New insights into the Tyrolean Iceman's origin and phenotype as inferred by whole-genome sequencing von Keller, Andreas, Graefen, Angela, Ball, Markus, Matzas, Mark, Boisguerin, Valesca, Maixner, Frank, Leidinger, Petra, Backes, Christina, Khairat, Rabab, Forster, Michael, Stade, Björn, Franke, Andre, Mayer, Jens, Spangler, Jessica, McLaughlin, Stephen, Shah, Minita, Lee, Clarence, Harkins, Timothy T., Sartori, Alexander, Moreno-Estrada, Andres, Henn, Brenna, Sikora, Martin, Semino, Ornella, Chiaroni, Jacques, Rootsi, Siiri, Myres, Natalie M., Cabrera, Vicente M., Underhill, Peter A., Bustamante, Carlos D., Vigl, Eduard Egarter, Samadelli, Marco, Cipollini, Giovanna, Haas, Jan, Katus, Hugo, O'Connor, Brian D., Carlson, Marc R.J., Meder, Benjamin, Blin, Nikolaus, Meese, Eckart, Pusch, Carsten M., Zink, Albert

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The complete form of X-linked congenital stationary night blindness is caused by mutations in a gene encoding a leucine-rich repeat protein von Pusch, Carsten M., Zeitz, Christina, Brandau, Oliver, Pesch, Katrin, Achatz, Helene, Feil, Silke, Scharfe, Curt, Maurer, Johannes, Jacobi, Felix K., Pinckers, Alfred, Andreasson, Sten, Hardcastle, Alison, Wissinger, Bernd, Berger, Wolfgang, Meindl, Alfons

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Comment on "The brain of LB1, Homo floresiensis" von Weber, Jochen, Czarnetzki, Alfred, Pusch, Carsten M

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Nonmuscle Myosin Heavy-Chain Gene MYH14 Is Expressed in Cochlea and Mutated in Patients Affected by Autosomal Dominant Hearing Impairment (DFNA4) von Donaudy, Francesca, Snoeckx, Rik, Pfister, Markus, Zenner, Hans-Peter, Blin, Nikolaus, Di Stazio, Mariateresa, Ferrara, Antonella, Lanzara, Carmen, Ficarella, Romina, Declau, Frank, Pusch, Carsten M., Nürnberg, Peter, Melchionda, Salvatore, Zelante, Leopoldo, Ballana, Ester, Estivill, Xavier, Van Camp, Guy, Gasparini, Paolo, Savoia, Anna

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Spiking of contemporary human template DNA with ancient DNA extracts induces mutations under PCR and generates nonauthentic mitochondrial sequences von Pusch, Carsten M, Bachmann, Lutz

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A genetic perspective on myopia von Jacobi, F K, Zrenner, E, Broghammer, M, Pusch, C M

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Substitutions in the Conserved C2C Domain of Otoferlin Cause DFNB9, a Form of Nonsyndromic Autosomal Recessive Deafness von Mirghomizadeh, F., Pfister, M., Apaydin, F., Petit, C., Kupka, S., Pusch, C.M., Zenner, H.P., Blin, N.

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Yersinial F1 antigen and the cause of Black Death von Pusch, Carsten M, Rahalison, Lila, Blin, Nikolaus, Nicholson, Graeme J, Czarnetzki, Alfred

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Archaeology and Prevalence of Paget's Disease von Pusch, Carsten M, Czarnetzki, Alfred

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Thirty distinct CACNA1F mutations in 33 families with incomplete type of XLCSNB and Cacna1f expression profiling in mouse retina von Wutz, Krisztina, Sauer, Christian, Zrenner, Eberhart, Lorenz, Birgit, Alitalo, Tiina, Broghammer, Martina, Hergersberg, Martin, Chapelle, Albert de La, Weber, Bernhard H F, Wissinger, Bernd, Meindl, Alfons, Pusch, Carsten M

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Fossil record of meningioma von Czarnetzki, Alfred, Schwaderer, Erwin, Pusch, Carsten M

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Segregation Patterns and Heteroplasmy Prevalence in Leber's Hereditary Optic Neuropathy von Jacobi, Felix K, Leo-Kottler, Beate, Mittelviefhaus, Karin, Zrenner, Eberhart, Meyer, Jens, Pusch, Carsten M, Wissinger, Bernd

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Down's syndrome in ancient Europe von Czarnetzki, A, Blin, N, Pusch, CM

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Genetic heterogeneity of deafness phenotypes linked to DFNA4 von Yang, Tao, Pfister, Markus, Blin, Nikolaus, Zenner, Hans P., Pusch, Carsten M., Smith, Richard J.H.

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Repair of degraded duplex DNA from prehistoric samples using Escherichia coli DNA polymerase I and T4 DNA ligase von Pusch, Carsten M., Giddings, Ian, Scholz, Michael

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Slow and Fast Rod ERG Pathways in Patients with X-Linked Complete Stationary Night Blindness Carrying Mutations in the NYX Gene von Scholl, Hendrik P. N, Langrova, Hana, Pusch, Carsten M, Wissinger, Bernd, Zrenner, Eberhart, Apfelstedt-Sylla, Eckart

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Palaeopathological and variant conditions of the Homo heidelbergensis type specimen (Mauer, Germany) von Czarnetzki, A., Jakob, T., Pusch, C.M.

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A Polymerase Chain Reaction Inhibitor of Ancient Hard and Soft Tissue DNA Extracts Is Determined as Human Collagen Type I von Scholz, Michael, Giddings, Ian, Pusch, Carsten M.

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PCR-induced sequence alterations hamper the typing of prehistoric bone samples for diagnostic achondroplasia mutations von Pusch, C M, Broghammer, M, Nicholson, G J, Nerlich, A G, Zink, A, Kennerknecht, I, Bachmann, L, Blin, N

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Isolation of the Mouse Nyctalopin Gene Nyx and Expression Studies in Mouse and Rat Retina von Pesch, Katrin, Zeitz, Christina, Fries, Julia E, Munscher, Stefanie, Pusch, Carsten M, Kohler, Konrad, Berger, Wolfgang, Wissinger, Bernd

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