Deleterious protein‐altering mutations in the SCN10A voltage‐gated sodium channel gene are associated with prolonged QT by Abou Ziki, M.D., Seidelmann, S.B., Smith, E., Atteya, G., Jiang, Y., Fernandes, R.G., Marieb, M.A., Akar, J.G., Mani, A.

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The pleiotropic effect of a deleterious DES mutation in familial atrial fibrillation and the role of PDE4DIP as a genetic modifier for heart block by Abou Ziki, M, Akar, J.A, Neogi, A.N, Abboud, J.A, Choueiri, S.C, Driscoll, T.D, Bhat, N.B, Ugwu, N.U, Liu, Y.L, Smith, E.S, Mani, A.M

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Men1 disruption in Nkx3.1-deficient mice results in ARlow/CD44+ microinvasive carcinoma development with the dysregulated AR pathway by Teinturier, Romain, Luo, Yakun, Decaussin-Petrucci, Myriam, Vlaeminck-Guillem, Virginie, Vacherot, Francis, Firlej, Virginie, Bonnavion, Rémy, Abou Ziki, Razan, Gherardi, Samuele, Goddard, Isabelle, Gadot, Nicolas, Bertolino, Philippe, Le Romancer, Muriel, Zhang, Chang Xian

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Prevalence of the Apolipoprotein E Arg145Cys Dyslipidemia At-Risk Polymorphism in African-Derived Populations by Abou Ziki, Maen D., BA, Strulovici-Barel, Yael, MS, Hackett, Neil R., PhD, Rodriguez-Flores, Juan L., PhD, Mezey, Jason G., PhD, Salit, Jacqueline, MS, Radisch, Sharon, MS, Hollmann, Charleen, PhD, Chouchane, Lotfi, MD, Malek, Joel, PhD, Zirie, Mahmoud A., MD, Jayyuosi, Amin, MD, Gotto, Antonio M., MD, DPhil, Crystal, Ronald G., MD

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Prevalence of the ApoE Arg145Cys Dyslipidemia At-risk Polymorphism in African-derived Populations by Abou Ziki, Maen D., Strulovici-Barel, Yael, Hackett, Neil R., Rodriguez-Flores, Juan L., Mezey, Jason G., Salit, Jacqueline, Radisch, Sharon, Hollmann, Charleen, Chouchane, Lotfi, Malek, Joel, Zirie, Mahmoud A., Jayyuosi, Amin, Gotto, Antonio M., Crystal, Ronald G.

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Severe extra-glandular involvement and pleural effusions complicating primary Sjogren’s syndrome: a case report by Abou Ziki, Maen D., Taoutel, Roy, Hong, Julian C., Podell, David N.

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