Works matching AU Schumacher, Johannes
Results: 75
Synthetische Analoga zeigen die essentiellen Strukturmotive von Lugdunin und seinen Protonentransport.
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- Angewandte Chemie, 2019, v. 131, n. 27, p. 9333, doi. 10.1002/ange.201901589
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- Article
MCM3AP and POMP Mutations Cause a DNA-Repair and DNA-Damage-Signaling Defect in an Immunodeficient Child.
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- Human Mutation, 2016, v. 37, n. 3, p. 257, doi. 10.1002/humu.22939
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Inhibition of RAS Activation Due to a Homozygous Ezrin Variant in Patients with Profound Intellectual Disability.
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- Human Mutation, 2015, v. 36, n. 2, p. 270, doi. 10.1002/humu.22737
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Comparison of the Real-World Reporting of Symptoms and Well-Being for the HER2-Directed Trastuzumab Biosimilar Ogivri With Registry Data for Herceptin in the Treatment of Breast Cancer: Prospective Observational Study (OGIPRO) of Electronic Patient-Reported Outcomes
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- JMIR Cancer, 2024, v. 10, n. 1, p. 1, doi. 10.2196/54178
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Re‐sequencing of candidate genes FOXF1, HSPA6, HAAO, and KYNU in 522 individuals with VATER/VACTERL, VACTER/VACTERL‐like association, and isolated anorectal malformation.
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- Birth Defects Research, 2022, v. 114, n. 10, p. 478, doi. 10.1002/bdr2.2008
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Exome sequencing in syndromic brain malformations identifies novel mutations in <italic>ACTB</italic>, and <italic>SLC9A6</italic>, and suggests <italic>BAZ1A</italic> as a new candidate gene.
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- Birth Defects Research, 2018, v. 110, n. 7, p. 587, doi. 10.1002/bdr2.1200
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Combination of Multi-Temporal Sentinel 2 Images and Aerial Image Based Canopy Height Models for Timber Volume Modelling.
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- Forests (19994907), 2019, v. 10, n. 9, p. 746, doi. 10.3390/f10090746
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- Article
Achalasia: will genetic studies provide insights?
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- Human Genetics, 2010, v. 128, n. 4, p. 353, doi. 10.1007/s00439-010-0874-8
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No evidence for DUP25 in patients with panic disorder using a quantitative real-time PCR approach.
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- Human Genetics, 2003, v. 114, n. 1, p. 115, doi. 10.1007/s00439-003-1022-5
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Mood-incongruent psychosis in bipolar disorder: conditional linkage analysis shows genome-wide suggestive linkage at 1q32.3, 7p13 and 20q13.31.
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- Bipolar Disorders, 2009, v. 11, n. 6, p. 610, doi. 10.1111/j.1399-5618.2009.00736.x
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Weakly time consistent concave valuations and their dual representations.
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- Finance & Stochastics, 2016, v. 20, n. 1, p. 123, doi. 10.1007/s00780-015-0285-8
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Solving Maxmin Optimization Problems via Population Games.
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- Journal of Optimization Theory & Applications, 2024, v. 201, n. 2, p. 760, doi. 10.1007/s10957-024-02415-4
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Within-canopy and ozone fumigation effects on δ13C and Δ18O in adult beech (Fagus sylvatica) trees: relation to meteorological and gas exchange parameters.
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- Tree Physiology, 2009, v. 29, n. 11, p. 1349, doi. 10.1093/treephys/tpp066
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Single-cell analysis reveals the spatial-temporal expression of genes associated with esophageal malformations.
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- Scientific Reports, 2024, v. 14, n. 1, p. 1, doi. 10.1038/s41598-024-53098-w
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Polymorphisms in DCDC2 and S100B associate with developmental dyslexia.
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- Journal of Human Genetics, 2015, v. 60, n. 7, p. 399, doi. 10.1038/jhg.2015.37
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The DISC locus and schizophrenia: evidence from an association study in a central European sample and from a meta-analysis across different European populations.
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- Human Molecular Genetics, 2009, v. 18, n. 14, p. 2719, doi. 10.1093/hmg/ddp204
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Brain-specific tryptophan hydroxylase 2 (TPH2): a functional Pro206Ser substitution and variation in the 5′-region are associated with bipolar affective disorder.
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- Human Molecular Genetics, 2008, v. 17, n. 1, p. 87
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- Article
A locus on 2p12 containing the co-regulated MRPL19 and C2ORF3 genes is associated to dyslexia.
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- Human Molecular Genetics, 2007, v. 16, n. 6, p. 667, doi. 10.1093/hmg/ddm009
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A genome screen for genes predisposing to bipolar affective disorder detects a new susceptibility locus on 8q.
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- Human Molecular Genetics, 2002, v. 11, n. 14, p. 1685, doi. 10.1093/hmg/11.14.1685
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Can long-range microsatellite data be used to predict short-range linkage disequilibrium?
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- Human Molecular Genetics, 2002, v. 11, n. 12, p. 1363, doi. 10.1093/hmg/11.12.1363
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The utility of forest attribute maps for automated Avalanche Terrain Exposure Scale (ATES) modelling.
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- Scandinavian Journal of Forest Research, 2022, v. 37, n. 4, p. 264, doi. 10.1080/02827581.2022.2096921
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Achalasie - Eine oft zu spät diagnostizierte und ätiologisch ungeklärte Krankheit.
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- Deutsches Ärzteblatt International, 2012, v. 109, n. 31/32, p. 534, doi. 10.3238/arztebl.2012.0534a
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Achalasie - eine oft zu spät diagnostizierte und ätiologisch ungeklärte Krankheit.
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- Deutsches Ärzteblatt International, 2012, v. 109, n. 12, p. 209, doi. 10.3238/arztebl.2012.0209
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- Article
Significance of anger suppression and preoccupied attachment in social anxiety disorder: a cross-sectional study.
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- BMC Psychiatry, 2021, v. 21, n. 1, p. 1, doi. 10.1186/s12888-021-03098-1
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Significance of anger suppression and preoccupied attachment in social anxiety disorder: a cross-sectional study.
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- BMC Psychiatry, 2021, v. 21, n. 1, p. 1, doi. 10.1186/s12888-021-03098-1
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An autoimmune disease risk variant: A trans master regulatory effect mediated by IRF1 under immune stimulation?
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- PLoS Genetics, 2021, v. 17, n. 7, p. 1, doi. 10.1371/journal.pgen.1009684
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Haplotype interaction analysis of unlinked regions.
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- Genetic Epidemiology, 2005, v. 29, n. 4, p. 313, doi. 10.1002/gepi.20096
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AI-based multi-PRS models outperform classical single-PRS models.
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- Frontiers in Genetics, 2023, p. 1, doi. 10.3389/fgene.2023.1217860
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Genetic regulatory effects modified by immune activation contribute to autoimmune disease associations.
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- Nature Communications, 2017, v. 8, n. 1, p. 1, doi. 10.1038/s41467-017-00366-1
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Characterizing the genetic basis of innate immune response in TLR4-activated human monocytes.
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- Nature Communications, 2014, v. 5, n. 10, p. 5236, doi. 10.1038/ncomms6236
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Genome-wide association study reveals two new risk loci for bipolar disorder.
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- Nature Communications, 2014, v. 5, n. 3, p. 3339, doi. 10.1038/ncomms4339
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Wall-to-wall tree type classification using airborne lidar data and CIR images.
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- International Journal of Remote Sensing, 2014, v. 35, n. 9, p. 3057, doi. 10.1080/01431161.2014.894670
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A systematic eQTL study of cis-trans epistasis in 210 HapMap individuals.
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- European Journal of Human Genetics, 2012, v. 20, n. 1, p. 97, doi. 10.1038/ejhg.2011.156
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Homozygosity mapping in 64 Syrian consanguineous families with non-specific intellectual disability reveals 11 novel loci and high heterogeneity.
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- European Journal of Human Genetics, 2011, v. 19, n. 11, p. 1161, doi. 10.1038/ejhg.2011.98
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Synthetic Lugdunin Analogues Reveal Essential Structural Motifs for Antimicrobial Action and Proton Translocation Capability.
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- Angewandte Chemie International Edition, 2019, v. 58, n. 27, p. 9234, doi. 10.1002/anie.201901589
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- Article
Synthetic Lugdunin Analogues Reveal Essential Structural Motifs for Antimicrobial Action and Proton Translocation Capability.
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- Angewandte Chemie International Edition, 2019, v. 58, n. 27, p. 9234, doi. 10.1002/anie.201901589
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- Article
Investigation of interaction between DCDC2 and KIAA0319 in a large German dyslexia sample.
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- Journal of Neural Transmission, 2008, v. 115, n. 11, p. 1587, doi. 10.1007/s00702-008-0124-6
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Analysis of Evolutionary Conservation, Expression Level, and Genetic Association at a Genome-wide Scale Reveals Heterogeneity Across Polygenic Phenotypes.
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- Molecular Biology & Evolution, 2024, v. 41, n. 7, p. 1, doi. 10.1093/molbev/msae115
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A note on Gollier's model for a collective pension scheme.
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- Journal of Pension Economics & Finance, 2021, v. 20, n. 2, p. 187, doi. 10.1017/S1474747220000013
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- Article
A genome screen for genes predisposingto bipolar affective disorder detects a new susceptibility locus on 8q.
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- Human Molecular Genetics, 2001, v. 10, n. 25, p. 2933, doi. 10.1093/hmg/10.25.2933
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- Article
Pathogen-specific innate immune response patterns are distinctly affected by genetic diversity.
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- Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-38994-5
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Identification of shared risk loci and pathways for bipolar disorder and schizophrenia.
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- PLoS ONE, 2017, v. 12, n. 2, p. 1, doi. 10.1371/journal.pone.0171595
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MicroRNA Expression Profiles in Superficial Esophageal Squamous Cell Carcinoma before Endoscopic Submucosal Dissection: A Pilot Study.
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- International Journal of Molecular Sciences, 2021, v. 22, n. 9, p. 4789, doi. 10.3390/ijms22094789
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Personality subtypes in adults with social anxiety disorder - novelty seeking makes the difference.
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- BMC Psychiatry, 2022, v. 22, n. 1, p. 1, doi. 10.1186/s12888-022-04484-z
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- Article
Murine genetic deficiency of neuronal nitric oxide synthase ( nNOS<sup>-/-</sup>) and interstitial cells of Cajal ( W/ W<sup>v</sup>): Implications for achalasia?
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- Journal of Gastroenterology & Hepatology, 2014, v. 29, n. 10, p. 1800, doi. 10.1111/jgh.12600
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Phenome-wide Mendelian randomisation analysis of 378,142 cases reveals risk factors for eight common cancers.
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- Nature Communications, 2024, v. 15, n. 1, p. 1, doi. 10.1038/s41467-024-46927-z
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- Article
LINEAR VERSUS NONLINEAR ALLOCATION RULES IN RISK SHARING UNDER FINANCIAL FAIRNESS.
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- Astin Bulletin, 2018, v. 48, n. 3, p. 995, doi. 10.1017/asb.2018.25
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The Aromatase Gene CYP19A1: Several Genetic and Functional Lines of Evidence Supporting a Role in Reading, Speech and Language.
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- Behavior Genetics, 2012, v. 42, n. 4, p. 509, doi. 10.1007/s10519-012-9532-3
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SNP Variations in the 7q33 Region Containing DGKI are Associated with Dyslexia in the Finnish and German Populations.
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- Behavior Genetics, 2011, v. 41, n. 1, p. 134, doi. 10.1007/s10519-010-9431-4
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Genome-wide transcriptome induced by Porphyromonas gingivalis LPS supports the notion of host-derived periodontal destruction and its association with systemic diseases.
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- Innate Immunity, 2016, v. 22, n. 1, p. 72, doi. 10.1177/1753425915616685
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