Two isoforms of the RAC-specific guanine nucleotide exchange factor TIAM2 act oppositely on transmission ratio distortion by the mouse t-haplotype von Charron, Yves, Willert, Jürgen, Lipkowitz, Bettina, Kusecek, Barica, Herrmann, Bernhard G, Bauer, Hermann

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Effect of inbreeding on intellectual disability revisited by trio sequencing von Kahrizi, Kimia, Hu, Hao, Hosseini, Masoumeh, Kalscheuer, Vera M., Fattahi, Zohreh, Beheshtian, Maryam, Suckow, Vanessa, Mohseni, Marzieh, Lipkowitz, Bettina, Mehvari, Sepideh, Mehrjoo, Zohreh, Akhtarkhavari, Tara, Ghaderi, Zhila, Rahimi, Maryam, Arzhangi, Sanaz, Jamali, Payman, Falahat Chian, Milad, Nikuei, Pooneh, Sabbagh Kermani, Farahnaz, Sadeghinia, Farnaz, Jazayeri, Roshanak, Tonekaboni, S. Hassan, Khoshaeen, Atefeh, Habibi, Haleh, Pourfatemi, Fatemeh, Mojahedi, Faezeh, Khodaie‐Ardakani, Mohammad‐Reza, Najafipour, Reza, Wienker, Thomas F., Najmabadi, Hossein, Ropers, Hans‐Hilger

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Up-regulation of glucocorticoid-regulated genes in a mouse model of Rett syndrome von Nuber, Ulrike A., Kriaucionis, Skirmantas, Roloff, Tim C., Guy, Jacky, Selfridge, Jim, Steinhoff, Christine, Schulz, Ralph, Lipkowitz, Bettina, Ropers, H. Hilger, Holmes, Megan C., Bird, Adrian

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Gene Expression Changes in the Course of Neural Progenitor Cell Differentiation von Gurok, Ulf, Steinhoff, Christine, Lipkowitz, Bettina, Ropers, H.-Hilger, Scharff, Constance, Nuber, Ulrike A

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Genetics of intellectual disability in consanguineous families von Hu, Hao, Kahrizi, Kimia, Musante, Luciana, Fattahi, Zohreh, Herwig, Ralf, Hosseini, Masoumeh, Oppitz, Cornelia, Abedini, Seyedeh Sedigheh, Suckow, Vanessa, Larti, Farzaneh, Beheshtian, Maryam, Lipkowitz, Bettina, Akhtarkhavari, Tara, Mehvari, Sepideh, Otto, Sabine, Mohseni, Marzieh, Arzhangi, Sanaz, Jamali, Payman, Mojahedi, Faezeh, Taghdiri, Maryam, Papari, Elaheh, Soltani Banavandi, Mohammad Javad, Akbari, Saeide, Tonekaboni, Seyed Hassan, Dehghani, Hossein, Ebrahimpour, Mohammad Reza, Bader, Ingrid, Davarnia, Behzad, Cohen, Monika, Khodaei, Hossein, Albrecht, Beate, Azimi, Sarah, Zirn, Birgit, Bastami, Milad, Wieczorek, Dagmar, Bahrami, Gholamreza, Keleman, Krystyna, Vahid, Leila Nouri, Tzschach, Andreas, Gärtner, Jutta, Gillessen-Kaesbach, Gabriele, Varaghchi, Jamileh Rezazadeh, Timmermann, Bernd, Pourfatemi, Fatemeh, Jankhah, Aria, Chen, Wei, Nikuei, Pooneh, Kalscheuer, Vera M., Oladnabi, Morteza, Wienker, Thomas F., Ropers, Hans-Hilger, Najmabadi, Hossein

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Deep sequencing reveals 50 novel genes for recessive cognitive disorders von Najmabadi, Hossein, Hu, Hao, Garshasbi, Masoud, Zemojtel, Tomasz, Abedini, Seyedeh Sedigheh, Chen, Wei, Hosseini, Masoumeh, Behjati, Farkhondeh, Haas, Stefan, Jamali, Payman, Zecha, Agnes, Mohseni, Marzieh, Püttmann, Lucia, Vahid, Leyla Nouri, Jensen, Corinna, Moheb, Lia Abbasi, Bienek, Melanie, Larti, Farzaneh, Mueller, Ines, Weissmann, Robert, Darvish, Hossein, Wrogemann, Klaus, Hadavi, Valeh, Lipkowitz, Bettina, Esmaeeli-Nieh, Sahar, Wieczorek, Dagmar, Kariminejad, Roxana, Firouzabadi, Saghar Ghasemi, Cohen, Monika, Fattahi, Zohreh, Rost, Imma, Mojahedi, Faezeh, Hertzberg, Christoph, Dehghan, Atefeh, Rajab, Anna, Banavandi, Mohammad Javad Soltani, Hoffer, Julia, Falah, Masoumeh, Musante, Luciana, Kalscheuer, Vera, Ullmann, Reinhard, Kuss, Andreas Walter, Tzschach, Andreas, Kahrizi, Kimia, Ropers, H. Hilger

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Different molecular mechanisms underlie placental overgrowth phenotypes caused by interspecies hybridization, cloning, and Esx1 mutation von Singh, Umashankar, Fohn, Laurel E., Wakayama, Teruhiko, Ohgane, Jun, Steinhoff, Christine, Lipkowitz, Bettina, Schulz, Ralph, Orth, Annie, Ropers, H. Hilger, Behringer, Richard R., Tanaka, Satoshi, Shiota, Kunio, Yanagimachi, Ryuzo, Nuber, Ulrike A., Fundele, Reinald

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Mutations of the aminoacyl‐tRNA‐synthetases SARS and WARS2 are implicated in the etiology of autosomal recessive intellectual disability von Musante, Luciana, Püttmann, Lucia, Kahrizi, Kimia, Garshasbi, Masoud, Hu, Hao, Stehr, Henning, Lipkowitz, Bettina, Otto, Sabine, Jensen, Lars R., Tzschach, Andreas, Jamali, Payman, Wienker, Thomas, Najmabadi, Hossein, Ropers, Hans Hilger, Kuss, Andreas W.

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Mutations of the aminoacyl-tRNA-synthetases SARS and WARS2 are implicated in the etiology of autosomal recessive intellectual disability: MUSANTE ET AL von Musante, Luciana, Püttmann, Lucia, Kahrizi, Kimia, Garshasbi, Masoud, Hu, Hao, Stehr, Henning, Lipkowitz, Bettina, Otto, Sabine, Jensen, Lars R., Tzschach, Andreas, Jamali, Payman, Wienker, Thomas, Najmabadi, Hossein, Ropers, Hans Hilger, Kuss, Andreas W.

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A novel ALDH5A1 mutation is associated with succinic semialdehyde dehydrogenase deficiency and severe intellectual disability in an Iranian family von Püttmann, Lucia, Stehr, Henning, Garshasbi, Masoud, Hu, Hao, Kahrizi, Kimia, Lipkowitz, Bettina, Jamali, Payman, Tzschach, Andreas, Najmabadi, Hossein, Ropers, Hans-Hilger, Musante, Luciana, Kuss, Andreas W.

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Hybridisation-based resequencing of 17 X-linked intellectual disability genes in 135 patients reveals novel mutations in ATRX, SLC6A8 and PQBP1 von JENSEN, Lars R, WEI CHEN, VAN ESCH, Hilde, CHELLY, Jamel, DE BROUWER, Arjan Pm, HACKETT, Anna, VAN DER HAAR, Sigrun, HENN, Wolfram, GECZ, Jozef, RIESS, Olaf, BONIN, Michael, REINHARDT, Richard, MOSER, Bettina, ROPERS, Hans-Hilger, KUSS, Andreas W, LIPKOWITZ, Bettina, SCHROEDER, Christopher, MUSANTE, Luciana, TZSCHACH, Andreas, KALSCHEUER, Vera M, MELONI, Ilaria, RAYNAUD, Martine

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Hybridisation-based resequencing of 17 X-linked intellectual disability genes in 135 patients reveals novel mutations in ATRX, SLC6A8 and PQBP1 von Jensen, Lars R, Chen, Wei, Moser, Bettina, Lipkowitz, Bettina, Schroeder, Christopher, Musante, Luciana, Tzschach, Andreas, Kalscheuer, Vera M, Meloni, Ilaria, Raynaud, Martine, Van Esch, Hilde, Chelly, Jamel, de Brouwer, Arjan P.M, Hackett, Anna, van der Haar, Sigrun, Henn, Wolfram, Gecz, Jozef, Riess, Olaf, Bonin, Michael, Reinhardt, Richard, Ropers, Hans-Hilger, Kuss, Andreas W

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MS 5-3: Gene expression changes in the course of neural progenitor cell differentiation von Gurok, Ulf, Steinhoff, Christine, Lipkowitz, Bettina, H-Hilger Ropers

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