| review article | Q7318358 |
| scholarly article | Q13442814 |
| P50 | author | Melissa Haendel | Q28368079 |
| Damian Smedley | Q44820039 | ||
| Pilar Cacheiro | Q57999105 | ||
| P2093 | author name string | International Mouse Phenotyping Consortium and the Monarch Initiative | |
| P2860 | cites work | The Monarch Initiative: an integrative data and analytic platform connecting phenotypes to genotypes across species | Q28584446 |
| Expanding the mammalian phenotype ontology to support automated exchange of high throughput mouse phenotyping data generated by large-scale mouse knockout screens | Q35228284 | ||
| Abundant pleiotropy in human complex diseases and traits. | Q35542127 | ||
| A mouse informatics platform for phenotypic and translational discovery. | Q36149437 | ||
| PhenoDigm: analyzing curated annotations to associate animal models with human diseases | Q36830807 | ||
| Appearances can be deceiving: phenotypes of knockout mice. | Q36856150 | ||
| Genetic pleiotropy in complex traits and diseases: implications for genomic medicine | Q37111321 | ||
| High-throughput discovery of novel developmental phenotypes | Q37629635 | ||
| Representation of rare diseases in health information systems: the Orphanet approach to serve a wide range of end users | Q38474579 | ||
| A bioimage informatics platform for high-throughput embryo phenotyping | Q39289789 | ||
| Disease model discovery from 3,328 gene knockouts by The International Mouse Phenotyping Consortium. | Q40145504 | ||
| A large scale hearing loss screen reveals an extensive unexplored genetic landscape for auditory dysfunction. | Q42375961 | ||
| Mouse Genome Database (MGD)-2018: knowledgebase for the laboratory mouse | Q47202657 | ||
| Landscape of Pleiotropic Proteins Causing Human Disease: Structural and System Biology Insights | Q47229935 | ||
| Identification of genetic elements in metabolism by high-throughput mouse phenotyping | Q47643645 | ||
| Absence of CFAP69 Causes Male Infertility due to Multiple Morphological Abnormalities of the Flagella in Human and Mouse. | Q52690495 | ||
| Identification of genes required for eye development by high-throughput screening of mouse knockouts | Q60300295 | ||
| Expansion of the Human Phenotype Ontology (HPO) knowledge base and resources | Q60950343 | ||
| Ensembl variation resources | Q61480444 | ||
| OMIM.org: leveraging knowledge across phenotype-gene relationships | Q93177837 | ||
| P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
| P4510 | describes a project that uses | ggplot2 | Q326489 |
| P433 | issue | 5-6 | |
| P921 | main subject | phenotype | Q104053 |
| animal disease model | Q64732998 | ||
| P1104 | number of pages | 8 | |
| P304 | page(s) | 143-150 | |
| P577 | publication date | 2019-05-24 | |
| 2019-06-01 | |||
| P1433 | published in | Mammalian Genome | Q1348949 |
| P1476 | title | New models for human disease from the International Mouse Phenotyping Consortium | |
| P478 | volume | 30 |
| Q89965056 | High Fidelity of Mouse Models Mimicking Human Genetic Skeletal Disorders |
| Q100954813 | High-throughput genotyping of high-homology mutant mouse strains by next-generation sequencing |
| Q89944661 | Inherited Eye Diseases with Retinal Manifestations through the Eyes of Homeobox Genes |
| Q90269934 | Principles of Genetic Engineering |
| Q89488064 | The Deep Genome Project |
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