Deficits in early neural tube identity found in CHARGE syndrome

by Parthiv Haldipur, Kathleen J Millen
Published 2013-12-01

Hippocampal granule cell dispersion: a non-specific finding in pediatric patients with no history of seizures

by Achira Roy, Kathleen J. Millen, Raj P. Kapur
Published 2020-04-01

Looking at cerebellar malformations through text-mined interactomes of mice and humans.

by Ivan Iossifov, Raul Rodriguez-Esteban, Ilya Mayzus, Kathleen J Millen, Andrey Rzhetsky
Published 2009-11-01

Genetic variation and population substructure in outbred CD-1 mice: implications for genome-wide association studies.

by Kimberly A Aldinger, Greta Sokoloff, David M Rosenberg, Abraham A Palmer, Kathleen J Millen
Published 2009-01-01

Foxc1 dependent mesenchymal signalling drives embryonic cerebellar growth

by Parthiv Haldipur, Gwendolyn S Gillies, Olivia K Janson, Victor V Chizhikov, Divakar S Mithal, Richard J Miller, Kathleen J Millen
Published 2014-12-01

Intermediate progenitors support migration of neural stem cells into dentate gyrus outer neurogenic niches

by Branden R Nelson, Rebecca D Hodge, Ray AM Daza, Prem Prakash Tripathi, Sebastian J Arnold, Kathleen J Millen, Robert F Hevner
Published 2020-04-01

PI3K-Yap activity drives cortical gyrification and hydrocephalus in mice

by Achira Roy, Rory M Murphy, Mei Deng, James W MacDonald, Theo K Bammler, Kimberly A Aldinger, Ian A Glass, Kathleen J Millen
Published 2019-05-01

Early dorsomedial tissue interactions regulate gyrification of distal neocortex

by Victor V. Chizhikov, Igor Y. Iskusnykh, Ekaterina Y. Steshina, Nikolai Fattakhov, Anne G. Lindgren, Ashwin S. Shetty, Achira Roy, Shubha Tole, Kathleen J. Millen
Published 2019-11-01

Phenotypic outcomes in Mouse and Human Foxc1 dependent Dandy-Walker cerebellar malformation suggest shared mechanisms

by Parthiv Haldipur, Derek Dang, Kimberly A Aldinger, Olivia K Janson, Fabien Guimiot, Homa Adle-Biasette, William B Dobyns, Joseph R Siebert, Rosa Russo, Kathleen J Millen
Published 2017-01-01

Mouse models of human PIK3CA-related brain overgrowth have acutely treatable epilepsy

by Achira Roy, Jonathan Skibo, Franck Kalume, Jing Ni, Sherri Rankin, Yiling Lu, William B Dobyns, Gordon B Mills, Jean J Zhao, Suzanne J Baker, Kathleen J Millen
Published 2015-12-01

Both rare and de novo copy number variants are prevalent in agenesis of the corpus callosum but not in cerebellar hypoplasia or polymicrogyria.

by Samin A Sajan, Liliana Fernandez, Sahar Esmaeeli Nieh, Eric Rider, Polina Bukshpun, Mari Wakahiro, Susan L Christian, Jean-Baptiste Rivière, Christopher T Sullivan, Jyotsna Sudi, Michael J Herriges, Alexander R Paciorkowski, A James Barkovich, Joseph T Glessner, Kathleen J Millen, Hakon Hakonarson, William B Dobyns, Elliott H Sherr
Published 2013-01-01

A novel intergenic ETnII-β insertion mutation causes multiple malformations in polypodia mice.

by Jessica A Lehoczky, Peedikayil E Thomas, Kevin M Patrie, Kailey M Owens, Lisa M Villarreal, Kenneth Galbraith, Joe Washburn, Craig N Johnson, Bryant Gavino, Alexander D Borowsky, Kathleen J Millen, Paul Wakenight, William Law, Margaret L Van Keuren, Galina Gavrilina, Elizabeth D Hughes, Thomas L Saunders, Lesil Brihn, Joseph H Nadeau, Jeffrey W Innis
Published 2013-01-01