2011
Microduplications in an autism multiplex family narrow the region of susceptibility for developmental disorders on 15q24 and implicate 7p21
Cukier H, Salyakina D, Blankstein S, Robinson J, Sacharow S, Ma D, Wright H, Abramson R, Menon R, Williams S, Haines J, Cuccaro M, Gilbert J, Pericak‐Vance M. Microduplications in an autism multiplex family narrow the region of susceptibility for developmental disorders on 15q24 and implicate 7p21. American Journal Of Medical Genetics Part B Neuropsychiatric Genetics 2011, 156: 493-501. PMID: 21480499, PMCID: PMC5490366, DOI: 10.1002/ajmg.b.31188.Peer-Reviewed Original Research
2007
Investigation of potential gene–gene interactions between apoe and reln contributing to autism risk
Ashley-Koch A, Jaworski J, Ma D, Mei H, Ritchie M, Skaar D, Delong G, Worley G, Abramson R, Wright H, Cuccaro M, Gilbert J, Martin E, Pericak-Vance M. Investigation of potential gene–gene interactions between apoe and reln contributing to autism risk. Psychiatric Genetics 2007, 17: 221-226. PMID: 17621165, DOI: 10.1097/ypg.0b013e32809c2f75.Peer-Reviewed Original ResearchApolipoproteins EAutistic DisorderCell Adhesion Molecules, NeuronalElectron Spin Resonance SpectroscopyExtracellular Matrix ProteinsFamilyFemaleGenetic Predisposition to DiseaseHumansMaleNerve Tissue ProteinsPolymorphism, GeneticPolymorphism, Single NucleotideReelin ProteinRisk AssessmentSerine EndopeptidasesUnited StatesWhite People