Stephen A. Murray

Jackson Laboratory — United States

Biochemistry, Genetics and Molecular Biology · Life Sciences

46h-index9.3kcitations220works8.62yr avg
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Research Topics

CRISPR and Genetic Engineering(34), Congenital heart defects research(19), Pluripotent Stem Cells Research(13), Genomics and Rare Diseases(13), Craniofacial Disorders and Treatments(13)

Publications209 total

Modeling patient variants of Cnot1 and Cdc42bpb results in distinct forms of congenital diaphragmatic hernia in mice
2026Open Access
Zfp750 prevents oral adhesions and promotes temporary epithelial fusions
2026Open Access
Efficient <i>in vivo</i> mammalian neuron editing using peptide-mediated CRISPR enzyme delivery
2025Open Access
Generation and characterization of a knockout mouse of an enhancer of <i>EBF3</i>
Biology Open·2025Open Access
Identifying genetic determinants of outer retinal function in mice using a large-scale gene-targeted screen
PLoS Genetics·2025Open Access
Shared and distinct cortical mechanisms for working memory and decision-making
2025Open Access
Caspase-11 drives macrophage hyperinflammation in models of Polg-related mitochondrial disease
Nature Communications·2025· 6 citedOpen Access
Alternating hemiplegia of childhood associated mutations in Atp1a3 reveal diverse neurological alterations in mice
Neurobiology of Disease·2025· 2 citedOpen Access
The contribution of de novo coding mutations to meningomyelocele
Nature·2025· 11 cited
A Scoping Review of Factors That Elevate the Risk of Anterior Cruciate Ligament Injury in Elite Male Field Team Sport Athletes
Applied Sciences·2025· 1 citedOpen Access
The spectrum of gene intolerance to variation: Insights from a rare disease cohort
2025· 2 citedOpen Access
A comprehensive atlas of AAV tropism in the mouse
Molecular Therapy·2025· 22 cited
Generation and Characterization of a Knockout Mouse of an Enhancer of <i>EBF3</i>
2025· 1 citedOpen Access
The ClinGen Syndromic Disorders Gene Curation Expert Panel: Assessing the clinical validity of 111 gene-disease relationships
Genetics in Medicine Open·2025Open Access
Alternating hemiplegia of childhood associated mutations in <i>Atp1a3</i> reveal diverse neurological alterations in mice
2024Open Access
The ClinGen Syndromic Disorders Gene Curation Expert Panel: Assessing the Clinical Validity of 111 Gene-Disease Relationships
2024· 1 citedOpen Access
Mutation in <i>Prkra</i> results in cerebellar abnormality and reduced eIF2α phosphorylation in a model of DYT-PRKRA
Disease Models & Mechanisms·2024· 4 citedOpen Access
Amphiphilic shuttle peptide delivers base editor ribonucleoprotein to correct the CFTR R553X mutation in well-differentiated airway epithelial cells
Nucleic Acids Research·2024· 5 citedOpen Access
A Comprehensive Atlas of AAV Tropism in the Mouse
2024· 4 citedOpen Access
A graph theoretical approach to experimental prioritization in genome-scale investigations
Mammalian Genome·2024· 3 citedOpen Access
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Frequent Co-authors

Leah Rae Donahue(7), Alan R. Boobis(7), Terrence F. Meehan(6), Lauryl M. J. Nutter(6), Kevin A. Peterson(6), Helen Parkinson(6), Robert E. Braun(6), Martin Hrabě de Angelis(6), Ann‐Marie Mallon(6), K. C. Kent Lloyd(6), Colin McKerlie(6), Damian Smedley(6), Ann M. Flenniken(5), Karen L. Svenson(5), Yann Hérault(5), David J. Adams(5), Arthur L. Beaudet(5), Nigel J. Gooderham(5), D. S. Davies(5), Mary E. Dickinson(4)