User profiles for Dan Lieber
Daniel LieberBiotech Verified email at post.harvard.edu Cited by 6182 |
[HTML][HTML] Analysis of 100,000 human cancer genomes reveals the landscape of tumor mutational burden
Background High tumor mutational burden (TMB) is an emerging biomarker of sensitivity to
immune checkpoint inhibitors and has been shown to be more significantly associated with …
immune checkpoint inhibitors and has been shown to be more significantly associated with …
Blood-based tumor mutational burden as a predictor of clinical benefit in non-small-cell lung cancer patients treated with atezolizumab
…, L Fehrenbacher, G Otto, C Malboeuf, DS Lieber… - Nature medicine, 2018 - nature.com
Although programmed death-ligand 1–programmed death 1 (PD-L1–PD-1) inhibitors are
broadly efficacious, improved outcomes have been observed in patients with high PD-L1 …
broadly efficacious, improved outcomes have been observed in patients with high PD-L1 …
[HTML][HTML] Global and local architecture of the mammalian microRNA–transcription factor regulatory network
microRNAs (miRs) are small RNAs that regulate gene expression at the posttranscriptional
level. It is anticipated that, in combination with transcription factors (TFs), they span a …
level. It is anticipated that, in combination with transcription factors (TFs), they span a …
Molecular diagnosis of infantile mitochondrial disease with targeted next-generation sequencing
…, SG Hershman, SC Lim, DS Lieber… - Science translational …, 2012 - science.org
Advances in next-generation sequencing (NGS) promise to facilitate diagnosis of inherited
disorders. Although in research settings NGS has pinpointed causal alleles using …
disorders. Although in research settings NGS has pinpointed causal alleles using …
[HTML][HTML] Clinical and analytical validation of FoundationOne®CDx, a comprehensive genomic profiling assay for solid tumors
…, J Thornton, DC Pavlick, GM Frampton, D Lieber… - PLoS …, 2022 - journals.plos.org
FoundationOne ® CDx (F1CDx) is a United States (US) Food and Drug Administration (FDA)-approved
companion diagnostic test to identify patients who may benefit from treatment in …
companion diagnostic test to identify patients who may benefit from treatment in …
[HTML][HTML] Analytical validation of a hybrid capture–based next-generation sequencing clinical assay for genomic profiling of cell-free circulating tumor DNA
Genomic profiling of circulating tumor DNA derived from cell-free DNA (cfDNA) in blood can
provide a noninvasive method for detecting genomic biomarkers to guide clinical decision …
provide a noninvasive method for detecting genomic biomarkers to guide clinical decision …
Targeted exome sequencing of suspected mitochondrial disorders
Objective: To evaluate the utility of targeted exome sequencing for the molecular diagnosis
of mitochondrial disorders, which exhibit marked phenotypic and genetic heterogeneity. …
of mitochondrial disorders, which exhibit marked phenotypic and genetic heterogeneity. …
Quality prediction in interlinked manufacturing processes based on supervised & unsupervised machine learning
D Lieber, M Stolpe, B Konrad, J Deuse, K Morik - Procedia Cirp, 2013 - Elsevier
In the context of a rolling mill case study, this paper presents a methodical framework based
on data mining for predicting the physical quality of intermediate products in interlinked …
on data mining for predicting the physical quality of intermediate products in interlinked …
Blood-based biomarkers for cancer immunotherapy: tumor mutational burden in blood (bTMB) is associated with improved atezolizumab (atezo) efficacy in 2L+ …
…, D Fabrizio, G Otto, C Malboeuf, D Lieber… - Annals of …, 2017 - annalsofoncology.org
Background: Atezo (anti–PD-L1) was FDA approved for 2L+ NSCLC based on results from
the randomized OAK and POPLAR trials, with atezo showing superior efficacy vs docetaxel (…
the randomized OAK and POPLAR trials, with atezo showing superior efficacy vs docetaxel (…
[PDF][PDF] Macrocytic anemia and mitochondriopathy resulting from a defect in sideroflexin 4
We used exome sequencing to identify mutations in sideroflexin 4 (SFXN4) in two children
with mitochondrial disease (the more severe case also presented with macrocytic anemia). …
with mitochondrial disease (the more severe case also presented with macrocytic anemia). …