Mutations in RAB39B Cause X-Linked Intellectual Disability and Early-Onset Parkinson Disease with α-Synuclein Pathology von Wilson, Gabrielle R., Sim, Joe C.H., McLean, Catriona, Giannandrea, Maila, Galea, Charles A., Riseley, Jessica R., Stephenson, Sarah E.M., Fitzpatrick, Elizabeth, Haas, Stefan A., Pope, Kate, Hogan, Kirk J., Gregg, Ronald G., Bromhead, Catherine J., Wargowski, David S., Lawrence, Christopher H., James, Paul A., Churchyard, Andrew, Gao, Yujing, Phelan, Dean G., Gillies, Greta, Salce, Nicholas, Stanford, Lynn, Marsh, Ashley P.L., Mignogna, Maria L., Hayflick, Susan J., Leventer, Richard J., Delatycki, Martin B., Mellick, George D., Kalscheuer, Vera M., D’Adamo, Patrizia, Bahlo, Melanie, Amor, David J., Lockhart, Paul J.

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Hemispheric cortical dysplasia secondary to a mosaic somatic mutation in MTOR von Leventer, Richard J, Scerri, Thomas, Marsh, Ashley P.L, Pope, Kate, Gillies, Greta, Maixner, Wirginia, MacGregor, Duncan, Harvey, A Simon, Delatycki, Martin B, Amor, David J, Crino, Peter, Bahlo, Melanie, Lockhart, Paul J

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Teaching NeuroImages: Imaging features of DCC-mediated mirror movements and isolated agenesis of the corpus callosum von Edwards, Timothy J, Marsh, Ashley P.L, Lockhart, Paul J, Richards, Linda J, Leventer, Richard J

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DCC Is Required for the Development of Nociceptive Topognosis in Mice and Humans von da Silva, Ronan V., Johannssen, Helge C., Wyss, Matthias T., Roome, R. Brian, Bourojeni, Farin B., Stifani, Nicolas, Marsh, Ashley P.L., Ryan, Monique M., Lockhart, Paul J., Leventer, Richard J., Richards, Linda J., Rosenblatt, Bernard, Srour, Myriam, Weber, Bruno, Zeilhofer, Hanns Ulrich, Kania, Artur

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The energetic brain - A review from students to students von Bordone, Melina Paula, Salman, Mootaz M., Titus, Haley E., Amini, Elham, Andersen, Jens V., Chakraborti, Barnali, Diuba, Artem V., Dubouskaya, Tatsiana G., Ehrke, Eric, Espindola de Freitas, Andiara, Braga de Freitas, Guilherme, Gonçalves, Rafaella A., Gupta, Deepali, Gupta, Richa, Ha, Sharon R., Hemming, Isabel A., Jaggar, Minal, Jakobsen, Emil, Kumari, Punita, Lakkappa, Navya, Marsh, Ashley P. L., Mitlöhner, Jessica, Ogawa, Yuki, Kumar, Paidi Ramesh, Ribeiro, Felipe C., Salamian, Ahmad, Saleem, Suraiya, Sharma, Sorabh, Silva, Joana M., Singh, Shripriya, Sulakhiya, Kunjbihari, Tefera, Tesfaye Wolde, Vafadari, Behnam, Yadav, Anuradha, Yamazaki, Reiji, Seidenbecher, Constanze I.

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DCC mutation update: Congenital mirror movements, isolated agenesis of the corpus callosum, and developmental split brain syndrome von Marsh, Ashley P. L., Edwards, Timothy J., Galea, Charles, Cooper, Helen M., Engle, Elizabeth C., Jamuar, Saumya S., Méneret, Aurélie, Moutard, Marie‐Laure, Nava, Caroline, Rastetter, Agnès, Robinson, Gail, Rouleau, Guy, Roze, Emmanuel, Spencer‐Smith, Megan, Trouillard, Oriane, Billette de Villemeur, Thierry, Walsh, Christopher A., Yu, Timothy W., Heron, Delphine, Sherr, Elliott H., Richards, Linda J., Depienne, Christel, Leventer, Richard J., Lockhart, Paul J.

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CUGC for pontocerebellar hypoplasia type 9 and spastic paraplegia-63 von Marsh, Ashley P L, Novarino, Gaia, Lockhart, Paul J, Leventer, Richard J

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Mutations in DCC cause isolated agenesis of the corpus callosum with incomplete penetrance von Marsh, Ashley P L, Heron, Delphine, Edwards, Timothy J, Quartier, Angélique, Galea, Charles, Nava, Caroline, Rastetter, Agnès, Moutard, Marie-Laure, Anderson, Vicki, Bitoun, Pierre, Bunt, Jens, Faudet, Anne, Garel, Catherine, Gillies, Greta, Gobius, Ilan, Guegan, Justine, Heide, Solveig, Keren, Boris, Lesne, Fabien, Lukic, Vesna, Mandelstam, Simone A, McGillivray, George, McIlroy, Alissandra, Méneret, Aurélie, Mignot, Cyril, Morcom, Laura R, Odent, Sylvie, Paolino, Annalisa, Pope, Kate, Riant, Florence, Robinson, Gail A, Spencer-Smith, Megan, Srour, Myriam, Stephenson, Sarah E M, Tankard, Rick, Trouillard, Oriane, Welniarz, Quentin, Wood, Amanda, Brice, Alexis, Rouleau, Guy, Attié-Bitach, Tania, Delatycki, Martin B, Mandel, Jean-Louis, Amor, David J, Roze, Emmanuel, Piton, Amélie, Bahlo, Melanie, Billette de Villemeur, Thierry, Sherr, Elliott H, Leventer, Richard J, Richards, Linda J, Lockhart, Paul J, Depienne, Christel

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Bi-allelic variants in SPATA5L1 lead to intellectual disability, spastic-dystonic cerebral palsy, epilepsy, and hearing loss von Richard, Elodie M., Bakhtiari, Somayeh, Marsh, Ashley P.L., Kaiyrzhanov, Rauan, Wagner, Matias, Shetty, Sheetal, Pagnozzi, Alex, Nordlie, Sandra M., Cornejo, Patricia, Magee, Helen, Liu, James, Norton, Bethany Y., Webster, Richard I., Hakonarson, Hakon, Li, Jiankang, Guo, Yiran, Jain, Mahim, Blesson, Alyssa, Rodan, Lance H., Abbott, Mary-Alice, Comi, Anne, Cohen, Julie S., Alhaddad, Bader, Meitinger, Thomas, Lenz, Dominic, Ziegler, Andreas, Kotzaeridou, Urania, Brunet, Theresa, Chassevent, Anna, Smith-Hicks, Constance, Ekstein, Joseph, Weiden, Tzvi, Hahn, Andreas, Zharkinbekova, Nazira, Turnpenny, Peter, Tucci, Arianna, Yelton, Melissa, Horvath, Rita, Gungor, Serdal, Hiz, Semra, Oktay, Yavuz, Lochmuller, Hanns, Zollino, Marcella, Morleo, Manuela, Marangi, Giuseppe, Nigro, Vincenzo, Torella, Annalaura, Pinelli, Michele, Amenta, Simona, Husain, Ralf A., Grossmann, Benita, Rapp, Marion, Steen, Claudia, Marquardt, Iris, Grimmel, Mona, Grasshoff, Ute, Korenke, G. Christoph, Owczarek-Lipska, Marta, Neidhardt, John, Radio, Francesca Clementina, Mancini, Cecilia, Claps Sepulveda, Dianela Judith, McWalter, Kirsty, Begtrup, Amber, Crunk, Amy, Guillen Sacoto, Maria J., Schnur, Rhonda E., Mancardi, Maria Margherita, Kreuder, Florian, Striano, Pasquale, Zara, Federico, Chung, Wendy K., Marks, Warren A., van Eyk, Clare L., Webber, Dani L., Corbett, Mark A., Harper, Kelly, Berry, Jesia G., MacLennan, Alastair H., Gecz, Jozef, Tartaglia, Marco, Salpietro, Vincenzo, Christodoulou, John, Kaslin, Jan, Padilla-Lopez, Sergio, Bilguvar, Kaya, Munchau, Alexander, Ahmed, Zubair M., Hufnagel, Robert B., Fahey, Michael C., Maroofian, Reza, Houlden, Henry, Mane, Shrikant M., Rad, Aboulfazl, Jin, Sheng Chih, Haack, Tobias B., Makowski, Christine, Hirsch, Yoel, Riazuddin, Saima, Kruer, Michael C.

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DCC regulates astroglial development essential for telencephalic morphogenesis and corpus callosum formation von Morcom, Laura, Gobius, Ilan, Marsh, Ashley Pl, Suarez, Rodrigo, Lim, Jonathan W. C., Bridges, Caitlin, Ye, Yunan, Fenlon, Laura R., Zagar, Yvrick, Douglass, Amelia M., Donahoo, Amber-Lee S., Fothergill, Thomas, Shaikh, Samreen, Kozulin, Peter, Edwards, Timothy J., Cooper, Helen M., Sherr, Elliott H., Chedotal, Alain, Leventer, Richard J., Lockhart, Paul J., Richards, Linda J.

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A novel AMPD2 mutation outside the AMP deaminase domain causes pontocerebellar hypoplasia type 9 von Marsh, Ashley P. L., Yap, Patrick, Tan, Tiong, Pope, Kate, White, Susan M., Chong, Belinda, Mcgillivray, George, Boys, Amber, Stephenson, Sarah E. M., Leventer, Richard J., Stark, Zornitza, Lockhart, Paul J.

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Investigating the role of somatic mutations in malformations of brain development von Leventer, Richard J., Scerri, Thomas, Marsh, Ashley P.L., Maixner, Wirginia, MacGregor, Duncan, Harvey, A. Simon, Delatycki, Martin B., Amor, David J., Bahlo, Melanie, Lockhart, Paul J.

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Heterozygous mutations in HSD17B4 cause juvenile peroxisomal D-bifunctional protein deficiency von Amor, David J, Marsh, Ashley P L, Storey, Elsdon, Tankard, Rick, Gillies, Greta, Delatycki, Martin B, Pope, Kate, Bromhead, Catherine, Leventer, Richard J, Bahlo, Melanie, Lockhart, Paul J

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Complete callosal agenesis, pontocerebellar hypoplasia, and axonal neuropathy due to AMPD2 loss von Marsh, Ashley P L, Lukic, Vesna, Pope, Kate, Bromhead, Catherine, Tankard, Rick, Ryan, Monique M, Yiu, Eppie M, Sim, Joe C H, Delatycki, Martin B, Amor, David J, McGillivray, George, Sherr, Elliott H, Bahlo, Melanie, Leventer, Richard J, Lockhart, Paul J

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