Researcher Portfolio
Dr. Haaf, Thomas
Dept. of Human Molecular Genetics (Head: Hans-Hilger Ropers), Max Planck Institute for Molecular Genetics, Max Planck Society
Researcher Profile
Position: Dept. of Human Molecular Genetics (Head: Hans-Hilger Ropers), Max Planck Institute for Molecular Genetics, Max Planck Society
Researcher ID: https://pure.mpg.de/cone/persons/resource/persons50182
Publications
: Bartsch, O., Gebauer, K., Lechno, S., van Esch, H., Froyen, G., Bonin, M., Jörg Seidel, J. S., Thamm-Mücke, B., Horn, D., Klopock, E., Hertzberg, C., Zechner, U., & Haaf, T. (2010). Four unrelated patients with Lubs X-linked mental retardation syndrome and different Xq28 duplications. American Journal of Medical Genetics Part A, 152A(2), 305-312,. doi:10.1002/ajmg.a.33198. [PubMan] : Haensel, J., Kohlschmidt, N., Pitz, S., Keilmann, A., Zenker, M., Ullmann, R., Haaf, T., & Bartsch, O. (2009). Case report supporting that the Barber-Say and ablepharon macrostomia syndromes could represent one disorder. American Journal of Medical Genetics Part A, 149(10), 2236-2240. doi:10.1002/ajmg.a.32993. [PubMan] : Bartsch, O., Vlccaronková, Z., Erdogan, F., Ullmann, R., Novotná, D., Spiegel, M., Beyer, V., Haaf, T., Zechner, U., & Seemanová, E. (2007). Two independent chromosomal rearrangements, a very small (550 kb) duplication of the 7q subtelomeric region and an atypical 17q11.2 (NF1) microdeletion, in a girl with neurofibromatosis. Cytogenetic and Genome Research, 119(1 - 2), 158-64. doi:10.1159/000109634. [PubMan] : Bartsch, O., Rasi, S., Delicado, A., Dyack, S., Neumann, L. M., Seemanová, E., Volleth, M., Haaf, T., & Kalscheuer, V. M. (2006). Evidence for a new contiguous gene syndrome, the chromosome 16p13.3 deletion syndrome alias severe Rubinstein–Taybi syndrome. Human Genetics, 120(3), 179-186. doi:10.1007/s00439-006-0215-0. [PubMan] : Tsend-Ayush, E., Grützner, F., Yue, Y., Grossmann, B., Hänsel, U., Sudbrak, R., & Haaf, T. (2004). Plasticity of human chromosome 3 during primate evolution. Genomics, 83(2), 193-202. doi:10.1016/j.ygeno.2003.08.012. [PubMan] : Lemmers, R. J. L. F., Osborn, M., Haaf, T., Rogers, M., Frants, R. R., Padberg, G. W., Cooper, D. N., van der Maarel, S. M., & Upadhyaya, M. (2003). D4F104S1 deletion in facioscapulohumeral muscular dystrophy - Phenotype, size, and detection. Neurology, 61(2), 178-183. [PubMan] : Grützner, F., Roest Crollius, H., Lütjens, G., Jaillon, O., Weissenbach, J., Ropers, H. H., & Haaf, T. (2002). Four-Hundred Million Years of Conserved Synteny of Human Xp and Xq Genes on Three Tetraodon Chromosomes. Genome Research, 12(9), 1316-1322. [PubMan] : Voigt, R., Maier-Weidmann, M., Lange, P. E., & Haaf, T. (2002). Chromosome 10p13-14 and 22q11 deletion screening in 100 patients with isolated and syndromic conotruncal heart defects. Journal of Medical Genetics, 39(4), e16-e16. [PubMan] : van Geel, M., Eichler, E. E., Beck, A. F., Shan, Z., Haaf, T., van der Maarel, S. M., Frants, R. R., & de Jong, P. J. (2002). A Cascade of Complex Subtelomeric Duplications during the Evolution of the Hominoid and Old World Monkey Genomes. American Journal of Human Genetics, 70(1), 269-278. [PubMan] : Raderschall, E., Bazarov, A., Cao, J., Lurz, R., Smith, A., Mann, W., Ropers, H. H., Sedivy, J. M., Golub, E. I., Fritz, E., & Haaf, T. (2002). Formation of higher-order nuclear Rad51 structures is functionally linked to p21 expression and protection from DNA damage-induced apoptosis. Journal of Cell Science, 115(1), 153-164. [PubMan] : Raderschall, E., Stout, K., Freier, S., Suckow, V., Schweiger, S., & Haaf, T. (2002). Elevated Levels of Rad51 Recombination Protein in Tumor Cells. Cancer Research, 62(1), 219-225. [PubMan] : Raderschall, E., Bazarov, A., Cao, J., Lurz, R., Smith, A., Mann, W., Ropers, H. H., Sedivy, J. M., Golub, E. I., Fritz, E., & Haaf, T. (2002). Formation of higher-order nuclear Rad51 structures is functionally linked to p21 expression and protection from DNA damage-induced apoptosis. Journal of Cell Science, 115(1), 153-164. [PubMan] : Hattori, M., Fujiyama, A., Taylor, T. D., Watanabe, H., Yada, T., Park, H.-S., Toyoda, A., Ishii, K., Totoki, Y., Choi, D.-K., Soeda, E., Ohki, M., Takagi, T., Sakaki, Y., Taudien, S., Blechschmidt, K., Polley, A., Menzel, U., Delabar, J., Kumpf, K., Lehmann, R., Patterson, D., Reichwald, K., Rump, A., Schillhabel, M., Schudy, A., Zimmermann, W., Rosenthal, A., Kudoh, J., Shibuya, K., Kawasaki, K., Asakawa, S., Shintani, A., Sasaki, T., Nagamine, K., Mitsuyama, S., Antonarakis, S. E., Minoshima, S., Shimizu, N., Nordsiek, G., Hornischer, K., Brandt, P., Scharfe, M., Schön, O., Desario, A., Reichelt, J., Kauer, G., Blöcker, H., Ramser, J., Beck, A., Klages, S., Hennig, S., Riesselmann, L., Dagand, E., Haaf, T., Wehrmeyer, S., Borzym, K., Gardiner, K., Nizetic, D., Francis, F., Lehrach, H., Reinhardt, R., & Yaspo, M.-L. (2000). The DNA sequence of human chromosome 21. Nature, 405. doi:10.1038/35012518. [PubMan]