Reaction time as an indicator of insufficient effort: Development and validation of an embedded performance validity parameter von Stevens, Andreas, Bahlo, Simone, Licha, Christina, Liske, Benjamin, Vossler-Thies, Elisabeth

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Leitlinie „Neuropsychologische Begutachtung von Neumann-Zielke, Ludger, Bahlo, Simone, Diebel, Andrea, Riepe, Johannes, Roschmann, Rupert, Schötzau-Fürwentsches, Peter, Wetzig, Lutz

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Familial cortical dysplasia caused by mutation in the mammalian target of rapamycin regulator NPRL3 von Sim, Joe C., Scerri, Thomas, Fanjul-Fernández, Miriam, Riseley, Jessica R., Gillies, Greta, Pope, Kate, van Roozendaal, Hanna, Heng, Julian I., Mandelstam, Simone A., McGillivray, George, MacGregor, Duncan, Kannan, Lakshminarayanan, Maixner, Wirginia, Harvey, A. Simon, Amor, David J., Delatycki, Martin B., Crino, Peter B., Bahlo, Melanie, Lockhart, Paul J., Leventer, Richard J.

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iPSC-derived retinal pigmented epithelial cells from patients with macular telangiectasia show decreased mitochondrial function von Eade, Kevin T, Ansell, Brendan Robert E, Giles, Sarah, Fallon, Regis, Harkins-Perry, Sarah, Nagasaki, Takayuki, Tzaridis, Simone, Wallace, Martina, Mills, Elizabeth A, Farashi, Samaneh, Johnson, Alec, Sauer, Lydia, Hart, Barbara, Diaz-Rubio, M Elena, Bahlo, Melanie, Metallo, Christian, Allikmets, Rando, Gantner, Marin L, Bernstein, Paul S, Friedlander, Martin

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Neonatal BCG vaccination is associated with a long-term DNA methylation signature in circulating monocytes von Bannister, Samantha, Kim, Bowon, Domínguez-Andrés, Jorge, Kilic, Gizem, Ansell, Brendan R E, Neeland, Melanie R, Moorlag, Simone J C F M, Matzaraki, Vasiliki, Vlahos, Amanda, Shepherd, Rebecca, Germano, Susie, Bahlo, Melanie, Messina, Nicole L, Saffery, Richard, Netea, Mihai G, Curtis, Nigel, Novakovic, Boris

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Genetic aetiologies for childhood speech disorder: novel pathways co-expressed during brain development von Kaspi, Antony, Hildebrand, Michael S., Jackson, Victoria E., Braden, Ruth, van Reyk, Olivia, Howell, Tegan, Debono, Simone, Lauretta, Mariana, Morison, Lottie, Coleman, Matthew J., Webster, Richard, Coman, David, Goel, Himanshu, Wallis, Mathew, Dabscheck, Gabriel, Downie, Lilian, Baker, Emma K., Parry-Fielder, Bronwyn, Ballard, Kirrie, Harrold, Eva, Ziegenfusz, Shaun, Bennett, Mark F., Robertson, Erandee, Wang, Longfei, Boys, Amber, Fisher, Simon E., Amor, David J., Scheffer, Ingrid E., Bahlo, Melanie, Morgan, Angela T.

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WWOX developmental and epileptic encephalopathy: Understanding the epileptology and the mortality risk von Oliver, Karen L., Trivisano, Marina, Mandelstam, Simone A., De Dominicis, Angela, Francis, David I., Green, Timothy E., Muir, Alison M., Chowdhary, Apoorva, Hertzberg, Christoph, Goldhahn, Klaus, Metreau, Julia, Prager, Christine, Pinner, Jason, Cardamone, Michael, Myers, Kenneth A., Leventer, Richard J., Lesca, Gaetan, Bahlo, Melanie, Hildebrand, Michael S., Mefford, Heather C., Kaindl, Angela M., Specchio, Nicola, Scheffer, Ingrid E.

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Divergent amino acid and sphingolipid metabolism in patients with inherited neuro-retinal disease von Green, Courtney R., Bonelli, Roberto, Ansell, Brendan R.E., Tzaridis, Simone, Handzlik, Michal K., McGregor, Grace H., Hart, Barbara, Trombley, Jennifer, Reilly, Mary M., Bernstein, Paul S., Egan, Catherine, Fruttiger, Marcus, Wallace, Martina, Bahlo, Melanie, Friedlander, Martin, Metallo, Christian M., Gantner, Marin L.

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Familial cortical dysplasia type IIA caused by a germline mutation in DEPDC5 von Scerri, Thomas, Riseley, Jessica R., Gillies, Greta, Pope, Kate, Burgess, Rosemary, Mandelstam, Simone A., Dibbens, Leanne, Chow, Chung W., Maixner, Wirginia, Harvey, Anthony Simon, Jackson, Graeme D., Amor, David J., Delatycki, Martin B., Crino, Peter B., Berkovic, Samuel F., Scheffer, Ingrid E., Bahlo, Melanie, Lockhart, Paul J., Leventer, Richard J.

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Callosal agenesis and congenital mirror movements: outcomes associated with DCC mutations von Spencer‐Smith, Megan, Knight, Jacquelyn L, Lacaze, Emmanuelle, Depienne, Christel, Lockhart, Paul J, Richards, Linda J, Heron, Delphine, Leventer, Richard J, Robinson, Gail A, Ceslis, Amelia, Gibson, Emily, Giraudat, Kim, McIlroy, Alissandra, Paul, Lynn K, Siffredi, Vanessa, Bahlo, Melanie, Barker, Megan, Blondiaux, Eleonore, Edwards, Timothy J, Garel, Catherine, Heide, Solveig, Keren, Boris, Mandelstam, Simone A, Marsh, Ashley PL, McGillivray, George, Mignot, Cyril, Moutard, Marie‐Laure, Nava, Caroline, Pope, Kate, Rastetter, Agnès, Stephenson, Sarah EM, Valence, Stéphanie, de Villemeur, Thierry Billette, Wood, Amanda, Anderson, Vicki, Sherr, Elliott H

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Dorsal language stream anomalies in an inherited speech disorder von Liégeois, Frédérique J, Turner, Samantha J, Mayes, Angela, Bonthrone, Alexandra F, Boys, Amber, Smith, Libby, Parry-Fielder, Bronwyn, Mandelstam, Simone, Spencer-Smith, Megan, Bahlo, Melanie, Scerri, Tom S, Hildebrand, Michael S, Scheffer, Ingrid E, Connelly, Alan, Morgan, Angela T

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Infantile‐onset myoclonic developmental and epileptic encephalopathy: A new RARS2 phenotype von de Valles‐Ibáñez, Guillem, Hildebrand, Michael S., Bahlo, Melanie, King, Chontelle, Coleman, Matthew, Green, Timothy E., Goldsmith, John, Davis, Suzanne, Gill, Deepak, Mandelstam, Simone, Scheffer, Ingrid E., Sadleir, Lynette G.

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Correction: Genetic aetiologies for childhood speech disorder: novel pathways co-expressed during brain development von Kaspi, Antony, Hildebrand, Michael S., Jackson, Victoria E., Braden, Ruth, van Reyk, Olivia, Howell, Tegan, Debono, Simone, Lauretta, Mariana, Morison, Lottie, Coleman, Matthew J., Webster, Richard, Coman, David, Goel, Himanshu, Wallis, Mathew, Dabscheck, Gabriel, Downie, Lilian, Baker, Emma K., Parry-Fielder, Bronwyn, Ballard, Kirrie, Harrold, Eva, Ziegenfusz, Shaun, Bennett, Mark F., Robertson, Erandee, Wang, Longfei, Boys, Amber, Fisher, Simon E., Amor, David J., Scheffer, Ingrid E., Bahlo, Melanie, Morgan, Angela T.

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Epidemiology and etiology of infantile developmental and epileptic encephalopathies in Tasmania von Ware, Tyson L., Huskins, Shannon R., Grinton, Bronwyn E., Liu, Yu‐Chi, Bennett, Mark F., Harvey, Michael, McMahon, Jacinta, Andreopoulos‐Malikotsinas, Danae, Bahlo, Melanie, Howell, Katherine B., Hildebrand, Michael S., Damiano, John A., Rosenfeld, Alexander, Mackay, Mark T., Mandelstam, Simone, Leventer, Richard J., Harvey, A. Simon, Freeman, Jeremy L., Scheffer, Ingrid E., Jones, Dean L., Berkovic, Samuel F.

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Mosaic uniparental disomy results in GM1 gangliosidosis with normal enzyme assay von Myers, Kenneth A., Bennett, Mark F., Chow, Chung W., Carden, Susan M., Mandelstam, Simone A., Bahlo, Melanie, Scheffer, Ingrid E.

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Comparative genomics revealed adaptive admixture in Cryptosporidium hominis in Africa von Tichkule, Swapnil, Jex, Aaron R, van Oosterhout, Cock, Sannella, Anna Rosa, Krumkamp, Ralf, Aldrich, Cassandra, Maiga-Ascofare, Oumou, Dekker, Denise, Lamshöft, Maike, Mbwana, Joyce, Rakotozandrindrainy, Njari, Borrmann, Steffen, Thye, Thorsten, Schuldt, Kathrin, Winter, Doris, Kremsner, Peter G, Oppong, Kwabena, Manouana, Prince, Mbong, Mirabeau, Gesase, Samwel, Minja, Daniel T R, Mueller, Ivo, Bahlo, Melanie, Nader, Johanna, May, Jürgen, Rakotozandrindrain, Raphael, Adegnika, Ayola Akim, Lusingu, John P A, Amuasi, John, Eibach, Daniel, Caccio, Simone Mario

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Comparative genomics revealed adaptive admixture in Cryptosporidium hominis in Africa von Tichkule, Swapnil, Jex, Aaron R., Van Oosterhout, Cock, Sannella, Anna Rosa, Krumkamp, Ralf, Aldrich, Cassandra, Maiga-Ascofare, Oumou, Dekker, Denise, Lamshöft, Maike, Mbwana, Joyce, Rakotozandrindrainy, Njari, Borrmann, Steffen, Thye, Thorsten, Schuldt, Kathrin, Winter, Doris, Kremsner, Peter G., Oppong, Kwabena, Manouana, Prince, Mbong, Mirabeau, Gesase, Samwel, Minja, Daniel T. R., Mueller, Ivo, Bahlo, Melanie, Nader, Johanna Lucia Thorbjørnsrud, May, Jürgen, Rakotozandrindrain, Raphael, Adegnika, Ayola Akim, Lusingu, John P. A., Amuasi, John, Eibach, Daniel, Caccio, Simone M

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Familial cortical dysplasia type IIA caused by a germline mutation in DEPDC 5 von Scerri, Thomas, Riseley, Jessica R., Gillies, Greta, Pope, Kate, Burgess, Rosemary, Mandelstam, Simone A., Dibbens, Leanne, Chow, Chung W., Maixner, Wirginia, Harvey, Anthony Simon, Jackson, Graeme D., Amor, David J., Delatycki, Martin B., Crino, Peter B., Berkovic, Samuel F., Scheffer, Ingrid E., Bahlo, Melanie, Lockhart, Paul J., Leventer, Richard J.

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Divergent amino acid and sphingolipid metabolism in patients with inherited neuro-retinal disease von Green, Courtney R, Bonelli, Roberto, Ansell, Brendan RE, Tzaridis, Simone, Handzlik, Michal K, McGregor, Grace H, Hart, Barbara, Trombley, Jennifer, Reilly, Mary M, Bernstein, Paul S, Egan, Catherine, Fruttiger, Marcus, Wallace, Martina, Bahlo, Melanie, Friedlander, Martin, Metallo, Christian M, Gantner, Marin L

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Comparative genomics revealed adaptive admixture in Cryptosporidium hominis in Africa von Tichkule, Swapnil, Jex, Aaron R, Van Oosterhout, Cock, Sannella, Anna Rosa, Krumkamp, Ralf, Aldrich, Cassandra, Maiga-Ascofare, Oumou, Dekker, Denise, Lamshöft, Maike, Mbwana, Joyce, Rakotozandrindrainy, Njari, Borrmann, Steffen, Thye, Thorsten, Schuldt, Kathrin, Winter, Doris, Kremsner, Peter G, Oppong, Kwabena, Manouana, Prince, Mbong, Mirabeau, Gesase, Samwel, Minja, Daniel T. R, Mueller, Ivo, Bahlo, Melanie, Nader, Johanna Lucia Thorbjørnsrud, May, Jürgen, Rakotozandrindrain, Raphael, Adegnika, Ayola Akim, Lusingu, John P. A, Amuasi, John, Eibach, Daniel, Caccio, Simone M

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