Sara Wells

Biochemistry, Genetics and Molecular Biology · Life Sciences

42h-index7.9kcitations197works12.62yr avg
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Research Topics

CRISPR and Genetic Engineering(28), Animal Genetics and Reproduction(18), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities(13), Genetics and Neurodevelopmental Disorders(12), Molecular Biology Techniques and Applications(11)

Publications192 total

Transcription Factor Binding and Individual Genetic Risk of Valproate Teratogenicity
Neurology·2026· 1 cited
Establishing standardized transthoracic echocardiography reference ranges for mouse models: insights into the impact of anesthesia, sex, and age
Frontiers in Cardiovascular Medicine·2025· 1 citedOpen Access
Hierarchical Deep Learning for Abnormality Classification in Mouse Skeleton Using Multiview X-Ray Images: Convolutional Autoencoders Versus ConvNeXt
Journal of Imaging·2025Open Access
Multi-modal comparative phenotyping of knock-in mouse models of frontotemporal dementia/amyotrophic lateral sclerosis
Disease Models & Mechanisms·2025· 3 citedOpen Access
The Sex Inclusive Research Framework to address sex bias in preclinical research proposals
Nature Communications·2025· 14 citedOpen Access
Establishing Comprehensive Transthoracic Echocardiography Reference Ranges for Mouse Models: Insights into the Impact of Anesthesia, Sex, and Age
2025Open Access
Characterization of quinazolinone calcilytic therapy for autosomal dominant hypocalcemia type 1 (ADH1)
Journal of Biological Chemistry·2025· 2 citedOpen Access
Evolutionary constrained genes associated with autism spectrum disorder across 2,054 nonhuman primate genomes
Molecular Autism·2025· 2 citedOpen Access
DYRK1A kinase triplication is the major cause of Otitis Media in Down Syndrome
2025Open Access
DYRK1A kinase triplication is the major cause of Otitis Media in Down Syndrome
2025· 1 citedOpen Access
DYRK1A kinase triplication is the major cause of Otitis Media in Down Syndrome
2024Open Access
Long-read transcriptomic identification of synaptic adaptation to amyloid pathology in the <i> App <sup>NL-G-F</sup> </i> knock-in mouse model of the earliest phase of Alzheimer’s disease
2024Open Access
Negative equity – the value of reporting negative results
Disease Models & Mechanisms·2024· 8 citedOpen Access
Improving laboratory animal genetic reporting: LAG-R guidelines
Nature Communications·2024· 15 citedOpen Access
An unbiased ranking of murine dietary models based on their proximity to human metabolic dysfunction-associated steatotic liver disease (MASLD)
Nature Metabolism·2024· 187 citedOpen Access
Pleiotropic brain function of whirlin identified by a novel mutation
iScience·2024· 2 citedOpen Access
Identification of cellular retinoic acid binding protein 2 (CRABP2) as downstream target of nuclear factor I/X (NFIX): implications for skeletal dysplasia syndromes
JBMR Plus·2024· 1 citedOpen Access
Phenotyping of genetically modified mice
2024
An introduction to laboratory animal genetics
2024· 2 cited
Recommendations for measuring and standardizing light for laboratory mammals to improve welfare and reproducibility in animal research
PLoS Biology·2024· 46 citedOpen Access
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Frequent Co-authors

Steve D. M. Brown(12), Lydia Teboul(9), Patrick M. Nolan(9), Roger Cox(9), Michael Cheeseman(9), Tertius Hough(8), Andy Greenfield(7), Ann‐Marie Mallon(6), Nick Warr(6), Heather Cater(5), Abraham Acevedo‐Arozena(5), Debora Bogani(5), Pam Siggers(5), Lauren Chessum(5), Gemma Codner(5), Andrew Parker(5), Michelle M. Simon(5), Michael R. Bowl(5), Michelle Stewart(4), Rachel Brixey(4)