the transmission disequilibrium test: application to autism exome sequence data.Am J Hum Genet2014
24451234MutPred Splice: machine learning-based prediction of exonic variants that disrupt splicing.Genome Biol2014
22949387Calibration of multiple in silico tools for predicting pathogenicity of mismatch repair gene missense substitutions.Hum Mutat2013
24315375SIRT5 regulates the mitochondrial lysine succinylome and metabolic networks.Cell Metab2013
23946335Factors influencing ascertainment bias of microsatellite allele sizes: impact on estimates of mutation rates.Genetics2013
23533597Evaluating purifying selection in the mitochondrial DNA of various mammalian species.PLoS One2013
23576753Label-free quantitative proteomics of the lysine acetylome in mitochondria identifies substrates of SIRT3 in metabolic pathways.Proc Natl Acad Sci U S A2013
22914216SimRare: a program to generate and analyze sequence-based data for association studies of quantitative and qualitative traits.Bioinformatics2012
21457906Comparing phylogeny and the predicted pathogenicity of protein variations reveals equal purifying selection across the global human mtDNA diversity.Am J Hum Genet2011
20052762In silico functional profiling of human disease-associated and polymorphic amino acid substitutions.Hum Mutat2010
20383776Power analysis for case-control association studies of samples with known family histories.Hum Genet2010
19734154Automated inference of molecular mechanisms of disease from amino acid substitutions.Bioinformatics2009
14687949Simian retrovirus serogroup 2 constitutive transport element recognizes the ribosomal L10-like protein and translocon gamma subunit-like protein in a yeast three-hybrid assay.Virus Res2004
12526174Development of simian retroviral vectors for gene delivery.Methods Mol Med2003
12907756Compromised reproductive function in adult female mice selectively expressing mutant ErbB-1 tyrosine kinase receptors in astroglia.Mol Endocrinol2003
12866411UV cross-linking/immunoprecipitation assay: glucocorticoid receptor-adrenergic receptor gene sequence interaction.Biotechniques2003
11796513Altered gene activity of epidermal growth factor receptor (ErbB-1) in the hypothalamus of aging female rat is linked to abnormal estrous cycles.Endocrinology2002
11956173Functional integrity of ErbB-4/-2 tyrosine kinase receptor complex in the hypothalamus is required for maintaining normal reproduction in young adult female rats.Endocrinology2002
11723238Agonist-mediated down-regulation of rat beta1-adrenergic receptor transcripts: role of potential post-transcriptional degradation factors.Mol Pharmacol2001
11325470Simian retrovirus vectors for gene transfer in nonhuman primate cells.Virus Res2001
11129642Simian retrovirus serogroup 5: partial gag-prt sequence and viral RNA distribution in an infected rhesus macaque.Virus Genes2000
10860867Rat beta 1-adrenergic receptor regulatory region containing consensus AP-2 elements recognizes novel transactivator proteins.Mol Cell Biol Res Commun2000
10544128Nucleocytoplasmic export of type D simian retrovirus genomic RNA: identification of important genetic subregions and interacting cellular proteins.Virology1999
9343671Rapid preparation and identification of insert-containing recombinant plasmid DNA.Biotechniques1997
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Collaborators

University of Washington
Co-authored papers 13
Center for Statistical Genetics, Columbia University Medical Center
Co-authored papers 12
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Indiana University
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University of Washington
Co-authored papers 4
Institute of Medical Genetics, Cardiff University
Co-authored papers 4
University of Washington
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University of Washington
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Vanderbilt University
Co-authored papers 3
University of Padova
Co-authored papers 3
University of Padua
Co-authored papers 3
University of Washington
Co-authored papers 3
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University of Padua
Co-authored papers 3
University of California berkeley
Co-authored papers 3
University of California San Diego
Co-authored papers 2
Medical Research Council Laboratory of Molecular Biology
Co-authored papers 2
University of California berkeley
Co-authored papers 2
Indiana University
Co-authored papers 2
Johns Hopkins University
Co-authored papers 2
Institute for Bioscience and Biotechnology Research
Co-authored papers 2
Icahn School of Medicine at Mount Sinai
Co-authored papers 2
Department of Pharmacy and Biotechnology, University of Bologna
Co-authored papers 2
Hematology and Clinical Immunology Unit, University of Padova
Co-authored papers 2
University College London
Co-authored papers 2
Huntsman Cancer Institute at the University of Utah
Co-authored papers 2
The Buck Institute for Research on Aging
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Stanford University
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Buck Institute for Research on Aging
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Department of Pharmacy and Biotechnology, University of Bologna
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