檢索結果 - Thomas Meitinger

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  1. 1
    Genome-wide association studies of atrial fibrillation: past, present, and future

    Genome-wide association studies of atrial fibrillation: past, present, and future 由 Moritz F. Sinner, Patrick T. Ellinor, Thomas Meitinger, Emelia J. Benjamin, Stefan Kääb

    出版 2011
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  2. 2
    Characterization of circular RNAs in human, mouse and rat hearts

    Characterization of circular RNAs in human, mouse and rat hearts 由 Stanislas Werfel, Stephan Nothjunge, Thomas Schwarzmayr, Tim-Matthias Strom, Thomas Meitinger, Stefan Engelhardt

    出版 2016
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  3. 3
    Lifetime risk of autosomal recessive neurodegeneration with brain iron accumulation (NBIA) disorders calculated from genetic databases

    Lifetime risk of autosomal recessive neurodegeneration with brain iron accumulation (NBIA) disorders calculated from genetic databases 由 Hana Kolářová, Jing Tan, Tim M. Strom, Thomas Meitinger, Matias Wagner, Thomas Klopstock

    出版 2022
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  4. 4
    A One Base Pair Deletion in the Canine ATP13A2 Gene Causes Exon Skipping and Late-Onset Neuronal Ceroid Lipofuscinosis in the Tibetan Terrier

    A One Base Pair Deletion in the Canine ATP13A2 Gene Causes Exon Skipping and Late-Onset Neuronal Ceroid Lipofuscinosis in the Tibetan Terrier 由 Anne Wöhlke, U. Philipp, Patricia Bock, Andreas Beineke, Peter Lichtner, Thomas Meitinger, O. Distl

    出版 2011
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  5. 5
    Whole genome sequencing of a single Bos taurus animal for single nucleotide polymorphism discovery

    Whole genome sequencing of a single Bos taurus animal for single nucleotide polymorphism discovery 由 Sebastian Eck, Anna Benet‐Pagès, Krzysztof Flisikowski, Thomas Meitinger, Ruedi Fries, Tim M. Strom

    出版 2009
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  6. 6
    Mitochondrial Genetic Variants Identified to Be Associated with BMI in Adults

    Mitochondrial Genetic Variants Identified to Be Associated with BMI in Adults 由 Antònia Flaquer, Clemens Baumbach, Jennifer Kriebel, Thomas Meitinger, Annette Peters, Mélanie Waldenberger, Harald Grallert, Konstantin Strauch

    出版 2014
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  7. 7
    The retinitis pigmentosa GTPase regulator, RPGR, interacts with the delta subunit of rod cyclic GMP phosphodiesterase

    The retinitis pigmentosa GTPase regulator, RPGR, interacts with the delta subunit of rod cyclic GMP phosphodiesterase 由 Marco Linari, Marius Ueffing, Forbes D.C. Manson, Alan F. Wright, Thomas Meitinger, Jörg D. Becker

    出版 1999
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  8. 8
    Pex Gene Deletions in Gy and Hyp Mice Provide Mouse Models for X-Linked Hypophosphatemia

    Pex Gene Deletions in Gy and Hyp Mice Provide Mouse Models for X-Linked Hypophosphatemia 由 Tim M. Strom, Fiona Francis, Bettina Lorenz, Annett Böddrich, Hans Lehrach, Michael J. Econs, Thomas Meitinger

    出版 1997
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  9. 9
    Infantile Leigh-like syndrome caused by SLC19A3 mutations is a treatable disease

    Infantile Leigh-like syndrome caused by SLC19A3 mutations is a treatable disease 由 Tobias B. Haack, Dirk Klee, Tim M. Strom, Ertan Mayatepek, Thomas Meitinger, Holger Prokisch, Felix Distelmaier

    出版 2014
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  10. 10
    Chronic recurrent multifocal osteomyelitis (CRMO): evidence for a susceptibility gene located on chromosome 18q21.3-18q22

    Chronic recurrent multifocal osteomyelitis (CRMO): evidence for a susceptibility gene located on chromosome 18q21.3-18q22 由 Astrid Golla, Annette Jansson, Juliane Ramser, Heide Hellebrand, R. Zahn, Thomas Meitinger, Bernd H. Belohradsky, Alfons Meindl

    出版 2002
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  11. 11
    Genetic Variation in Soluble Epoxide Hydrolase ( <i>EPHX2</i> ) Is Associated With an Increased Risk of Ischemic Stroke in White Europeans

    Genetic Variation in Soluble Epoxide Hydrolase ( <i>EPHX2</i> ) Is Associated With an Increased Risk of Ischemic Stroke in White Europeans 由 Andreas Gschwendtner, Stephan Ripke, Tobias Freilinger, Peter Lichtner, Bertram Müller‐Myhsok, H.‐Erich Wichmann, Thomas Meitinger, Martin Dichgans

    出版 2008
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  12. 12
    Hypothetical LOC387715 is a second major susceptibility gene for age-related macular degeneration, contributing independently of complement factor H to disease risk

    Hypothetical LOC387715 is a second major susceptibility gene for age-related macular degeneration, contributing independently of complement factor H to disease risk 由 Andrea Rivera, Sheila Fisher, Lars G. Fritsche, Claudia N. Keilhauer, Peter Lichtner, Thomas Meitinger, Bernhard H. F. Weber

    出版 2005
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  13. 13
    Exome sequencing revealed a splice site variant in the IQCE gene underlying post-axial polydactyly type A restricted to lower limb

    Exome sequencing revealed a splice site variant in the IQCE gene underlying post-axial polydactyly type A restricted to lower limb 由 Muhammad Umair, Khadim Shah, Bader Alhaddad, Tobias B. Haack, Elisabeth Graf, Tim M. Strom, Thomas Meitinger, Wasim Ahmad

    出版 2017
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  14. 14
    The epsilon-sarcoglycan gene (SGCE), mutated in myoclonus-dystonia syndrome, is maternally imprinted

    The epsilon-sarcoglycan gene (SGCE), mutated in myoclonus-dystonia syndrome, is maternally imprinted 由 Monika Grabowski, Alexander Zimprich, Bettina Lorenz‐Depiereux, Vera M. Kalscheuer, Friedrich Asmus, Thomas Gasser, Thomas Meitinger, Tim M. Strom

    出版 2003
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  15. 15
    The Parkinson disease causing LRRK2 mutation I2020T is associated with increased kinase activity

    The Parkinson disease causing LRRK2 mutation I2020T is associated with increased kinase activity 由 Christian Johannes Gloeckner, Norbert Kinkl, Annette Schumacher, Ralf J. Braun, Eric O’Neill, Thomas Meitinger, Walter Kölch, Holger Prokisch, Marius Ueffing

    出版 2005
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  16. 16
    Lifetime risk of autosomal recessive mitochondrial disorders calculated from genetic databases

    Lifetime risk of autosomal recessive mitochondrial disorders calculated from genetic databases 由 Jing Tan, Matias Wagner, Sarah L. Stenton, Tim M. Strom, Saskia B. Wortmann, Holger Prokisch, Thomas Meitinger, Konrad Oexle, Thomas Klopstock

    出版 2020
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  17. 17
    Fatal neonatal encephalopathy and lactic acidosis caused by a homozygous loss-of-function variant in COQ9

    Fatal neonatal encephalopathy and lactic acidosis caused by a homozygous loss-of-function variant in COQ9 由 Katharina Danhauser, Diran Herebıan, Tobias B. Haack, Richard J. Rodenburg, Tim M. Strom, Thomas Meitinger, Dirk Klee, Ertan Mayatepek, Holger Prokisch, Felix Distelmaier

    出版 2015
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  18. 18
    Assessment of the genomic variation in a cattle population by re-sequencing of key animals at low to medium coverage

    Assessment of the genomic variation in a cattle population by re-sequencing of key animals at low to medium coverage 由 Sandra Jansen, Bernhard Aigner, Hubert Pausch, Michał Wysocki, Sebastian Eck, Anna Benet‐Pagès, Elisabeth Graf, Thomas Wieland, Tim M. Strom, Thomas Meitinger, Ruedi Fries

    出版 2013
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  19. 19
    Copy-Number Variations Measured by Single-Nucleotide–Polymorphism Oligonucleotide Arrays in Patients with Mental Retardation

    Copy-Number Variations Measured by Single-Nucleotide–Polymorphism Oligonucleotide Arrays in Patients with Mental Retardation 由 Janine Wagenstaller, Stephanie Spranger, Bettina Lorenz‐Depiereux, Bernd Kazmierczak, Michaela Nathrath, Dagmar Wahl, Babett Heye, Dieter Gläser, Volkmar Liebscher, Thomas Meitinger, Tim M. Strom

    出版 2007
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  20. 20
    CLOCK Gene Variants Associate with Sleep Duration in Two Independent Populations

    CLOCK Gene Variants Associate with Sleep Duration in Two Independent Populations 由 Karla V. Allebrandt, Maris Teder‐Laving, Mahmut Akyol, Irene Pichler, Bertram Müller-Myhsok, Peter P. Pramstaller, Martha Merrow, Thomas Meitinger, Andreas Metspalu, Till Roenneberg

    出版 2010
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