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List of works by S. Wells

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

scientific article

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

scientific article published on 12 October 2017

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

scientific article published on 14 August 2017

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

scientific article

Analysis of motor dysfunction in Down Syndrome reveals motor neuron degeneration.

scientific article

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.

scientific article published on 8 November 2017

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

scientific article published on 26 June 2017

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

scientific article published on 07 March 2019

EuroPhenome: a repository for high-throughput mouse phenotyping data

scientific article

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

scientific article published on 12 August 2020

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

scientific article published on 31 January 2020

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

scientific article published on 21 December 2018

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

scientific article published on 18 January 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

scientific article published on 28 December 2020

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

scientific article published in 2022

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

scientific article

Perspectives on Cognitive Phenotypes and Models of Vascular Disease

scientific article published on 05 May 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

scientific article published on 15 June 2020

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