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Author Details

Braden Boone
HudsonAlpha Institute for Biotechnology
1999
32
24
PMIDPaper TitleJournal TitlePublished Year
34645491Artificial intelligence enables comprehensive genome interpretation and nomination of candidate diagnoses for rare genetic diseases.Genome Med2021
34645491Artificial intelligence enables comprehensive genome interpretation and nomination of candidate diagnoses for rare genetic diseases.Genome Med2021
32027465Targeted Identification of Protein Interactions in Eukaryotic mRNA Translation.Proteomics2020
32027465Targeted Identification of Protein Interactions in Eukaryotic mRNA Translation.Proteomics2020
30323017Next-Generation Sequencing Strategies.Cold Spring Harb Perspect Med2019
30323017Next-Generation Sequencing Strategies.Cold Spring Harb Perspect Med2019
29847298Genetic Risk for Subsequent Neoplasms Among Long-Term Survivors of Childhood Cancer.J Clin Oncol2018
30095213Reversible deficits in apical transporter trafficking associated with deficiency in diacylglycerol acyltransferase.Traffic2018
29847298Genetic Risk for Subsequent Neoplasms Among Long-Term Survivors of Childhood Cancer.J Clin Oncol2018
30095213Reversible deficits in apical transporter trafficking associated with deficiency in diacylglycerol acyltransferase.Traffic2018
28030809Genomic regulation of invasion by STAT3 in triple negative breast cancer.Oncotarget2017
28535339Ecophysiological Examination of the Lake Erie Microcystis Bloom in 2014: Linkages between Biology and the Water Supply Shutdown of Toledo, OH.Environ Sci Technol2017
28398289A high-throughput molecular data resource for cutaneous neurofibromas.Sci Data2017
28030809Genomic regulation of invasion by STAT3 in triple negative breast cancer.Oncotarget2017
28398289A high-throughput molecular data resource for cutaneous neurofibromas.Sci Data2017
28535339Ecophysiological Examination of the Lake Erie Microcystis Bloom in 2014: Linkages between Biology and the Water Supply Shutdown of Toledo, OH.Environ Sci Technol2017
25700176Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways.Science2015
25700176Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways.Science2015
27135684Modern Methods for Delineating Metagenomic Complexity.Cell Syst2015
27135689Geospatial Resolution of Human and Bacterial Diversity with City-Scale Metagenomics.Cell Syst2015
26594662Geospatial Resolution of Human and Bacterial Diversity with City-Scale Metagenomics.Cell Syst2015
26594662Geospatial Resolution of Human and Bacterial Diversity with City-Scale Metagenomics.Cell Syst2015
27135684Modern Methods for Delineating Metagenomic Complexity.Cell Syst2015
27135689Geospatial Resolution of Human and Bacterial Diversity with City-Scale Metagenomics.Cell Syst2015
24984783Intragenic motifs regulate the transcriptional complexity of Pkhd1/PKHD1.J Mol Med (Berl)2014
24984783Intragenic motifs regulate the transcriptional complexity of Pkhd1/PKHD1.J Mol Med (Berl)2014
22495311Patterns and rates of exonic de novo mutations in autism spectrum disorders.Nature2012
22495311Patterns and rates of exonic de novo mutations in autism spectrum disorders.Nature2012
23482460Targeted genome enrichment for efficient purification of endosymbiont DNA from host DNA.Symbiosis2012
23042115De novo gene mutations highlight patterns of genetic and neural complexity in schizophrenia.Nat Genet2012
23482460Targeted genome enrichment for efficient purification of endosymbiont DNA from host DNA.Symbiosis2012
23042115De novo gene mutations highlight patterns of genetic and neural complexity in schizophrenia.Nat Genet2012
21822266Exome sequencing supports a de novo mutational paradigm for schizophrenia.Nat Genet2011
21822266Exome sequencing supports a de novo mutational paradigm for schizophrenia.Nat Genet2011
19834031Identification of genes and pathways involved in retinal neovascularization by microarray analysis of two animal models of retinal angiogenesis.Invest Ophthalmol Vis Sci2010
19781859A microarray analysis of temporal gene expression profiles in thermally injured human skin.Burns2010
21057224Genomic profiling of C/EBPβ2 transformed mammary epithelial cells: a role for nuclear interleukin-1β.Cancer Biol Ther2010
19834493Disruption of PPARgamma signaling results in mouse prostatic intraepithelial neoplasia involving active autophagy.Cell Death Differ2010
19834031Identification of genes and pathways involved in retinal neovascularization by microarray analysis of two animal models of retinal angiogenesis.Invest Ophthalmol Vis Sci2010
21057224Genomic profiling of C/EBPβ2 transformed mammary epithelial cells: a role for nuclear interleukin-1β.Cancer Biol Ther2010
19781859A microarray analysis of temporal gene expression profiles in thermally injured human skin.Burns2010
19834493Disruption of PPARgamma signaling results in mouse prostatic intraepithelial neoplasia involving active autophagy.Cell Death Differ2010
19038492Identification of genes, including the gene encoding p27Kip1, regulated by serine 276 phosphorylation of the p65 subunit of NF-kappaB.Cancer Lett2009
19038492Identification of genes, including the gene encoding p27Kip1, regulated by serine 276 phosphorylation of the p65 subunit of NF-kappaB.Cancer Lett2009
20027305Androgen regulated genes in human prostate xenografts in mice: relation to BPH and prostate cancer.PLoS One2009
20027305Androgen regulated genes in human prostate xenografts in mice: relation to BPH and prostate cancer.PLoS One2009
17989729Gene profiling of keloid fibroblasts shows altered expression in multiple fibrosis-associated pathways.J Invest Dermatol2008
17989729Gene profiling of keloid fibroblasts shows altered expression in multiple fibrosis-associated pathways.J Invest Dermatol2008
18297134Gene expression profiling of a mouse model of pancreatic islet dysmorphogenesis.PLoS One2008
18297134Gene expression profiling of a mouse model of pancreatic islet dysmorphogenesis.PLoS One2008
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Collaborators

HudsonAlpha Institute for Biotechnology
Co-authored papers 18
Vanderbilt University Medical Center
Co-authored papers 8
Co-authored papers 3
Co-authored papers 3
Feil Family Brain and Mind Research Institute.
Co-authored papers 3
David Geffen School of Medicine, university of california los angeles
Co-authored papers 3
Institute for Next Generation Healthcare
Co-authored papers 3
Center for Genomics and Systems Biology
Co-authored papers 3
Icahn School of Medicine at Mount Sinai
Co-authored papers 3
Co-authored papers 2
HudsonAlpha Institute for Biotechnology, Heersink School of Medicine
Co-authored papers 2
Co-authored papers 2
HudsonAlpha Institute for Biotechnology
Co-authored papers 2
Huntsman Cancer Institute, University of Utah
Co-authored papers 1
Co-authored papers 1
Co-authored papers 1
Baylor College of Medicine
Co-authored papers 1
Harvard Medical School
Co-authored papers 1
Co-authored papers 1
McGill University, Canada Montreal Neurological Institute and Hospital
Co-authored papers 1
Co-authored papers 1
Co-authored papers 1
Co-authored papers 1
Institute for Genomic Medicine, Columbia University Irving Medical Center
Co-authored papers 1
Co-authored papers 1
Pacific Northwest National Laboratory (PNNL)
Co-authored papers 1
Co-authored papers 1
Harvard Medical School
Co-authored papers 1
university of massachusetts amherst Chan Medical School
Co-authored papers 1
Changhai Hospital, Second Military Medical University
Co-authored papers 1