Three phases of DiGeorge/22q11 deletion syndrome pathogenesis during brain development: Patterning, proliferation, and mitochondrial functions of 22q11 genes by Meechan, D.W., Maynard, T.M., Tucker, E.S., LaMantia, A.-S.

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Mitochondrial localization and function of a subset of 22q11 deletion syndrome candidate genes by Maynard, T.M., Meechan, D.W., Dudevoir, M.L., Gopalakrishna, D., Peters, A.Z., Heindel, C.C., Sugimoto, T.J., Wu, Y., Lieberman, J.A., LaMantia, A.-S.

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Cognitive ability is associated with altered medial frontal cortical circuits in the LgDel mouse model of 22q11.2DS by Meechan, D W, Rutz, H L H, Fralish, M S, Maynard, T M, Rothblat, L A, LaMantia, A-S

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Specific mesenchymal/epithelial induction of olfactory receptor, vomeronasal, and gonadotropin‐releasing hormone (GnRH) neurons by Rawson, N.E., Lischka, F. W., Yee, K.K., Peters, A.Z., Tucker, E.S., Meechan, D.W., Zirlinger, M., Maynard, T.M., Burd, G.B., Dulac, C., Pevny, L., LaMantia, A.‐S.

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Gene dosage in the developing and adult brain in a mouse model of 22q11 deletion syndrome by Meechan, D.W., Maynard, T.M., Wu, Y., Gopalakrishna, D., Lieberman, J.A., LaMantia, A.-S.

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Limited influence of olanzapine on adult forebrain neural precursors in vitro by Councill, J.H., Tucker, E.S., Haskell, G.T., Maynard, T.M., Meechan, D.W., Hamer, R.M., Lieberman, J.A., LaMantia, A.-S.

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Oesophageal cancer survival in Europe: A EUROCARE-4 study by Gavin, A.T, Francisci, S, Foschi, R, Donnelly, D.W, Lemmens, V, Brenner, H, Anderson, L.A

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