Pentchev, K.; Ono, K.; Herwig, R.; Ideker, T.; Kamburov, A.: Evidence mining and novelty assessment of protein-protein interactions with the ConsensusPathDB plugin for Cytoscape. (2010)

Sudmant, P. H.; Kitzman, J. O.; Antonacci, F.; Alkan, C.; Malig, M.; Tsalenko, A.; Sampas, N.; Bruhn, L.; Shendure, J.; 1000 Genomes Project, 1. G. P. et al.; Eichler, E. E.; Abecasis, G. R.; Altshuler, D. L.; Auton, A.; Brooks, L. D.; Durbin, R. M.; Gibbs, R. A.; Hurles, M. E.; McVean, G. A.: Diversity of human copy number variation and multicopy genes. Science 330 (6004), S. 641 - 646 (2010)

Wolfrum, K.; Wang, Y.; Prigione, A.; Sperling, K.; Lehrach, H.; Adjaye, J.: The LARGE principle of cellular reprogramming: lost, acquired and retained gene expression in foreskin and amniotic fluid-derived human iPS cells. PLoS ONE 5 (10), S. e13703 - e13703 (2010)

Durbin, R. M.; Abecasis, G. R.; Altshuler, D. L.; Auton, A.; Brooks, L. D.; Gibbs, R. A.; Hurles, M. E.; McVean, G. A.; Sudbrak, R. e. a.: A map of human genome variation from population-scale sequencing. Nature 467 (7319), S. 1061 - 1073 (2010)

Darvish, H. ..; Nieh, S. E.; Monajemi, G. B.; Mohseni, M.; Ghasemi-Firouzabadi, S.; Abedini, S. S.; Bahman, I.; P Jamali, P.; Azimi, S.; Mojahedi, F. et al.; Dehghan, A.; Shafeghati, Y.; Jankhah, A.; Falah, M.; Soltani Banavandi, M. J.; Ghani-Kakhi, M.; Garshasbi, M.; Rakhshani, F.; Naghavi, A.; Tzschach, A.; Neitzel, H.; Ropers, H.-H.; Kuss, A. W.; Behjati, F.; Kahrizi, K.; Najmabadi, H.: A clinical and molecular genetic study of 112 Iranian families with primary microcephaly. Journal of Medical Genetics. 47 (12), S. 823 - 828 (2010)

Bertram, L.; Lill, C. M.; Tanzi, R. E.: The genetics of Alzheimer disease: back to the future. Neuron 68 (2), S. 270 - 281 (2010)

Albrecht, B.; de Brouwer, A. P.; Lefeber, D. J.; Cremer, K.; Hausser, I.; Rossen, N.; Wortmann, S. B.; Wevers, R. A.; Kornak, U.; Morava, E.: MACS syndrome: A combined collagen and elastin disorder due to abnormal Golgi trafficking. American Journal of Medical Genetics. Part A. 152A (11), S. 2916 - 2918 (2010)

Kantaputra, P. N.; Mundlos, S.; Sripathomsawat, W.: A novel homozygous Arg222Trp missense mutation in WNT7A in two sisters with severe Al-Awadi/Raas-Rothschild/Schinzel phocomelia syndrome. American Journal of Medical Genetics Part A 152A (11), S. 2832 - 2837 (2010)

Bhushan, S.; Meyer, H.; Starosta, A. L.; Becker, T.; Mielke, T.; Berninghausen, O.; Sattler, M.; Wilson, D. N.; Beckmann, R.: Structural basis for translational stalling by human cytomegalovirus and fungal arginine attenuator peptide. (2010)

Kim, H.-G.; Ahn, J.-W.; Kurth, I.; Ullmann, R.; Kim, H.-T.; Kulharya, A.; Ha, K.-S.; Itokawa, Y.; Meliciani, I.; Wolfgang Wenzel, W. W. et al.; Lee, D.; Rosenberger, G.; Ozata, M.; Bick, D. P.; Sherins, R. J.; Nagase, T.; Tekin, M.; Kim, S.-H.; Kim, C.-H.; Ropers, H.-H.; Gusella, J. F.; Kalscheuer, V. M.; Choi, C. Y.; Layman, L. C.: WDR11, a WD protein that interacts with transcription factor EMX1, is mutated in idiopathic hypogonadotropic hypogonadism and Kallmann syndrome. American Society of Human Genetics 87 (4), S. 465 - 479 (2010)

Hein, G.; Silani, G.; Preuschoff, K.; Batson, C. D.; Singer, T.: Neural responses to ingroup and outgroup members' suffering predict individual differences in costly helping. Neuron 68 (1), S. 149 - 160 (2010)

Müller, H.; Schmidt, D.; Steinbrink, S.; Mirgorodskaya, E.; Lehmann, V.; Habermann, K.; Dreher, F.; Gustavsson, N.; Kessler, T.; Lehrach, H. et al.; Herwig, R.; Gobom, J.; Ploubidou, A.; Boutros, M.; Lange, B. M.: Proteomic and functional analysis of the mitotic Drosophila centrosome. The EMBO Journal 29 (19), S. 3344 - 3357 (2010)

Scherthan, H.; Sfeir, A.; Lange, T.: Rap1-independent telomere attachment and bouqet formation in mammalian meiosis. Chromosoma 119 (5), S. online - online (2010)

Endele, S.; Rosenberger, G.; Geider, K.; Popp, B.; Tamer, C.; Stefanova, I.; Milh, M.; Kortüm, F.; Fritsch, A.; Pientka, F. K. et al.; Hellenbroich, Y.; Kalscheuer, V. M.; Kohlhase, J.; Moog, U.; Rappold, G.; Rauch, A.; Ropers, H.-H.; von Spiczak, S.; Tönnies, H.; Villeneuve, N.; Villard, L.; Zabel, B.; Zenker, M.; Laube, B.; Reis, A.; Wieczorek, D.; Van Maldergem, L.; Kutsche, K.: Mutations in GRIN2A and GRIN2B encoding regulatory subunits of NMDA receptors cause variable neurodevelopmental phenotypes. Nature Genetics. 42 (11), S. 1021 - 1026 (2010)

Kerick, M.; Timmermann, B.; Schweiger, M. R.: High-throughput sequencing of frozen and paraffin-embedded tumor and normal tissue. Pathologe 31 (suppl 2), S. 255 - 257 (2010)

Makrantonaki, E.; Schonknecht, P.; Hossini, A. M.; Kaiser, E.; Katsouli, M. M.; Adjaye, J.; Schroder, J.; Zouboulis, C. C.: Skin and brain age together: The role of hormones in the ageing process. Experimental Gerontology 45 (10), S. 801 - 813 (2010)

Rybczynski, M.; Mir, T. S.; Sheikhzadeh, S.; Bernhardt, A. M.; Schad, C.; Treede, H.; Veldhoen, S.; Groene, E. F.; Kühne, K.; Koschyk, D. et al.; Robinson, P. N.; Berger, J.; Reichenspurner, H.; Meinertz, T.; von Kodolitsch, Y.: Frequency and age-related course of mitral valve dysfunction in the Marfan syndrome. American Journal of Cardiol 106 (7), S. 1048 - 1053 (2010)

Warnatz, H. J.; Querfurth, R.; Guerasimova, A.; Cheng, X.; Haas, S. A.; Hufton, A. L.; Manke, T.; Vanhecke, D.; Nietfeld, W.; Vingron, M. et al.; Janitz, M.; Lehrach, H.; Yaspo, M. L.: Functional analysis and identification of cis-regulatory elements of human chromosome 21 gene promoters. Nucleic Acids Research 38 (18), S. 6112 - 6123 (2010)

Bertram, L.; Heekeren, H.: Obesity and the brain: a possible genetic link. Alzheimer's Research & Therapy 2 (5), S. 2:27 - 2:27 (2010)

Mertes, F.; Biens, K.; Lehrach, H.; Wagner, M.; Dahl, A.: High-throughput Universal Probe Salmonella Serotyping (UPSS) by nanoPCR. J Microbiol Methods 83 (2), S. 217 - 223 (2010)