2016
CYP2A6 metabolism in the development of smoking behaviors in young adults
Olfson E, Bloom J, Bertelsen S, Budde JP, Breslau N, Brooks A, Culverhouse R, Chan G, Chen L, Chorlian D, Dick DM, Edenberg HJ, Hartz S, Hatsukami D, Hesselbrock VM, Johnson EO, Kramer JR, Kuperman S, Meyers JL, Nurnberger J, Porjesz B, Saccone NL, Schuckit MA, Stitzel J, Tischfield JA, Rice JP, Goate A, Bierut LJ. CYP2A6 metabolism in the development of smoking behaviors in young adults. Addiction Biology 2016, 23: 437-447. PMID: 28032407, PMCID: PMC5491369, DOI: 10.1111/adb.12477.Peer-Reviewed Original ResearchConceptsNicotine dependenceSlow metabolizersDaily smokersYoung adultsSmoking behaviorCYP2A6 variationNicotine metabolismRole of CYP2A6Adult daily smokersDevelopment of dependenceCollaborative Genetics StudyGenetics of AlcoholismSmoking milestonesCytochrome P450 2A6Young adult daily smokersNormal metabolizersCollaborative studyDaily smokingFirst cigaretteSecondary analysisCYP2A6 variantsMetabolizersYoung adulthoodP450 2A6Conflicting resultsThe significant impact of education, poverty, and race on Internet-based research participant engagement
Hartz SM, Quan T, Ibiebele A, Fisher SL, Olfson E, Salyer P, Bierut LJ. The significant impact of education, poverty, and race on Internet-based research participant engagement. Genetics In Medicine 2016, 19: 240-243. PMID: 27467456, PMCID: PMC5274598, DOI: 10.1038/gim.2016.91.Peer-Reviewed Original Research
2015
Rare, low frequency and common coding variants in CHRNA5 and their contribution to nicotine dependence in European and African Americans
Olfson E, Saccone NL, Johnson EO, Chen LS, Culverhouse R, Doheny K, Foltz SM, Fox L, Gogarten SM, Hartz S, Hetrick K, Laurie CC, Marosy B, Amin N, Arnett D, Barr RG, Bartz TM, Bertelsen S, Borecki IB, Brown MR, Chasman DI, van Duijn CM, Feitosa MF, Fox ER, Franceschini N, Franco OH, Grove ML, Guo X, Hofman A, Kardia SL, Morrison AC, Musani SK, Psaty BM, Rao DC, Reiner AP, Rice K, Ridker PM, Rose LM, Schick UM, Schwander K, Uitterlinden AG, Vojinovic D, Wang JC, Ware EB, Wilson G, Yao J, Zhao W, Breslau N, Hatsukami D, Stitzel JA, Rice J, Goate A, Bierut LJ. Rare, low frequency and common coding variants in CHRNA5 and their contribution to nicotine dependence in European and African Americans. Molecular Psychiatry 2015, 21: 601-607. PMID: 26239294, PMCID: PMC4740321, DOI: 10.1038/mp.2015.105.Peer-Reviewed Original Research
2012
Rare and Common Variants in CARD14, Encoding an Epidermal Regulator of NF-kappaB, in Psoriasis
Jordan CT, Cao L, Roberson ED, Duan S, Helms CA, Nair RP, Duffin KC, Stuart PE, Goldgar D, Hayashi G, Olfson EH, Feng BJ, Pullinger CR, Kane JP, Wise CA, Goldbach-Mansky R, Lowes MA, Peddle L, Chandran V, Liao W, Rahman P, Krueger GG, Gladman D, Elder JT, Menter A, Bowcock AM. Rare and Common Variants in CARD14, Encoding an Epidermal Regulator of NF-kappaB, in Psoriasis. American Journal Of Human Genetics 2012, 90: 796-808. PMID: 22521419, PMCID: PMC3376540, DOI: 10.1016/j.ajhg.2012.03.013.Peer-Reviewed Original ResearchMeSH KeywordsCARD Signaling Adaptor ProteinsCase-Control StudiesEpidermisGene Expression RegulationGenetic Predisposition to DiseaseGuanylate CyclaseHLA-C AntigensHumansKeratinocytesMembrane ProteinsMutation, MissenseNF-kappa BPolymorphism, GeneticPsoriasisSkinTranscriptomeTumor Necrosis Factor-alphaWhite People