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| 36792746 | The case for standardizing gene nomenclature in vertebrates. | Nature | 2023 |
| 36866529 | The Gene Ontology knowledgebase in 2023. | Genetics | 2023 |
| 36864549 | From multiallele fish to nonstandard environments, how ZFIN assigns phenotypes, human disease models, and gene expression annotations to genes. | Genetics | 2023 |
| 36792746 | The case for standardizing gene nomenclature in vertebrates. | Nature | 2023 |
| 36866529 | The Gene Ontology knowledgebase in 2023. | Genetics | 2023 |
| 36864549 | From multiallele fish to nonstandard environments, how ZFIN assigns phenotypes, human disease models, and gene expression annotations to genes. | Genetics | 2023 |
| 35166825 | Zebrafish information network, the knowledgebase for Danio rerio research. | Genetics | 2022 |
| 35789323 | Multiomic atlas with functional stratification and developmental dynamics of zebrafish cis-regulatory elements. | Nat Genet | 2022 |
| 35788411 | Affinity purification of in vivo assembled whirlin-associated protein complexes from the zebrafish retina. | J Proteomics | 2022 |
| 35166825 | Zebrafish information network, the knowledgebase for Danio rerio research. | Genetics | 2022 |
| 35789323 | Multiomic atlas with functional stratification and developmental dynamics of zebrafish cis-regulatory elements. | Nat Genet | 2022 |
| 35788411 | Affinity purification of in vivo assembled whirlin-associated protein complexes from the zebrafish retina. | J Proteomics | 2022 |
| 33170210 | The Zebrafish Information Network: major gene page and home page updates. | Nucleic Acids Res | 2021 |
| 34113007 | Heterozygous loss-of-function variants significantly expand the phenotypes associated with loss of GDF11. | Genet Med | 2021 |
| 33724412 | A fish with no sex: gonadal and adrenal functions partition between zebrafish NR5A1 co-orthologs. | Genetics | 2021 |
| 33826717 | Erratum to: A fish with no sex: gonadal and adrenal functions partition between zebrafish NR5A1 co-orthologs. | Genetics | 2021 |
| 33170210 | The Zebrafish Information Network: major gene page and home page updates. | Nucleic Acids Res | 2021 |
| 34450031 | COPB2 loss of function causes a coatopathy with osteoporosis and developmental delay. | Am J Hum Genet | 2021 |
| 33826717 | Erratum to: A fish with no sex: gonadal and adrenal functions partition between zebrafish NR5A1 co-orthologs. | Genetics | 2021 |
| 33724412 | A fish with no sex: gonadal and adrenal functions partition between zebrafish NR5A1 co-orthologs. | Genetics | 2021 |
| 34450031 | COPB2 loss of function causes a coatopathy with osteoporosis and developmental delay. | Am J Hum Genet | 2021 |
| 34113007 | Heterozygous loss-of-function variants significantly expand the phenotypes associated with loss of GDF11. | Genet Med | 2021 |
| 32544203 | yippee like 3Â (ypel3) is a novel gene required for myelinating and perineurial glia development. | PLoS Genet | 2020 |
| 33104717 | Correction: yippee like 3 (ypel3) is a novel gene required for myelinating and perineurial glia development. | PLoS Genet | 2020 |
| 32544203 | yippee like 3Â (ypel3) is a novel gene required for myelinating and perineurial glia development. | PLoS Genet | 2020 |
| 33232675 | BICRA, a SWI/SNF Complex Member, Is Associated with BAF-Disorder Related Phenotypes in Humans and Model Organisms. | Am J Hum Genet | 2020 |
| 33104717 | Correction: yippee like 3 (ypel3) is a novel gene required for myelinating and perineurial glia development. | PLoS Genet | 2020 |
| 33232675 | BICRA, a SWI/SNF Complex Member, Is Associated with BAF-Disorder Related Phenotypes in Humans and Model Organisms. | Am J Hum Genet | 2020 |
| 30407545 | The Zebrafish Information Network: new support for non-coding genes, richer Gene Ontology annotations and the Alliance of Genome Resources. | Nucleic Acids Res | 2019 |
| 30407545 | The Zebrafish Information Network: new support for non-coding genes, richer Gene Ontology annotations and the Alliance of Genome Resources. | Nucleic Acids Res | 2019 |
| 30287385 | Cog4 is required for protrusion and extension of the epithelium in the developing semicircular canals. | Mech Dev | 2019 |
| 30773277 | Bi-allelic Variants in TONSL Cause SPONASTRIME Dysplasia and a Spectrum of Skeletal Dysplasia Phenotypes. | Am J Hum Genet | 2019 |
| 30773277 | Bi-allelic Variants in TONSL Cause SPONASTRIME Dysplasia and a Spectrum of Skeletal Dysplasia Phenotypes. | Am J Hum Genet | 2019 |
| 30287385 | Cog4 is required for protrusion and extension of the epithelium in the developing semicircular canals. | Mech Dev | 2019 |
| 29369744 | Changes to Extender, Cryoprotective Medium, and In Vitro Fertilization Improve Zebrafish Sperm Cryopreservation. | Zebrafish | 2018 |
| 30304647 | Effect of Genetic Diagnosis on Patients with Previously Undiagnosed Disease. | N Engl J Med | 2018 |
| 30290151 | A Recurrent De Novo Heterozygous COG4 Substitution Leads to Saul-Wilson Syndrome, Disrupted Vesicular Trafficking, and Altered Proteoglycan Glycosylation. | Am J Hum Genet | 2018 |
| 30380418 | Grxcr1 Promotes Hair Bundle Development by Destabilizing the Physical Interaction between Harmonin and Sans Usher Syndrome Proteins. | Cell Rep | 2018 |
| 29369744 | Changes to Extender, Cryoprotective Medium, and In Vitro Fertilization Improve Zebrafish Sperm Cryopreservation. | Zebrafish | 2018 |
| 29777677 | Usherin defects lead to early-onset retinal dysfunction in zebrafish. | Exp Eye Res | 2018 |
| 30290151 | A Recurrent De Novo Heterozygous COG4 Substitution Leads to Saul-Wilson Syndrome, Disrupted Vesicular Trafficking, and Altered Proteoglycan Glycosylation. | Am J Hum Genet | 2018 |
| 30304647 | Effect of Genetic Diagnosis on Patients with Previously Undiagnosed Disease. | N Engl J Med | 2018 |
| 30380418 | Grxcr1 Promotes Hair Bundle Development by Destabilizing the Physical Interaction between Harmonin and Sans Usher Syndrome Proteins. | Cell Rep | 2018 |
| 29777677 | Usherin defects lead to early-onset retinal dysfunction in zebrafish. | Exp Eye Res | 2018 |
| 27899582 | The Zebrafish Model Organism Database: new support for human disease models, mutation details, gene expression phenotypes and searching. | Nucleic Acids Res | 2017 |
| 28340351 | Bedside Back to Bench: Building Bridges between Basic and Clinical Genomic Research. | Cell | 2017 |
| 28838067 | Zebrafish Models of Human Disease: Gaining Insight into Human Disease at ZFIN. | ILAR J | 2017 |
| 28874452 | Model Organisms Facilitate Rare Disease Diagnosis and Therapeutic Research. | Genetics | 2017 |
| 27899582 | The Zebrafish Model Organism Database: new support for human disease models, mutation details, gene expression phenotypes and searching. | Nucleic Acids Res | 2017 |
| 28129854 | Zebrafish models of human eye and inner ear diseases. | Methods Cell Biol | 2017 |