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Author Details

Erich Jaeger
Illumina Inc.
2001
21
15
PMIDPaper TitleJournal TitlePublished Year
35953477Ultra-deep sequencing validates safety of CRISPR/Cas9 genome editing in human hematopoietic stem and progenitor cells.Nat Commun2022
35953477Ultra-deep sequencing validates safety of CRISPR/Cas9 genome editing in human hematopoietic stem and progenitor cells.Nat Commun2022
36514120Structural variant analysis of a cancer reference cell line sample using multiple sequencing technologies.Genome Biol2022
36514120Structural variant analysis of a cancer reference cell line sample using multiple sequencing technologies.Genome Biol2022
34504346Toward best practice in cancer mutation detection with whole-genome and whole-exome sequencing.Nat Biotechnol2021
34504347Establishing community reference samples, data and call sets for benchmarking cancer mutation detection using whole-genome sequencing.Nat Biotechnol2021
34504346Toward best practice in cancer mutation detection with whole-genome and whole-exome sequencing.Nat Biotechnol2021
34504347Establishing community reference samples, data and call sets for benchmarking cancer mutation detection using whole-genome sequencing.Nat Biotechnol2021
30698692New de novo assembly of the Atlantic bottlenose dolphin (Tursiops truncatus) improves genome completeness and provides haplotype phasing.Gigascience2019
30698692New de novo assembly of the Atlantic bottlenose dolphin (Tursiops truncatus) improves genome completeness and provides haplotype phasing.Gigascience2019
28650462Haplotype phasing of whole human genomes using bead-based barcode partitioning in a single tube.Nat Biotechnol2017
28650462Haplotype phasing of whole human genomes using bead-based barcode partitioning in a single tube.Nat Biotechnol2017
27271295Extensive sequencing of seven human genomes to characterize benchmark reference materials.Sci Data2016
27271295Extensive sequencing of seven human genomes to characterize benchmark reference materials.Sci Data2016
25634010Diagnostic Mutation Profiling and Validation of Non-Small-Cell Lung Cancer Small Biopsy Samples using a High Throughput Platform.J Thorac Oncol2015
25634010Diagnostic Mutation Profiling and Validation of Non-Small-Cell Lung Cancer Small Biopsy Samples using a High Throughput Platform.J Thorac Oncol2015
25985263Comprehensive transcriptome analysis using synthetic long-read sequencing reveals molecular co-association of distant splicing events.Nat Biotechnol2015
25985263Comprehensive transcriptome analysis using synthetic long-read sequencing reveals molecular co-association of distant splicing events.Nat Biotechnol2015
23552698Genomic copy number alterations in clear cell renal carcinoma: associations with case characteristics and mechanisms of VHL gene inactivation.Oncogenesis2012
23552698Genomic copy number alterations in clear cell renal carcinoma: associations with case characteristics and mechanisms of VHL gene inactivation.Oncogenesis2012
21641572A methyl-deviator epigenotype of estrogen receptor-positive breast carcinoma is associated with malignant biology.Am J Pathol2011
22022277Von Hippel-Lindau (VHL) inactivation in sporadic clear cell renal cancer: associations with germline VHL polymorphisms and etiologic risk factors.PLoS Genet2011
21641572A methyl-deviator epigenotype of estrogen receptor-positive breast carcinoma is associated with malignant biology.Am J Pathol2011
22022277Von Hippel-Lindau (VHL) inactivation in sporadic clear cell renal cancer: associations with germline VHL polymorphisms and etiologic risk factors.PLoS Genet2011
20069569Identification and functional relevance of de novo DNA methylation in cancerous B-cell populations.J Cell Biochem2010
20137853TP53, EGFR, and KRAS mutations in relation to VHL inactivation and lifestyle risk factors in renal-cell carcinoma from central and eastern Europe.Cancer Lett2010
20069569Identification and functional relevance of de novo DNA methylation in cancerous B-cell populations.J Cell Biochem2010
20137853TP53, EGFR, and KRAS mutations in relation to VHL inactivation and lifestyle risk factors in renal-cell carcinoma from central and eastern Europe.Cancer Lett2010
19155300Large-scale profiling of archival lymph nodes reveals pervasive remodeling of the follicular lymphoma methylome.Cancer Res2009
19155300Large-scale profiling of archival lymph nodes reveals pervasive remodeling of the follicular lymphoma methylome.Cancer Res2009
18635227von Hippel-Lindau gene status and response to vascular endothelial growth factor targeted therapy for metastatic clear cell renal cell carcinoma.J Urol2008
18676741Improved identification of von Hippel-Lindau gene alterations in clear cell renal tumors.Clin Cancer Res2008
18635227von Hippel-Lindau gene status and response to vascular endothelial growth factor targeted therapy for metastatic clear cell renal cell carcinoma.J Urol2008
18676741Improved identification of von Hippel-Lindau gene alterations in clear cell renal tumors.Clin Cancer Res2008
16827904Clinical response to therapy targeted at vascular endothelial growth factor in metastatic renal cell carcinoma: impact of patient characteristics and Von Hippel-Lindau gene status.BJU Int2006
16827904Clinical response to therapy targeted at vascular endothelial growth factor in metastatic renal cell carcinoma: impact of patient characteristics and Von Hippel-Lindau gene status.BJU Int2006
14618610Inhibition of prostate cancer metastatic colonization by approximately 4.2 Mb of human chromosome 12.Int J Cancer2004
14618610Inhibition of prostate cancer metastatic colonization by approximately 4.2 Mb of human chromosome 12.Int J Cancer2004
12618387Molecular evolution of the Escherichia coli chromosome. VI. Two regions of high effective recombination.Genetics2003
12618387Molecular evolution of the Escherichia coli chromosome. VI. Two regions of high effective recombination.Genetics2003
12085966Metastasis suppression in prostate cancer.Cancer Metastasis Rev2001
12085966Metastasis suppression in prostate cancer.Cancer Metastasis Rev2001
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Collaborators

Chongqing Aier Eye Hospital
Co-authored papers 4
Feil Family Brain and Mind Research Institute.
Co-authored papers 4
Co-authored papers 4
Illumina Inc.
Co-authored papers 4
Nanfang Hospital and Basic Medical College, Southern Medical University
Co-authored papers 3
National Cancer Institute, National Institutes of Health
Co-authored papers 3
Human Phenome Institute and Shanghai Cancer Center, Fudan University
Co-authored papers 3
Immuneering Corporation
Co-authored papers 3
Departments of Bioinformatics and Clinical Genomics, Illumina Inc.
Co-authored papers 3
National Center for Biotechnology Information, National Institutes of Health
Co-authored papers 3
Co-authored papers 3
National Center for Toxicological Research
Co-authored papers 2
Co-authored papers 2
Co-authored papers 2
Johns Hopkins School of Medicine, National Cancer Institute, Princeton University, University of Colorado Anschutz Medical Campus, University of Pittsburgh, University of Washington
Co-authored papers 2
From Foundation Medicine
Co-authored papers 2
Co-authored papers 2
Co-authored papers 2
Co-authored papers 2
Co-authored papers 2
Center for Cancer Research, National Cancer Institute, National Institutes of Health
Co-authored papers 2
Institute for Molecular Medicine Finland (FIMM), University of Helsinki
Co-authored papers 2
Co-authored papers 2
Co-authored papers 2
Center for Devices and Radiological Health
Co-authored papers 2
University of California san francisco
Co-authored papers 2
Center for Cancer Research, National Cancer Institute, National Institutes of Health
Co-authored papers 2
Illumina Inc.
Co-authored papers 2
Uppsala University
Co-authored papers 2
Virginia Tech
Co-authored papers 2