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Author Details
Full Name
Lars M Steinmetz
Affiliation
Stanford University
ORCID
Career Start Year
1998
Papers
193
H Index
68
Expertise
CM4AI Collaborator
Nevan J Krogan (CM4AI)
PMID
Paper Title
Journal Title
Published Year
36909618
A scalable, GMP-compatible, autologous organotypic cell therapy for Dystrophic Epidermolysis Bullosa.
bioRxiv
2023
37562410
Pooled Genome-Scale CRISPR Screens in Single Cells.
Annu Rev Genet
2023
37483015
Large scale microfluidic CRISPR screening for increased amylase secretion in yeast.
Lab Chip
2023
37704604
Gut barrier defects, intestinal immune hyperactivation and enhanced lipid catabolism drive lethality in NGLY1-deficient Drosophila.
Nat Commun
2023
37217719
Atlas of mRNA translation and decay for bacteria.
Nat Microbiol
2023
37463913
Mislocalization of pathogenic RBM20 variants in dilated cardiomyopathy is caused by loss-of-interaction with Transportin-3.
Nat Commun
2023
37066398
Gut barrier defects, increased intestinal innate immune response, and enhanced lipid catabolism drive lethality in <i>N</i> -glycanase 1 deficient <i>Drosophila</i>.
bioRxiv
2023
36653465
Cardiac splicing as a diagnostic and therapeutic target.
Nat Rev Cardiol
2023
36779527
Cell sorters see things more clearly now.
Mol Syst Biol
2023
34663920
High-throughput functional characterization of protein phosphorylation sites in yeast.
Nat Biotechnol
2022
35938400
Transcription Factor GATA4 Regulates Cell Type-Specific Splicing Through Direct Interaction With RNA in Human Induced Pluripotent Stem Cell-Derived Cardiac Progenitors.
Circulation
2022
36367695
Deep phenotyping of two preclinical mouse models and a cohort of RBM20 mutation carriers reveals no sex-dependent disease severity in <i>RBM20</i> cardiomyopathy.
Am J Physiol Heart Circ Physiol
2022
36266340
NIMA-related kinase 9 regulates the phosphorylation of the essential myosin light chain in the heart.
Nat Commun
2022
36293084
Genotype Complements the Phenotype: Identification of the Pathogenicity of an LMNA Splice Variant by Nanopore Long-Read Sequencing in a Large DCM Family.
Int J Mol Sci
2022
35918316
Transcriptomic diversity in human medullary thymic epithelial cells.
Nat Commun
2022
35258337
KIR<sup>+</sup>CD8<sup>+</sup> T cells suppress pathogenic T cells and are active in autoimmune diseases and COVID-19.
Science
2022
35100419
Assembly-dependent translation of subunits 6 (Atp6) and 9 (Atp9) of ATP synthase in yeast mitochondria.
Genetics
2022
34878535
Patient-derived gene and protein expression signatures of NGLY1 deficiency.
J Biochem
2022
35239377
Transcriptional neighborhoods regulate transcript isoform lengths and expression levels.
Science
2022
35050652
High-speed fluorescence image-enabled cell sorting.
Science
2022
33094674
Rpb4 and Puf3 imprint and post-transcriptionally control the stability of a common set of mRNAs in yeast.
RNA Biol
2021
33826901
The chaperone-binding activity of the mitochondrial surface receptor Tom70 protects the cytosol against mitoprotein-induced stress.
Cell Rep
2021
33649320
Identification of leukemic and pre-leukemic stem cells by clonal tracking from single-cell transcriptomics.
Nat Commun
2021
33568224
CRISPRi screens reveal genes modulating yeast growth in lignocellulose hydrolysate.
Biotechnol Biofuels
2021
33813118
Recommendations for accurate genotyping of SARS-CoV-2 using amplicon-based sequencing of clinical samples.
Clin Microbiol Infect
2021
34981055
Human KIR <sup>+</sup> CD8 <sup>+</sup> T cells target pathogenic T cells in Celiac disease and are active in autoimmune diseases and COVID-19.
bioRxiv
2021
34849874
Regulation of Msh4-Msh5 association with meiotic chromosomes in budding yeast.
Genetics
2021
34731027
High-Throughput Nucleotide Resolution Predictions of Assay Limitations Increase the Reliability and Concordance of Clinical Tests.
JCO Clin Cancer Inform
2021
34575212
RBM20-Related Cardiomyopathy: Current Understanding and Future Options.
J Clin Med
2021
34536502
Case-control study evaluating risk factors for SARS-CoV-2 outbreak amongst healthcare personnel at a tertiary care center.
Am J Infect Control
2021
34623901
Integrated single-cell transcriptomics and epigenomics reveals strong germinal center-associated etiology of autoimmune risk loci.
Sci Immunol
2021
34244519
Single-molecule, full-length transcript isoform sequencing reveals disease-associated RNA isoforms in cardiomyocytes.
Nat Commun
2021
33330942
A functional connection between translation elongation and protein folding at the ribosome exit tunnel in Saccharomyces cerevisiae.
Nucleic Acids Res
2021
32483332
Targeted Perturb-seq enables genome-scale genetic screens in single cells.
Nat Methods
2020
31871321
Combined single-cell and spatial transcriptomics reveal the molecular, cellular and spatial bone marrow niche organization.
Nat Cell Biol
2020
31733337
Liver-specific deletion of Ngly1 causes abnormal nuclear morphology and lipid metabolism under food stress.
Biochim Biophys Acta Mol Basis Dis
2020
33226342
Combined transient ablation and single-cell RNA-sequencing reveals the development of medullary thymic epithelial cells.
Elife
2020
32796939
GOTI, a method to identify genome-wide off-target effects of genome editing in mouse embryos.
Nat Protoc
2020
32905764
iPSC Modeling of RBM20-Deficient DCM Identifies Upregulation of RBM20 as a Therapeutic Strategy.
Cell Rep
2020
32816037
TIF-Seq2 disentangles overlapping isoforms in complex human transcriptomes.
Nucleic Acids Res
2020
32265286
Loss of N-Glycanase 1 Alters Transcriptional and Translational Regulation in K562 Cell Lines.
G3 (Bethesda)
2020
32293132
A Circulating Bioreactor Reprograms Cancer Cells Toward a More Mesenchymal Niche.
Adv Biosyst
2020
30871351
Regional Variation in RBM20 Causes a Highly Penetrant Arrhythmogenic Cardiomyopathy.
Circ Heart Fail
2019
33654857
Yeast Single-cell RNA-seq, Cell by Cell and Step by Step.
Bio Protoc
2019
31659326
Biological plasticity rescues target activity in CRISPR knock outs.
Nat Methods
2019
31740578
Chromatin-sensitive cryptic promoters putatively drive expression of alternative protein isoforms in yeast.
Genome Res
2019
30925180
Evolthon: A community endeavor to evolve lab evolution.
PLoS Biol
2019
30819928
Cytosine base editor generates substantial off-target single-nucleotide variants in mouse embryos.
Science
2019
30992377
Select sequencing of clonally expanded CD8<sup>+</sup> T cells reveals limits to clonal expansion.
Proc Natl Acad Sci U S A
2019
30718850
Sensitive high-throughput single-cell RNA-seq reveals within-clonal transcript correlations in yeast populations.
Nat Microbiol
2019
1 - 50 of 193
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row(s) 1 - 30 of 30
Collaborators
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Stanford University
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Technische Universitat Munchen
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Shantou University Medical College
Co-authored papers
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Michelle Nguyen
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Co-authored papers
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Co-authored papers
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Stanford University
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Co-authored papers
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Harvard Medical School
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Michael Gotthardt
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Universitetsbyen 81, Aarhus University
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Heidelberg University
Co-authored papers
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Adam M Deutschbauer
Lawrence Berkeley National Laboratory
Co-authored papers
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Universitat Pompeu Fabra
Co-authored papers
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Lars Juhl Jensen
Novo Nordisk Foundation Center for Protein Research, University of Copenhagen
Co-authored papers
3
Mariona Nadal-Ribelles
Universitat Pompeu Fabra (UPF)
Co-authored papers
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Francesc Posas
Universitat Pompeu Fabra
Co-authored papers
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Jan O Korbel
European Bioinformatics Institute (EMBL-EBI)
Co-authored papers
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Victoria N Parikh
Stanford University
Co-authored papers
3
Robin Andersson
University of Copenhagen
Co-authored papers
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Peer Bork
University of Wurzburg
Co-authored papers
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Jorge R Oksenberg
Co-authored papers
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Charles Boone
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