Periventricular heterotopia and the genetics of neuronal migration in the cerebral cortex.

le Fox, J W, Walsh, C A
Foilsithe 1999

AGE-FRIENDLY COMMUNITY STRATEGIES: A RESEARCH-BASED APPROACH ADOPTED IN GUANGZHOU, CHINA

le Lai, D.W., Zhang, Q., Hewson, J., Walsh, C.A., Tong, H.L.
Foilsithe in Innov Aging (2017)

Cytokine expression by cultured osteoblasts from patients with osteoporotic fractures

le Walsh, C A, Birch, Mark A, Fraser, William D, Ginty, Andrew F, Gallagher, James A
Foilsithe 2000

Disorders of Microtubule Function in Neurons: Imaging Correlates

le Mutch, C.A., Poduri, A., Sahin, M., Barry, B., Walsh, C.A., Barkovich, A.J.
Foilsithe in AJNR Am J Neuroradiol (2016)

Slapping and spanking in childhood and its association with lifetime prevalence of psychiatric disorders in a general population sample

le MacMillan, H L, Boyle, M H, Wong, M Y, Duku, E K, Fleming, J E, Walsh, C A
Foilsithe 1999

Congenital Microcephaly with a Simplified Gyral Pattern: Associated Findings and Their Significance

le Adachi, Y., Poduri, A., Kawaguch, A., Yoon, G., Salih, M.A., Yamashita, F., Walsh, C.A., Barkovich, A.J.
Foilsithe 2011

Novel susceptibility locus at chromosome 6q16.3-22.31 in a family with GEFS+

le Poduri, A, Wang, Y, Gordon, D, Barral-Rodriguez, S, Barker-Cummings, C, Ulgen, A, Chitsazzadeh, V, Hill, R S., Risch, N, Hauser, W A., Pedley, T A., Walsh, C A., Ottman, R
Foilsithe 2009

FLNA genomic rearrangements cause periventricular nodular heterotopia

le Clapham, K.R., Yu, T.W., Ganesh, V.S., Barry, B., Chan, Y., Mei, D., Parrini, E., Funalot, B., Dupuis, L., Nezarati, M.M., du Souich, C., van Karnebeek, C., Guerrini, R., Walsh, C.A.
Foilsithe 2012

The CC2D1A, a member of a new gene family with C2 domains, is involved in autosomal recessive non‐syndromic mental retardation

le Basel‐Vanagaite, L, Attia, R, Yahav, M, Ferland, R J, Anteki, L, Walsh, C A, Olender, T, Straussberg, R, Magal, N, Taub, E, Drasinover, V, Alkelai, A, Bercovich, D, Rechavi, G, Simon, A J, Shohat, M
Foilsithe 2006

Using whole exome sequencing to identify inherited causes of autism

le Yu, T.W., Chahrour, M.H., Coulter, M.E., Jiralerspong, S., Okamura-Ikeda, K., Ataman, B., Schmitz-Abe, K., Harmin, D.A., Adli, M., Malik, A.N., D’Gama, A.M., Lim, E.T., Sanders, S.J., Mochida, G.H., Partlow, J.N., Sunu, C.M., Felie, J.M., Rodriguez, J., Nasir, R.H., Ware, J., Joseph, R.M., Hill, R.S., Kwan, B.Y., Al-Saffar, M., Mukaddes, N.M., Hashmi, A., Balkhy, S., Gascon, G.G., Hisama, F.M., LeClair, E., Poduri, A., Oner, O., Al-Saad, S., Al-Awadi, S.A., Bastaki, L., Ben-Omran, T., Teebi, A., Al-Gazali, L., Eapen, V., Stevens, C.R., Rappaport, L., Gabriel, S.B., Markianos, K., State, M.W., Greenberg, M.E., Taniguchi, H., Braverman, N.E., Morrow, E.M., Walsh, C.A.
Foilsithe 2013