Related references
Note: Only part of the references are listed.Post-synaptic scaffold protein TANC2 in psychiatric and somatic disease risk
Lillian Garrett et al.
DISEASE MODELS & MECHANISMS (2022)
Pleiotropy data resource as a primer for investigating co-morbidities/multi-morbidities and their role in disease
Violeta Munoz-Fuentes et al.
MAMMALIAN GENOME (2022)
Identifying genetic determinants of inflammatory pain in mice using a large-scale gene-targeted screen
Janine M. Wotton et al.
PAIN (2022)
Skeletal screening IMPC/KOMP using μCT and computer automated cryohistology: Application to the Efna4 KO mouse line
David W. Rowe et al.
BONE (2021)
Open Targets Platform: supporting systematic drug-target identification and prioritisation
David Ochoa et al.
NUCLEIC ACIDS RESEARCH (2021)
LAMA: automated image analysis for the developmental phenotyping of mouse embryos
Neil R. Horner et al.
DEVELOPMENT (2021)
100,000 Genomes Pilot on Rare-Disease Diagnosis in Health Care - Preliminary Report
Damian Smedley et al.
NEW ENGLAND JOURNAL OF MEDICINE (2021)
A resource of targeted mutant mouse lines for 5,061 genes
Marie-Christine Birling et al.
NATURE GENETICS (2021)
Soft windowing application to improve analysis of high-throughput phenotyping data
Hamed Haselimashhadi et al.
BIOINFORMATICS (2020)
The Monarch Initiative in 2019: an integrative data and analytic platform connecting phenotypes to genotypes across species
Kent A. Shefchek et al.
NUCLEIC ACIDS RESEARCH (2020)
High-throughput phenotyping reveals expansive genetic and structural underpinnings of immune variation
Lucie Abeler-Dorner et al.
NATURE IMMUNOLOGY (2020)
Human and mouse essentiality screens as a resource for disease gene discovery
Pilar Cacheiro et al.
NATURE COMMUNICATIONS (2020)
High-throughput discovery of genetic determinants of circadian misalignment
Tao Zhang et al.
PLOS GENETICS (2020)
A Genome-Wide Screen in Mice To Identify Cell-Extrinsic Regulators of Pulmonary Metastatic Colonisation
Louise van der Weyden et al.
G3-GENES GENOMES GENETICS (2020)
A trans-eQTL network regulates osteoclast multinucleation and bone mass
Marie Pereira et al.
ELIFE (2020)
Mouse mutant phenotyping at scale reveals novel genes controlling bone mineral density
Anna L. Swan et al.
PLOS GENETICS (2020)
Machine learning-based automated phenotyping of inflammatory nocifensive behavior in mice
Janine M. Wotton et al.
MOLECULAR PAIN (2020)
New models for human disease from the International Mouse Phenotyping Consortium
Pilar Cacheiro et al.
MAMMALIAN GENOME (2019)
Mouse screen reveals multiple new genes underlying mouse and human hearing loss
Neil J. Ingham et al.
PLOS BIOLOGY (2019)
Large-scale neuroanatomical study uncovers 198 gene associations in mouse brain morphogenesis
Stephan C. Collins et al.
NATURE COMMUNICATIONS (2019)
Mouse Genome Database (MGD) 2019
Carol J. Bult et al.
NUCLEIC ACIDS RESEARCH (2019)
OMIM.org: leveraging knowledge across phenotype-gene relationships
Joanna S. Amberger et al.
NUCLEIC ACIDS RESEARCH (2019)
Expansion of the Human Phenotype Ontology (HPO) knowledge base and resources
Sebastian Koehler et al.
NUCLEIC ACIDS RESEARCH (2019)
The International Mouse Phenotyping Consortium (IMPC): a functional catalogue of the mammalian genome that informs conservation
Violeta Munoz-Fuentes et al.
CONSERVATION GENETICS (2018)
High-throughput mouse phenomics for characterizing mammalian gene function
Steve D. M. Brown et al.
NATURE REVIEWS GENETICS (2018)
Identification of genetic elements in metabolism by high-throughput mouse phenotyping
Jan Rozman et al.
NATURE COMMUNICATIONS (2018)
Identification of genes required for eye development by high-throughput screening of mouse knockouts
Bret A. Moore et al.
COMMUNICATIONS BIOLOGY (2018)
Efficient gene targeting in mouse zygotes mediated by CRISPR/Cas9-protein
Chris J. Jung et al.
TRANSGENIC RESEARCH (2017)
Disease model discovery from 3,328 gene knockouts by The International Mouse Phenotyping Consortium
Terrence F. Meehan et al.
NATURE GENETICS (2017)
Prevalence of sexual dimorphism in mammalian phenotypic traits
Natasha A. Karp et al.
NATURE COMMUNICATIONS (2017)
A large scale hearing loss screen reveals an extensive unexplored genetic landscape for auditory dysfunction
Michael R. Bowl et al.
NATURE COMMUNICATIONS (2017)
Clinical Practice Guidelines for Rare Diseases: The Orphanet Database
Sonia Pavan et al.
PLOS ONE (2017)
High-throughput discovery of novel developmental phenotypes
Mary E. Dickinson et al.
NATURE (2016)
Analysis of mammalian gene function through broad-based phenotypic screens across a consortium of mouse clinics
Martin Hrabe de Angelis et al.
NATURE GENETICS (2015)
High-throughput screening of mouse gene knockouts identifies established and novel skeletal phenotypes
Robert Brommage et al.
BONE RESEARCH (2014)
Genome-wide Generation and Systematic Phenotyping of Knockout Mice Reveals New Roles for Many Genes
Jacqueline K. White et al.
CELL (2013)
PhenoDigm: analyzing curated annotations to associate animal models with human diseases
Damian Smedley et al.
DATABASE-THE JOURNAL OF BIOLOGICAL DATABASES AND CURATION (2013)
The mammalian phenotype ontology: enabling robust annotation and comparative analysis
Cynthia L. Smith et al.
WILEY INTERDISCIPLINARY REVIEWS-SYSTEMS BIOLOGY AND MEDICINE (2009)
Share Paper
