Author

Elisabeth M. Busch‐Nentwich

Observed names: Busch-Nentwich, Elisabeth, Busch-Nentwich, Elisabeth M, Busch-Nentwich, Elisabeth M., Busch‐Nentwich, Elisabeth M, Busch−Nentwich, Elisabeth, E. Busch-Nentwich, Elisabeth Busch-Nentwich, Elisabeth Busch-Nentwich (23944), Elisabeth Busch-nentwich, Elisabeth M Busch-Nentwich, Elisabeth M. Busch-Nentwich, Elisabeth M. Busch-nentwich, M.Busch-Nentwich, Elisabeth, Nentwich, Elisabeth Busch, Nentwich, Elisabeth M. Busch

Institution: Queen Mary University of London

Observed institutions: Queen Mary University of London, University of Cambridge, European Synchrotron Radiation Facility, Wellcome Sanger Institute, Vollum Institute, Max Planck Institute for Developmental Biology, Molecular Immunity Unit, Wellcome Trust

ORCID: 0000-0001-6450-744X

Observed ORCID: 0000-0001-6450-744X

OpenAlex ID: A5026550780

A systematic genome-wide analysis of zebrafish protein-coding gene function

2013 · Ross N. W. Kettleborough, Elisabeth M. Busch-Nentwich, et al. · Nature · 621

Placentation defects are highly prevalent in embryonic lethal mouse mutants

2018 · Vicente Perez-Garcia, Elena Fineberg, et al. · Nature · 371

A high-resolution mRNA expression time course of embryonic development in zebrafish

2017 · Richard J White, John E Collins, et al. · eLife · 361

Vesicular Glutamate Transporter 3 Is Required for Synaptic Transmission in Zebrafish Hair Cells

2008 · Nikolaus Obholzer, Sean Wolfson, et al. · Journal of Neuroscience · 324

Control of Crystal Size and Lattice Formation by Starmaker in Otolith Biomineralization

2003 · Christian Söllner, Manfred Burghammer, et al. · Science · 318

scRNA-Seq reveals distinct stem cell populations that drive hair cell regeneration after loss of Fgf and Notch signaling

2019 · Mark E. Lush, Daniel C. Diaz, et al. · eLife · 169

mRNA processing in mutant zebrafish lines generated by chemical and CRISPR-mediated mutagenesis produces unexpected transcripts that escape nonsense-mediated decay

2017 · Jennifer L. Anderson, Timothy S. Mulligan, et al. · PLoS Genetics · 112

geminiEncodes a Zebrafish L-Type Calcium Channel That Localizes at Sensory Hair Cell Ribbon Synapses

2004 · Samuel Sidi, Elisabeth Busch-Nentwich, et al. · Journal of Neuroscience · 101

Organ-specific requirements for Hdac1 in liver and pancreas formation

2008 · Emily S. Noël, Antonio Casal-Sueiro, et al. · Developmental Biology · 81

mTOR-regulated mitochondrial metabolism limits mycobacterium-induced cytotoxicity

2022 · Antonio J. Pagán, Lauren J. Lee, et al. · Cell · 80

Chemokine receptor trafficking coordinates neutrophil clustering and dispersal at wounds in zebrafish

2019 · Caroline Coombs, Antonios Georgantzoglou, et al. · Nature Communications · 70

The deafness genedfna5is crucial forugdhexpression and HA production in the developing ear in zebrafish

2004 · Elisabeth Busch-Nentwich, Christian Söllner, et al. · Development · 66

Large-scale mapping of mutations affecting zebrafish development

2007 · Robert Geisler, Gerd-Jörg Rauch, et al. · BMC Genomics · 65

Integration of Tmc1/2 into the mechanotransduction complex in zebrafish hair cells is regulated by Transmembrane O-methyltransferase (Tomt)

2017 · Timothy Erickson, Clive P Morgan, et al. · eLife · 63

Genetic Screen for Postembryonic Development in the Zebrafish (Danio rerio): Dominant Mutations Affecting Adult Form

2017 · Katrin Henke, Jacob M Daane, et al. · Genetics · 62

Zebrafish models for nemaline myopathy reveal a spectrum of nemaline bodies contributing to reduced muscle function

2015 · Tamar E. Sztal, Mo Zhao, et al. · Acta Neuropathologica · 55

The zebrafish dystrophic mutantsoftymaintains muscle fibre viability despite basement membrane rupture and muscle detachment

2009 · Arie S. Jacoby, Elisabeth Busch-Nentwich, et al. · Development · 54

KDM2A integrates DNA and histone modification signals through a CXXC/PHD module and direct interaction with HP1

2016 · Julie Borgel, Marek Tyl, et al. · Nucleic Acids Research · 47

Xirp Proteins Mark Injured Skeletal Muscle in Zebrafish

2012 · Cécile Otten, Peter F. van der Ven, et al. · PLoS ONE · 46

A point mutation decouples the lipid transfer activities of microsomal triglyceride transfer protein

2020 · Meredith H. Wilson, Sujith Rajan, et al. · PLoS Genetics · 43

Pla2g12b drives expansion of triglyceride-rich lipoproteins

2024 · James H. Thierer, Ombretta Foresti, et al. · Nature Communications · 42

The gene regulatory basis of genetic compensation during neural crest induction

2019 · Christopher M. Dooley, Neha Wali, et al. · PLoS Genetics · 41

PRL3-DDX21 Transcriptional Control of Endolysosomal Genes Restricts Melanocyte Stem Cell Differentiation

2020 · Jeanette A. Johansson, Kerrie L. Marie, et al. · Developmental Cell · 40

Digenic inheritance involving a muscle-specific protein kinase and the giant titin protein causes a skeletal muscle myopathy

2024 · Ana Töpf, Dan Cox, et al. · Nature Genetics · 34

Selenoprotein deficiency disorder predisposes to aortic aneurysm formation

2023 · Erik Schoenmakers, Federica Marelli, et al. · Nature Communications · 27

Works count: 139

Citation count: 3,697

H-index: 27

I10-index: 45