«SNX8 modulates the innate immune response to RNA viruses by regulating the aggregation of VISA». Cellular & Molecular Immunology: 1–10. PMID31511639. doi:10.1038/s41423-019-0285-2
Glenner. «Alzheimer's disease: Initial report of the purification and characterization of a novel cerebrovascular amyloid protein». Biochemical and Biophysical Research Communications. 120: 885–890. PMID6375662. doi:10.1016/S0006-291X(84)80190-4
«Delineation of a less than 200 kb minimal deleted region for cardiac malformations on chromosome 7p22». American Journal of Medical Genetics Part A. 155: 1729–1734. PMID21671376. doi:10.1002/ajmg.a.34041
«7p22.3 microdeletion disrupting SNX8 in a patient presenting with intellectual disability but no tetralogy of Fallot». American Journal of Medical Genetics Part A. 164: 2133–2135. PMID24715298. doi:10.1002/ajmg.a.36566
«SNX8: A candidate gene for 7p22 cardiac malformations including tetralogy of fallot». American Journal of Medical Genetics Part A. 164: 554–556. PMID24311514. doi:10.1002/ajmg.a.36242
«Small 7p22.3 microdeletion: Case report of Snx8 haploinsufficiency and neurological findings». European Journal of Medical Genetics. 103772 páginas. PMID31568860. doi:10.1016/j.ejmg.2019.103772
«Correspondence regarding SNX8 haploinsufficiency and its potential for cardiac anomalies including tetralogy of Fallot». American Journal of Medical Genetics Part A. 164: 2136–2137. PMID24733602. doi:10.1002/ajmg.a.36572
«SNX8 modulates the innate immune response to RNA viruses by regulating the aggregation of VISA». Cellular & Molecular Immunology: 1–10. PMID31511639. doi:10.1038/s41423-019-0285-2
Glenner. «Alzheimer's disease: Initial report of the purification and characterization of a novel cerebrovascular amyloid protein». Biochemical and Biophysical Research Communications. 120: 885–890. PMID6375662. doi:10.1016/S0006-291X(84)80190-4
«Delineation of a less than 200 kb minimal deleted region for cardiac malformations on chromosome 7p22». American Journal of Medical Genetics Part A. 155: 1729–1734. PMID21671376. doi:10.1002/ajmg.a.34041
«7p22.3 microdeletion disrupting SNX8 in a patient presenting with intellectual disability but no tetralogy of Fallot». American Journal of Medical Genetics Part A. 164: 2133–2135. PMID24715298. doi:10.1002/ajmg.a.36566
«SNX8: A candidate gene for 7p22 cardiac malformations including tetralogy of fallot». American Journal of Medical Genetics Part A. 164: 554–556. PMID24311514. doi:10.1002/ajmg.a.36242
«Small 7p22.3 microdeletion: Case report of Snx8 haploinsufficiency and neurological findings». European Journal of Medical Genetics. 103772 páginas. PMID31568860. doi:10.1016/j.ejmg.2019.103772
«Correspondence regarding SNX8 haploinsufficiency and its potential for cardiac anomalies including tetralogy of Fallot». American Journal of Medical Genetics Part A. 164: 2136–2137. PMID24733602. doi:10.1002/ajmg.a.36572