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Author Details

Stephen A Murray
Columbia University.
2005
78
31
PMIDPaper TitleJournal TitlePublished Year
36527789Efficient in vivo neuronal genome editing in the mouse brain using nanocapsules containing CRISPR-Cas9 ribonucleoproteins.Biomaterials2023
37579143Focused ultrasound-mediated brain genome editing.Proc Natl Acad Sci U S A2023
37503148DISCOVERY AND VALIDATION OF GENES DRIVING DRUG-INTAKE AND RELATED BEHAVIORAL TRAITS IN MICE.bioRxiv2023
37380661Author Correction: MusMorph, a database of standardized mouse morphology data for morphometric meta-analyses.Sci Data2023
37341808The spontaneous mouse mutant low set ears (Lse) is caused by tandem duplication of Fgf3 and Fgf4.Mamm Genome2023
36971348Identification of a heterogeneous and dynamic ciliome during embryonic development and cell differentiation.Development2023
37131609Spatial transcriptome profiling uncovers metabolic regulation of left-right patterning.bioRxiv2023
37294348Comprehensive ECG reference intervals in C57BL/6N substrains provide a generalizable guide for cardiac electrophysiology studies in mice.Mamm Genome2023
37066300A single-cell transcriptional timelapse of mouse embryonic development, from gastrula to pup.bioRxiv2023
36712096Focused ultrasound-mediated brain genome editing.Res Sq2023
36669109TMEM161B modulates radial glial scaffolding in neocortical development.Proc Natl Acad Sci U S A2023
34482425Annotated expression and activity data for murine recombinase alleles and transgenes: the CrePortal resource.Mamm Genome2022
35614082MusMorph, a database of standardized mouse morphology data for morphometric meta-analyses.Sci Data2022
35461561Mouse mutagenesis and phenotyping to generate models of development and disease.Curr Top Dev Biol2022
35552317Identifying genetic determinants of inflammatory pain in mice using a large-scale gene-targeted screen.Pain2022
36307211Autosomal recessive LRP1-related syndrome featuring cardiopulmonary dysfunction, bone dysmorphology, and corneal clouding.Cold Spring Harb Mol Case Stud2022
35288709Systematic reconstruction of cellular trajectories across mouse embryogenesis.Nat Genet2022
35284927Auriculocondylar syndrome 2 results from the dominant-negative action of PLCB4 variants.Dis Model Mech2022
34698892Progress towards completing the mutant mouse null resource.Mamm Genome2022
34870374Overlapping roles for PLK1 and aurora A during meiotic centrosome biogenesis in mouse spermatocytes.EMBO Rep2021
33828315The NIH Somatic Cell Genome Editing program.Nature2021
33715275The Mafb cleft-associated variant H131Q is not required for palatogenesis in the mouse.Dev Dyn2021
33615678Overlapping roles for PLK1 and Aurora A during meiotic centrosome biogenesis in mouse spermatocytes.EMBO Rep2021
32955381Machine learning-based automated phenotyping of inflammatory nocifensive behavior in mice.Mol Pain2020
32094912Chromatin interaction analyses elucidate the roles of PRC2-bound silencers in mouse development.Nat Genet2020
33370286Mouse mutant phenotyping at scale reveals novel genes controlling bone mineral density.PLoS Genet2020
33214242<i>Snx3</i> is important for mammalian neural tube closure via its role in canonical and non-canonical WNT signaling.Development2020
30659012Large-scale discovery of mouse transgenic integration sites reveals frequent structural variation and insertional mutagenesis.Genome Res2019
30854487Erratum: Author Correction: Identification of genes required for eye development by high-throughput screening of mouse knockouts.Commun Biol2019
29348434Identification of genetic elements in metabolism by high-throughput mouse phenotyping.Nat Commun2018
30100824The International Mouse Phenotyping Consortium (IMPC): a functional catalogue of the mammalian genome that informs conservation.Conserv Genet2018
30372477Sebaceous gland abnormalities in fatty acyl CoA reductase 2 (Far2) null mice result in primary cicatricial alopecia.PLoS One2018
29423138Developmental constraint through negative pleiotropy in the zygomatic arch.Evodevo2018
29569026The Genetic Landscape of Hypoplastic Left Heart Syndrome.Pediatr Cardiol2018
29600991Response to "Unexpected mutations after CRISPR-Cas9 editing in vivo".Nat Methods2018
27892606SVEP1 plays a crucial role in epidermal differentiation.Exp Dermatol2017
28280930CRISPRtools: a flexible computational platform for performing CRISPR/Cas9 experiments in the mouse.Mamm Genome2017
28352650Point mutations in murine <i>Nkx2-5</i> phenocopy human congenital heart disease and induce pathogenic Wnt signaling.JCI Insight2017
28119373Of mice and CRISPR: The post-CRISPR future of the mouse as a model system for the human condition.EMBO Rep2017
29026089A large scale hearing loss screen reveals an extensive unexplored genetic landscape for auditory dysfunction.Nat Commun2017
28756587Phenotyping first-generation genome editing mutants: a new standard?Mamm Genome2017
28650954Prevalence of sexual dimorphism in mammalian phenotypic traits.Nat Commun2017
28650483Disease model discovery from 3,328 gene knockouts by The International Mouse Phenotyping Consortium.Nat Genet2017
28700664Systematic screening for skin, hair, and nail abnormalities in a large-scale knockout mouse program.PLoS One2017
28530678The complex genetics of hypoplastic left heart syndrome.Nat Genet2017
28739660A Gene Implicated in Activation of Retinoic Acid Receptor Targets Is a Novel Renal Agenesis Gene in Humans.Genetics2017
28817352ARHGAP29 Mutation Is Associated with Abnormal Oral Epithelial Adhesions.J Dent Res2017
28069890APOBEC1 complementation factor (A1CF) is dispensable for C-to-U RNA editing in vivo.RNA2017
26234751Discovery and characterization of spontaneous mouse models of craniofacial dysmorphology.Dev Biol2016
27626380High-throughput discovery of novel developmental phenotypes.Nature2016
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Collaborators

Kent C Lloyd
University of California davis
Co-authored papers 12
Robert E Braun
University of Maine
Co-authored papers 12
Ann-Marie Mallon
The Turing Institute
Co-authored papers 11
Colin McKerlie
The Hospital for Sick Children
Co-authored papers 11
Karen L Svenson
Co-authored papers 11
Jacqueline K White
Wellcome Trust Sanger Institute
Co-authored papers 10
John R Seavitt
Baylor College of Medicine
Co-authored papers 10
Helen Parkinson
European Bioinformatics Institute
Co-authored papers 10
Anne M Dickinson
Translational and Clinical Research Institute, Newcastle University
Co-authored papers 10
Steve D M Brown
Mary Lyon Centre Harwell Science and Innovation Campus Oxfordshire UK.
Co-authored papers 10
Ann M Flenniken
Lunenfeld-Tanenbaum Research Institute, Mount Sinai Hospital
Co-authored papers 10
Lauryl M J Nutter
The Hospital for Sick Children
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Terrence F Meehan
European Bioinformatics Institute
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Sara Wells
Mary Lyon Centre at Medical Research Council
Co-authored papers 9
Martin Hrab?? de Angelis
German Center for Diabetes Research (DZD e.V.)
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Jeremy Mason
European Molecular Biology Laboratory - European Bioinformatics Institute
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Yann Herault
Institut Clinique de la Souris (ICS), Universite de Strasbourg, CNRS, INSERM
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Lynette Bower
University of California davis
Co-authored papers 8
Monica J Justice
The Hospital for Sick Children
Co-authored papers 7
Luis Santos
The Turing Institute
Co-authored papers 7
Mark Moore
Co-authored papers 7
Paul Flicek
European Bioinformatics Institute
Co-authored papers 7
Arthur L Beaudet
Baylor College of Medicine
Co-authored papers 7
David B West
Children's Hospital Oakland Research Institute
Co-authored papers 7
Damian Smedley
William Harvey Research Institute, Queen Mary University of London
Co-authored papers 7
Cathleen Lutz
JAX Center for Precision Genetics
Co-authored papers 6
Xiang Gao
Nanjing Biomedical Research Institute, Nanjing University
Co-authored papers 6
Laura G Reinholdt
Co-authored papers 6
Wolfgang Wurst
Institute of Developmental Genetics, German Research Center for Environmental Health
Co-authored papers 5
Tania Sorg
Universite de Strasbourg, CNRS, INSERM, Institut de La Clinique de La Souris
Co-authored papers 5
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