Deficits in early neural tube identity found in CHARGE syndrome by Parthiv Haldipur, Kathleen J Millen

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Neonatal subarachnoid hemorrhage disrupts multiple aspects of cerebellar development by David F. Butler, Jonathan Skibo, Christopher M. Traudt, Kathleen J. Millen, Kathleen J. Millen

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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

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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

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Dynamics of levitated nanospheres: towards the strong coupling regime by T S Monteiro, J Millen, G A T Pender, Florian Marquardt, D Chang, P F Barker

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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

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The effect of diagnostic delays on the drop-out rate and the total delay to diagnosis of tuberculosis. by Stephen J Millen, Pieter W Uys, John Hargrove, Paul D van Helden, Brian G Williams

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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

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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

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Non-synaptic Cell-Autonomous Mechanisms Underlie Neuronal Hyperactivity in a Genetic Model of PIK3CA-Driven Intractable Epilepsy by Achira Roy, Victor Z. Han, Victor Z. Han, Angela M. Bard, Devin T. Wehle, Devin T. Wehle, Stephen E. P. Smith, Stephen E. P. Smith, Jan-Marino Ramirez, Jan-Marino Ramirez, Jan-Marino Ramirez, Jan-Marino Ramirez, Franck Kalume, Franck Kalume, Franck Kalume, Kathleen J. Millen, Kathleen J. Millen

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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

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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

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The IFIH1-A946T risk variant promotes diabetes in a sex-dependent manner by Amanda J. Stock, Pierina Gonzalez Paredes, Luciana Previato de Almeida, Stanley D. Kosanke, Srinivaas Chetlur, Hannah Budde, Paul Wakenight, Theresa A. Zwingman, Aaron B.I. Rosen, Eric J. Allenspach, Eric J. Allenspach, Kathleen J. Millen, Kathleen J. Millen, Jane H. Buckner, David J. Rawlings, David J. Rawlings, David J. Rawlings, Jacquelyn A. Gorman

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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

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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

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P008 Real-world analysis of the clinical and economic impact of 21-gene recurrence score (RS) testing in early-stage node positive breast cancer in Ireland by I.M. Browne, R.A. McLaughlin, R.S. Prichard, D.P. McCartan, S.J. Millen, M.J. Higgins, J.P. Crown, B.T. Hennessy, C.M. Quinn, P.G. Morris, J.M. Walshe

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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

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Spiny mice activate unique transcriptional programs after severe kidney injury regenerating organ function without fibrosis by Daryl M. Okamura, Chris M. Brewer, Paul Wakenight, Nadia Bahrami, Kristina Bernardi, Amy Tran, Jill Olson, Xiaogang Shi, Szu-Ying Yeh, Adrian Piliponsky, Sarah J. Collins, Elizabeth D. Nguyen, Andrew E. Timms, James W. MacDonald, Theo K. Bammler, Branden R. Nelson, Kathleen J. Millen, David R. Beier, Mark W. Majesky

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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

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Real-World Analysis of the Clinical and Economic Impact of the 21-Gene Recurrence Score (RS) in Invasive Lobular Early-Stage Breast Carcinoma in Ireland by Lynda M. McSorley, Mehala Tharmabala, Fathiya Al Rahbi, Fergus Keane, Denis Evoy, James G. Geraghty, Jane Rothwell, Damian P. McCartan, Megan Greally, Miriam O’Connor, Deirdre O’Mahony, Maccon Keane, Michael John Kennedy, Seamus O’Reilly, Steve J. Millen, John P. Crown, Catherine M. Kelly, Ruth S. Prichard, Cecily M. Quinn, Janice M. Walshe

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