Ohcanbohtosat - Kennerknecht, Ingo

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  1. 1
    Clinical utility gene card for: Ehlers–Danlos syndrome types I–VII

    Clinical utility gene card for: Ehlers–Danlos syndrome types I–VII Dahkki Mayer, Karin, Kennerknecht, Ingo, Steinmann, Beat

    Almmustuhtton 2010
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  2. 2
    Clinical utility gene card for: Ehlers–Danlos syndrome types I–VII and variants - update 2012

    Clinical utility gene card for: Ehlers–Danlos syndrome types I–VII and variants - update 2012 Dahkki Mayer, Karin, Kennerknecht, Ingo, Steinmann, Beat

    Almmustuhtton 2013
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  3. 3
    The Early Time Course of Compensatory Face Processing in Congenital Prosopagnosia

    The Early Time Course of Compensatory Face Processing in Congenital Prosopagnosia Dahkki Stollhoff, Rainer, Jost, Jürgen, Elze, Tobias, Kennerknecht, Ingo

    Almmustuhtton 2010
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  4. 4
    Deficits in Long-Term Recognition Memory Reveal Dissociated Subtypes in Congenital Prosopagnosia

    Deficits in Long-Term Recognition Memory Reveal Dissociated Subtypes in Congenital Prosopagnosia Dahkki Stollhoff, Rainer, Jost, Jürgen, Elze, Tobias, Kennerknecht, Ingo

    Almmustuhtton 2011
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  5. 5
    Galactose uncovers face recognition and mental images in congenital prosopagnosia: The first case report

    Galactose uncovers face recognition and mental images in congenital prosopagnosia: The first case report Dahkki Esins, Janina, Schultz, Johannes, Bülthoff, Isabelle, Kennerknecht, Ingo

    Almmustuhtton 2014
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  6. 6
    Face Perception and Test Reliabilities in Congenital Prosopagnosia in Seven Tests

    Face Perception and Test Reliabilities in Congenital Prosopagnosia in Seven Tests Dahkki Esins, Janina, Schultz, Johannes, Stemper, Claudia, Kennerknecht, Ingo, Bülthoff, Isabelle

    Almmustuhtton 2016
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  7. 7
    Neoplasia in Cri du Chat Syndrome from Italian and German Databases

    Neoplasia in Cri du Chat Syndrome from Italian and German Databases Dahkki Guala, Andrea, Spunton, Marianna, Kalantari, Silvia, Kennerknecht, Ingo, Danesino, Cesare

    Almmustuhtton 2017
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  8. 8
    Corrigendum: Do congenital prosopagnosia and the other-race effect affect the same face recognition mechanisms?

    Corrigendum: Do congenital prosopagnosia and the other-race effect affect the same face recognition mechanisms? Dahkki Esins, Janina, Schultz, Johannes, Stemper, Claudia, Kennerknecht, Ingo, Wallraven, Christian, Bülthoff, Isabelle

    Almmustuhtton 2015
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  9. 9
    Face Processing in Developmental Prosopagnosia: Altered Neural Representations in the Fusiform Face Area

    Face Processing in Developmental Prosopagnosia: Altered Neural Representations in the Fusiform Face Area Dahkki Haeger, Alexa, Pouzat, Christophe, Luecken, Volker, N’Diaye, Karim, Elger, Christian, Kennerknecht, Ingo, Axmacher, Nikolai, Dinkelacker, Vera

    Almmustuhtton 2021
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  10. 10
    MBTPS2 mutations cause defective regulated intramembrane proteolysis in X-linked osteogenesis imperfecta

    MBTPS2 mutations cause defective regulated intramembrane proteolysis in X-linked osteogenesis imperfecta Dahkki Lindert, Uschi, Cabral, Wayne A., Ausavarat, Surasawadee, Tongkobpetch, Siraprapa, Ludin, Katja, Barnes, Aileen M., Yeetong, Patra, Weis, Maryann, Krabichler, Birgit, Srichomthong, Chalurmpon, Makareeva, Elena N., Janecke, Andreas R., Leikin, Sergey, Röthlisberger, Benno, Rohrbach, Marianne, Kennerknecht, Ingo, Eyre, David R., Suphapeetiporn, Kanya, Giunta, Cecilia, Marini, Joan C., Shotelersuk, Vorasuk

    Almmustuhtton 2016
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  11. 11
    Genotype–phenotype correlations in Down syndrome identified by array CGH in 30 cases of partial trisomy and partial monosomy chromosome 21

    Genotype–phenotype correlations in Down syndrome identified by array CGH in 30 cases of partial trisomy and partial monosomy chromosome 21 Dahkki Lyle, Robert, Béna, Frédérique, Gagos, Sarantis, Gehrig, Corinne, Lopez, Gipsy, Schinzel, Albert, Lespinasse, James, Bottani, Armand, Dahoun, Sophie, Taine, Laurence, Doco-Fenzy, Martine, Cornillet-Lefèbvre, Pascale, Pelet, Anna, Lyonnet, Stanislas, Toutain, Annick, Colleaux, Laurence, Horst, Jürgen, Kennerknecht, Ingo, Wakamatsu, Nobuaki, Descartes, Maria, Franklin, Judy C, Florentin-Arar, Lina, Kitsiou, Sophia, Aït Yahya-Graison, Emilie, Costantine, Maher, Sinet, Pierre-Marie, Delabar, Jean M, Antonarakis, Stylianos E

    Almmustuhtton 2009
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  12. 12
    Next‐generation sequencing reveals the mutational landscape of clinically diagnosed Usher syndrome: copy number variations, phenocopies, a predominant target for translational read‐through, and PEX26 mutated in Heimler syndrome

    Next‐generation sequencing reveals the mutational landscape of clinically diagnosed Usher syndrome: copy number variations, phenocopies, a predominant target for translational read... Dahkki Neuhaus, Christine, Eisenberger, Tobias, Decker, Christian, Nagl, Sandra, Blank, Cornelia, Pfister, Markus, Kennerknecht, Ingo, Müller‐Hofstede, Cornelie, Charbel Issa, Peter, Heller, Raoul, Beck, Bodo, Rüther, Klaus, Mitter, Diana, Rohrschneider, Klaus, Steinhauer, Ute, Korbmacher, Heike M., Huhle, Dagmar, Elsayed, Solaf M., Taha, Hesham M., Baig, Shahid M., Stöhr, Heidi, Preising, Markus, Markus, Susanne, Moeller, Fabian, Lorenz, Birgit, Nagel‐Wolfrum, Kerstin, Khan, Arif O., Bolz, Hanno J.

    Almmustuhtton 2017
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