Publikationen von Bettina Lipkowitz

Hao Hu, Kimia Kahrizi, Luciana Musante, Zohreh Fattahi, Ralf Herwig, Masoumeh Hosseini, Cornelia Oppitz, Seyedeh Sedigheh Abedini, Vanessa Suckow, Larti Farzaneh, Maryam Beheshtian, Bettina Lipkowitz, Tara Akhtarkhavari, Sepideh Mehvari, Sabine Otto, Marzieh Mohseni, Sanaz Arzhangi, Payman Jamali, Faezeh Mojahedi, Maryam Taghdiri, Elaheh Papari, Mohammad Javad Soltani Banavandi, Saeide Akbari, Seyed Hassan Tonekaboni, Hossein Dehghani, Mohammad Reza Ebrahimpou, Ingrid Bader, Behzad Davarnia, Monika Cohen, Hossein Khodaei, Beate Albrecht, Sarah Azimi, Birgit Zirn, Milad Bastami, Dagmar Wieczorek, Gholamreza Bahrami, Krystyna Keleman, Leila Nouri Vahid, Bernd Timmermann, Fatemeh Pourfatemi, Aria Jankhah, Wei Chen, Pooneh Nikuei, Vera M. Kalscheuer, Morteza Oladnabi, Thomas F. Wienker, Hans-Hilger Ropers, and Hossein Najmabadi, "Genetics of intellectual disability in consanguineous families," Molecular Psychiatry 24 (7), 1027-1039 (2019).

Yves Charron, Jürgen Willert, Bettina Lipkowitz, Barica Kusecek, Bernhard G. Herrmann, and Hermann Bauer, "Two isoforms of the RAC-specific guanine nucleotide exchange factor TIAM2 act oppositely on transmission ratio distortion by the mouse t-haplotype," PLOS Genetics 15 (2), e1007964 (2019).

Kimia Kahrizi, Hao Hu, Masoumeh Hosseini, Vera M. Kalscheuer, Zohreh Fattahi, Maryam Beheshtian, Vanessa Suckow, Marzieh Mohseni, Bettina Lipkowitz, Sepideh Mehvari, Zohreh Mehrjoo, Tara Akhtarkhavari, Zhila Ghaderi, Maryam Rahimi, Sanaz Arzhangi, Payman Jamali, Milad Falahat Chian, Pooneh Nikuei , Farahnaz Sabbagh Kermani, Farnaz Sadeghinia, Roshanak Jazayeri , Seyed Hassan Tonekaboni, Atefeh Khoshaeen, Haleh Habibi, Fatemeh Pourfatemi, Faezeh Mojahedi , Mohammad‐Reza Khodaie‐Ardakani, Reza Najafipour, Thomas F. Wienker, Hossein Najmabadi , and Hans-Hilger Ropers, "Effect of inbreeding on intellectual disability revisited by Trio sequencing," Clinical Genetics: an international journal of genetics in medicine 95 (1), 151-159 (2019).

L. Puettmann, H. Stehr, M. Garshasbi, H. Hu, K. Kahrizi, B. Lipkowitz, P. Jamali, A. Tzschach, H. Najmabadi, H. H. Ropers, L. Musante, and A. W. Kuss, "A novel ALDH5A1 mutation is associated with succinic semialdehyde dehydrogenase deficiency and severe intellectual disability in an Iranian family," American Journal of Medical Genetics Part A 161A (8), 1915-1922 (2013).

L. R. Jensen, W. Chen, B. Moser, B. Lipkowitz, C. Schroeder, L. Musante, A. Tzschach, V. M. Kalscheuer, I. Meloni, M. Raynaud, H. van Esch, J. Chelly, A. P. de Brouwer, A. Hackett, S. van der Haar, W. Henn, J. Gecz, O. Riess, M. Bonin, R. Reinhardt, H. H. Ropers, and A. W. Kuss, "Hybridisation-based resequencing of 17 X-linked intellectual disability genes in 135 patients reveals novel mutations in ATRX, SLC6A8 and PQBP1," Eur J Hum Genet 19 (6), 717-20 (2011).

H. Najmabadi, H. Hu, M. Garshasbi, T. Zemojtel, S. S. Abedini, W. Chen, M. Hosseini, F. Behjati, S. Haas, P. Jamali, A. Zecha, M. Mohseni, L. Puttmann, L. N. Vahid, C. Jensen, L. A. Moheb, M. Bienek, F. Larti, I. Mueller, R. Weissmann, H. Darvish, K. Wrogemann, V. Hadavi, B. Lipkowitz, S. Esmaeeli-Nieh, D. Wieczorek, R. Kariminejad, S. G. Firouzabadi, M. Cohen, Z. Fattahi, I. Rost, F. Mojahedi, C. Hertzberg, A. Dehghan, A. Rajab, M. J. Banavandi, J. Hoffer, M. Falah, L. Musante, V. Kalscheuer, R. Ullmann, A. W. Kuss, A. Tzschach, K. Kahrizi, and H. H. Ropers, "Deep sequencing reveals 50 novel genes for recessive cognitive disorders," Nature 478 (7367), 57-63 (2011).

Ulrike A. Nuber, Skirmantas Kriaucionis, Tim C. Roloff, Jacky Guy, Jim Selfridge, Christine Steinhoff, Ralph Schulz, Bettina Lipkowitz, H. Hilger Ropers, Megan C. Holmes, and Adrian Bird, "Up-regulation of glucocorticoid-regulated genes in a mouse model of Rett syndrome," Human Molecular Genetics 14 (15), 2247-2256 (2005).

Ulf Gurok, Christine Steinhoff, Bettina Lipkowitz, Hans-Hilger Ropers, Constance Scharff, and Ulrike A. Nuber, "Gene expression changes in the course of neural progenitor cell differentiation," Journal of Neuroscience 24 (26), 5982-6002 (2004).

Umashankar Singh, Laurel E. Fohn, Teruhiko Wakayama, Jun Ohgane, Christine Steinhoff, Bettina Lipkowitz, Ralph Schulz, Annie Orth, Hans-Hilger Ropers, Richard R. Behringer, Satoshi Tanaka, Kunio Shiota, Ryuzo Yanagimachi, Ulrike A. Nuber, and Reinald Fundele, "Different molecular mechanisms underlie placental overgrowth phenotypes caused by interspecies hybridization, cloning, and Esx1 mutation," Developmental Dynamics 230 (1), 149-164 (2004).