Risultati della ricerca - Bertram Müller‐Myhsok

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  1. 1
    Rapid Simulation of P Values for Product Methods and Multiple-Testing Adjustment in Association Studies

    Rapid Simulation of P Values for Product Methods and Multiple-Testing Adjustment in Association Studies di Shaun R. Seaman, Bertram Müller‐Myhsok

    Pubblicazione 2005
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  2. 2
    Connexin 26 R143W Mutation Associated with Recessive Nonsyndromic Sensorineural Deafness in Africa

    Connexin 26 R143W Mutation Associated with Recessive Nonsyndromic Sensorineural Deafness in Africa di G W Brobby, Bertram Müller‐Myhsok, Rolf D. Horstmann

    Pubblicazione 1998
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  3. 3
    Advancing social behavioral neuroscience by integrating ethology and comparative psychology methods through machine learning

    Advancing social behavioral neuroscience by integrating ethology and comparative psychology methods through machine learning di Joeri Bordes, Lucas Miranda, Bertram Müller‐Myhsok, Mathias V. Schmidt

    Pubblicazione 2023
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  4. 4
    Systematic Review of Functional MRI Applications for Psychiatric Disease Subtyping

    Systematic Review of Functional MRI Applications for Psychiatric Disease Subtyping di Lucas Miranda, Riya Paul, Benno Pütz, Nikolaos Koutsouleris, Bertram Müller‐Myhsok

    Pubblicazione 2021
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  5. 5
    Integration of a polygenic score into guideline-recommended prediction of cardiovascular disease

    Integration of a polygenic score into guideline-recommended prediction of cardiovascular disease di Ling Li, Shichao Pang, Fabian Starnecker, Bertram Müller‐Myhsok, Heribert Schunkert

    Pubblicazione 2024
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  6. 6
    Genomewide Linkage Analysis Identifies Polymorphism in the Human Interferon-γ Receptor Affecting Helicobacter pylori Infection

    Genomewide Linkage Analysis Identifies Polymorphism in the Human Interferon-γ Receptor Affecting Helicobacter pylori Infection di Thorsten Thye, Gerd Burchard, Manfred Nilius, Bertram Müller‐Myhsok, Rolf D. Horstmann

    Pubblicazione 2003
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  7. 7
    Heritability of MRI Lesion Volume in CADASIL

    Heritability of MRI Lesion Volume in CADASIL di Christian Opherk, Nils Peters, Markus Holtmannspötter, Andreas Gschwendtner, Bertram Müller‐Myhsok, Martin Dichgans

    Pubblicazione 2006
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  8. 8
    Early Onset of Severe Familial Amyotrophic Lateral Sclerosis with a SOD-1 Mutation: Potential Impact of CNTF as a Candidate Modifier Gene

    Early Onset of Severe Familial Amyotrophic Lateral Sclerosis with a SOD-1 Mutation: Potential Impact of CNTF as a Candidate Modifier Gene di Ralf Giess, Bettina Holtmann, M. Braga, T. Grimm, Bertram Müller‐Myhsok, Klaus V. Toyka, Michael Sendtner

    Pubblicazione 2002
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  9. 9
    Evidence for the Late MMN as a Neurophysiological Endophenotype for Dyslexia

    Evidence for the Late MMN as a Neurophysiological Endophenotype for Dyslexia di Nina Neuhoff, Jennifer Bruder, Jürgen Bartling, Andreas Warnke, Helmut Remschmidt, Bertram Müller‐Myhsok, Gerd Schulte‐Körne

    Pubblicazione 2012
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  10. 10
    Population Bias in Polygenic Risk Prediction Models for Coronary Artery Disease

    Population Bias in Polygenic Risk Prediction Models for Coronary Artery Disease di Damian Gola, Jeanette Erdmann, Kristi Läll, Reedik Mägi, Bertram Müller‐Myhsok, Heribert Schunkert, Inke R. König

    Pubblicazione 2020
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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 di Andreas Gschwendtner, Stephan Ripke, Tobias Freilinger, Peter Lichtner, Bertram Müller‐Myhsok, H.‐Erich Wichmann, Thomas Meitinger, Martin Dichgans

    Pubblicazione 2008
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  12. 12
    De Novo Rearrangements Found in 2% of Index Patients with Spinal Muscular Atrophy: Mutational Mechanisms, Parental Origin, Mutation Rate, and Implications for Genetic Counseling

    De Novo Rearrangements Found in 2% of Index Patients with Spinal Muscular Atrophy: Mutational Mechanisms, Parental Origin, Mutation Rate, and Implications for Genetic Counseling di Brunhilde Wirth, Thorsten Schmidt, Eric Hahnen, Sabine Rudnik–Schöneborn, Michael Krawczak, Bertram Müller-Myhsok, Jutta Schönling, Klaus Zerres

    Pubblicazione 1997
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  13. 13
    Evidence for Linkage of Spelling Disability to Chromosome 15

    Evidence for Linkage of Spelling Disability to Chromosome 15 di Gerd Schulte‐Körne, T. Grimm, Markus M. Nöthen, Bertram Müller‐Myhsok, Sven Cichon, Ina R. Vogt, Peter Propping, Helmut Remschmidt

    Pubblicazione 1998
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  14. 14
    Epidemiology of amebiasis in a region of high incidence of amebic liver abscess in central Vietnam.

    Epidemiology of amebiasis in a region of high incidence of amebic liver abscess in central Vietnam. di Joerg Blessmann, Pham Van Linh, Phuong Anh Ton Nu, Hao Duong Thi, Bertram Müller‐Myhsok, Heidrun Buß, Egbert Tannich

    Pubblicazione 2002
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  15. 15
    Polymorphisms in GRIK4, HTR2A, and FKBP5 Show Interactive Effects in Predicting Remission to Antidepressant Treatment

    Polymorphisms in GRIK4, HTR2A, and FKBP5 Show Interactive Effects in Predicting Remission to Antidepressant Treatment di Sonja Horstmann, Susanne Lucae, Andreas Menke, Johannes M. Hennings, Marcus Ising, Darina Roeske, Bertram Müller-Myhsok, Herta Flor, Elisabeth B. Binder

    Pubblicazione 2009
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  16. 16
    “DNA Methylation signatures in panic disorder”

    “DNA Methylation signatures in panic disorder” di Stella Iurato, Tania Carrillo‐Roa, Janine Arloth, Darina Czamara, Laura Diener-Hölzl, Jennifer Lange, Bertram Müller‐Myhsok, Elisabeth B. Binder, Angelika Erhardt

    Pubblicazione 2017
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  17. 17
    Gender-Specific Association of Galanin Polymorphisms with HPA-Axis Dysregulation, Symptom Severity, and Antidepressant Treatment Response

    Gender-Specific Association of Galanin Polymorphisms with HPA-Axis Dysregulation, Symptom Severity, and Antidepressant Treatment Response di Paul G. Unschuld, Marcus Ising, Darina Roeske, Angelika Erhardt, Michael Specht, Stefan Kloiber, Manfred Uhr, Bertram Müller‐Myhsok, Herta Flor, Elisabeth B. Binder

    Pubblicazione 2010
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  18. 18
    CLOCK Gene Variants Associate with Sleep Duration in Two Independent Populations

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

    Pubblicazione 2010
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  19. 19
    Genome-Wide Association Study of Antidepressant Treatment-Emergent Suicidal Ideation

    Genome-Wide Association Study of Antidepressant Treatment-Emergent Suicidal Ideation di Andreas Menke, Katharina Domschke, Darina Czamara, Torsten Klengel, Johannes M. Hennings, Susanne Lucae, Bernhard T. Baune, Volker Arolt, Bertram Müller‐Myhsok, Herta Flor, Elisabeth B. Binder

    Pubblicazione 2011
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  20. 20
    Gene Expression Patterns Associated with Posttraumatic Stress Disorder Following Exposure to the World Trade Center Attacks

    Gene Expression Patterns Associated with Posttraumatic Stress Disorder Following Exposure to the World Trade Center Attacks di Rachel Yehuda, Guiqing Cai, Julia A. Golier, Casey Sarapas, Sandro Galea, Marcus Ising, Theo Rein, James Schmeidler, Bertram Müller‐Myhsok, Herta Flor, Joseph D. Buxbaum

    Pubblicazione 2009
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