Jens Reeder

Biochemistry, Genetics and Molecular Biology · Life Sciences

23h-index48.4kcitations39works0.02yr avg
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Research Topics

RNA and protein synthesis mechanisms(10), Genomics and Phylogenetic Studies(9), RNA modifications and cancer(9), Gut microbiota and health(6), RNA Research and Splicing(6)

Publications39 total

Multi-ancestry GWAS analysis identifies two novel loci associated with diabetic eye disease and highlights APOL1 as a high risk locus in patients with diabetic macular edema
PLoS Genetics·2023· 7 citedOpen Access
Enrichment of oral-derived bacteria in inflamed colorectal tumors and distinct associations of Fusobacterium in the mesenchymal subtype
Cell Reports Medicine·2023· 45 citedOpen Access
Multi-ancestry GWAS analysis identifies two novel loci associated with diabetic eye disease and highlights <i>APOL1</i> as a high risk locus in patients with diabetic macular edema
2023Open Access
A whole genome sequencing study of moderate to severe asthma identifies a lung function locus associated with asthma risk
Scientific Reports·2022· 16 citedOpen Access
Germline genetic polymorphisms influence tumor gene expression and immune cell infiltration
Proceedings of the National Academy of Sciences·2018· 127 citedOpen Access
Enabling genome-wide association testing with multiple diseases and no healthy controls
Gene·2018· 10 citedOpen Access
A whole genome sequencing association study of severe, uncontrolled asthma
Genes and Environment·2018· 1 citedOpen Access
Analysis of protein-altering variants in telomerase genes and their association with MUC5B common variant status in patients with idiopathic pulmonary fibrosis: a candidate gene sequencing study
The Lancet Respiratory Medicine·2018· 191 cited
Previously reported placebo-response-associated variants do not predict patient outcomes in inflammatory disease Phase III trial placebo arms
Genes and Immunity·2018· 5 citedOpen Access
Identifying and mitigating batch effects in whole genome sequencing data
BMC Bioinformatics·2017· 64 citedOpen Access
Additional file 3: of Identifying and mitigating batch effects in whole genome sequencing data
Figshare·2017Open Access
Recurrent Loss of NFE2L2 Exon 2 Is a Mechanism for Nrf2 Pathway Activation in Human Cancers
Cell Reports·2016· 207 citedOpen Access
scikit-bio: scikit-bio 0.4.2: Maintenance release
Zenodo (CERN European Organization for Nuclear Research)·2016Open Access
GMAP and GSNAP for Genomic Sequence Alignment: Enhancements to Speed, Accuracy, and Functionality
Methods in molecular biology·2016· 478 cited
scikit-bio: scikit-bio 0.4.1: TabularMSA and phylogenitc diversity metrics
Zenodo (CERN European Organization for Nuclear Research)·2015Open Access
Cognitive Deficits, Changes in Synaptic Function, and Brain Pathology in a Mouse Model of Normal Aging
eNeuro·2015· 73 citedOpen Access
qiime: QIIME 1.9.1
Zenodo (CERN European Organization for Nuclear Research)·2015Open Access
A comprehensive transcriptional portrait of human cancer cell lines
Nature Biotechnology·2014· 701 cited
Spectrum of diverse genomic alterations define non–clear cell renal carcinoma subtypes
Nature Genetics·2014· 353 citedOpen Access
Integrated exome and transcriptome sequencing reveals ZAK isoform usage in gastric cancer
Nature Communications·2014· 95 citedOpen Access
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Frequent Co-authors

Rob Knight(9), William F. Forrest(9), Tushar Bhangale(8), Jennifer Tom(8), Robert Giegerich(7), Julie Hunkapiller(7), Brian L. Yaspan(7), Kiran Mukhyala(6), Matthew J. Brauer(6), Amy Cowgill(5), Jan Vogel(5), Robert Graham(5), Peter M. Haverty(4), Oleg Mayba(4), Thomas D. Wu(4), Zora Modrušan(4), Somasekar Seshagiri(4), Karen T. Cuenco(4), Arthur Wüster(4), Timothy W. Behrens(4)