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Author Details

Jeffrey A Rosenfeld
Cancer Institute of New Jersey
2004
44
22
PMIDPaper TitleJournal TitlePublished Year
35357935A complete reference genome improves analysis of human genetic variation.Science2022
34692584RNA-seq profile of African American men with a clinically localized prostate cancer.Prostate Int2021
33712587Shotgun transcriptome, spatial omics, and isothermal profiling of SARS-CoV-2 infection reveals unique host responses, viral diversification, and drug interactions.Nat Commun2021
32133155Single-cell sperm transcriptomes and variants from fathers of children with and without autism spectrum disorder.NPJ Genom Med2020
31951591IGF2 drives formation of ileal neuroendocrine tumors in patients and mice.Endocr Relat Cancer2020
31860080Whole Genome Sequencing and Assembly of the Asian Honey Bee Apis dorsata.Genome Biol Evol2020
32699374Author Correction: A robust benchmark for detection of germline large deletions and insertions.Nat Biotechnol2020
32923111Genomic and immunologic correlates of LAG-3 expression in cancer.Oncoimmunology2020
32541955A robust benchmark for detection of germline large deletions and insertions.Nat Biotechnol2020
31536510TCF4 induces enzalutamide resistance via neuroendocrine differentiation in prostate cancer.PLoS One2019
27866013A whole genome gene content phylogenetic analysis of anopheline mosquitoes.Mol Phylogenet Evol2017
28154808Patient-Derived Xenograft Models of Non-Small Cell Lung Cancer and Their Potential Utility in Personalized Medicine.Front Oncol2017
28241792Genome content analysis yields new insights into the relationship between the human malaria parasite Plasmodium falciparum and its anopheline vectors.BMC Genomics2017
28978720Gamma Secretase Inhibition by BMS-906024 Enhances Efficacy of Paclitaxel in Lung Adenocarcinoma.Mol Cancer Ther2017
28575287An essential domain of an early-diverged RNA polymerase II functions to accurately decode a primitive chromatin landscape.Nucleic Acids Res2017
26836631Genome assembly and geospatial phylogenomics of the bed bug Cimex lectularius.Nat Commun2016
26549428Insect genome content phylogeny and functional annotation of core insect genomes.Mol Phylogenet Evol2016
27617305The mitogenome of the bed bug <i>Cimex lectularius</i> (Hemiptera: Cimicidae).Mitochondrial DNA B Resour2016
25725478High throughput sequencing analysis of Trypanosoma brucei DRBD3/PTB1-bound mRNAs.Mol Biochem Parasitol2015
26862572Data for constructing insect genome content matrices for phylogenetic analysis and functional annotation.Data Brief2015
26100517The impact of read length on quantification of differentially expressed genes and splice junction detection.Genome Biol2015
24586155Inflammatory monocytes orchestrate innate antifungal immunity in the lung.PLoS Pathog2014
25150835Multi-platform assessment of transcriptome profiling using RNA-seq in the ABRF next-generation sequencing study.Nat Biotechnol2014
24764495Response to 'pervasive sequence patents cover the entire human genome' - authors' reply.Genome Med2014
23325106Implication of a rare deletion at distal 16p11.2 in schizophrenia.JAMA Psychiatry2013
24079746Crowdfunding genomics and bioinformatics.Genome Biol2013
24092746Integrative annotation of variants from 1092 humans: application to cancer genomics.Science2013
24253340Genome-wide association study implicates NDST3 in schizophrenia and bipolar disorder.Nat Commun2013
23522065Pervasive sequence patents cover the entire human genome.Genome Med2013
21920466Mycobacterium tuberculosis spoligotypes that may derive from mixed strain infections are revealed by a novel computational approach.Infect Genet Evol2012
22811759Limitations of the human reference genome for personalized genomics.PLoS One2012
22445448Random roots and lineage sorting.Mol Phylogenet Evol2012
22306824E value cutoff and eukaryotic genome content phylogenetics.Mol Phylogenet Evol2012
22277159Implications for health and disease in the genetic signature of the Ashkenazi Jewish population.Genome Biol2012
22344438A systematic survey of loss-of-function variants in human protein-coding genes.Science2012
22179743Condensin dysfunction in human cells induces nonrandom chromosomal breaks in anaphase, with distinct patterns for both unique and repeated genomic regions.Chromosoma2012
34875790The mega-matrix tree of life: using genome-scale horizontal gene transfer and sequence evolution data as information about the vertical history of life.Cladistics2011
20488869Novel multi-nucleotide polymorphisms in the human genome characterized by whole genome and exome sequencing.Nucleic Acids Res2010
19335899Determination of enriched histone modifications in non-genic portions of the human genome.BMC Genomics2009
19786836Investigating repetitively matching short sequencing reads: the enigmatic nature of H3K9me3.Epigenetics2009
18552846Combinatorial patterns of histone acetylations and methylations in the human genome.Nat Genet2008
19139635Using whole genome presence/absence data to untangle function in 12 Drosophila genomes.Fly (Austin)2008
16861208Reciprocal illumination in the gene content tree of life.Syst Biol2006
15271781ORFcurator: molecular curation of genes and gene clusters in prokaryotic organisms.Bioinformatics2004
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Collaborators

Feil Family Brain and Mind Research Institute.
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Baylor College of Medicine
Co-authored papers 4
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Johns Hopkins University
Co-authored papers 4
National Human Genome Research Institute, National Institutes of Health
Co-authored papers 3
National Human Genome Research Institute, National Institutes of Health
Co-authored papers 3
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HudsonAlpha Institute for Biotechnology
Co-authored papers 3
Institute for Computational Biomedicine
Co-authored papers 3
National Human Genome Research Institute, National Institutes of Health
Co-authored papers 3
National Institute of Standards and Technology
Co-authored papers 3
National Institute of Standards and Technology
Co-authored papers 3
Chongqing Aier Eye Hospital
Co-authored papers 3
Co-authored papers 3
Charles-Bruneau Cancer Center, Centre Hospitalier Universitaire (CHU) Sainte-Justine
Co-authored papers 2
Center for Biomedical Informatics, Brown University
Co-authored papers 2
Prairie View A&M University
Co-authored papers 2
Baylor College of Medicine Human Genome Sequencing Center
Co-authored papers 2
Wellcome Sanger Institute
Co-authored papers 2
Chengdu First People's Hospital
Co-authored papers 2
Institute of Human Genetics, University Hospital Bonn
Co-authored papers 2
University of Geneva
Co-authored papers 2
University of Texas MD Anderson Cancer Center
Co-authored papers 2
University of Michigan Medical School ann arbor
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Institute for Computational Biomedicine, Weill Cornell Medicine of Cornell University
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Yale University
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