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Sara Wells

universites de strasbourg etablissements associes
H-index:42
Citation Count:7,938
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Establishing standardized transthoracic echocardiography reference ranges for mouse models: insights into the impact of anesthesia, sex, and age
2025-12-190
OA
Hierarchical Deep Learning for Abnormality Classification in Mouse Skeleton Using Multiview X-Ray Images: Convolutional Autoencoders Versus ConvNeXt

基于多视角X射线图像的小鼠骨骼异常分类的层次化深度学习:卷积自编码器与ConvNeXt

2025-10-070
OAAI
The Sex Inclusive Research Framework to address sex bias in preclinical research proposals

性包容研究框架:用于解决预临床研究方案中的性别偏见

2025-04-221
OA
Characterization of quinazolinone calcilytic therapy for autosomal dominant hypocalcemia type 1 (ADH1)
2025-04-010
OAAI
Evolutionary constrained genes associated with autism spectrum disorder across 2,054 nonhuman primate genomes
2025-01-230
OAAI
Negative equity - the value of reporting negative results
2024-08-303
OAAI
Improving laboratory animal genetic reporting: LAG-R guidelines
2024-07-025
OAAI
An unbiased ranking of murine dietary models based on their proximity to human metabolic dysfunction-associated steatotic liver disease (MASLD)

基于与人类代谢功能障碍相关的脂肪变性肝病 (MASLD) 的接近程度,对小鼠饮食模型进行无偏排名

2024-06-1233
OA
Identification of cellular retinoic acid binding protein 2 (CRABP2) as downstream target of nuclear factor I/X (NFIX): implications for skeletal dysplasia syndromes
2024-05-151
OAAI
Long-read sequencing for fast and robust identification of correct genome-edited alleles: PCR-based and Cas9 capture methods
2024-03-081
OAAI
Dual-Stream Spatiotemporal Networks with Feature Sharing for Monitoring Animals in the Home Cage
SENSORS
IF3.5
2023-11-301
OAAI
Shiga toxin targets the podocyte causing hemolytic uremic syndrome through endothelial complement activation

志贺毒素通过内皮补体激活靶向足细胞引起溶血性尿毒症综合征

MED
IF11.8
2023-11-013
OAAI
A Mouse Model with a Frameshift Mutation in the Nuclear Factor I/X (NFIX) Gene Has Phenotypic Features of Marshall-Smith Syndrome
2023-03-304
OAAI
Early embryonic lethality in complex I associated p.L104PNubpl mutant mice
2022-10-243
OAAI
Perspectives on Cognitive Phenotypes and Models of Vascular Disease
2022-07-015
OA
Gadd45g is required for timely Sry expression independently of RSPO1 activity
2022-06-015
OAAI
Extensive identification of genes involved in congenital and structural heart disorders and cardiomyopathy
2022-02-1728
OAAI
Neuroplastin genetically interacts with Cadherin 23 and the encoded isoform Np55 is sufficient for cochlear hair cell function and hearing
2022-01-316
OAAI
Comprehensive phenotypic analysis of the Dp1Tyb mouse strain reveals a broad range of Down syndrome-related phenotypes
2021-10-1815
OAAI