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Lista de obras de S. Wells

A comparative phenotypic and genomic analysis of C57BL/6J and C57BL/6N mouse strains

artículo científico publicado en 2013

A large scale hearing loss screen reveals an extensive unexplored genetic landscape for auditory dysfunction.

artículo científico publicado en 2017

A mutation in Nischarin causes otitis media via LIMK1 and NF-κB pathways

artículo científico publicado en 2017

Analysis of mammalian gene function through broad-based phenotypic screens across a consortium of mouse clinics

artículo científico publicado en 2015

Analysis of motor dysfunction in Down Syndrome reveals motor neuron degeneration

artículo científico publicado en 2018

Clarin-2 is essential for hearing by maintaining stereocilia integrity and function

scientific article published on 26 August 2019

Corrigendum: High-throughput discovery of novel developmental phenotypes.

artículo científico publicado en 2017

Disease model discovery from 3,328 gene knockouts by The International Mouse Phenotyping Consortium.

artículo científico publicado en 2017

Erratum: Author Correction: Identification of genes required for eye development by high-throughput screening of mouse knockouts

artículo científico publicado en 2019

EuroPhenome: a repository for high-throughput mouse phenotyping data

artículo científico publicado en 2010

Forward genetics identifies a novel sleep mutant with sleep state inertia and REM sleep deficits

artículo científico publicado en 2020

Human and mouse essentiality screens as a resource for disease gene discovery

artículo científico publicado en 2020

Identification of genes required for eye development by high-throughput screening of mouse knockouts

artículo científico publicado en 2018

Identification of genetic elements in metabolism by high-throughput mouse phenotyping

artículo científico publicado en 2018

LAMA: automated image analysis for the developmental phenotyping of mouse embryos

scientific article published on 11 February 2021

Loss of Bardet-Biedl syndrome proteins causes synaptic aberrations in principal neurons

scientific article published on 03 September 2019

Mouse mutant phenotyping at scale reveals novel genes controlling bone mineral density

artículo científico publicado en 2020

Neuroplastin genetically interacts with Cadherin 23 and the encoded isoform Np55 is sufficient for cochlear hair cell function and hearing

artículo científico publicado en 2022

Novel gene function revealed by mouse mutagenesis screens for models of age-related disease.

artículo científico publicado en 2016

Perspectives on Cognitive Phenotypes and Models of Vascular Disease

artículo científico publicado en 2022

The Deep Genome Project

scientific article published on 03 February 2020

The occurrence of tarsal injuries in male mice of C57BL/6N substrains in multiple international mouse facilities

artículo científico publicado en 2020

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